Cremanthodium ellisii

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Internal ID	UUID643fcc314eab1625647075
Scientific name	Cremanthodium ellisii
Authority	(Hook.f.) Kitam.
First published in	Enum. Fl. Pl. Nepal 3: 22 (1982): (1982)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Senecio maximowiczii	Franch.	Bull. Soc. Bot. France 39: 287 (1892)
Cremanthodium plantagineum	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg xxvii. (1881) 481.
Cremanthodium plantagineum f. albidum	R.D.Good	Journal of the Linnean Society, Botany 48(322): 293-294 1929
Senecio fletcheri	Hemsl.	Bull. Misc. Inform. Kew 1896: 212 (1896)
Cremanthodium plantagineum f. ellissii	(Hook.f.) R.D.Good	J. Linn. Soc., Bot. 48: 293. 1929
Cremanthodium ellisii	(Hook.f.) Seybold & Kull	Bot. Jahrb. Syst. 105(2): 269 (1985)
Senecio paberensis	Franch.	Bull. Soc. Bot. France 39: 288 (1892)
Cremanthodium fletcheri	Hemsl.	J. Linn. Soc., Bot. 35: 185 (1902)
Senecio kunawarensis	N.C.Nair	Fl. Bashahr Himal. 164, nom. (1977)
Werneria ellisii	Hook.f.	Fl. Brit. India 3(8): 357 (1881)
Senecio goringensis	Hemsl.	Bull. Misc. Inform. Kew 1896: 212 (1896)
Cremanthodium goringense	Hemsl.	J. Linn. Soc., Bot. 35: 185 (1902)
Cremanthodium oblongatum var. villosior	C.B.Clarke	Compositae Indica 168 1876
Senecio arnicoides var. frigida	Hook.f.	351 1881
Cremanthodium plantagineum var. maximowiczii	(Franch.) Aswal	in B.S. Aswal & B.N. Mehrotra, Fl. Lahaul-Spiti 348 (1994):.
Cremanthodium plantagineum f. goringense	(Hemsl.) R.D.Good	Journal of the Linnean Society, Botany 48(322): 293-294 1929

Common names Top

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Language	Common/alternative name
Chinese	垂头菊
Chinese	狭叶垂头菊
Chinese	车前状垂头菊
Chinese	车前状头菊
Chinese	俄尕

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Cremanthodium ellisii var. ramosum	(Ling) Ling & S.W.Liu	Acta Biol. Plateau Sin. 3: 65 (1984) (1984)

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - Qinghai
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya
  - Nepal
  - West Himalaya

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000059773
Tropicos	50046893
KEW	urn:lsid:ipni.org:names:910462-1
The Plant List	gcc-16846
Open Tree Of Life	98475
NCBI Taxonomy	186945
IPNI	910462-1
iNaturalist	706623
GBIF	3137314

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

Comparative analyses of five complete chloroplast genomes from the endemic genus Cremanthodium (Asteraceae) in Himalayan and adjacent areas

Zhong W, Du X, Wang X, Cao L, Mu Z, Zhong G

Physiol Mol Biol Plants

27-Feb-2023

PMCID:	PMC10073364
doi:	10.1007/s12298-023-01292-x
PMID:	37033762

Plant Resources Utilization among Different Ethnic Groups of Ladakh in Trans-Himalayan Region

Haq SM, Yaqoob U, Calixto ES, Rahman IU, Hashem A, Abd_Allah EF, Alakeel MA, Alqarawi AA, Abdalla M, Hassan M, Bussmann RW, Abbasi AM, Ur Rahman S, Ijaz F

Biology (Basel)

26-Aug-2021

PMCID:	PMC8468708
doi:	10.3390/biology10090827
PMID:	34571704

Four Eremophil-9-en-8-one Derivatives from Cremanthodium stenactinium Samples Collected in China

Saito Y, Ichihara M, Okamoto Y, Gong X, Kuroda C, Tori M

Molecules

19-Dec-2011

PMCID:	PMC6264706
doi:	10.3390/molecules161210645
PMID:	22183888

Nor-lignan and sesquiterpenes from Cremanthodium ellisii.

