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Internal ID UUID643fdf1e68d3c524567944
Scientific name Podocytisus caramanicus
Authority Boiss. & Heldr.
First published in P.E.Boissier, Diagn. Pl. Orient.9: 7 (1849)

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Synonyms Top

Scientific name Authority First published in
Laburnum caramanicum (Boiss. & Heldr.) Benth. & Hook.f. Gen. Pl.1: 481 (1865)
Cytisus caramanicus Nyman Consp. Fl. Eur.: 155 (1878)

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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-0000213929
Tropicos 13054046
KEW urn:lsid:ipni.org:names:515441-1
The Plant List ild-8994
Open Tree Of Life 179595
Observations.org 120749
NCBI Taxonomy 359571
IPNI 515441-1
GBIF 2981476
EPPO LABCA
EOL 704087
Elurikkus 347551
USDA GRIN 311179
CMAUP NPO7867

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 CentralĀ®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
From Biodiversity to Musketry: Detection of Plant Diversity in Pre-Industrial Peloponnese during the Flora Graeca Expedition Chimona C, Papadopoulou S, Kolyva F, Mina M, Rhizopoulou S Life (Basel) 23-Nov-2022
PMCID:PMC9785030
doi:10.3390/life12121957
PMID:36556322
Developing nutritional component chrysin as a therapeutic agent: Bioavailability and pharmacokinetics consideration, and ADME mechanisms Gao S, Siddiqui N, Etim I, Du T, Zhang Y, Liang D Biomed Pharmacother 24-Aug-2021
PMCID:PMC8653576
doi:10.1016/j.biopha.2021.112080
PMID:34449320
Effect of 7-O-beta-D-glucopyranosylchrysin and its aglycone chrysin isolated from Podocytisus caramanicus on estrogen receptor alpha transcriptional activity. Berthier A, Girard C, Grandvuillemin A, Muyard F, Skaltsounis AL, Jouvenot M, Delage-Mourroux R Planta Med 01-Nov-2007
doi:10.1055/S-2007-990248
PMID:17948189

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 / Biphenols
1,1'-Binaphthalene-4,4',5,5'-tetrol 10087226 Click to see C1=CC2=C(C=CC(=C2C(=C1)O)O)C3=C4C=CC=C(C4=C(C=C3)O)O 318.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Taraxasterol 115250 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Ergone 167799 Click to see CC(C)C(C)C=CC(C)C1CCC2=C3C=CC4=CC(=O)CCC4(C3CCC12C)C 392.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterone 9801811 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(+)-Mellein 10921069 Click to see CC1CC2=C(C(=CC=C2)O)C(=O)O1 178.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, octadecyl ester 149044 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 446.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown https://doi.org/10.1055/S-2007-990248
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1055/S-2007-990248
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-phenyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 15558424 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1055/S-2007-990248
Chrysin-7beta-monoglucoside 5490092 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1055/S-2007-990248
Kaempferol-7-rhamnoside 25079965 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein 5281708 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 254.24 unknown https://doi.org/10.1055/S-2007-990248
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
3-Genistein-8-C-glucoside 5472471 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown https://doi.org/10.1055/S-2007-990248
Genistein 8-C-glucoside 5281757 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown https://doi.org/10.1055/S-2007-990248
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-Methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 3733033 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1055/S-2007-990248
Ononin 442813 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1055/S-2007-990248

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