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Tephrosia sinapou

Tephrosia sinapou - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fdd1caf6d7148908935
Scientific name Tephrosia sinapou
Authority (Buc'hoz) A.Chev.
First published in Compt. Rend. Hebd. Séances Acad. Sci.180: 1522 (1925)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tephrosia emarginata Kunth F.W.H.von Humboldt, A.J.A.Bonpland & C.S.Kunth, Nov. Gen. Sp.6: 461 (1824)
Cracca schiedeana (Schltdl.) Standl. Contr. U.S. Natl. Herb.23: 474 (1922)
Tephrosia schiedeana Schltdl. Linnaea12: 299 (1838)
Cracca toxicaria (Sw.) Kuntze Revis. Gen. Pl.1: 175 (1891)
Galega sinapou Buc'hoz Hist. Univ. Règne Vég.10: t. 4 (1777)
Galega toxicaria Sw. Prodr. Veg. Ind. Occ.: 108 (1788)
Galega sericea Lam. Encycl. [J. Lamarck & al.] 2(2): 596. 1788 [14 Apr 1788]
Tephrosia toxicaria (Sw.) Pers. Syn. Pl.2: 329 (1807)

Common names Top

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Language Common/alternative name
English hoarypea

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
  • Africa
    • East Tropical Africa
      • Tanzania
    • West-central Tropical Africa
      • Zaïre
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
    • Caribbean
      • Dominican Republic
      • Haiti
      • Trinidad-Tobago
    • Central America
      • El Salvador
      • Honduras
      • Nicaragua
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000204324
USDA Plants TESI2
Tropicos 13003501
INPN 729281
KEW urn:lsid:ipni.org:names:250423-2
The Plant List ild-5063
Open Tree Of Life 3920315
IPNI 250423-2
iNaturalist 280757
GBIF 5341992
USDA GRIN 80177

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
Unequivocal assignments of flavonoids from Tephrosia sp. (Fabaceae). Arriaga AM, Lima JQ, Vasconcelos JN, de Oliveira MC, Andrade-Neto M, Santiago GM, Uchoa DE, Malcher GT, Mafezoli J, Braz-Filho R Magn Reson Chem 01-Jun-2009
doi:10.1002/MRC.2422
PMID:19306481
221. The active principles of leguminous fish-poison plants. Part V. Derris malaccensis and Tephrosia toxicaria Stanley H. Harper Royal Society of Chemistry (RSC) 21-Apr-2004
doi:10.1039/JR9400001178
Potential cncer chemopreventive flavonoids from the stems of Tephrosia toxicaria. Jang DS, Park EJ, Kang YH, Hawthorne ME, Vigo JS, Graham JG, Cabieses F, Fong HH, Mehta RG, Pezzuto JM, Kinghorn AD J Nat Prod 01-Sep-2003
doi:10.1021/NP0302100
PMID:14510590

