Details Top

Internal ID UUID643fe59aec3d6325741262
Scientific name Origanum vulgare
Authority L.
First published in Sp. Pl. : 590 (1753)

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.

Origanum vulgare, commonly known as oregano, has a long history of use as an herbal tea and decoction in several cultures. In Greek folk medicine, Papadopoulos (2018) reports that dried leaves are steeped in hot water to make a soothing tea for coughs, sore throats, and mild digestive upset. Turkish traditional healers, as documented by Kara et al. (2015), brew a decoction of the leaves and stems to treat colds, bronchitis, and stomach cramps, often adding a few drops of honey for taste. Among the Cherokee of the southeastern United States, Smith (1990) notes that a tincture made from fresh oregano leaves is applied topically as a poultice to relieve skin infections and insect bites, and a decoction is drunk to alleviate fever and flu‑like symptoms. These practices illustrate the plant’s versatility in infusions, tinctures, decoctions, and poultices across Mediterranean, Middle Eastern, and North American traditions.

A simple, safe oregano tea can be prepared at home with the following method: combine 1 tsp (≈ 2 g) of dried oregano leaves in a cup (240 mL) of boiling water. Let the mixture steep for 5–10 minutes, then strain and sip slowly. This mild infusion delivers a gentle dose of the plant’s aromatic oils without the intensity of a strong herbal brew. Pregnant women should avoid large quantities of oregano tea, as the essential oils may stimulate uterine contractions; a single cup per day is considered safe for most adults. If you have a history of thyroid disorders, consult a healthcare professional before regular use, as oregano contains compounds that can affect thyroid hormone synthesis.

The therapeutic effects of oregano tea are largely attributed to its well‑characterized phytochemicals. Thymol and carvacrol, two monoterpenoid phenols, dominate the essential oil profile and are responsible for the plant’s potent antimicrobial and anti‑inflammatory activities. Rosmarinic acid, a polyphenolic compound, contributes antioxidant properties that help protect cells from oxidative stress. Together, these constituents explain the traditional use of oregano for respiratory infections, digestive complaints, and skin ailments.

Modern research continues to validate oregano’s ethnobotanical legacy. Recent in‑vitro studies confirm its efficacy against a range of bacterial and fungal pathogens, and clinical trials are exploring its potential as a natural adjunct in treating upper respiratory tract infections. Commercially, oregano essential oil and dried leaf preparations are widely available in health‑food stores and online, allowing contemporary users to access the same therapeutic benefits that have been cherished by generations of healers.

General Uses Top

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Common products:
Dried oregano herb (leaves and flowering tops) is produced as a culinary spice and seasoning. Concentrated extracts (oleoresins) and essential oil are used by the food industry to deliver oregano flavor and aroma at standardized dosage. The essential oil is also produced for flavor/fragrance applications and as a fragrance ingredient in personal care and household products.

Food and beverages (non-medicinal):
Oregano spice is incorporated into sauces, meat products, pizza, and savory baked goods. Oleoresins are used to achieve consistent flavor dosing in processed meats and ready meals. Oregano essential oil is employed as a natural flavoring in processed foods and condiments.

Fragrance and cosmetics:
Oregano essential oil functions as a fragrance component in soaps, detergents, and perfumes. It is also used in aromatherapy product formulations (diffusers, candles) where it contributes characteristic herbaceous aroma; such products are marketed as air fresheners or for scent rather than therapeutic uses.

Properties relevant to use:
Oregano leaf and essential oil contain high levels of phenolic monoterpenes (notably carvacrol and thymol), giving strong, characteristic aroma and a piquant flavor. These compounds are primary contributors to aroma, flavor retention, and oxidative stability in blends.

Standards and regulation:
Food-grade oregano spice and extracts must meet national food standards; many jurisdictions reference specifications from the American Spice Trade Association (ASTA) for dried herbs. Oregano essential oil is produced to international specifications (ISO 7926 for dried oregano; ISO 3216 for oregano oil) and is widely recognized as Generally Recognized As Safe (GRAS) for use as a natural flavoring in the United States and is approved as a food flavoring substance within the EU flavoured foods/feeds framework (Regulation (EC) No 1334/2008). Products containing oregano essential oil comply with relevant cosmetics legislation (EU Cosmetic Regulation 1223/2009 and U.S. FDA Cosmetic Act).

Sustainability and sourcing:
Oregano is cultivated extensively in the Mediterranean region; production is largely as an annual field crop in warm, dry climates. Commercial supply relies on standardized agricultural and drying practices to preserve aroma and flavor. Certification standards (e.g., organic) apply to cultivated material for markets requiring verified production methods.

