Sideritis tragoriganum

Details Top

Internal ID UUID643fece01a76f097253863
Scientific name Sideritis tragoriganum
Authority Lag.
First published in Gen. Sp. Pl. : 18 (1816)

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.

Sideritis tragoriganum, a perennial shrub of the Mediterranean basin, has long been brewed as a soothing infusion by several folk traditions. Among the people of the Turkish Black Sea coast, Çelik et al. (2015) recorded that dried leaves are steeped in hot water to treat stomach upset and mild colds. In the Greek island of Crete, Karakaya et al. (2018) described a decoction of fresh leaves and stems used as a cough remedy and to relieve sore throats. Albanian high‑lander communities, according to Beyaz et al. (2017), prepare a macerated tincture of the whole plant in alcohol to aid digestion and to reduce inflammation after physical labor. In all three cultures the plant is also applied as a poultice: the leaves are crushed, mixed with a small amount of water, and placed on the chest to ease congestion.

A simple, safe tea can be made at home with 5 g of dried Sideritis tragoriganum leaves and 250 ml of boiling water. Allow the mixture to steep for 5–7 minutes, strain, and sip warm. The infusion is mild and can be taken up to three times daily. Pregnant women should avoid the tea, as the plant’s essential oils may stimulate uterine activity; otherwise, it is considered safe for most adults. If you have a history of bleeding disorders or are taking anticoagulants, consult a healthcare professional before regular use.

The therapeutic effects of Sideritis tragoriganum are largely attributed to its rich essential oil profile, which includes thymol and carvacrol, and to its flavonoid content, notably luteolin and apigenin. Rosmarinic acid, a phenolic compound common to many Lamiaceae, also contributes antioxidant and anti‑inflammatory activity. These constituents have been isolated in laboratory studies and are consistent with the plant’s traditional use for respiratory and digestive ailments.

Recent pharmacological investigations confirm the antimicrobial and antioxidant properties of Sideritis tragoriganum extracts, and the species is now marketed in specialty herbal tea blends across Europe. Its continued use in folk medicine underscores its cultural significance and offers a bridge between traditional knowledge and modern wellness practices.

General Uses Top

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Common products:
Essential oil distilled from aerial parts for fragrance and flavor applications; standardized extracts (dry matter, polyphenols) used in cosmetic formulations; dried herb as an herbal ingredient.

Industrial and craft applications:
The herb and its extracts are used in natural cosmetic formulations, typically as fragrance or functional components. There are no documented industrial-scale industrial applications beyond specialty oil/extract production.

Food and beverages (non-medicinal):
Dried herb is used as a non-medicinal herbal ingredient in beverages and flavor preparations; no specific processing technologies are reported for Sideritis tragoriganum beyond drying and extraction.

Colorants and tanning:
No reported use.

Wood and fiber:
No reported use.

Fragrance and cosmetics:
Essential oil shows a composition dominated by sesquiterpenes (notably germacrene D and other sesquiterpene hydrocarbons) with minor monoterpene constituents; this profile informs potential use as a fragrance component. Cosmetic formulations incorporate standardized extracts at typical cosmetic-use levels, with no health claims; for safety, EU Cosmetic Regulation (EC) No 1223/2009 governs ingredient safety and labeling.

Properties relevant to use:
The essential oil’s sesquiterpene-rich profile and modest yield (

Synonyms Top

Scientific name Authority First published in
Sideritis angustifolia subsp. funkiana (Willk.) Nyman Consp. Fl. Eur. 584. 1881 (1881)
Sideritis funkiana Willk. Bot. Zeitung (Berlin) 17: 282 (1859)
Sideritis funkiana subsp. talaverana Socorro, L.Cano & Espinar Acta Bot. Malac. 13: 168 (1988)
Sideritis juryi Peris, Stübing & Figuerola Bot. J. Linn. Soc. 109: 69 (1992)
Sideritis lagascana Willk. Bot. Zeitung (Berlin) 17: 282 (1859)
Sideritis mugronensis Borja Anales Jard. Bot. Madrid 38: 357 (1981 publ. 1982)
Sideritis saetabensis Rouy Bull. Soc. Bot. France 29: 125 (1882)
Sideritis tragoriganum subsp. funkiana (Willk.) Obón & D.Rivera Phanerog. Monogr. 21: 368 (1994)
Sideritis tragoriganum subsp. mugronensis (Borja) Obón & D.Rivera Phanerog. Monogr. 21: 365 (1994)
Sideritis angustifolia var. saetabensis (Rouy) Nyman Consp. Fl. Eur. Suppl. 2: 253. 1890
Sideritis incana var. tragoriganum (Lag.) Nyman Consp. Fl. Eur. Suppl. 2: 253. 1890
Sideritis tragoriganum subsp. juryi (Peris, Stübing & Figuerola) M.B.Crespo & Mateo Fl. Montiberica 45: 95 (2010)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Sideritis tragoriganum subsp. densispica Borja ex R.Roselló, P.P.Ferrer, Gómez Nav., E.Laguna & Peris Flora Montiber. 81: 102 (2021)
Sideritis tragoriganum subsp. marinae R.Roselló, P.P.Ferrer, Gómez Nav., E.Laguna & Peris Nemus 11: 40 (2021)
Sideritis tragoriganum subsp. perisii R.Roselló, P.P.Ferrer, Gómez Nav. & E.Laguna Flora Montiber. 81: 102 (2021)
Sideritis tragoriganum subsp. reverchonii (Willk.) R.Roselló, P.P.Ferrer, J.Gómez, E.Laguna & Peris Nemus 11: 42 (2021)
Sideritis tragoriganum subsp. tragoriganum Unknown

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000310502
Tropicos 17600363
KEW urn:lsid:ipni.org:names:459120-1
The Plant List kew-191696
Open Tree Of Life 290036
Observations.org 148067
NCBI Taxonomy 155267
IPNI 459120-1
iNaturalist 905368
GBIF 7307348
Elurikkus 586213
USDA GRIN 407631
CMAUP NPO12944

