CAS 2443767-35-7

BPR1K871

CAS : 2443767-35-7

Formule : C₂₅H₂₈ClN₇O₂S

Degré de pureté : 98%

Masse moléculaire : 526.0535

Ref: IN-DA01TP4J

1-(3-Chlorophenyl)-3-(5-(2-((7-(3-(Dimethylamino)Propoxy)Quinazolin-4-Yl)Amino)Ethyl)Thiazol-2-Yl)Urea

CAS : 2443767-35-7

1-(3-Chlorophenyl)-3-(5-(2-((7-(3-(Dimethylamino)Propoxy)Quinazolin-4-Yl)Amino)Ethyl)Thiazol-2-Yl)Urea

Degré de pureté : 98%

Masse moléculaire : 526.05g/mol

Ref: 54-OR1023304

BPR1K871

CAS : 2443767-35-7

BPR1K871, a preclinical development candidate for anti-cancer therapy [1], is a potent, selective dual inhibitor targeting FLT3 and AURKA, with IC50 values of

Formule : C₂₅H₂₈ClN₇O₂S

Couleur et forme : Solid

Masse moléculaire : 526.05

Ref: TM-T10592

BPR1K871

CAS : 2443767-35-7

BPR1K871 is a synthetic, orally bioavailable anticancer compound that has potent anticancer activity. It is a multi-kinase inhibitor that inhibits the activity of aurora kinases A and B, AKT, ERK1/2, and JNK. BPR1K871 also inhibits the enzymatic activity of PDGFRβ kinase, which is involved in the proliferation of cancer cells. BPR1K871 has been shown to have no significant impurities and is stable in human plasma. This compound has been shown to have potent anticancer activity in preclinical studies with no toxicity to normal cells.

Formule : C₂₅H₂₈ClN₇O₂S

Degré de pureté : Min. 95%

Masse moléculaire : 526.1 g/mol

Ref: 3D-TXD76735