Valproate pivoxil

Anti-PAGR1 PAXIP1 associated glutamate-rich protein 1, 100ul

Anti-PAGR1 PAXIP1 associated glutamate-rich protein 1, 100ul

A widely used cell-permeable autophagic sequestration blocker that effectly protects cerebellar granule cells from apoptosis following serum/potassium deprivation. Although a known class III PI3K inhibitor (IC 50 = 4.

A cell-permeable morpholino-thienopyrimidine compound that acts as a potent and isoform-selective inhibitor of PI 3-Ks (IC 50 = 2 nM, 16 nM, 660 nM, and 220 nM for p110&#945, p110&#946 p110&#947, and PI 3-K C2&#946, respectively) and inhibits

A cell-permeable p53 inhibitor that exhibits 10-fold higher potency (ED 50 = 30 nM in protecting etoposide-induced cortical neuron death) and 50% longer half-life ( t 1/2 = 6h in neuron culture medium at 37&#176C) than Pifithrin-&#945 (Cat. No.

Pimodivir (VX-787) is an orally bioavailable inhibitor of influenza A virus polymerases through interaction with the viral PB2 subunit.In VitroPimodivir rescues macrophages from virus-mediated death at non-cytotoxic concentrations 24 hpi.

Pimodivir (VX-787) is an orally bioavailable inhibitor of influenza A virus polymerases through interaction with the viral PB2 subunit.In VitroPimodivir rescues macrophages from virus-mediated death at non-cytotoxic concentrations 24 hpi. The EC 50

InformationPiroxicam Piroxicam (CP 16171) is a non-selective COX inhibitor, used in the treatment of rheumatoid and osteoarthritis.In vitroPiroxicam induces activation of extracellular signal-regulated kinase (ERK) in neurones and phosphorylation of

Pivalopril is a new orally active angiotensin converting enzyme ( ACE ) inhibitor.In VivoPivalopril is a new compound with a hindered sulfur group that has been compared to Captopril for oral angiotensin-converting enzyme (ACE) inhibition in rats

Pivalopril is a new orally active angiotensin converting enzyme ( ACE ) inhibitor.In VivoPivalopril is a new compound with a hindered sulfur group that has been compared to Captopril for oral angiotensin-converting enzyme (ACE) inhibition in rats

Selective PI3Kδ Inhibitor 1 (compound 7n) is an inhibitor of PI3Kδ with an IC50 of 0.9 nM and &gt:1000-fold selectivity against other class I PI3K isoforms [PI3K α/γ/β=3670/1460/21300 nM].InformationSelective PI3Kδ Inhibitor 1 (compound 7n) is an

Selective PI3Kδ Inhibitor 1 (compound 7n) is an inhibitor of PI3Kδ with an IC50 of 0.9 nM and &gt:1000-fold selectivity against other class I PI3K isoforms [PI3K α/γ/β=3670/1460/21300 nM].InformationSelective PI3Kδ Inhibitor 1 (compound 7n) is an