Scientific name	Authority	First published in
Linosyris montana	DC.	Prodr. 5: 352 (1836)
Chrysocoma montana	Vahl	Symb. Bot. i. 70
Jasonia montana	(Vahl) Botsch.	Novosti Sist. Vyssh. Rast. 365 (1964)
Varthemia conyzoides	Boiss.	Diagn. Pl. Orient. , ser. 2, 3: 10 (1856)
Inula conyzoides	DC.	Prodr. 7(1): 283 (1838)
Varthemia montana	Boiss.	Fl. Orient. 3: 212 (1875)

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	كتيلة جبلية

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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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
  - Egypt

Asia-temperate click to expand
- Arabian Peninsula
  - Saudi Arabia
- Western Asia
  - Palestine
  - Sinai

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000065727
KEW	urn:lsid:ipni.org:names:192779-1
The Plant List	gcc-2263
Open Tree Of Life	7051731
NCBI Taxonomy	1458965
IPNI	192779-1
iNaturalist	634007
GBIF	3089831
CMAUP	NPO5020

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

Polyphenols of the Inuleae-Inulinae and Their Biological Activities: A Review

Malarz J, Michalska K, Stojakowska A

Molecules

27-Apr-2024

PMCID:	PMC11085778
doi:	10.3390/molecules29092014
PMID:	38731504

Antimicrobial Potential of Different Isolates of Chaetomium globosum Combined with Liquid Chromatography Tandem Mass Spectrometry Chemical Profiling

Goda MS, El-Kattan N, Abdel-Azeem MA, Allam KA, Badr JM, Nassar NA, Almalki AJ, Alharbi M, Elhady SS, Eltamany EE

Biomolecules

21-Nov-2023

PMCID:	PMC10742071
doi:	10.3390/biom13121683
PMID:	38136556

Fungal Endophytes: Microfactories of Novel Bioactive Compounds with Therapeutic Interventions; A Comprehensive Review on the Biotechnological Developments in the Field of Fungal Endophytic Biology over the Last Decade

Gupta A, Meshram V, Gupta M, Goyal S, Qureshi KA, Jaremko M, Shukla KK

Biomolecules

25-Jun-2023

PMCID:	PMC10377637
doi:	10.3390/biom13071038
PMID:	37509074

An insight into endophytic antimicrobial compounds: an updated analysis

Digra S, Nonzom S

Plant Biotechnol Rep

14-Mar-2023

PMCID:	PMC10013304
doi:	10.1007/s11816-023-00824-x
PMID:	37359493

In Vitro Cultures and Volatile Organic Compound Production in Chiliadenus montanus (Vhal.) Brullo

Abu-Darwish D, Shibli R, Al-Abdallat AM

Plants (Basel)

17-May-2022

PMCID:	PMC9148159
doi:	10.3390/plants11101326
PMID:	35631753

Trichoderma: An Eco-Friendly Source of Nanomaterials for Sustainable Agroecosystems

Alghuthaymi MA, Abd-Elsalam KA, AboDalam HM, Ahmed FK, Ravichandran M, Kalia A, Rai M

J Fungi (Basel)

02-Apr-2022

PMCID:	PMC9027617
doi:	10.3390/jof8040367
PMID:	35448598

Phenolic and flavonoid contents and antioxidant activity of an endophytic fungus Nigrospora sphaerica (EHL2), inhabiting the medicinal plant Euphorbia hirta (dudhi) L.

Gautam VS, Singh A, Kumari P, Nishad JH, Kumar J, Yadav M, Bharti R, Prajapati P, Kharwar RN

Arch Microbiol

17-Jan-2022

PMCID:	PMC8763303
doi:	10.1007/s00203-021-02650-7
PMID:	35039945

Targeting Mammalian 5-Lipoxygenase by Dietary Phenolics as an Anti-Inflammatory Mechanism: A Systematic Review

Giménez-Bastida JA, González-Sarrías A, Laparra-Llopis JM, Schneider C, Espín JC

Int J Mol Sci

25-Jul-2021

PMCID:	PMC8348464
doi:	10.3390/ijms22157937
PMID:	34360703

Harnessing Bacterial Endophytes for Promotion of Plant Growth and Biotechnological Applications: An Overview

