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Euchresta horsfieldii

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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 UUID643fd99ac1ff4358031969
Scientific name Euchresta horsfieldii
Authority (Lesch.) Benn.
First published in Pl. Jav. Rar.: 148 (1840)

Description Top

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Synonyms Top

Scientific name Authority First published in
Euchresta horsfeldii (Lesch.) Benn.
Euchresta strigillosa C.Y.Wu Acta Phytotax. Sin.6: 249 (1957)
Andira horsfieldii Lesch. Ann. Mus. Hist. Nat.16: 481 (1810)
Euchresta horsfieldii var. horsfieldii (Lesch.) Benn.
Euchresta horsfieldii var. bhutanica H.Ohashi
Euchresta strigillosa C.Y.Wu Acta Phytotax. Sin. 6: 249 (1957)
Geoffroea horsfieldii (Lesch.) Oken Allg. Naturgesch.3(2): 1784 (1841)
Euchresta horsfieldii var. laotica Dy Phon Bull. Mus. Natl. Hist. Nat., B, Adansonia3: 118 (1981)

Common names Top

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Language Common/alternative name
Chinese 苦参
Chinese 伏毛山豆根

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-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
    • Indo-China
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Philippines
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000186315
Tropicos 13051766
KEW urn:lsid:ipni.org:names:494673-1
The Plant List ild-32755
Open Tree Of Life 908594
NCBI Taxonomy 53879
IPNI 494673-1
iNaturalist 347762
GBIF 2951871
EOL 643928

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
Phytosomes as an Emerging Nanotechnology Platform for the Topical Delivery of Bioactive Phytochemicals Alharbi WS, Almughem FA, Almehmady AM, Jarallah SJ, Alsharif WK, Alzahrani NM, Alshehri AA Pharmaceutics 15-Sep-2021
PMCID:PMC8465302
doi:10.3390/pharmaceutics13091475
PMID:34575551
Corrigendum N/A Appl Plant Sci 07-Jun-2019
PMCID:PMC6580981
doi:10.1002/aps3.1252
PMID:31236311
Development of 10 single‐copy nuclear DNA markers for Euchresta horsfieldii (Fabaceae), a rare medicinal plant Priyadi A, Feng C, Kang M, Huang H Appl Plant Sci 21-Sep-2018
PMCID:PMC6159642
doi:10.1002/aps3.1178
PMID:30276026
Phylogenetic analysis in genus Euchresta based on secondary metabolites Nobuyasu Matsuura, Munekazu Iinuma, Toshiyuki Tanaka Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(94)90075-2
Isoflavones from stems of Euchresta horsfieldii Mizuo Mizuno, Nobuyasu Matsuura, Munekazu Iinuma, Toshiyuki Tanaka, Chamlong Phengklai Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85211-W
(+)-5α,9α-dihydroxymatrine, a new lupin alkaloid from Euchresta horsfeldii Shigeru Ohmiya, Kimio Higashiyama, Hirotaka Otomasu, Isamu Murakoshi, Joju Haginiwa Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84277-6
Flavonoids in the roots of Euchresta horsfieldii in Thailand Mizuo Mizuno, Toshiyuki Tanaka, Koh-Ichi Tamura, Nobuyasu Matsuura, Munekazu Iinuma, Chamlong Phengklai Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85208-W
Two flavanones from Euchresta horsfieldii Mizuo Mizuno, Toshiyuki Tanaka, Nobuyasu Matsuura, Munekazu Iinuma, Chen Cheih Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85236-9