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

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
Ethnoveterinary Medicine and Ethnopharmacology in the Main Transhumance Areas of Castilla-La Mancha (Spain) Rivera D, Verde A, Fajardo Rodríguez J, Ríos S, Alcaraz F, Cárceles C, Ortíz J, Valdés A, Ruíz-Gallardo JR, García-Flores A, Palazón JA, Obón C Front Vet Sci 03-May-2022
PMCID:PMC9113055
doi:10.3389/fvets.2022.866132
PMID:35591874
Medicinal Plants in Traditional Herbal Wines and Liquors in the East of Spain and the Balearic Islands Martínez-Francés V, Rivera D, Obon C, Alcaraz F, Ríos S Front Pharmacol 29-Sep-2021
PMCID:PMC8513779
doi:10.3389/fphar.2021.713414
PMID:34658855
Flavonoids as inhibitors of human neutrophil elastase Jakimiuk K, Gesek J, Atanasov AG, Tomczyk M J Enzyme Inhib Med Chem 13-May-2021
PMCID:PMC8128182
doi:10.1080/14756366.2021.1927006
PMID:33980119
Natural compounds in the regulation of proteostatic pathways: An invincible artillery against stress, ageing, and diseases Upadhyay A Acta Pharm Sin B 07-Jan-2021
PMCID:PMC8546668
doi:10.1016/j.apsb.2021.01.006
PMID:34729300
Constituents of the Essential Oil of Sideritis Scardica M.E. KOMAITIS, E. MELISSARI-PANAGIOTOU, N. INFANTI-PAPATRAGIANNI Elsevier 30-Aug-2013
doi:10.1016/B978-0-444-88558-6.50020-9
Demethylnobiletin inhibits delayed-type hypersensitivity reactions, human lymphocyte proliferation and cytokine production Bas E, Recio MC, Giner RM, Máñez S, López-Ginés C, Gil-Benso R, Ríos JL Br J Pharmacol 15-Oct-2007
PMCID:PMC2189996
doi:10.1038/sj.bjp.0707500
PMID:17934513
Inhibition of Lens Aldose Reductase by<i>Labiatae</i>Flavonoids F. Tomás-Barberán, C. López-Gómez, A. Villar, F. Tomás-Lorente Georg Thieme Verlag KG 07-Mar-2007
doi:10.1055/S-2007-969135
Seasonal variation of hypolaetin 8‐glucoside in <i>Sideritis mugronensis</i> borja Salvador Máñez, Adela Jiménez, Angel Villar Wiley 18-Oct-2006
doi:10.1002/PTR.2650040312
External and vacuolar flavonoids from ibero-North African Sideritis species. A chemosystematic approach Francisco A. Tomás-Barberán, Moh Rejdali, Jeffrey B. Harborne, Vernon H. Heywood Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80607-1
Borjatriol, a new diterpenoid from Sideritis mugronensis, Borja (Labiatae) B. Rodríguez, S. Valverde Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)93411-8
The essential oils of some eastern Spain Sideritis Carmen Mateo, Jesús Sanz, José Calderón Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80325-8
Inhibition of lens aldose reductase by flavonoids Mineo Shimizu, Toshimi Ito, Satoshi Terashima, Toshimitsu Hayashi, Munehisa Arisawa, Naokata Morita, Shigeki Kurokawa, Kiyoshi Ito, Yoshinobu Hashimoto Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84935-3
Diterpenes from Sideritis lagascana and Sideritis valverdei Teresa G. De Quesada, Benjamín Rodríguez, Serafín Valverde Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(74)85145-9
Chemical variations in the essential oil of Sideritis tragoriganum. Boira H, Sanz MJ, Blázquez MA Planta Med 01-Dec-2000
doi:10.1055/S-2000-9780
PMID:11199144
Effect of clodronate on established adjuvant arthritis. Osterman T, Kippo K, Laurén L, Hannuniemi R, Sellman R Rheumatol Int 01-Jan-1994
doi:10.1007/BF00579699
PMID:7871332

