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Request The Product List ofTGF beta Receptor (TGFBR) TGF beta Receptor (TGFBR)

Cat. No. Product Name Information
PC-61455

TASP0382088

ALK5 inhibitor

A potent, selective ALK5 inhibitor with IC50 of 4.8 nM, >100-fold selectivity over 95 different kinases.
PC-61454

TP-0427736

ALK5 inhibitor

TP-0427736 (TP0427736) is a novel potent and selective ALK5 inhibitor with IC50 of 2.72 nM, displays 300-fold selecitvity over ALK3.
PC-61453

ALK5-IN-16i

ALK5 inhibitor

ALK5-IN-16i is a potent and selective ALK5 inhibitor with IC50 of 5.5 nM, displays 300-fold selecitvity over ALK3.
PC-61448

IN-1233 phosphate

ALK5 inhibitor

IN-1233 phosphate is a potent and selective TGF-βRI (ALK5) inhibitor with IC50 of 34 nM, prevents tissue hyperplasia in the rat urethra or common iliac artery.
PC-61447

IN-1233

ALK5 inhibitor

IN-1233 is a potent and selective TGF-βRI (ALK5) inhibitor with IC50 of 34 nM, prevents tissue hyperplasia in the rat urethra or common iliac artery.
PC-61446

EW-7195

ALK5 inhibitor

A novel potent and selective TGF-βRI (ALK5) inhibitor with IC50 of 4.83 nM, dispalys >300-fold selectivity over p38α.
PC-60916

San78-130

ALK1 inhibitor

San78-130 is a potent, selective activin receptor-like Kinase 1 (ALK1) inhibitor with IC50 of 62 nM, with greater selectivity compared with L-783277.
PC-60915

L-783277

ALK1 inhibitor

L-783277 is a resorcylic lactone type covalent kinase inhibitor that inhibits ALK1 with IC50 of 125 nM, also inhibits FLT3, VEGFR2, VEGFR3, MEK2 with IC50 of 1-10 nM.
PC-60770

VU 0469381

ALK2 inhibitor

VU 0469381 (ML347) is a potent, sellective BMP receptor ALK2 antaognist with Ki of 32 nM, with no affinity for ALK3/4/5/6.
PC-60769

VU 0465350

ALK3 inhibitor

VU 0465350 is a potent, specific BMP receptor activin receptor-like kinase 3 (ALK3) antaognist with Ki of 92.3 nM.
PC-60768

VU 0364849

ALK3 inhibitor

VU 0364849 (DMH2) is a potent, specific BMP receptor activin receptor-like kinase 3 (ALK3) antaognist with Ki of 5.4 nM.
PC-70054

IN-1130

ALK5 inhibitor

IN-1130 is a potent, highly selective ALK5 inhibitor, inhibits the purified kinase domain of ALK5-mediated Smad3 phosphorylation with an IC50 of 5.3 nM.

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