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L-Phenylalanyl-L-methionyl-L-histidyl-L-asparaginyl-L-leucyl-D-tryptophyl-L-lysyl-L-histidyl-L-leucyl-L-seryl-L-seryl-L-methionyl-L-alpha-glutamyl-L-arginyl-L-valyl-L-alpha-glutamyl-L-tryptophyl-L-leucyl-L-arginyl-L-lysyl-L-lysyl-L-leucyl-L-glutaminyl-L-a | CAS:118102-98-0
L-Phenylalanyl-L-methionyl-L-histidyl-L-asparaginyl-L-leucyl-D-tryptophyl-L-lysyl-L-histidyl-L-leucyl-L-seryl-L-seryl-L-methionyl-L-alpha-glutamyl-L-arginyl-L-valyl-L-alpha-glutamyl-L-tryptophyl-L-leucyl-L-arginyl-L-lysyl-L-lysyl-L-leucyl-L-glutaminyl-L-a
  • 名称:L-苯丙氨酰-L-蛋氨酰-L-组氨酰-L-天冬氨酰胺酰-L-亮氨酰-D-色氨酰-L-赖氨酰-L-组氨酰-L-亮氨酰-L-丝氨酰-L-丝氨酰-L-蛋氨酰-L-alpha-谷氨酰-L-精氨酰-L-缬氨酰-L-alpha-谷氨酰-L-色氨酰-L-亮氨酰-L-精氨酰-L-赖氨酰-L-赖氨酰-L-亮氨酰-L-谷氨酰胺酰-L-alpha-天冬氨酰-L-缬氨酰-L-组氨酰-L-天冬氨酰胺酰-L-酪氨酰胺 | L-Phenylalanyl-L-methionyl-L-histidyl-L-asparaginyl-L-leucyl-D-tryptophyl-L-lysyl-L-histidyl-L-leucyl-L-seryl-L-seryl-L-methionyl-L-alpha-glutamyl-L-arginyl-L-valyl-L-alpha-glutamyl-L-tryptophyl-L-leucyl-L-arginyl-L-lysyl-L-lysyl-L-leucyl-L-glutaminyl-L-a
  • CAS号:118102-98-0
  • 别名:[D-Trp12,Tyr34]-bPTH-(7-34)NH2
  • 分子式:C165H251N49O40S2
  • 分子量:3625.20
  • EINESC号:

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物理化学性质

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Mutagenicity of chloroolefins in the Salmonella/mammalian microsome test. III. Metabolic activation of the allylic chloropropenes allyl chloride, 1,3-dichloropropene, 2,3-dichloro-1-propene, 1,2,3-trichloropropene, 1,1,2,3-tetrachloro-2-propene and hexachloropropene by S9 mix via two different metabolic pathways.T Neudecker et al.Mutation research, 170(1-2), 1-9 (1986-04-01) Effects of a heterogeneous set of xenobiotics on RNA synthesis of yeast cells.I Cascorbi et al.Ecotoxicology and environmental safety, 30(3), 252-258 (1995-04-01) Metabolism of 2,3-dichloro-1-propene in the rat. Consideration of bioactivation mechanisms.E Eder et al.Drug metabolism and disposition: the biological fate of chemicals, 16(1), 60-68 (1988-01-01) Evidence for a radical mechanism of the dechlorination of chlorinated propenes mediated by the tetrachloroethene reductive dehalogenase of Sulfurospirillum muftivorans.Roland P H Schmitz et al.Environmental science & technology, 41(21), 7370-7375 (2007-11-30) Disposition of [14C]2,3-dichloropropene in Fischer-344 rats after oral or intraperitoneal administration.M A Medinsky et al.Toxicology letters, 23(1), 119-125 (1984-10-01) Effect of vapor concentration on the disposition of inhaled 2,3-dichloropropene in Fischer-344 rats.J S Dutcher et al.Fundamental and applied toxicology : official journal of the Society of Toxicology, 5(5), 997-1005 (1985-10-01) Halogenated derivatives QSAR model using spectral moments to predict haloacetic acids (HAA) mutagenicity.Alfonso Pérez-Garrido et al.Bioorganic & medicinal chemistry, 16(10), 5720-5732 (2008-04-15) Disposition and metabolism of 2,3-[14C]dichloropropene in rats after inhalation.J A Bond et al.Toxicology and applied pharmacology, 78(1), 47-54 (1985-03-30) Subchronic inhalation toxicity and reproductive assessment in rats of three chlorinated propenes.F R Johannsen et al.Journal of toxicology and environmental health, 33(3), 291-302 (1991-07-01)
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