Defactinib-hydrochloride-VS-6063-hydrochloride-DataSheet-生命科學(xué)試劑-MedChemExpress

1、Hotline: 400-820-3792Inhibitors Agonists Screening Librarieswww.MedChemEDefactinib hydrochlorideCat. No.: HY-12289ACAS No.: 1073160-26-5Synonyms: VS-6063 hydrochloride; PF 04554878 hydrochloride分式: CHClFNOS分量: 546.95作靶點(diǎn): FAK作通路: Protein Tyrosine Kinase/RTK儲存式: Powder -20C 3 years4C 2 yearsIn solvent

2、 -80C 6 months-20C 1 month溶解性數(shù)據(jù)體外實(shí)驗(yàn) DMSO : 30 mg/mL (54.85 mM; Need ultrasonic)Mass Solvent1 mg 5 mg 10 mg Concentration制備儲備液1 mM 1.8283 mL 9.1416 mL 18.2832 mL5 mM 0.3657 mL 1.8283 mL 3.6566 mL10 mM 0.1828 mL 0.9142 mL 1.8283 mL請根據(jù)產(chǎn)品在不同溶劑中的溶解度，選擇合適的溶劑配制儲備液，并請注意儲備液的保存式和期限。BIOLOGICAL ACTIVITY物活性 Defa

3、ctinib hydrochloride (VS-6063 hydrochloride; PF 04554878 hydrochloride)種新型 FAK 抑制劑，抑制 FAK 在 Tyr397 位點(diǎn)磷酸化，這種作具有時(shí)間和劑量依賴性。IC50 & Target FAK 1體外研究Defactinib (VS-6063) inhibits FAK phosphorylation at the Tyr397 site in a time- and dose-dependent manner.1/3 Master of Small Molecules 您邊的抑制劑師www.MedChemERPP

4、A data shows that Defactinib reduces levels of AKT and YB-1 in taxane-resistant cell lines. Theexpression of pFAK (Tyr397) is statistically significantly inhibited by Defactinib in a dose-dependent mannerin all cell lines. Defactinib inhibits pFAK (Tyr397) expression within 3 hours, with a gradual r

5、eturn ofexpression by 48 hours 1.體內(nèi)研究 Defactinib (VS-6063) doses of 25 mg/kg twice a day or greater statistically significantly inhibits pFAK(Tyr397) at 3 hours, with return of expression noted by 24 hours. Therefore, administration of Defactinib at 25mg/kg twice a day is selected as the dosing sche

6、dule for subsequent therapy experiments. For therapyexperiments, female nude mice bearing HeyA8 tumors in the peritoneal cavity are randomly divided into 4groups (n=10 per group): 1) vehicle orally twice daily and phosphate-buffered saline intraperitoneally weekly(control); 2) Defactinib 25 mg/kg or

7、ally twice daily; 3) PTX intraperitoneally weekly; and 4) both VDefactinib25 mg/kg orally twice daily and PTX intraperitoneally weekly. There is an 87.4% reduction in tumor weight byPTX monotherapy in the HeyA8 model, and combination therapy resulted in the greatest tumor weightreduction, with a 97.

8、9% reduction (P=0.05 compared with PTX). In the SKOV3ip1 model, a 92.7% tumorweight reduction is observed in the combination group compared with PTX (P 1.PROTOCOLAnimal Mice 1Administration 1 To determine the antitumor effects of Defactinib, SKOV3ip1, SKOV3-TR, HeyA8, and HeyA8-MDR cells areinjected

9、 intraperitoneally. One week after tumor cell injection, mice are randomly assigned to 4 groups of 10mice (control, PTX alone, Defactinib alone, and PTX with Defactinib); treatment is initiated at 3-4 weeksfollowing injection. PTX at 2 mg/kg (SKOV3ip1 and SKOV3-TR) or 2.5 mg/kg (HeyA8 and HeyA8-MDR)

10、 isgiven intraperitoneally weekly; Defactinib at 25 mg/kg is given orally twice every day. Control mice receivedHBSS intraperitoneally once a week and vehicle orally twice every day. Mice are monitored daily for adverseeffects of therapy and are killed on day 35 (SKOV3ip1 or SKOV3-TR), day 28 (HeyA8

11、 or HeyA8-MDR), orwhen any of the mice seemed moribund. Total body weight, tumor incidence and mass, and the number oftumor nodules are recorded. Tumors are either fixed in formalin or embedded in paraffin or snap frozen inoptimal cutting temperature (OCT) compound in liquid nitrogen.MCE has not ind

12、ependently confirmed the accuracy of these methods. They are for reference only.戶使本產(chǎn)品發(fā)表的科研獻(xiàn) Science. 2017 Dec 1;358(6367). Nat Commun. 2019 Aug 16;10(1):3708. J Exp Clin Cancer Res. 2018 Jul 28;37(1):175. Sci Rep. 2019 May 20;9(1):7617. J Int Med Res. 2018 Apr;46(4):1311-1325.See more customer validations on HYPERLINK / www.MedChemEREFERENCES2/3 Master of Small Molecules 您邊的抑制劑師www.MedChemE1. Kang Y, et al. Role of focal adhesion kinase in regulating YB-1-mediated resistance in ovarian cancer. J Natl Cancer Inst. 2013 Oct2;105(19):1485-95.McePdfHeig