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Chemical Compound Review

BW-501C     N'-[3-(2- chlorophenoxy)propyl]-2...

Synonyms: BW501, BW 501, BW 501C, AC1L58RM, BW 501C67, ...
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High impact information on N'-[3-(2-chlorophenoxy)propyl]-2-phenylazanyl-ethanimidamide

  • 4. Pretreatment with the peripherally acting 5-HT(2) receptor antagonist BW 501C67 (0.1 mg kg(-1) i.v.) had no effect on the DOI-induced inhibition of 5-HT cell firing, but completely blocked the DOI-induced rise in mean arterial blood pressure [1].
  • Pretreatment with the 5-HT1C receptor agonist/5-HT2 receptor antagonist m-chlorophenylpiperazine (1 mg/kg i.v.) tended to decrease the EPI-releasing effect of d-Fen, whereas that with the peripheral 5-HT1C/5-HT2 receptor antagonist BW 501C67 (0.5 mg/kg i.v.) did not alter the EPI-releasing effect of d-Fen [2].
  • However, the antiserotoninergic drug BW 501C and the histamine H2-receptor antagonist cimetidine each caused short-term suppression of tumour growth [3].
 

Gene context of N'-[3-(2-chlorophenoxy)propyl]-2-phenylazanyl-ethanimidamide

 

Analytical, diagnostic and therapeutic context of N'-[3-(2-chlorophenoxy)propyl]-2-phenylazanyl-ethanimidamide

References

 
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