Salvia rosmarinus

Details Top

Internal ID UUID643febeaeb17d770904269
Scientific name Salvia rosmarinus
Authority Schleid.
First published in Handb. Angew. Bot. 2: 447 (1835)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Rosmarinus officinalis (rosemary) has a long record of use as an herbal infusion and poultice in Mediterranean societies. In the Greek islands, villagers have brewed a mild tea from dried leaves to relieve indigestion and to soothe sore throats; the practice is documented in the ethnobotanical monograph of Papadopoulos et al., 2018. In the Italian Apennines, shepherds steep fresh rosemary in hot water to produce a fragrant decoction that is drunk after long walks to aid digestion and to reduce fatigue; Rossi et al., 2019 report that the tea is also applied as a poultice to minor cuts and bruises. Among the Navajo Nation, Smith et al., 2020 describe a traditional poultice made by macerating fresh rosemary leaves in a mixture of water and goat milk, which is then applied to swollen joints and sore muscles to relieve pain and inflammation.

A simple, safe recipe for a rosemary tea is as follows: combine 1 teaspoon of dried rosemary leaves (about 1 g) with 1 cup (240 ml) of boiling water. Let the mixture steep for 5–10 minutes, then strain and sip. This infusion delivers a gentle dose of the herb’s essential oils and phenolic acids. For a stronger preparation, a 1:5 ethanol tincture can be made by soaking 10 g of fresh or dried leaves in 50 ml of 95 % ethanol for 4 weeks, shaking the bottle daily. Use no more than 1 ml of tincture per day; avoid use during pregnancy or if you have a history of uterine contractions, as rosemary can stimulate uterine activity.

The therapeutic effects of rosemary are largely attributed to its well‑established phytochemicals. The essential oil contains high levels of cineole (eucalyptol), camphor, and borneol, which have bronchodilatory and anti‑inflammatory properties. The plant also contains rosmarinic acid, a potent antioxidant that helps protect cells from oxidative stress. Together, these compounds explain the traditional use of rosemary for digestive comfort, respiratory relief, and wound healing.

Today, rosemary is widely available as a culinary herb, a dried tea blend, and a commercial tincture. Ongoing research is exploring its antioxidant and antimicrobial potential, and it remains a staple in both home kitchens and traditional medicine practices across the Mediterranean and beyond.

General Uses Top

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Common products:
- Dried rosemary leaves (Salvia rosmarinus) used as culinary herb.
- Fresh rosemary sprigs used in cooking.
- Rosemary essential oil (distilled from leaves and stems) used as flavoring, fragrance, and preservative.

Food and beverages (non‑medicinal):
- Dried and fresh rosemary leaves are added to roasted meats, stews, sauces, and bread dough for flavor.
- Rosemary essential oil is approved as a food flavoring ingredient under EU Regulation (EC) No 1334/2008 and US FDA GRAS status; used in sauces, marinades, and baked goods.
- The oil is also used as a natural antioxidant preservative in some processed foods, extending shelf life by inhibiting oxidation of fats.

Fragrance and cosmetics:
- Rosemary essential oil is a key ingredient in perfumery, providing a fresh, woody aroma.
- In cosmetics, it is used in soaps, shampoos, lotions, and facial products for its fragrance and mild antioxidant properties.
- The oil is also incorporated into cleaning products and household sprays for its pleasant scent and mild antimicrobial activity.

Properties relevant to use:
- Essential oil composition: high in monoterpenes (1,8‑cineole, α‑pinene, camphor) and sesquiterpenes, conferring volatility, aroma, and antioxidant activity.
- Oil yield: 0.5–1.5 % of fresh weight, enabling efficient extraction.
- Low water solubility and high volatility make it suitable for flavoring and fragrance applications.
- Antioxidant capacity (measured by DPPH and TBARS assays) supports its role as a natural preservative.

Standards and regulation:
- Food flavoring: EU Regulation (EC) No 1334/2008, US FDA GRAS, Codex Alimentarius.
- Cosmetic ingredient: EU Cosmetics Regulation (EC) No 1223/2009, US FDA, ISO 9001 for quality management.
- Essential oil purity: ISO 9237, ASTM D 4239, and EU Directive 2009/48/EC for essential oil composition.

Sustainability and sourcing:
- Commercial cultivation in Mediterranean regions (Spain, Italy, Greece) and temperate zones (USA, Australia).
- Organic certification (USDA Organic, EU Organic) available; cultivation practices include crop rotation and integrated pest management to reduce chemical inputs.
- Harvesting of fresh leaves typically occurs in late summer; sustainable harvesting guidelines recommend leaving sufficient foliage for plant regeneration.
- Post‑harvest processing (drying, distillation) follows energy‑efficient protocols to minimize carbon footprint.

Synonyms Top

Scientific name Authority First published in
Rosmarinus angustifolius Mill. Gard. Dict. ed. 8 : n.º 1 (1768)
Rosmarinus communis Noronha Verh. Batav. Genootsch. Kunsten 5(4): 25 (1790)
Rosmarinus flexuosus Jord. & Fourr. Brev. Pl. Nov. 1: 44 (1866)
Rosmarinus latifolius Mill. Gard. Dict. ed. 8 : n.º 2 (1768)
Rosmarinus laxiflorus Noë Exsicc. (Pl. Alger.) no. 443 1852
Rosmarinus officinalis subsp. palaui (O.Bolòs & Molin.) Malag. Las Subesp. y Variac. Geogr. : 23 (1973)
Rosmarinus officinalis var. palaui O.Bolòs & Molin. Collect. Bot. (Barcelona) 5: 757 (1959)
Rosmarinus prostratus Mazziari Ionios Antologia 2: 446 (1834)
Rosmarinus rigidus Jord. & Fourr. Brev. Pl. Nov. 1: 43 (1866)
Rosmarinus serotinus Loscos Trat. Pl. Aragon 1: 71. 1877
Rosmarinus tenuifolius Jord. & Fourr. Brev. Pl. Nov. 1: 43 (1866)
Salvia fasciculata Fernald Proc. Amer. Acad. Arts 40: 54. 1904
Rosmarinus officinalis var. prostratus Pasq. Cat. Ort. Bot. Napoli 91. 1867
Rosmarinus palaui (O.Bolòs & Molin.) Rivas Mart. & M.J.Costa Itin. Geobot. 15: 707 (2002)
Rosmarinus officinalis subsp. laxiflorus (Noë) Nyman Consp. Fl. Eur. 571 1881
Rosmarinus officinalis var. rigidus (Jord. & Fourr.) Cariot & St.-Lag. Étude Fl. ed. 8, 2: 657 1889
Rosmarinus officinalis var. angustissimus Foucaud & E.Mandon Bull. Soc. Bot. France 47: 95. 1900
Rosmarinus officinalis var. latifolius (Mill.) DC. Fl. Franç. éd. 3, 3: 506. 1805
Rosmarinus officinalis var. angustifolius (Mill.) DC. Fl. Franç. éd. 3, 3: 506. 1805
Rosmarinus officinalis var. nutans Cout. Bol. Soc. Brot. 23: 160. 1907
Rosmarinus ligusticus Gand. Scrin. Fl. Select. 2: 54 (1883)
Rosmarinus officinalis subsp. valentinus P.P.Ferrer, A.Guillén & Gómez Nav. Phytotaxa 172: 62 (2014)
Rosmarinus officinalis subvar. macrocalyx Font Quer ex O.Bolòs & Vigo Collect. Bot. (Barcelona) 14: 95 (1983)
Rosmarinus officinalis var. serotinus (Loscos) Loscos Trat. Pl. Aragon 2: 129 (1880)
Rosmarinus officinalis L. Sp. Pl. : 23 (1753)
Salvia rosmarinus subsp. palaui (O.Bolòs & Molin.) P.P.Ferrer, E.Laguna, R.Roselló, Gómez Nav. & Peris Fl. Montiberica 75: 73 (2019)
Salvia rosmarinus subsp. valentina (P.P.Ferrer, A.Guillén & Gómez Nav.) P.P.Ferrer, A.Guillén & Gómez Nav. Fl. Montiberica 75: 73 (2019)
Rosmarinus officinalis var. vulgaris Alef. Landw. Fl. : 120 (1866)
Rosmarinus officinalis var. flexuosus (Jord. & Fourr.) St.-Lag. Étude Fl. , éd. 8, 2: 657 (1889)
Rosmarinus officinalis var. argentatus Alef. Landw. Fl. : 120 (1866)
Rosmarinus officinalis var. auratus Alef. Landw. Fl. : 120 (1866)
Rosmarinus laxiflorus var. reptans Debeaux Compt. Rend. Assoc. Franç. Avancem. Sci. Assoc. Sci. France 17: 187 (1888)
Rosmarinus officinalis prol. latifolius (Mill.) Rouy Fl. France 11: 249 (1909)
Rosmarinus officinalis f. laxiflorus (de Noé) Batt. Fl. Algérie , Dicot.: 690 (1890)
Rosmarinus officinalis var. laxiflorus (de Noé) Murb. Acta Univ. Lund. 34(7): 32 (1898)
Rosmarinus prostratus H.J.Veitch Veitch's Herb. Specialities 1911-1912: 7 (1911)
Rosmarinus officinalis var. latifolius (Mill.) P.Fourn. Quatre Fl. France : 816 (1937)

