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Internal ID UUID643fdc0308124839621319
Scientific name Euchresta tubulosa
Authority Dunn
First published in J. Linn. Soc., Bot.35: 492 (1903)

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Common names Top

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Language Common/alternative name
Chinese 管萼山豆根
Chinese 鄂豆根

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Varieties (abbr. var.) Top

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Name Authority First published in
Euchresta tubulosa var. brevituba C.Chen Acta Phytotax. Sin.30: 50 (1992)
Euchresta tubulosa var. longiracemosa (S.Lee & H.Q.Wen) C.Chen Acta Phytotax. Sin.30: 50 (1992)
Euchresta tubulosa var. tubulosa Dunn Unknown

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Forms (abbr. f.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000198724
Tropicos 13058179
KEW urn:lsid:ipni.org:names:494678-1
The Plant List ild-45235
Open Tree Of Life 3923553
NCBI Taxonomy 2172547
IPNI 494678-1
GBIF 2951866
EOL 648877

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
Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity Cely-Veloza W, Kato MJ, Coy-Barrera E ACS Omega 28-Jul-2023
PMCID:PMC10413377
doi:10.1021/acsomega.3c02179
PMID:37576649
Characterization of the first chloroplast genome of Euchresta tubulosa Dunn and its phylogenetic analysis Zhuo W, Ren F, Wang L, Chen S, Chen Y, Huang H Mitochondrial DNA B Resour 09-Sep-2021
PMCID:PMC8439238
doi:10.1080/23802359.2021.1972866
PMID:34532578
Preparative Separation of Alkaloids from Stem of Euchresta tubulosa Dunn. by High-Speed Counter-Current Chromatography Using Stepwise Elution Li W, Wang H, Dong A Molecules 16-Dec-2019
PMCID:PMC6943640
doi:10.3390/molecules24244602
PMID:31888219
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
Flavonoids and a benzofuran in roots of Euchresta tubulosa Nobuyasu Matsuura, Munekazu Iinuma, Toshiyuki Tanaka, Mizuo Mizuno Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85477-9

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
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
6-Furo[2,3-f][1,3]benzodioxol-6-yl-2,2,8,8-tetramethylpyrano[2,3-f]chromene 163049367 Click to see CC1(C=CC2=CC(=C3C(=C2O1)C=CC(O3)(C)C)C4=CC5=CC6=C(C=C5O4)OCO6)C 402.40 unknown https://doi.org/10.1016/0031-9422(93)85477-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2R)-2-(2,2-dimethylchromen-6-yl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 163056879 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC5=C(C=C4)OC(C=C5)(C)C)O)C 472.60 unknown https://doi.org/10.1016/0031-9422(93)85477-9
(2S)-2-(2,2-dimethylchromen-6-yl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 163056880 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC5=C(C=C4)OC(C=C5)(C)C)O)C 472.60 unknown https://doi.org/10.1016/0031-9422(93)85477-9
Euchrenone a15 42607938 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC5=C(C=C4)OC(C=C5)(C)C)O)C 472.60 unknown https://doi.org/10.1016/0031-9422(93)85477-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(8R)-8-(2,2-dimethylchromen-6-yl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 162939035 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC5=C(C=C4)OC(C=C5)(C)C)O)C=CC(O2)(C)C)C 472.60 unknown https://doi.org/10.1016/0031-9422(93)85477-9
(8S)-8-(2,2-dimethylchromen-6-yl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 162939034 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC5=C(C=C4)OC(C=C5)(C)C)O)C=CC(O2)(C)C)C 472.60 unknown https://doi.org/10.1016/0031-9422(93)85477-9
Euchrenone a14 42607937 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC5=C(C=C4)OC(C=C5)(C)C)O)C=CC(O2)(C)C)C 472.60 unknown https://doi.org/10.1016/0031-9422(93)85477-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/0305-1978(94)90075-2
Vitexin-2''-O-rhamnoside 129661210 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/0305-1978(94)90075-2
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Euchretin B 15138441 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)OC4=C(C(=C(C=C34)O)O)CC=C(C)C)C 436.50 unknown https://doi.org/10.1016/0031-9422(93)85477-9
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
11,17-Dihydroxy-7,7,20,20-tetramethyl-10-(3-methylbut-2-enyl)-2,8,19,25-tetraoxahexacyclo[12.11.0.03,12.04,9.015,24.018,23]pentacosa-1(14),3,5,9,11,15,17,21,23-nonaen-13-one 85617815 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(O3)OC5=C6C=CC(OC6=C(C=C45)O)(C)C)C=CC(O2)(C)C)C 500.50 unknown https://doi.org/10.1016/0031-9422(93)85477-9
11,17-Dihydroxy-7,7,20,20-tetramethyl-4-(3-methylbut-2-enyl)-2,6,19,25-tetraoxahexacyclo[12.11.0.03,12.05,10.015,24.018,23]pentacosa-1(14),3(12),4,8,10,15,17,21,23-nonaen-13-one 85617813 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C5=CC(=C6C(=C5O4)C=CC(O6)(C)C)O)O)C=CC(O2)(C)C)C 500.50 unknown https://doi.org/10.1016/0031-9422(93)85477-9
5-Hydroxy-3-(5-hydroxy-2,2-dimethylchromen-6-yl)-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one 163024072 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=C(C5=C(C=C4)OC(C=C5)(C)C)O)C=CC(O2)(C)C)C 486.60 unknown https://doi.org/10.1016/0031-9422(93)85477-9
5-Hydroxy-7-(5-hydroxy-2,2-dimethylchromen-6-yl)-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one 163094428 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C5=C(C=C4)OC(C=C5)(C)C)O)O)C=CC(O2)(C)C)C 486.60 unknown https://doi.org/10.1016/0031-9422(93)85477-9
6,7,21-Trihydroxy-17,17-dimethyl-8,20-bis(3-methylbut-2-enyl)-10,12,18-trioxapentacyclo[11.8.0.03,11.04,9.014,19]henicosa-1(21),3(11),4,6,8,13,15,19-octaen-2-one 163047260 Click to see CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)OC4=C5C=CC(OC5=C(C(=C4C3=O)O)CC=C(C)C)(C)C)C 502.60 unknown https://doi.org/10.1016/0031-9422(93)85477-9
Euchretin A 10368763 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)OC4=C5C=CC(OC5=C(C=C34)O)(C)C)CC=C(C)C)O)C 502.60 unknown https://doi.org/10.1016/0031-9422(93)85477-9
Euchretin C 44260102 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)OC4=C(C(=C(C=C34)O)O)CC=C(C)C)CC=C(C)C)O)C 504.60 unknown https://doi.org/10.1016/0305-1978(94)90075-2
https://doi.org/10.1016/0031-9422(93)85477-9

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