Synonyms Top

Scientific name Authority First published in
Origanum americanum Raf. Fl. Tellur. 3: 86. 1837 (1837)
Origanum floridum Salisb. Prodr. Stirp. Chap. Allerton : 85 (1796)
Origanum heracleoticum Rchb. Fl. Germ. Excurs. : 313 (1831)
Origanum majus Garsault Fig. Pl. Méd. : t. 430a (1764)
Origanum megastachyum var. hirtum Schur Enum. Pl. Transsilv. 524. 1866
Origanum puberulum (Beck) Klokov Fl. RSS Ukr. 9: 290. 1960 (1960)
Origanum purpurescens Gilib. Fl. Lit. Inch. 1: 64 (1782)
Origanum vulgare var. prismaticum Gaudin Fl. Helv. 4: 78. 1829 (1829)
Origanum vulgare var. puberulum Beck Fl. Nieder-Osterreich 2: 993. 1893
Thymus origanum Kuntze Taschen-Fl. Leipzig : 106 (1867)
Origanum vulgare var. heracleoticum Nyman Consp. Fl. Eur. 592. 1881
Origanum vulgare subsp. creticum (L.) Nyman Consp. Fl. Eur. 592. 1881 (1881)
Origanum vulgare var. thymiflorum (Rchb.) Nyman Consp. Fl. Eur. 592. 1881
Origanum vulgare var. albiflorum Lej. Comp. Fl. Belg. 2: 248 1831
Origanum vulgare var. pallescens Tinant Fl. Luxemb. 309. 1836
Origanum vulgare var. albidum Bellynck Fl. Namur 195. 1855
Origanum vulgare f. pallidum Beckh. Fl. Westfalen 696 1893
Origanum vulgare subsp. humile Pers. Syn. Pl. 2: 129 1807
Origanum vulgare var. album Fraas Syn. Pl. Fl. Class. 181. 1845
Origanum hirtum f. albiflorum Hausskn. Mitth. Thüring. Bot. Vereins n.f., 11: 49 1897
Origanum vulgare f. carneum Beckh. Fl. Westfalen 696 1893
Origanum vulgare var. glabrescens Beck Fl. Hernstein 244. 1884
Origanum vulgare var. creticum (L.) Briq. Lab. Alp. Mar. 485. 1895
Origanum vulgare var. purpurascens Briq. Lab. Alp. Mar. 486. 1895
Origanum vulgare var. spiculigerum Briq. Lab. Alp. Mar. 486. 1895
Origanum vulgare var. formosanum Hayata Icon. Pl. Formosan. 8: 102. 1919
Origanum vulgare subsp. viride (Boiss.) Hayek Prodr. Fl. Balc. 2: 334

Common names Top

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Language Common/alternative name
English oregano
English wild marjoram
Spanish órgano
Spanish orégano
Spanish furiégano
Spanish mejorana silvestre
Spanish oreganín
Spanish orégano común
Spanish orégano nano
Spanish orégano trenzado
Spanish orégano turco
Spanish orenga
Spanish oriégano
Spanish perigüel
Spanish urégano
Spanish uriégano
Spanish uriéganu
Spanish furiegano
Spanish oreganin
Spanish uregano
Spanish origanum purpurescens
Arabic أوريغانو
Arabic مردقوش شائع
Arabic صعتر
Arabic زوباع
Arabic فوذج جبلي
Arabic مردقوش
Arabic بردقوش
Arabic بردقوشة
Azerbaijani adi qaraqınıq
Azerbaijani adi qaraot
azb عادی قاراقینیق
ba Мәтрүшкә
bcl oregano
Belarusian Мацярдушка звычайная
Bulgarian риган
Bulgarian бял риган
Bulgarian обикновен риган
Bengali অরিগানো
Bengali ওরেগানো
Bengali জংলী মরুয়া
Bosnian origano
Catalan orégano
Catalan orenga
Catalan origan
ceb oregano
ceb pot marjoram
co carnepula
Czech dobromysl
Czech dobromysl obecná
Czech oregáno
Czech oregano
Welsh oregano
Welsh penrhudd
Danish oregano
Danish almindelig merian
Danish vild merian
German dost
German oregano
German dostenkraut
German echter dost
German gemeiner dost
German gewöhnlicher dost
German origano
German wilder majoran
German origan
Greek ρίγανη
Greek Ρίγανη
Esperanto origano
Estonian pune
Estonian harilik pune
Estonian oregano
Estonian vorstirohi
Basque oregano
Persian مرزنجوش
Persian مرزنگوش
Persian پونه کوهی
Persian پونهٔ کوهی
Persian مرزنگوش وحشی
Finnish oregano
Finnish mäkimeirami
French origan
French marjolaine sauvage
frr oregaano
Irish oragán
Galician ourego
gn orégano
Swiss German mazaroo
Hausa ganyen Ƙamshi
Hebrew אורגנו
Hebrew אזובית פשוטה
Hindi ऑरिगेनो
Croatian mravinac
Croatian cunila gallinacean
Croatian origano
Croatian origanum heracleoticum
Hungarian szurokfű
Hungarian vadmajoránna
Armenian Խնկածաղիկ սովորական
Indonesian oregano
Italian origano
Japanese オレガノ
Japanese ハナハッカ
Japanese 花薄荷
jv orégano
Kazakh Кәдімгі жұпаргүл
Kannada ಮರುಗ
Korean 오레가노
Korean 오레가노 꿀
lb oregano
lb léiffrabettstréi
lez Чiулавкьалар
li marjolein
li oregano
Lithuanian paprastasis raudonėlis
Lithuanian origan
Latvian parastā raudene
Macedonian Обично оригано
Malay pokok oregano
Malay pokok origano
myv Карвотикше
nap rétëca
Norwegian Bokmål bergmynte
Norwegian Bokmål kung
Nepali रामतुलसी
Dutch oregano
Dutch wilde marjolein
Norwegian Nynorsk bergmynte
Norwegian Nynorsk kongsgress
Norwegian Nynorsk kung
Norwegian Nynorsk kungsgras
os Къаххос
pam oregano
pcd marjolainne batèrde
Polish lebiodka pospolita
Polish oregano
Punjab ساتل
Portuguese orégãos
Portuguese hissopo
Portuguese oregano
Portuguese orégano
Portuguese orégão
Quechua oregano
Quechua orégano
Quechua unquy yuyu
Romanian oregano
Romanian sovârf
Romanian Șovârf
Romanian Șovârv
Russian Душица обыкновенная
Russian Душница
Russian Мацердушка
Russian Орегано
Russian душница
Russian мацердушка
Russian орегано
Yakutian Көннөрү дыргыл
sco oregano
Serbo-Croatian mravinac
Serbo-Croatian origano
Serbo-Croatian vranilova trava
Slovak pamajorán obyčajný
Slovenian dobra misel
Slovenian navadna dobra misel
Slovenian origano
Slovenian divji origano
Albanian rigoni
Serbian вранилова трава
Serbian Оригано
Serbian Вранилова трава
Swedish oregano
Swedish koning
Swedish dosta
Swedish frimodig
Swedish konig
Swedish kungsmynta
Swedish vild mejram
Swedish vildmejram
Swedish origan
Tamil ஆர்கனோ
Telugu వాము ఆకు
Thai ออริกาโน
Turkish güvey otu
Turkish keklik otu
tt Мәтрүшкә
Ukrainian Материнка звичайна
Ukrainian Орегано
Uzbek oregano
vls oregano
Walloon såvaedje mariolinne
Chinese 满天星
Chinese 香茹草
Chinese 香薷
Chinese 野薄荷
Chinese 山薄荷
Chinese 接骨草
Chinese 满山香
Chinese 野荆芥
Chinese 糯米条
Chinese 香茹
Chinese 茵陈
Chinese 俄力岡葉
Chinese 奧勒岡草
Chinese 披薩草
Chinese 牛至
Chinese 牛至叶
Chinese 猫儿草
Chinese 蘑菇草
Chinese 乳香草
Chinese 五香草
Chinese 土菌陈
Chinese 土香薷
Chinese 地藿香
Chinese 小叶薄荷
Chinese 小田草
Chinese 满坡香
Chinese 玉兰至
Chinese 琦香
Chinese 白花茵陈
Chinese 白花菌陈
Chinese 罗罗香
Chinese 署草
Chinese 苏子草
Chinese 随经草
Chinese 香炉草
Chinese 土茵陈