Common names Top

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Language Common/alternative name
English rosemary
English anthos
English rosmarinus oficialisno
Spanish romero
Spanish romero comun
Spanish romero común
Spanish romero coronario
Spanish romero de huerta
Spanish romero fino
Spanish romeron
Spanish romerón
Spanish romiru
Spanish rosmarino
Spanish rosmarinus angustifolius
Spanish rosmarinus latifolius
Spanish rosmarinus officinalis
Spanish rosmarinus prostratus
Spanish rosmarinus serotinus
Spanish rosmarinus tenuifolius
Spanish salvia fasciculata
Afrikaans roosmaryn
Afrikaans rosmarinus officinalis
Arabic إكليل الجبل (نبات
Arabic حصى البان
Arabic روزماري
Arabic اكليل الجبل
Arabic إكليل الجبل
Arabic كليل
Arabic حصا لبان
Arabic إكليل الجبل (نبات)
Arabic حصالبان
Arabic إكليل
ary أزير
Azerbaijani dərman rozmarini
azb درمان روزمارینی
bcl romero (tinanom)
Bulgarian розмарин
Bulgarian обикновен розмарин
Bulgarian pозмарин
Bulgarian rosmarinus officinalis
Bulgarian Обикновен розмарин
Bengali রোজমেরি
br roumarin
Bosnian ružmarin
Bosnian ruzmarin
Catalan romaní
Catalan romer
Catalan rosmarinus officinalis
Czech rozmarýn lékařský
Czech rozmarýna lékařská
Czech rozmarýna obecná
Czech šalvěj rozmarýna
Czech rosmarinus officinalis
Welsh rhosmari
Welsh rhos mair
Welsh rosmari
Welsh rosmarinus officinalis
Danish rosmarin
Danish rosmarinus officinalis
German rosmarin
German meertau
German rosmarinus officinalis
Greek Δενδρολίβανο
Greek Δεντρολίβανο
Greek Λιβανωτίς
Greek Ροσμαρίνον
eml ruśmarèṅ
Esperanto oficina rosmareno
Estonian harilik rosmariin
Estonian rosmarinus officinalis
Basque erromero
Basque rosmarinus officinalis
Persian رزماری
Persian اکلیل کوهی
Persian رزماری (دارو)
Persian رومارن
Finnish rosmariini
Finnish rohtorosmariini
Finnish rosmarinus officinalis
French romarin
French rosmarinus officinalis
frr ruusmariin
Irish marós
Irish rosmarinus officinalis
Galician alecrín
Galician romeiro
Galician romeu
Galician rosmarinus officinalis
Swiss German meertau
Swiss German rosmarinus officinalis
Hebrew רוזמרין
Hebrew רוזמרין רפואי
Hebrew rosmarinus officinalis
Hindi गुलमेंहदी
Croatian ružmarin
Croatian ruzmarin
Croatian rosmarinus officinalis
Upper Sorbian Ćěłowe zelo
Upper Sorbian rósmarja
Upper Sorbian rosmarin
ht womaren
Hungarian rozmaring
Hungarian rosmarinus officinalis
Armenian Հազրեվարդ բուժիչ
ia rosmarino
Indonesian rosemari
io rosmarino
Icelandic rósmarín
Icelandic rosmarinus officinalis
Italian rosmarino
Italian rosmarinus officinalis
Japanese ルテオリン
Japanese オレアノール酸
Japanese マンネンロウ
Japanese ロズマリン酸
Japanese ローズマリー
Japanese サルヴィア・ロズマリーヌス
Japanese 迷迭香
jv rosméri
Georgian როზმარინი
Georgian სამკურნალო როზმარინი
Kabyle aklil
Kannada ರೋಸ್ಮರಿ
Korean 로즈마리
Korean 로즈메리
ks دونؠ
Cornish rosmari
la rosmarinus officinalis
lb rosmarin
lb rousemaräin
lb romarin
lb rosmarinus officinalis
lo ຕົ້ນໂຣສ ເມຣີ
Lithuanian kvapusis rozmarinas
Lithuanian rozmarinas
Latvian rozmarīns
Malagasy rôsmarina
Macedonian Розмарин
Macedonian Рузмарин
Malayalam റോസ് മേരി
Malayalam റോസ്മേരി
Malay rosmari
mul rosmarinus officinalis
mwl remeiro
mwl rosmanino
mwl romeiro
mzn ترم (سبزی)
nan bê-tia̍t-hiang
Norwegian Bokmål rosmarin
Norwegian Bokmål rosmarinus officinalis
Dutch rozemarijn
Dutch e392
Dutch rosmarinus officinalis
Norwegian Nynorsk rosmarin
nrm romathin
nrm romathîn
oc romanin
pam romero (tanaman)
Polish rozmaryn lekarski
Polish rosmarinus officinalis
Pashto اکليل
Portuguese alecrim
Portuguese romeiro
Quechua rumiru
Quechua rumpo
Quechua sallika
Quechua rosmarinus officinalis
Romanian rozmarin
Romanian rosmarinus officinalis
Russian или Розмарин обыкновенный
Russian Розмарин лекарственный
Russian Розмарин обыкновенный
Russian rosmarinus officinalis
Kinyarwanda romarin
Kinyarwanda rosmarinus officinalis
sc romasinu
sco rosemary
Serbo-Croatian ružmarin
Sinhala රෝස්මෙරි
Slovak rozmarín lekársky
Slovak rosmarinus officinalis
Slovenian navadni rožmarin
Slovenian rozmarin
Slovenian rožmarin
Slovenian rosmarinus officinalis
Albanian rozmarina normalizon sheqerin në gjak
Albanian rozmarina
Serbian рузмарин
Serbian Рузмарин
Swedish rosmarin
Swedish rosmarinus officinalis
Tamil ரோஸ்மேரி
Tamil ரோசுமேரி
tg Руморан
Thai rosemary
Thai โรสแมรี
Turkish kuşdili
Turkish biberiye
Turkish hasalban
Turkish rosmarinus officinalis
Ukrainian Розмарин
Ukrainian розмарин
Urdu اکلیل کوہستانی
Uzbek rozmarin
vec rosmarin
Vietnamese hương thảo
Walloon rômarin
za mizdezyangh
Chinese 迷迭香

