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Scorzonera divaricata

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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 UUID643fd01f45ef2967593798
Scientific name Scorzonera divaricata
Authority Turcz.
First published in Bull. Soc. Imp. Naturalistes Moscou 5: 200 (1832)

Description Top

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Synonyms Top

Scientific name Authority First published in
Scorzonera divaricata var. intricatissima Maxim. Bulletin de l'Academie Imperiale des Sciences de St-Petersbourg 32(4): 494 1888
Scorzonera roylei DC. Prodr. 7(1): 125 (1838)
Scorzonera divaricata var. tatewakii Kitam. Acta Phytotax. Geobot. 40: 143 (1989)

Common names Top

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Language Common/alternative name
Chinese 叉枝鸦葱
Chinese 拐轴鸦葱
Chinese 拐軸鴉蔥

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000096383
Tropicos 2733484
KEW urn:lsid:ipni.org:names:243149-1
The Plant List gcc-52528
Open Tree Of Life 923825
NCBI Taxonomy 1205778
IPNI 243149-1
iNaturalist 1148347
GBIF 3111123
EOL 6246052
USDA GRIN 402018

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
Dihydrocaffeic Acid—Is It the Less Known but Equally Valuable Phenolic Acid? Zieniuk B Biomolecules 18-May-2023
PMCID:PMC10216370
doi:10.3390/biom13050859
PMID:37238728
New Insights Into the Relationships Within Subtribe Scorzonerinae (Cichorieae, Asteraceae) Using Hybrid Capture Phylogenomics (Hyb-Seq) Hatami E, Jones KE, Kilian N Front Plant Sci 01-Jul-2022
PMCID:PMC9298463
doi:10.3389/fpls.2022.851716
PMID:35873957
Perennial Flowering Plants Sustain Natural Enemy Populations in Gobi Desert Oases of Southern Xinjiang, China Liu Y, Liu B, Li Q, Sun M, Li M, Wyckhuys KA, Wang P, Lu Y Insects 20-Apr-2022
PMCID:PMC9145401
doi:10.3390/insects13050399
PMID:35621735
Phytochemical Composition and Biological Activities of Scorzonera Species Lendzion K, Gornowicz A, Bielawski K, Bielawska A Int J Mol Sci 12-May-2021
PMCID:PMC8151016
doi:10.3390/ijms22105128
PMID:34066212
Activity strategy and pattern of the Siberian jerboa (Orientallactaga sibirica) in the Alxa desert region, China Ji Y, Yuan S, Fu H, Yang S, Bu F, Li X, Wu X PeerJ 10-Mar-2021
PMCID:PMC7955674
doi:10.7717/peerj.10996
PMID:33854836
New chlorogenic acid derivatives and triterpenoids from Scorzonera aucheriana ERİK İ, COŞKUNÇELEBİ K, MAKBUL S, YAYLI N Turk J Chem 17-Feb-2021
PMCID:PMC7925298
doi:10.3906/kim-2009-17
PMID:33679163
Ethnomedicinal Plants Traditionally Used for the Treatment of Jaundice (Icterus) in Himachal Pradesh in Western Himalaya—A Review Raghuvanshi D, Dhalaria R, Sharma A, Kumar D, Kumar H, Valis M, Kuča K, Verma R, Puri S Plants (Basel) 25-Jan-2021
PMCID:PMC7910824
doi:10.3390/plants10020232
PMID:33504029
Phytolith‐occluded carbon sequestration potential in three major steppe types along a precipitation gradient in Northern China Qi L, Sun T, Guo X, Guo Y, Li FY Ecol Evol 04-Jan-2021
PMCID:PMC7863665
doi:10.1002/ece3.7155
PMID:33598143
Folk nomenclature of plants in Cistanche deserticola-associated community in South Gobi, Mongolia Mandakh U, Battseren M, Ganbat D, Ayanga T, Adiya Z, Borjigidai A, Long C Plant Divers 06-Oct-2020
PMCID:PMC7936101
doi:10.1016/j.pld.2020.09.008
PMID:33733011
Changes in traditional ecological knowledge of forage plants in immigrant villages of Ningxia, China Ma Y, Luo B, Zhu Q, Ma D, Wen Q, Feng J, Xue D J Ethnobiol Ethnomed 16-Dec-2019
PMCID:PMC6916113
doi:10.1186/s13002-019-0333-0
PMID:31842902
Ethnopharmacological Approaches for Therapy of Jaundice: Part I Tewari D, Mocan A, Parvanov ED, Sah AN, Nabavi SM, Huminiecki L, Ma ZF, Lee YY, Horbańczuk JO, Atanasov AG Front Pharmacol 15-Aug-2017
PMCID:PMC5559545
doi:10.3389/fphar.2017.00518
PMID:28860989
Efficacy of Venom from Tentacle of Jellyfish Stomolophus meleagris (Nemopilema nomurai) against the Cotton Bollworm Helicoverpa armigera Yu H, Li R, Dong X, Xing R, Liu S, Li P Biomed Res Int 04-Aug-2014
PMCID:PMC4137687
doi:10.1155/2014/315853
PMID:25162008
Interactive Effects of Warming and Increased Precipitation on Community Structure and Composition in an Annual Forb Dominated Desert Steppe Hou Y, Zhou G, Xu Z, Liu T, Zhang X PLoS One 19-Jul-2013
PMCID:PMC3716769
doi:10.1371/journal.pone.0070114
PMID:23894600
Biologically active natural products from Mongolian medicinal plants Scorzonera divaricata and Scorzonera pseudodivaricata. Tsevegsuren N, Edrada R, Lin W, Ebel R, Torre C, Ortlepp S, Wray V, Proksch P J Nat Prod 01-Jun-2007
doi:10.1021/NP070013R
PMID:17542634

