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Saussurea parviflora

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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 UUID643fcf2f4c1f4917620287
Scientific name Saussurea parviflora
Authority (Poir.) DC.
First published in Ann. Mus. Natl. Hist. Nat. 16: 200 (1810)

Description Top

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Synonyms Top

Scientific name Authority First published in
Saussurea serrata DC. Ann. Mus. Natl. Hist. Nat. 16: 199 (1810)
Saussurea atriplicifolia M.Bieb. ex Besser Flora 17(1, Beibl.): 15 (1834)
Saussurea atriplicifolia Fisch. ex Herder Byulleten Moskovskogo Obshchestva Ispytatelij Prirody, Otdel Biologicheskii 41(3): 19 1868
Saussurea parviflora var. cinerascens Hand.-Mazz. Acta Horti Gothoburgensis 12(9): 316-317 1938
Saussurea chowana F.H.Chen Bull. Fan Mem. Inst. Biol. , Bot. 8: 119 (1938)
Saussurea parviflora var. cuspidata Hand.-Mazz. Acta Horti Gothoburgensis 12(9): 316 1938
Serratula parviflora Poir. Encycl. 6: 554 (1805)
Saussurea parviflora var. contracta (Ledeb.) Lipsch. Bot. Zhurn. (Moscow & Leningrad) 57(6): 682 (1972)

Common names Top

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Language Common/alternative name
Chinese 小花风毛菊
Chinese 小花風毛菊

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Inner Mongolia
      • Qinghai
      • Xinjiang
    • Middle Asia
      • Kazakhstan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000088123
Tropicos 2717680
KEW urn:lsid:ipni.org:names:242516-1
The Plant List gcc-44467
Open Tree Of Life 40100
Observations.org 137725
NCBI Taxonomy 238949
IPNI 242516-1
iNaturalist 521263
GBIF 5404641
EOL 6211608

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
Analysis of the Potential Range of Anticlea sibirica L. (Kunth) and Its Changes under Moderate Climate Change in the 21st Century Fedorov N, Kutueva A, Muldashev A, Verkhozina A, Lashchinskiy N, Martynenko V Plants (Basel) 28-Nov-2022
PMCID:PMC9738958
doi:10.3390/plants11233270
PMID:36501310
Eudesmane derivatives and other constituents from Saussurea parviflora. Yang ZD, Gao K, Jia ZJ Phytochemistry 01-Apr-2003
doi:10.1016/S0031-9422(02)00758-6
PMID:12648535

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 / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Arctigenin 64981 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
Arctigenin, (+)- 28125531 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
l-Arctigenin 230232 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
> Lignans, neolignans and related compounds / Lignan glycosides
3-[(4-Hydroxy-3-methoxyphenyl)methyl]-4-[[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl]oxolan-2-one 74105540 Click to see COC1=C(C=CC(=C1)CC2C(COC2=O)CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O 520.50 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
Matairesinol monoglucoside 23757184 Click to see COC1=C(C=CC(=C1)CC2C(COC2=O)CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O 520.50 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
Matairesinoside 486612 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O 520.50 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
2,3-Dihydroxypropyl hexadecanoate 14900 Click to see CCCCCCCCCCCCCCCC(=O)OCC(CO)O 330.50 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
11,12,13-Trihydroxy-4(15),8-eudesmadiene-9-one 639678 Click to see CC12CCCC(=C)C1CC(=CC2=O)C(CO)(CO)O 266.33 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
8a-methyl-5-methylidene-3-(1,2,3-trihydroxypropan-2-yl)-4a,6,7,8-tetrahydro-4H-naphthalen-1-one 73880808 Click to see CC12CCCC(=C)C1CC(=CC2=O)C(CO)(CO)O 266.33 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,4aS,5S,8aS,9aR)-5,8a-dimethyl-3-methylidene-3a,4,4a,5,9,9a-hexahydrobenzo[f][1]benzofuran-2,6-dione 162974718 Click to see CC1C2CC3C(CC2(C=CC1=O)C)OC(=O)C3=C 246.30 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
(3R,3aR,4aS,5S,8S,8aR,9aR)-3,5,8a-trimethyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,3a,4,4a,5,6,7,8,9,9a-decahydrobenzo[f][1]benzofuran-2-one 162879907 Click to see CC1CCC(C2(C1CC3C(C(=O)OC3C2)C)C)OC4C(C(C(C(O4)CO)O)O)O 414.50 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
3,5,8a-Trimethyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,3a,4,4a,5,6,7,8,9,9a-decahydrobenzo[f][1]benzofuran-2-one 162879906 Click to see CC1CCC(C2(C1CC3C(C(=O)OC3C2)C)C)OC4C(C(C(C(O4)CO)O)O)O 414.50 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
5,8a-Dimethyl-3-methylidene-3a,4,4a,5,9,9a-hexahydrobenzo[f][1]benzofuran-2,6-dione 162974716 Click to see CC1C2CC3C(CC2(C=CC1=O)C)OC(=O)C3=C 246.30 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
Dehydrofarinosin 329302 Click to see CC12CC3C(CC1C(=C)C(=O)C=C2)C(=C)C(=O)O3 244.28 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
Encelin 72540 Click to see CC12CC3C(CC1C(=C)C(=O)C=C2)C(=C)C(=O)O3 244.28 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a-dodecahydro-1H-picen-3-yl) octadecanoate 162864887 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CC(C2(C(C1(C)C)CCC3(C2=CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C)O 707.20 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
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/10.1016/S0031-9422(02)00758-6
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/10.1016/S0031-9422(02)00758-6
Octadecanoic acid 1beta-hydroxyurs-9(11),12-diene-3beta-yl ester 12085701 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CC(C2(C(C1(C)C)CCC3(C2=CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C)O 707.20 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
> 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/10.1016/S0031-9422(02)00758-6
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(02)00758-6
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(02)00758-6
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
6-Hydroxy-7-methoxychromen-4-one 15406743 Click to see COC1=C(C=C2C(=O)C=COC2=C1)O 192.17 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/S0031-9422(02)00758-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
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/S0031-9422(02)00758-6

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