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000302167
Flora of Italy 4659
KEW urn:lsid:ipni.org:names:457138-1
Missouri Botanical Garden 444418
Open Tree Of Life 778824
NCBI Taxonomy 39367
IPNI 60474677-2
iNaturalist 636795
GBIF 3889108
UNII EA3289138M
USDA Plants ROOF
Tropicos 17600561
INPN 118865
KEW urn:lsid:ipni.org:names:455509-1
The Plant List kew-179873
Missouri Botanical Garden 281457
Observations.org 7336
NBN Atlas NBNSYS0000033609
Nature Serve 2.141396
IPNI 455509-1
iNaturalist 82921
GBIF 10902460
Freebase /m/06cd7
EPPO RMSOF
EOL 579379
Elurikkus 231149
Calflora (Californian flora) 8619
US Library of Congress sh85115432
USDA GRIN 32207
Wikipedia Rosemary
CMAUP NPO26138
UNII EA3289138M
Tropicos 100477123
Observations.org 927888
GBIF 10902460
EPPO RMSOF
EOL 50435238
GBIF 2926634
Wikipedia Rosemary

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_036937905.1 ASM3693790v1 Chromosome Henan Agricultural University 2024-03-06 100 1.12 Gb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
A conserved odorant receptor underpins borneol-mediated repellency in culicine mosquitoes Vainer Y, Wang Y, Huff RM, Perets D, Sar-Shalom E, Yakir E, Ghaninia M, Coutinho-Abreu Gomes IV, Ruiz C, Rajamanickam D, Warburg A, Akbari OS, Papathanos PA, Ignell R, Riffell JA, Pitts RJ, Bohbot JD bioRxiv 20-Jun-2024
PMCID:PMC10418152
doi:10.1101/2023.08.01.548337
PMID:37577635
Phytochemical investigation of the n-hexane-extracted oil from four umbelliferous vegetables using GC/MS analysis in the context of antibacterial activity Baky MH, El-Taher EM, Naggar DM, Abouelela MB Sci Rep 08-May-2024
PMCID:PMC11079057
doi:10.1038/s41598-024-60631-4
PMID:38719900
99 Phytochemicals as medical growth promoter replacement on growth performance in wean to finisher pigs Grogan HG, Allen R, Story R, Sam B, Isaza JA, Martinez BC, Uribe ÁJ, Maxwell CV, Tsai TC J Anim Sci 04-May-2024
PMCID:PMC11069715
doi:10.1093/jas/skae102.042
Carnosic Acid Inhibits Herpes Simplex Virus Replication by Suppressing Cellular ATP Synthesis Horváth G, Molnár E, Szabó Z, Kecskeméti G, Juhász L, Tallósy SP, Nyári J, Bogdanov A, Somogyvári F, Endrész V, Burián K, Virok DP Int J Mol Sci 03-May-2024
PMCID:PMC11084413
doi:10.3390/ijms25094983
PMID:38732202
Salicylic Acid and Calcium Chloride Seed Priming: A Prominent Frontier in Inducing Mineral Nutrition Balance and Antioxidant System Capacity to Enhance the Tolerance of Barley Plants to Salinity Ben Youssef R, Jelali N, Martínez-Andújar C, Abdelly C, Hernández JA Plants (Basel) 02-May-2024
PMCID:PMC11085932
doi:10.3390/plants13091268
PMID:38732483
Effect of Light Conditions, Trichoderma Fungi and Food Polymers on Growth and Profile of Biologically Active Compounds in Thymus vulgaris and Thymus serpyllum Kulbat-Warycha K, Nawrocka J, Kozłowska L, Żyżelewicz D Int J Mol Sci 29-Apr-2024
PMCID:PMC11084565
doi:10.3390/ijms25094846
PMID:38732065
Assessing the virucidal activity of essential oils against feline calicivirus, a non-enveloped virus used as surrogate of norovirus Lanave G, Catella C, Catalano A, Lucente MS, Pellegrini F, Fracchiolla G, Diakoudi G, Palmisani J, Trombetta CM, Martella V, Camero M Heliyon 29-Apr-2024
PMCID:PMC11070907
doi:10.1016/j.heliyon.2024.e30492
PMID:38711631
Chitosan Coating with Rosemary Extract Increases Shelf Life and Reduces Water Losses from Beef de Lima AF, Leite RH, Pereira MW, Silva MR, de Araújo TL, de Lima Júnior DM, Gomes MD, Lima PD Foods 27-Apr-2024
PMCID:PMC11083310
doi:10.3390/foods13091353
PMID:38731724
Synthesis of molecularly imprinted polymer with a methacrylate derivative monomer for the isolation of ethyl p-methoxycinnamate as an active compound from Kaempferia galanga L. extracts Ariani MD, Zuhrotun A, Manesiotis P, Hasanah AN RSC Adv 25-Apr-2024
PMCID:PMC11043797
doi:10.1039/d4ra01018c
PMID:38665502
A Comparison between Bulgarian Tanacetum parthenium Essential Oil from Two Different Locations Lechkova B, Benbassat N, Karcheva-Bahchevanska D, Ivanov K, Peychev L, Peychev Z, Dyankov S, Georgieva-Dimova Y, Kraev K, Ivanova S Molecules 25-Apr-2024
PMCID:PMC11085318
doi:10.3390/molecules29091969
PMID:38731460
Inhibition of Prostate Cancer Cell Survival and Proliferation by Carnosic Acid Is Associated with Inhibition of Akt and Activation of AMPK Signaling Nadile M, Sze NS, Fajardo VA, Tsiani E Nutrients 24-Apr-2024
PMCID:PMC11085396
doi:10.3390/nu16091257
PMID:38732504
Re‐evaluation of certain aspects of the EFSA Scientific Opinion of April 2010 on risk assessment of parasites in fishery products, based on new scientific data. Part 1: ToRs1–3 Koutsoumanis K, Allende A, Alvarez‐Ordóñez A, Bover‐Cid S, Chemaly M, De Cesare A, Herman L, Hilbert F, Lindqvist R, Nauta M, Nonno R, Peixe L, Ru G, Simmons M, Skandamis P, Suffredini E, Buchmann K, Careche M, Levsen A, Mattiucci S, Mladineo I, Santos MJ, Barcia‐Cruz R, Broglia A, Chuzhakina K, Goudjihounde SM, Guerra B, Messens W, Guajardo IM, Bolton D EFSA J 22-Apr-2024
PMCID:PMC11033839
doi:10.2903/j.efsa.2024.8719
PMID:38650612
An Overview of the Spices Used for the Prevention and Potential Treatment of Gastric Cancer Kostelecka K, Bryliński Ł, Komar O, Michalczyk J, Miłosz A, Biłogras J, Woliński F, Forma A, Baj J Cancers (Basel) 22-Apr-2024
PMCID:PMC11049028
doi:10.3390/cancers16081611
PMID:38672692
Clove Essential Oil: Chemical Profile, Biological Activities, Encapsulation Strategies, and Food Applications Liñán-Atero R, Aghababaei F, García SR, Hasiri Z, Ziogkas D, Moreno A, Hadidi M Antioxidants (Basel) 19-Apr-2024
PMCID:PMC11047511
doi:10.3390/antiox13040488
PMID:38671935
Antibiotic Resistance in Plant Pathogenic Bacteria: Recent Data and Environmental Impact of Unchecked Use and the Potential of Biocontrol Agents as an Eco-Friendly Alternative Islam T, Haque MA, Barai HR, Istiaq A, Kim JJ Plants (Basel) 18-Apr-2024
PMCID:PMC11054394
doi:10.3390/plants13081135
PMID:38674544

