Year |
Citation |
Score |
2020 |
Reddi R, Ganji RJ, Marapaka AK, Bala SC, Yerra NV, Haque N, Addlagatta A. Puromycin, a selective inhibitor of PSA acts as a substrate for other M1 family aminopeptidases: Biochemical and structural basis. International Journal of Biological Macromolecules. PMID 33045297 DOI: 10.1016/j.ijbiomac.2020.10.035 |
0.769 |
|
2015 |
Aeluri R, Ganji RJ, Marapaka AK, Pillalamarri V, Alla M, Addlagatta A. Highly functionalized tetrahydropyridines are cytotoxic and selective inhibitors of human puromycin sensitive aminopeptidase. European Journal of Medicinal Chemistry. 106: 26-33. PMID 26513642 DOI: 10.1016/J.Ejmech.2015.10.026 |
0.78 |
|
2015 |
Arya T, Reddi R, Kishor C, Ganji RJ, Bhukya S, Gumpena R, McGowan S, Drag M, Addlagatta A. Identification of the molecular basis of inhibitor selectivity between the human and streptococcal type i methionine aminopeptidases Journal of Medicinal Chemistry. 58: 2350-2357. PMID 25699713 DOI: 10.1021/Jm501790E |
0.726 |
|
2015 |
Ganji RJ, Reddi R, Gumpena R, Marapaka AK, Arya T, Sankoju P, Bhukya S, Addlagatta A. Structural basis for the inhibition of M1 family aminopeptidases by the natural product actinonin: Crystal structure in complex with E. coli aminopeptidase N. Protein Science : a Publication of the Protein Society. 24: 823-31. PMID 25644575 DOI: 10.1002/Pro.2653 |
0.733 |
|
2014 |
Manda BR, Alla M, Ganji RJ, Addlagatta A. Discovery of Tröger's base analogues as selective inhibitors against human breast cancer cell line: design, synthesis and cytotoxic evaluation. European Journal of Medicinal Chemistry. 86: 39-47. PMID 25140752 DOI: 10.1016/J.Ejmech.2014.08.044 |
0.656 |
|
2014 |
Reddi R, Arya T, Kishor C, Gumpena R, Ganji RJ, Bhukya S, Addlagatta A. Selective targeting of the conserved active site cysteine of Mycobacterium tuberculosis methionine aminopeptidase with electrophilic reagents. The Febs Journal. 281: 4240-8. PMID 24841365 DOI: 10.1111/Febs.12847 |
0.709 |
|
2013 |
Rapolu S, Alla M, Ganji RJ, Saddanapu V, Kishor C, Bommena VR, Addlagatta A. Synthesis, cytotoxicity and hDHFR inhibition studies of 2H-pyrido[1,2-a]pyrimidin-2-ones Medchemcomm. 4: 817. DOI: 10.1039/C3Md00013C |
0.725 |
|
2012 |
Gumpena R, Kishor C, Ganji RJ, Jain N, Addlagatta A. Glu121-Lys319 salt bridge between catalytic and N-terminal domains is pivotal for the activity and stability of Escherichia coli aminopeptidase N. Protein Science : a Publication of the Protein Society. 21: 727-36. PMID 22411732 DOI: 10.1002/Pro.2060 |
0.747 |
|
2012 |
Subba Reddy BV, Rajeswari N, Sarangapani M, Prashanthi Y, Ganji RJ, Addlagatta A. Iodine-catalyzed condensation of isatin with indoles: a facile synthesis of di(indolyl)indolin-2-ones and evaluation of their cytotoxicity. Bioorganic & Medicinal Chemistry Letters. 22: 2460-3. PMID 22386528 DOI: 10.1016/J.Bmcl.2012.02.011 |
0.629 |
|
2011 |
Gumpena R, Kishor C, Ganji RJ, Addlagatta A. Discovery of α,β- and α,γ-diamino acid scaffolds for the inhibition of M1 family aminopeptidases. Chemmedchem. 6: 1971-6. PMID 22025387 DOI: 10.1002/Cmdc.201100298 |
0.774 |
|
2010 |
Gumpena R, Kishor C, Ganji RJ, Addlagatta A. Discovery of alpha, beta- and alpha, gamma-Diamino Acid Scaffolds for the Inhibition of M1 Family Aminopeptidases Chemmedchem. 6: 1971-1976. DOI: 10.2210/Pdb3Ked/Pdb |
0.719 |
|
Show low-probability matches. |