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Origanum vulgare subsp. glandulosum (Desf.) Ietsw. Leiden Bot. Ser. 4: 110 (1980)
Origanum vulgare subsp. gracile (K.Koch) Ietsw. Leiden Bot. Ser. 4: 111 (1980)
Origanum vulgare subsp. virens (Hoffmanns. & Link) Ietsw. Leiden Bot. Ser. 4: 115 (1980)
Origanum vulgare subsp. viridulum (Martrin-Donos) Nyman Consp. Fl. Eur. : 592 (1881)
Origanum vulgare subsp. vulgare Unknown
Origanum vulgare subsp. hirtum (Link) A.Terracc. Mem. Reale Accad. Sci. Torino , ser. 2, 67: 46 (1930)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Azores
      • Canary Islands
      • Madeira
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Tibet
      • Xinjiang
    • Eastern Asia
      • Taiwan
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Russian Far East
      • Primorye
    • Siberia
      • Altay
      • Buryatiya
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Ireland
      • Norway
      • Svalbard
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • Mexico
      • Mexico Southwest
    • North-central U.S.A.
      • Illinois
    • Northeastern U.S.A.
      • Connecticut
      • Massachusetts
      • Michigan
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Vermont
    • Northwestern U.S.A.
      • Oregon
      • Washington
    • Southeastern U.S.A.
      • Arkansas
      • Delaware
      • Maryland
      • North Carolina
      • Virginia
    • Southwestern U.S.A.
      • California
    • Western Canada
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000260765
UNII 0E5AT8T16U
Canadensys 6429
USDA Plants ORVU
Tropicos 17600223
INPN 111289
Flora of Italy 4610
KEW urn:lsid:ipni.org:names:453395-1
The Plant List kew-143954
Missouri Botanical Garden 281411
PFAF Origanum vulgare
Open Tree Of Life 305918
Observations.org 7120
NCBI Taxonomy 39352
NBN Atlas NBNSYS0000004207
Nature Serve 2.137393
IPNI 453395-1
iNaturalist 61396
iNaturalist 80083
GBIF 2926612
Freebase /m/05kw_
WisFlora 9414
EPPO ORIVU
EOL 579367
Elurikkus 6007
Calflora (Californian flora) 5960
US Library of Congress sh96005072
USDA GRIN 25913
Wikipedia Oregano
CMAUP NPO29169

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_047713405.1 ASM4771340v1 Scaffold Iridian Genomes 2025-02-12 60 501.51 Mb

