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Telitoxicum peruvianum

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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 UUID64404950cc460904448541
Scientific name Telitoxicum peruvianum
Authority Moldenke
First published in Brittonia 3: 45 (1938)

Description Top

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Synonyms Top

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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
    • Western South America
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001083921
Tropicos 20600372
KEW urn:lsid:ipni.org:names:250115-2
The Plant List tro-20600372
Open Tree Of Life 576472
NCBI Taxonomy 461639
IPNI 250115-2
GBIF 3829689
EOL 5518053

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
Total Syntheses of Telisatin A, Telisatin B and Lettowianthine Nimgirawath S, Udomputtimekakul P Molecules 26-Feb-2009
PMCID:PMC6253876
doi:10.3390/molecules14030917
PMID:19255550
The Alkaloids of Telitoxicum peruvianum Mary D. Menachery, Michael P. Cava American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50015A014
Telisatin A, Telisatin B, and Telitoxinone, Three New Aporphinoids from Telitoxicum peruvianum Mary D. Menachery, Geoffrey W. Blake, Robert C. Gourley, Alan Freyer American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50126A025

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 / Aporphines
14-Hydroxy-12-imino-8,15,16-trimethoxy-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2,4,6,8,13,15-heptaen-11-one 135475270 Click to see COC1=C2C3=C(C4=CC=CC=C41)C(=C(C(=C3C(=N)C(=O)N2)O)OC)OC 352.30 unknown https://doi.org/10.1021/NP50126A025
15,16-Dimethoxy-11-azapentacyclo[9.6.2.02,7.08,19.014,18]nonadeca-1(17),2,4,6,8(19),14(18),15-heptaene-9,10-dione 101691125 Click to see COC1=C(C2=C3C(=C1)C4=CC=CC=C4C5=C3N(CC2)C(=O)C5=O)OC 333.30 unknown https://doi.org/10.1021/NP50126A025
16-Amino-15-methoxy-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2,4,6,9,11,13,15-octaen-8-one 11832657 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC=CC=C42)N 276.29 unknown https://doi.org/10.1021/NP50015A014
5-Hydroxy-14,15,16-trimethoxy-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2(7),3,5,9,11,13(17),14-octaen-8-one 135703596 Click to see COC1=C(C(=C2C3=C(C=C(C=C3)O)C(=O)C4=NC=CC1=C24)OC)OC 337.30 unknown https://doi.org/10.1021/NP50015A014
7H-Dibenzo(de,g)quinolin-7-one, 9-hydroxy-1,2-dimethoxy- 157207 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=C2C=CC(=C4)O)OC 307.30 unknown https://doi.org/10.1021/NP50015A014
Lysicamine 122691 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC=CC=C42)OC 291.30 unknown https://doi.org/10.1021/NP50015A014
Teladiazoline 189692 Click to see COC1=C(C(=C2C3=CC=CC=C3C(=O)C4=NC=CC1=C24)N)OC 306.30 unknown https://doi.org/10.1021/NP50015A014
Telisatin B 10784920 Click to see COC1=C(C(=C2C3=CC=CC=C3C4=C5C2=C1CCN5C(=O)C4=O)OC)OC 363.40 unknown https://doi.org/10.1021/NP50126A025
> Organoheterocyclic compounds / Isoquinolines and derivatives
Indeno(1,2,3-ij)isoquinolin-9-ol, 5,6-dimethoxy- 157208 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C4=C2C=CC(=C4)O)OC 279.29 unknown https://doi.org/10.1021/NP50015A014
Norruffscine 135778936 Click to see COC1=C(C(=C2C3=C(C=C(C=C3)O)C4=NC=CC1=C24)OC)OC 309.30 unknown https://doi.org/10.1021/NP50015A014

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