*Five Years Citation in Google scholar (2016 - 2020) is. 1451*   *    IJPR IS INDEXED IN ELSEVIER EMBASE & EBSCO *       

logo

INTERNATIONAL JOURNAL OF PHARMACEUTICAL RESEARCH

A Step Towards Excellence
Published by : Advanced Scientific Research
ISSN
0975-2366
Current Issue
Article In Press
No Data found.
ADOBE READER

(Require Adobe Acrobat Reader to open, If you don't have Adobe Acrobat Reader)

Index Page 1
Click here to Download
IJPR 9[3] July - September 2017 Special Issue

July - September 9[3] 2017

Click to download
 

Article Detail

Label
Label
Synthesis and Anti-Cancer (Cytotoxic) Activity of Novel Thiazoloquinazolines Derivatives

Author: UPLOADED BY-ADMIN, PANNEER SELVAM T, VIJAYARAJ KUMAR P
Abstract: A series of 6,7,8,9 Tetra hydro-5H-5-phenyl-2-benzylidine-3-substituted hydrazino thiazolo (2, 3-b) quinazoline (6a-o) have been synthesized to meet the structural requirements essential for anti-cancer properties. The synthesized series of heterocycles, 6,7,8,9 Tetra hydro-5H-5-phenyl-2-benzylidine-3-substituted hydrazino thiazolo (2, 3-b) quinazoline (6a-o) by the reaction of 6,7,8,9 Tetra hydro-5H-5- phenyl thiazolo (2, 3-b) quinazolin-3(2H)-one 3 with appropriate hydrazine hydrate and ketones / aldehydes in the presence of anhydrous sodium acetate and glacial acetic acid as presented in scheme. Their anti-cancer activity was evaluated by MTT assay. The 6,7,8,9 Tetra hydro-5H-5-phenyl-2-benzylidine-3- (N´-3-pentylidenehydrazino) thiazolo (2, 3-b) quinazoline (6b) and 6,7,8,9 Tetra hydro-5H-5-phenyl-2-benzylidine-3-(N´-2-pentylidenehydrazino) thiazolo (2, 3-b) quinazoline (6c) exhibited the most potent anti-cancer activity.
Keyword: Thiazolo quinazoline; Benzylidine thiazolo quinazoline, Anti-cancer activity.
Download: Request For Article
 




ONLINE SUBMISSION
USER LOGIN


Username
Password
Login | Register
News & Events
SCImago Journal & Country Rank

Terms and Conditions
Disclaimer
Refund Policy
Instrucations for Subscribers
Privacy Policy

Copyrights Form

0.12
2018CiteScore
 
8th percentile
Powered by  Scopus
Google Scholar

hit counters free