PNU-282987 200 mg | 99.00%
TargetMol
PNU-282987 is a selective α7 nicotinic acetylcholine receptor(α7 nAChR) agonist with Ki of 26 nM; no affinity for α1β1γδ and α3β4 nAChRs (IC50 ≥ 60 μM).
More Information Supplier PagePNU-282987
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PNU-282987 100 mg | 99.00%
TargetMol
PNU-282987 is a selective α7 nicotinic acetylcholine receptor(α7 nAChR) agonist with Ki of 26 nM; no affinity for α1β1γδ and α3β4 nAChRs (IC50 ≥ 60 μM).
More Information Supplier PagePNU-282987
PNU-282987 25 mg | 99.00%
TargetMol
PNU-282987 is a selective α7 nicotinic acetylcholine receptor(α7 nAChR) agonist with Ki of 26 nM; no affinity for α1β1γδ and α3β4 nAChRs (IC50 ≥ 60 μM).
More Information Supplier PagePNU-282987
Triptolide 50 mg | 98.52%
TargetMol
Triptolide is a diterpenes trioxide, immunosuppressive agent extracted from the Chinese herb Tripterygium wilfordii.
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Zebularine 100 mg | 100.00%
TargetMol
Zebularine is a DNA methylation inhibitor. Acts as a transition state analog inhibitor of cytidine deaminase by binding to the active size as covalent hydrates. It also inhibits cytidine deaminase (Ki: 2 μM, in a cell-free assay).
More Information Supplier PageZebularine
Zebularine 25 mg | 100.00%
TargetMol
Zebularine is a DNA methylation inhibitor. Acts as a transition state analog inhibitor of cytidine deaminase by binding to the active size as covalent hydrates. It also inhibits cytidine deaminase (Ki: 2 μM, in a cell-free assay).
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Wiskostatin 25 mg | 98.00%
TargetMol
Wiskostatin is a selective inhibitor of N-WASP, a ubiquitously expressed member of the Wiskott-Aldrich Syndrome protein (WASp) family that regulates actin polymerization.
More Information Supplier PageWiskostatin
HDAC-IN-7 25 mg | Purity Not Available
TargetMol
HDAC-IN-7 (Chidamide impurity) is an impurity of Chidamide. Chidamide is a potent and orally bioavailable inhibitor of HDAC enzymes class I (HDAC1/2/3) and class IIb (HDAC10).
More Information Supplier PageHDAC-IN-7
HDAC-IN-7 2 mg | Purity Not Available
TargetMol
HDAC-IN-7 (Chidamide impurity) is an impurity of Chidamide. Chidamide is a potent and orally bioavailable inhibitor of HDAC enzymes class I (HDAC1/2/3) and class IIb (HDAC10).
More Information Supplier PageHDAC-IN-7
SB-3CT 100 mg | 98.97%
TargetMol
SB-3CT is a potent and specific gelatinase inhibitor for MMP-2(Ki=13.9 nM) and MMP-9(Ki=600 nM).
More Information Supplier PageSB-3CT
