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Clathrotropis glaucophylla

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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 UUID6440446f5c928768954655
Scientific name Clathrotropis glaucophylla
Authority R.S.Cowan
First published in Bol. Soc. Venez. Ci. Nat.15: 99 (1954)

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
  • Southern America
    • Brazil
      • Brazil North
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001051055
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

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
(-)-Thermospine 442967 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1002/CHIN.200317183
(+)-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 C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 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,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 C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 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 CC(C1CC(CC2N1CC3CC2CN4C3=CC=CC4=O)O)O 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 C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 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 C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Epibaptifoline 91747695 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Thermopsine 92768 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Thermospine 638234 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(+)-Cytisine 683511 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 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 CN1CC2CC(C1CC=C)CN3C2=CC=CC3=O 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)-3,4,5,6-tetrahydro-1H-1,5-methanopyrido[1,2-a][1,5]diazocin-8(2H)-one 6713952 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 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 C=CCCN1CC2CC(C1)C3=CC=CC(=O)N3C2 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, 1,2,3,4,5,6-hexahydro-3-methyl-4-(2-propenyl)- 157031 Click to see CN1CC2CC(C1CC=C)CN3C2=CC=CC3=O 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 C=CCCN1CC2CC(C1)C3=CC=CC(=O)N3C2 244.33 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Citizin 22407 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Cytisinicline 10235 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
N-Methylcytisine 670971 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
N-Methylcytisine 234566 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1016/S0031-9422(02)00394-1
Rhombifoline 92795 Click to see C=CCCN1CC2CC(C1)C3=CC=CC(=O)N3C2 244.33 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 C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/S0031-9422(02)00394-1

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