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Tephrosia fulvinervis

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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
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Details Top

Internal ID UUID643fdcbdde228159659456
Scientific name Tephrosia fulvinervis
Authority Hochst. ex A.Rich.
First published in Tent. Fl. Abyss.1: 187 (1847)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cracca fulvinervis (Hochst. ex A.Rich.) Kuntze Revis. Gen. Pl.1: 175 (1891)

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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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-0000202384
Tropicos 13033439
KEW urn:lsid:ipni.org:names:520576-1
The Plant List ild-4874
Open Tree Of Life 3920228
IPNI 520576-1
GBIF 5342238
EOL 687536

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
Natural occurrence of Tephrosia flavones Saboor Ahmad Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(86)80037-1
Flavonoids from Tephrosia fulvinervis E. Venkata Rao, G. Venkataratnam, C. Vilain Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83056-3
Fulvinervin C, a flavone from Tephrosia fulvinervis G. Venkataratnam, E.Venkata Rao, C. Vilain Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81327-8
Flavonoids and isoflavonoids from Tephrosia fulvinervis and Tephrosia pentaphylla Ermias Dagne, Abiy Yenesew, Peter G. Waterman Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80308-5

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 / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydropyrano[2,3-h]chromen-4-one 101321355 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC=CC=C4)O)C 390.50 unknown https://doi.org/10.1016/S0031-9422(00)83056-3
Fulvinervin A 42607884 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC=CC=C4)O)C 390.50 unknown https://doi.org/10.1016/S0031-9422(00)81327-8
https://doi.org/10.1016/S0031-9422(00)83056-3
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
5-Hydroxy-6-(3-hydroxy-3-methyl-1-butenyl)-8,8-dimethyl-2-phenyl-4h,8h-benzo[1,2-b:3,4-b']dipy ran-4-one 74977432 Click to see CC1(C=CC2=C3C(=C(C(=C2O1)C=CC(C)(C)O)O)C(=O)C=C(O3)C4=CC=CC=C4)C 404.50 unknown https://doi.org/10.1016/S0031-9422(00)81327-8
5-Hydroxy-8,8-dimethyl-6-(3-methylbuta-1,3-dienyl)-2-phenylpyrano[2,3-h]chromen-4-one 74977431 Click to see CC(=C)C=CC1=C2C(=C3C(=C1O)C(=O)C=C(O3)C4=CC=CC=C4)C=CC(O2)(C)C 386.40 unknown https://doi.org/10.1016/S0031-9422(00)83056-3
Fulvinervin B 44257641 Click to see CC(=C)C=CC1=C2C(=C3C(=C1O)C(=O)C=C(O3)C4=CC=CC=C4)C=CC(O2)(C)C 386.40 unknown https://doi.org/10.1016/S0031-9422(00)83056-3
Fulvinervin C 44257642 Click to see CC1(C=CC2=C3C(=C(C(=C2O1)C=CC(C)(C)O)O)C(=O)C=C(O3)C4=CC=CC=C4)C 404.50 unknown https://doi.org/10.1016/0031-9422(86)80037-1
https://doi.org/10.1016/S0031-9422(00)81327-8
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
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(89)80308-5
Maackiain 91510 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(89)80308-5
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(-)-Deguelin;(-)-cis-Deguelin 606171 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown https://doi.org/10.1016/0031-9422(89)80308-5
(6aS,12aS)-12a-hydroxy-2,3,9-trimethoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one 133564748 Click to see COC1=CC2=C(C=C1)C(=O)C3(C(O2)COC4=CC(=C(C=C43)OC)OC)O 358.30 unknown https://doi.org/10.1016/0031-9422(89)80308-5
[1]Benzopyrano[3,4-b][1]benzopyran-12(6H)-one, 6a,12a-dihydro-2,3,9-trimethoxy-, (6aS-cis)- 14427371 Click to see COC1=CC2=C(C=C1)C(=O)C3C(O2)COC4=CC(=C(C=C34)OC)OC 342.30 unknown https://doi.org/10.1016/0031-9422(89)80308-5
12a-Hydroxymunduserone 14427372 Click to see COC1=CC2=C(C=C1)C(=O)C3(C(O2)COC4=CC(=C(C=C43)OC)OC)O 358.30 unknown https://doi.org/10.1016/0031-9422(89)80308-5
6-Hydroxy-9,10-dimethoxy-3,3-dimethyl-13,13a-dihydro-3H,7aH-pyrano[2,3-c:6,5-f']dichromen-7-one 243723 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C 410.40 unknown https://doi.org/10.1016/0031-9422(89)80308-5
alpha-Toxicarol 442826 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C 410.40 unknown https://doi.org/10.1016/0031-9422(89)80308-5
Deguelin 107935 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown https://doi.org/10.1016/0031-9422(89)80308-5
Mundoserone 3083809 Click to see COC1=CC2=C(C=C1)C(=O)C3C(O2)COC4=CC(=C(C=C34)OC)OC 342.30 unknown https://doi.org/10.1016/0031-9422(89)80308-5
Munduserone 315227 Click to see COC1=CC2=C(C=C1)C(=O)C3C(O2)COC4=CC(=C(C=C34)OC)OC 342.30 unknown https://doi.org/10.1016/0031-9422(89)80308-5
rel-(7aR,13aR)-9,10-Dimethoxy-3,3-dimethyl-13,13a-dihydro-3H-pyrano[2,3-c:6,5-f']dichromen-7(7aH)-one 184223 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown https://doi.org/10.1016/0031-9422(89)80308-5

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