Codeine/menthol/pheniramine/phenylephrine

Description(S)-(+)-2-Methoxy-2-phenylethanol can be used:As a starting material for the synthesis ofN-substituted 6,7-benzomorphan based opioid receptor agonists.As a ligand in the preparation of organolanthanoid complexes.As starting material for

(S)-(+)-Dimethindene maleate, an enantiomer, is a potent M2-selective muscarinic receptor antagonist (pA2 = 7.86/7.74: pKi = 7.78). (S)-(+)-Dimethindene maleate shows lower affinities for the muscarinic M1 (pA2 = 6.83/6.36: pKi = 7.08), the M3 (pA2

A PAF receptor agonist with potency comparable to PAF C-18 and PAF C-16 chromogenic substrate used in Cayman&rsquos PAF-AH Assay Kit (Item No. 760901).

4-PPBP maleate is a potent σ1 receptor (ligand) agonist. 4-PPBP maleate can be considered a selective, non-competitive NR1a/2B NMDA receptor antagonist in the context of Xenopus oocytes expression. 4-PPBP maleate has neuroprotective properties.

4-PPBP maleate is a potent σ1 receptor (ligand) agonist. 4-PPBP maleate can be considered a selective, non-competitive NR1a/2B NMDA receptor antagonist in the context of Xenopus oocytes expression. 4-PPBP maleate has neuroprotective properties.

4-PPBP maleate is a potent σ1 receptor (ligand) agonist. 4-PPBP maleate can be considered a selective, non-competitive NR1a/2B NMDA receptor antagonist in the context of Xenopus oocytes expression. 4-PPBP maleate has neuroprotective properties.

4-PPBP maleate is a potent σ1 receptor (ligand) agonist. 4-PPBP maleate can be considered a selective, non-competitive NR1a/2B NMDA receptor antagonist in the context of Xenopus oocytes expression. 4-PPBP maleate has neuroprotective properties.

4-PPBP maleate is a potent σ1 receptor (ligand) agonist. 4-PPBP maleate can be considered a selective, non-competitive NR1a/2B NMDA receptor antagonist in the context of Xenopus oocytes expression. 4-PPBP maleate has neuroprotective properties.

DescriptionTraceless Staudinger ligation reagent with borane protecting group.The borane group stabilizes the phosphine against oxidation and can be easily removed with mild basic or acidic conditions to yield the active phosphine.After reaction

Acetylthiomethyl-diphenylphosphine borane complex is a traceless Staudinger ligation reagent with borane protecting group. The borane group works to stabilize the phosphine against oxidation and then it can be easily removed with mild basic or

Anti-DNAH10OS dynein, axonemal, heavy chain 10 opposite stra

Anti-MANSC4 MANSC domain containing 4, 25ul UN 1687 6.1 PG2