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Carpesium lipskyi

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fca9f5fc7d062751257
Scientific name Carpesium lipskyi
Authority C.Winkl.
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada xiv. (1895) 68.

Description Top

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Synonyms Top

Scientific name Authority First published in
Carpesium lipskyi var. potaninii C.Winkl. Trudy Imperatorskago S.-Peterburgskago Botanicheskago Sada 14(1): 68-69 1895
Carpesium lipskyi var. hotonense C.Winkl. Trudy Imperatorskago S.-Peterburgskago Botanicheskago Sada 14(1): 69 1895
Carpesium lipskyi var. przewalskii C.Winkl. Trudy Imperatorskago S.-Peterburgskago Botanicheskago Sada 14(1): 69 1895

Common names Top

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Language Common/alternative name
Chinese 高原天名精
Chinese 高山金挖耳
Chinese 贡布美多露米

Subspecies (abbr. subsp./ssp.) Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Qinghai

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000039860
Tropicos 2745455
KEW urn:lsid:ipni.org:names:189350-1
The Plant List gcc-138552
Open Tree Of Life 6056713
Observations.org 293676
NCBI Taxonomy 1898829
IPNI 189350-1
iNaturalist 633992
GBIF 3094837

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
Antiprostate Cancer Activity of Ineupatolide Isolated from Carpesium cernuum L. Huang YS, Mao JX, Zhang L, Guo HW, Yan C, Chen M Biomed Res Int 29-Apr-2021
PMCID:PMC8105106
doi:10.1155/2021/5515961
PMID:33996996
Karyotypes of nineteen species of Asteraceae in the Hengduan Mountains and adjacent regions Sun W, Ma X, Zhang J, Su F, Zhang Y, Li Z Plant Divers 24-Aug-2017
PMCID:PMC6112298
doi:10.1016/j.pld.2017.08.001
PMID:30159511
Natural Resource Monitoring of Rheum tanguticum by Multilevel Remote Sensing Xie C, Song J, Suo F, Li X, Li Y, Yu H, Xu X, Luo K, Li Q, Xin T, Guan M, Xu X, Miki E, Takeda O, Chen S Evid Based Complement Alternat Med 02-Jul-2014
PMCID:PMC4101945
doi:10.1155/2014/618902
PMID:25101134
Germacranolides from Carpesium lipskyi. Shi YP, Guo W, Jia ZJ Planta Med 01-Feb-1999
doi:10.1055/S-2006-960452
PMID:17260245
Two new aromatic monoterpene derivatives from Carpesium lipskyi. Shi YP, Guo W, Yang C, Jia ZJ Planta Med 01-Oct-1998
doi:10.1055/S-2006-957550
PMID:17253309

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
> Benzenoids / Phenol ethers / Anisoles
[(2R)-3-acetyloxy-2-hydroxy-2-(2-methoxy-4-methylphenyl)propyl] 2-methylpropanoate 163030567 Click to see CC1=CC(=C(C=C1)C(COC(=O)C)(COC(=O)C(C)C)O)OC 324.40 unknown https://doi.org/10.1055/S-2006-957550
[2-Hydroxy-2-(2-methoxy-4-methylphenyl)-3-(2-methylpropanoyloxy)propyl] 2-methylpropanoate 100916618 Click to see CC1=CC(=C(C=C1)C(COC(=O)C(C)C)(COC(=O)C(C)C)O)OC 352.40 unknown https://doi.org/10.1055/S-2006-957550
[3-Acetyloxy-2-hydroxy-2-(2-methoxy-4-methylphenyl)propyl] 2-methylpropanoate 100916619 Click to see CC1=CC(=C(C=C1)C(COC(=O)C)(COC(=O)C(C)C)O)OC 324.40 unknown https://doi.org/10.1055/S-2006-957550
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(6,10-dimethyl-3-methylidene-2,9-dioxo-4,5,6,7,8,10,11,11a-octahydro-3aH-cyclodeca[b]furan-5-yl) 2-methylbut-2-enoate 162918654 Click to see CC=C(C)C(=O)OC1CC2C(CC(C(=O)CCC1C)C)OC(=O)C2=C 348.40 unknown https://doi.org/10.1055/S-2006-960452
(9-Acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,6,7,8,9,11a-octahydrocyclodeca[b]furan-5-yl) 2-methylbut-2-enoate 162904900 Click to see CC=C(C)C(=O)OC1CC2C(C=C(C(CCC1C)OC(=O)C)C)OC(=O)C2=C 390.50 unknown https://doi.org/10.1055/S-2006-960452
[(3aS,5S,6R,10S,11aR)-6,10-dimethyl-3-methylidene-2,9-dioxo-4,5,6,7,8,10,11,11a-octahydro-3aH-cyclodeca[b]furan-5-yl] (Z)-2-methylbut-2-enoate 162918655 Click to see CC=C(C)C(=O)OC1CC2C(CC(C(=O)CCC1C)C)OC(=O)C2=C 348.40 unknown https://doi.org/10.1055/S-2006-960452
[(3aS,5S,6R,9S,10E,11aR)-9-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,6,7,8,9,11a-octahydrocyclodeca[b]furan-5-yl] (Z)-2-methylbut-2-enoate 162904901 Click to see CC=C(C)C(=O)OC1CC2C(C=C(C(CCC1C)OC(=O)C)C)OC(=O)C2=C 390.50 unknown https://doi.org/10.1055/S-2006-960452
[(5S,6R,10S,11aR)-6,10-dimethyl-3-methylidene-2,9-dioxo-4,5,6,7,8,10,11,11a-octahydro-3aH-cyclodeca[b]furan-5-yl] (Z)-2-methylbut-2-enoate 100988384 Click to see CC=C(C)C(=O)OC1CC2C(CC(C(=O)CCC1C)C)OC(=O)C2=C 348.40 unknown https://doi.org/10.1055/S-2006-960452
[(5S,6R,10Z,11aR)-9-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,6,7,8,9,11a-octahydrocyclodeca[b]furan-5-yl] (Z)-2-methylbut-2-enoate 100988385 Click to see CC=C(C)C(=O)OC1CC2C(C=C(C(CCC1C)OC(=O)C)C)OC(=O)C2=C 390.50 unknown https://doi.org/10.1055/S-2006-960452
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1055/S-2006-960452
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/10.1055/S-2006-960452
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/10.1055/S-2006-960452
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
CID 45273057 45273057 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(O2)C=C(C=C3OC)O 300.30 unknown https://doi.org/10.1055/S-2006-960452
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-5-hydroxy-7-methoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one 14057197 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC)O 300.30 unknown https://doi.org/10.1055/S-2006-960452
5-Hydroxy-7-methoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one 321346 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC)O 300.30 unknown https://doi.org/10.1055/S-2006-960452

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