Eid AM, Fouda A, Abdel-Rahman MA, Salem SS, Elsaied A, Oelmüller R, Hijri M, Bhowmik A, Elkelish A, Hassan SE

Plants (Basel)

07-May-2021

PMCID:	PMC8151188
doi:	10.3390/plants10050935
PMID:	34067154

A sulfated polyphenols-rich extract from Sabal yapa exhibits antitumor activities in Ehrlich ascites carcinoma

Fahmi AA, El Raey MA, Ibrahim AY, Abdelfattah MA, Abdelmageed AM, Sobeh M

Saudi J Biol Sci

21-Feb-2021

PMCID:	PMC8117008
doi:	10.1016/j.sjbs.2021.02.056
PMID:	34012333

Farnesane-Type Sesquiterpenoids with Antibiotic Activity from Chiliadenus lopadusanus

Masi M, Roscetto E, Cimmino A, Catania MR, Surico G, Evidente A

Antibiotics (Basel)

02-Feb-2021

PMCID:	PMC7913021
doi:	10.3390/antibiotics10020148
PMID:	33540688

Jaceidin Flavonoid Isolated from Chiliadenus montanus Attenuates Tumor Progression in Mice via VEGF Inhibition: In Vivo and In Silico Studies

Elhady SS, Eltamany EE, Shaaban AE, Bagalagel AA, Muhammad YA, El-Sayed NM, Ayyad SN, Ahmed AA, Elgawish MS, Ahmed SA

Plants (Basel)

14-Aug-2020

PMCID:	PMC7464537
doi:	10.3390/plants9081031
PMID:	32823927

Anti-rheumatoid Activity of Secondary Metabolites Produced by Endophytic Chaetomium globosum

Abdel-Azeem AM, Zaki SM, Khalil WF, Makhlouf NA, Farghaly LM

Front Microbiol

20-Sep-2016

PMCID:	PMC5029229
doi:	10.3389/fmicb.2016.01477
PMID:	27703452

Endophytic Actinobacteria and the Interaction of Micromonospora and Nitrogen Fixing Plants

