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Ochrosia acuminata

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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 UUID643fe4bae9c78195147122
Scientific name Ochrosia acuminata
Authority Trimen
First published in Ann. Jard. Bot. Buitenzorg 12: 231 (1895)

Description Top

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Synonyms Top

Scientific name Authority First published in
Neisosperma acuminatum (Trimen ex Valeton) Fosberg & Sachet Adansonia , n.s., 17: 28 (1977)

Common names Top

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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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No germination or propagation data was added yet.

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-0000253094
Tropicos 100230483
KEW urn:lsid:ipni.org:names:80487-1
The Plant List kew-136690
IPNI 80487-1
GBIF 3618101
USDA GRIN 25474

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)!
Title Authors Publication Released IDs
New indole alkaloids from the roots of Ochrosia acuminata. Salim AA, Garson MJ, Craik DJ J Nat Prod 01-Oct-2004
doi:10.1021/NP049812P
PMID:15497947
Antitumor Agents LXIX. Alkaloids of Ochrosia acuminata1. Lin YM, Juichi M, Wu RY, Lee KH Planta Med 01-Dec-1985
doi:10.1055/S-2007-969602
PMID:17345297

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 / Corynanthean-type alkaloids
methyl (1R,9S,10S,12S,13E,16S,17R,18S)-13-ethylidene-18-hydroxy-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6-triene-17-carboxylate 11870794 Click to see CC=C1CN2C3CC1C4(C2CC5(C3NC6=CC=CC=C65)C4O)C(=O)OC 352.40 unknown https://doi.org/10.1021/NP049812P
> Alkaloids and derivatives / Macroline alkaloids
Methyl (12S,14S,15E)-15-ethylidene-13-(hydroxymethyl)-3-methyl-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 134716706 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)(CO)C(=O)OC 366.50 unknown https://doi.org/10.1021/NP049812P
methyl (1S,12S,13R,14S,15E,17S)-15-ethylidene-13-(hydroxymethyl)-17-oxido-3-aza-17-azoniapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 163185031 Click to see CC=C1C[N+]2(C3CC1C(C2CC4=C3NC5=CC=CC=C45)(CO)C(=O)OC)[O-] 368.40 unknown https://doi.org/10.1021/NP049812P
methyl (1S,12S,13R,14S,15E)-15-ethylidene-13-(hydroxymethyl)-17-oxido-3-aza-17-azoniapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 11268654 Click to see CC=C1C[N+]2(C3CC1C(C2CC4=C3NC5=CC=CC=C45)(CO)C(=O)OC)[O-] 368.40 unknown https://doi.org/10.1021/NP049812P
methyl (1S,14S,15Z)-15-ethylidene-13-(hydroxymethyl)-17-oxido-3-aza-17-azoniapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate 101357660 Click to see CC=C1C[N+]2(C3CC1C(C2CC4=C3NC5=CC=CC=C45)(CO)C(=O)OC)[O-] 368.40 unknown https://doi.org/10.1021/NP049812P
Sarpagan-16-carboxylic acid, 17-hydroxy-1-methyl-, methyl ester, (16R)- 12444908 Click to see CC=C1CN2C3CC1C(C2CC4=C3N(C5=CC=CC=C45)C)(CO)C(=O)OC 366.50 unknown https://doi.org/10.1021/NP049812P
> Alkaloids and derivatives / Yohimbine alkaloids
Isoreserpiline 161345 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC 412.50 unknown https://doi.org/10.1021/NP049812P
Reserpiline 67228 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC 412.50 unknown https://doi.org/10.1021/NP049812P
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
(5Z)-2-(5-bromo-1H-indole-3-carbonyl)-5-[(6-hydroxy-1H-indol-3-yl)methylidene]-1H-imidazol-4-one 10456352 Click to see C1=CC2=C(C=C1O)NC=C2C=C3C(=O)N=C(N3)C(=O)C4=CNC5=C4C=C(C=C5)Br 449.30 unknown https://doi.org/10.1021/NP049812P
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / 1,3-dicarbonyl compounds / Beta-diketones
2-(4-Butanoyl-3,5-dioxooxolan-2-yl)acetic acid 163037595 Click to see CCCC(=O)C1C(=O)C(OC1=O)CC(=O)O 228.20 unknown https://doi.org/10.1021/NP049812P
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
9-Methoxyellipticine 72512 Click to see CC1=C2C=CN=CC2=C(C3=C1NC4=C3C=C(C=C4)OC)C 276.30 unknown https://doi.org/10.1055/S-2007-969602
https://doi.org/10.1021/NP049812P
Ellipticine 3213 Click to see CC1=C2C=CN=CC2=C(C3=C1NC4=CC=CC=C43)C 246.31 unknown https://doi.org/10.1021/NP049812P
https://doi.org/10.1055/S-2007-969602
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(1S,18S,19S,20S)-19-ethenyl-18-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15-pentaen-14-one 159304057 Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=CC=CC=C6N4 498.50 unknown https://doi.org/10.1021/NP049812P
Strictosamide 10345799 Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=CC=CC=C6N4 498.50 unknown https://doi.org/10.1021/NP049812P

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