Desmethylflunitrazepam

Desmethylflunitrazepam
Systematic (IUPAC) name
5-(2-fluorophenyl)-7-nitro-1,3-dihydro-1,4-benzodiazepin-2-one
Clinical data
Legal status
Identifiers
CAS Number 2558-30-7
PubChem CID 520217
ChemSpider 453770
Chemical data
Formula C15H10FN3O3
Molar mass 299.26 g·mol−1

Desmethylflunitrazepam (Ro05-4435, fonazepam) is a benzodiazepine that is a metabolite of flunitrazepam.[1][2][3] It has an IC50 value of 1.499 nM for the GABAA receptor.[4][5]

See also

References

  1. Ruud W. Busker, Gerard M.J.Beijersbergen van Henegouwen, Brigitta M.C. Kwee, Jos H.M. Winkens (May 1987). "Photobinding of flunitrazepam and its major photo-decomposition product N-desmethylflunitrazepam". International Journal of Pharmaceutics 36 (2–3): 113–120. doi:10.1016/0378-5173(87)90145-1.
  2. Janet K Coller, Andrew A Somogyi, Felix Bochner (November 1998). "Quantification of flunitrazepam's oxidative metabolites, 3-hydroxyflunitrazepam and desmethylflunitrazepam, in hepatic microsomal incubations by high-performance liquid chromatography". Journal of Chromatography B: Biomedical Sciences and Applications 719 (1–2): 87–92. doi:10.1016/S0378-4347(98)00383-1. PMID 9869368.
  3. Tansel Kilicarslan, Robert L. Haining, Allan E. Rettie, Usanda Busto, Rachel F. Tyndale, Edward M. Sellers (April 2001). "Flunitrazepam Metabolism by Cytochrome P450s 2C19 and 3A4". Drug Metabolism and Disposition 29 (4): 460–465. PMID 11259331.
  4. Desmond J. Maddalena, Graham A. R. Johnston (February 1995). "Prediction of Receptor Properties and Binding Affinity of Ligands to Benzodiazepine/GABAA Receptors Using Artificial Neural Networks". Journal of Medicinal Chemistry 38 (4): 715–724. doi:10.1021/jm00004a017. PMID 7861419.
  5. Sung-Sau So, Martin Karplus (December 1996). "Genetic Neural Networks for Quantitative Structure−Activity Relationships:  Improvements and Application of Benzodiazepine Affinity for Benzodiazepine/GABAA Receptors". Journal of Medicinal Chemistry 39 (26): 5246–5256. doi:10.1021/jm960536o. PMID 8978853.
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