sn-50

SN50 is a cell permeable NF-κB translocation inhibitor.

SN50 acetate is a cell permeable inhibitor of NF-κB translocation.

SN50 TFA is a cell-permeable inhibitor of NF-κB and attenuates alveolar hypercoagulation and fibrinolysis inhibition in acute respiratory distress syndrome mice through inhibiting NF-κB p65 translocation. SN50 TFA can be used in studies about ARDS.

SN50 trifluoroacetate is a useful organic compound for research related to life sciences and the catalog number is T64720.

MSN-50, an inhibitor of Bax and Bak oligomerization, inhibits liposome permeabilization, prevents genotoxic cell death and promotes neuroprotection.

ASN-500 is a human monoclonal antibody (mAb) targeting the F/FusionglycoproteinF0. It is useful in the study of respiratory syncytial virus infections.

SN50M (NF-κB Control) is a synthetic peptide containing a hydrophobic region and a mutant nuclear localization sequence that enters cells but does not inhibit NF-κB nuclear translocation or induce apoptosis.

1-O-Hexadecyl-sn-glycerol is a biologically active alkyl glyceryl ether that exhibits protective effects against UVB-induced cellular damage by reducing keratinocyte death, reactive oxygen species (ROS) generation, and prostaglandin E2 synthesis in normal human epidermal keratinocytes (NHEKs). additionally, at a concentration of 50 μM, 1-O-Hexadecyl-sn-glycerol significantly enhances coronary flow and left ventricular developed pressure while reducing malondialdehyde (MDA) formation in an ex vivo rat heart model of ischemia and reperfusion injury, thereby demonstrating both cytoprotective and cardioprotective properties.

AP-1, a miniaturized proteolysis-targeting chimera (PROTAC) incorporating an anaplastic lymphoma kinase (ALK) ligand connected to (±)-thalidomide via an ultrashort linker, effectively degrades ALK fusion proteins such as NPM-ALK in Karpas-299 cells and EML4-ALK and ALKF1174L in SN-N-SH and NCI H3122 cells, respectively. Concentrations ranging from 10 to 300 nM are sufficient for its action, which is hindered by the proteasome inhibitor MG-132. Demonstrating selectivity, AP-1 exhibits cytotoxicity towards ALK-dependent Karpas-299 cells with an IC50 value of 0.1265 nM, while showing significantly less toxicity to non-ALK-dependent THP-1 cells (IC50 = 2,704 nM). Furthermore, it effectively reduces tumor volume in NCI H3122 mouse xenograft models at doses of 25, 50, and 100 mg/kg.

1,3-Dioleoyl glycerol, a diacylglycerol with oleic acid at the sn-1 and sn-3 positions, activates protein kinase C (PKC) by approximately 30% at a concentration of 50 μM.

1,3-Dioleoyl Glycerol (Standard) is the standard substance of 1,3-Dioleoyl Glycerol, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. 1,3-Dioleoyl glycerol, a diacylglycerol with oleic acid at the sn-1 and sn-3 positions, activates protein kinase C (PKC) by approximately 30% at a concentration of 50 μM.