Flucindole
![]() | |
| Clinical data | |
|---|---|
| Other names | WIN-35150; WIN35150; WIN-35,150; 5,7-Difluoro-N,N-dimethyl-α,2-dimethylene-tryptamine |
| Routes of administration | Oral |
| ATC code |
|
| Legal status | |
| Legal status |
|
| Identifiers | |
| |
| CAS Number | |
| PubChem CID | |
| ChemSpider |
|
| UNII | |
| KEGG |
|
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C14H16F2N2 |
| Molar mass | 250.293 g·mol−1 |
| 3D model (JSmol) | |
| |
| |
| (verify) | |
Flucindole (INNTooltip International Nonproprietary Name, USANTooltip United States Adopted Name; developmental code name WIN-35150) is an antipsychotic of the tetrahydrocarbazolamine family with a tricyclic cyclized tryptamine structure that was never marketed.[1][2] It is the 6,8-difluoro derivative of ciclindole.[3] The drug is about 5 to 10 times more potent than ciclindole both in vitro and in vivo.[2]
See also
References
- ^ Elks, J. (2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 556. ISBN 978-1-4757-2085-3. Retrieved 2 November 2024.
- ^ a b Wood PL, McQuade PS (1984). "Ciclindole and flucindole: novel tetrahydrocarbazolamine neuroleptics". Progress in Neuro-Psychopharmacology & Biological Psychiatry. 8 (4–6): 773–7. doi:10.1016/0278-5846(84)90057-5. PMID 6152347. S2CID 39252411.
- ^ Edelson J, Benziger DP (1980). "Disposition of a series of tetrahydrocarbazoles". Drug Metabolism Reviews. 11 (2): 263–89. doi:10.3109/03602538008994027. PMID 7011760.
| Tryptamines |
|
|---|---|
| 4-Hydroxytryptamines and esters/ethers |
|
| 5-Hydroxy- and 5-methoxytryptamines |
|
| N-Acetyltryptamines |
|
| α-Alkyltryptamines |
|
| Cyclized tryptamines |
|
| Isotryptamines | |
| Related compounds |
|
| |
| Classes | |
|---|---|
| Antidepressants (Tricyclic antidepressants (TCAs)) |
|
| Antihistamines |
|
| Antipsychotics |
|
| Anticonvulsants | |
| Anticholinergics |
|
| Others |
|
This article is issued from Wikipedia. The text is available under Creative Commons Attribution-Share Alike 4.0 unless otherwise noted. Additional terms may apply for the media files.
