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Hsp90-Cdc37-IN-3
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。
Hsp90-Cdc37-IN-3图片
CAS NO:2361009-68-7
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
Hsp90-Cdc37-IN-3 (Compound 9) 是一种具有抗癌活性 (anticancer) 的新型 celastrol–imidazole 衍生物。Hsp90-Cdc37-IN-3 通过共价结合抑制Hsp90Cdc37,诱导细胞凋亡 (apoptosis)。
生物活性

Hsp90-Cdc37-IN-3 (Compound 9) is a novel celastrol–imidazole derivative withanticanceractivity. Hsp90-Cdc37-IN-3 inhibitsHsp90Cdc37by covalent-binding, and inducesapoptosis[1].

IC50& Target

Hsp90-Cdc37

 

体外研究
(In Vitro)

Hsp90-Cdc37-IN-3 (Compound 9) (24 h) shows broad-spectrum antitumor potential with IC50values of 0.54, 0.59, 0.57, and 0.57 μM against A549, HTC116, U2OS, and MDA-MB231 cells, respectively[1].
Hsp90-Cdc37-IN-3 (0-5 μM, 12 h) inhibits Hsp90–Cdc37 and influences the function of apoptosis-related proteins by covalently combining with both Hsp90 and Cdc37[1].
Hsp90-Cdc37-IN-3 (0-0.8 μM, 48 h) induces apoptosis significantly in A549 cells[1].
Hsp90-Cdc37-IN-3 (0-0.4 μM, 24 h) arrests the cell cycle in the G0/G1phase in a dose-dependent manner[1].

Western Blot Analysis[1]

Cell Line:A549
Concentration:1.25, 2.5, and 5 μM
Incubation Time:12 h
Result:Downregulated the levels of Hsp90–Cdc37 clients (p-Akt and Cdk4) in a dose-dependent manner, and the levels of apoptosis-related proteins (Bax, Bcl-2, cleaved caspase-3, and cleaved PARP) were significantly regulated.

Apoptosis Analysis[1]

Cell Line:A549
Concentration:0.2, 0.4, and 0.8 μM
Incubation Time:48 h
Result:Induced apoptosis significantly.

Cell Cycle Analysis[1]

Cell Line:A549
Concentration:0.1, 0.2, and 0.4 μM
Incubation Time:24 h
Result:Arrested the cell cycle in the G0/G1phase in a dose-dependent manner.
体内研究
(In Vivo)

Hsp90-Cdc37-IN-3 (Compound 9) (0-1 mg/kg; i.p.; once a day, 21 days) shows strong antitumor activity with no significant toxicity[1].

Animal Model:Female BALB/c nude mice at 6 weeks old[1].
Dosage:0.5 mg/kg or 1 mg/kg. Mice were inoculated subcutaneously with A549 cells (1*107in 100 μL of PBS for each mouse).
Administration:Intraperitoneal injection, once a day, 21 days
Result:Decreased tumor weight and enhanced TIR without show toxicity.
分子量

638.19

Formula

C35H44ClN3O6

CAS 号

2361009-68-7

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.