Codeine/guaifenesin/pseudoephed/triprolidine

3-AMINO-N-(4-{[(4 6-DIMETHYL-2-PYRIMIDINYL)AMINO]SULFONYL}PHENYL)-6 7 8 9-TETRAHYDRO-5H-CYCLOHEPTA[B]THIENO[3 2-E]PYRIDINE-2-CA-

4-Hydroxy-8-(trifluoromethyl)quinolone (8-(Trifluoromethyl)-4-quinolinol) is a heterocyclic building block. Various 4-hydroxy-8-trifluoromethyl-quinoline derivatives have been prepared via multi step reactions and were tested for their antimicrobial

4-Hydroxy-8-(trifluoromethyl)quinolone (8-(Trifluoromethyl)-4-quinolinol) is a heterocyclic building block. Various 4-hydroxy-8-trifluoromethyl-quinoline derivatives have been prepared via multi step reactions and were tested for their antimicrobial

4-NAPHTHALEN-2-YL-PYRIMIDINE-

MF: 342.30 CAS: 3459-18-5

4-PYRROLIDIN-1-YL-2-THIOPHEN-2-YL-QUINOLINE-

Application 5&#8242-Guanidinonaltrindole di(trifluoroacetate) salt hydrate (GNTI) has been used as a selective &#954 opioid receptor antagonist: to study the influence of opioid receptor types on the anti-hyperalgesic effect of dipeptidyl

5-BRMO-3-FLRO-2-methoxyPYRIDN 97% 250mg

Application Reactant for preparation of: Inhibitors of mammalian target of rapamycin (mTOR ) protein Inhibitors of the AcrAB-TolC efflux pump Inhibitors of Gli1-mediated transcription in the Hedgehog pathway Potent DNA-topoisomerase II poisons and

7-Methoxy-1-indanone, 95% 250mg

A-425619, a potent and selective TRPV1 receptor antagonist, is effective in alleviating acute and chronic inflammatory pain and postoperative pain.

A-425619, a potent and selective TRPV1 receptor antagonist, is effective in alleviating acute and chronic inflammatory pain and postoperative pain.