Year |
Citation |
Score |
2023 |
Kim W, Tripathi M, Kim C, Vardhineni S, Cha Y, Kandi SK, Feitosa M, Kholiya R, Sah E, Thakur A, Kim Y, Ko S, Bhatia K, Manohar S, Kong YB, et al. An optimized Nurr1 agonist provides disease-modifying effects in Parkinson's disease models. Nature Communications. 14: 4283. PMID 37463889 DOI: 10.1038/s41467-023-39970-9 |
0.538 |
|
2015 |
Thakur A, Linga Reddy P, Tripathi M, Rawat DS. Facile construction of 3-indolochromenes and 3-indoloxanthenes via EDDF catalyzed one-pot three component reactions New Journal of Chemistry. 39: 6253-6260. DOI: 10.1039/C5Nj01288K |
0.687 |
|
2015 |
Tripathi M, Khan SI, Thakur A, Ponnan P, Rawat DS. 4-Aminoquinoline-pyrimidine-aminoalkanols: Synthesis, in vitro antimalarial activity, docking studies and ADME predictions New Journal of Chemistry. 39: 3474-3483. DOI: 10.1039/C5Nj00094G |
0.683 |
|
2015 |
Rajesh UC, Kholiya R, Thakur A, Rawat DS. [TBA][Gly] ionic liquid promoted multi-component synthesis of 3-substituted indoles and indolyl-4H-chromenes Tetrahedron Letters. 56: 1790-1793. DOI: 10.1016/J.Tetlet.2015.02.058 |
0.624 |
|
2014 |
Manohar S, Thakur A, Khan SI, Sun G, Ni N, Wang B, Rawat DS. Synthesis of unsymmetrical c5-curcuminoids as potential anticancer agents Letters in Drug Design and Discovery. 11: 138-149. DOI: 10.2174/15701808113109990061 |
0.666 |
|
2014 |
Thakur A, Khan SI, Rawat DS. Synthesis of piperazine tethered 4-aminoquinoline-pyrimidine hybrids as potent antimalarial agents Rsc Advances. 4: 20729-20736. DOI: 10.1039/C4Ra02276A |
0.597 |
|
2014 |
Thakur A, Manohar S, Vélez Gerena CE, Zayas B, Kumar V, Malhotra SV, Rawat DS. Novel 3,5-bis(arylidiene)-4-piperidone based monocarbonyl analogs of curcumin: Anticancer activity evaluation and mode of action study Medchemcomm. 5: 576-586. DOI: 10.1039/C3Md00399J |
0.677 |
|
2013 |
Thakur A, Tripathi M, Rajesh UC, Rawat DS. Ethylenediammonium diformate (EDDF) in PEG600: an efficient ambiphilic novel catalytic system for the one-pot synthesis of 4H-pyrans via Knoevenagel condensation Rsc Advances. 3: 18142. DOI: 10.1039/C3Ra42410C |
0.704 |
|
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