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Crotalaria ramosissima

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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 UUID643fd75686649341088838
Scientific name Crotalaria ramosissima
Authority Roxb.
First published in Fl. Ind. ed. 1832, 3: 268 (1832)

Description Top

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Synonyms Top

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Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Crotalaria ramosissima var. ramnadensis A.A.Ansari Crotalaria India: 249 (2008)
Crotalaria ramosissima var. ramosissima

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000174080
The Plant List ild-20196
Open Tree Of Life 3927841
NCBI Taxonomy 1978219
IPNI 110311-3
GBIF 2942321
EOL 640359

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
Synthesis and evaluation of novel chromanone and quinolinone analogues of uniflorol as anti-leishmanial agents Castro H, Cruz T, de Aguiar Amaral P, da Silva Cardoso P, Alsaffar A, Farrell P, Tomás AM, Barlow JW Heliyon 20-Mar-2020
PMCID:PMC7096758
doi:10.1016/j.heliyon.2020.e03614
PMID:32258470
Cinnamic Acid Bornyl Ester Derivatives from Valeriana wallichii Exhibit Antileishmanial In Vivo Activity in Leishmania major-Infected BALB/c Mice Masic A, Valencia Hernandez AM, Hazra S, Glaser J, Holzgrabe U, Hazra B, Schurigt U PLoS One 10-Nov-2015
PMCID:PMC4640567
doi:10.1371/journal.pone.0142386
PMID:26554591
A new trimethoxychalcone from Crotalaria ramosissima. Rao MS, Narukulla R Fitoterapia 01-Sep-2007
doi:10.1016/J.FITOTE.2007.03.011
PMID:17616261
Prenylated chalcones isolated from Crotalaria genus inhibits in vitro growth of the human malaria parasite Plasmodium falciparum. Narender T, Shweta, Tanvir K, Rao MS, Srivastava K, Puri SK Bioorg Med Chem Lett 16-May-2005
doi:10.1016/J.BMCL.2005.03.081
PMID:15929201
Further dihydrochalcones from Crotolaria ramosissima J.K. Kumar, T. Narender, M.S. Rao, P.S. Rao, G. Tóth, B. Balázs, H. Duddeck FapUNIFESP (SciELO) 25-Apr-2005
doi:10.1590/S0103-50531999000400004
Crotaramosmin, a New Prenylated Flavanone from Crotalaria ramosissima Md. Khalilullah, V. M. Sharma, P. S. Rao, K. Raghava Raju American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50080A013
Munchiwarin, a prenylated chalcone from crotalaria trifoliastrum. Yang SW, Cordell GA, Lotter H, Wagner H, Mouly BC, Appa Rao AVN, Rao PS J Nat Prod 01-Oct-1998
doi:10.1021/NP970223B
PMID:9784166
A revised structure for crotaramosmin from crotolaria ramosissima. Rao MS, Rao PS, Toth G, Balazs B, Duddeck H J Nat Prod 01-Sep-1998
doi:10.1021/NP980043H
PMID:9748387

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
(2R)-5-hydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 163043722 Click to see CC(=CCC1=C(C2=C(C=C1)OC(CC2=O)C3=CC=C(C=C3)O)O)C 324.40 unknown https://doi.org/10.1021/NP970223B
Crotaramosmin 42607840 Click to see CC(=CCC1=C(C2=C(C=C1)OC(CC2=O)C3=CC=C(C=C3)O)O)C 324.40 unknown https://doi.org/10.1021/NP50080A013
https://doi.org/10.1021/NP980043H
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-(5-Hydroxy-2,2-Dimethylchromen-6-Yl)-3-(4-Hydroxyphenyl)Propan-1-One 9973521 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)CCC3=CC=C(C=C3)O)C 324.40 unknown https://doi.org/10.1016/J.BMCL.2005.03.081
Crotaramin 11325222 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)CCC3=CC=C(C=C3)OC)C 338.40 unknown https://doi.org/10.1016/J.BMCL.2005.03.081
https://doi.org/10.1590/S0103-50531999000400004
Crotin (chalcone) 11473265 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)CCC3=CC(=C(C=C3)O)O)C 340.40 unknown https://doi.org/10.1016/J.BMCL.2005.03.081
https://doi.org/10.1590/S0103-50531999000400004
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-(5-hydroxy-2,2-dimethylchromen-6-yl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one 66571756 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)C 396.40 unknown https://doi.org/10.1016/J.FITOTE.2007.03.011
1-(5-Hydroxy-2,2-dimethylchromen-6-yl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one 77145044 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)C 396.40 unknown https://doi.org/10.1016/J.FITOTE.2007.03.011
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retrochalcones
Trimethoxy-chalcone 54454091 Click to see COC1=C(C(=C(C=C1)C=CC(=O)C2=CC=CC=C2)OC)OC 298.30 unknown https://doi.org/10.1016/J.FITOTE.2007.03.011

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