Su BN, Zhu QX, Jia ZJ

Phytochemistry

01-Apr-2000

doi:	10.1016/S0031-9422(99)00584-1
PMID:	10820839

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lignans, neolignans and related compounds
4-[(1Z,3S)-1-(4-methoxyphenyl)penta-1,4-dien-3-yl]phenol	162970870	Click to see COC1=CC=C(C=C1)C=CC(C=C)C2=CC=C(C=C2)O	266.30	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
4-[(1Z)-1-(4-methoxyphenyl)penta-1,4-dien-3-yl]phenol	5319736	Click to see COC1=CC=C(C=C1)C=CC(C=C)C2=CC=C(C=C2)O	266.30	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
4-[1-(4-Methoxyphenyl)penta-1,4-dien-3-yl]phenol	74071366	Click to see COC1=CC=C(C=C1)C=CC(C=C)C2=CC=C(C=C2)O	266.30	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
4'-O-Methylnyasol	23626544	Click to see COC1=CC=C(C=C1)C=CC(C=C)C2=CC=C(C=C2)O	266.30	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[(1S,2R,3S,4S,5S,6S)-3-acetyloxy-5-[(3R,5S)-3,6-dihydroxy-6-methyl-5-(2-methylpropanoyloxy)hept-1-en-2-yl]-2,6-dihydroxy-2-methyl-4-(2-methylpropanoyloxy)cyclohexyl] (Z)-2-methylbut-2-enoate	162874337	Click to see CC=C(C)C(=O)OC1C(C(C(C(C1(C)O)OC(=O)C)OC(=O)C(C)C)C(=C)C(CC(C(C)(C)O)OC(=O)C(C)C)O)O	600.70	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
[(1S,2R,3S,4S,5S,6S)-3-acetyloxy-5-[(3S,5S)-5,6-dihydroxy-6-methyl-3-(2-methylpropanoyloxy)hept-1-en-2-yl]-2,6-dihydroxy-2-methyl-4-(2-methylpropanoyloxy)cyclohexyl] (Z)-2-methylbut-2-enoate	162981084	Click to see CC=C(C)C(=O)OC1C(C(C(C(C1(C)O)OC(=O)C)OC(=O)C(C)C)C(=C)C(CC(C(C)(C)O)O)OC(=O)C(C)C)O	600.70	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
[(1S,2S,3R,4S,5S,6S)-2-acetyloxy-6-[(3S,5S)-5,6-dihydroxy-6-methyl-3-(2-methylpropanoyloxy)hept-1-en-2-yl]-3,5-dihydroxy-3-methyl-4-(2-methylpropanoyloxy)cyclohexyl] 2-methylpropanoate	163060095	Click to see CC(C)C(=O)OC1C(C(C(C(C1OC(=O)C)(C)O)OC(=O)C(C)C)O)C(=C)C(CC(C(C)(C)O)O)OC(=O)C(C)C	588.70	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
[(1S,2S,3S,4S,5S,6S)-2-acetyloxy-5-hydroxy-4-[(3S,5S)-6-hydroxy-6-methyl-3,5-bis(2-methylpropanoyloxy)hept-1-en-2-yl]-1-methyl-7-oxabicyclo[4.1.0]heptan-3-yl] 2-methylpropanoate	163043246	Click to see CC(C)C(=O)OC1C(C(C2C(C1OC(=O)C)(O2)C)O)C(=C)C(CC(C(C)(C)O)OC(=O)C(C)C)OC(=O)C(C)C	570.70	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
[2-Acetyloxy-5-hydroxy-4-[6-hydroxy-6-methyl-3,5-bis(2-methylpropanoyloxy)hept-1-en-2-yl]-1-methyl-7-oxabicyclo[4.1.0]heptan-3-yl] 2-methylpropanoate	101420371	Click to see CC(C)C(=O)OC1C(C(C2C(C1OC(=O)C)(O2)C)O)C(=C)C(CC(C(C)(C)O)OC(=O)C(C)C)OC(=O)C(C)C	570.70	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
[2-Acetyloxy-6-[5,6-dihydroxy-6-methyl-3-(2-methylpropanoyloxy)hept-1-en-2-yl]-3,5-dihydroxy-3-methyl-4-(2-methylpropanoyloxy)cyclohexyl] 2-methylpropanoate	101426260	Click to see CC(C)C(=O)OC1C(C(C(C(C1OC(=O)C)(C)O)OC(=O)C(C)C)O)C(=C)C(CC(C(C)(C)O)O)OC(=O)C(C)C	588.70	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
[3-Acetyloxy-5-[3,6-dihydroxy-6-methyl-5-(2-methylpropanoyloxy)hept-1-en-2-yl]-2,6-dihydroxy-2-methyl-4-(2-methylpropanoyloxy)cyclohexyl] 2-methylbut-2-enoate	162874336	Click to see CC=C(C)C(=O)OC1C(C(C(C(C1(C)O)OC(=O)C)OC(=O)C(C)C)C(=C)C(CC(C(C)(C)O)OC(=O)C(C)C)O)O	600.70	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
[3-Acetyloxy-5-[5,6-dihydroxy-6-methyl-3-(2-methylpropanoyloxy)hept-1-en-2-yl]-2,6-dihydroxy-2-methyl-4-(2-methylpropanoyloxy)cyclohexyl] 2-methylbut-2-enoate	162981083	Click to see CC=C(C)C(=O)OC1C(C(C(C(C1(C)O)OC(=O)C)OC(=O)C(C)C)C(=C)C(CC(C(C)(C)O)O)OC(=O)C(C)C)O	600.70	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
14-(5-Ethyl-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-ene-5,9-diol	5318414	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C	430.70	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
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/S0031-9422(99)00584-1
24-Ethylcholest-5-en-3beta-ol	22012	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/S0031-9422(99)00584-1
7beta-Hydroxysitosterol	12309569	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C	430.70	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
Beta-Sitosterol	222284	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/S0031-9422(99)00584-1
Ikshusterol	161816	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C	430.70	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	12315422	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
5-Hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl)oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one	5377847	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O	578.50	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
Isorhoifolin	9851181	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O	578.50	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1
Luteolin 7-o-rutinoside	10461109	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(99)00584-1

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Cremanthodium ellisii

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top