Glucagon hydrochloride

(S)-V-0219 hydrochloride is an enantiomer of V-0219 ( HY-143312 ). V-0219 is an orally active and positive allosteric modulator (PAM) of the GLP Receptor -1 ( GLP-1R ). (S)-V-0219 hydrochloride activates calcium fluxes in HEK cells stably expressing

(S)-V-0219 hydrochloride is an enantiomer of V-0219 ( HY-143312 ). V-0219 is an orally active and positive allosteric modulator (PAM) of the GLP Receptor -1 ( GLP-1R ). (S)-V-0219 hydrochloride activates calcium fluxes in HEK cells stably expressing

1,3,4,6-Tetra-O-acetyl-2-amino-2-deoxy-α-D-glucopyranose Hydrochloride is a potential metabolic inhibitor of cellular-membrane glycoconjugates.

1-Benzyl-APDC hydrochloride is a selective ligand of mGlu6 receptor.

1-Benzyl-APDC hydrochloride is a selective ligand of mGlu6 receptor.

15(S)-15-methyl Prostaglandin F2α is a metabolically stable analog of PGF2α. It is a potent uterine stimulant and abortifacient which can be given intramuscularly to induce labor. It induces luteolysis and reduces serum progesterone concentrations

15(S)-15-methyl Prostaglandin F2α is a metabolically stable analog of PGF2α. It is a potent uterine stimulant and abortifacient which can be given intramuscularly to induce labor. It induces luteolysis and reduces serum progesterone concentrations

15(S)-15-methyl Prostaglandin F2α is a metabolically stable analog of PGF2α. It is a potent uterine stimulant and abortifacient which can be given intramuscularly to induce labor. It induces luteolysis and reduces serum progesterone concentrations

15(S)-15-methyl Prostaglandin F2α is a metabolically stable analog of PGF2α. It is a potent uterine stimulant and abortifacient which can be given intramuscularly to induce labor. It induces luteolysis and reduces serum progesterone concentrations

Other Notes Important D -glucopyranose derivative for glucosylations and other reactions Preparation of the &#945-glucopyranosyl chloride Synthesis of 1-C-&#945- D -glucopyranose derivatives

2-Hydroxysaclofen is a potent γ-amino-butyric-acid-B (GABAB) receptor antagonist. 2-Hydroxysaclofen can abolish nicotine-induced hypolocomotor effects and increases the antinociceptive effects. 2-Hydroxysaclofen can stimulate luteinizing hormone

2-Hydroxysaclofen is a potent γ-amino-butyric-acid-B (GABAB) receptor antagonist. 2-Hydroxysaclofen can abolish nicotine-induced hypolocomotor effects and increases the antinociceptive effects. 2-Hydroxysaclofen can stimulate luteinizing hormone