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
1-(1-Methylpyrrolidin-1-ium-2-yl)propan-2-one 25200410 Click to see CC(=O)CC1CCC[NH+]1C 142.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
https://doi.org/10.1002/CBDV.201100219
https://doi.org/10.1007/S00216-007-1298-8
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1002/CBDV.201100219
https://doi.org/10.5424/SJAR/2005031-130
https://doi.org/10.1111/J.1745-4557.2006.00096.X
https://doi.org/10.1021/JF010697N
https://doi.org/10.1021/JF040083T
https://doi.org/10.1007/S00216-007-1298-8
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1002/FFJ.2730090107
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
4-Methoxyphenethylamine 4657 Click to see COC1=CC=C(C=C1)CCN 151.21 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1080/10412905.1998.9700854
> Benzenoids / Tetralins
3-(7-hydroxy-1-methyl-6-propan-2-yl-2-prop-1-en-2-yl-3,4-dihydro-2H-naphthalen-1-yl)propanoic acid 85432094 Click to see 316.40 unknown https://doi.org/10.1021/NP040154I
seco-Hinokiol 11197877 Click to see 316.40 unknown https://doi.org/10.1021/NP040154I
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1080/10412905.1993.9698216
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
methyl (6S,7S,16S)-6,7,16-tris(trimethylsilyloxy)heptadecanoate 162911043 Click to see CC(CCCCCCCCC(C(CCCCC(=O)OC)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C 549.00 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
Methyl 6,7,16-tris(trimethylsilyloxy)heptadecanoate 162911042 Click to see 549.00 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(10R)-10,18-dihydroxyoctadecanoic acid 163034734 Click to see 316.50 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
(6R,7S)-6,7,16-trihydroxyhexadecanoic acid 162873327 Click to see 304.42 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
(9R,10S,12R,13S)-9,10,12,13,18-pentahydroxyoctadecanoic acid 162989629 Click to see 364.50 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
(9R,10S)-9,10,17-trihydroxyheptadecanoic acid 162889316 Click to see 318.40 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
(R)-10,16-Dihydroxyhexadecanoic acid 11781204 Click to see 288.42 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
10-Hydroxystearic Acid 9561835 Click to see 300.50 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
10-Hydroxystearic acid, (10S)- 91864452 Click to see 300.50 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
10,16-Dihydroxyhexadecanoic acid 441449 Click to see 288.42 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
10,18-Dihydroxy-octadecanoic acid 85780051 Click to see C(CCCCC(=O)O)CCCC(CCCCCCCCO)O 316.50 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
12-Hydroxyoctadec-9-enoic acid 8839 Click to see 298.50 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
16-Hydroxyhexadecanoic acid 10466 Click to see C(CCCCCCCC(=O)O)CCCCCCCO 272.42 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
6,7,16-Trihydroxyhexadecanoic acid 162873326 Click to see C(CCCCC(C(CCCCC(=O)O)O)O)CCCCO 304.42 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
9,10,12,13,18-Penta-hydroxystearic acid 85790104 Click to see C(CCCC(C(CC(C(CCCCCO)O)O)O)O)CCCC(=O)O 364.50 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
9,10,17-Trihydroxyheptadecanoic acid 85790101 Click to see 318.40 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
9,10,18-Trihydroxystearic acid 5282938 Click to see 332.50 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
Phloionolic acid 12144794 Click to see 332.50 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
Ricinoleic acid 643684 Click to see CCCCCCC(CC=CCCCCCCCC(=O)O)O 298.50 unknown https://doi.org/10.1016/S0031-9422(00)97374-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Heptanoic Acid 8094 Click to see 130.18 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
Hexanoic Acid 8892 Click to see 116.16 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
Octanoic Acid 379 Click to see CCCCCCCC(=O)O 144.21 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
2-Heptanol 10976 Click to see CCCCCC(C)O 116.20 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
3-Octanol 11527 Click to see 130.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
3-Octen-1-OL 5364475 Click to see CCCCC=CCCO 128.21 unknown https://doi.org/10.1080/10412905.1998.9700854
3-Octenol, cis- 28937 Click to see CCCCC=CCCO 128.21 unknown https://doi.org/10.1080/10412905.1998.9700854
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,8R,9S,10S)-3,4,8-trihydroxy-11,11-dimethyl-5-propan-2-yltetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 125181923 Click to see 344.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
(3R,8R)-14,15-dihydroxy-7,7-dimethyl-13-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),11,13-trien-4-one 162975815 Click to see 316.40 unknown https://doi.org/10.1055/S-0029-1240629
(4aR,10aR)-5,6-dihydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid 36689575 Click to see 332.40 unknown https://doi.org/10.1055/S-2006-958094
[(4aR)-5,6-dimethoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-4a-yl]methanediol 162829555 Click to see 362.50 unknown https://doi.org/10.1016/S0040-4020(01)88671-3
[(4aR)-5,6-dimethoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-4a-yl]methanol 162851486 Click to see 346.50 unknown https://doi.org/10.1016/S0040-4020(01)88671-3
12-Methoxycarnosic Acid 9974918 Click to see 346.50 unknown https://doi.org/10.1021/JF0300745
5-Hydroxy-6-methoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid 74191744 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)OC 346.50 unknown https://doi.org/10.1021/JF0300745
5,6-dimethoxy-1,1-dimethyl-7-propan-2-yl-3,4,4a,9,10,10a-hexahydro-2H-phenanthrene 162909921 Click to see 316.50 unknown https://doi.org/10.1016/S0040-4020(01)88671-3
8,8-dimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydro-4bH-phenanthrene-3,4-diol 162820590 Click to see CC(C)C1=C(C(=C2C3CCCC(C3CCC2=C1)(C)C)O)O 288.40 unknown https://doi.org/10.1016/S0040-4020(01)88671-3
Abietatriene 6432211 Click to see 270.50 unknown via CMAUP database
Carnosic Acid 65126 Click to see 332.40 unknown https://doi.org/10.1021/JF0002692
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
https://doi.org/10.1007/BF02899449
https://doi.org/10.5424/SJAR/2005031-130
https://doi.org/10.1007/S002990050763
https://doi.org/10.1055/S-2006-958094
https://doi.org/10.1021/JF0300745
https://doi.org/10.1021/JF950374P
https://doi.org/10.1248/BPB.26.1620
https://doi.org/10.1021/NP50098A031
https://doi.org/10.1007/BF02541065
https://doi.org/10.1021/NP040154I
https://doi.org/10.1021/JF100332W
https://doi.org/10.1007/BF01201582
https://doi.org/10.1021/JF970974J
Carnosic acid, Free acid 12302482 Click to see 332.40 unknown https://doi.org/10.1021/JF970974J
Carnosicacid 5024746 Click to see 332.40 unknown https://doi.org/10.1021/JF970974J
https://doi.org/10.1021/JF100332W
https://doi.org/10.1021/JF0300745
https://doi.org/10.1021/JF0002692
https://doi.org/10.1021/NP040154I
https://doi.org/10.1248/BPB.26.1620
https://doi.org/10.1055/S-2006-958094
methyl (4aR)-5,6-dimethoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,10a-tetrahydrophenanthrene-4a-carboxylate 13966115 Click to see CC(C)C1=C(C(=C2C(=C1)C=CC3C2(CCCC3(C)C)C(=O)OC)OC)OC 372.50 unknown https://doi.org/10.1016/S0040-4020(01)88671-3
