Soulamea soulameoides

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Internal ID UUID68f8f4d6a7e45015739102
Scientific name Soulamea soulameoides
Authority (A.Gray) Noot.
First published in Fl. Males., Ser. 1, Spermat. 6: 221 (1963), in obs.

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Synonyms Top

Scientific name Authority First published in
Amaroria soulameoides A.Gray U.S. Expl. Exped., Phan. 15: 356. t. 40 (1854)

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
Tropicos 100287333
KEW urn:lsid:ipni.org:names:813567-1
The Plant List kew-2633227
Open Tree Of Life 708237
NCBI Taxonomy 43721
IPNI 813567-1
iNaturalist 812617
GBIF 3709231
Wikipedia Amaroria_soulameoides
World Flora Online wfo-0000492115

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)!
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Title Authors Publication Released IDs
Crystal and molecular structure of amarorine monohydrate, a new phenolic alkaloid from Amaroria soulameoides Peter J. Clarke, Kenneth Jewers, Haydn F. Jones Royal Society of Chemistry (RSC) 23-Apr-2004
doi:10.1039/P19800001614
Plant anticancer agents XXIX. Cleomiscosin A from Simaba multiflora, Soulamea soulameoides, and Matayba arborescens. Arisawa M, Handa SS, McPherson DD, Lankin DC, Cordell GA, Fong HH, Farnsworth NR J Nat Prod 01-Mar-1984
doi:10.1021/NP50032A011
PMID:6736970
Plant anticancer agents XXV. Constituents of Soulamea soulameoides. Handa SS, Kinghorn AD, Cordell GA, Farnsworth NR J Nat Prod 01-May-1983
doi:10.1021/NP50027A011
PMID:6619884

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 / Indolonaphthyridine alkaloids
11-hydroxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one 5281405 Click to see C1=CC2=C(C3=C4N2C(=O)C=CC4=NC=C3)C(=C1)O 236.22 unknown https://doi.org/10.1039/P19800001614
11-Hydroxycanthin-6-one 337601 Click to see C1=CC(=O)C2=C3C=CNC4=C3N(C2=C1)C(=O)C=C4 236.22 unknown https://doi.org/10.1021/NP50027A011
Amaroridine 14463028 Click to see COC1=CC=CC2=C1C3=C4N2C(=O)C=CC4=NC=C3 250.25 unknown https://doi.org/10.1039/P19800001614
> Lignans, neolignans and related compounds / Coumarinolignans
(2S)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 5315965 Click to see 386.40 unknown https://doi.org/10.1021/NP50032A011
CID 335652 335652 Click to see 386.40 unknown https://doi.org/10.1021/NP50027A011
https://doi.org/10.1021/NP50032A011
Cleomiscosin A 442510 Click to see 386.40 unknown https://doi.org/10.1021/NP50027A011
https://doi.org/10.1021/NP50032A011
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
Glaucarubolone 441797 Click to see 394.40 unknown https://doi.org/10.1021/NP50027A011
Holacanthone 158475 Click to see 436.50 unknown https://doi.org/10.1021/NP50027A011
Isobrucein A 441802 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)OC)O)O)C)O 522.50 unknown https://doi.org/10.1021/NP50027A011
Picrasin B 12313355 Click to see CC1CC(C(=O)C2(C1CC3C4(C2C(=O)C(=C(C4CC(=O)O3)C)OC)C)C)O 376.40 unknown https://doi.org/10.1021/NP50027A011

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