Allanblackia stuhlmannii - Unknown
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Internal ID UUID6440085931be2051449811
Scientific name Allanblackia stuhlmannii
Authority Engl.
First published in Nat. Pflanzenfam. , Nachtr. 1: 249 (1897)

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Synonyms Top

Scientific name Authority First published in
Allanblackia sacleuxii Hua Bull. Mus. Hist. Nat. (Paris) 2: 155 (1897)
Stearodendron stuhlmannii Engl. Notizbl. Königl. Bot. Gart. Berlin 1: 43. 1895

Common names Top

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Language Common/alternative name
Spanish allanblackia sacleuxii
Spanish stearodendron stuhlmannii
Chinese 斯氏阿兰藤黄
Chinese 斯氏阿蘭藤黃

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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-0000525993
Tropicos 7801549
KEW urn:lsid:ipni.org:names:427050-1
The Plant List kew-2628591
Open Tree Of Life 6099612
IUCN Red List 34745
IPNI 427050-1
iNaturalist 130861
GBIF 3713122
Freebase /m/02w0cl8
EOL 5710519
USDA GRIN 456284
Wikipedia Allanblackia_stuhlmannii

Genomes (via NCBI) Top

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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
Antimicrobial and antileishmanial xanthones from the stem bark of Allanblackia gabonensis (Guttiferae). Azebaze AG, Ouahouo BM, Vardamides JC, Valentin A, Kuete V, Acebey L, Beng VP, Nkengfack AE, Meyer M Nat Prod Res 10-Mar-2008
doi:10.1080/14786410701855811
PMID:18322848
Leishmanicidal and cholinesterase inhibiting activities of phenolic compounds from Allanblackia monticola and Symphonia globulifera. Lenta BN, Vonthron-Sénécheau C, Weniger B, Devkota KP, Ngoupayo J, Kaiser M, Naz Q, Choudhary MI, Tsamo E, Sewald N Molecules 20-Jul-2007
PMCID:PMC6149078
doi:10.3390/12081548
PMID:17960072
A prenylated xanthone from Allanblackia floribunda. Nkengfack AE, Azebaze GA, Vardamides JC, Fomum ZT, van Heerden FR Phytochemistry 01-Jun-2002
doi:10.1016/S0031-9422(02)00036-5
PMID:12031429
Guttiferone F, the first prenylated benzophenone from Allanblackia stuhlmannii. Fuller RW, Blunt JW, Boswell JL, Cardellina JH 2nd, Boyd MR J Nat Prod 01-Jan-1999
doi:10.1021/NP9801514
PMID:9917299

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 / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Guttiferon F 76971996 Click to see CC(=CCC1CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C(C2=O)(C1(C)C)CC=C(C)C)CC(CC=C(C)C)C(=C)C)C 602.80 unknown https://doi.org/10.1021/NP9801514
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
[(2R,3S,4S,5R,6R)-6-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-9,14-dihydroxy-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl acetate 162964060 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3CCC45CC46CCC7(C(C(CC7(C6CC(C5C3(C)C)O)C)O)C8(CCC(O8)C(C)(C)O)C)C)COC(=O)C)O)O)O 841.00 unknown https://doi.org/10.1080/14786410701855811
https://doi.org/10.1021/NP9801514
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149078/
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,5-Trihydroxyxanthone 5281663 Click to see C1=CC2=C(C(=C1)O)OC3=CC(=CC(=C3C2=O)O)O 244.20 unknown https://doi.org/10.1016/S0031-9422(02)00036-5
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Bilirubins
Biliverdin 5280353 Click to see CC1=C(C(=CC2=C(C(=C(N2)C=C3C(=C(C(=O)N3)C)C=C)C)CCC(=O)O)NC1=CC4=NC(=O)C(=C4C)C=C)CCC(=O)O 582.60 unknown https://doi.org/10.1016/S0031-9422(02)00036-5
https://doi.org/10.1021/NP9801514
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Fukugetin 5464454 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)O)O 556.50 unknown https://doi.org/10.1016/S0031-9422(02)00036-5
Talbotaflavone 5315272 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O 540.50 unknown https://doi.org/10.1016/S0031-9422(02)00036-5
Volkensiflavone 5480834 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O 540.50 unknown https://doi.org/10.1016/S0031-9422(02)00036-5

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