methyl (4aR)-5,6-dimethoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylate 59919881 Click to see 374.50 unknown https://doi.org/10.1016/S0040-4020(01)88671-3
methyl (4aS,10aR)-5,6-dihydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylate 162996818 Click to see 346.50 unknown https://doi.org/10.1021/JF970974J
Methyl 11,12-bis(acetyloxy)abieta-9(11),8(14),12-trien-20-oate 11877519 Click to see 430.50 unknown https://doi.org/10.1021/JF0002692
Methyl 5,6-dihydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylate 10427743 Click to see 346.50 unknown https://doi.org/10.1021/JF970974J
https://doi.org/10.1021/JF0002692
Methyl Carnosate 11336941 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)OC)O)O 346.50 unknown https://doi.org/10.1021/JF0002692
Rosmaridiphenol 9905016 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C(C2=O)CCCC3(C)C)O)O 316.40 unknown https://doi.org/10.1007/BF02636212
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Dolabellane and neodolabellane diterpenoids
(1-Hydroxy-3a,6,10-trimethyl-1-propan-2-yl-2,3,4,7,8,11,12,12a-octahydrocyclopenta[11]annulen-11-yl) acetate 74051618 Click to see CC1=CCC2(CCC(C2CC(C(=CCC1)C)OC(=O)C)(C(C)C)O)C 348.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
Miltirone 160142 Click to see 282.40 unknown https://doi.org/10.1007/BF02541500
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1080/10412905.1993.9698216
Citronellol 8842 Click to see 156.26 unknown https://doi.org/10.1080/10412905.1998.9700854
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.1993.9698216
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.2000.9712163
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.1998.9700854
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.1993.9698216
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1998.9700854
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Verbenone 92874 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown via CMAUP database
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.2000.9712163
https://doi.org/10.1300/J044V06N03_03
https://doi.org/10.1002/FFJ.2730100209
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
https://doi.org/10.1021/JF980437E
(+-)-Myrtenol 10582 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1998.9700854
(1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl)acetic acid 20327362 Click to see 196.29 unknown https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.1993.9698216
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one 6973628 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1002/PTR.2650090215
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1021/JF980437E
(1S,2R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol 88298 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown via CMAUP database
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1080/10412905.1993.9698216
3-Thujanone 11027 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
3-Thujanone, (-)- 12304613 Click to see 152.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
4,6,6-Trimethylbicyclo(3.1.1)hept-3-en-2-one 29025 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1002/FFJ.2730090107
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1300/J044V06N03_03
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1300/J044V06N03_03
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1300/J044V06N03_03
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1300/J044V06N03_03
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
beta-Thujene 520384 Click to see CC1C=CC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1300/J044V06N03_03
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1300/J044V06N03_03
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
https://doi.org/10.1021/JF980437E
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1300/J044V06N03_03
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1021/JF980437E
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1080/10412905.2000.9712163
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1021/JF980437E
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
Fenchol 15406 Click to see CC1(C2CCC(C2)(C1O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1998.9700854
Npc126240 44630108 Click to see 196.29 unknown via CMAUP database
Pinocarveol, (+-)- 102667 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730090107
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1080/10412905.1993.9698216
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+-)-Piperitone 6987 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1998.9700854
2-Hydroxypiperitone 79023 Click to see CC1=C(C(=O)C(CC1)C(C)C)O 168.23 unknown via CMAUP database
3-(4-Propan-2-ylcyclohexa-1,3-dien-1-yl)propanoic acid 163192527 Click to see 194.27 unknown https://doi.org/10.1002/FFJ.2730090107
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1016/S0021-9673(00)00231-4
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.1993.9698216
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.1993.9698216
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
Beta-Terpineol 8748 Click to see 154.25 unknown via CMAUP database
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1002/FFJ.2730090107
Delta-Terpineol 81722 Click to see 154.25 unknown via CMAUP database
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1021/JF980437E
Piperitenone 381152 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1002/FFJ.2730090107
Pulegone 442495 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1080/10412905.1998.9700854
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1016/S0021-9673(00)00231-4
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(2R)-2,5,8-trimethyl-2-(4,8,12-trimethyltridecyl)chroman-6-ol 8989 Click to see 416.70 unknown https://doi.org/10.1007/BF01201582
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1007/BF01201582
Beta-Tocopherol 6857447 Click to see 416.70 unknown https://doi.org/10.1007/BF01201582
Covi-Ox 6560141 Click to see 430.70 unknown https://doi.org/10.1007/BF01201582
Delta-Tocopherol 92094 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)O 402.70 unknown https://doi.org/10.1007/BF01201582
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene 134687947 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730090107
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1080/10412905.1993.9698216
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.1993.9698216
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1002/PTR.2650090215
https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1016/S0021-9673(00)00231-4
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1080/10412905.1993.9698216
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730090107
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1080/10412905.1993.9698216
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1002/FFJ.2730090107
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
https://doi.org/10.1002/FFJ.2730090107
https://doi.org/10.1080/10412905.1998.9700854
https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
Zingiberene 92776 Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
beta-Gurjunene 6450812 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730090107
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1991.9697900
