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Schizozygia coffaeoides

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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 UUID643fec6ae2ed8966066420
Scientific name Schizozygia coffaeoides
Authority Baill.
First published in Bull. Mens. Soc. Linn. Paris 1: 752 (1888)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Northeast Tropical Africa
      • Somalia
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
    • West-central Tropical Africa
      • Zaïre
    • Western Indian Ocean
      • Comoros

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000306904
Tropicos 1805130
KEW urn:lsid:ipni.org:names:81764-1
The Plant List kew-188193
Open Tree Of Life 136540
NCBI Taxonomy 184394
IUCN Red List 143720183
IPNI 81764-1
GBIF 3614729

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Alkaloide aus <i>Schizozygia caffaeoides</i> (B<scp>OJ</scp>.) B<scp>AILL</scp>. II. Die Struktur des Schizozygins U. Renner, H. Fritz Wiley 23-Dec-2004
doi:10.1002/HLCA.19650480208
Revised structure of isoschizogamine Josef Hájíček, Jan Taimr, Miloš Buděšínský Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(97)10588-3
Antimicrobial activities of a new schizozygane indoline alkaloid from Schizozygia coffaeoides and the revised structure of isoschizogaline. Kariba RM, Houghton PJ, Yenesew A J Nat Prod 01-Apr-2002
doi:10.1021/NP010298M
PMID:11975502
Identity of pericalline, tabernoschizine, apparicine and gomezine. Fransworth NR, Fong HH J Pharm Sci 01-Jan-1970
doi:10.1002/JPS.2600580241
PMID:5779884
[Alkaloids from Schizozygia caffaeoides (Boj.) Baill]. RENNER U, KERNWEISZ P Experientia 01-Jan-1970
doi:10.1007/BF02151358
PMID:13981674

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 / Schizozygine alkaloids
(1R,11R,15R,16S)-7,8-dimethoxy-4,14-diazahexacyclo[12.4.3.01,15.04,16.05,10.011,16]henicosa-5,7,9,19-tetraen-3-one 163047661 Click to see COC1=C(C=C2C(=C1)C3CCN4CC=CC56C4C3(N2C(=O)C5)CC6)OC 352.40 unknown https://doi.org/10.1007/BF02151358
(1S,11S,15S,16R)-7-methoxy-4,14-diazahexacyclo[12.4.3.01,15.04,16.05,10.011,16]henicosa-5(10),6,8,19-tetraen-3-one 101967173 Click to see COC1=CC2=C(C=C1)C3CCN4CC=CC56C4C3(N2C(=O)C5)CC6 322.40 unknown https://doi.org/10.1007/BF02151358
(1S,2R,18S,19R)-2-hydroxy-8,10-dioxa-4,17-diazaheptacyclo[15.4.3.01,18.04,19.05,13.07,11.014,19]tetracosa-5,7(11),12,14,22-pentaen-3-one 10043462 Click to see C1CC23C4C15C=CCN4CC=C2C6=CC7=C(C=C6N3C(=O)C5O)OCO7 350.40 unknown https://doi.org/10.1021/NP010298M
CID 26204194 26204194 Click to see C1CN2CC=CC34C2C5(C1C6=CC7=C(C=C6N5C(=O)C3)OCO7)CC4 336.40 unknown https://doi.org/10.1002/HLCA.19650480208
Schizozygin 44631038 Click to see C1CC23CCC45C2N(C1)CCC4C6=CC7=C(C=C6N5CC3)OCO7 324.40 unknown https://doi.org/10.1021/NP010298M
> Benzenoids / Benzene and substituted derivatives / Benzazocines
Pericalline 6436240 Click to see CC=C1CN2CCC1C(=C)C3=C(C2)C=C4C=CNC4=C3 264.40 unknown https://doi.org/10.1002/JPS.2600580241
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
methyl 2-[(1R,9R,16S,19S)-5-methoxy-2,12-diazapentacyclo[10.6.1.01,9.03,8.016,19]nonadeca-3(8),4,6,14-tetraen-16-yl]acetate 101973943 Click to see COC1=CC2=C(C=C1)C3CCN4CC=CC5(C4C3(N2)CC5)CC(=O)OC 354.40 unknown https://doi.org/10.1007/BF02151358
> Organoheterocyclic compounds / Quinolines and derivatives / Aminoquinolines and derivatives
(1S,8R,16S,17R)-11,12-dimethoxy-5,15-diazahexacyclo[13.4.2.01,16.05,16.08,17.09,14]henicosa-2,9,11,13-tetraen-21-one 23955822 Click to see COC1=C(C=C2C(=C1)C3CCN4CC=CC56C4(C3CC5)N2C(=O)C6)OC 352.40 unknown https://doi.org/10.1007/BF02151358
(1S,8R,16S,17S)-11,12-dimethoxy-5,15-diazahexacyclo[13.4.2.01,16.05,16.08,17.09,14]henicosa-2,9,11,13-tetraen-21-one 101933315 Click to see COC1=C(C=C2C(=C1)C3CCN4CC=CC56C4(C3CC5)N2C(=O)C6)OC 352.40 unknown https://doi.org/10.1016/S0040-4039(97)10588-3
(1S,8R,16S,17S)-12-methoxy-5,15-diazahexacyclo[13.4.2.01,16.05,16.08,17.09,14]henicosa-2,9(14),10,12-tetraen-21-one 101182033 Click to see COC1=CC2=C(C=C1)C3CCN4CC=CC56C4(C3CC5)N2C(=O)C6 322.40 unknown https://doi.org/10.1021/NP010298M
(1S,8R,16S)-11,12-dimethoxy-5,15-diazahexacyclo[13.4.2.01,16.05,16.08,17.09,14]henicosa-2,9,11,13-tetraen-21-one 163192892 Click to see COC1=C(C=C2C(=C1)C3CCN4CC=CC56C4(C3CC5)N2C(=O)C6)OC 352.40 unknown https://doi.org/10.1007/BF02151358
Isoschizogaline 636755 Click to see COC1=CC2=C(C=C1)C3CCN4CC=CC56C4(C3CC5)N2C(=O)C6 322.40 unknown https://doi.org/10.1021/NP010298M
https://doi.org/10.1007/BF02151358

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