| Year |
Citation |
Score |
| 2024 |
Tang SA, Fults A, Boyd SR, Gattu N, Tran KA, Fan J, MacKenzie KR, Palzkill T, Young DW, Chamakuri S. Expanding Complex Morpholines Using Systematic Chemical Diversity. Organic Letters. PMID 38506470 DOI: 10.1021/acs.orglett.4c00528 |
0.318 |
|
| 2023 |
Jimmidi R, Chamakuri S, Lu S, Ucisik MN, Chen PJ, Bohren KM, Moghadasi SA, Versteeg L, Nnabuife C, Li JY, Qin X, Chen YC, Faver JC, Nyshadham P, Sharma KL, et al. DNA-encoded chemical libraries yield non-covalent and non-peptidic SARS-CoV-2 main protease inhibitors. Communications Chemistry. 6: 164. PMID 37542196 DOI: 10.1038/s42004-023-00961-y |
0.774 |
|
| 2021 |
Chamakuri S, Lu S, Ucisik MN, Bohren KM, Chen YC, Du HC, Faver JC, Jimmidi R, Li F, Li JY, Nyshadham P, Palmer SS, Pollet J, Qin X, Ronca SE, et al. DNA-encoded chemistry technology yields expedient access to SARS-CoV-2 M inhibitors. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 34426525 DOI: 10.1073/pnas.2111172118 |
0.768 |
|
| 2019 |
Chamakuri S, Jain P, Guduru SRK, Arney JW, MacKenzie KR, Santini C, Young DW. Correction to Synthesis of Enantiomerically Pure 6-Substituted-Piperazine-2-Acetic Acid Esters as Intermediates for Library Production. The Journal of Organic Chemistry. PMID 30855144 DOI: 10.1021/Acs.Joc.9B00594 |
0.374 |
|
| 2019 |
Jain P, Raji IO, Chamakuri S, MacKenzie KR, Ebright BT, Santini C, Young DW. Synthesis of Enantiomerically Pure 5-Substituted-Piperazine-2-Acetic Acid Esters as Intermediates for Library Production. The Journal of Organic Chemistry. PMID 30848904 DOI: 10.1021/Acs.Joc.9B00148 |
0.414 |
|
| 2018 |
Guduru SKR, Chamakuri S, Raji IO, MacKenzie KR, Santini C, Young DW. Synthesis of Enantiomerically Pure 3-Substituted-Piperazine-2-Acetic Acid Esters as Intermediates for Library Production. The Journal of Organic Chemistry. PMID 30180575 DOI: 10.1021/Acs.Joc.8B01708 |
0.43 |
|
| 2018 |
Chamakuri S, Jain P, Guduru SKR, Arney JW, MacKenzie K, Santini C, Young DW. Synthesis of Enantiomerically Pure 6-Substituted-Piperazine-2-Acetic Acid Esters as Intermediates for Library Production. The Journal of Organic Chemistry. PMID 29751727 DOI: 10.1021/Acs.Joc.8B00854 |
0.466 |
|
| 2017 |
Jogula S, Soorneedi AR, Gaddam J, Chamakuri S, Deora GS, Indarapu RK, Ramgopal MK, Dravida S, Arya P. Geldanamycin-inspired compounds induce direct trans-differentiation of human mesenchymal stem cells to neurons. European Journal of Medicinal Chemistry. 135: 110-116. PMID 28441579 DOI: 10.1016/J.Ejmech.2017.03.082 |
0.604 |
|
| 2015 |
Chamakuri S, Jogula S, Arya P. Regio- and Stereocontrolled Dieckmann Approach to Treprostinil-Inspired, Polycyclic Scaffold For Building Macrocyclic Diversity. Acs Combinatorial Science. 17: 437-41. PMID 26167941 DOI: 10.1021/Acscombsci.5B00076 |
0.712 |
|
| 2014 |
Aeluri M, Chamakuri S, Dasari B, Guduru SK, Jimmidi R, Jogula S, Arya P. Small molecule modulators of protein-protein interactions: selected case studies. Chemical Reviews. 114: 4640-94. PMID 24673632 DOI: 10.1021/Cr4004049 |
0.419 |
|
| 2013 |
Reddy Guduru SK, Chamakuri S, Chandrasekar G, Kitambi SS, Arya P. Tetrahydroquinoline-derived macrocyclic toolbox: the discovery of antiangiogenesis agents in zebrafish assay. Acs Medicinal Chemistry Letters. 4: 666-70. PMID 24900727 DOI: 10.1021/Ml400026N |
0.726 |
|
| 2013 |
Chamakuri S, Guduru SKR, Pamu S, Chandrasekar G, Kitambi SS, Arya P. A Modular Approach to Build Macrocyclic Diversity in Aminoindoline Scaffolds Identifies Antiangiogenesis Agents from a Zebrafish Assay European Journal of Organic Chemistry. 2013: 3959-3964. DOI: 10.1002/Ejoc.201300409 |
0.658 |
|
| 2010 |
Kumar KS, Chamakuri S, Vishweshwar P, Iqbal J, Pal M. AlCl3-induced (hetero)arylation of thienopyrimidine ring: a new synthesis of 4-substituted thieno[2,3-d]pyrimidines Tetrahedron Letters. 51: 3269-3273. DOI: 10.1016/J.Tetlet.2010.04.057 |
0.387 |
|
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