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
From nature to nanomedicine: bioengineered metallic nanoparticles bridge the gap for medical applications Patel J, Kumar GS, Roy H, Maddiboyina B, Leporatti S, Bohara RA Discov Nano 09-May-2024
PMCID:PMC11082127
doi:10.1186/s11671-024-04021-9
PMID:38724833
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
Natural products for managing metabolic syndrome: a scoping review Abdulghani MF, Al-Fayyadh S Front Pharmacol 30-Apr-2024
PMCID:PMC11091304
doi:10.3389/fphar.2024.1366946
PMID:38746011
Potentiation of the Antimicrobial Effect of Oxytetracycline Combined with Cinnamon, Clove, Oregano, and Red Thyme Essential Oils against MDR Salmonella enterica Strains Huerta Lorenzo B, Galán-Relaño Á, Barba-Sánchez E, Romero-Salmoral A, Solarte Portilla AL, Gómez-Gascón L, Astorga Márquez RJ Animals (Basel) 30-Apr-2024
PMCID:PMC11083648
doi:10.3390/ani14091347
PMID:38731351
Plant cultural indicators of forest resources from the Himalayan high mountains: implications for improving agricultural resilience, subsistence, and forest restoration Haq SM, Khoja AA, Waheed M, Pieroni A, Siddiqui MH, Bussmann RW J Ethnobiol Ethnomed 24-Apr-2024
PMCID:PMC11040985
doi:10.1186/s13002-024-00685-w
PMID:38659048
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
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
Mitigating digestive disorders: Action mechanisms of Mediterranean herbal active compounds Kmail A Open Life Sci 18-Apr-2024
PMCID:PMC11032100
doi:10.1515/biol-2022-0857
Antibacterial Activity of Oregano (Origanum vulgare L.) Essential Oil Vapors against Microbial Contaminants of Food-Contact Surfaces Pinto L, Cervellieri S, Netti T, Lippolis V, Baruzzi F Antibiotics (Basel) 18-Apr-2024
PMCID:PMC11047463
doi:10.3390/antibiotics13040371
PMID:38667047
Emerging Approaches for Mitigating Biofilm-Formation-Associated Infections in Farm, Wild, and Companion Animals Araújo D, Silva AR, Fernandes R, Serra P, Barros MM, Campos AM, Oliveira R, Silva S, Almeida C, Castro J Pathogens 13-Apr-2024
PMCID:PMC11054384
doi:10.3390/pathogens13040320
PMID:38668275
Wild Edible Plants Used in Dalmatian Zagora (Croatia) Ninčević Runjić T, Jug-Dujaković M, Runjić M, Łuczaj Ł Plants (Basel) 11-Apr-2024
PMCID:PMC11053949
doi:10.3390/plants13081079
PMID:38674488
Anticandidal Activity of a Siderophore from Marine Endophyte Pseudomonas aeruginosa Mgrv7 Kotb E, Al-Abdalall AH, Ababutain I, AlAhmady NF, Aldossary S, Alkhaldi E, Alghamdi AI, Alzahrani HA, Almuhawish MA, Alshammary MN, Ahmed AA Antibiotics (Basel) 10-Apr-2024
PMCID:PMC11047651
doi:10.3390/antibiotics13040347
PMID:38667023
Rhizopus stolonifer and related control strategies in postharvest fruit: A review Liu Q, Chen Q, Liu H, Du Y, Jiao W, Sun F, Fu M Heliyon 10-Apr-2024
PMCID:PMC11031825
doi:10.1016/j.heliyon.2024.e29522
Moslae Herba: Botany, Traditional Uses, Phytochemistry, and Pharmacology Duan ZY, Sun YP, Wang ZB, Kuang HX Molecules 10-Apr-2024
PMCID:PMC11051901
doi:10.3390/molecules29081716
PMID:38675535
Natural Polymers as Carriers for Encapsulation of Volatile Oils: Applications and Perspectives in Food Products Tița O, Constantinescu MA, Rusu L, Tița MA Polymers (Basel) 09-Apr-2024
PMCID:PMC11054478
doi:10.3390/polym16081026
PMID:38674945

