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Rhabdodendron macrophyllum

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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
Collections

Details Top

Internal ID UUID64404d7dae53c758521259
Scientific name Rhabdodendron macrophyllum
Authority (Spruce ex Benth.) Huber
First published in Bol. Mus. Goeldi Hist. Nat. Ethnogr. v. 428 (1909).

Description Top

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Synonyms Top

Scientific name Authority First published in
Lecostomon macrophyllum Spruce ex Benth. Hooker's J. Bot. Kew Gard. Misc. 5: 296 (1853)
Rhabdodendron columnare Gilg & Pilg. Verh. Bot. Vereins Prov. Brandenburg 47: 152 (1905)
Lecostemon macrophyllum Spruce ex Benth. Hooker's J. Bot. Kew Gard. Misc. 5: 296 1853

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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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001132684
Tropicos 28100032
KEW urn:lsid:ipni.org:names:218867-2
The Plant List tro-28100032
Open Tree Of Life 760100
NCBI Taxonomy 169278
IPNI 775047-1
iNaturalist 853712
GBIF 3880536
EPPO RBDMA
USDA GRIN 450611

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
Ellagic acid derivatives from Rhabdodendron macrophyllum Wilson Wolter Filho, Arnaldo I. Da Rocha, Massayoshi Yoshida, Otto R. Gottlieb Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83107-6
Chemosystematics of Rhabdodendron Wilson Wolter-Filho, Arnaldo I. Da Rocha, Massayoshi Yoshida, Otto R. Cottlieb Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97983-4

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
3-Acetyloxy-9,10,16-trihydroxyhexadecanoic acid 163015444 Click to see CC(=O)OC(CCCCCC(C(CCCCCCO)O)O)CC(=O)O 362.50 unknown https://doi.org/10.1016/S0031-9422(00)97983-4
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(4aR,6aS,6bS,8aS,10S,12aS,14aS,14bS)-10-acetyloxy-2,2,6b,9,9,12a,14a-heptamethyl-1,3,4,5,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydropicene-4a-carboxylic acid 641666 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
(4aS,6aS,6bR,8aR,10S,12aR,14aS,14bS)-10-acetyloxy-2,2,6b,9,9,12a,14a-heptamethyl-1,3,4,5,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydropicene-4a-carboxylic acid 162903734 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
Acetylaleuritolic acid 429885 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 38349948 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
(4aS,6aR,6aS,6bR,8aS,9R,10S,12aR,14bS)-10-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 40477245 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bS)-10-hydroxy-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 25728252 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
10,11-Dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 5320146 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
https://doi.org/10.1016/S0031-9422(00)97983-4
alpha-Hederagenin 258538 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
https://doi.org/10.1016/S0031-9422(00)97983-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R)-1-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 71716352 Click to see CC(C)C(=C)CCC(CO)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97983-4
(1S,3R,6S,8S,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methyl-5-methylideneheptan-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 12760140 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
15-(1-Hydroxy-6-methyl-5-methylideneheptan-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 78157055 Click to see CC(C)C(=C)CCC(CO)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97983-4
3beta-24-Methylenecycloartan-3-ol 544165 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
7,7,12,16-Tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadec-8-en-6-ol 162820419 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CC=C5C3(C4)CCC(C5(C)C)O)C)C 438.70 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3,3',4-Tri-O-methylflavellagic acid 14412544 Click to see COC1=C(C=C2C3=C1OC(=O)C4=C3C(=C(C(=C4O)OC)OC)OC2=O)O 360.30 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
https://doi.org/10.1016/S0031-9422(00)97983-4
3,3',4,4'-Tetra-O-methylellagic acid 12313147 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)OC)C(=O)O2)OC 358.30 unknown https://doi.org/10.1016/S0031-9422(00)83107-6
5,13-Dihydroxy-6,7,12,14-tetramethoxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(14),4(16),5,7,11(15),12-hexaene-3,10-dione 14412545 Click to see COC1=C(C(=C2C3=C1C(=O)OC4=C(C(=C(C(=C34)C(=O)O2)O)OC)OC)OC)O 390.30 unknown https://doi.org/10.1016/S0031-9422(00)83107-6

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