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Design and synthesis of spiro derivatives of parthenin as novel anti-cancer agents

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Title Design and synthesis of spiro derivatives of parthenin as novel anti-cancer agents
 
Creator Reddy, Doma Mahendhar
Qazi, Naveed A.
Sawant, Sanghpal D.
Bandey, Abid H.
Srinivas, Jada
Shankar, Mannepalli
Singh, Shashank K.
Verma, Monika
Chashoo, Gousia
Saxena, Arpita
Mondhe, Dilip
Saxena, Ajit K.
Sethi, V.K.
Taneja, Subhash C.
Qazi, Gulam N.
Sampath Kumar, H.M.
 
Subject Chemical Sciences
 
Description Several novel spiro derivatives of parthenin (1) have been synthesized by the dipolar cycloaddition using various dipoles viz; benzonitrile oxides, nitrones and azides with exocyclic double bond of C ring(a-methylene-g-butyrolactone). Majority of the compounds exhibited improved anti-cancer activity compared to the parthenin, when screened for their in vitro cytotoxicity against three human cancer cell lines viz., SW-620, DU-145 and PC-3. In vivo screening of select analog revealed improved anti-cancer activity with low mammalian toxicity as compared to parthenin. The results of the cytotoxicity pattern of these derivatives reveals the SAR of these sesquiterpinoid lactones and possible role of a,b-unsaturated ketone of parthenin in inhibiting NF-kB. A mechanistic correlation of anti-cancer activity along with
in vivo and western blotting experiments has been described.
 
Date 2011
 
Type Article
PeerReviewed
 
Format application/pdf
 
Identifier http://iiim.csircentral.net/236/1/10.1016j.ejmech.2011.04.030.pdf
Reddy, Doma Mahendhar and Qazi, Naveed A. and Sawant, Sanghpal D. and Bandey, Abid H. and Srinivas, Jada and Shankar, Mannepalli and Singh, Shashank K. and Verma, Monika and Chashoo, Gousia and Saxena, Arpita and Mondhe, Dilip and Saxena, Ajit K. and Sethi, V.K. and Taneja, Subhash C. and Qazi, Gulam N. and Sampath Kumar, H.M. (2011) Design and synthesis of spiro derivatives of parthenin as novel anti-cancer agents. European Journal of Medicinal Chemistry, 46 (8). pp. 3210-3217. ISSN 02235234
 
Relation http://dx.doi.org/10.1016/j.ejmech.2011.04.030
http://iiim.csircentral.net/236/