Trujillo ME, Riesco R, Benito P, Carro L

Front Microbiol

01-Dec-2015

PMCID:	PMC4664631
doi:	10.3389/fmicb.2015.01341
PMID:	26648923

Jasonone, a Nor-sesquiterepene from Jasonia montana

Abou El-Hamd H. Mohamed

Walter de Gruyter GmbH

16-Feb-2015

doi:	10.1515/ZNB-2007-0119

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 / Benzene and substituted derivatives / Xylenes / m-Xylenes
2-(Butoxymethyl)-2-(2,4-dimethylphenyl)oxirane	163004469	Click to see CCCCOCC1(CO1)C2=C(C=C(C=C2)C)C	234.33	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
> Benzenoids / Phenol esters
[(2R)-2-[4-methyl-2-(2-methylpropanoyloxy)phenyl]oxiran-2-yl]methyl 2-methylpropanoate	25837754	Click to see CC1=CC(=C(C=C1)C2(CO2)COC(=O)C(C)C)OC(=O)C(C)C	320.40	unknown	via CMAUP database
> Benzenoids / Phenol ethers
(2R)-2-[[(2S)-butan-2-yl]oxymethyl]-2-[2-[(2R)-butan-2-yl]oxy-4-methylphenyl]oxirane	163072811	Click to see CCC(C)OCC1(CO1)C2=C(C=C(C=C2)C)OC(C)CC	292.40	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
2-(Butan-2-yloxymethyl)-2-(2-butan-2-yloxy-4-methylphenyl)oxirane	163072810	Click to see CCC(C)OCC1(CO1)C2=C(C=C(C=C2)C)OC(C)CC	292.40	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
(3E,6E)-2,6-Dimethyl-8-acetoxy-3,6-octadien-2-ol	14191351	Click to see CC(=CCOC(=O)C)CC=CC(C)(C)O	212.28	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
(7-Hydroxy-3,7-dimethylocta-2,5-dienyl) acetate	129684587	Click to see CC(=CCOC(=O)C)CC=CC(C)(C)O	212.28	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2E,6R)-3,7-dimethylocta-2,7-diene-1,6-diol	11229042	Click to see CC(=C)C(CCC(=CCO)C)O	170.25	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
(2R,3E,6E)-2,6-dimethylocta-3,6-diene-1,2,8-triol	162903140	Click to see CC(=CCO)CC=CC(C)(CO)O	186.25	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
(2S,3E,6E)-2,6-dimethylocta-3,6-diene-1,2,8-triol	162903139	Click to see CC(=CCO)CC=CC(C)(CO)O	186.25	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
2,6-Dimethylocta-3,6-diene-1,2,8-triol	129684633	Click to see CC(=CCO)CC=CC(C)(CO)O	186.25	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
3,7-Dimethylocta-2,7-diene-1,6-diol	71349850	Click to see CC(=C)C(CCC(=CCO)C)O	170.25	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(2R,5R)-5-(2-hydroxypropan-2-yl)-2-methyl-2-(4-oxopentyl)cyclohexan-1-one	11172838	Click to see CC(=O)CCCC1(CCC(CC1=O)C(C)(C)O)C	254.36	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
5-(2-Hydroxypropan-2-yl)-2-methyl-2-(4-oxopentyl)cyclohexan-1-one	13895700	Click to see CC(=O)CCCC1(CCC(CC1=O)C(C)(C)O)C	254.36	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(6E)-10-hydroxy-2,6,10-trimethyldodeca-6,11-dien-4-one	102125253	Click to see CC(C)CC(=O)CC(=CCCC(C)(C=C)O)C	238.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.027
(6R,9E)-11-methoxy-3,7,11-trimethyldodeca-1,9-diene-3,6,7-triol	102125252	Click to see CC(C)(C=CCC(C)(C(CCC(C)(C=C)O)O)O)OC	286.41	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.027
3-methyl-5-[(3R,6S)-4-methylidene-6-(2-methylprop-1-enyl)dioxan-3-yl]pent-1-en-3-ol	102125250	Click to see CC(=CC1CC(=C)C(OO1)CCC(C)(C=C)O)C	252.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.027
3-methyl-5-[(3S,6S)-4-methylidene-6-(2-methylprop-1-enyl)dioxan-3-yl]pent-1-en-3-ol	102125251	Click to see CC(=CC1CC(=C)C(OO1)CCC(C)(C=C)O)C	252.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.027
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4S,4aR,6S,8aR)-4,8a-dimethyl-6-prop-1-en-2-yl-2,3,4a,5,7,8-hexahydro-1H-naphthalene-1,4,6-triol	102125249	Click to see CC(=C)C1(CCC2(C(CCC(C2C1)(C)O)O)C)O	254.36	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.027
(3R,4aR,8aR)-3-(2-hydroxypropan-2-yl)-8a-methyl-5-methylidene-2,3,4,6,7,8-hexahydro-1H-naphthalen-4a-ol	14705655	Click to see CC12CCCC(=C)C1(CC(CC2)C(C)(C)O)O	238.37	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
(3R,4aS,8aR)-3-(2-hydroxypropan-2-yl)-8a-methyl-5-methylidene-2,3,4,6,7,8-hexahydro-1H-naphthalen-4a-ol	14705656	Click to see CC12CCCC(=C)C1(CC(CC2)C(C)(C)O)O	238.37	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
1,4,7-Eudesmanetriol	101634632	Click to see CC(C)C1(CCC2(C(CCC(C2C1)(C)O)O)C)O	256.38	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.027
