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Cullen drupaceum

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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 UUID643fd9b4b9543311456408
Scientific name Cullen drupaceum
Authority (Bunge) C.H.Stirt.

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
German tumlu psoralea

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

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-0000186902
KEW urn:lsid:ipni.org:names:908578-1
The Plant List ild-33404
Open Tree Of Life 3919784
GBIF 2948954
EOL 643289
USDA GRIN 312051
IPNI 908578-1

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
Flavonoids ofPsoralea drupaceae andReseda luteola M. P. Yuldashev, �. Kh. Batirov, V. M. Malikov, N. P. Yuldashevaa Springer Science and Business Media LLC 01-Apr-2005
doi:10.1007/BF01374036
Phenolic components of the unsaponifiable fraction of the lipids of Psorlea drupaceae G. K. Nikonov, N. A. Artamonova Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630133
The structure of drupanol — A new phenol from Psoralea drupaceae L. A. Golovina, G. K. Nikonov Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00580876
The structures of drupacin and drupanin — New components of Psoralea drupaceae L. A. Golovina, G. K. Nikonov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565783

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
> Alkaloids and derivatives / Cephalotaxus alkaloids
(1S,11R,12R,13S,15R)-13-methoxy-5,7,21-trioxa-19-azahexacyclo[11.7.1.02,10.04,8.011,15.015,19]henicosa-2,4(8),9-trien-12-ol 133645824 Click to see COC12CC34CCCN3CC(O1)C5=CC6=C(C=C5C4C2O)OCO6 331.40 unknown https://doi.org/10.1007/BF00565783
> Benzenoids / Benzene and substituted derivatives / Styrenes
4-[(4R)-4-ethenyl-4,7-dimethylocta-1,6-dien-2-yl]phenol 163008220 Click to see CC(=CCC(C)(CC(=C)C1=CC=C(C=C1)O)C=C)C 256.40 unknown https://doi.org/10.1007/BF00580876
Drupanol 129685892 Click to see CC(=CCC(C)(CC(=C)C1=CC=C(C=C1)O)C=C)C 256.40 unknown https://doi.org/10.1007/BF00580876
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Bakuchiol 5468522 Click to see CC(=CCCC(C)(C=C)C=CC1=CC=C(C=C1)O)C 256.40 unknown https://doi.org/10.1007/BF00630133
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(4-Hydroxy-3-(3-methyl-2-butenyl)phenyl)-2-propenoic acid 6440361 Click to see CC(=CCC1=C(C=CC(=C1)C=CC(=O)O)O)C 232.27 unknown https://doi.org/10.1007/BF00565783
3-[4-Hydroxy-3-(3-methylbut-2-enyl)phenyl]prop-2-enoic acid 154365 Click to see CC(=CCC1=C(C=CC(=C1)C=CC(=O)O)O)C 232.27 unknown https://doi.org/10.1007/BF00565783
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Methoxycoumarin 10748 Click to see COC1=CC2=C(C=C1)C=CC(=O)O2 176.17 unknown https://doi.org/10.1007/BF00630133
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown https://doi.org/10.1007/BF00630133
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Angelicin 10658 Click to see C1=CC2=C(C=CO2)C3=C1C=CC(=O)O3 186.16 unknown https://doi.org/10.1007/BF01374036
https://doi.org/10.1007/BF00630133
Isobergapten 68082 Click to see COC1=C2C=CC(=O)OC2=C3C=COC3=C1 216.19 unknown https://doi.org/10.1007/BF00630133
Pimpinellin 4825 Click to see COC1=C(C2=C(C=CO2)C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1007/BF00630133
Sphondin 108104 Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)C=CO2 216.19 unknown https://doi.org/10.1007/BF00630133
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown https://doi.org/10.1007/BF01374036
https://doi.org/10.1007/BF00630133
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1007/BF00630133
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1007/BF00630133
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1007/BF00630133
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 4-hydroxycoumarins
4-Hydroxycoumarin 54682930 Click to see C1=CC=C2C(=C1)C(=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/BF00630133
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/BF00630133
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)- 4183640 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1007/BF01374036
Daidzin 107971 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1007/BF01374036

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