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MedChemexpress

货号: HY-12501

ITI214 (free base)

  • 1160521-50-5
  • C29H26FN7O
  • 98%
  • 7日

销 售 价 ¥2333.00 /mg

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  • MSDS
信息更新时间:2018.06.10
  • ITI214 (free base)
  • 98%
  • 2mg
  • 1 mg
  • 7日
  • HY-12501
化合物信息 [查看化合物百科]
化合物英文学名 (6aR,9aS)-5,6a,7,8,9,9a-hexahydro-5-methyl-3-(phenylamino)-2-((4-(6-fluoropyridin-2-yl)phenyl)methyl)cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidin-4(2H)-one 化合物中文学名 (6aR,9aS)-5,6a,7,8,9,9a-hexahydro-5-methyl-3-(phenylamino)-2-((4-(6-fluoropyridin-2-yl)phenyl)methyl)cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidin-4(2H)-one
CAS号 1160521-50-5 分子式 C29H26FN7O
分子量 507.561 精确质量 507.218
LogP 4.046 PSA 82.03
详细描述
产品描述:ITI-214 (free base) is a picomolar PDE1 inhibitor with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters, and ion channels, exhibits potent PDE1 inhibitory activity (Ki = 58 pM). IC50 value: 58 pM (Ki) Target: PDE1 in vitro: ITI-214 exhibits picomolar inhibitory potency for PDE1, demonstrates excellent selectivity against all other PDE families. ITI214 exhibits excellent selectivity over other PDE family members. For instance, the Ki values of ITI214 against recombinant full-length human PDE1A, PDE1B, and PDE1C are 33 pM, 380 pM, and 35 pM, respectively. ITI214 is profiled in a panel of enzymes, receptors, transporters, and ion channels from Caliper at 10 μM, which is over 170000 times higher than its Ki for PDE1, and demonstrates good selectivity. [1] in vivo: ITI214 possesses a good overall profile with balanced physicochemical properties, excellent potency and selectivity, and good pharmacokinetics. ITI214 is found to significantly enhance memory performance in the test with a minimum effective dose of 3 mg/kg. [1]
产品链接:http://www.medchemexpress.com/IKK_epsilon_-IN-1.html
产品链接:http://www.medchemexpress.cn/iti214-free-base.html

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ITI214 (free base)

1160521-50-5

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