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Cat. No. Product Name Information
PC-42525

GW788388

ALK5 inhibitor

GW788388 is a potent, selective, and orally active TGF-β type I receptor (ALK5) inhibitor with IC50 of 18 nM in binding assay.
PC-42582

A 83-01

TGF-βRI inhibitor

A 83-01 is a potent, selective TGF-beta type I receptor ALK-5, ALK-4 and ALK-7 inhibitor with IC50 of 12, 45 and 7.5 nM, respectively.
PC-42887

LY2109761

TGF-β RI/II inhibitor

LY2109761 is a potent, selective and orally active TGF-β RI/II dual inhibitor with Ki of 38/300 nM, respectively.
PC-45993

A 77-01

ALK5 inhibitor

A 77-01 is a potent inhibitor of TGF-β type I receptor superfamily activin-like kinase ALK5 with IC50 of 25 nM.
PC-45058

LDN-214117

ALK2 inhibitor

LDN-214117 (LDN214117) is a potent and selective ALK2 inhibitor with a biochemical IC50 of 24 nM, a cell-based IC50 for BMP6 of 100 nM.
PC-42176

FT011

Collagen synthesis inhibitor

FT011 (SHP-627) is an anti-fibrotic agent that prevents TGF-beta-stimulated production of collagen in cultured renal mesangial cells (55-70% inhibition at 30 uM).
PC-45749

Vactosertib

ALK5 inhibitor

Vactosertib (EW-7197, TEW-7197) is a highly potent, selective inhibitor of TGF-β type I receptor kinase (TGF-βRI, ALK5) with IC50 of 11 nM.
PC-27461

Finbosertib

ALK5 inhibitor

Finbosertib is a potent, selecitve inhibitor of transforming growth factor-β receptor I (Activin receptor-like kinase 5, TGFβRI/ALK5).
PC-26849

ALK5 inhibitor 20

ALK5 inhibitor

ALK5 inhibitor 20 is a potent, selective and lung-restricted ALK5 inhibitor with pKi of 10.13, shows persistent and lung-restricted target engagement in a pharmacodynamic model, shows remarkable efficacy in idiopathic pulmonary fibrosis (IPF).
PC-26694

M4K2308

ALK2 inhibitor

M4K2308 is a potent, selective inhibitor of ALK2 with IC50 of 2 nM, >100-fold selectivity over ALK5.
PC-24983

YH395A

TGF-βRI inhibitor

YH395A is a specific inhibitor of TGFβ receptor 1 (TGFβR1) with MST KD of 35.6 uM, abrogates Smad-dependent signaling in TNBC.
PC-24982

YR-290

TGF-βRI inhibitor

YR-290 is a specific inhibitor of TGFβ receptor 1 (TGFβR1) with IC50 of 137 nM, exhibits anticancer activity of IC50 value of 9.13 μM against A549 cell.

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