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CEP-32496 (hydrochloride)

    
98%

CEP-32496 (hydrochloride)

源叶(MedMol)
Y65366 一键复制产品信息
1227678-26-3
C24H23ClF3N5O5
553.9182
Agerafenib hydrochloride
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
Y65366-5mg
98%

¥2270.00

货期:2-4周 - - - -
Y65366-10mg
98%

¥3320.00

货期:2-4周 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
体内研究: Oral administration of Agerafenib (CEP-32496) to Colo-205 tumor xenograft-bearing mice results in significant inhibition of pMEK in tumor cell lysates. For instance, a single 30 mg/kg (po) dose of Agerafenib (CEP-32496) leads to a 50 and 75% inhibition of normalized pMEK in tumor lysates at the 2 and 6 h postdose time point, respectively (p<0.03), while a 55 mg/kg (po) dose resulted in a 75% to 57% (p<0.03) inhibition of pMEK at 2 through 10 h post administration, with normalization to baseline by 24 h. Agerafenib (CEP-32496) exhibits an exceptional PK profile in mouse, dog, and cynomolgus monkey. Administration of Agerafenib (CEP-32496) to beagle dogs (single dose of 1 mg/kg iv and 10 mg/kg po) results in low clearance (CL=5.0 (mL/min)/kg) and excellent bioavailability (%F=100). Similarly, in cynomolgus monkey, the administration of Agerafenib (CEP-32496) (single dose of 1 mg/kg iv and 10 mg/kg po) leads to high oral exposure due to low clearance (CL=6.7 mL/min/kg) and excellent bioavailability (%F=100).
溶解性: 10  mM  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.805 ml 9.027 ml 18.053 ml
5 mM 0.361 ml 1.805 ml 3.611 ml
10 mM 0.181 ml 0.903 ml 1.805 ml
50 mM 0.036 ml 0.181 ml 0.361 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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