| Year |
Citation |
Score |
| 2018 |
Muppidi A, Lee SJ, Hsu CH, Zou H, Lee C, Pflimlin E, Mahankali M, Yang P, Chao E, Ahmad I, Crameri A, Wang D, Woods A, Shen W. Design and Synthesis of Potent, Long-Acting Lipidated Relaxin-2 Analogs. Bioconjugate Chemistry. PMID 30543420 DOI: 10.1021/Acs.Bioconjchem.8B00764 |
0.588 |
|
| 2018 |
Yang P, Zou H, Lee C, Muppidi A, Chao E, Fu Q, Luo X, Wang D, Schultz PG, Shen W. A Stapled, Long-Acting Glucagon-like Peptide 2 Analog with Efficacy in Dextran Sodium Sulfate-Induced Mouse Colitis Models. Journal of Medicinal Chemistry. PMID 29528634 DOI: 10.1021/Acs.Jmedchem.7B00768 |
0.728 |
|
| 2016 |
Muppidi A, Zou H, Yang PY, Chao E, Sherwood L, Nunez V, Woods AK, Schultz PG, Lin Q, Shen W. Design of Potent and Proteolytically Stable Oxyntomodulin Analogs. Acs Chemical Biology. 11: 324-8. PMID 26727558 DOI: 10.1021/Acschembio.5B00787 |
0.676 |
|
| 2014 |
Muppidi A, Doi K, Ramil CP, Wang HG, Lin Q. Synthesis of cell-permeable stapled BH3 peptide-based Mcl-1 inhibitors containing simple aryl and vinylaryl cross-linkers. Tetrahedron. 70: 7740-7745. PMID 25267861 DOI: 10.1016/J.Tet.2014.05.104 |
0.646 |
|
| 2014 |
Muppidi A, Zhang H, Curreli F, Li N, Debnath AK, Lin Q. Design of antiviral stapled peptides containing a biphenyl cross-linker. Bioorganic & Medicinal Chemistry Letters. 24: 1748-51. PMID 24613163 DOI: 10.1016/J.Bmcl.2014.02.038 |
0.657 |
|
| 2014 |
Muppidi A, Doi K, Edwardraja S, Pulavarti SV, Szyperski T, Wang HG, Lin Q. Targeted delivery of ubiquitin-conjugated BH3 peptide-based Mcl-1 inhibitors into cancer cells. Bioconjugate Chemistry. 25: 424-32. PMID 24410055 DOI: 10.1021/Bc4005574 |
0.668 |
|
| 2012 |
Muppidi A, Doi K, Edwardraja S, Drake EJ, Gulick AM, Wang HG, Lin Q. Rational design of proteolytically stable, cell-permeable peptide-based selective Mcl-1 inhibitors. Journal of the American Chemical Society. 134: 14734-7. PMID 22920569 DOI: 10.1021/Ja306864V |
0.682 |
|
| 2011 |
Muppidi A, Li X, Chen J, Lin Q. Conjugation of spermine enhances cellular uptake of the stapled peptide-based inhibitors of p53-Mdm2 interaction. Bioorganic & Medicinal Chemistry Letters. 21: 7412-5. PMID 22047690 DOI: 10.1016/J.Bmcl.2011.10.009 |
0.69 |
|
| 2011 |
Muppidi A, Wang Z, Li X, Chen J, Lin Q. Achieving cell penetration with distance-matching cysteine cross-linkers: a facile route to cell-permeable peptide dual inhibitors of Mdm2/Mdmx. Chemical Communications (Cambridge, England). 47: 9396-8. PMID 21773579 DOI: 10.1039/C1Cc13320A |
0.645 |
|
| 2011 |
Madden MM, Muppidi A, Li Z, Li X, Chen J, Lin Q. Synthesis of cell-permeable stapled peptide dual inhibitors of the p53-Mdm2/Mdmx interactions via photoinduced cycloaddition. Bioorganic & Medicinal Chemistry Letters. 21: 1472-5. PMID 21277201 DOI: 10.1016/J.Bmcl.2011.01.004 |
0.744 |
|
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