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Palbociclib Isethionate 10 mg | Purity Not Available
TargetMol
Palbociclib Isethionate (PD 0332991 isethionate) is a selective inhibitor of CDK4/6 (IC50s: 11/16 nM). It exhibits no inhibition against a panel of 36 additional protein kinases.
More Information Supplier PagePalbociclib Isethionate 50 mg | Purity Not Available
TargetMol
Palbociclib Isethionate (PD 0332991 isethionate) is a selective inhibitor of CDK4/6 (IC50s: 11/16 nM). It exhibits no inhibition against a panel of 36 additional protein kinases.
More Information Supplier PageRGFP966 2 mg | 99.77%
TargetMol
RGFP966 is an HDAC3 inhibitor (IC50: 0.08 μM) and does not affect other HDACs at concentrations up to 15 μM.
More Information Supplier PageRGFP966 25 mg | 99.77%
TargetMol
RGFP966 is an HDAC3 inhibitor (IC50: 0.08 μM) and does not affect other HDACs at concentrations up to 15 μM.
More Information Supplier PageDdr1-In-1 25 mg | Purity Not Available
TargetMol
DDR1-IN-1 is an effective and specific DDR1 receptor tyrosine kinase inhibitor (IC50: 105 nM), about 3-fold selectivity over DDR2.
More Information Supplier PageDdr1-In-1 2 mg | Purity Not Available
TargetMol
DDR1-IN-1 is an effective and specific DDR1 receptor tyrosine kinase inhibitor (IC50: 105 nM), about 3-fold selectivity over DDR2.
More Information Supplier PageSANT-1 100 mg | 100.00%
TargetMol
SANT-1 directly binds to Smoothened (Smo) receptor (Kd: 1.2 nM) and inhibits Smo agonist effects (IC50: 20 nM).
More Information Supplier PageNSC 228155 50 mg | 99.84%
TargetMol
NSC 228155 is an activator of EGFR, binding to the sEGFR dimerization domain II and modulate EGFR tyrosine phosphorylation.
More Information Supplier PageNSC 228155 25 mg | 99.84%
TargetMol
NSC 228155 is an activator of EGFR, binding to the sEGFR dimerization domain II and modulate EGFR tyrosine phosphorylation.
More Information Supplier Page