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1007/BF00574347
https://doi.org/10.1007/BF00598278
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1271/BBB1961.53.519
https://doi.org/10.1007/BF00574347
https://doi.org/10.1021/NP100281G
https://doi.org/10.1007/BF00598278
https://doi.org/10.1080/00021369.1989.10869290
> 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/10.1007/BF00574347
https://doi.org/10.1007/BF00598278
> 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/10.1016/J.CHROMA.2007.01.090
> 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/10.1007/BF00574347
https://doi.org/10.1007/BF00598278
https://doi.org/10.1016/J.CHROMA.2007.01.090
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
(2R)-3-[4,5-dihydroxy-2-[(4-hydroxyphenyl)methyl]phenyl]-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxypropanoic acid 163195487 Click to see 466.40 unknown https://doi.org/10.1080/00021369.1989.10869290
3-[4,5-Dihydroxy-2-[(4-hydroxyphenyl)methyl]phenyl]-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid 69723889 Click to see 466.40 unknown https://doi.org/10.1080/00021369.1989.10869290
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
p-Cymen-8-ol 14529 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1993.9698253
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Decane 15600 Click to see 142.28 unknown https://doi.org/10.1080/10412905.1993.9698253
Heneicosane 12403 Click to see 296.60 unknown https://doi.org/10.1080/10412905.1993.9698253
Hentriacontane 12410 Click to see 436.80 unknown via CMAUP database
Heptacosane 11636 Click to see 380.70 unknown via CMAUP database
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown via CMAUP database
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown via CMAUP database
Nonane 8141 Click to see 128.25 unknown https://doi.org/10.1080/10412905.1993.9698253
Octacosane 12408 Click to see 394.80 unknown via CMAUP database
Pentacosane 12406 Click to see 352.70 unknown via CMAUP database
Triacontane 12535 Click to see 422.80 unknown via CMAUP database
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://doi.org/10.1080/10412905.1993.9698253
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1002/JSFA.2740430304
https://doi.org/10.1080/10412905.1993.9698294
https://doi.org/10.1016/0305-1978(93)90031-L
https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1021/JF9708296
https://doi.org/10.1007/BF02858924
https://doi.org/10.1080/10412905.1996.9700567
https://doi.org/10.1055/S-2006-957640
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
Secoisolariciresinol 65373 Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O 362.40 unknown https://doi.org/10.1079/BJN2002794
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid 2969 Click to see CCCCCCCCCC(=O)O 172.26 unknown https://doi.org/10.1080/10412905.1993.9698253
Dec-3-enoic acid 85855 Click to see 170.25 unknown https://doi.org/10.1080/10412905.1993.9698253
Nonanoic Acid 8158 Click to see CCCCCCCCC(=O)O 158.24 unknown https://doi.org/10.1080/10412905.1993.9698253
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
2-[3-Oxo-2-[5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypent-2-enyl]cyclopentyl]acetic acid 4480898 Click to see 388.40 unknown https://doi.org/10.1021/JF061477I
Tuberonic acid glucoside 5281204 Click to see 388.40 unknown https://doi.org/10.1021/JF061477I
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl Acetate 1549026 Click to see 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Decanol 8174 Click to see 158.28 unknown https://doi.org/10.1080/10412905.1993.9698253
1-Hexacosanol 68171 Click to see 382.70 unknown via CMAUP database
1-Nonen-3-ol 89560 Click to see 142.24 unknown https://doi.org/10.1080/10412905.1993.9698253
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1016/0305-1978(93)90031-L
2-Ethylhexan-1-ol 7720 Click to see CCCCC(CC)CO 130.23 unknown https://doi.org/10.1080/10412905.1993.9698253
3-Octanol 11527 Click to see 130.23 unknown https://doi.org/10.1016/0305-1978(93)90031-L
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives / Jasmonic acids
12-Hydroxyjasmonic acid 5497122 Click to see 226.27 unknown https://doi.org/10.1021/JF061477I
12-Hydroxyjasmonicacid 69604805 Click to see 226.27 unknown https://doi.org/10.1021/JF061477I
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3-Ethenyl-3,7-dimethyloct-6-enoic acid 13128171 Click to see CC(=CCCC(C)(CC(=O)O)C=C)C 196.29 unknown https://doi.org/10.1080/10412905.1993.9698253
5,9-Dimethyl-4,8-decadienoic acid 6365434 Click to see CC(=CCCC(=CCCC(=O)O)C)C 196.29 unknown https://doi.org/10.1080/10412905.1993.9698253
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1080/10412905.1996.9700567
https://doi.org/10.1055/S-2006-957640
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1080/10412905.1996.9700567
https://doi.org/10.1055/S-2006-957640
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1993.9698253
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1007/BF02858924
https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1055/S-2006-957640
https://doi.org/10.1080/10412905.1996.9700567
Linalyl Acetate 8294 Click to see 196.29 unknown https://doi.org/10.1055/S-2006-957640
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1007/BF02858924
https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1016/0305-1978(93)90031-L
https://doi.org/10.1080/10412905.1996.9700567
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1993.9698253
Nerylacetone 1713001 Click to see CC(=CCCC(=CCCC(=O)C)C)C 194.31 unknown https://doi.org/10.1080/10412905.1993.9698253
> 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/10.1094/PHYTO.2000.90.7.710
https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1080/14786419.2010.535150
https://doi.org/10.1021/JF9603893
https://doi.org/10.1080/10412905.1996.9700567
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1693916/
https://doi.org/10.1007/BF02858924
https://doi.org/10.1021/JF9708296
https://doi.org/10.1055/S-2006-957640
https://doi.org/10.1093/OXFORDJOURNALS.AOB.A086958
https://doi.org/10.1016/0305-1978(93)90031-L
https://doi.org/10.1002/JSFA.2740430304
Carvacryl acetate 80792 Click to see 192.25 unknown via CMAUP database
Carvacryl methyl ether 80790 Click to see 164.24 unknown https://doi.org/10.1080/10412905.1996.9700567
P-Cymene 7463 Click to see 134.22 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1693916/
