Y-27632 dihydrochloride 10 mg | 98.80%
TargetMol
Y-27632 is a selective inhibitor of ROCKs including p160ROCK (Ki: 140 nM) and ROCK2 (IC50: 800 nM).
More Information Supplier PageY-27632 dihydrochloride
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Y-27632 dihydrochloride 50 mg | 98.80%
TargetMol
Y-27632 is a selective inhibitor of ROCKs including p160ROCK (Ki: 140 nM) and ROCK2 (IC50: 800 nM).
More Information Supplier PageY-27632 dihydrochloride
MK-2206 dihydrochloride 100 mg | 99.69%
TargetMol
MK-2206 is a highly specific inhibitor of Akt1/2/3 (IC50: 8/12/65 nM in cell-free assays) and no effect on the activities of 250 other protein kinases.
More Information Supplier PageMK-2206 dihydrochloride
MK-2206 dihydrochloride 10 mg | 99.69%
TargetMol
MK-2206 is a highly specific inhibitor of Akt1/2/3 (IC50: 8/12/65 nM in cell-free assays) and no effect on the activities of 250 other protein kinases.
More Information Supplier PageMK-2206 dihydrochloride
Niraparib tosylate 2 mg | Purity Not Available
TargetMol
MK-4827(Niraparib) tosylate (with IC50 of 3.8 nM/2.1 nM) is a selective PARP1/PARP2 inhibitor.
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LLY-507 100 mg | Purity Not Available
TargetMol
LLY-507 is an effective, cell-active, and specific inhibitor of protein-lysine Methyltransferase SMYD2.
More Information Supplier PageLLY-507
LLY-507 2 mg | Purity Not Available
TargetMol
LLY-507 is an effective, cell-active, and specific inhibitor of protein-lysine Methyltransferase SMYD2.
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HLCL-61 hydrochloride 200 mg | 99.91%
TargetMol
HLCL-61 hydrochloride is a potent and selective PRMT5 inhibitor for the treatment of acute myeloid leukemia.
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HLCL-61 hydrochloride 50 mg | 99.91%
TargetMol
HLCL-61 hydrochloride is a potent and selective PRMT5 inhibitor for the treatment of acute myeloid leukemia.
More Information Supplier PageHLCL-61 hydrochloride
HLCL-61 hydrochloride 10 mg | 99.91%
TargetMol
HLCL-61 hydrochloride is a potent and selective PRMT5 inhibitor for the treatment of acute myeloid leukemia.
More Information Supplier PageHLCL-61 hydrochloride