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Cabari glaucophylla

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 UUID68f915ac70c2c857265910
Scientific name Cabari glaucophylla
Authority (R.S.Cowan) Gregório & D.B.O.S.Cardoso
First published in Bot. J. Linn. Soc. 205(1): 12 2023

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Clathrotropis glaucophylla R.S.Cowan Bol. Soc. Venez. Ci. Nat. 15: 99 (1954)

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
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
Tropicos 13008149
KEW urn:lsid:ipni.org:names:59777-2
The Plant List ild-12013
Open Tree Of Life 3919896
IUCN Red List 19891420
IPNI 59777-2
iNaturalist 139399
GBIF 2939636
EOL 418857
World Flora Online wfo-1000060937

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
Quinolizidine Alkaloids from the Curare Adjuvant Clathrotropis glaucophylla. Anne‐Lise Sagen, Juerg Gertsch, Rita Becker, Joerg Heilmann, Otto Sticher Wiley 29-Jun-2005
doi:10.1002/CHIN.200317183
Quinolizidine alkaloids from the curare adjuvant Clathrotropis glaucophylla. Sagen AL, Gertsch J, Becker R, Heilmann J, Sticher O Phytochemistry 01-Dec-2002
doi:10.1016/S0031-9422(02)00394-1
PMID:12453529

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 / Lupin alkaloids / Anagyrine-type alkaloids
(-)-Thermopsine 638234 Click to see 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
(+)-Thermopsine 682648 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
(10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 10246 Click to see 244.33 unknown https://doi.org/10.1002/CHIN.200317183
(1R,9R,10R,12R,14S)-12-hydroxy-14-[(1S)-1-hydroxyethyl]-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 51027988 Click to see CC(C1CC(CC2N1CC3CC2CN4C3=CC=CC4=O)O)O 304.40 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
(1R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 6920824 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
(1S,9R,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 442967 Click to see 244.33 unknown https://doi.org/10.1002/CHIN.200317183
(1S,9S,10R,12S)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 131676079 Click to see 260.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
(1S,9S,10S,12S,14R)-12-hydroxy-14-[(1S)-1-hydroxyethyl]-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 15939932 Click to see CC(C1CC(CC2N1CC3CC2CN4C3=CC=CC4=O)O)O 304.40 unknown https://doi.org/10.1002/CHIN.200317183
12-Hydroxy-14-(1-hydroxyethyl)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 73201095 Click to see 304.40 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
12-Hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 621307 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
7,14-Methano-4H,6H-dipyrido[1,2-a:1',2'-E][1,5]diazocin-4-one, 7,7a,8,9,10,11,13,14-octahydro-, [7R-(7alpha,7aalpha,14alpha)]- 91746595 Click to see 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Anagyrine 5351589 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Baptifoline 160543 Click to see 260.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Epibaptifoline 91747695 Click to see 260.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Thermopsine 92768 Click to see 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(-)-Cytisine 6713952 Click to see 190.24 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
(1R,5S)-3-(3-Buten-1-yl)-1,2,3,4,5,6-hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one 92795 Click to see 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
(1R,9R,10R)-11-methyl-10-prop-2-enyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 102247462 Click to see 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 1747617 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
(1R,9S,10R)-11-methyl-10-prop-2-enyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 162959883 Click to see CN1CC2CC(C1CC=C)CN3C2=CC=CC3=O 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
(1S,5R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one 683511 Click to see 190.24 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
(1S,9R)-11-but-3-enyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 7067420 Click to see 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
1,2,3,4,5,6-hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one 22407 Click to see 190.24 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
1,5-Methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one, 1,2,3,4,5,6-hexahydro-3-methyl-4-(2-propenyl)- 157031 Click to see 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
1,5-Methano-8H-pyrido[1,2-a][1,5]diazocin-8-one, 3-(3-butenyl)-1,2,3,4,5,6-hexahydro-, (1R)- 547355 Click to see 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Caulophylline 234566 Click to see 204.27 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Cytisine 10235 Click to see 190.24 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
N-Methylcytisine 670971 Click to see 204.27 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Tinctorine 442968 Click to see CN1CC2CC(C1CC=C)CN3C2=CC=CC3=O 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,9R,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one 14379239 Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O 246.35 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Hydrorhombinine 7018997 Click to see 248.36 unknown https://doi.org/10.1016/S0031-9422(02)00394-1

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