Scientific name	Authority	First published in
Rhagadiolus koelpinia	F.W.Schmidt	Samml. Phys.-Oekon. Aufsatze 1: 265. 1795
Lapsana koelpinia	L.f.	Suppl. Pl. : 248 (1782)
Koelpinia latifolia	C.Winkl.	Trudy Imp. S.-Peterburgsk. Bot. Sada xi. (1890) 284.
Rhagadiolus koelpinia	F.W.Schmidt	Samml. Phys. Aufsätze Böhm. Naturgesch. i. (1795) 265

Common names Top

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Language	Common/alternative name
Chinese	蝎尾菊

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Arabian Peninsula
  - Gulf States
  - Kuwait
  - Oman
  - Saudi Arabia
- Caucasus
  - Transcaucasus
- China
  - Tibet
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Western Asia
  - Afghanistan
  - Cyprus
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Sinai
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan
  - West Himalaya

Europe click to expand
- Eastern Europe
  - Central European Russia
  - South European Russia
  - Ukraine
- Southwestern Europe
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000083622
Tropicos	2702745
INPN	610671
KEW	urn:lsid:ipni.org:names:227574-1
The Plant List	gcc-401
Open Tree Of Life	1016037
Observations.org	132097
NCBI Taxonomy	122539
IPNI	227574-1
iNaturalist	513620
GBIF	3144493
EPPO	KOPLI
CMAUP	NPO5795

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

Classification, biosynthesis, and biological functions of triterpene esters in plants

Liu J, Yin X, Kou C, Thimmappa R, Hua X, Xue Z

Plant Commun

13-Feb-2024

PMCID:	PMC11009366
doi:	10.1016/j.xplc.2024.100845
PMID:	38356259

Variations in root architecture traits and their association with organ mass fraction of common annual ephemeral species in the desert of northern Xinjiang

Wang T, Liu B, Zhang X, Wang M, Tan D

Ecol Evol

07-Feb-2024

PMCID:	PMC10847883
doi:	10.1002/ece3.10908
PMID:	38327684

Plant as an Alternative Source of Antifungals against Aspergillus Infections: A Review

Tan LF, Yap VL, Rajagopal M, Wiart C, Selvaraja M, Leong MY, Tan PL

Plants (Basel)

08-Nov-2022

PMCID:	PMC9697101
doi:	10.3390/plants11223009
PMID:	36432738

New Insights Into the Relationships Within Subtribe Scorzonerinae (Cichorieae, Asteraceae) Using Hybrid Capture Phylogenomics (Hyb-Seq)

Hatami E, Jones KE, Kilian N

Front Plant Sci

01-Jul-2022

PMCID:	PMC9298463
doi:	10.3389/fpls.2022.851716
PMID:	35873957

Ecological significance of floristic composition and life forms of Riyadh region, Central Saudi Arabia

Al Shaye NA, Masrahi YS, Thomas J

Saudi J Biol Sci

17-Apr-2019

PMCID:	PMC6933222
doi:	10.1016/j.sjbs.2019.04.009
PMID:	31889814

Diversity of desert rangelands of Tunisia

Gamoun M, Belgacem AO, Louhaichi M

Plant Divers

20-Aug-2018

PMCID:	PMC6224667
doi:	10.1016/j.pld.2018.06.004
PMID:	30740567

Phytochemical standardization and biological activities of certain desert plants growing in Saudi Arabia

Al-Saleem MS, Awaad AS, Alothman MR, Alqasoumi SI

Saudi Pharm J

13-Dec-2017

PMCID:	PMC6111233
doi:	10.1016/j.jsps.2017.12.011
PMID:	30166916

Floristic diversity and vegetation analysis of Wadi Arar: A typical desert Wadi of the Northern Border region of Saudi Arabia

Osman AK, Al-Ghamdi F, Bawadekji A

Saudi J Biol Sci

18-Feb-2014

PMCID:	PMC4250517
doi:	10.1016/j.sjbs.2014.02.001
PMID:	25473364

The Relationship between Diaspore Characteristics with Phylogeny, Life History Traits, and Their Ecological Adaptation of 150 Species from the Cold Desert of Northwest China

Liu HL, Zhang DY, Duan SM, Wang XY, Song MF

ScientificWorldJournal

30-Jan-2014

PMCID:	PMC3925582
doi:	10.1155/2014/510343
PMID:	24605054

Floristic composition and vegetation analysis in Hail region north of central Saudi Arabia

El-Ghanim WM, Hassan LM, Galal TM, Badr A

Saudi J Biol Sci

13-Feb-2010

PMCID:	PMC3730706
doi:	10.1016/j.sjbs.2010.02.004
PMID:	23961067

Coumarins ofKoelpinia linearis

S. F. Dzhumyrko

Springer Science and Business Media LLC

20-Nov-2004

doi:	10.1007/BF00564819

Novel Nor and Seco Triterpenoids from Koelpinia linearis

W. A. Shah, M. Ya. Dar, M. A. Qurishi

Springer Science and Business Media LLC

27-Apr-2004

doi:	10.1023/B:CONC.0000025461.14074.F0

5β,24α-Stigmasta-8,22-dien-3β-ol, a sterol from Koelpinia linearis

W.A. Shah, M.A. Qurishi, S.K. Koul, K.L. Dhar

Elsevier BV

30-Apr-2003

doi:	10.1016/0031-9422(95)00620-6

Unusual homologous long-chain alkanoic acid esters of lupeol from Koelpinia linearis

T.K. Razdan, P.K. Kachroo, M.A. Qurishi, A.K. Kalla, E.S. Waight

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(95)00687-7

Koelpinin-A, B and C--three triterpenoids from Koelpinia linearis.

