Synthesis, SAR and selectivity of 2-acyl- and 2-cyano-1-hetarylalkyl-guanidines at the four histamine receptor subtypes: a bioisosteric approach-Reference-Cited by-同舟云学术

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Synthesis, SAR and selectivity of 2-acyl- and 2-cyano-1-hetarylalkyl-guanidines at the four histamine receptor subtypes: a bioisosteric approach

Published:2014 Issue:1 Volume:5 Page:72-81
ISSN:2040-2503
Container-title:Med. Chem. Commun.
language:en
Short-container-title:Med. Chem. Commun.

Author:

Geyer Roland,Igel Patrick,Kaske Melanie,Elz Sigurd,Buschauer Armin

Publisher

Royal Society of Chemistry (RSC)

Subject

Pharmaceutical Science,Biochemistry,Drug Discovery,Molecular Medicine,Pharmacology,Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/MD/C3MD00245D

Reference58 articles.

1. Genomics Meets Histamine Receptors: New Subtypes, New Receptors

2. Molecular and cellular analysis of human histamine receptor subtypes

3. Species-dependent activities of G-protein-coupled receptor ligands: lessons from histamine receptor orthologs

4. Histamine H3 Receptor Antagonists Go to Clinics

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1. Abolishing Dopamine D2long/D3 Receptor Affinity of Subtype-Selective Carbamoylguanidine-Type Histamine H2 Receptor Agonists;Journal of Medicinal Chemistry;2021-06-10

2. POxAP Precatalysts and the Negishi Cross-Coupling Reaction;Synthesis;2019-10-28

3. Synthesis and biological evaluation of heteroalicyclic cyanoguanidines at histamine receptors;Archiv der Pharmazie;2019-07-29

4. Online investigation of reaction acceleration and reaction mechanism by thermospray ionization mass spectrometry;International Journal of Mass Spectrometry;2019-01

5. Routes to drug design via bioisosterism of carboxyl and sulfonamide groups;Future Medicinal Chemistry;2017-12

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