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2-Bromo-6-cyanopyrazine | CAS:859064-02-1
2-Bromo-6-cyanopyrazine
  • 名称:2-溴-6-氰基吡嗪 | 2-Bromo-6-cyanopyrazine
  • CAS号:859064-02-1
  • 别名:
  • 分子式:C5H2BrN3
  • 分子量:183.99
  • EINESC号:

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物理化学性质

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Disposition of phencyclidine in mice after smoke exposure.A S Freeman et al.Drug metabolism and disposition: the biological fate of chemicals, 10(6), 680-684 (1982-11-01) Effects of drug and chemical pretreatments on biliary excretion of phenylcyclohexene in the rat.F C Law et al.Drug and chemical toxicology, 7(3), 273-282 (1984-01-01) Identification of in vitro rat metabolites of 1-phenylcyclohexene.C E Cook et al.Drug metabolism and disposition: the biological fate of chemicals, 12(2), 186-192 (1984-03-01) Interaction between phencyclidine and its pyrolysis product, 1-phenylcyclohexene.A K Chaturvedi et al.Pharmacology, biochemistry, and behavior, 30(4), 1035-1043 (1988-08-01) Toxicity of 1-phenylcyclohexene and its interaction with phencyclidine.C Y Hu et al.Toxicology and applied pharmacology, 76(3), 403-413 (1984-12-01) Structure-activity relationships of phenylcyclohexene and biphenyl antitubulin compounds against plant and mammalian cells.D H Young et al.Bioorganic & medicinal chemistry letters, 11(11), 1393-1396 (2001-05-30) Phenylcyclohexene and phenylcyclohexadiene substituted compounds having retinoid antagonist activity.R L Beard et al.Bioorganic & medicinal chemistry letters, 11(6), 765-768 (2001-03-30) Metabolic disposition and irreversible binding of 1-phenylcyclohexene in rats.S Chakrabarti et al.Toxicology and applied pharmacology, 69(2), 179-184 (1983-06-30) Quantification of phencyclidine in mainstream smoke and identification of phenylcyclohex-1-ene as pyrolysis product.A S Freeman et al.Journal of pharmaceutical sciences, 70(9), 1002-1004 (1981-09-01) In vitro metabolism of 1-phenyl-1-cyclohexene, a pyrolysis product of phencyclidine.B R Martin et al.Drug metabolism and disposition: the biological fate of chemicals, 10(6), 685-689 (1982-11-01) Phencyclidine and phenylcyclohexene disposition after smoking phencyclidine.C E Cook et al.Clinical pharmacology and therapeutics, 31(5), 635-641 (1982-05-01)
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