BRD4770 5 mg | 99.82%
TargetMol
BRD4770 is a histone methyltransferase G9a inhibitor and induces cell senescence.
More Information Supplier PageBRD4770
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BRD4770 50 mg | 99.82%
TargetMol
BRD4770 is a histone methyltransferase G9a inhibitor and induces cell senescence.
More Information Supplier PageBRD4770
BRD4770 25 mg | 99.82%
TargetMol
BRD4770 is a histone methyltransferase G9a inhibitor and induces cell senescence.
More Information Supplier PageBRD4770
BRD4770 10 mg | 99.82%
TargetMol
BRD4770 is a histone methyltransferase G9a inhibitor and induces cell senescence.
More Information Supplier PageBRD4770
BRD4770 100 mg | 99.82%
TargetMol
BRD4770 is a histone methyltransferase G9a inhibitor and induces cell senescence.
More Information Supplier PageBRD4770
Atglistatin 10 mg | 99.81%
TargetMol
Atglistatin is a highly effective, specific and competitive ATGL inhibitor with an IC50 of ~0.7 μM for inhibition of lipolysis in vitro, and no toxicity when the concentration up to 50 μM.
More Information Supplier PageAtglistatin
Atglistatin 100 mg | 99.81%
TargetMol
Atglistatin is a highly effective, specific and competitive ATGL inhibitor with an IC50 of ~0.7 μM for inhibition of lipolysis in vitro, and no toxicity when the concentration up to 50 μM.
More Information Supplier PageAtglistatin
Omipalisib 5 mg | 99.16%
TargetMol
GSK2126458 is a small-molecule pyridylsulfonamide inhibitor of phosphatidylinositol 3-kinase (PI3K) with potential antineoplastic activity.
More Information Supplier PageOmipalisib
Omipalisib 10 mg | 99.16%
TargetMol
GSK2126458 is a small-molecule pyridylsulfonamide inhibitor of phosphatidylinositol 3-kinase (PI3K) with potential antineoplastic activity.
More Information Supplier PageOmipalisib
XMD17-109 5 mg | Purity Not Available
TargetMol
XMD17-109 is a new selective ERK-5 inhibitor (EC50: 4.2 uM, HEK293 cells).
More Information Supplier PageXMD17-109
