Conivaptan hydrochloride

Ethyl 1-benzyl-3-oxo-4-piperidinecarboxylate hydrochloride was used as building block for the syntheses of receptor agonists and antagonists.

Ethyl 1-benzyl-3-oxo-4-piperidinecarboxylate hydrochloride was used as building block for the syntheses of receptor agonists and antagonists.

Ethyl 1-benzyl-3-oxo-4-piperidinecarboxylate hydrochloride was used as building block for the syntheses of receptor agonists and antagonists.

DescriptionFmoc-L-photo-methionine is a diazirine-containing, Fmoc-protectedmethionine amino acid and multifunctional photo-crosslinker. Its incorporation into peptides or small-molecule probes and tools allows for photoaffinity labeling of cellular

Forodesine hydrochloride (BCX-1777 hydrochloride) is a highly potent and orally active purine nucleoside phosphorylase (PNP) inhibitor with IC 50 values ranging from 0.48 to 1.57 nM for human, mouse, rat, monkey and dog PNP . Forodesine

Forodesine hydrochloride (BCX-1777 hydrochloride) is a highly potent and orally active purine nucleoside phosphorylase (PNP) inhibitor with IC 50 values ranging from 0.48 to 1.57 nM for human, mouse, rat, monkey and dog PNP . Forodesine

Forodesine hydrochloride (BCX-1777 hydrochloride) is a highly potent and orally active purine nucleoside phosphorylase (PNP) inhibitor with IC 50 values ranging from 0.48 to 1.57 nM for human, mouse, rat, monkey and dog PNP . Forodesine

Forodesine hydrochloride (BCX-1777 hydrochloride) is a highly potent and orally active purine nucleoside phosphorylase (PNP) inhibitor with IC 50 values ranging from 0.48 to 1.57 nM for human, mouse, rat, monkey and dog PNP . Forodesine

Forodesine hydrochloride (BCX-1777 hydrochloride) is a highly potent and orally active purine nucleoside phosphorylase (PNP) inhibitor with IC 50 values ranging from 0.48 to 1.57 nM for human, mouse, rat, monkey and dog PNP . Forodesine

H3R antagonist 1 hydrochloride is a histamine receptor 3 ( H3R ) inverse agonist extracted from patent WO2013107336A1, compound example 2.In VitroTreatment with H3R antagonist 1 hydrochloride, which is a H3R inverse agonist, promotes oligodendrocyte

H3R antagonist 1 hydrochloride is a histamine receptor 3 ( H3R ) inverse agonist extracted from patent WO2013107336A1, compound example 2.In VitroTreatment with H3R antagonist 1 hydrochloride, which is a H3R inverse agonist, promotes oligodendrocyte

H3R antagonist 1 hydrochloride is a histamine receptor 3 ( H3R ) inverse agonist extracted from patent WO2013107336A1, compound example 2.In VitroTreatment with H3R antagonist 1 hydrochloride, which is a H3R inverse agonist, promotes oligodendrocyte