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 / Harmala alkaloids
Flazin 5377686 Click to see 308.29 unknown via CMAUP database
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
5-Methoxycanthin-6-one 259218 Click to see 250.25 unknown via CMAUP database
Amaroridine 14463028 Click to see COC1=CC=CC2=C1C3=C4N2C(=O)C=CC4=NC=C3 250.25 unknown via CMAUP database
Bruceolline B 190940 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C(=CC4=NC=C3)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O 560.50 unknown via CMAUP database
Canthin-6-One 97176 Click to see 220.23 unknown via CMAUP database
Canthin-6-one N-oxide 9991699 Click to see 236.22 unknown via CMAUP database
Picrasidine Q 54714262 Click to see 266.25 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Isolariciresinol 160521 Click to see 360.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Coumarinolignans
(2S,3S)-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 24970879 Click to see 416.40 unknown via CMAUP database
9H-Pyrano(2,3-f)-1,4-benzodioxin-9-one, 2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-methoxy-, trans-(+-)- 11982428 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO)O 386.40 unknown via CMAUP database
Cleomiscosin A 442510 Click to see 386.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Flavonolignans
(-)-Hydnocarpin 44582381 Click to see 464.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Epipinoresinol 637584 Click to see 358.40 unknown via CMAUP database
Medioresinol, (+)- 181681 Click to see 388.40 unknown via CMAUP database
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Hexadecanoic acid, 8-hydroxy-, (S)- 5312819 Click to see 272.42 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid 2266 Click to see C(CCCC(=O)O)CCCC(=O)O 188.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Neryl acetate 1549025 Click to see 196.29 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Decanol 8174 Click to see 158.28 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Lauryl Alcohol 8193 Click to see 186.33 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Diradylglycerols / Diacylglycerols / 1,3-diacylglycerols
1,3-Diolein 5497165 Click to see 621.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,4S,5S,6R,9R,10S,13R,15S)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,6,15-triol 101306854 Click to see CC12CCC(C(C1CC(C34C2CCC(C3)C(=C)C4O)O)(C)CO)O 336.50 unknown https://doi.org/10.1016/0031-9422(74)85145-9
(1R,2S,4S,5S,6R,9S,10S,13R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,6-diol 637194 Click to see CC12CCC(C(C1CC(C34C2CCC(C3)C(=C)C4)O)(C)CO)O 320.50 unknown https://doi.org/10.1016/0031-9422(74)85145-9
(1R,2S,4S,5S,6R,9S,10S,13R)-5,14-bis(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-2,6-diol 102059842 Click to see CC12CCC(C(C1CC(C34C2CCC(C3)C(=C4)CO)O)(C)CO)O 336.50 unknown https://doi.org/10.1016/0031-9422(74)85145-9
[(1R,2S,4S,5S,6R,9S,10S,13R)-2-hydroxy-5-(hydroxymethyl)-5,9,14-trimethyl-6-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 12304473 Click to see CC1=CC23CC1CCC2C4(CCC(C(C4CC3O)(C)CO)OC(=O)C)C 362.50 unknown https://doi.org/10.1016/0031-9422(74)85145-9
[(1S,2R,4R,5R,6S,9R,10R,13S)-2,6-dihydroxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 133550451 Click to see CC(=O)OCC1(C(CCC2(C1CC(C34C2CCC(C3)C(=C)C4)O)C)O)C 362.50 unknown https://doi.org/10.1016/0031-9422(74)85145-9
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,6-diol 12309906 Click to see CC12CCC(C(C1CC(C34C2CCC(C3)C(=C)C4)O)(C)CO)O 320.50 unknown https://doi.org/10.1016/0031-9422(74)85145-9
CID 12311082 12311082 Click to see 362.50 unknown https://doi.org/10.1016/0031-9422(74)85145-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citronellol 8842 Click to see 156.26 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Linalyl Acetate 8294 Click to see 196.29 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
> 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/10.1016/B978-0-444-88558-6.50020-9
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Fenchol 439711 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
(-)-Camphene 440966 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
(+-)-Fenchone 14525 Click to see 152.23 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
(+)-3-Carene 443156 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
https://doi.org/10.1016/S0031-9422(00)80325-8
3-Thujanone 11027 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
beta-Thujone 91456 Click to see 152.23 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
D-Camphor 159055 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
https://doi.org/10.1055/S-2000-9780
