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Cat.No.  Name Information
M21630 NMS-P515 NMS-P515 is a potent inhibitor of PARP-1 both in biochemical (Kd: 0.016 μM) and cellular (IC50: 0.027 μM) assays.
M21629 3,3-Dimethyl-1-butanol (liquid) 3,3-Dimethyl-1-butanol (DMB) is an indirect inhibitors of TMAO, which can reduce plasma TMAO levels. 3,3-Dimethyl-1-butanol is a branched alkanol, which can be used as a ligand in the preparation of nickel based single-molecule magnets.
M21628 2'-Fucosyllactose 2'-Fucosyllactose (2'-FL) is an oligosaccharide that could be derived from human milk. 2'-Fucosyllactose regulates the expression of CD14, alleviates colitis and regulates the gut microbiome. 2'-Fucosyllactose stimulates T cells to increase IFN-γ production and decreases IL-6, IL-17, and TNF-α production of cytokines.
M21627 Tautomycetin Tautomycetin is a potent and specifical PP1 inhibitor with the potential apoptosis-inducing activity. Tautomycetin inhibits purified PP1 and PP2A enzymes with IC50s of 1.6 nM and 62 nM, respectively.
M21626 Cadisegliatin (TTP-399) Cadisegliatin (TTP-399) is a potential, orally active liver-selective glucokinase (GK) activator. Cadisegliatin has antihyperglycaemic activity. Cadisegliatin can be used for the research of type 2 diabetes.
M21625 CAM833 CAM833 is a potent orthosteric inhibitor of the interaction between BRCA2 and RAD51 with a Kd of 366 nM against the ChimRAD51 protein. CAM833 also inhibits RAD51 oligomerization.
M21624 Timentin (Ticarcillin/Clavunate, 15:1)
M21623 Clavulanate Potassium Clavulanate potassium is a potent β-lactamase inhibitor and acts as an antibiotic.




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