Koul S, Razdan TK, Andotra CS, Kalla AK, Koul S, Taneja SC, Dhar KL

Phytochemistry

01-Jan-2000

doi:	10.1016/S0031-9422(99)00490-2
PMID:	10680188

Phytochemical Profile Top

Add a new one!

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 / Naphthalenes
Microstegiol	403772	Click to see CC1=C2CCCC(C3(C2=C(C=C1)C=C(C3=O)C(C)C)O)(C)C	298.40	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Aethiopinone	157301	Click to see CC1=C(C2=C(C=C1)C=C(C(=O)C2=O)C(C)C)CCCC(=C)C	296.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
1-Oxoferruginol	15241260	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(C(=O)CCC3(C)C)C)O	300.40	unknown	via CMAUP database
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	via CMAUP database
Salviviridinol	102005790	Click to see CC(C)C1=C(C(=C2C(=C1)C(C(C3C2(CCCC3(C)C)C)O)O)O)OC	348.50	unknown	via CMAUP database
Sugiol	94162	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O	300.40	unknown	via CMAUP database
Viridone	102005792	Click to see CC(C)C1=CC2=CC(=C3C(CCCC3(C2=C(C1=O)O)C)(C)C)OC	328.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
[(3S,4aR,6aR,8aR,12aR,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-yl] acetate	5458941	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
Taraxerol acetate	94225	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
Taraxeryl acetate	5205968	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,4R,5aS,5bR,7aR,9S,11aR,11bR)-5a,5b,8,8,11a-pentamethyl-1-propan-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12-dodecahydro-1H-cyclopenta[a]chrysene-4,9-diol	101021047	Click to see CC(C)C1CCC2=C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
(1S,4R,5aS,5bR,7aS,9S,11aR,11bR)-5a,5b,8,8,11a-pentamethyl-1-propan-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12-dodecahydro-1H-cyclopenta[a]chrysene-4,9-diol	163071852	Click to see CC(C)C1CCC2=C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
(1S,5aS,5bR,7aR,9S,11aR,11bS)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-propan-2-yl-1,2,3,5,6,7,7a,9,10,11,11b,12-dodecahydrocyclopenta[a]chrysen-4-one	162933931	Click to see CC(C)C1CCC2=C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2=O)C)C)(C)C)O)C	424.70	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) heptadecanoate	14486638	Click to see CCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C	679.20	unknown	https://doi.org/10.1016/0031-9422(95)00687-7
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) octadecanoate	14486641	Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C	693.20	unknown	https://doi.org/10.1016/0031-9422(95)00687-7
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) pentadecanoate	14486633	Click to see CCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C	651.10	unknown	https://doi.org/10.1016/0031-9422(95)00687-7
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) tetradecanoate	14486630	Click to see CCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C	637.10	unknown	https://doi.org/10.1016/0031-9422(95)00687-7
(3S,6aR,6bR,8aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicen-3-ol	11611623	Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C	426.70	unknown	via CMAUP database
(4-hydroxy-5a,5b,8,8,11a-pentamethyl-1-propan-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12-dodecahydro-1H-cyclopenta[a]chrysen-9-yl) acetate	162881004	Click to see CC(C)C1CCC2=C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC(=O)C)C	468.70	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] heptadecanoate	14486640	Click to see CCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C	679.20	unknown	https://doi.org/10.1016/0031-9422(95)00687-7
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] octadecanoate	14486643	Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C	693.20	unknown	https://doi.org/10.1016/0031-9422(95)00687-7
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] pentadecanoate	14486635	Click to see CCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C	651.10	unknown	https://doi.org/10.1016/0031-9422(95)00687-7
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] tetradecanoate	14486632	Click to see CCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C	637.10	unknown	https://doi.org/10.1016/0031-9422(95)00687-7
[(1S,4R,5aS,5bR,7aR,9S,11aR,11bS)-4-hydroxy-5a,5b,8,8,11a-pentamethyl-1-propan-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12-dodecahydro-1H-cyclopenta[a]chrysen-9-yl] acetate	162881006	Click to see CC(C)C1CCC2=C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC(=O)C)C	468.70	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
5a,5b,8,8,11a-pentamethyl-1-propan-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12-dodecahydro-1H-cyclopenta[a]chrysene-4,9-diol	163071851	Click to see CC(C)C1CCC2=C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-propan-2-yl-1,2,3,5,6,7,7a,9,10,11,11b,12-dodecahydrocyclopenta[a]chrysen-4-one	162933930	Click to see CC(C)C1CCC2=C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2=O)C)C)(C)C)O)C	424.70	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
