Chemistry:Sarmazenil

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Short description: Chemical compound
Sarmazenil
Sarmazenil.svg
Clinical data
AHFS/Drugs.comInternational Drug Names
ATCvet code
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC15H14ClN3O3
Molar mass319.75 g·mol−1
3D model (JSmol)
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Sarmazenil (Ro15-3505) is a drug from the benzodiazepine family. It acts as a partial inverse agonist of benzodiazepine receptors,[1] meaning that it causes the opposite effects to most benzodiazepine drugs, and instead acts as an anxiogenic and convulsant. It is used in veterinary medicine to reverse the effects of benzodiazepine sedative drugs in order to rapidly re-awaken anesthetized animals.[2][3][4]

See also

References

  1. "Molecular structure and stereoelectronic properties of sarmazenil--a weak inverse agonist at the omega modulatory sites (benzodiazepine receptors): comparison with bretazenil and flumazenil". Bioorganic & Medicinal Chemistry 6 (10): 1745–57. October 1998. doi:10.1016/S0968-0896(98)00117-5. PMID 9839004. 
  2. "[Clinical investigations of an i.m. combination anesthesia with fentanylclimazolam/xylazine and postoperative i.v. antagonism with naloxone/sarmazenil/yohimbine in guinea pigs]" (in German). Tierarztliche Praxis 24 (1): 85–7. February 1996. PMID 8720962. 
  3. "A Zoletil-Rompun mixture as an alternative to the use of opioids for immobilization of feral red deer". Journal of Wildlife Diseases 36 (4): 663–9. October 2000. doi:10.7589/0090-3558-36.4.663. PMID 11085427. 
  4. "Partial antagonism of tiletamine-zolazepam anesthesia in cheetah". Journal of Wildlife Diseases 38 (2): 468–72. April 2002. doi:10.7589/0090-3558-38.2.468. PMID 12038151. 

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See also
Receptor/signaling modulators
GABAA receptor positive modulators
GABA metabolism/transport modulators

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