Literature DB >> 34931967

Mannich Bases: Centrality in Cytotoxic Drug Design.

Neha V Bhilare1, Vinayak S Marulkar1, Pramodkumar J Shirote1, Shailaja A Dombe2, Vilas J Pise1, Pallavi L Salve1, Shantakumar M Biradar1, Vishal D Yadav2, Prakash D Jadhav2, Anjali A Bodhe2, Smita P Borkar2, Prachi M Ghadge3, Pournima A Shelar4, Apurva V Jadhav2, Kirti C Godse3.   

Abstract

Mannich bases identified by Professor Carl Mannich have been the most extensively explored scaffolds for more than 100 years now. The versatile biological roles that they play have promoted their applications in many clinical conditions. The present review highlights the application of Mannich bases as cytotoxic agents, categorizing them into synthetic, semisynthetic, and prodrugs classes, and gives an exhaustive account of the work reported in the last two decades. The methods of synthesis of these cytotoxic agents, their anti-cancer potential in various cell lines, and promising leads for future drug development have also been discussed. Structure-activity relationships, along with the targets on which these cytotoxic Mannich bases act, have been included as well. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

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Keywords:  Mannich bases; aminomethylation; cytotoxicity; n-mannich bases; o-mannich bases; prodrugs; structure activity relationship

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Year:  2022        PMID: 34931967     DOI: 10.2174/1573406418666211220124119

Source DB:  PubMed          Journal:  Med Chem        ISSN: 1573-4064            Impact factor:   2.745


  1 in total

1.  Synthesis of 4-Hydroxyquinolines as Potential Cytotoxic Agents.

Authors:  Oszkár Csuvik; Nikoletta Szemerédi; Gabriella Spengler; István Szatmári
Journal:  Int J Mol Sci       Date:  2022-08-26       Impact factor: 6.208

  1 in total

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