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
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-1,3-bis[3-(3,4-dihydroxyphenyl)propanoyloxy]-4-hydroxy-5-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxycyclohexane-1-carboxylic acid 16736244 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2O)OC(=O)CCC3=CC(=C(C=C3)O)O)(C(=O)O)OC(=O)CCC4=CC(=C(C=C4)O)O)O 696.60 unknown https://doi.org/10.1021/NP070013R
(1R,3R,4S,5R)-1,4-bis[3-(3,4-dihydroxyphenyl)propanoyloxy]-3-hydroxy-5-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxycyclohexane-1-carboxylic acid 102318967 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2OC(=O)CCC3=CC(=C(C=C3)O)O)O)(C(=O)O)OC(=O)CCC4=CC(=C(C=C4)O)O)O 696.60 unknown https://doi.org/10.1021/NP070013R
1,3-Bis[3-(3,4-dihydroxyphenyl)propanoyloxy]-4-hydroxy-5-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]cyclohexane-1-carboxylic acid 73316176 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2O)OC(=O)CCC3=CC(=C(C=C3)O)O)(C(=O)O)OC(=O)CCC4=CC(=C(C=C4)O)O)O 696.60 unknown https://doi.org/10.1021/NP070013R
1,4-Bis[3-(3,4-dihydroxyphenyl)propanoyloxy]-3-hydroxy-5-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]cyclohexane-1-carboxylic acid 162879440 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2OC(=O)CCC3=CC(=C(C=C3)O)O)O)(C(=O)O)OC(=O)CCC4=CC(=C(C=C4)O)O)O 696.60 unknown https://doi.org/10.1021/NP070013R
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1021/NP070013R
Feruloylpodospermic acid A 44424296 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2O)OC(=O)CCC3=CC(=C(C=C3)O)O)(C(=O)O)OC(=O)CCC4=CC(=C(C=C4)O)O)O 696.60 unknown https://doi.org/10.1021/NP070013R
Feruloylpodospermic acid B 44424298 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2OC(=O)CCC3=CC(=C(C=C3)O)O)O)(C(=O)O)OC(=O)CCC4=CC(=C(C=C4)O)O)O 696.60 unknown https://doi.org/10.1021/NP070013R
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1021/NP070013R
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1021/NP070013R
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 154497089 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/NP070013R

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