Codeine/guaifenesin/phenylpropanolamine

(-)-Bebeerine is a cyclic natural product alkaloid. (-)-Bebeerine is described to noncompetitively block neuromuscular transmission through interaction with the nicotinic acetylcholine receptor. (-)-Bebeerine is also described as an identifier of

(-)-Bebeerine is a cyclic natural product alkaloid. (-)-Bebeerine is described to noncompetitively block neuromuscular transmission through interaction with the nicotinic acetylcholine receptor. (-)-Bebeerine is also described as an identifier of

(-)-Bebeerine is a cyclic natural product alkaloid. (-)-Bebeerine is described to noncompetitively block neuromuscular transmission through interaction with the nicotinic acetylcholine receptor. (-)-Bebeerine is also described as an identifier of

(R)-SLV 319 is the inactive enantiomer of SLV 319 with 100-fold less affinity for the CB1 receptor than (S)-SLV 319.

(Rac)-Tavapadon ((Rac)-PF-06649751) is a potent and selective noncatechol dopamine D1 receptor agonist. (Rac)-Tavapadon displays potent full agonism in the GS activation assay as well as partial agonism in the β-arrestin2 recruitment assay (GS-cAMP,

A mixture of the potent and selective CB1 receptor antagonist SLV 319 (Ki = 7.8 nM) and its distomer, SLV 319 (+)-enantiomer.

A mixture of the potent and selective CB1 receptor antagonist SLV 319 (Ki = 7.8 nM) and its distomer, SLV 319 (+)-enantiomer.

A mixture of the potent and selective CB1 receptor antagonist SLV 319 (Ki = 7.8 nM) and its distomer, SLV 319 (+)-enantiomer.

1-Piperidin-1-ylcyclopentanecarbonitrile.

Other Notes Reagent for introducing the Pbf protection in the guanidine group of arginine

2-Hydroxy-5-nitropyridine

Usually used in the synthesis of SR 48968, a potent, competitive and selective non-peptide antagonist of the neurokinin A (NK2) receptor, tachykinin NK3 receptor antagonist SR 142801, (R)-N-[ 1-[3-[