Year |
Citation |
Score |
2016 |
Kadam KS, Gandhi T, Gupte A, Gangopadhyay AK, Sharma R. Alkyl Nitrites: Novel Reagents for One-Pot Synthesis of 3,5-Disubstituted Isoxazoles from Aldoximes and Alkynes Synthesis (Germany). DOI: 10.1055/S-0035-1561464 |
0.338 |
|
2015 |
Kadam KS, Gandhi T, Reddy MM, Gupte A, Sharma R. Synthesis, characterization, and DGAT1 inhibition of new 5-piperazinethiazole and 5-piperidinethiazole analogs Journal of Heterocyclic Chemistry. 52: 802-814. DOI: 10.1002/Jhet.2194 |
0.407 |
|
2014 |
Kandre S, Bhagat PR, Reddy MM, Dalal R, Dixit A, Deshmukh NJ, Anthony J, Bose J, Anupindi R, Sharma R, Gupte A. Synthesis and evaluation of cyclohexane carboxylic acid head group containing isoxazole and thiazole analogs as DGAT1 inhibitors. European Journal of Medicinal Chemistry. 79: 203-15. PMID 24735646 DOI: 10.1016/J.Ejmech.2014.03.077 |
0.447 |
|
2013 |
Kadam KS, Jadhav RD, Kandre S, Guha T, Reddy MM, Brahma MK, Deshmukh NJ, Dixit A, Doshi L, Srinivasan S, Devle J, Damre A, Nemmani KV, Gupte A, Sharma R. Evaluation of thiazole containing biaryl analogs as diacylglycerol acyltransferase 1 (DGAT1) inhibitors. European Journal of Medicinal Chemistry. 65: 337-47. PMID 23735282 DOI: 10.1016/J.Ejmech.2013.05.006 |
0.484 |
|
2012 |
Jadhav RD, Kadam KS, Kandre S, Guha T, Reddy MMK, Brahma MK, Deshmukh NJ, Dixit A, Doshi L, Potdar N, Enose AA, Vishwakarma RA, Sivaramakrishnan H, Srinivasan S, Nemmani KVS, ... Gupte A, et al. Synthesis and biological evaluation of isoxazole, oxazole, and oxadiazole containing heteroaryl analogs of biaryl ureas as DGAT1 inhibitors European Journal of Medicinal Chemistry. 54: 324-342. PMID 22683241 DOI: 10.1016/J.Ejmech.2012.05.016 |
0.487 |
|
2011 |
Motiwala H, Kandre S, Birar V, Kadam KS, Rodge A, Jadhav RD, Mahesh Kumar Reddy M, Brahma MK, Deshmukh NJ, Dixit A, Doshi L, Gupte A, Gangopadhyay AK, Vishwakarma RA, Srinivasan S, et al. Exploration of pyridine containing heteroaryl analogs of biaryl ureas as DGAT1 inhibitors Bioorganic and Medicinal Chemistry Letters. 21: 5812-5817. PMID 21868220 DOI: 10.1016/J.Bmcl.2011.07.109 |
0.488 |
|
2009 |
Gupte A, Buolamwini JK. Synthesis and biological evaluation of phloridzin analogs as human concentrative nucleoside transporter 3 (hCNT3) inhibitors. Bioorganic & Medicinal Chemistry Letters. 19: 917-21. PMID 19097778 DOI: 10.1016/J.Bmcl.2008.11.112 |
0.689 |
|
2009 |
Gupte A, Buolamwini JK. CoMFA and CoMSIA 3D-QSAR studies on S(6)-(4-nitrobenzyl)mercaptopurine riboside (NBMPR) analogs as inhibitors of human equilibrative nucleoside transporter 1 (hENT1). Bioorganic & Medicinal Chemistry Letters. 19: 314-8. PMID 19091561 DOI: 10.1016/J.Bmcl.2008.11.092 |
0.644 |
|
2007 |
Gupte A, Buolamwini JK. Novel C2-purine position analogs of nitrobenzylmercaptopurine riboside as human equilibrative nucleoside transporter 1 inhibitors. Bioorganic & Medicinal Chemistry. 15: 7726-37. PMID 17881236 DOI: 10.1016/J.Bmc.2007.08.058 |
0.669 |
|
2005 |
Gupte A, Buolamwini JK, Yadav V, Chu CK, Naguib FN, el Kouni MH. 6-Benzylthioinosine analogues: promising anti-toxoplasmic agents as inhibitors of the mammalian nucleoside transporter ENT1 (es). Biochemical Pharmacology. 71: 69-73. PMID 16310172 DOI: 10.1016/J.Bcp.2005.10.031 |
0.645 |
|
2004 |
Gupte A, Buolamwini JK. Novel halogenated nitrobenzylthioinosine analogs as es nucleoside transporter inhibitors. Bioorganic & Medicinal Chemistry Letters. 14: 2257-60. PMID 15081020 DOI: 10.1016/J.Bmcl.2004.02.016 |
0.69 |
|
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