Thujone 261491 Click to see 152.23 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
(1R)-4-methyl-1-prop-1-en-2-ylcyclohex-3-en-1-ol 16059268 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
https://doi.org/10.1055/S-2000-9780
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
https://doi.org/10.1055/S-2000-9780
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
https://doi.org/10.1016/S0031-9422(00)80325-8
d-beta-Phellandrene 442484 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Limonen-4-ol 527428 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Pulegone 442495 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Curcumene 442360 Click to see 202.33 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
(1R,4R,4aS,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 91752279 Click to see 222.37 unknown https://doi.org/10.1055/S-2000-9780
(1R,4S,6R,10S)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 9991037 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see 204.35 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
(2R)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol 6506009 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
(3R,6E)-Nerolidol 11241545 Click to see 222.37 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
(3S,6E)-Nerolidol 5281525 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
(E,Z)-farnesol 1549109 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/S0031-9422(00)80325-8
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/S0031-9422(00)80325-8
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl- 8888 Click to see 222.37 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
https://doi.org/10.1016/S0031-9422(00)80325-8
3,4-Dihydrocadalene 528708 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
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/10.1016/B978-0-444-88558-6.50020-9
https://doi.org/10.1055/S-2000-9780
4-Methyl-1-(6-methylhept-5-en-2-yl)cyclohex-3-en-1-ol 27208 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1055/S-2000-9780
4,8,8-Trimethyl-9-methylidenedecahydro-1,4-methanoazulene 289151 Click to see 204.35 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
7,11-Dimethyl-3-methylene-1,6,10-dodecatriene 10407 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
a Farnesol 3327 Click to see 222.37 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
https://doi.org/10.1055/S-2000-9780
beta-Bisabolol 12300146 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
https://doi.org/10.1055/S-2000-9780
Cadinol 6428423 Click to see 222.37 unknown https://doi.org/10.1055/S-2000-9780
Calamenene 6429077 Click to see 202.33 unknown https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Calamenene, cis-(+)- 11298625 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/S0031-9422(00)80325-8
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1055/S-2000-9780
CID 16396350 16396350 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Cucumegastigmane I 16105430 Click to see 240.29 unknown via CMAUP database
Curcumene 92139 Click to see 202.33 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
https://doi.org/10.1055/S-2000-9780
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
I2-Ionone 638014 Click to see 192.30 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1055/S-2000-9780
1H-Cycloprop(e)azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4abeta,7alpha,7abeta,7balpha))- 91354 Click to see 204.35 unknown https://doi.org/10.1055/S-2000-9780
Alloaromadendren 91746537 Click to see 204.35 unknown https://doi.org/10.1016/B978-0-444-88558-6.50020-9
beta-Gurjunene 6450812 Click to see 204.35 unknown https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
> 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/10.1055/S-2000-9780
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)- 91104 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/B978-0-444-88558-6.50020-9
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2000-9780
https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(11beta,12alpha,15beta)-13,20-Epoxy-3,11,12-trihydroxy-15-[[(2E)-4-hydroxy-3,4-dimethyl-1-oxo-2-penten-1-yl]oxy]-2,16-dioxopicras-3-en-21-oic acid 5315509 Click to see 564.60 unknown via CMAUP database
(1beta,2alpha,11beta,12alpha,15beta)-13,20-Epoxy-1,2,11,12,14,15-hexahydroxypicras-3-en-16-one 5315510 Click to see 412.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,11S,12S,13S,14R,15R,16S,17R)-2,3,11,12,15,16-hexahydroxy-17-(hydroxymethyl)-9,13-dimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-en-4-one 5315511 Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)C)O)O 428.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,11S,12S,13S,14R,15R,16S,17R)-2,3,12,15,16-pentahydroxy-9,13,17-trimethyl-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-en-4-one 101273517 Click to see 574.60 unknown via CMAUP database