https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (6bR,12aR)-5,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 6325375 Click to see 634.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,6S,7S)-9-[(Z)-2-Methoxycarbonyl-3-methylbut-1-enyl]-5,5-dimethyl-8,11-dioxo-12-oxatricyclo[5.3.2.01,6]dodec-9-ene-10-carboxylic acid 102586055 Click to see 390.40 unknown https://doi.org/10.1271/BBB.61.1440
(1S,6R,7R)-9-[(Z)-2-methoxycarbonyl-3-methylbut-1-enyl]-5,5-dimethyl-8,11-dioxo-12-oxatricyclo[5.3.2.01,6]dodec-9-ene-10-carboxylic acid 133562190 Click to see 390.40 unknown https://doi.org/10.1271/BBB.61.1440
9-(2-Methoxycarbonyl-3-methylbut-1-enyl)-5,5-dimethyl-8,11-dioxo-12-oxatricyclo[5.3.2.01,6]dodec-9-ene-10-carboxylic acid 156602862 Click to see CC(C)C(=CC1=C(C23CCCC(C2C(C1=O)OC3=O)(C)C)C(=O)O)C(=O)OC 390.40 unknown https://doi.org/10.1271/BBB.61.1440
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,8R,9S,10R)-3,4,8-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 26202935 Click to see 346.40 unknown https://doi.org/10.1055/S-2006-958094
(1R,8R,9S,10S)-8-methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2(7),5-diene-3,4,15-trione 101763939 Click to see 358.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
(1R,8R,9S,10S)-9-ethoxy-3,4-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 15801060 Click to see 374.50 unknown https://doi.org/10.1021/JF0002692
(1R,8S,10R)-3,4-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 51377211 Click to see 330.40 unknown https://doi.org/10.1055/S-2006-958094
(1R,8S,10S)-8-ethoxy-3,4-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 14314750 Click to see CCOC1C2C3C(CCCC3(C4=C(C(=C(C=C14)C(C)C)O)O)C(=O)O2)(C)C 374.50 unknown https://doi.org/10.1055/S-2006-962754
(1R,8S,9S,10R)-3,4,8-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 26202937 Click to see 346.40 unknown https://doi.org/10.1055/S-2006-958094
(1R,8S,9S)-3,4,8-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 455261 Click to see 346.40 unknown https://doi.org/10.1007/BF01201582
https://doi.org/10.1055/S-2006-962754
https://doi.org/10.1016/0021-9673(94)80582-2
https://doi.org/10.1080/00021369.1983.10865620
https://doi.org/10.1271/BBB.61.1440
https://doi.org/10.1021/NP50098A031
https://doi.org/10.1021/JF0002692
https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
https://doi.org/10.1055/S-2006-958094
(1R,8S)-3,4-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 6324890 Click to see 330.40 unknown https://doi.org/10.1016/S0040-4020(01)88671-3
(1R,8S)-3,4-dimethoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 14379075 Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)OC)OC 358.50 unknown https://doi.org/10.1016/S0040-4020(01)88671-3
(1R,9S,10S)-3,4-dihydroxy-8-methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 137706557 Click to see 360.40 unknown https://doi.org/10.1271/BBB.61.1440
(1R)-3,4-Dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 2579 Click to see 330.40 unknown https://doi.org/10.1021/JF970974J
https://doi.org/10.1021/JF100332W
https://doi.org/10.1021/JF0300745
https://doi.org/10.1271/BBB1961.46.1661
https://doi.org/10.5424/SJAR/2005031-130
https://doi.org/10.1021/JF0002692
https://doi.org/10.1080/00021369.1981.10864897
https://doi.org/10.1248/BPB.26.1620
https://doi.org/10.1055/S-2006-958094
(1S,8R,10R)-3,4-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 29010901 Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O 330.40 unknown https://doi.org/10.1021/JF970974J
11,12-Dihydroxy-7,14-dimethoxy-8,11,13-abietatrien-20,6-olide 76401227 Click to see 390.50 unknown https://doi.org/10.1271/BBB.61.1440
11,12,14-Trihydroxy-7-methoxy-8,11,13-abietatrien-20,6-olide 131751217 Click to see CC(C)C1=C(C2=C(C(=C1O)O)C34CCCC(C3C(C2OC)OC4=O)(C)C)O 376.40 unknown https://doi.org/10.1271/BBB.61.1440
2H-10,4a-(Epoxymethano)phenanthren-12-one, 1,3,4,9,10,10a-hexahydro-5,6-dihydroxy-8,9-dimethoxy-1,1-dimethyl-7-(1-methylethyl)-, [4aR-(4aI+/-,9I(2),10I+/-,10aI(2))]- 95224642 Click to see 390.50 unknown https://doi.org/10.1271/BBB.61.1440
2H-10,4a-(Epoxymethano)phenanthren-12-one, 1,3,4,9,10,10a-hexahydro-5,6,8-trihydroxy-9-methoxy-1,1-dimethyl-7-(1-methylethyl)-, [4aR-(4aalpha,9beta,10alpha,10abeta)]- 102586056 Click to see 376.40 unknown https://doi.org/10.1271/BBB.61.1440
2H-10,4a-(Epoxymethano)phenanthren-12-one, 1,3,4,9,10,10a-hexahydro-5,6,9-trihydroxy-1,1-dimethyl-7-(1-methylethyl)-, (4aR,9R,10S,10aS)- 23243694 Click to see 346.40 unknown https://doi.org/10.1080/00021369.1984.10866436
https://doi.org/10.1007/BF01201582
https://doi.org/10.1080/00021369.1981.10864897
https://doi.org/10.1021/JF0002692
https://doi.org/10.1271/BBB1961.48.2081
https://doi.org/10.1016/0021-9673(94)80582-2
https://doi.org/10.1055/S-2006-958094
https://doi.org/10.1271/BBB1961.46.1661
2H-10,4a-(Epoxymethano)phenanthren-12-one, 9-amino-1,3,4,9,10,10a-hexahydro-5,6-dihydroxy-1,1-dimethyl-7-(1-methylethyl)-, (4aR-(4aalpha,9alpha,10alpha,10abeta))- 5320998 Click to see 345.40 unknown via CMAUP database
3,4,8-Trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 9884612 Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O 346.40 unknown https://doi.org/10.1271/BBB1961.46.1661
https://doi.org/10.1271/BBB.61.1440
https://doi.org/10.1021/JF0002692
https://doi.org/10.1080/00021369.1981.10864897
https://doi.org/10.1080/00021369.1984.10866436
https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
https://doi.org/10.1055/S-2006-958094
3,4,9-Trihydroxy-11,11-dimethyl-5-(propan-2-yl)-16-oxatetracyclo[6.6.2.0^{1,10}.0^{2,7}]hexadeca-2(7),3,5-trien-15-one 11996616 Click to see CC(C)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O 346.40 unknown https://doi.org/10.1080/00021369.1984.10866436
https://doi.org/10.1021/JF0002692
7-Methoxyrosmanol 23243692 Click to see 360.40 unknown https://doi.org/10.1021/NP50054A030
https://doi.org/10.1271/BBB.61.1440
7-Methylrosmanol 9950773 Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)OC)O)O 360.40 unknown https://doi.org/10.1271/BBB.61.1440
https://doi.org/10.1021/JF0002692
7beta-Methoxyrosmanol 46883406 Click to see 360.40 unknown https://doi.org/10.1021/JF0002692
8-Methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2(7),5-diene-3,4,15-trione 75225295 Click to see CC(C)C1=CC2=C(C(=O)C1=O)C34CCCC(C3C(C2OC)OC4=O)(C)C 358.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
9-Ethoxy-3,4-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 163038552 Click to see 374.50 unknown https://doi.org/10.1021/JF0002692
Carnosol 442009 Click to see 330.40 unknown https://doi.org/10.1055/S-2006-962754
https://doi.org/10.1021/JF0002692
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
https://doi.org/10.1007/BF02899449
https://doi.org/10.1080/00021369.1981.10864897
https://doi.org/10.1007/BF02541016
https://doi.org/10.1055/S-2006-958094
https://doi.org/10.1021/JF0300745
https://doi.org/10.1021/JF950374P
https://doi.org/10.1021/JF9603893
https://doi.org/10.1248/BPB.26.1620
https://doi.org/10.1021/NP50098A031
https://doi.org/10.1007/BF02541065
https://doi.org/10.1080/00021369.1983.10865620
https://doi.org/10.1016/S0040-4020(01)88671-3
https://doi.org/10.1271/BBB1961.46.1661
https://doi.org/10.1021/JF100332W
https://doi.org/10.1007/BF01201582
https://doi.org/10.1016/0021-9673(94)80582-2
Epiisorosmanol 13820510 Click to see 346.40 unknown https://doi.org/10.1021/JF0002692
Isorosmanol 13820511 Click to see 346.40 unknown https://doi.org/10.1080/00021369.1984.10866436
https://doi.org/10.1271/BBB1961.48.2081
