您好,欢迎来到化工原料网! [登录] [免费注册]
化工原料网
位置:首页 > 产品库 > Dalpiciclib
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
Dalpiciclib
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Dalpiciclib图片
CAS NO:1637781-04-4
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议

产品名称
SHR-6390
产品介绍
Dalpiciclib (SHR-6390) 是一种具有口服活性和高选择性的CDK4/6抑制剂,IC50值分别为 12.4 nM 和 9.9 nM。Dalpiciclib 对乳腺癌和食道鳞状细胞癌显示出抗肿瘤活性。
生物活性

Dalpiciclib (SHR-6390) is an orally active and highly selective inhibitor ofCDK4and 6withIC50values of 12.4 nM and 9.9 nM, respectively[1][2]. Dalpiciclib shows antitumor activity against breastcancerand esophageal squamous cell carcinoma[1][2][3][4].

IC50& Target[1]

CDK4

12.4 nM (IC50)

CDK6

9.9 nM (IC50)

体外研究
(In Vitro)

Dalpiciclib (0-4 μM, 72 h) inhibits cell proliferation in a dose-dependent manner[3].
Dalpiciclib (0-10 μM, 6 d) inhibits the proliferation of retinoblastoma-positive tumor cell lines[4].

Cell Proliferation Assay[3]

Cell Line:Eca 109, Eca 9706, and KYSE-510 ESCC cell lines
Concentration:0-4 μM
Incubation Time:72 hours
Result:Inhibited cell proliferation in a dose-dependent manner, with Eca 109 being the relative sensitive one and Eca 9706 being the relative resistant one.

Cell Viability Assay[4]

Cell Line:MCF7, MCF7/TR, BT-474/T cell lines
Concentration:0-10 μM
Incubation Time:6 days
Result:Inhibited MCF7/TR cells, parental MCF7 cells and BT-474/T resistant cells with the IC50values of 229.5, 115.4 and 210.7 nM, respectively.
体内研究
(In Vivo)

Dalpiciclib (oral gavage; 150 mg/kg; once weekly; 3 weeks) shows antitumor activity against ESCC xenografts[3].
Dalpiciclib combined with Paclitaxel (PTX) or Cisplatin (CDDP) offer synergistic inhibitory effects in ESCC xenografts[3].
Dalpiciclib (oral gavage; 37.5 mg/kg, 75 mg/kg, 150 mg/kg; once daily; 30 days) shows antitumor activity in human xenograft models[4].

Animal Model:NOD/SCID mice (ESCC PDXs models)[3]
Dosage:150 mg/kg
Administration:Oral gavage; 150 mg/kg; once weekly; 3 weeks
Result:Suppressed the growth of tumor.
Animal Model:5-week-old female Balb/cA-nude mice subcutaneously inoculated MCF7/ARO, COLO 205 and U87MG[4]
Dosage:37.5 mg/kg, 75 mg/kg, 150 mg/kg
Administration:Oral gavage; 37.5 mg/kg, 75 mg/kg, 150 mg/kg; once daily; 30 days
Result:Caused regression of all tumor xenografts at the highest dose tested.
Clinical Trial
分子量

446.54

Formula

C25H30N6O2

CAS 号

1637781-04-4

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.