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Internal ID UUID643ff7e1b6c9d359670942
Scientific name Psorospermum aurantiacum
Authority Engl.
First published in Bot. Jahrb. Syst. 55: 383 (1919)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • West Tropical Africa
      • Nigeria
    • West-central Tropical Africa
      • Cameroon

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000395028
Tropicos 50052139
KEW urn:lsid:ipni.org:names:429026-1
The Plant List kew-2408824
Open Tree Of Life 6101562
IPNI 429026-1
iNaturalist 429486
GBIF 3714729
EOL 42014230

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)!
Title Authors Publication Released IDs
Psorantin, a unique methylene linked dimer of vismin and kenganthranol E, two anthranoid derivatives from the fruits of Psorospermum aurantiacum (Hypericaceae) Simeon F. Kouam, Yves L.N. Njonkou, Guy Merlin Kuigoua, Bonaventure T. Ngadjui, Hidayat Hussain, Ivan R. Green, Barbara Schulz, Karsten Krohn Elsevier BV 24-Jul-2010
doi:10.1016/J.PHYTOL.2010.07.003

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 / Anthracenes
(3R)-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-3,8,9-trihydroxy-3-methyl-2,4-dihydroanthracen-1-one 162935401 Click to see CC(=CCCC(=CCOC1=CC(=C2C(=C1)C=C3CC(CC(=O)C3=C2O)(C)O)O)C)C 410.50 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.003
6-(3,7-Dimethylocta-2,6-dienoxy)-3,8,9-trihydroxy-3-methyl-2,4-dihydroanthracen-1-one 354179 Click to see CC(=CCCC(=CCOC1=CC(=C2C(=C1)C=C3CC(CC(=O)C3=C2O)(C)O)O)C)C 410.50 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.003
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.003
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.003
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/10.1016/J.PHYTOL.2010.07.003
Friedelanol 101341 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.003
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.PHYTOL.2010.07.003
Friedelinol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.003
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
cyclo[DL-Phe-DL-N(Me)Phe-DL-Val-DL-N(Me)Val-DL-Val] 76523789 Click to see CC(C)C1C(=O)NC(C(=O)N(C(C(=O)NC(C(=O)N(C(C(=O)N1)C(C)C)C)C(C)C)CC2=CC=CC=C2)C)CC3=CC=CC=C3 619.80 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.003
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
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.PHYTOL.2010.07.003
> Organoheterocyclic compounds / Naphthopyrans
(11R)-5,7,11-trihydroxy-2,2,9-trimethyl-10,12-bis(3-methylbut-2-enyl)-11H-naphtho[2,3-g]chromen-6-one 162951015 Click to see CC1=CC(=C2C(=C1CC=C(C)C)C(C3=C(C2=O)C(=C4C=CC(OC4=C3CC=C(C)C)(C)C)O)O)O 474.60 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.003
(1R,3'R,4'S,10S,11R,12S,13S)-4',5',5',6,10,12-hexamethylspiro[14-oxatetracyclo[9.3.2.01,10.02,7]hexadeca-2(7),3,5,8-tetraene-13,2'-oxolane]-3',5-diol 162874973 Click to see CC1C2CCC3(C2(C=CC4=C3C=CC(=C4C)O)C)OC15C(C(C(O5)(C)C)C)O 384.50 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.003

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