Ranitidine bismuth citrate

Application 2,3- Bis (2-pyridyl)pyrazine (dpp) has been employed: as building block for supermolecular molecules in the preparation of luminescent complexes Ru(bpy) 2 (dpp) 2+ and (bpy) 2 Ru-(dpp)Ru(bpp) 2 4+ [bpy=2,2&#8242-bipyridine] in the

Application Bismuth(III) iodide or Bismuth triiodide are nontoxic and hence they are used as environmentally friendly catalysts. It can be used as a catalyst in the: Chemoselective deprotection of acetals and ketals in water.

Application Bismuth(III) iodide or Bismuth triiodide are nontoxic and hence they are used as environmentally friendly catalysts. It can be used as a catalyst in the: Chemoselective deprotection of acetals and ketals in water.

FTI-2153 is a potent and highly selective inhibitor of farnesyltransferase (FTase) , with an IC 50 of 1.4 nM. FTI-2153 is &gt:3000-fold more potent at blocking H-Ras ( IC 50 , 10 nM) than Rap1A processing. Anti-cancer activity.In VitroFTI-2153,

FTI-2153 is a potent and highly selective inhibitor of farnesyltransferase (FTase) , with an IC 50 of 1.4 nM. FTI-2153 is &gt:3000-fold more potent at blocking H-Ras ( IC 50 , 10 nM) than Rap1A processing. Anti-cancer activity.In VitroFTI-2153,

FTI-2153 is a potent and highly selective inhibitor of farnesyltransferase (FTase) , with an IC 50 of 1.4 nM. FTI-2153 is &gt:3000-fold more potent at blocking H-Ras ( IC 50 , 10 nM) than Rap1A processing. Anti-cancer activity.In VitroFTI-2153,

FTI-2153 is a potent and highly selective inhibitor of farnesyltransferase (FTase) , with an IC 50 of 1.4 nM. FTI-2153 is &gt:3000-fold more potent at blocking H-Ras ( IC 50 , 10 nM) than Rap1A processing. Anti-cancer activity.In VitroFTI-2153,

FTI-2153 is a potent and highly selective inhibitor of farnesyltransferase (FTase) , with an IC 50 of 1.4 nM. FTI-2153 is &gt:3000-fold more potent at blocking H-Ras ( IC 50 , 10 nM) than Rap1A processing. Anti-cancer activity.In VitroFTI-2153,

FTI-2153 is a potent and highly selective inhibitor of farnesyltransferase (FTase) , with an IC 50 of 1.4 nM. FTI-2153 is &gt:3000-fold more potent at blocking H-Ras ( IC 50 , 10 nM) than Rap1A processing. Anti-cancer activity.In VitroFTI-2153,

A potent competitive inhibitor of cytidine deaminase. Used in combination with cytosine arabinoside (Ara-C) to assess the anti-leukemic activity and anti-tumor activity of Ara-C in in vitro studies.

Application Salsalate was used to study the effect on palmitate-induced insulin resistance and hepatic steatosis in obese rats. Biochem/physiol Actions Salsalate is a nonsteroidal anti-inflammatory drug (NSAID), a nonacetylated salicylate with

Application Salsalate was used to study the effect on palmitate-induced insulin resistance and hepatic steatosis in obese rats. Biochem/physiol Actions Salsalate is a nonsteroidal anti-inflammatory drug (NSAID), a nonacetylated salicylate with