Kuldip Upadhyay
Affiliations: | ICMR-National Institute of Occupational Health |
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Upadhyay KD, Dodia NM, Khunt RC, et al. (2019) Evaluation and in vivo efficacy study of Pyrano[3,2-c]quinoline analogues as TNF-α inhibitors. Chemical Biology & Drug Design |
Upadhyay KD, Shah AK. (2019) Evaluation of Pyrano[3,2 C] Quinoline Analogues as Anticancer Agents. Anti-Cancer Agents in Medicinal Chemistry |
Upadhyay KD, Dodia NM, Khunt RC, et al. (2018) Synthesis and Biological Screening of Pyrano[3,2-]quinoline Analogues as Anti-inflammatory and Anticancer Agents. Acs Medicinal Chemistry Letters. 9: 283-288 |
Manvar A, Upadhyay K, Patel GR, et al. (2014) Targeting Tuberculosis Through Diversity Oriented Synthesis (DOS) of Hydrazide Frameworks and Evaluation of Mycobacterium Activity Thereof Current Organic Chemistry. 18: 2646-2651 |
Chaniyara R, Thakrar S, Kakadiya R, et al. (2014) DBU-catalyzed multicomponent synthesis: Facile access of 4,5,6,9-tetrahydro-pyrido[3,2-c]quinolines Journal of Heterocyclic Chemistry. 51: 466-474 |
Upadhyay K, Manvar A, Loddo R, et al. (2013) Erratum to: Syntheses and in vitro biological screening of 1-aryl-10 H -[1,2,4]triazolo[3′,4′:3,4][1,2,4]triazino[5,6- b ]indoles Medicinal Chemistry Research. 22: 3687-3687 |
Upadhyay K, Manvar A, Rawal K, et al. (2012) Evaluation of structurally diverse benzoazepines clubbed with coumarins as Mycobacterium tuberculosis agents. Chemical Biology & Drug Design. 80: 1003-8 |
Upadhyay K, Manvar A, Loddo R, et al. (2012) Syntheses and in vitro biological screening of 1-aryl-10H-[1,2,4]triazolo[3′,4′:3,4][1,2,4]triazino[5,6-b]indoles Medicinal Chemistry Research. 22: 3675-3686 |
Upadhyay K, Bavishi A, Thakrar S, et al. (2011) Synthesis and biological evaluation of 4-styrylcoumarin derivatives as inhibitors of TNF-α and IL-6 with anti-tubercular activity. Bioorganic & Medicinal Chemistry Letters. 21: 2547-9 |
Virsdoia V, Shaikh MS, Manvar A, et al. (2010) Screening for in vitro antimycobacterial activity and three-dimensional quantitative structure-activity relationship (3D-QSAR) study of 4-(arylamino)coumarin derivatives. Chemical Biology & Drug Design. 76: 412-24 |