BI 882370

BI 882370 구조식 이미지
카스 번호:
1392429-79-6
상품명:
BI 882370
동의어(영문):
CS-2615;BI 882370;BI882370;BI-882370;BI-882370,Raf,BI882370,inhibit,Inhibitor,Raf kinases,BI 882370;1-Propanesulfonamide, N-[3-[5-[(1-ethyl-4-piperidinyl)methylamino]-3-(5-pyrimidinyl)-1H-pyrrolo[3,2-b]pyridin-1-yl]-2,4-difluorophenyl]-;N-(3-(5-((1-Ethylpiperidin-4-yl)(methyl)amino)-3-(pyrimidin-5-yl)-1H-pyrrolo[3,2-b]pyridin-1-yl)-2,4-difluorophenyl)propane-1-sulfonamide
CBNumber:
CB53358255
분자식:
C28H33F2N7O2S
포뮬러 무게:
569.67
MOL 파일:
1392429-79-6.mol

BI 882370 속성

끓는 점
649.6±65.0 °C(Predicted)
밀도
1.37±0.1 g/cm3(Predicted)
저장 조건
Store at -20°C
용해도
DMSO:5.0(Max Conc. mg/mL);8.78(Max Conc. mM)
물리적 상태
결정성 고체
산도 계수 (pKa)
5.48±0.10(Predicted)
색상
Off-white to gray

안전

BI 882370 C화학적 특성, 용도, 생산

개요

BI-882370 is an orally bioavailable RAF inhibitor with IC50 values of 0.8, 0.8, and 0.6 nM for B-RAFV600E, wild-type B-RAF, and C-RAF in the DFG-out inactive conformation, respectively. It is selective for RAF over a panel of kinases, including LCK, KIT, Src, LYNA, LYNB, and PDGFR (IC50s = 49, 415, 485, 750, 715, and 1,220 nM, respectively). It inhibits proliferation of human B-RAF-mutant melanoma cells when used at concentrations ranging from 1 to 10 nM. It reduces tumor growth in multiple B-RAF-mutant melanoma and colorectal carcinoma mouse xenograft models when administered at a dose of 25 mg/kg twice per day. BI-882370, alone and in combination with trametinib , induces tumor regression in an A375 melanoma mouse xenograft model with no resistance developing within three or five weeks, respectively.

BI 882370 준비 용품 및 원자재

원자재

준비 용품


BI 882370 공급 업체

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