Design, synthesis and H1-antihistaminic activity of novel 1-substituted-4-(3-chlorophenyl)-[1,2,4] triazolo [4,3-a] quinazolin-5(4H)-ones
In the present study a series of 1-substituted-4-(3-chlorophenyl)-[1,2,4] triazolo [4,3-a] quinazolin-5(4H)-ones were synthesized and screened for their H1-antihistaminic activity. The synthesized compounds were characterized by IR, 1H-NMR, mass spectral data and purity of the compounds was determin...
Main Authors: | Manavalan Gobinath, Natesan Subramanian, Veerachamy Alagarsamy |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2015-05-01
|
Series: | Journal of Saudi Chemical Society |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1319610312000361 |
Similar Items
-
CSACI position statement: Newer generation H1-antihistamines are safer than first-generation H1-antihistamines and should be the first-line antihistamines for the treatment of allergic rhinitis and urticaria
by: Michael N. Fein, et al.
Published: (2019-10-01) -
Antihistamines suppress upregulation of histidine decarboxylase gene expression with potencies different from their binding affinities for histamine H1 receptor in toluene 2,4-diisocyanate-sensitized rats
by: Hiroyuki Mizuguchi, et al.
Published: (2016-04-01) -
Choice of an antihistamine administration route in the treatment of allergic diseases
by: L V Luss
Published: (2016-03-01) -
Use of antihistamines in a physician's clinical practice
by: L V Luss
Published: (2014-08-01) -
Antihistamine drugs, quinuclidine derivatives, in allergic diseases. What is their benefit?
by: L V Luss, et al.
Published: (2013-01-01)