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Psorospermum laurentii

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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 UUID644069494015a409821943
Scientific name Psorospermum laurentii
Authority (De Wild.) Byng & Christenh.
First published in Global Fl. 0.254861111. 2018

Description Top

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Synonyms Top

Scientific name Authority First published in
Vismia laurentii De Wild. Ann. Mus. Congo Belge, Bot. , sér. 5, 2: 311 (1908)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001425159
KEW urn:lsid:ipni.org:names:77185673-1
Open Tree Of Life 6101614
IPNI 77185673-1
GBIF 9785486
CMAUP NPO14855

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
Laurentixanthone C: A New Antifungal and Algicidal Xanthone from Stem Bark of Vismia laurentii Michel F. Tala, Karsten Krohn, Hidayat Hussain, Simeon F. Kouamc, Hippolyte K. Wabo, Pierre Tane, Barbara Schulz, Qunxiu Hu Walter de Gruyter GmbH 16-Feb-2015
doi:10.1515/ZNB-2007-0413
Anthraquinones from the fruits of Vismia laurentii. Noungoue DT, Antheaume C, Chaabi M, Lenta Ndjakou B, Ngouela S, Lobstein A, Tsamo E Phytochemistry 01-Feb-2008
doi:10.1016/J.PHYTOCHEM.2007.10.026
PMID:18067931
Prenylated anthraquinones and other constituents from the seeds of Vismia laurentii. Wabo HK, Kouam SF, Krohn K, Hussain H, Tala MF, Tane P, Ree Tv, Hu Q, Schulz B Chem Pharm Bull (Tokyo) 01-Nov-2007
doi:10.1248/CPB.55.1640
PMID:17978527
Laurentixanthones A and B, antimicrobial xanthones from Vismia laurentii. Nguemeving JR, Azebaze AG, Kuete V, Eric Carly NN, Beng VP, Meyer M, Blond A, Bodo B, Nkengfack AE Phytochemistry 01-Jul-2006
doi:10.1016/J.PHYTOCHEM.2006.03.018
PMID:16740282
Anthraquinones from Vismia species Maria do Carmo, M. Miraglia, Antonio A.L. Mesquita, M. de Jesus, C. Varejão, Otto R. Gottlieb, Hugo E. Gottlieb Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)84067-8