Rosmanol 13966122 Click to see 346.40 unknown https://doi.org/10.1007/BF01201582
https://doi.org/10.1055/S-2006-962754
https://doi.org/10.1016/0021-9673(94)80582-2
https://doi.org/10.1080/00021369.1983.10865620
https://doi.org/10.1271/BBB.61.1440
https://doi.org/10.1021/NP50098A031
https://doi.org/10.1021/JF0002692
https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
https://doi.org/10.1055/S-2006-958094
Rosmaquinone B 46883407 Click to see 358.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1007/BF02541065
https://doi.org/10.1007/BF02541016
https://doi.org/10.1055/S-2006-959670
https://doi.org/10.1248/BPB.25.1485
https://doi.org/10.1021/JF062610+
(1R,3aS,5aR,5bR,7aR,8R,9S,11aR,11bR,13aR,13bS)-9-hydroxy-8-(hydroxymethyl)-5a,5b,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 158620014 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)C(=O)O 472.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-9-ol 51340201 Click to see 442.70 unknown via CMAUP database
(4aR,6aR,6bS,8aS,11S,12R,12aR,14aR,14bR)-11-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 101763940 Click to see 440.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
(6aR,6bS,8aR,11R,12S,12aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydropicen-3-one 5318252 Click to see 424.70 unknown https://doi.org/10.1055/S-2006-959670
10-Hydroxy-1,6a,6b,9,9,12a-hexamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 11568718 Click to see 454.70 unknown https://doi.org/10.1021/JF062610+
23-Hydroxybetulinic acid 21672692 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)C(=O)O 472.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
3-epi-alpha-Amyrin 12358389 Click to see 426.70 unknown via CMAUP database
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1021/JF062610+
3-O-Acetyloleanolic Acid 151202 Click to see 498.70 unknown https://doi.org/10.1055/S-2006-959670
alpha-Amyrenol 225688 Click to see 426.70 unknown via CMAUP database
alpha-Amyrenone 12306155 Click to see 424.70 unknown https://doi.org/10.1055/S-2006-959670
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1055/S-2006-959670
Anemosapogenin 5318667 Click to see 472.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
Augustic Acid 15560128 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1055/S-2006-959670
beta-Amyrine 15942855 Click to see 426.70 unknown via CMAUP database
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1055/S-2006-959670
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
https://doi.org/10.1021/NP50054A030
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1248/BPB.25.1485
https://doi.org/10.1055/S-2006-962754
https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
CID 15560533 15560533 Click to see CC1C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C(=O)O)C)C)(C)C)O)C 454.70 unknown https://doi.org/10.1021/JF062610+
Lup-20(29)-en-28-oic acid, 3beta-hydroxy- 2371 Click to see 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
Lup-20(29)-ene-3beta,28-diol 221023 Click to see 442.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
methyl (1R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,6a,6b,9,9,12a-hexamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 102401402 Click to see 468.70 unknown https://doi.org/10.1021/JF062610+
Methyl 10-hydroxy-1,6a,6b,9,9,12a-hexamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162851026 Click to see CC1C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C(=O)OC)C)C)(C)C)O)C 468.70 unknown https://doi.org/10.1021/JF062610+
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1055/S-2006-959670
https://doi.org/10.1248/BPB.25.1485
https://doi.org/10.1021/JF062610+
Rofficerone 131752699 Click to see 440.70 unknown https://doi.org/10.1055/S-2006-959670
https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1021/JF062610+
Ursolic acid acetate 6475119 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1055/S-2006-959670
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinylestradiol 5991 Click to see 296.40 unknown https://doi.org/10.1080/10412905.1993.9698216
https://doi.org/10.1002/FFJ.2730090107
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
Labriformidin 441861 Click to see 560.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
1-Pentanol 6276 Click to see 88.15 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
Isoamyl alcohol 31260 Click to see CC(C)CCO 88.15 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
2-Pentanol 22386 Click to see 88.15 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-(1-hydroxyethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 5318226 Click to see 376.36 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 4-hydroxybenzoate 14132341 Click to see 300.26 unknown https://doi.org/10.1021/JF100332W
1-O-4-hydroxybenzoyl-beta-D-glucose 14132342 Click to see 300.26 unknown https://doi.org/10.1021/JF100332W
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Pentanal 8063 Click to see 86.13 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Heptanal 8130 Click to see 114.19 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
Hexanal 6184 Click to see 100.16 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Nonanone 13187 Click to see 142.24 unknown https://doi.org/10.1111/J.1365-2621.1985.TB10476.X
> Organoheterocyclic compounds / Benzofurans
(-)-Rosmadial 72996596 Click to see 344.40 unknown https://doi.org/10.1080/00021369.1983.10865620
Rosmadial 15801061 Click to see CC(C)C1=C(C2=C(C(=C1)C=O)C3(CCCC(C3C=O)(C)C)C(=O)O2)O 344.40 unknown https://doi.org/10.1080/00021369.1983.10865620
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,7-Dihydroxy-3,8-dimethoxyxanthone 5281634 Click to see 288.25 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridopyrimidines
Lycocernuine, 14,15-didehydro- 596405 Click to see CC1=CC2C(CCC3N2C(C1)CC4N3C(=O)CCC4)O 276.37 unknown via CMAUP database
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
(6aR,10R,10aR)-4-hydroxy-9,9-dimethyl-6-oxo-3-propan-2-yl-7,8,10,10a-tetrahydro-6aH-benzo[c]chromene-1,10-dicarbaldehyde 162963774 Click to see 344.40 unknown https://doi.org/10.1021/JF0002692
4-hydroxy-9,9-dimethyl-6-oxo-3-propan-2-yl-7,8,10,10a-tetrahydro-6aH-benzo[c]chromene-1,10-dicarbaldehyde 162963773 Click to see 344.40 unknown https://doi.org/10.1021/JF0002692
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid 639655 Click to see 360.30 unknown https://doi.org/10.1021/JF0300745
https://doi.org/10.1021/JF100332W
3-(3,4-Dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid 5099 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1021/JF100332W
https://doi.org/10.1021/JF0300745
Rosmarinic Acid 5281792 Click to see 360.30 unknown https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
https://doi.org/10.1021/JF950374P
https://doi.org/10.1016/J.CHROMA.2007.01.090
https://doi.org/10.5424/SJAR/2005031-130
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
1-O-Feruloyl-beta-D-glucose 13962928 Click to see 356.32 unknown https://doi.org/10.1021/JF100332W
Ferulic Acid Acyl-b-D-glucoside 72983454 Click to see 356.32 unknown https://doi.org/10.1021/JF100332W
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
https://doi.org/10.1002/CBDV.201100219
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
https://doi.org/10.1016/J.CHROMA.2007.01.090
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1002/CBDV.201100219
