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Dorstenia zenkeri

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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 UUID6440182f07471902648769
Scientific name Dorstenia zenkeri
Authority Engl.
First published in Monogr. Afrik. Pflanzen-Fam. 1: 14 (1898)

Description Top

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Synonyms Top

Scientific name Authority First published in
Dorstenia laurentii De Wild. Miss. Ém. Laurent : 69 (1905)
Dorstenia laurentii var. brevipedicellata De Wild. Pl. Nov. Horti Then. 1(7): 1907

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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-0000654725
Tropicos 100326500
KEW urn:lsid:ipni.org:names:851670-1
The Plant List kew-2775955
Open Tree Of Life 6108093
Observations.org 341353
NCBI Taxonomy 2605016
IPNI 851670-1
iNaturalist 934896
GBIF 3762584
Elurikkus 409621

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
Chalcone Scaffolds, Bioprecursors of Flavonoids: Chemistry, Bioactivities, and Pharmacokinetics Rudrapal M, Khan J, Dukhyil AA, Alarousy RM, Attah EI, Sharma T, Khairnar SJ, Bendale AR Molecules 26-Nov-2021
PMCID:PMC8659147
doi:10.3390/molecules26237177
PMID:34885754
Chalcones and other constituents of Dorstenia prorepens and Dorstenia zenkeri. Abegaz BM, Ngadjui BT, Dongo E, Ngameni B, Nindi MN, Bezabih M Phytochemistry 01-Apr-2002
doi:10.1016/S0031-9422(01)00483-6
PMID:11937170

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
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(01)00483-6
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown https://doi.org/10.1016/S0031-9422(01)00483-6
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(3R)-3,5-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one 163190234 Click to see CC1(C(CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)O)C 340.40 unknown https://doi.org/10.1016/S0031-9422(01)00483-6
(E)-1-[(3S)-3,5-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one 162893333 Click to see CC1(C(CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)O)C 340.40 unknown https://doi.org/10.1016/S0031-9422(01)00483-6
1-(3,5-Dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-3-(4-hydroxyphenyl)prop-2-en-1-one 74819183 Click to see CC1(C(CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)O)C 340.40 unknown https://doi.org/10.1016/S0031-9422(01)00483-6
1-(5-Hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-3-(4-hydroxyphenyl)prop-2-en-1-one 403813 Click to see CC1(CCC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(01)00483-6
5-Hydroxy-6-(4-hydroxycinnamoyl)-2,2-dimethylchromene 3662729 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C 322.40 unknown https://doi.org/10.1016/S0031-9422(01)00483-6
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/10.1016/S0031-9422(01)00483-6
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/10.1016/S0031-9422(01)00483-6

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