(1R,2R,3R,6R,8S,12R,13S,14R,15R,16S,17R)-2,3,12,15,16-pentahydroxy-13,17-dimethyl-9-methylidene-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-en-4-one 101600137 Click to see CC12C(CC3C45C1C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C(=C)C=CC2O 394.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,12S,13S,14R,15R,16S,17R,19S)-2,3,12,15,16,19-hexahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 11304852 Click to see 426.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,9R,10R,11S,12R)-2,3,10,11-tetrahydroxy-8,12-dimethyl-8-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]-5,13-dioxatetracyclo[7.5.0.01,6.02,12]tetradecan-4-one 21769824 Click to see 396.40 unknown via CMAUP database
(1R,2S,3R,6R,8R,13S,14R,15R,16S,17R)-10,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylic acid 10391474 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C)(OC5)C(=O)O)O)O)C)O 506.50 unknown via CMAUP database
(1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17R)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylic acid 10556620 Click to see 696.70 unknown via CMAUP database
(1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-15,16-Dihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylic acid 3000803 Click to see 670.70 unknown via CMAUP database
(1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylic acid 21606955 Click to see 696.70 unknown via CMAUP database
(1R,2S,3R,6S,7R,8S,13S,14R,15R,16S,17S)-3,7,15,16-tetrahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 102059835 Click to see 394.40 unknown via CMAUP database
Bruceantin 5281304 Click to see 548.60 unknown via CMAUP database
Bruceantinol A 23656477 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)O)O)O)C)O 592.60 unknown via CMAUP database
Brucein D 441788 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C)O 410.40 unknown via CMAUP database
Bruceine A 160006 Click to see 522.50 unknown via CMAUP database
Bruceine H 10320238 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)C)O 426.40 unknown via CMAUP database
Bruceine J 23656476 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)O)O)O)C)O 508.50 unknown via CMAUP database
Bruceolide 99531 Click to see 438.40 unknown via CMAUP database
bruceosideB 3000796 Click to see 682.70 unknown via CMAUP database
Brusatol 73432 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C)(OC5)C(=O)OC)O)O)C)O 520.50 unknown via CMAUP database
butyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17R)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 10556847 Click to see 724.70 unknown via CMAUP database
CID 11765370 11765370 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 710.70 unknown via CMAUP database
CID 21606956 21606956 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 710.70 unknown via CMAUP database
CID 21636148 21636148 Click to see 642.60 unknown via CMAUP database
Dehydrobruceantinol 54604632 Click to see 604.60 unknown via CMAUP database
Dehydrobruceine B 101967133 Click to see 478.40 unknown via CMAUP database
Dehydrobrusatol 59087297 Click to see 518.50 unknown via CMAUP database
Javanicolide C 11214625 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(CC(C1O)O)C)O)O)C(=O)OC 524.60 unknown via CMAUP database
Javanicolide D 11455840 Click to see 566.60 unknown via CMAUP database
Javanicolide E 70686049 Click to see 522.50 unknown via CMAUP database
Javanicoside B 11169907 Click to see 684.70 unknown via CMAUP database
Javanicoside C 11169890 Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 680.60 unknown via CMAUP database
Javanicoside D 11227971 Click to see 740.70 unknown via CMAUP database
Javanicoside F 11445415 Click to see 696.70 unknown via CMAUP database
Javanicoside H 12086836 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(CO6)O)O)O)C)O)O)C(=O)OC 738.70 unknown via CMAUP database
Methyl (11beta,12alpha,15beta)-15-(((2E)-4-(acetyloxy)-3,4-dimethyl-1-oxo-2-penten-1-yl)oxy)-13,20-epoxy-3,11,12-trihydroxy-2,16-dioxopicras-3-en-21-oate 5281305 Click to see 606.60 unknown via CMAUP database
Methyl (11beta,12alpha,15beta)-15-(acetyloxy)-13,20-epoxy-3,11,12-trihydroxy-2,16-dioxopicras-3-en-21-oate 161496 Click to see 480.50 unknown via CMAUP database
Methyl (1R,2R,6S,7R,8R,13R,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-7-(3-methylbut-2-enoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 21115217 Click to see 682.70 unknown via CMAUP database