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoic acid	12304100	Click to see CC12CCCC(=C)C1CC(CC2)C(=C)C(=O)O	234.33	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
2-(4a,8-Dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl)prop-2-enoic acid	13819151	Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C(=O)O	248.32	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
2-(8-Hydroxy-4a,8-dimethyldecahydro-2-naphthalenyl)acrylic acid	496073	Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O	252.35	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
2-(8a-hydroxy-4a-methyl-8-methylidene-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl)prop-2-enoic acid	14705650	Click to see CC12CCCC(=C)C1(CC(CC2)C(=C)C(=O)O)O	250.33	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
2-(8a-Hydroxy-4a,8-dimethyl-1,2,3,4,5,6-hexahydronaphthalen-2-yl)prop-2-enoic acid	14705652	Click to see CC1=CCCC2(C1(CC(CC2)C(=C)C(=O)O)O)C	250.33	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
2-[(2R,4aR,8aR)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid	12304103	Click to see CC12CCCC(=C)C1CC(CC2)C(=C)C(=O)O	234.33	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
2-[(2R,4aR,8aS)-8a-hydroxy-4a,8-dimethyl-1,2,3,4,5,6-hexahydronaphthalen-2-yl]prop-2-enoic acid	14705653	Click to see CC1=CCCC2(C1(CC(CC2)C(=C)C(=O)O)O)C	250.33	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
2-[(2R,4aR,8S,8aR)-8a-hydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8-octahydronaphthalen-2-yl]prop-2-enoic acid	101589316	Click to see CC1CCCC2(C1(CC(CC2)C(=C)C(=O)O)O)C	252.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.027
2-[(2R,4aS,7R,8aS)-7,8a-dihydroxy-4a-methyl-8-methylidene-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid	13895639	Click to see CC12CCC(CC1(C(=C)C(CC2)O)O)C(=C)C(=O)O	266.33	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
2-[(2R,4aS,7R)-7-acetyloxy-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid	162816978	Click to see CC1=C2CC(CCC2(CCC1OC(=O)C)C)C(=C)C(=O)O	292.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.027
2-[(2R,4aS,7R)-7-methoxy-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid	102125248	Click to see CC1=C2CC(CCC2(CCC1OC)C)C(=C)C(=O)O	264.36	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.027
2-[(2R,4aS,7S)-7-methoxy-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid	102125247	Click to see CC1=C2CC(CCC2(CCC1OC)C)C(=C)C(=O)O	264.36	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.027
2-[(4aR,8R,8aR)-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid	137795140	Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O	252.35	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
2-[(8aR)-2,4a-dimethyl-8-methylidene-3,4,5,6,7,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid	5316106	Click to see CC12CCCC(=C)C1CC(CC2)(C)C(=C)C(=O)O	248.36	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
5alpha-Hydroxycostic acid	14705651	Click to see CC12CCCC(=C)C1(CC(CC2)C(=C)C(=O)O)O	250.33	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
5beta-Hydroxycostic acid	637286	Click to see CC12CCCC(=C)C1(CC(CC2)C(=C)C(=O)O)O	250.33	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
Costic acid	6451579	Click to see CC12CCCC(=C)C1CC(CC2)C(=C)C(=O)O	234.33	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
ent-Intermedeol	6566044	Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C	222.37	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
Ilicic acid	11876195	Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O	252.35	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
Isointermedeol	527217	Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C	222.37	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
Methyl 2-(4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl)prop-2-enoate	13819152	Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C(=O)OC	262.34	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
methyl 2-[(2R,4aS)-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl]prop-2-enoate	13819153	Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C(=O)OC	262.34	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
Pterodonoic acid	11054003	Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C(=O)O	248.32	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