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
(+)-Thermopsine 682648 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/S0031-9422(00)84277-6
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(+)-Cytisine 683511 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/S0031-9422(00)84277-6
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 1747617 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1016/S0031-9422(00)84277-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 149043 Click to see CCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 418.60 unknown https://doi.org/10.1016/0031-9422(90)85208-W
Hexadecyl ferulate 6440079 Click to see CCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 418.60 unknown https://doi.org/10.1016/0031-9422(90)85208-W
https://doi.org/10.1016/0031-9422(90)85236-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
eriosemaone A 11742973 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=C(C=C(C=C4)O)O)O)C 422.50 unknown https://doi.org/10.1016/0031-9422(90)85208-W
Euchrenone a9 14704583 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=C(C=C(C=C4)O)O)O)C 422.50 unknown https://doi.org/10.1016/0031-9422(90)85208-W
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 5318894 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)O)C 424.50 unknown https://doi.org/10.1016/0305-1978(94)90075-2
https://doi.org/10.1016/0031-9422(90)85208-W
(2R)-7-hydroxy-2-[2-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162919461 Click to see CC(=CCC1=CC(=C(C=C1OC)O)C2CC(=O)C3=C(O2)C(=C(C=C3)O)CC=C(C)C)C 422.50 unknown https://doi.org/10.1016/0031-9422(90)85236-9
(2R)-7-hydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 129360227 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C(=C(C=C3)O)CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1016/0031-9422(90)85236-9
(2S)-7-hydroxy-2-[2-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 163189669 Click to see CC(=CCC1=CC(=C(C=C1OC)O)C2CC(=O)C3=C(O2)C(=C(C=C3)O)CC=C(C)C)C 422.50 unknown https://doi.org/10.1016/0031-9422(90)85236-9
(2S)-Euchrenone A7 44593508 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C 340.40 unknown https://doi.org/10.1016/0031-9422(90)85236-9
(S)-4',7-Dihydroxy-3',8-diprenylflavanone 480768 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C(=C(C=C3)O)CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1016/0031-9422(90)85236-9
2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 9979767 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)O)C 424.50 unknown https://doi.org/10.1016/0031-9422(90)85208-W
Euchrenone a8 14704601 Click to see CC(=CCC1=CC(=C(C=C1OC)O)C2CC(=O)C3=C(O2)C(=C(C=C3)O)CC=C(C)C)C 422.50 unknown https://doi.org/10.1016/0031-9422(90)85236-9
Euchrenone-a7 10291003 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C 340.40 unknown https://doi.org/10.1016/0031-9422(90)85236-9
Glabrol 11596309 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C(=C(C=C3)O)CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1016/0031-9422(90)85236-9
Kushenol E 127234 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)O)C 424.50 unknown https://doi.org/10.1016/0305-1978(94)90075-2
https://doi.org/10.1016/0031-9422(90)85208-W
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257674 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0305-1978(94)90075-2
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Tephrosol 14704585 Click to see COC1=C(C=C2C(=C1)C3=C(C4=CC5=C(C=C4O3)OCO5)C(=O)O2)O 326.26 unknown https://doi.org/10.1016/0031-9422(90)85208-W
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(1R,12R)-15-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 102060272 Click to see COC1=C(C=C2C(=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5)O 314.29 unknown https://doi.org/10.1016/0031-9422(90)85208-W
15-Methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 14704584 Click to see COC1=C(C=C2C(=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5)O 314.29 unknown https://doi.org/10.1016/0031-9422(90)85208-W
3-Hydroxy-8,9-methylenedioxypterocarpane 363863 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown https://doi.org/10.1016/0031-9422(90)85211-W
https://doi.org/10.1016/0031-9422(90)85236-9
Sophoracarpan B 14704594 Click to see COC1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 314.29 unknown https://doi.org/10.1016/0031-9422(90)85211-W
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
4'-O-methylalpinumisoflavone 15596285 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)OC)C 350.40 unknown https://doi.org/10.1016/0031-9422(90)85208-W
5-hydroxy-10-[(2R)-2-hydroxy-3-methylbut-3-enyl]-7-(4-hydroxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one 163186580 Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)O 420.50 unknown https://doi.org/10.1016/0031-9422(90)85211-W
5-hydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-8,8-dimethylpyrano[2,3-h]chromen-4-one 163015412 Click to see CC(=C)C(CC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C=CC(O2)(C)C)O 420.50 unknown https://doi.org/10.1016/0031-9422(90)85211-W
6,8-Diprenylgenistein 480783 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC=C(C)C)O)C 406.50 unknown https://doi.org/10.1016/0031-9422(90)85211-W
https://doi.org/10.1016/0031-9422(90)85208-W
Euchrenone b6 14704590 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CCC(C)(C)O)OC=C(C3=O)C4=CC=C(C=C4)O)O)C 422.50 unknown https://doi.org/10.1016/0031-9422(90)85211-W
Euchrenone b7 14704592 Click to see CC1(C=CC2=C3C(=C(C(=C2O1)CCC(C)(C)O)O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C 422.50 unknown https://doi.org/10.1016/0031-9422(90)85211-W
Euchrenone b8 14704591 Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)O 420.50 unknown https://doi.org/10.1016/0031-9422(90)85211-W
Euchrenone b9 14704593 Click to see CC(=C)C(CC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C=CC(O2)(C)C)O 420.50 unknown https://doi.org/10.1016/0031-9422(90)85211-W
Osajin 95168 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C=CC(O2)(C)C)C 404.50 unknown https://doi.org/10.1016/0031-9422(90)85208-W
https://doi.org/10.1016/0031-9422(90)85211-W
Warangalone 5379679 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 404.50 unknown https://doi.org/10.1016/0031-9422(90)85208-W
https://doi.org/10.1016/0305-1978(94)90075-2
https://doi.org/10.1016/0031-9422(90)85211-W
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
8-O-methylretusin 5319771 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC)O 298.29 unknown https://doi.org/10.1016/0031-9422(90)85211-W
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
4'-O-Methylderrone 15596286 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC=C(C3=O)C4=CC=C(C=C4)OC)O)C 350.40 unknown https://doi.org/10.1016/0031-9422(90)85208-W

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