Germanicol	122857	Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
Koelpinin B	101021048	Click to see CC(C)C1CCC2=C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC(=O)C)C	468.70	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
Koelpinin C	101021049	Click to see CC(C)C1CCC2=C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2=O)C)C)(C)C)O)C	424.70	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
Lup-20(29)-ene-2alpha,3beta-diol	15127233	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C	442.70	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Lupeol palmitate	161739	Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C	665.10	unknown	https://doi.org/10.1016/0031-9422(95)00687-7
Olean-13(18)-ene-2beta,3beta-diol	101686479	Click to see CC1(CCC2(CCC3(C(=C2C1)CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C)C)C	442.70	unknown	via CMAUP database
Olean-18-en-3-ol	609334	Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
Sambuculin a	14486636	Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C	665.10	unknown	https://doi.org/10.1016/0031-9422(95)00687-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives
1-(9-Hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-1-yl)ethanone	13996054	Click to see CC(=O)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	428.70	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
29-Nor-20-oxolupeol	490365	Click to see CC(=O)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	428.70	unknown	https://doi.org/10.1016/S0031-9422(99)00490-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Viridinol	102005791	Click to see CC(C)C1=C(C2=CC(C3C(CCCC3(C2=C(C1=O)O)C)(C)C)O)OC	346.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,5R,10S,13R,14R,17R)-17-[(Z,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,7,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	162933765	Click to see CCC(C=CC(C)C1CCC2C1(CCC3=C2CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/0031-9422(95)00620-6
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,7,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	73188822	Click to see CCC(C=CC(C)C1CCC2C1(CCC3=C2CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/0031-9422(95)00620-6
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(95)00620-6
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(2S,4aR,5S,8aR)-5-[(2E)-2-[(2S,4aR,7R,8S,8aR)-2,4a,7,8-tetramethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ylidene]ethyl]-1,1,4a-trimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-ol	162876079	Click to see CC1CCC2(CCC(C(=CCC3C(=C)CCC4C3(CCC(C4(C)C)O)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1023/B:CONC.0000025461.14074.F0
(2S,4aR,5S,8aR)-5-[2-[(4aR,7R,8S,8aR)-2,4a,7,8-tetramethyl-4,5,6,7,8,8a-hexahydro-3H-naphthalen-1-yl]ethyl]-1,1,4a-trimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-ol	162940054	Click to see CC1CCC2(CCC(=C(C2C1C)CCC3C(=C)CCC4C3(CCC(C4(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1023/B:CONC.0000025461.14074.F0
5-[2-(2,4a,7,8-tetramethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ylidene)ethyl]-1,1,4a-trimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-ol	162876078	Click to see CC1CCC2(CCC(C(=CCC3C(=C)CCC4C3(CCC(C4(C)C)O)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1023/B:CONC.0000025461.14074.F0
5-[2-(2,4a,7,8-tetramethyl-4,5,6,7,8,8a-hexahydro-3H-naphthalen-1-yl)ethyl]-1,1,4a-trimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-ol	162940053	Click to see CC1CCC2(CCC(=C(C2C1C)CCC3C(=C)CCC4C3(CCC(C4(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1023/B:CONC.0000025461.14074.F0
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2S,4aR,5S,6S,8aR)-5-[(2E)-2-[(4aS,7R,8R,8aR)-7-hydroxy-4a,7,8-trimethyl-3,4,5,6,8,8a-hexahydro-2H-naphthalen-1-ylidene]ethyl]-1,1,4a,6-tetramethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-2-ol	163053369	Click to see CC1CCC2C(C(CCC2(C1CC=C3CCCC4(C3C(C(CC4)(C)O)C)C)C)O)(C)C	430.70	unknown	https://doi.org/10.1023/B:CONC.0000025461.14074.F0
5-[2-(7-hydroxy-4a,7,8-trimethyl-3,4,5,6,8,8a-hexahydro-2H-naphthalen-1-ylidene)ethyl]-1,1,4a,6-tetramethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-2-ol	163053368	Click to see CC1CCC2C(C(CCC2(C1CC=C3CCCC4(C3C(C(CC4)(C)O)C)C)C)O)(C)C	430.70	unknown	https://doi.org/10.1023/B:CONC.0000025461.14074.F0
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
[(8bS)-4,8b-dimethyl-3-(methylcarbamoyl)-2,3a-dihydro-1H-pyrrolo[2,3-b]indol-7-yl] N-methylcarbamate	3083935	Click to see CC12CCN(C1N(C3=C2C=C(C=C3)OC(=O)NC)C)C(=O)NC	318.37	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Cichoriin	442101	Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)OC3C(C(C(C(O3)CO)O)O)O	340.28	unknown	https://doi.org/10.1007/BF00564819
Esculin	5281417	Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O	340.28	unknown	https://doi.org/10.1007/BF00564819
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O	178.14	unknown	https://doi.org/10.1007/BF00564819

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Koelpinia linearis

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