3a-(hydroxymethyl)-6-(2-hydroxypropan-2-yl)-8a-methyl-2,3,5,6,7,8-hexahydro-1H-azulen-4-one	163192703	Click to see CC12CCCC1(C(=O)CC(CC2)C(C)(C)O)CO	254.36	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
beta-D-Glucopyranoside, 5-methyl-2-(1-methylethyl)phenyl	88687	Click to see CC1=CC(=C(C=C1)C(C)C)OC2C(C(C(C(O2)CO)O)O)O	312.36	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
Glucopyranoside,2-ipr-5-ME phenyl	14239340	Click to see CC1=CC(=C(C=C1)C(C)C)OC2C(C(C(C(O2)CO)O)O)O	312.36	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids
[(2R,3S,4S,5R)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl 2-[(2R,4aS)-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl]prop-2-enoate	162816983	Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C(=O)OCC3C(C(C(C(O3)O)O)O)O	410.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.027
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
(5-Hydroxy-3,6-dimethylhepta-2,6-dienyl) acetate	163087203	Click to see CC(=C)C(CC(=CCOC(=O)C)C)O	198.26	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
[(2E,5R)-5-hydroxy-3,6-dimethylhepta-2,6-dienyl] acetate	163087204	Click to see CC(=C)C(CC(=CCOC(=O)C)C)O	198.26	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
Acetic acid 3-methyl-5-[(R)-3,3-dimethyloxiranyl]-2-pentenyl ester	12701271	Click to see CC(=CCOC(=O)C)CCC1C(O1)(C)C	212.28	unknown	via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
methyl (1R,2R,4aS)-1-hydroxy-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalene-2-carboxylate	14705659	Click to see CC1=C2C(C(CCC2(CCC1=O)C)C(=O)OC)O	252.31	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
methyl (1S,2S,4aR)-1-hydroxy-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalene-2-carboxylate	163046494	Click to see CC1=C2C(C(CCC2(CCC1=O)C)C(=O)OC)O	252.31	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
Methyl 1-hydroxy-4a,8-dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalene-2-carboxylate	14705658	Click to see CC1=C2C(C(CCC2(CCC1=O)C)C(=O)OC)O	252.31	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
Edeine F	194407	Click to see C1=CC=C(C=C1)C(CN)C(=O)N(C(CN)C(=O)NC(CCCC(C(CC(=O)NC(=O)CNCCCNCCCCN=C(N)N)O)N)C(=O)O)C(=O)CC(N)O	780.90	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
1-Hydroxy-4,8a-dimethyl-1,2,3,3a,4,5,7,8-octahydroazulen-6-one	13994041	Click to see CC1CC(=O)CCC2(C1CCC2O)C	196.29	unknown	https://doi.org/10.1515/ZNB-2007-0119
2-(3a-acetyl-3-hydroxy-7a-methyl-2,3,4,5,6,7-hexahydro-1H-inden-5-yl)prop-2-enoic acid	14165747	Click to see CC(=O)C12CC(CCC1(CCC2O)C)C(=C)C(=O)O	266.33	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
2-[(3S,3aR,5R,7aS)-3a-acetyl-3-hydroxy-7a-methyl-2,3,4,5,6,7-hexahydro-1H-inden-5-yl]prop-2-enoic acid	189528	Click to see CC(=O)C12CC(CCC1(CCC2O)C)C(=C)C(=O)O	266.33	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
Jasonone	10943421	Click to see CC1CC(=O)CCC2(C1CCC2O)C	196.29	unknown	https://doi.org/10.1515/ZNB-2007-0119
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(3aR,6R)-6-(2-hydroxypropan-2-yl)-3a-methyl-3,4,5,6,7,9-hexahydro-2H-cyclopenta[8]annulen-8-one	11031886	Click to see CC12CCC=C1CC(=O)CC(CC2)C(C)(C)O	236.35	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
(3aR)-6-(2-hydroxypropan-2-yl)-3a-methyl-3,4,5,6,7,9-hexahydro-2H-cyclopenta[8]annulen-8-one	162896309	Click to see CC12CCC=C1CC(=O)CC(CC2)C(C)(C)O	236.35	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
1-[(3S,3aR,5R,7aS)-3-hydroxy-5-(2-hydroxypropan-2-yl)-7a-methyl-2,3,4,5,6,7-hexahydro-1H-inden-3a-yl]ethanone	14705661	Click to see CC(=O)C12CC(CCC1(CCC2O)C)C(C)(C)O	254.36	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
1-[3-hydroxy-5-(2-hydroxypropan-2-yl)-7a-methyl-2,3,4,5,6,7-hexahydro-1H-inden-3a-yl]ethanone	14705660	Click to see CC(=O)C12CC(CCC1(CCC2O)C)C(C)(C)O	254.36	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
6-(2-hydroxypropan-2-yl)-3a-methyl-3,4,5,6,7,9-hexahydro-2H-cyclopenta[8]annulen-8-one	14191352	Click to see CC12CCC=C1CC(=O)CC(CC2)C(C)(C)O	236.35	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
8-hydroxy-4a,8-dimethyl-4,5,6,7-tetrahydro-3H-naphthalen-2-one	72746331	Click to see CC12CCCC(C1=CC(=O)CC2)(C)O	194.27	unknown	https://doi.org/10.1515/ZNB-2007-0119
Teuhetenone A	15153216	Click to see CC12CCCC(C1=CC(=O)CC2)(C)O	194.27	unknown	https://doi.org/10.1515/ZNB-2007-0119