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Anthracenes
(10S)-10-[(9R)-4,5-dihydroxy-2-methoxy-7-methyl-3-[(E)-3-methylbut-1-enyl]-10-oxo-9H-anthracen-9-yl]-1,8-dihydroxy-3-methoxy-6-methyl-2-[(E)-3-methylbut-1-enyl]-10H-anthracen-9-one 163079573 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2C4C5=CC(=C(C(=C5C(=O)C6=C4C=C(C=C6O)C)O)C=CC(C)C)OC)OC)C=CC(C)C)O 674.80 unknown https://doi.org/10.1515/ZNB-2007-0413
https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
10-[4,5-dihydroxy-2-methoxy-7-methyl-3-(3-methylbut-1-enyl)-10-oxo-9H-anthracen-9-yl]-1,8-dihydroxy-3-methoxy-6-methyl-2-(3-methylbut-1-enyl)-10H-anthracen-9-one 73321763 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2C4C5=CC(=C(C(=C5C(=O)C6=C4C=C(C=C6O)C)O)C=CC(C)C)OC)OC)C=CC(C)C)O 674.80 unknown https://doi.org/10.1515/ZNB-2007-0413
https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
3-(3,7-dimethylocta-2,6-dienoxy)-1,8-dihydroxy-6-methyl-10H-anthracen-9-one 54536756 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2)C=C(C=C3O)OCC=C(C)CCC=C(C)C 392.50 unknown https://doi.org/10.1248/CPB.55.1640
6-Geranyloxy-3-methyl-1,8-dihydroxyanthrone 23661636 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2)C=C(C=C3O)OCC=C(C)CCC=C(C)C 392.50 unknown https://doi.org/10.1248/CPB.55.1640
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Laurenquinone A 23661635 Click to see CC1=CC2=C(C(=C1C(=O)OC)O)C(=O)C3=C(C(=C(C=C3C2=O)O)CC=C(C)C)O 396.40 unknown https://doi.org/10.1248/CPB.55.1640
https://doi.org/10.1016/J.PHYTOCHEM.2007.10.026
Laurenquinone B 24750385 Click to see CC1=CC2=C(C(=C1C(=O)OC)O)C(=O)C3=C(C4=C(C=C3C2=O)OC(C=C4)(C)C)O 394.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.10.026
https://doi.org/10.1248/CPB.55.1640
Methyl 9-(acetyloxymethyl)-5,7-dihydroxy-2,2-dimethyl-6,11-dioxonaphtho[3,2-g]chromene-8-carboxylate 24814168 Click to see CC(=O)OCC1=CC2=C(C(=C1C(=O)OC)O)C(=O)C3=C(C4=C(C=C3C2=O)OC(C=C4)(C)C)O 452.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.10.026
> Benzenoids / Anthracenes / Anthraquinones
1,4,8-Trihydroxy-2-methoxy-6-methylanthracene-9,10-dione 85926407 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=CC(=C3O)OC)O 300.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.10.026
1,8-Dihydroxy-3-methoxy-6-methyl-2-(3-methylbut-1-enyl)anthracene-9,10-dione 628167 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)C=CC(C)C)O 352.40 unknown https://doi.org/10.1515/ZNB-2007-0413
https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
3-(3,7-Dimethylocta-2,6-dienyloxy)-1,8-dihydroxy-6-methyl-9,10-anthraquinone 333635 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OCC=C(C)CCC=C(C)C 406.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
Geranyloxyemodin 5785070 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OCC=C(C)CCC=C(C)C 406.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown https://doi.org/10.1248/CPB.55.1640
Vismiaquinone 5378723 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)C=CC(C)C)O 352.40 unknown https://doi.org/10.1515/ZNB-2007-0413
https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
vismiaquinone B 14729072 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)CC(=O)C(C)C)O 368.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
https://doi.org/10.1016/J.PHYTOCHEM.2007.10.026
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Dammara-20,24-dien-3 beta-ol 13893944 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1515/ZNB-2007-0413
Dammaradienol 13893946 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1515/ZNB-2007-0413
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.55.1640
https://doi.org/10.1016/0031-9422(81)84067-8
https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
https://doi.org/10.1016/0031-9422(81)84067-8
https://doi.org/10.1248/CPB.55.1640
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
Poriferasterol 5281330 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1-Hydroxy-6,7-dimethoxyxanthone 14189054 Click to see COC1=C(C=C2C(=C1)C(=O)C3=C(C=CC=C3O2)O)OC 272.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
Euxanthone 5281631 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 228.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
Laurentixanthone B 16081684 Click to see COC1=C(C(=C(C2=C1C(=O)C3=C(C=CC=C3O2)O)OC)OC)OC 332.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
5,8,10-Trihydroxy-2,2-dimethyl-9,12-bis(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one 16724087 Click to see CC(=CCC1=C(C=C2C(=C1O)OC3=C(C2=O)C(=C4C=CC(OC4=C3CC=C(C)C)(C)C)O)O)C 462.50 unknown https://doi.org/10.1515/ZNB-2007-0413
5,9,10-Trihydroxy-2,2-dimethyl-12-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one 11859087 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=CC(=C4O)O)O)C=CC(O2)(C)C)C 394.40 unknown https://doi.org/10.1248/CPB.55.1640
LaurentixanthoneA 16081685 Click to see CC(=CCC1=C2C(=CC=C1)C(=O)C3=C(O2)C4=C(C=C3O)OC(C=C4)(C)C)C 362.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
6-Deoxyisojacareubin 5464641 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC=C4O)O)C 310.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018
> 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 https://doi.org/10.1016/J.PHYTOCHEM.2006.03.018

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