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Aspidosperma pyricollum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fea7218541212947455
Scientific name Aspidosperma pyricollum
Authority Müll.Arg.
First published in Fl. Bras. 6(1): 58 (1860)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Aspidosperma longipetiolatum Kuhlm. Anais Reunião Sul-Amer. Bot. 3: 86 (1938 publ. 1940)
Aspidosperma pyricollum var. obovatum Müll.Arg. Fl. Bras. 6(1): 58 (1860)
Macaglia pyricolla Kuntze Revis. Gen. Pl. 2: 416. 1891 [5 Nov 1891]

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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Distribution (via POWO/KEW) Top

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000291454
Tropicos 1800147
KEW urn:lsid:ipni.org:names:77436-1
The Plant List kew-17342
Open Tree Of Life 5784597
IUCN Red List 149203001
IPNI 77436-1
GBIF 7316886
Freebase /m/011smm7k
Wikipedia Aspidosperma_pyricollum

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
Indole alkaloid biosynthesis. III James P. Kutney, Vern R. Nelson, Donald C. Wigfield American Chemical Society (ACS) 10-Mar-2005
doi:10.1021/JA01043A042
Alkaloid studies LV. 19-Dehydroyohimbine, a novel alkaloid from Aspidosperma pyricollum. Arndt RR, Djerassi C Experientia 01-Jan-1970
doi:10.1007/BF02151532
PMID:5868480
Alkaloid studies. XXIII. Isolation of four new Aspidosperma cylindrocarpin, refractine, pyrifoline, and pyrifolidine alkaloids. GILBERT B, ANTONACCIO LD, ARCHER AA, DJERASSI C Experientia 01-Jan-1970
doi:10.1007/BF02170260
PMID:13849988

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/BF02151532
> Alkaloids and derivatives / Corynanthean-type alkaloids
methyl (1S,18R,19R,20R)-18-hydroxy-1,3,11,12,14,17,18,19,20,21-decahydroyohimban-19-carboxylate 163190310 Click to see 352.40 unknown https://doi.org/10.1007/BF02151532
Methyl 18-hydroxy-1,3,11,12,14,17,18,19,20,21-decahydroyohimban-19-carboxylate 14166904 Click to see 352.40 unknown https://doi.org/10.1007/BF02151532
> Alkaloids and derivatives / Vallesaman alkaloids
(13R,14E)-14-Ethylidene-12-methylidene-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene 6912322 Click to see 264.40 unknown https://doi.org/10.1021/JA01043A042
> 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/10.1007/BF02151532
Yohimbine 8969 Click to see 354.40 unknown https://doi.org/10.1007/BF02151532
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Conanine-type alkaloids
Kurcholessine 20054951 Click to see 404.60 unknown https://doi.org/10.1007/BF02151532
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1R,12S,16R)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.02,10.03,8]hexadeca-2(10),3,5,7-tetraene 11108306 Click to see CCC1C2CCN(C1C3=C(C2=C)NC4=CC=CC=C43)C 266.40 unknown https://doi.org/10.1007/BF02170260
Uleine 252320 Click to see CCC1C2CCN(C1C3=C(C2=C)NC4=CC=CC=C43)C 266.40 unknown https://doi.org/10.1021/JA01043A042
https://doi.org/10.1007/BF02170260

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