New high affinity H 3 receptor agonists without a basic side chain

R Kitbunnadaj, M Hoffmann, SA Fratantoni…

Index: Bioorganic and Medicinal Chemistry, , vol. 13, # 23 p. 6309 - 6323

Full Text: HTML

Citation Number: 13

Abstract

... Bioorganic & Medicinal Chemistry. ... a Leiden/Amsterdam Center of Drug Research (LACDR), Division of Medicinal Chemistry, Department of ... b Department of Pharmaceutical Chemistry and Pharmacognosy, Faculty of Pharmaceutical Sciences, Naresuan University, Phitsanulok ...

Related Articles:

Fadrozole hydrochloride: a potent, selective, nonsteroidal inhibitor of aromatase for the treatment of estrogen-dependent disease

[Journal of Medicinal Chemistry, , vol. 34, # 2 p. 725 - 736]

[125I] Iodoproxyfan and related compounds: a reversible radioligand and novel classes of antagonists with high affinity and selectivity for the histamine H3 receptor

[Journal of medicinal chemistry, , vol. 39, # 6 p. 1220 - 1226]

A new type of carboxypeptidase A inhibitors designed using an imidazole as a zinc coordinating ligand

[Bioorganic and Medicinal Chemistry, , vol. 5, # 10 p. 1989 - 1998]

Towards non-peptide ANG II AT1 receptor antagonists based on urocanic acid: rational design, synthesis and biological evaluation

[Amino Acids, , vol. 40, # 2 p. 411 - 420]

Towards non-peptide ANG II AT1 receptor antagonists based on urocanic acid: rational design, synthesis and biological evaluation

[Amino Acids, , vol. 40, # 2 p. 411 - 420]

More Articles...