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Machaerium incorruptibile

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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 UUID643fd7c3979e6889060695
Scientific name Machaerium incorruptibile
Authority (Vell.) Benth.
First published in Comm. Legum. Gen.: 37 (1837)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tipuana mucronata (Vogel) J.F.Macbr. Candollea6: 10 (1934)
Machaerium fluminense Rudd Phytologia25: 400 (1973)
Nissolia incorruptibilis Vell. Fl. Flumin.: 297 (1829)
Machaerium mucronatum Vogel Linnaea11: 191 (1837)
Machaerium incorruptibile Allem. in Trab. Soc. Vell. [1852] 56.

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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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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-0000175482
KEW urn:lsid:ipni.org:names:505471-1
The Plant List ild-21641
Open Tree Of Life 3926971
Observations.org 398904
NCBI Taxonomy 1963797
IUCN Red List 177826885
IPNI 505473-1
GBIF 5355071
EPPO MCJIN
EOL 641528
Elurikkus 525949
USDA GRIN 436809

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
Triterpenoids isolated from Machaerium incorruptibile H.Magalhães Alves, V.H. Arndt, W.D. Ollis, W.B. Eyton, O.R. Gottlieb, M.Taveira Magalhães Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)86130-0

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 / Triterpenoids
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 345510 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)86130-0
(4aS,6aS,6aS,6bR,8aR,10S,12aR,14bS)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 12882368 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/10.1016/S0031-9422(00)86130-0
(8a-Formyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 14829105 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C 482.70 unknown https://doi.org/10.1016/S0031-9422(00)86130-0
[8a-(Hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 14010963 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C 484.80 unknown https://doi.org/10.1016/S0031-9422(00)86130-0
10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 619165 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/10.1016/S0031-9422(00)86130-0
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)86130-0
O-Acetyloleanolic aldehyde 14829106 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C 482.70 unknown https://doi.org/10.1016/S0031-9422(00)86130-0
Olean-12-ene-3beta,28-diol 3-acetate 14010964 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C 484.80 unknown https://doi.org/10.1016/S0031-9422(00)86130-0

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