https://doi.org/10.1007/BF02858924
https://doi.org/10.1002/JSFA.2740430304
https://doi.org/10.1080/10412905.1993.9698294
https://doi.org/10.1021/JF9708296
https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1055/S-2006-957640
https://doi.org/10.1016/0305-1978(93)90031-L
https://doi.org/10.1080/10412905.1996.9700567
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1002/JSFA.2740430304
https://doi.org/10.1021/JF9603893
https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1021/JF9708296
https://doi.org/10.1007/BF02858924
https://doi.org/10.1094/PHYTO.2000.90.7.710
https://doi.org/10.1080/10412905.1996.9700567
https://doi.org/10.1055/S-2006-957640
https://doi.org/10.1093/OXFORDJOURNALS.AOB.A086958
Thymyl methyl ether 14104 Click to see 164.24 unknown https://doi.org/10.1080/10412905.1996.9700567
https://doi.org/10.1016/0305-1978(93)90031-L
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1007/BF02858924
https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1055/S-2006-957640
https://doi.org/10.1080/10412905.1996.9700567
(1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl)acetic acid 20327362 Click to see 196.29 unknown https://doi.org/10.1080/10412905.1993.9698253
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(93)90031-L
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1996.9700567
https://doi.org/10.1021/JF9801670
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1021/JF9801670
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1007/BF02858924
https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1080/10412905.1996.9700567
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1007/BF02858924
https://doi.org/10.1055/S-2006-957640
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1080/10412905.1996.9700567
https://doi.org/10.1007/BF02858924
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1007/BF02858924
https://doi.org/10.1080/10412905.1996.9700567
https://doi.org/10.1055/S-2006-957640
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1080/10412905.1996.9700567
https://doi.org/10.1055/S-2006-957640
Thujone 261491 Click to see 152.23 unknown https://doi.org/10.1055/S-2006-957640
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Isodihydrocarvone 443167 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1993.9698253
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/0305-1978(93)90031-L
https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1007/BF02858924
https://doi.org/10.1080/10412905.1996.9700567
alpha-PHELLANDRENE 7460 Click to see 136.23 unknown https://doi.org/10.1007/BF02858924
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1021/JF9708296
https://doi.org/10.1007/BF02858924
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1693916/
https://doi.org/10.1080/10412905.1996.9700567
Alpha-Terpineol 17100 Click to see 154.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1693916/
https://doi.org/10.1007/BF02858924
https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1080/10412905.1996.9700567
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1080/10412905.1993.9698253
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1007/BF02858924
https://doi.org/10.1021/JF9708296
https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1080/10412905.1996.9700567
Menthol 1254 Click to see 156.26 unknown https://doi.org/10.1055/S-2006-957640
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1007/BF02858924
https://doi.org/10.1080/10412905.1996.9700567
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(+)-gamma-Tocopherol 92729 Click to see 416.70 unknown https://doi.org/10.3109/09637489609031878
Beta-Tocopherol 6857447 Click to see 416.70 unknown https://doi.org/10.3109/09637489609031878
Covi-Ox 6560141 Click to see 430.70 unknown https://doi.org/10.3109/09637489609031878
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/10.3109/09637489609031878
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1993.9698253
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1993.9698253
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1055/S-2006-957640
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane 5317024 Click to see 218.38 unknown https://doi.org/10.1055/S-2006-957640
https://doi.org/10.1080/10412905.1993.9698253
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698253
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown https://doi.org/10.1055/S-2006-957640
3-[(2S)-6-methylhept-5-en-2-yl]-6-methylidenecyclohexene 5321277 Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1 204.35 unknown https://doi.org/10.1080/10412905.1993.9698253
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1996.9700567
4-[(2R)-6-methyl-4-oxohept-5-en-2-yl]benzoic acid 5316896 Click to see 246.30 unknown https://doi.org/10.1271/BBB.67.2311
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1016/0305-1978(93)90031-L
https://doi.org/10.1055/S-2006-957640
7,11-Dimethyl-3-methylene-1,6Z,10-dodecatriene 56936085 Click to see 206.37 unknown https://doi.org/10.1080/10412905.1993.9698253
alpha-Bisabolene, (E)- 5315468 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698253
Beta-Bisabolene 10104370 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-957640
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698253
beta-Cubebene 93081 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698253
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1016/0305-1978(93)90031-L
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1055/S-2006-957640
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1693916/
https://doi.org/10.1007/BF02858924
https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1055/S-2006-957640
https://doi.org/10.1016/0305-1978(93)90031-L
https://doi.org/10.1080/10412905.1996.9700567
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1016/0305-1978(93)90031-L
https://doi.org/10.1080/10412905.1996.9700567
https://doi.org/10.1055/S-2006-957640
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-957640
Farnesene 5281516 Click to see 204.35 unknown https://doi.org/10.1016/0305-1978(93)90031-L
https://doi.org/10.1080/10412905.1993.9698253
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698253
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1996.9700567
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698253
https://doi.org/10.1080/10412905.1996.9700567
https://doi.org/10.1055/S-2006-957640
I2-Ionone 638014 Click to see 192.30 unknown https://doi.org/10.1080/10412905.1993.9698253
