包装 | 价格(元) |
500 µg | 电议 |
1mg | 电议 |
Canonical SMILES | O=C(N1)NN=C1CN(CCO2)C(C3=C([2H])C([2H])=C(F)C([2H])=C3[2H])C2OC(C)C4=CC(C(F)(F)F)=CC(C(F)(F)F)=C4 |
分子式 | C23H17D4F7N4O3 |
分子量 | 538.5 |
溶解度 | DMF: 25 mg/ml,DMSO: 16 mg/ml,Ethanol: 3 mg/ml |
储存条件 | -20°C |
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. |
Shipping Condition | Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request |
产品描述 | rac-Aprepitant-d4is intended for use as an internal standard for the quantification of aprepitant by GC- or LC-MS. Aprepitant an antiemetic compound and antagonist of the neurokinin-1 (NK1) receptor (Ki= 3 nM; IC50= 0.09 nM for the human receptor).1,2It is selective for NK1over NK3receptors (Ki= 454.1 nM for human NK3).1In vivo, aprepitant (1 mg/kg) prevents plasma extravasation into the esophagus of guinea pigs induced by substance P .3It also reduces NK1-agonist-induced foot tapping in gerbils. Formulations containing aprepitant have been used to prevent chemotherapy-induced nausea and vomiting. 1.Bissantz, C., Bohnert, C., Hoffmann, T., et al.Identification of a crucial amino acid in the helix position 6.51 of human tachykinin neurokinin 1 and 3 receptors contributing to the insurmountable mode of antagonism by dual NK1/NK3 antagonistsJ. Med. Chem.55(11)5061-5076(2012) 2.Finke, P.E., Meurer, L.C., Levorse, D.A., et al.Cyclopentane-based human NK1 antagonists. Part 1: Discovery and initial SARBioorg. Med. Chem. Lett.16(17)4497-4503(2006) 3.Meurer, L.C., Finke, P.E., Owens, K.A., et al.Cyclopentane-based human NK1 antagonists. Part 2: Development of potent, orally active, water-soluble derivativesBioorg. Med. Chem. Lett.16(17)4504-4511(2006) |