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SD-208 5mg  | Purity Not Available

Selleck Chemicals

SD-208 is a selective TGF-βRI (ALK5) inhibitor with IC50 of 48 nM, >100-fold selectivity over TGF-βRII.

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PI-3065 25mg  | Purity Not Available

Selleck Chemicals

PI-3065 is a selective p110δ inhibitor with IC50 of 15 nM, >70-fold selectivity over other PI3K family members.

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GSK1324726A (I-BET726) 25mg  | Purity Not Available

Selleck Chemicals

GSK1324726A (I-BET726) is a highly selective inhibitor of BET family proteins with IC50 of 41 nM, 31 nM, and 22 nM for BRD2, BRD3, and BRD4, respectively.

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GSK1324726A (I-BET726) 5mg  | Purity Not Available

Selleck Chemicals

GSK1324726A (I-BET726) is a highly selective inhibitor of BET family proteins with IC50 of 41 nM, 31 nM, and 22 nM for BRD2, BRD3, and BRD4, respectively.

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SD-208 100mg  | Purity Not Available

Selleck Chemicals

SD-208 is a selective TGF-βRI (ALK5) inhibitor with IC50 of 48 nM, >100-fold selectivity over TGF-βRII.

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Lomitapide Mesylate 10mg  | Purity Not Available

Selleck Chemicals

Lomitapide Mesylate(AEGR-733 Mesylate,BMS-2138 Mesylate) is a potent microsomal triglyceride transfer protein (MTP) inhibitor, used in the treatment of familial hypercholesterolemia.

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Lomitapide Mesylate 50mg  | Purity Not Available

Selleck Chemicals

Lomitapide Mesylate(AEGR-733 Mesylate,BMS-2138 Mesylate) is a potent microsomal triglyceride transfer protein (MTP) inhibitor, used in the treatment of familial hypercholesterolemia.

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Lomitapide 100mg  | Purity Not Available

Selleck Chemicals

Lomitapide (AEGR-733, BMS-201038) is a potent microsomal triglyceride transfer protein (MTP) inhibitor, used in the treatment of familial hypercholesterolemia.

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Lomitapide 25mg  | Purity Not Available

Selleck Chemicals

Lomitapide (AEGR-733, BMS-201038) is a potent microsomal triglyceride transfer protein (MTP) inhibitor, used in the treatment of familial hypercholesterolemia.

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Cerdulatinib (PRT062070) hydrochloride 200mg  | Purity Not Available

Selleck Chemicals

Cerdulatinib (PRT-062070, PRT2070) hydrochloride is an oral active, multi-targeted tyrosine kinase inhibitor with IC50 of 12 nM/6 nM/8 nM/0.5 nM and 32 nM for JAK1/JAK2/JAK3/TYK2 and Syk, respectively. Also inhibits 19 other tested kinases with IC50 less than 200 nM.

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