Synthesis and histamine H1-receptor antagonist activity of 4-(diphenylmethyl)-1-piperazine derivatives with a terminal heteroaryl or cycloalkyl amide fragment-Reference-Cited by-同舟云学术

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Synthesis and histamine H1-receptor antagonist activity of 4-(diphenylmethyl)-1-piperazine derivatives with a terminal heteroaryl or cycloalkyl amide fragment

Published:1996-01 Issue:10 Volume:31 Page:813-818
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Orjales A,Gil-Sánchez JC,Alonso-Cires L,Labeaga L,Mosquera R,Berisa A,Ucelay M,Innerárity A,Corcóstegui R

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference16 articles.

1. Pharmacokinetic-Pharmacodynamic Relationships of H1-Antihistamines

2. A new classification of H1-receptor antagonists

3. Cetirizine

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Neuropharmacological Potential of Different Piperazine Analogs: A Recent Prospective;Mini-Reviews in Organic Chemistry;2024-01-16

2. A Profound Insight into the Structure-activity Relationship of Ubiquitous Scaffold Piperazine: An Explicative Review;Medicinal Chemistry;2024-01

3. The Neuropharmacological Potential of Piperazine Derivatives: A Mini- Review;Mini-Reviews in Organic Chemistry;2022-11

4. Piperazine: A Promising Scaffold with Analgesic and Anti-inflammatory Potential;Drug Research;2020-12-17

5. ChemInform Abstract: Synthesis and Histamine H1-Receptor Antagonist Activity of 4-( Diphenylmethyl)-1-piperazine Derivatives with a Terminal Heteroaryl or Cycloalkyl Amide Fragment.;ChemInform;2010-08-04

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