Benzimidazoles
Sigma Aldrich Fine Chemicals Biosciences Pantoprazole sodium hydrate >=98% (HPLC) | 718635-09-7 | 10MG
Pantoprazole sodium hydrate >=98% (HPLC) | Purity: >=98% (HPLC) | 718635-09-7 | 10MG
Cayman Chemical Omeprazole sulfIde-d3 1mg
A pre-mRNA splicing modulator corrects aberrant splicing in a SPREADD using HeLa cells expressing IKBKAP with an IVS20 6TC point mutation restores the modification of cytoplasmic tRNAs with uridine in the wobble position in primary human fibroblasts from patients with FD to the same level as in primary human fibroblasts from carriers of the FD mutation at 2 UM increases the levels of correctly spliced PARK7 mRNA in neural precursor cells differentiated from fibroblasts of patients with the homozygous PARK7 c.192GC exonic splicing mutation in combination with phenylbutyric acid intratumoral administration decreases tumor volume and increases survival and the number of tumor-infiltrating CD8 T cells in an MC-38 murine colon carcinoma model
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
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-d3 5mg
A chalcone derivative and an inhibitor of the MD-2-LPS interaction inhibits the interaction between MD-2 and LPS in a cell-free assay at 0.1 UM inhibits LPS-induced increases in the levels of Tnf-a and Il-6 secreted from isolated and washed MPMs (IC50s 4.27 and 2.09 UM respectively) inhibits LPS-induced Nf-KB DNA binding in MPMs at 5 and 20 UM inhibits the growth of various cancer cells (GI50s 0.019-0.32 UM respectively) reduces tumor volume and weight in a HeLa cervical mouse xenograft model at 10 mg/kg for three days prevents LPS-induced increases in BALF total protein levels and CD68 macrophage and neutrophil infiltration in a mouse model of LPS-induced acute lung injury at 20 mg/kg per day reduces MPO activity in isolated neutrophils in the same model
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%
U.S. Pharmacopeia Albendazole, 54965-21-8, MFCD00083232, 200 mg
Empirical Formula (Hill Notation): C12H15N3O2S, Molecular Weight: 265.33, Synonym: Methyl 5-(propylthio)-2-benzimidazolecarbamate.
1H-Benzimidazole-2-sulfonic Acid 98%, Thermo Scientific™
CAS: 40828-54-4 Molecular Formula: C7H6N2O3S Molecular Weight (g/mol): 198.196 InChI Key: GWXQTTKUYBEZBP-UHFFFAOYSA-N Synonym: 1h-benzoimidazole-2-sulfonic acid,1h-benzo d imidazole-2-sulfonic acid,benzimidazole-2-sulfonic acid,1h-1,3-benzodiazole-2-sulfonic acid,2-benzimidazolesulfonic acid,cambridge id 5140822,1h-benzimidazolesulfonic acid,1h-benzimidazole-2-sulfonicacid,1h-benzimidazole-2-sulfonic acid,9ci PubChem CID: 1572160 IUPAC Name: 1H-benzimidazole-2-sulfonic acid SMILES: C1=CC=C2C(=C1)NC(=N2)S(=O)(=O)O