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S83882

Imidafenacin

源叶(MedMol) 98%
  • 英文名:
  • Imidafenacin
  • 别名:
  • 咪达那新;咪达那新 [IMIDAFENACIN];4-(2-甲基-1H-咪唑-1-基)-2,2-二苯基丁酰胺;咪达那新;4-(2-METHYL-1H-IMIDAZOL-1-YL)-2,2-DIPHENYLBUTANAMIDE;Imidafenacin;2-Methyl-α,α-diphenyl-1H-iMidazole-1-butanaMide;4-(2-Methyl-1-iMidazolyl)-
  • CAS号:
  • 170105-16-5
  • 分子式:
  • C20H21N3O
  • 分子量:
  • 319.4
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S83882-100mg 98% ¥383.00元 9 - - - EA 加入购物车
源叶(MedMol) S83882-250mg 98% ¥700.00元 7 - - - EA 加入购物车
源叶(MedMol) S83882-1g 98% ¥2000.00元 4 - - - EA 加入购物车
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  • 提示:详情请下载说明书。
  • 产品描述: Imidafenacin(KRP-197; ONO-8025) is a potent and selective inhibitor of M3 receptors with Kb of 0.317 nM; less potent for M2 receptors(IC50=4.13 nM). IC50 value: 0.3 nM(M3) [1] in vitro: KRP-197 showed equipotent anti-M2 and anti-M3 activity and decreased subtype-selectivity. in vivo: Intraduodenal administration of KRP-197 (0.04±0.30 mg/kg) inhibited bladder contraction dose-dependently, and the ED30 value was 0.11 mg/kg. The inhibitory action of KRP-197 on the bladder contraction was 19 times as potent as that of oxybutynin. KRP-197 showed preventive action against the decrease in bladder capacity induced by carbachol (ED50 0.074 mg/kg, intragastric administration), and the potency of the inhibitory action was 15-fold greater than that of oxybutynin. The learning-inhibitory doses of intravenous oxybutynin hydrochloride and tolterodine tartrate were 0.3 and 3 mg/kg in sham-operated rats and 0.1 and 1 mg/kg in nbM-lesioned rats, respectively. Thus, the learning impairments by those antimuscarinics were more sensitive in nbM-lesioned rats than in sham-operated rats. On the other hand, intravenous administration of imidafenacin had no influence on learning in either case of the rats. In normal rats, however, intracerebroventricular administration of imidafenacin impaired learning to the same degree as that of oxybutynin hydrochloride
  • 靶点: mAChR;AChR
  • 参考文献:
    1. Miyachi H, et al. Synthesis and antimuscarinic activity of a series of 4-(1-Imidazolyl)-2,2-diphenylbutyramides: discovery of potent and subtype-selective antimuscarinic agents. Bioorg Med Chem. 1999 Jun;7(6):1151-61. 2. Yamazaki T, et al. Imidafenacin has no influence on learning in nucleus basalis of Meynert-lesioned rats. Naunyn Schmiedebergs Arch Pharmacol. 2013 Dec;386(12):1095-102.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 3.131 ml 15.654 ml 31.309 ml
    5 mM 0.626 ml 3.131 ml 6.262 ml
    10 mM 0.313 ml 1.565 ml 3.131 ml
    50 mM 0.063 ml 0.313 ml 0.626 ml
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