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(1S,6R,9R)-6-methyl-2,10-dimethylidene-12-oxatricyclo[7.3.1.01,6]tridecan-11-one	11020766	Click to see CC12CCCC(=C)C13CC(CC2)C(=C)C(=O)O3	232.32	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
(1S,6R)-6-methyl-2,10-dimethylidene-12-oxatricyclo[7.3.1.01,6]tridecan-11-one	162912447	Click to see CC12CCCC(=C)C13CC(CC2)C(=C)C(=O)O3	232.32	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
6-Methyl-2,10-dimethylidene-12-oxatricyclo[7.3.1.01,6]tridecan-11-one	14705657	Click to see CC12CCCC(=C)C13CC(CC2)C(=C)C(=O)O3	232.32	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
methyl (2S)-2-[(1S,2R,5R,6R,11S,12R,14S,15R,17S,18S)-6-(furan-3-yl)-11,14,17-trihydroxy-1,5,15-trimethyl-8,13-dioxo-7-oxapentacyclo[13.2.1.02,11.05,10.012,17]octadec-9-en-18-yl]-2-hydroxyacetate	102375914	Click to see CC12CCC3C4(C(C5(CC4(C(C3(C1=CC(=O)OC2C6=COC=C6)O)C(=O)C5O)O)C)C(C(=O)OC)O)C	516.50	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
Methyl 2-hydroxy-3,3-dimethoxy-4-methyl-1,9-dioxocyclopenta[b]quinoline-2-carboxylate	101998853	Click to see CN1C2=CC=CC=C2C(=O)C3=C1C(C(C3=O)(C(=O)OC)O)(OC)OC	347.30	unknown	https://doi.org/10.1016/0031-9422(88)83035-8
> Phenylpropanoids and polyketides / Coumarins and derivatives
[1-Hydroxy-1-(7-methoxy-2-oxochromen-8-yl)-3-methylbut-3-en-2-yl] 3-methylbutanoate	14779477	Click to see CC(C)CC(=O)OC(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O)C(=C)C	360.40	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Patuletin	5281678	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O	332.26	unknown	https://doi.org/10.1016/0031-9422(89)80084-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-[3-(2,4-Dihydroxyphenoxy)-4-hydroxyphenyl]-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one	74394441	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)OC5=C(C=C(C=C5)O)O)O)O)O	556.50	unknown	https://doi.org/10.1016/0031-9422(90)85296-R
6''-O-Acetylastragalin	10435673	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	490.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2014.03.027
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Quercetin 3,3'-dimethyl ether	5316900	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O	330.29	unknown	https://doi.org/10.1016/0031-9422(89)80084-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Quercetin 3,4'-dimethyl ether	5380905	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O	330.29	unknown	https://doi.org/10.1016/0031-9422(89)80084-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Centaureidin	5315773	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O	360.30	unknown	https://doi.org/10.1016/0031-9422(89)80084-6
Jaceidin	5464461	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O	360.30	unknown	https://doi.org/10.1016/0031-9422(89)80084-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4'-Hydroxy-3,5,6,7,3'-pentamethoxyflavone	14376231	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC)O	388.40	unknown	https://doi.org/10.1016/0031-9422(89)80084-6
Artemetin	5320351	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC	388.40	unknown	https://doi.org/10.1016/0031-9422(89)80084-6
Casticin	5315263	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O	374.30	unknown	https://doi.org/10.1016/0031-9422(89)80084-6
chrysoplenol D	5280699	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC	360.30	unknown	https://doi.org/10.1016/0031-9422(89)80084-6
Chrysosplenetin	5281608	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O	374.30	unknown	https://doi.org/10.1016/0031-9422(89)80084-6
Hexamethylquercetagetin	386331	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC)OC	402.40	unknown	https://doi.org/10.1016/0031-9422(89)80084-6
Pachypodol	5281677	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O	344.30	unknown	https://doi.org/10.1016/0031-9422(89)80084-6
Penduletin	5320462	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)OC	344.30	unknown	https://doi.org/10.1016/0031-9422(89)80084-6
Velutin	5464381	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)OC)O	314.29	unknown	https://doi.org/10.1016/0031-9422(88)83035-8

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Chiliadenus montanus

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