cycloclavine: isolated from the seeds of the African morning glory (Ipomea hildebrandtii): structure in first source
ID Source | ID |
---|---|
PubMed CID | 24823847 |
SCHEMBL ID | 15828351 |
MeSH ID | M0560403 |
Synonym |
---|
cycloclavine |
xrq6tj7kl8 , |
SCHEMBL15828351 |
Q15633927 |
1h-cycloprop[c]indolo[4,3-ef]indole, 1a,2,3,3a,4,6-hexahydro-1a,3-dimethyl-, (1ar,3ar,9br)- |
(+)-cycloclavine |
(8beta,10s)-6,8-dimethyl-8,10-cycloergoline |
8,10-cycloergoline, 6,8-dimethyl-, (8beta,10s)- |
(2s,4s,7r)-4,6-dimethyl-6,11-diazapentacyclo[7.6.1.02,4.02,7.012,16]hexadeca-1(16),9,12,14-tetraene |
DTXSID701045769 |
Cycloclavine is a clavine-type Ergot alkaloid. It has a unique pentacyclic skeleton featuring a 3-azabicyclo[3.1.0]hexane substructure.
Excerpt | Reference | Relevance |
---|---|---|
"Cycloclavine is a clavine-type Ergot alkaloid noteworthy for its unique pentacyclic skeleton featuring a 3-azabicyclo[3.1.0]hexane substructure. " | ( A Modular Formal Total Synthesis of (±)-Cycloclavine. Netz, N; Opatz, T, 2016) | 2.14 |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 7 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.
| This Compound (23.01) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 7 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |