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BI 882370

CAS No.
1392429-79-6
Chemical Name:
BI 882370
Synonyms
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
Molecular Formula:
C28H33F2N7O2S
Molecular Weight:
569.67
MDL Number:
MFCD31618072
MOL File:
1392429-79-6.mol
Last updated:2023-09-04 15:50:00

BI 882370 Properties

Boiling point 649.6±65.0 °C(Predicted)
Density 1.37±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO:5.0(Max Conc. mg/mL);8.78(Max Conc. mM)
form A crystalline solid
pka 5.48±0.10(Predicted)
FDA UNII V32TR55QP9

BI 882370 price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 24273 BI-882370 ≥95% 1392429-79-6 1mg $32 2024-03-01 Buy
Cayman Chemical 24273 BI-882370 ≥95% 1392429-79-6 5mg $139 2024-03-01 Buy
Cayman Chemical 24273 BI-882370 ≥95% 1392429-79-6 10mg $243 2024-03-01 Buy
Cayman Chemical 24273 BI-882370 ≥95% 1392429-79-6 25mg $533 2024-03-01 Buy
ChemScene CS-0030522 BI-882370 99.16% 1392429-79-6 50mg $550 2021-12-16 Buy
Product number Packaging Price Buy
24273 1mg $32 Buy
24273 5mg $139 Buy
24273 10mg $243 Buy
24273 25mg $533 Buy
CS-0030522 50mg $550 Buy

BI 882370 Chemical Properties,Uses,Production

Description

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 Preparation Products And Raw materials

Raw materials

Preparation Products

BI 882370 Suppliers

Global( 40)Suppliers
Supplier Tel Email Country ProdList Advantage
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6313 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471 sales@sarms4muscle.com China 10523 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 52927 58
Wuhan Jingkang en Biomedical Technology Co., Ltd
+8613720134139 orders@jknbiochem.com China 4398 58
Shanghai Boyle Chemical Co., Ltd. sales@boylechem.com China 2923 55
Shanghai Lollane Biological Technology Co.,Ltd. 021-52996696,15000506266 15000506266 China 4153 55
BOC Sciences 16314854226 info@bocsci.com United States 9926 65
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9709 58
ShangHai Biochempartner Co.,Ltd 17754423994 17754423994 2853530910@QQ.com China 8012 62

BI 882370 Spectrum

BI 882370 BI882370;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]- CS-2615 BI-882370,Raf,BI882370,inhibit,Inhibitor,Raf kinases,BI 882370 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 1392429-79-6 C28H33F2N7O2S