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 / Benzoic acid esters
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown https://doi.org/10.1021/NP0302100
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 7092730 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1021/NP0302100
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1021/NP0302100
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1021/NP0302100
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
(2S)-2-cyclohexa-1,5-dien-1-yl-5-hydroxy-7-methoxy-8-[(E)-3-oxobut-1-enyl]-2,3-dihydrochromen-4-one 163189172 Click to see CC(=O)C=CC1=C(C=C(C2=C1OC(CC2=O)C3=CCCC=C3)O)OC 340.40 unknown https://doi.org/10.1021/NP0302100
2-Cyclohexa-1,5-dien-1-yl-5-hydroxy-7-methoxy-8-(3-oxobut-1-enyl)-2,3-dihydrochromen-4-one 162938573 Click to see CC(=O)C=CC1=C(C=C(C2=C1OC(CC2=O)C3=CCCC=C3)O)OC 340.40 unknown https://doi.org/10.1021/NP0302100
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Benzyl cinnamate 5273469 Click to see C1=CC=C(C=C1)COC(=O)C=CC2=CC=CC=C2 238.28 unknown https://doi.org/10.1021/NP0302100
Benzylcinnamate 7652 Click to see C1=CC=C(C=C1)COC(=O)C=CC2=CC=CC=C2 238.28 unknown https://doi.org/10.1021/NP0302100
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one 604512 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1021/NP0302100
Marmesin 334704 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1021/NP0302100
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1021/NP0302100
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5-hydroxy-7-methoxy-8-[(E)-3-oxo-1-butenyl]flavanone 10980660 Click to see CC(=O)C=CC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC 338.40 unknown https://doi.org/10.1021/NP0302100
5-Hydroxy-7-methoxy-8-(3-oxobut-1-enyl)-2-phenyl-2,3-dihydrochromen-4-one 73808139 Click to see CC(=O)C=CC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC 338.40 unknown https://doi.org/10.1021/NP0302100
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
5-Hydroxy-8,8-dimethyl-2-phenyl-2,3-dihydropyrano[2,3-h]chromen-4-one 13940732 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC(CC3=O)C4=CC=CC=C4)O)C 322.40 unknown https://doi.org/10.1021/NP0302100
https://doi.org/10.1002/MRC.2422
Obovatin 13940733 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC(CC3=O)C4=CC=CC=C4)O)C 322.40 unknown https://doi.org/10.1002/MRC.2422
https://doi.org/10.1021/NP0302100
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1021/NP0302100
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(12H)-one, 1,2-dihydro-8,9-dimethoxy-2-(1-methylethenyl)-, (R)- 99190 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC 392.40 unknown https://doi.org/10.1002/MRC.2422
(1R,14R)-11,14-dihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.0^{3,12.0^{4,9.0^{15,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one 13846202 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C 426.40 unknown https://doi.org/10.1021/NP0302100
(1R,14S)-11,14-dihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one 162980813 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C 426.40 unknown https://doi.org/10.1021/NP0302100
(1R,5R,6S,14R)-6,11,14-trihydroxy-5,17,18-trimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),10,15,17,19-hexaen-13-one 162889174 Click to see CC1(C(C(C2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)OC)O)C 474.50 unknown https://doi.org/10.1021/NP0302100
(1R,5S,6S,14R)-6,11,14-trihydroxy-5,17,18-trimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),10,15,17,19-hexaen-13-one 162889173 Click to see CC1(C(C(C2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)OC)O)C 474.50 unknown https://doi.org/10.1021/NP0302100
(1S,14R)-11,14-dihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one 124355889 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C 426.40 unknown https://doi.org/10.1021/NP0302100
11-Hydroxytephrosin 155725 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C 426.40 unknown https://doi.org/10.1021/NP0302100
4',5'-Dihydro-11,5'-dihydroxy-4'-methoxytephrosin 11762505 Click to see CC1(C(C(C2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)OC)O)C 474.50 unknown https://doi.org/10.1021/NP0302100
5-Hydroxy-8,9-dimethoxy-2-(prop-1-en-2-yl)-1,2,12,12a-tetrahydrofuro[2',3':7,8][1]benzopyrano[2,3-c][1]benzopyran-6(6aH)-one 3665545 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O 410.40 unknown https://doi.org/10.1021/NP0302100
https://doi.org/10.1039/JR9400001178
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/10.1021/NP0302100
6,11,14-Trihydroxy-5,17,18-trimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),10,15,17,19-hexaen-13-one 73090323 Click to see CC1(C(C(C2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)OC)O)C 474.50 unknown https://doi.org/10.1021/NP0302100
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/10.1021/NP0302100
Dehydrorotenone 303993 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC 392.40 unknown https://doi.org/10.1002/MRC.2422
Dehydrotoxicarol 5491616 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)O)C 408.40 unknown https://doi.org/10.1021/NP0302100
Sumatrol 442824 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O 410.40 unknown https://doi.org/10.1039/JR9400001178
https://doi.org/10.1021/NP0302100
Villosol 5490819 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)O 408.40 unknown https://doi.org/10.1021/NP0302100
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1021/NP0302100
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1021/NP0302100

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