Benzimidazoles
Sigma Aldrich Fine Chemicals Biosciences Omeprazole solid500MG
Omeprazole is a benzimidazole derivative a weak base and is lipophilic in nature. This compound is pH sensitive and does not exists in its original form at low pH.
Cayman Chemical Omeprazole sulfon-d3 1mg
A taurine-conjugated form of hyocholic acid inhibits precipitation of cholesterol crystals by stabilizing cholesterol in the liquid-crystalline phase prevents cholestasis and cellular necrosis induced by taurolithocholic acid in isolated rat livers levels are increased in the urine of patients with hepatitis B-induced cirrhosis
Cayman Chemical Omeprazole-d3 1mg
A selective inhibitor of PI3Ka (Ki 0 2 nM) is 133- 20- and 51-fold selective for PI3Ka over PI3KB PI3K and PI3KY respectively inhibits proliferation of MCF7-neo/HER2 and PC3 cells (EC50s 0 1 and 2 2 M respectively) induces tumor regression in a KPL-4 mouse xenograft model at 6 25 mg/kg reduces tumor growth tumor vasculature and the number of liver and lymph node metastases in the RIP1-Tag2 transgenic mouse model of pancreatic neuroendocrine tumors
TARGETMOL CHEMICALS INC Albendazole sulfoxide 500MG
Also available in 1 mL, 50 mg, 100 mg, 200 mg and bulk. Please contact Fisher for quotes. Albendazole sulfoxide (Ricobendazole) is a metabolite of Albendazole, an anthelmintic. Purity 98.04%
Cayman Chemical Albendazole 25g
An inactive metabolite of TXA2 serum levels positively correlate with platelet COX-1 activation urinary levels reflect intrarenal TXA2 synthesis
Cayman Chemical Omeprazole sulfIde 100mg
Source Recombinant protein expressed in E coli citrullinated with human recombinant PAD4 Amino acids 1-103 (full-length) MW 11 5 kDa
eMolecules Medchem Express / Omeprazole-d3 / 1mg / 446272053 / HY-B0113S / / 922731-01-9 / MFCD21647386 / 348.440 / C17H19N3O3S
Medchem Express / Omeprazole-d3 / 1mg / 446272053 / HY-B0113S / / 922731-01-9 / MFCD21647386 / 348.440 / C17H19N3O3S
Cayman Chemical Omeprazole sulfon 25mg
A serotonin synthesis inhibitor that is used for tracing pools of neuronal serotonin as a competitive inhibitor of tryptophan binding to albumin and as a substrate for the serotonin neural transporter
Cayman Chemical Omeprazole sulfon 10mg
A serotonin synthesis inhibitor that is used for tracing pools of neuronal serotonin as a competitive inhibitor of tryptophan binding to albumin and as a substrate for the serotonin neural transporter
Cayman Chemical Omeprazole sulfon 50mg
A serotonin synthesis inhibitor that is used for tracing pools of neuronal serotonin as a competitive inhibitor of tryptophan binding to albumin and as a substrate for the serotonin neural transporter
Cayman Chemical Omeprazole sulfIde 250mg
A c-Met inhibitor (Ki 4 8 nM) 1000-fold selective for c-Met over a panel of 150 kinases inhibits the proliferation of and induces apoptosis in GTL-16 cells (IC50s 12 and 31 nM respectively) inhibits HGF-induced migration of H441 cells (IC50 11 nM) reduces tumor growth in a GTL-16 mouse xenograft model at 1-30 mg/kg
Cayman Chemical 4-desmethoxy Omeprazole 10mg
A suppressor of IQ electron leak (IC50 70 nM) diminishes endogenous oxidative damage in primary astrocytes reduces stress-induced signaling in a cardiomyocyte cell model and protects against ischemia-reperfusion injury in perfused mouse heart
Cayman Chemical 4-desmethoxy Omeprazole 25mg
A suppressor of IQ electron leak (IC50 70 nM) diminishes endogenous oxidative damage in primary astrocytes reduces stress-induced signaling in a cardiomyocyte cell model and protects against ischemia-reperfusion injury in perfused mouse heart
Cayman Chemical Omeprazole-d3 500ug
A lignan with diverse biological activities inhibits polymerization of isolated chicken brain tubulin (IC50 0 6 UM) induces mitotic arrest at the G2/M phase in CCRF CEM cells from 0 01 to 5 Ug/ml is protective against HSV-1 infection in Vero cells at 5 UM inhibits proliferation of several DLBCL cell lines (IC50s 0 0098-0 017 UM) a starting material in the semisynthesis of etoposide and teniposide
Cayman Chemical Albendazole 5g
An anticonvulsant inhibits the activation of Nav1 1 at 100 UM inhibits Nav1 1 but not Nav1 2 Nav1 3 and Nav1 6 opening and increases the action potential threshold in primary rat hippocampal neurons inhibits CAVA (Ki 343 8 nM) but not CAI and CAII (Kis 10000 nM for both) prolongs the preictal phase and reduces seizure-like event frequency in an in vitro model of epileptiform activity in rat hippocampal slices at 100 UM inhibits pentylenetetrazole-induced seizures in a mouse model of epilepsy (ED50 54 mg/kg i p ) reduces kainic acid-induced neuronal cell death in the mouse hippocampal CA3 region when used at doses of 25 50 and 100 mg/kg