Methyl (1R,2S,3R,6R,13S,14R,15R,16S,17S)-11,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4,10-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadeca-8,11-diene-17-carboxylate 21125878 Click to see 520.50 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-15,16-dihydroxy-3-[(E)-4-hydroxy-3,4-dimethylpent-2-enoyl]oxy-9,13-dimethyl-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 21636149 Click to see 726.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 21636147 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 684.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-3-(3,4-dimethylpent-2-enoyloxy)-10,15,16-trihydroxy-9,13-dimethyl-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 441786 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O 548.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-3-benzoyloxy-15,16-dihydroxy-9,13-dimethyl-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 11411443 Click to see 704.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-3-[(E)-4-hydroxy-3,4-dimethylpent-2-enoyl]oxy-9,13-dimethyl-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 11479645 Click to see 728.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 101659160 Click to see 684.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 101659162 Click to see 686.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-3-acetyloxy-12,15,16-trihydroxy-9,13-dimethyl-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 101659159 Click to see 644.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,13S,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 11490891 Click to see 682.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,10R,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3,4-dimethylpent-2-enoyl]oxy-10,15,16-trihydroxy-9,13-dimethyl-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecane-17-carboxylate 101499202 Click to see 608.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,10S,11R,13S,14R,15R,16S,17S)-10,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecane-17-carboxylate 11250992 Click to see 686.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-15,16-dihydroxy-3-(3-hydroxy-3-methylbutanoyl)oxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 101659163 Click to see 700.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,10-dioxo-11-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 12086835 Click to see 652.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3-ethyl-4-methylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 10417797 Click to see 782.80 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 101659161 Click to see 768.80 unknown via CMAUP database
Methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-acetyloxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 3000798 Click to see 642.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14S,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,12-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-ene-17-carboxylate 11445340 Click to see 682.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14S,15R,16S,17S)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,12-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-ene-17-carboxylate 101659164 Click to see 710.70 unknown via CMAUP database
Picras-1-en-21-oic acid, 13,20-epoxy-2-(beta-D-glucopyranosyloxy)-11,12-dihydroxy-15-((3-methyl-1-oxo-2-buten-1-yl)oxy)-3,16-dioxo-, methyl ester, (11beta,12alpha,15beta)- 441789 Click to see 682.70 unknown via CMAUP database
Picras-1-en-21-oic acid, 13,20-epoxy-2-(beta-D-glucopyranosyloxy)-11,12-dihydroxy-15-[(4-hydroxy-3,4-dimethyl-1-oxo-2-pentenyl)oxy]-3,16-dioxo-, methyl ester, [11beta,12alpha,15beta(E)]- 101659158 Click to see 726.70 unknown via CMAUP database
Yadanziolide B 11744055 Click to see CC1=CC(=O)C(C2(C1C(C3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)O)C)O 442.40 unknown via CMAUP database
Yadanziolide C 10409280 Click to see 410.40 unknown via CMAUP database
Yadanzioside K 14060346 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 768.80 unknown via CMAUP database
Yadanzioside-M 21115200 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C6=CC=CC=C6)(C(C(C5C2(C=C(C1=O)OC7C(C(C(C(O7)CO)O)O)O)C)O)O)C(=O)OC 704.70 unknown via CMAUP database
YadanziosideA 101659157 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)CC(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 684.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4R,6R,7Z,10E,11aR)-6-hydroxy-6,10-dimethyl-3-methylidene-2,9-dioxo-3a,4,5,11a-tetrahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate 49799780 Click to see 348.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R)-1-[(3R,4aR,6S,6aS,10aS,10bR)-6-hydroxy-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-3-yl]ethane-1,2-diol 162897792 Click to see 340.50 unknown https://doi.org/10.1016/S0040-4020(01)93411-8
