Potassium iodide/sodium bicarbonate/theobromine

(1S 2S 5S)-BICYCLO[3.2.

(E)-Osmundacetone is the isomer of Osmundacetone. Osmundacetone significantly suppresses the phosphorylation of MAPKs, including JNK , ERK , and p38 kinases. Osmundacetone has a neuroprotective effect against oxidative stress.Form:Solid.

(E)-Osmundacetone is the isomer of Osmundacetone. Osmundacetone significantly suppresses the phosphorylation of MAPKs, including JNK , ERK , and p38 kinases. Osmundacetone has a neuroprotective effect against oxidative stress.Form:Solid.

(E)-Osmundacetone is the isomer of Osmundacetone. Osmundacetone significantly suppresses the phosphorylation of MAPKs, including JNK , ERK , and p38 kinases. Osmundacetone has a neuroprotective effect against oxidative stress.Form:Solid.

(E)-Osmundacetone is the isomer of Osmundacetone. Osmundacetone significantly suppresses the phosphorylation of MAPKs, including JNK , ERK , and p38 kinases. Osmundacetone has a neuroprotective effect against oxidative stress.Form:Solid.

Product Introduction(R)-(+)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthalene is an axially dissymmetric bis(triaryl)phosphine ligand for asymmetric reactions. ApplicationUseful ligand for transition metal catalyzed asymmetric reactions, including

Product Introduction(R)-(+)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthalene is an axially dissymmetric bis(triaryl)phosphine ligand for asymmetric reactions. ApplicationUseful ligand for transition metal catalyzed asymmetric reactions, including

Product Introduction(R)-(+)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthalene is an axially dissymmetric bis(triaryl)phosphine ligand for asymmetric reactions. ApplicationUseful ligand for transition metal catalyzed asymmetric reactions, including

(S)-Willardiine is a potent agonist of AMPA/kainate receptors with EC50 of 44.8 uM.IC50 value: 44.8 uM(EC50)Target: AMPA/kainate receptor agonistin vitro: The (S)- but not (R)-isomers of willardiine and 5-bromowillardiine were potent agonists,

(S)-Willardiine is a potent agonist of AMPA/kainate receptors with EC50 of 44.8 uM.IC50 value: 44.8 uM(EC50)Target: AMPA/kainate receptor agonistin vitro: The (S)- but not (R)-isomers of willardiine and 5-bromowillardiine were potent agonists,

An alkaloid metabolite of nicotine as well as a major product of its pyrolysis binds comparably to CYP2A6 and CYP2A13 (Kis = 7.5 and 5.6 &microM, respectively), but appears to more effectively inactivate CYP2A6.

1-CHLORO-4-IODO-NAPHTHALENE-