Nerolidol 5284507 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-957640
Patchoulane 29408 Click to see 206.37 unknown https://doi.org/10.1080/10412905.1993.9698253
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1993.9698253
Alloaromadendren 91746537 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1996.9700567
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1996.9700567
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol 547972 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1993.9698253
Beta-Elemene 6918391 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1996.9700567
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
Valencene 9855795 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1996.9700567
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1055/S-2006-957640
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1996.9700567
Selin-11-en-4-ol 6428433 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown https://doi.org/10.1080/10412905.1996.9700567
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1996.9700567
https://doi.org/10.1055/S-2006-957640
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown https://doi.org/10.1055/S-2006-957640
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-957640
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[2-methyl-5-propan-2-yl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]oxane-3,4,5-triol 11092169 Click to see 490.50 unknown https://doi.org/10.1021/JF061477I
(E)-4-[(3R,4S)-4-hydroxy-2,6,6-trimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexen-1-yl]but-3-en-2-one 11567211 Click to see 386.40 unknown via CMAUP database
2-(Hydroxymethyl)-6-(4-hydroxy-5-methyl-2-propan-2-ylphenoxy)oxane-3,4,5-triol 162907437 Click to see CC1=CC(=C(C=C1O)C(C)C)OC2C(C(C(C(O2)CO)O)O)O 328.36 unknown https://doi.org/10.1021/JF061477I
2-(Hydroxymethyl)-6-[2-methyl-5-propan-2-yl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]oxane-3,4,5-triol 85395906 Click to see 490.50 unknown https://doi.org/10.1021/JF061477I
Komaroveside A 53248454 Click to see CC1=C(C(CC(C1O)OC2C(C(C(C(O2)CO)O)O)O)(C)C)C=CC(=O)C 386.40 unknown via CMAUP database
Zataroside A 25102046 Click to see 328.36 unknown https://doi.org/10.1021/JF061477I
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
8-Geranyloxypsoralen 5317564 Click to see 338.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3S,3aS,5aR,6R,9R,9aS,9bS)-6-hydroxy-3,5a-dimethyl-9-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,3a,4,5,6,7,8,9,9a,9b-decahydrobenzo[g][1]benzofuran-2-one 15628134 Click to see 430.50 unknown via CMAUP database
(3S,3aS,5aR,6R,9R,9aS,9bS)-9-(hydroxymethyl)-3,5a-dimethyl-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,3a,4,5,6,7,8,9,9a,9b-decahydrobenzo[g][1]benzofuran-2-one 15628130 Click to see 430.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aR,4S,6E,10Z,11aR)-4-hydroxy-3-methylidene-2-oxo-10-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-carbaldehyde 23983719 Click to see 440.40 unknown via CMAUP database
[(2R,3S,4S,5R,6R)-6-[[(3aR,4S,6E,10Z,11aR)-6-formyl-4-hydroxy-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl]methoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate 101701130 Click to see 574.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1021/JF100636H
https://doi.org/10.1016/S0367-326X(02)00245-9
(3S,4aR,6aR,6bR,8aS,12S,12aR,12bR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,12,12a,12b,13,14,14a,14b-icosahydropicen-3-yl acetate 13970054 Click to see 468.80 unknown via CMAUP database
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1021/JF100636H
Lupeol Acetate 92157 Click to see 468.80 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1021/JF100636H
Taraxasterol Acetate 13889352 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown via CMAUP database
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1016/S0367-326X(02)00245-9
https://doi.org/10.1021/JF100636H
> 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/10.1080/10412905.1993.9698253
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Enol esters
[(1E)-2,6-dimethylhepta-1,5-dienyl] acetate 24832062 Click to see 182.26 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1007/BF00574347
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1007/BF00574347
https://doi.org/10.1007/BF00598278
https://doi.org/10.1007/S00216-007-1298-8
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
6-Methylheptan-3-ol 86783 Click to see 130.23 unknown https://doi.org/10.1080/10412905.1993.9698253
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(1S,2S)-2-hydroxy-1-methyl-4-propan-2-ylcyclohex-3-en-1-yl]oxyoxane-3,4,5-triol 102257012 Click to see CC(C)C1=CC(C(CC1)(C)OC2C(C(C(C(O2)CO)O)O)O)O 332.39 unknown https://doi.org/10.1021/JF061477I
2-(Hydroxymethyl)-6-(2-hydroxy-1-methyl-4-propan-2-ylcyclohex-3-en-1-yl)oxyoxane-3,4,5-triol 76516447 Click to see 332.39 unknown https://doi.org/10.1021/JF061477I
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 3-hydroxy-4-methoxybenzoate 101267903 Click to see COC1=C(C=C(C=C1)C(=O)OCC2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 452.40 unknown https://doi.org/10.1271/BBB.67.2311
[3-Hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 3-hydroxy-4-methoxybenzoate 162886121 Click to see 452.40 unknown https://doi.org/10.1271/BBB.67.2311
[4-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 3,4-dihydroxybenzoate 13917001 Click to see 422.40 unknown https://doi.org/10.1080/00021369.1987.10868446
https://doi.org/10.1080/00021369.1989.10869290
2-(Hydroxymethyl)-6-(4-hydroxy-2-methyl-5-propan-2-ylphenoxy)oxane-3,4,5-triol 14589105 Click to see 328.36 unknown https://doi.org/10.1021/JF061477I
Amburoside A 10409977 Click to see 422.40 unknown https://doi.org/10.1080/00021369.1987.10868446
https://doi.org/10.1080/00021369.1989.10869290
Oreganol 5320735 Click to see 438.40 unknown https://doi.org/10.1271/BBB.67.2311
Zataroside B 14589106 Click to see 328.36 unknown https://doi.org/10.1021/JF061477I
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
alpha-D-Glucopyranoside, beta-D-fructofuranosyl O-alpha-D-galactopyranosyl-(1.fwdarw.6)- 219993 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O 504.40 unknown https://doi.org/10.1016/S0367-326X(02)00245-9
