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Caragana conferta

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fd9b3aa14c151584576
Scientific name Caragana conferta
Authority Benth. ex Baker
First published in J.D.Hooker, Fl. Brit. India2: 116 (1876)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Aspalathus confertus (Benth. ex Baker) Kuntze Revis. Gen. Pl.1: 161 (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-0000186887
Tropicos 13049168
KEW urn:lsid:ipni.org:names:483814-1
The Plant List ild-33391
Open Tree Of Life 78091
NCBI Taxonomy 626677
IUCN Red List 19892732
IPNI 483814-1
iNaturalist 139445
GBIF 2943223
EOL 643744

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
Caragisides A – C, New Isoflavone Glucosides from <i>Caragana conferta</i> with Inhibition of Platelet Aggregation Amna Nisar Khan, Itrat Fatima, Abdul Malik, Huma Rasheed Wiley 14-Mar-2011
doi:10.1002/HLCA.201000210
Phenolic substances of Caragana conferta and their superoxide scavenging activity R. Khan, A. Malik, M. I. Qadir, A. Adhikari, M. I. Choudhary Springer Science and Business Media LLC 08-Nov-2010
doi:10.1007/S10600-010-9725-Z
Conferols A and B, new anti-inflammatory 4-hydroxyisoflavones from Caragana conferta. Khan R, Malik A, Adhikari A, Qadir MI, Choudhary MI Chem Pharm Bull (Tokyo) 01-Apr-2009
doi:10.1248/CPB.57.415
PMID:19336940

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.57.415
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1248/CPB.57.415
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
Phenolphthalein 4764 Click to see C1=CC=C2C(=C1)C(=O)OC2(C3=CC=C(C=C3)O)C4=CC=C(C=C4)O 318.30 unknown https://doi.org/10.1007/S10600-010-9725-Z
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Scutellarein 4'-methyl ether 11174076 Click to see 300.26 unknown https://doi.org/10.1007/S10600-010-9725-Z
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
7,5'-Dihydroxy-2'-methoxyisoflavone 50907453 Click to see 284.26 unknown https://doi.org/10.1007/S10600-010-9725-Z
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
7-hydroxy-3-[4-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 52914106 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1002/HLCA.201000210
7-Hydroxy-3-[4-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 163037489 Click to see 446.40 unknown https://doi.org/10.1002/HLCA.201000210
7-methoxy-3-(4-methoxyphenyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 52914010 Click to see 460.40 unknown https://doi.org/10.1002/HLCA.201000210
7-Methoxy-3-(4-methoxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163036803 Click to see 460.40 unknown https://doi.org/10.1002/HLCA.201000210
methyl 3-(7-methoxy-4-oxochromen-3-yl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 52914107 Click to see 488.40 unknown https://doi.org/10.1002/HLCA.201000210
Methyl 3-(7-methoxy-4-oxochromen-3-yl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 163006954 Click to see COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC(=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)C(=O)OC 488.40 unknown https://doi.org/10.1002/HLCA.201000210
Npc198030 3733033 Click to see 430.40 unknown https://doi.org/10.1002/HLCA.201000210
Ononin 442813 Click to see 430.40 unknown https://doi.org/10.1002/HLCA.201000210
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 2-O-methylated isoflavonoids
Conferol A 42604344 Click to see 288.29 unknown https://doi.org/10.1248/CPB.57.415
Conferol B 42604345 Click to see 270.32 unknown https://doi.org/10.1248/CPB.57.415
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Formononetin 5280378 Click to see 268.26 unknown https://doi.org/10.1007/S10600-010-9725-Z

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