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Swartzia arborescens

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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
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Details Top

Internal ID UUID643fd5901464f571436376
Scientific name Swartzia arborescens
Authority (Aubl.) Pittier
First published in J. Washington Acad. Sci.11: 157 (1921)

Description Top

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Synonyms Top

Scientific name Authority First published in
Swartzia triphylla (Sw.) Willd. Sp. Pl., ed. 4, 2: 1220 (1799)
Possira triphylla Sw. Prodr. Veg. Ind. Occ.: 82 (1788)
Swartzia triphyllata Willd.
Possira arborescens Aubl. Hist. Pl. Guiane: 934 (1775)
Swartzia dodecandra (Vahl) Willd. Sp. Pl., ed. 4, 2: 1220 (1799)
Swartzia bifida Steud. Flora26: 757 (1843)
Tounatea arborescens (Aubl.) Britton Bull. Torrey Bot. Club16: 325 (1889)
Tunatea arborescens (Aubl.) Kuntze
Rittera dodecandra Vahl Symb. Bot.2: 60 (1791)
Swartzia parviflora DC. Mém. Légum.: 403 (1826)
Rittera triphylla Sw. ex Steud. Nomencl. Bot. [Steudel], ed. 2. 2: 460. 1841
Tounatea dodecandra (Willd.) Taub. Bot. Centralbl.47: 390 (1891)
Swartzia rariflora Hoehne Relat. Commiss. Linhas Telegr. Estratég. Matto Grosso Amazonas5(12): 16 (1922)
Tunatea dodecandra (Vahl) Kuntze
Deguelia arborescens Spreng. Syst. Veg. ed. 16, 4(2): 269 (1827)
Possira dodecandra Poir. J.B.A.M.de Lamarck, Encycl.5: 571 (1804)
Rittera triphylla Forsyth f. Bot. Nomencl.: 289 (1794)

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000164095
Tropicos 13001674
INPN 733779
KEW urn:lsid:ipni.org:names:519836-1
The Plant List ild-10510
Open Tree Of Life 39689
NCBI Taxonomy 450057
IUCN Red List 170267960
IPNI 246584-2
iNaturalist 431657
GBIF 5352087
EOL 418188
USDA GRIN 437165

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)!
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Title Authors Publication Released IDs
Swartziarboreols A-E, Five New Cassane Diterpenoids from Swartzia arborescens (Aubl.) Pittier Michel Koch, Bernadette Orphelin, Michèle Brum-Bousquet, François Tillequin, Christian Moretti The Japan Institute of Heterocyclic Chemistry 31-Mar-2009
doi:10.3987/COM-95-7249

