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Hedysarum theinum

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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 UUID643fde12bee2b928450093
Scientific name Hedysarum theinum
Authority Krasnob.
First published in Bot. Zhurn. (Moscow & Leningrad)70: 970 (1985)

Description Top

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Synonyms Top

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Common names Top

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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
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
    • Mongolia
      • Mongolia
    • Siberia
      • Altay

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000209188
Tropicos 50042122
KEW urn:lsid:ipni.org:names:906252-1
The Plant List ild-55209
Open Tree Of Life 3922437
Observations.org 147597
NCBI Taxonomy 2419554
IPNI 906252-1
GBIF 2960861
EOL 681941
Elurikkus 341894
CMAUP NPO8435

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
Current state of populations of Rhodiola rosea L. (Crassulaceae) in East Kazakhstan Kubentayev SA, Zhumagul MZ, Kurmanbayeva MS, Alibekov DT, Kotukhov JA, Sitpayeva GT, Mukhtubayeva SK, Izbastina KS Bot Stud 07-Nov-2021
PMCID:PMC8572951
doi:10.1186/s40529-021-00327-4
PMID:34746988
Modern Trends in the In Vitro Production and Use of Callus, Suspension Cells and Root Cultures of Medicinal Plants Babich O, Sukhikh S, Pungin A, Ivanova S, Asyakina L, Prosekov A Molecules 09-Dec-2020
PMCID:PMC7763305
doi:10.3390/molecules25245805
PMID:33316965
Isolation and identification of 4′,6-dimethoxy-7-hydroxyisoflavone from roots of Hedysarum theinum cultivated in vitro I. V. Nechepurenko, N. I. Komarova, I. N. Kuzovkina, M. Yu. Vdovitchenko, M. P. Polovinka, N. F. Salakhutdinov Springer Science and Business Media LLC 11-Aug-2009
doi:10.1007/S10600-009-9327-9
Low-molecular-weight phenolic compounds from Hedysarum theinum roots I. V. Nechepurenko, M. P. Polovinka, N. I. Komarova, D. V. Korchagina, N. F. Salakhutdinov, S. B. Nechepurenko Springer Science and Business Media LLC 22-Apr-2008
doi:10.1007/S10600-008-0009-9
Components of the ethylacetate extract of Hedysarum theinum roots I. V. Nechepurenko, N. P. Polovinka, O. I. Sal’nikova, L. M. Pokrovskii, N. I. Komarova, N. F. Salakhutdinov, S. B. Nechepurenko Springer Science and Business Media LLC 19-Apr-2007
doi:10.1007/S10600-007-0052-Y

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1007/S10600-008-0009-9
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(+)-Rhododendrol 919204 Click to see CC(CCC1=CC=C(C=C1)O)O 166.22 unknown https://doi.org/10.1007/S10600-008-0009-9
https://doi.org/10.1007/S10600-007-0052-Y
4-(3-Hydroxybutyl)phenol 97790 Click to see CC(CCC1=CC=C(C=C1)O)O 166.22 unknown https://doi.org/10.1007/S10600-007-0052-Y
https://doi.org/10.1007/S10600-008-0009-9
4-(4-Hydroxyphenyl)-2-butanone 21648 Click to see CC(=O)CCC1=CC=C(C=C1)O 164.20 unknown https://doi.org/10.1007/S10600-007-0052-Y
https://doi.org/10.1007/S10600-008-0009-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechin 73160 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1007/S10600-008-0009-9
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1007/S10600-008-0009-9
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1007/S10600-008-0009-9
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
9-Methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol 623060 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1007/S10600-007-0052-Y
https://doi.org/10.1007/S10600-008-0009-9
Medicarpin 336327 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1007/S10600-007-0052-Y
https://doi.org/10.1007/S10600-008-0009-9
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
8-Hydroxydaidzein 5466139 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3O)O)O 270.24 unknown https://doi.org/10.1007/S10600-008-0009-9
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
[3,4,5-Trihydroxy-6-[3-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl acetate 162902421 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC3=C(C=C2)C(=O)C(=CO3)C4=CC=C(C=C4)OC)O)O)O 472.40 unknown https://doi.org/10.1007/S10600-008-0009-9
6''-O-Acetylononin 102463148 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC3=C(C=C2)C(=O)C(=CO3)C4=CC=C(C=C4)OC)O)O)O 472.40 unknown https://doi.org/10.1007/S10600-008-0009-9
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(+)-Vestitol 177149 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown https://doi.org/10.1007/S10600-008-0009-9
Vestitol 92503 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown https://doi.org/10.1007/S10600-007-0052-Y
https://doi.org/10.1007/S10600-008-0009-9
Vestitol, (-)- 182259 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown https://doi.org/10.1007/S10600-007-0052-Y
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afrormosin 5281704 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O 298.29 unknown https://doi.org/10.1007/S10600-009-9327-9
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1007/S10600-008-0009-9
https://doi.org/10.1007/S10600-007-0052-Y

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