Hedysarum sachalinense

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Internal ID	UUID643fd987a145a303210662
Scientific name	Hedysarum sachalinense
Authority	B.Fedtsch.
First published in	Sborn. President Akad. Nauk V. L. Komarov, reimpr.: 737 (1939)

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Synonyms Top

Scientific name	Authority	First published in
Hedysarum hedysaroides subsp. sachalinense	(B.Fedtsch.) Vorosch.	Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol., n.s., 96(1): 133 (1991)

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Varieties (abbr. var.) 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
- Russian Far East
  - Sakhalin

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000185999
Tropicos	13056871
KEW	urn:lsid:ipni.org:names:498073-1
The Plant List	ild-32336
PFAF	Hedysarum sachalinense
Open Tree Of Life	3922432
Observations.org	142163
IPNI	498073-1
GBIF	2960851
EOL	643680
Elurikkus	341887
CMAUP	NPO3331

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)!

Title

Authors

Publication

Released

IDs

Phenolic compounds ofHedysarum sachalinense andH. Brandtii

V. I. Glyzin, A. I. Ban'kovskii, N. S. Pavlova

Springer Science and Business Media LLC

20-Nov-2004

doi:	10.1007/BF00567331

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 / Gallic acid and derivatives
[(1R,2R)-1-(7-methoxy-1,3-benzodioxol-5-yl)-2-methyl-3-oxobutyl] 3,4,5-trimethoxybenzoate	11859073	Click to see CC(C(C1=CC2=C(C(=C1)OC)OCO2)OC(=O)C3=CC(=C(C(=C3)OC)OC)OC)C(=O)C	446.40	unknown	via CMAUP database
[(1S,2R)-2-methyl-3-oxo-1-(3,4,5-trimethoxyphenyl)butyl] 7-methoxy-1,3-benzodioxole-5-carboxylate	11859072	Click to see CC(C(C1=CC(=C(C(=C1)OC)OC)OC)OC(=O)C2=CC3=C(C(=C2)OC)OCO3)C(=O)C	446.40	unknown	via CMAUP database
Tsangin C	56661913	Click to see CC(C(C1=CC(=C(C(=C1)OC)OC)OC)OC(=O)C2=CC(=C(C(=C2)OC)OC)OC)C(=O)C	462.50	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
4Alpha,5Alpha-Epoxybeilschmin A	71454057	Click to see CC1C(OC2(C1(O2)C)C3=CC4=C(C(=C3)OC)OCO4)C5=CC(=C(C(=C5)OC)OC)OC	430.40	unknown	via CMAUP database
4Alpha,5Alpha-Epoxybeilschmin B	71459474	Click to see CC1C(OC2(C1(O2)C)C3=CC(=C(C(=C3)OC)OC)OC)C4=CC(=C(C(=C4)OC)OC)OC	446.50	unknown	via CMAUP database
Beilschmin D	71455792	Click to see CC1C(OC2(C1(O2)C)C3=CC4=C(C(=C3)OC)OCO4)C5=CC6=C(C(=C5)OC)OCO6	414.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
Beilschmin A	22297613	Click to see CC1C(C(OC1C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC)C	416.50	unknown	via CMAUP database
Beilschmin B	14352170	Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C	432.50	unknown	via CMAUP database
beilschminol A, rel-	54671632	Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)O)C3=CC4=C(C(=C3)OC)OCO4)C	402.40	unknown	via CMAUP database
rel-(7S,8S,7'R,8'R)-3,3',4,4',5,5'-hexamethoxy-7.O.7',8.8'-lignan	21827796	Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C	432.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl linoleate	5284421	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC	294.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
alpha-Tocopherolquinone	2734086	Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C	446.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Tanacetene	5321610	Click to see CC(=CCCC=C(C)CCC=C(C)C)C	206.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
alpha-Tocospiro-B	21674157	Click to see CC1=C(C(C2(C1=O)CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)(C(=O)C)O)C	462.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene	638072	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Ergosta-4,6,8(14),22-tetraen-3-one	6441416	Click to see CC(C)C(C)C=CC(C)C1CCC2=C3C=CC4=CC(=O)CCC4(C3CCC12C)C	392.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
3-Hydroxystigmast-5-en-7-one	160608	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C	428.70	unknown	via CMAUP database
6alpha-Hydroxystigmast-4-en-3-one	9867274	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C	428.70	unknown	via CMAUP database
6beta-Hydroxystigmast-4-en-3-one	9823926	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C	428.70	unknown	via CMAUP database
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
Stigmast-4-en-3-one	5484202	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	via CMAUP database
Stigmast-4-ene-3,6-dione	5490007	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(=O)CCC34C)C)C(C)C	426.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Endiandramide A	54669853	Click to see CC(C)CNC(=O)C1C=CC2CC3C(C4C3C2C1C=C4)CC5=CC6=C(C=C5)OCO6	405.50	unknown	via CMAUP database
tsangibeilin A, rac-	54671628	Click to see C1C2C=CC(C3C2C4C1C(C4C=C3)CCCC5=CC6=C(C=C5)OCO6)C(=O)O	378.50	unknown	via CMAUP database
tsangibeilin B, rel-	54671629	Click to see C1C2C=CC(C3C2C4C1C(C4C=C3)CC5=CC6=C(C=C5)OCO6)C(=O)O	350.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,6,7-Tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one	5358385	Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O	422.30	unknown	https://doi.org/10.1007/BF00567331
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1007/BF00567331
3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	12308704	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1007/BF00567331
3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	5320668	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1007/BF00567331
Avicularin	5490064	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1007/BF00567331
Isoquercitin	10813969	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1007/BF00567331

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Hedysarum sachalinense

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