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 / Phenanthrenes and derivatives
(1S,5aR,9aS)-10-hydroxy-1-(hydroxymethyl)-11-methoxy-6,6,9a-trimethyl-1,4,5,5a,8,9-hexahydronaphtho[1,2-g][2]benzofuran-3,7-dione 127027433 Click to see CC1(C2CCC3=C4C(=C(C(=C3C2(CCC1=O)C)O)OC)C(OC4=O)CO)C 374.40 unknown https://doi.org/10.3987/COM-95-7249
(5aR,9aS)-10-hydroxy-1-(hydroxymethyl)-11-methoxy-6,6,9a-trimethyl-1,4,5,5a,8,9-hexahydronaphtho[1,2-g][2]benzofuran-3,7-dione 15762193 Click to see CC1(C2CCC3=C4C(=C(C(=C3C2(CCC1=O)C)O)OC)C(OC4=O)CO)C 374.40 unknown https://doi.org/10.3987/COM-95-7249
10-Hydroxy-1-(hydroxymethyl)-11-methoxy-6,6,9a-trimethyl-1,4,5,5a,8,9-hexahydronaphtho[1,2-g][2]benzofuran-3,7-dione 162916892 Click to see CC1(C2CCC3=C4C(=C(C(=C3C2(CCC1=O)C)O)OC)C(OC4=O)CO)C 374.40 unknown https://doi.org/10.3987/COM-95-7249
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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/10.3987/COM-95-7249
Oleanolic acid acetate 6708573 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.3987/COM-95-7249
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.3987/COM-95-7249
> Organoheterocyclic compounds / Naphthopyrans
(1R,6aR,10aS)-1,11-dihydroxy-12-methoxy-7,7,10a-trimethyl-2,5,6,6a,9,10-hexahydro-1H-naphtho[1,2-h]isochromene-4,8-dione 162843056 Click to see CC1(C2CCC3=C4C(=C(C(=C3C2(CCC1=O)C)O)OC)C(COC4=O)O)C 374.40 unknown https://doi.org/10.3987/COM-95-7249
(6aR,10aS)-1,11-dihydroxy-12-methoxy-7,7,10a-trimethyl-2,5,6,6a,9,10-hexahydro-1H-naphtho[1,2-h]isochromene-4,8-dione 15762192 Click to see CC1(C2CCC3=C4C(=C(C(=C3C2(CCC1=O)C)O)OC)C(COC4=O)O)C 374.40 unknown https://doi.org/10.3987/COM-95-7249
(6aR,10aS)-11-hydroxy-12-methoxy-7,7,10a-trimethyl-2,5,6,6a,9,10-hexahydro-1H-naphtho[1,2-h]isochromene-4,8-dione 15762189 Click to see CC1(C2CCC3=C4C(=C(C(=C3C2(CCC1=O)C)O)OC)CCOC4=O)C 358.40 unknown https://doi.org/10.3987/COM-95-7249
(6aR,10aS)-11-Hydroxy-12-methoxy-7,7,10a-trimethyl-5,6a,7,9,10,10a-hexahydro-4H-phenanthro[1,2-c]pyran-4,8(6H)-dione 15762190 Click to see CC1(C2CCC3=C(C2(CCC1=O)C)C(=C(C4=C3C(=O)OC=C4)OC)O)C 356.40 unknown https://doi.org/10.3987/COM-95-7249
1,11-dihydroxy-12-methoxy-7,7,10a-trimethyl-2,5,6,6a,9,10-hexahydro-1H-naphtho[1,2-h]isochromene-4,8-dione 162843055 Click to see CC1(C2CCC3=C4C(=C(C(=C3C2(CCC1=O)C)O)OC)C(COC4=O)O)C 374.40 unknown https://doi.org/10.3987/COM-95-7249
11-hydroxy-12-methoxy-7,7,10a-trimethyl-2,5,6,6a,9,10-hexahydro-1H-naphtho[1,2-h]isochromene-4,8-dione 162923788 Click to see CC1(C2CCC3=C4C(=C(C(=C3C2(CCC1=O)C)O)OC)CCOC4=O)C 358.40 unknown https://doi.org/10.3987/COM-95-7249
11-Hydroxy-12-methoxy-7,7,10a-trimethyl-5,6,6a,8,9,10-hexahydronaphtho[1,2-h]isochromen-4-one 162859354 Click to see CC1(CCCC2(C1CCC3=C2C(=C(C4=C3C(=O)OC=C4)OC)O)C)C 342.40 unknown https://doi.org/10.3987/COM-95-7249
11-hydroxy-12-methoxy-7,7,10a-trimethyl-6,6a,9,10-tetrahydro-5H-naphtho[1,2-h]isochromene-4,8-dione 92030715 Click to see CC1(C2CCC3=C(C2(CCC1=O)C)C(=C(C4=C3C(=O)OC=C4)OC)O)C 356.40 unknown https://doi.org/10.3987/COM-95-7249
Swartziarboreol C 15762191 Click to see CC1(CCCC2(C1CCC3=C2C(=C(C4=C3C(=O)OC=C4)OC)O)C)C 342.40 unknown https://doi.org/10.3987/COM-95-7249
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afrormosin 5281704 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O 298.29 unknown https://doi.org/10.3987/COM-95-7249

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