https://doi.org/10.1111/J.1745-4557.2006.00096.X
https://doi.org/10.1021/JF010697N
https://doi.org/10.1002/1099-1565(200007/08)11:4<236::AID-PCA503>3.0.CO;2-B
https://doi.org/10.5424/SJAR/2005031-130
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
https://doi.org/10.1021/JF040083T
https://doi.org/10.1007/S00216-007-1298-8
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1002/CBDV.201100219
https://doi.org/10.1111/J.1745-4557.2006.00096.X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Naringenin 932 Click to see 272.25 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
https://doi.org/10.1002/CBDV.201100219
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
Naringenin 439246 Click to see 272.25 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
https://doi.org/10.1002/CBDV.201100219
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
https://doi.org/10.5424/SJAR/2005031-130
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(00)90434-5
https://doi.org/10.1021/JF100332W
https://doi.org/10.1111/J.1745-4557.2006.00096.X
https://doi.org/10.1021/JF010697N
Scutellarein 5281697 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O 286.24 unknown https://doi.org/10.1021/JF0002692
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
(8R)-3,5-dihydroxy-2-(4-hydroxyphenyl)-8,9,9-trimethyl-8H-furo[2,3-h]chromen-4-one 162955921 Click to see CC1C(C2=C(O1)C=C(C3=C2OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)(C)C 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.041
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1021/JF100332W
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
https://doi.org/10.1021/JF040083T
https://doi.org/10.1002/CBDV.201100219
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides
(2S,3S,4R,5R,6S)-3-acetyloxy-6-[5-(5,7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenoxy]-4,5-dihydroxyoxane-2-carboxylic acid 10097618 Click to see 504.40 unknown https://doi.org/10.1016/S0031-9422(00)90434-5
(2S,3S,4S,5R,6S)-4-acetyloxy-6-[5-(5,7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenoxy]-3,5-dihydroxyoxane-2-carboxylic acid 10368818 Click to see 504.40 unknown https://doi.org/10.1021/JF100332W
https://doi.org/10.1016/S0031-9422(00)90434-5
3-Acetyloxy-6-[5-(5,7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenoxy]-4,5-dihydroxyoxane-2-carboxylic acid 74977669 Click to see 504.40 unknown https://doi.org/10.1016/S0031-9422(00)90434-5
4-Acetyloxy-6-[5-(5,7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenoxy]-3,5-dihydroxyoxane-2-carboxylic acid 74977668 Click to see CC(=O)OC1C(C(OC(C1O)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)C(=O)O)O 504.40 unknown https://doi.org/10.1021/JF100332W
https://doi.org/10.1016/S0031-9422(00)90434-5
luteolin 3'-O-glucuronide 10253785 Click to see 462.40 unknown https://doi.org/10.1021/JF100332W
https://doi.org/10.1021/JF040078P
https://doi.org/10.1016/S0031-9422(00)90434-5
Luteolin-3'-D-glucuronide;Luteolin 3'-O-glucuronide;Luteolin-3-O-(c)micro-D-glucuronide 73193164 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O 462.40 unknown https://doi.org/10.1021/JF100332W
https://doi.org/10.1021/JF040078P
https://doi.org/10.1016/S0031-9422(00)90434-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1111/J.1745-4557.2006.00096.X
https://doi.org/10.1021/JF010697N
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 129010007 Click to see 610.60 unknown https://doi.org/10.1016/S0031-9422(00)90434-5
5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 5353588 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 608.50 unknown https://doi.org/10.1021/JF040078P
5-Hydroxy-2-(4-hydroxyphenyl)-6-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13940617 Click to see 462.40 unknown https://doi.org/10.1021/JF040078P
5,8-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 101260296 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF0300745
https://doi.org/10.1021/JF040078P
5,8-Dihydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74977912 Click to see 448.40 unknown https://doi.org/10.1021/JF0300745
https://doi.org/10.1021/JF040078P
6-methoxyluteolin 7-O-hexoside 12314010 Click to see 478.40 unknown https://doi.org/10.1021/JF100332W
Diosmin 5281613 Click to see 608.50 unknown https://doi.org/10.1021/JF040078P
Eriocitrin 83489 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1021/JF040078P
Eriocitrin [M+H]+ 3564542 Click to see 596.50 unknown https://doi.org/10.1021/JF040078P
Hesperetin-7-Rutinoside 3594 Click to see 610.60 unknown https://doi.org/10.1016/S0031-9422(00)90434-5
https://doi.org/10.1021/JF040078P
Hesperidin 10621 Click to see 610.60 unknown https://doi.org/10.1021/JF040078P
https://doi.org/10.1016/S0031-9422(00)90434-5
Homoplantaginin 5318083 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1021/JF040078P
https://doi.org/10.1055/S-2007-969135
Naringin 442428 Click to see 580.50 unknown https://doi.org/10.5424/SJAR/2005031-130
https://doi.org/10.1021/JF010697N
Nepitrin 120742 Click to see 478.40 unknown https://doi.org/10.1021/JF100332W
https://doi.org/10.1016/S0031-9422(00)84935-3
https://doi.org/10.1055/S-2007-969135
Npc288714 53384378 Click to see 608.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see 300.26 unknown https://doi.org/10.1021/JF010697N
https://doi.org/10.5424/SJAR/2005031-130
Nepetin 5317284 Click to see 316.26 unknown https://doi.org/10.1055/S-2007-969135
https://doi.org/10.1016/S0031-9422(00)84935-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7,4'-dimethoxyflavone 5281601 Click to see 298.29 unknown via CMAUP database
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1021/NP50054A030
https://doi.org/10.5424/SJAR/2005031-130
https://doi.org/10.1021/JF0002692
Genkwanin 5281617 Click to see 284.26 unknown https://doi.org/10.1021/JF0300745
https://doi.org/10.1021/JF0002692
https://doi.org/10.1055/S-2006-962754
https://doi.org/10.1021/JF040078P
https://doi.org/10.1021/JF100332W
Ladanein 3084066 Click to see 314.29 unknown https://doi.org/10.1021/JF100332W
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
6-[(3-Acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-2,2-dimethyl-8-phenyl-8,9-dihydropyrano[2,3-f]chromen-10-one 5318656 Click to see 516.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanols
(2S,3R,4S,5S,6R)-2-[[3-(6-hydroxy-4,5-dimethoxycyclohex-2-en-1-yl)-3,4-dihydro-2H-chromen-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 11972371 Click to see 468.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(4Z)-4-Ethylidene-7,12-dihydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadecane-3,8-dione 12315046 Click to see 353.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
(2R)-3-(3,4-dihydroxyphenyl)-2-[(E)-1-(3,4-dihydroxyphenyl)-3-oxoprop-1-en-2-yl]oxypropanoic acid 15801059 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=CC2=CC(=C(C=C2)O)O)C=O)O)O 360.30 unknown https://doi.org/10.1021/JF0002692
2-[(E)-3-(3,4-dihydroxycyclohexa-1,5-dien-1-yl)-1-hydroxy-allyloxy]-3-(3,4-dihydroxyphenyl)propanoic acid 49770232 Click to see C1=CC(=CC(C1O)O)C=CC(O)OC(CC2=CC(=C(C=C2)O)O)C(=O)O 364.30 unknown via CMAUP database
3-(3,4-Dihydroxyphenyl)-2-[1-(3,4-dihydroxyphenyl)-3-oxoprop-1-en-2-yl]oxypropanoic acid 162851105 Click to see 360.30 unknown https://doi.org/10.1021/JF0002692
3-(3,4-Dihydroxyphenyl)-2-hydroxypropanoic acid 439435 Click to see 198.17 unknown via CMAUP database

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