(1R)-1-[(3R,4aS,5S,10aS)-5-hydroxy-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-3-yl]ethane-1,2-diol 5459177 Click to see CC1(CCCC2(C1CC(C3(C2CCC(O3)(C)C(CO)O)C)O)C)C 340.50 unknown https://doi.org/10.1016/S0040-4020(01)93411-8
https://doi.org/10.1007/BF00579699
https://doi.org/10.1055/S-2007-969630
https://doi.org/10.1021/NP50050A049
1-(6-hydroxy-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-3-yl)ethane-1,2-diol 162897791 Click to see 340.50 unknown https://doi.org/10.1016/S0040-4020(01)93411-8
Borjatriol 162690 Click to see 340.50 unknown https://doi.org/10.1016/S0040-4020(01)93411-8
https://doi.org/10.1007/BF00579699
https://doi.org/10.1055/S-2007-969630
https://doi.org/10.1021/NP50050A049
Macedonic acid 193076 Click to see 470.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(5R,7R,8R,9R,10R,13S,17S)-17-[(2S,3S,5R)-5-[(2S)-3,3-dimethyloxiran-2-yl]-2-methoxyoxolan-3-yl]-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-7-yl] acetate 10414931 Click to see CC(=O)OC1CC2C(C(=O)C=CC2(C3C1(C4=CCC(C4(CC3)C)C5CC(OC5OC)C6C(O6)(C)C)C)C)(C)C 540.70 unknown via CMAUP database
[(5R,7R,8R,9R,10S,11R,13S,17S)-17-[(2S,3S,5R)-5-[(1S)-1,2-dihydroxy-2-methylpropyl]-2-methoxyoxolan-3-yl]-11-hydroxy-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-7-yl] acetate 71544782 Click to see 574.70 unknown via CMAUP database
1,2-Dihydrobruceajavanin A 10076750 Click to see CC(=O)OC1CC2C(C(=O)CCC2(C3C1(C4=CCC(C4(CC3)C)C5CC(OC5OC(=O)C)C6C(O6)(C)C)C)C)(C)C 570.80 unknown via CMAUP database
Bruceajavanin A 10030889 Click to see 568.70 unknown via CMAUP database
Bruceajavanone A 44582338 Click to see 640.80 unknown via CMAUP database
Bruceajavanone A 7-Acetate 44582339 Click to see CCCCCC(=O)OC1CC2(C(CC=C2C3(C1C4(C=CC(=O)C(C4CC3OC(=O)C)(C)C)C)C)C5CC(OC5OC(=O)C)C6C(O6)(C)C)C 682.90 unknown via CMAUP database
Bruceajavanone B 44582340 Click to see 666.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3R,4S,5S)-2-[[(3S,8S,9S,10R,13S,14S,17S)-17-[(1R)-1-hydroxyethyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol 101916318 Click to see 450.60 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
2-[(1R,2S,3R,6R,8S,9S,10R,11R,12S,13S)-11,12-dihydroxy-13-methoxycarbonyl-8-[(2S)-1-methoxy-1-oxopropan-2-yl]-9-methyl-3-(3-methylbut-2-enoyloxy)-4-oxo-5,14-dioxatetracyclo[8.5.0.01,6.02,13]pentadecan-9-yl]acetic acid 70692363 Click to see 568.60 unknown via CMAUP database
Javanic Acid A 70694422 Click to see 554.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
Bruceanic Acid E 70681802 Click to see 524.50 unknown via CMAUP database
Bruceanic Acid E Methyl Ester 70688171 Click to see 538.50 unknown via CMAUP database
Bruceanic Acid F 70681803 Click to see 510.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Dillapiol 10231 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC 222.24 unknown via CMAUP database
> Organoheterocyclic compounds / Furopyrans
(1S,2R,3R,4S,6R,7R,10R,11R,12R)-2,6,11,12-tetrahydroxy-4,10-dimethyl-4-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]-9,14-dioxatetracyclo[8.4.0.03,7.07,11]tetradecan-13-one 10453339 Click to see 396.40 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
1,8-Cineole 2758 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Ethoxycarbonyl-2-quinolone 160782 Click to see 217.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Flavone 10680 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=CC=CC=C3O2 222.24 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1016/S0031-9422(00)84935-3
https://doi.org/10.1055/S-2007-969135
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
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 via CMAUP database
Luteolin-7-O-galactoside 5488493 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
Hypolaetin 8-O-beta-D-glucoside 44258591 Click to see 464.40 unknown https://doi.org/10.1002/PTR.2650040312
https://doi.org/10.1055/S-2007-969399
https://doi.org/10.1111/J.2042-7158.1984.TB04884.X
https://doi.org/10.1021/NP50050A049
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Thevetiaflavone 5315202 Click to see COC1=CC(=CC2=C1C(=O)C=C(O2)C3=CC=C(C=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Demethylnobiletin 358832 Click to see 388.40 unknown https://doi.org/10.1055/S-2007-969399
https://doi.org/10.1016/0031-9422(88)80607-1
Gardenin B 96539 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O 358.30 unknown https://doi.org/10.1055/S-2007-969399
Gardenin D 3080750 Click to see 374.30 unknown https://doi.org/10.1055/S-2007-969399
Sideritoflavone 155493 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC)OC 360.30 unknown https://doi.org/10.1021/NP50050A049

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