Protease Inhibitors and Phosphatase Inhibitors
MilliporeSigma™ Calbiochem™ BAY 11-7085
Has biological properties very similar to those of BAY 11-7082. In addition, BAY 11-7085 shows potent anti-inflammatory properties in vivo.
MilliporeSigma™ Calbiochem™ DNA Repair Pathway Inhibitor, NS-123
The DNA Repair Pathway Inhibitor, NS-123, also referenced under CAS 101860-83-7, modulates DNA Repair Pathway. This small molecule/inhibitor is primarily used for Cell Structure applications.
MilliporeSigma™ Calbiochem™ Ifenprodil Hemitartrate
A partial non-competitive antagonist highly selective for GluN1/N2B subtype NMDA receptors (IC50
MilliporeSigma™ Calbiochem™ L-Serine-O-phosphate
A potent agonist for group III mGlu receptor subtype 4, 6, and 8.
MilliporeSigma™ Calbiochem™ 14-3-3 Antagonist II, BV02
The 14-3-3 Antagonist II, BV02 controls the biological activity of 14-3-3.
Novus Biologicals™ Etoposide Inhibitor
Low molecular weight, organic compound that may help regulate biological process.
MilliporeSigma™ Calbiochem™ VEGFR2 Kinase Inhibitor III
The VEGFR2 Kinase Inhibitor III, also referenced under CAS 204005-46-9, controls the biological activity of VEGFR2 Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
MilliporeSigma™ Calbiochem™ PKM2 Activator III
A cell-permeable quinoline-sulfonamide that acts as a potent allosteric PKM2 activator both in cell-free enzymatic assays (AC50 = 17nM with 40 ng PKM2/200μL) and in cultures (AC50 = 45nM in A549 cells) via a high affinity, 2:1 stoichiometric binding, effectively locking PKM2 in an active tetrameric state resistant to known intracellular negative regulators of FBP-activated PKM2 te
MilliporeSigma™ Calbiochem™ Proprotein Convertase Inhibitor
The Proprotein Convertase Inhibitor controls the biological activity of Proprotein Convertase. This small molecule/inhibitor is primarily used for Cell Signaling applications.
MilliporeSigma™ Calbiochem™ HSP90α Inhibitor, PU-29F
A cell-permeable 6-amino-purine based compound that selectively binds to HSP90a (EC50 = 5.4 μM) and inhibits its activity cancer cells.
MilliporeSigma™ Calbiochem™ InhibitorSelect™ FGF Signaling Pathway Inhibitor Panel
A panel containing 14 potent, selective, reversible and cell-permeable inhibitors useful for the study of multiple signaling pathways activated by FGF: 1 mg of Akt Inhibitor VIII, Isozyme-Selective, Akti-1/2 (Cat
Novus Biologicals™ MSC 2032964A Inhibitor
Low molecular weight, organic compound that may help regulate biological process.
MilliporeSigma™ Calbiochem™ Hexamethonium Bromide
A potent antagonist of nicotinic acetylcholine receptors (nAChRs) at pre-ganglionic sites in both the sympathetic and parasympathetic nervous systems.
MilliporeSigma™ Calbiochem™ FTI-276
A highly potent and selective CAAX peptidomimetic of the carboxyl terminal of Ras proteins that inhibits farnesyl transferase (FTase) in vitro (IC50 = 500 pM).