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Molecular Diversity|June 29, 2014
N-Polybenzylated alicyclic 1,2-diamines: cytotoxicity and G1 phase arrest in cancer cell lineAntonio Caldarelli, Valeria De Biasio, Giovanni B Giovenzana, et al.Molecular Diversity|February 6, 2015
Efficient one-pot protocol for diverse pyrazolylphosphonates by multi-component reactions: their antioxidant and antibacterial activitiesSo Rang Kang, Yong Rok LeeMolecular Diversity|March 11, 2015
Predicting antiprotozoal activity of benzyl phenyl ether diamine derivatives through QSAR multi-target and molecular topologyRamon Garcia-Domenech, Riccardo Zanni, Maria Galvez-Llompart, et al.Molecular Diversity|June 28, 2020
Design and in vitro analysis of SIRT2 inhibitor targeting Parkinson's diseaseAmrendra Pratap Singh, Lokesh Nigam, Yudhishthir Yadav, et al.Molecular Diversity|August 15, 2012
Rationalizing lead optimization by consensus 2D- CoMFA CoMSIA GRIND (3D) QSAR guided fragment hopping in search of γ-secretase inhibitorsPrabu Manoharan, Nanda GhoshalMolecular Diversity|August 16, 2012
Synthesis and evaluation of functionalized indoles as antimycobacterial and anticancer agentsGökçe Cihan-Üstündağ, Gültaze CapanMolecular Diversity|January 24, 2015
One-step synthesis of azole- and benzazole-based sulfonamides in aqueous mediaHassan Zali-Boeini, Zhaleh Najafi, Bahareh Abtahi, et al.Molecular Diversity|September 22, 2012
Molecular docking and receptor-specific 3D-QSAR studies of acetylcholinesterase inhibitorsPran Kishore Deb, Anuradha Sharma, Poonam Piplani, et al.Molecular Diversity|September 20, 2012
Catalyst-free synthesis of quinazolin-4-ones from (hetero)aryl-guanidines: application to the synthesis of pyrazolo[4,3-f]quinazolin-9-ones, a new family of DYRK1A inhibitorsJulien Debray, Simon Bonte, Olivier Lozach, et al.Molecular Diversity|July 4, 2012
Exploring a sulfone linker utilizing trimethyl aluminum as a cleavage reagent: solid-phase synthesis of sulfonamides and ureasTsai-Wen Chung, Chih-Hau Chen, Chu-Chung Lin, et al.Pageof 290