Synthesis of 2-(Bis (2-Chloroethyl)Amino)-N-(5-Substitutedphenyl)- 1,3,4- Thiadiazol-2-Yl)Acetohydrazide And Evaluation of Anticancer Activity

Title:Synthesis of 2-(Bis (2-Chloroethyl)Amino)-N-(5-Substitutedphenyl)- 1,3,4- Thiadiazol-2-Yl)Acetohydrazide And Evaluation of Anticancer Activity

Volume: 14 Issue: 3

Author(s): Byran Gowramma*, Thaggikuppe K. Praveen, Subramanian Gomathy, Rajagopal Kalirajan, Baswan Babu and Nagappan Krishnavenic

Affiliation:

• Department of Pharmaceutical Chemistry, JSS College of Pharmacy, Jagadguru Sri Shivarathreeswara University, Mysore, Udhagamandalam 643001, Tamil Nadu,India

Keywords: Anticancer activity, 1, 3, 4-thiadiazole, daltons lymphoma ascites (DLA) cell line, 5-flurouracil, in vitro and in vivo screening.

Abstract: Objective: The objective of this study was to synthesize a series of 1,3,4-thiadiazole derivative and evaluate their possible in vitro and in vivo anticancer activity.

Method: Compounds 7a-f have been synthesized by chlorination of 2-[bis(2-hydroxyethyl)amino]-N-[5- substituted phenyl)-1,3,4-thiadiazol-2-yl]acetohydrazide with phosphorous oxychloride and phosphorous pentachloride. Synthesis of the targeted compounds was (7a-f) confirmed through their MP, IR, 1HNMR and mass spectrum studies.

Results: Compounds 7a and 7d showed considerable anticancer activity against Hep-2 cell lines and, therefore, selected for the in vitro studies and DLA cell line for the in vivo studies.

Conclusion: It may be concluded that the presence of nitro and chloro phenyl substituted 1,3,4- thiadiazoles showed significant anticancer activity.

Cite this article as:

Gowramma Byran*, Praveen K. Thaggikuppe, Gomathy Subramanian, Kalirajan Rajagopal, Babu Baswan and Krishnavenic Nagappan, Synthesis of 2-(Bis (2-Chloroethyl)Amino)-N-(5-Substitutedphenyl)- 1,3,4- Thiadiazol-2-Yl)Acetohydrazide And Evaluation of Anticancer Activity, Current Bioactive Compounds 2018; 14 (3) . https://dx.doi.org/10.2174/1573407213666170428110528