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1397219-81-6

中文名稱 BS181
英文名稱 BS-181 HCl
CAS 1397219-81-6
分子式 C22H33ClN6
分子量 416.991
MOL 文件 1397219-81-6.mol
更新日期 2024/10/28 11:14:35
1397219-81-6 結(jié)構(gòu)式 1397219-81-6 結(jié)構(gòu)式

基本信息

中文別名
BS-181 鹽酸鹽
化合物BS-181 HCL
英文別名
CS-979
BS181
BS 181
BS-181 HCl USP/EP/BP
N5-(6-aminohexyl)-N7-benzyl-3-isopropylpyrazolo[1,5-a]pyrimidine-5,7-diamine hydrochloride
所屬類別
生物化工:CDK 抑制劑

物理化學(xué)性質(zhì)

儲存條件Keep in dark place,Inert atmosphere,2-8°C
溶解度insoluble in H2O; ≥20.85 mg/mL in DMSO; ≥6.49 mg/mL in EtOH with ultrasonic
形態(tài)固體
顏色White to off-white

圖譜信息

常見問題列表

生物活性
BS-181 hydrochloride 是一種高度選擇性的 CDK7 抑制劑,IC50 值為 21 nM,對 CDK7 的選擇性是對 CDK1,2,4,5,6 和 9 的 40 多倍。
靶點(diǎn)

CDK7/CycH/MAT1

0.021 μM (IC 50 )

CDK2/Cyc E

0.88 μM (IC 50 )

CDK5/p35NCK

3 μM (IC 50 )

CDK9/cycT

4.2 μM (IC 50 )

CDK1/cycB

8.1 μM (IC 50 )

CDK4/Cyc D1

33 μM (IC 50 )

CDK6/cycD1

47 μM (IC 50 )

體外研究

BS-181 promotes cell cycle arrest and inhibits cancer cell growth, and growth is inhibited for all cell lines tested, with IC 50 values ranging from 11.5 to 37 μM. BS-181 inhibits RB phosphorylation at Ser 795 and Ser 821 with an apparent IC 50 of 15 μM, similar to the IC 50 obtained for P-Ser2 inhibition. BS-181 treatment of MCF-7 cells leads to G1 arrest at and apoptosis. BS-181 inhibits GC cell and normal gastric epithelial RGM-1 cell line growth with inhibitory concentration (IC 50 ) ranging from 17 to 22 μM and 6.5 μM, respectively. BS-181 significantly inhibits cell migration and invasion ability in a dose-dependent manner.

體內(nèi)研究

BS-181 (5 mg/kg, 10 mg/kg, i.p.) inhibits the growth of MCF-7 tumors in nude mice. Intravenous (i.v) and i.p administration of 10 mg/kg BS-181 shows rapid clearance. BS-181 (10 mg/kg/d or 20 mg/kg/d, i.p.) significantly inhibits the growth of tumor in a dose-dependent manner compared to the control group.

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