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Chemical Compound Review

Protactyl     N,N-dimethyl-3-phenothiazin- 10-yl-propan-1...

Synonyms: Ampazine, Berophen, Fraction, Promazin, Promwill, ...
 
 
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Disease relevance of PROMAZINE HYDROCHLORIDE

 

High impact information on PROMAZINE HYDROCHLORIDE

 

Chemical compound and disease context of PROMAZINE HYDROCHLORIDE

 

Biological context of PROMAZINE HYDROCHLORIDE

 

Anatomical context of PROMAZINE HYDROCHLORIDE

  • Rabbit erythrocyte membrane interaction with promazine and calcium [20].
  • The increase of neurotensin-IR material of nucleus accumbens was elicited also by chloropromazine (6 mg/kg), trifluoroperazine (2 mg/kg) and pimozide (1.5 mg/kg) while promazine (10 mg/kg) and promethazine (25 mg/kg) were ineffective [21].
  • 6. In a primary culture of human hepatocytes, TCDD (a CYP1A subfamily inducer), as well as rifampicin (mainly a CYP3A4 inducer) induced the formation of promazine 5-sulphoxide and N-desmethylpromazine [22].
  • The aim of the present study was to determine optimum conditions for studying promazine and perazine metabolism in rat liver microsomes, and to investigate the influence of specific cytochrome P-450 inhibitors on 5-sulfoxidation and N-demethylation of these neuroleptics [23].
  • In conclusion, all the three SSRIs administered chronically in pharmacological doses, increase the concentrations of promazine in the blood plasma and brain of rats by inhibiting different metabolic pathways of the neuroleptic [24].
 

Associations of PROMAZINE HYDROCHLORIDE with other chemical compounds

 

Gene context of PROMAZINE HYDROCHLORIDE

  • Of the other isoforms studied, CYP2C9 and CYP3A4 contribute to a lesser degree to promazine 5-sulphoxidation and N-demethylation, respectively [22].
  • Moreover, the observed reaction-dependent effects of promazine and sertindole provide indirect evidence that CYP1A2 is not the only isoenzyme important for the metabolism of caffeine, which requires further pharmacological and clinical consideration [29].
  • In this study the in vivo and in vitro effects of the clinically important phenothiazines promazine (PZ) and chlorpromazine (CPZ) on drug oxidations catalysed by specific cytochrome P450 (P450) enzymes were investigated in the rat [30].
  • 1. The aim of the present study was to identify human cytochrome p-450 isoforms (CYPs) involved in 5-sulphoxidation and N-demethylation of the simplest phenothiazine neuroleptic promazine in human liver [22].
  • Inhibition and induction of cytochrome P450 2B1 in rat liver by promazine and chlorpromazine [30].
 

Analytical, diagnostic and therapeutic context of PROMAZINE HYDROCHLORIDE

References

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  23. The contribution of cytochrome P-450 isoenzymes to the metabolism of phenothiazine neuroleptics. Daniel, W.A., Syrek, M., Haduch, A. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology. (2002) [Pubmed]
  24. The influence of selective serotonin reuptake inhibitors on the plasma and brain pharmacokinetics of the simplest phenothiazine neuroleptic promazine in the rat. Daniel, W.A., Syrek, M., Wójcikowski, J. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology. (1999) [Pubmed]
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