GW 9662-<wbr/>d<sub>5</sub>

GW 9662-d5

CAT N°: 9000497
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From 82.00 69.70

The peroxisome proliferator-activated receptor ? (PPAR?) is the nuclear receptor responsible for transducing the therapeutic activity of the thiazolidinediones (TZDs). TZDs are a group of structurally related synthetic PPAR? agonists with antidiabetic actions in vivo.{7575,8224} Rosiglitazone is a prototypical TZD and has served as a reference compound for this class.{8241} There are many PPAR? agonists, including 15-deoxy-?12,14-prostaglandin J2 and azelaoyl PAF, which are naturally derived.{8461,8930} However, only a few antagonists have been reported.{8953} GW 9662 blocks the PPAR?-induced differentiation of monocytes to osteoclasts by >90% at a dose of 0.1 µM.{9318} It is therefore a much more potent antagonist than BADGE, which is another reported PPAR? antagonist.{9318}

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