Ixeridium gracile

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Scientific Literature

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Details Top

Internal ID	UUID643fcc6265828780947684
Scientific name	Ixeridium gracile
Authority	(DC.) Pak & Kawano
First published in	Mem. Coll. Sci. Kyoto Imp. Univ., Ser. B, Biol. 15(1-2): 45 (1992): (1992)

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Synonyms Top

Scientific name	Authority	First published in
Ixeris gracilis	(DC.) Stebbins	J. Bot. 75: 50 (1937)
Lactuca gracilis	DC.	Prodr. 7(1): 140 (1838)
Chondrilla gracilis	Wall.	Numer. List : n.° 3267 (1831)
Ixeridium gracile	(DC.) C.Shih	Acta Phytotax. Sin. 31: 545 (1993), isonym; (1993)

Common names Top

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Language	Common/alternative name
Chinese	粉苞苣
Chinese	细叶小苦荬
Chinese	细叶小苦荬(等叶苦荬）
Chinese	细叶苦荬
Chinese	纤细苦荬菜

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Ixeridium gracile var. khasianum	(C.B.Clarke ex Hook.f.) Karthik. & Moorthy	Fl. Pl. India : 241 (2009)

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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 South-central
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya
  - Nepal
- Indo-China
  - Vietnam

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000062068
Tropicos	50117672
KEW	urn:lsid:ipni.org:names:972100-1
The Plant List	gcc-19078
Open Tree Of Life	5536662
NCBI Taxonomy	1325988
IPNI	972100-1
GBIF	3100769

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

Kaempferol: Antimicrobial Properties, Sources, Clinical, and Traditional Applications

Periferakis A, Periferakis K, Badarau IA, Petran EM, Popa DC, Caruntu A, Costache RS, Scheau C, Caruntu C, Costache DO

Int J Mol Sci

30-Nov-2022

PMCID:	PMC9740324
doi:	10.3390/ijms232315054
PMID:	36499380

Crowberry inhibits cell proliferation and migration through a molecular mechanism that includes inhibition of DEK and Akt signaling in cholangiocarcinoma

Wang X, Zhou X, Zhang L, Zhang X, Yang C, Piao Y, Zhao J, Jin L, Jin G, An R, Ren X

Chin Med

13-Jun-2022

PMCID:	PMC9190153
doi:	10.1186/s13020-022-00623-6
PMID:	35698073

Effect of sheep grazing on seed circulation on the Loess Plateau

Wang S, Hu A, Hou F

Ecol Evol

17-Nov-2021

PMCID:	PMC8668805
doi:	10.1002/ece3.8368
PMID:	34938511

Traditional use and management of NTFPs in Kangchenjunga Landscape: implications for conservation and livelihoods

Uprety Y, Poudel RC, Gurung J, Chettri N, Chaudhary RP

J Ethnobiol Ethnomed

03-May-2016

PMCID:	PMC4855762
doi:	10.1186/s13002-016-0089-8
PMID:	27142597

Soil Biota Reduce Allelopathic Effects of the Invasive Eupatorium adenophorum

Zhu X, Zhang J, Ma K

PLoS One

28-Sep-2011

PMCID:	PMC3182202
doi:	10.1371/journal.pone.0025393
PMID:	21980442

Advances of Modern Chromatographic and Electrophoretic Methods in Separation and Analysis of Flavonoids

Liu EH, Qi LW, Cao J, Li P, Li CY, Peng YB

Molecules

16-Oct-2008

PMCID:	PMC6245463
doi:	10.3390/molecules13102521
PMID:	18927516

Triterpenoids and steroids from Ixeridium gracile

Xue-Mei Ma, Duo-Long Di, Yan-Ping Shi

Springer Science and Business Media LLC

01-Oct-2008

doi:	10.1007/S10600-008-9078-Z

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(18alpha,19alpha)-5alpha-Urs-20(30)-ene-3beta-ol palmitate	14055767	Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(C(=C)CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C)C	665.10	unknown	https://doi.org/10.1007/S10600-008-9078-Z
(3S,4aS,6aR,6bS,8aS,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,12,12a,14,14a-dodecahydro-1H-picen-3-ol	162998487	Click to see CC1C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC=C1C)C)C)C)(C)C)O)C	424.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
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]chrysene-9,11,12-triol	75069370	Click to see CC(=C)C1CCC2(C1C3CC(C4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)O)C	458.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,12,12a,14,14a-dodecahydro-1H-picen-3-ol	162998486	Click to see CC1C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC=C1C)C)C)C)(C)C)O)C	424.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
4,4,6a,6b,8a,12,14b-Heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol	610148	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	2371	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
beta-Ursolic acid	220774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Dammara-20,24-dien-3 beta-ol	13893944	Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)C	426.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Dammaradienol	13893946	Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)C	426.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Lup-20(29)-en-3-ol, (3beta)-	521518	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Methyl betulate	423298	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)OC	470.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Methyl betulinate	73493	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)OC	470.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Nepetidin	12083275	Click to see CC(=C)C1CCC2(C1C3CC(C4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)O)C	458.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Olean-12-en-3beta-ol	225689	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Taraxasterol	115250	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Taraxasterol palmitate	14055766	Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(C(=C)CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C)C	665.10	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Urs-12-en-3beta-ol	225688	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
> Lipids and lipid-like molecules / Steroids and steroid derivatives / C24-propyl sterols and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	90694767	Click to see CCC(CCC(C)C1CCC2C1(C=CC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	163080571	Click to see CCC(CCC(C)C1CCC2C1(C=CC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z
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/10.1007/S10600-008-9078-Z
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/10.1007/S10600-008-9078-Z
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1007/S10600-008-9078-Z

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Ixeridium gracile

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