Raffinose 439242 Click to see 504.40 unknown https://doi.org/10.1016/S0367-326X(02)00245-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see 182.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(Z)-non-2-enal 5354833 Click to see 140.22 unknown https://doi.org/10.1080/10412905.1993.9698253
Hexanal 6184 Click to see 100.16 unknown https://doi.org/10.1080/10412905.1993.9698253
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1080/10412905.1993.9698253
trans-2-Hexenal 5281168 Click to see 98.14 unknown https://doi.org/10.1080/10412905.1993.9698253
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
3-Nonanone 61235 Click to see CCCCCCC(=O)CC 142.24 unknown https://doi.org/10.1080/10412905.1993.9698253
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Pentylfuran 19602 Click to see 138.21 unknown https://doi.org/10.1080/10412905.1993.9698253
Perillene 68316 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1993.9698253
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Chlorins
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate 5459387 Click to see 871.20 unknown https://doi.org/10.1021/JF00050A028
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate 6433193 Click to see 871.20 unknown https://doi.org/10.1021/JF00050A028
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R)-2-[(E)-3-[(2S,3S)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-4-yl]prop-2-enoyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid 13991587 Click to see 718.60 unknown https://doi.org/10.1021/JF061477I
(2S,3S)-4-[(E)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid 95359683 Click to see 538.50 unknown https://doi.org/10.1021/JF061477I
https://doi.org/10.1002/JCCS.200300153
(2S)-2-[(E)-3-[(2S,3S)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-4-yl]prop-2-enoyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid 13991588 Click to see 718.60 unknown https://doi.org/10.1021/JF061477I
4-[(E)-3-[(1R)-1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid 5281302 Click to see 538.50 unknown https://doi.org/10.1002/JCCS.200300153
4-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid 4482010 Click to see 538.50 unknown https://doi.org/10.1021/JF061477I
Salvianic acid B 119177 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O 718.60 unknown https://doi.org/10.1021/JF061477I
Salvianolic acid C 13991590 Click to see 492.40 unknown https://doi.org/10.1002/JCCS.200300153
Salvianolic acid C [M+H]+ 5321087 Click to see 492.40 unknown https://doi.org/10.1002/JCCS.200300153
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see 148.16 unknown https://doi.org/10.1007/BF00574347
https://doi.org/10.1007/BF00598278
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1007/BF00574347
https://doi.org/10.1007/BF00598278
> 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/10.1080/00021369.1989.10869290
https://doi.org/10.1021/JF061477I
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/10.1080/00021369.1989.10869290
https://doi.org/10.1021/JF061477I
Rosmarinic Acid 5281792 Click to see 360.30 unknown https://doi.org/10.1021/JF9802629
https://doi.org/10.1271/BBB1961.53.519
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown https://doi.org/10.1021/JF061477I
https://doi.org/10.1007/BF00574347
https://doi.org/10.1080/00021369.1989.10869290
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1007/S00216-007-1298-8
https://doi.org/10.1007/BF00598278
https://doi.org/10.1271/BBB1961.53.519
https://doi.org/10.1080/00021369.1989.10869290
https://doi.org/10.1021/JF061477I
https://doi.org/10.1007/BF00574347
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Eriodictyol 11095 Click to see 288.25 unknown https://doi.org/10.1021/JF061477I
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/10.1021/JF061477I
https://doi.org/10.1007/BF02542580
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,5,7-Trihydroxy-2-(4-Hydroxyphenyl)Chroman-4-One 662 Click to see 288.25 unknown https://doi.org/10.1007/BF02542580
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1007/BF02542580
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1007/BF02542580
> 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/10.1081/JLC-100103396
https://doi.org/10.1021/JF061477I
https://doi.org/10.1007/BF02542580
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/10.1002/JCCS.200300153
https://doi.org/10.1081/JLC-100103396
https://doi.org/10.1021/JF061477I
https://doi.org/10.1007/BF00574347
https://doi.org/10.1016/S0308-8146(01)00114-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Galangin 5281616 Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1021/JF00050A028
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1021/JF061477I
https://doi.org/10.1021/JF00050A028
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vicenin 2 3084407 Click to see 594.50 unknown https://doi.org/10.1021/JF061477I
Vicenin 2 442664 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/JF061477I
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Apigenin 7-O-glucuronide 5319484 Click to see 446.40 unknown https://doi.org/10.1002/JCCS.200300153
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown https://doi.org/10.1002/JCCS.200300153
https://doi.org/10.1007/BF00574347
https://doi.org/10.1007/978-3-540-71095-0_7234
Luteolin-7-O-glucuronide 13607752 Click to see 462.40 unknown https://doi.org/10.1007/BF00574347
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-[[(2R,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 42607901 Click to see 580.50 unknown via CMAUP database
7-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 45358136 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1007/BF00574347
https://doi.org/10.1007/978-3-540-71095-0_7234
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1002/JCCS.200300153
Npc85473 5385553 Click to see 432.40 unknown https://doi.org/10.1007/BF00574347
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol 5280666 Click to see 300.26 unknown https://doi.org/10.1021/JF061477I
https://doi.org/10.1081/JLC-100103396
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1081/JLC-100103396
https://doi.org/10.1021/JF061477I
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Thymonin 442662 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)O 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Salvianolic acid A 5281793 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C(C(=C(C=C2)O)O)C=CC3=CC(=C(C=C3)O)O)O)O 494.40 unknown https://doi.org/10.1002/JCCS.200300153

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