Aspidosperma discolor - Unknown
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Internal ID UUID643fea5ed8f1c813083653
Scientific name Aspidosperma discolor
Authority A.DC.
First published in Prodr. 8: 398 (1844)

Description Top

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Aspidosperma macrocarpon, also known as the timber tree, is a species native to Brazil. It is mentioned in the book Flora Brasiliensis, written by Carl Friedrich Philipp von Martius. This plant is known for its use in timber production and is an important part of Brazil's natural ecosystem. Its inclusion in Flora Brasiliensis highlights its significance and contribution to the country's biodiversity.

Synonyms Top

Scientific name Authority First published in
Macaglia discolor Kuntze Revis. Gen. Pl. 2: 416 (1891)
Aspidosperma francisii A.DC. Prodr. 8: 398 (1844)
Aspidosperma discolor var. parvifolium Müll.Arg. Fl. Bras. 6(1): 60 (1860)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000290579
Tropicos 1800107
KEW urn:lsid:ipni.org:names:77354-1
The Plant List kew-17257
Open Tree Of Life 5784602
IUCN Red List 149206908
IPNI 77354-1
GBIF 7317048
Freebase /m/0268886
EOL 6852134
Wikipedia Aspidosperma_discolor

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
[On the alkaloids from Aspidosperma discolor A. DC]. Dastoor NJ, Gorman AA, Schmid H Helv Chim Acta 01-Jan-1970
doi:10.1002/HLCA.19670500129
PMID:5593208
THE ALKALOIDS OF ASPIDOSPERMA DISCOLOR A. DC. FERREIRA JM, GILBERT B, OWELLEN RJ, DJERASSI C Experientia 01-Jan-1970
doi:10.1007/BF02151003
PMID:14101518
[On the alkaloids of Aspidosperma discolor A. DC]. DASTOOR N, SCHMID H Experientia 01-Jan-1970
doi:10.1007/BF02150415
PMID:14025199

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 / Aspidospermatan-type alkaloids
1-[(1R,9R,12S,19S)-12-ethyl-6-hydroxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5-trien-8-yl]ethanone 162933069 Click to see CCC12CCCN3C1C4(CC3)C(CC2)N(C5=C4C=CC=C5O)C(=O)C 340.50 unknown https://doi.org/10.1007/BF02151003
1-[(1R,9R,12S,19S)-12-ethyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6-trien-8-yl]ethanone 162915600 Click to see CCC12CCCN3C1C4(CC3)C(CC2)N(C5=CC=CC=C45)C(=O)C 324.50 unknown https://doi.org/10.1007/BF02151003
1-[(1R,9R,12S,19S)-12-ethyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6-trien-8-yl]propan-1-one 162911876 Click to see CCC(=O)N1C2CCC3(CCCN4C3C2(CC4)C5=CC=CC=C51)CC 338.50 unknown https://doi.org/10.1007/BF02151003
Aspidospermidine, 1-acetyl- 580310 Click to see CCC12CCCN3C1C4(CC3)C(CC2)N(C5=CC=CC=C45)C(=O)C 324.50 unknown https://doi.org/10.1007/BF02151003
Palosine, 17-demethoxy- 579957 Click to see CCC(=O)N1C2CCC3(CCCN4C3C2(CC4)C5=CC=CC=C51)CC 338.50 unknown https://doi.org/10.1007/BF02151003
> Alkaloids and derivatives / Yohimbine alkaloids
beta-Yohimbine 2866 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1002/HLCA.19670500129
Elliptamine 234846 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC 412.50 unknown https://doi.org/10.1007/BF02150415
https://doi.org/10.1002/HLCA.19670500129
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/10.1007/BF02150415
methyl (1R,15R,16S,20S)-6,7-dimethoxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate 12304341 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC 412.50 unknown https://doi.org/10.1002/HLCA.19670500129
Rauvanin 201052 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC 412.50 unknown https://doi.org/10.1002/HLCA.19670500129
Yohimbine 8969 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1002/HLCA.19670500129
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Conanine-type alkaloids
Kurcholessine 20054951 Click to see CC1C(CCC2(C1(CC(C3C2CCC45C3CCC4C(N(C5)C)C)O)O)C)N(C)C 404.60 unknown https://doi.org/10.1007/BF02151003
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
2-(3-Ethenyl-10-methoxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl)ethanol 162911840 Click to see COC1=CC2=C(C=C1)C3=C(N2)C4CC(C(CN4CC3)C=C)CCO 326.40 unknown https://doi.org/10.1007/BF02150415
2-(3-Ethyl-10-methoxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl)ethanol 14414973 Click to see CCC1CN2CCC3=C(C2CC1CCO)NC4=C3C=CC(=C4)OC 328.40 unknown https://doi.org/10.1007/BF02150415
2-[(2R,3R,12bS)-3-ethyl-10-methoxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]ethanol 14414974 Click to see CCC1CN2CCC3=C(C2CC1CCO)NC4=C3C=CC(=C4)OC 328.40 unknown https://doi.org/10.1007/BF02150415
2-[(2R,3S,12bS)-3-ethenyl-10-methoxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]ethanol 163189739 Click to see COC1=CC2=C(C=C1)C3=C(N2)C4CC(C(CN4CC3)C=C)CCO 326.40 unknown https://doi.org/10.1007/BF02150415
> Organoheterocyclic compounds / Indolizidines
Isoreserpiline pseudoindoxyl 637152 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C(=O)C5=CC(=C(C=C5N4)OC)OC 428.50 unknown https://doi.org/10.1007/BF02150415
methyl 5',6'-dimethoxy-1-methyl-3'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,2'-1H-indole]-4-carboxylate 73880680 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C(=O)C5=CC(=C(C=C5N4)OC)OC 428.50 unknown https://doi.org/10.1007/BF02150415

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