Year |
Citation |
Score |
2019 |
Poudel YB, Rao C, Kotapati S, Deshpande M, Thevanayagam L, Pan C, Cardarelli J, Chowdari N, Kaspady M, Samikannu R, Kuppusamy P, Saravanakumar P, Arunachalam PN, Deshpande S, Rangan V, et al. Design, synthesis and biological evaluation of phenol-linked uncialamycin antibody-drug conjugates. Bioorganic & Medicinal Chemistry Letters. 126782. PMID 31767265 DOI: 10.1016/J.Bmcl.2019.126782 |
0.329 |
|
2016 |
Nicolaou KC, Wang Y, Lu M, Mandal D, Pattanayak MR, Yu R, Shah AA, Chen JS, Zhang H, Crawford JJ, Pasunoori L, Poudel YB, Chowdari NS, Pan C, Nazeer A, et al. Streamlined Total Synthesis of Uncialamycin and Its Application to the Synthesis of Designed Analogues for Biological Investigations. Journal of the American Chemical Society. PMID 27266267 DOI: 10.1021/Jacs.6B04339 |
0.473 |
|
2015 |
Lee K, Poudel YB, Glinkerman CM, Boger DL. Total synthesis of dihydrolysergic acid and dihydrolysergol: development of a divergent synthetic strategy applicable to rapid assembly of D-ring analogs. Tetrahedron. 71: 5897-5905. PMID 26273113 DOI: 10.1016/J.Tet.2015.05.093 |
0.788 |
|
2015 |
Lee K, Poudel YB, Glinkerman CM, Boger DL. Total synthesis of dihydrolysergic acid and dihydrolysergol: Development of a divergent synthetic strategy applicable to rapid assembly of D-ring analogs Tetrahedron. DOI: 10.1016/j.tet.2015.05.093 |
0.489 |
|
2014 |
Kraft MB, Poudel YB, Kedei N, Lewin NE, Peach ML, Blumberg PM, Keck GE. Synthesis of a des-B-ring bryostatin analogue leads to an unexpected ring expansion of the bryolactone core. Journal of the American Chemical Society. 136: 13202-8. PMID 25207434 DOI: 10.1021/Ja5078188 |
0.793 |
|
2013 |
Kedei N, Lewin NE, Géczy T, Selezneva J, Braun DC, Chen J, Herrmann MA, Heldman MR, Lim L, Mannan P, Garfield SH, Poudel YB, Cummins TJ, Rudra A, Blumberg PM, et al. Biological profile of the less lipophilic and synthetically more accessible bryostatin 7 closely resembles that of bryostatin 1. Acs Chemical Biology. 8: 767-77. PMID 23369356 DOI: 10.1021/Cb300671S |
0.688 |
|
2013 |
Breazzano SP, Poudel YB, Boger DL. A Pd(0)-mediated indole (macro)cyclization reaction. Journal of the American Chemical Society. 135: 1600-6. PMID 23298368 DOI: 10.1021/Ja3121394 |
0.775 |
|
2013 |
Kedei N, Telek A, Michalowski AM, Kraft MB, Li W, Poudel YB, Rudra A, Petersen ME, Keck GE, Blumberg PM. Comparison of transcriptional response to phorbol ester, bryostatin 1, and bryostatin analogs in LNCaP and U937 cancer cell lines provides insight into their differential mechanism of action. Biochemical Pharmacology. 85: 313-24. PMID 23146662 DOI: 10.1016/J.Bcp.2012.10.028 |
0.719 |
|
2012 |
Keck GE, Poudel YB, Rudra A, Stephens JC, Kedei N, Lewin NE, Blumberg PM. Role of the C8 gem-dimethyl group of bryostatin 1 on its unique pattern of biological activity. Bioorganic & Medicinal Chemistry Letters. 22: 4084-8. PMID 22579485 DOI: 10.1016/J.Bmcl.2012.04.073 |
0.731 |
|
2012 |
Kedei N, Telek A, Michalowski AM, Kraft MB, Li W, Poudel YB, Rudra A, Petersen ME, Keck GE, Blumberg PM. Abstract 3815: Comparison of transcriptional response to phorbol ester, bryostatin 1, and bryostatin analogues in LNCaP and U937 cancer cell lines provides insight into their differential mechanism of action Cancer Research. 72: 3815-3815. DOI: 10.1158/1538-7445.Am2012-3815 |
0.721 |
|
2011 |
Keck GE, Poudel YB, Cummins TJ, Rudra A, Covel JA. Total synthesis of bryostatin 1. Journal of the American Chemical Society. 133: 744-7. PMID 21175177 DOI: 10.1021/Ja110198Y |
0.791 |
|
2011 |
Keck GE, Poudel YB, Cummins TJ, Rudra A, Covel JA. Synthesis of Bryostatin 1 Synfacts. 2011: 464-464. DOI: 10.1055/S-0030-1259787 |
0.738 |
|
2010 |
Keck GE, Poudel YB, Rudra A, Stephens JC, Kedei N, Lewin NE, Peach ML, Blumberg PM. Molecular modeling, total synthesis, and biological evaluations of C9-deoxy bryostatin 1. Angewandte Chemie (International Ed. in English). 49: 4580-4. PMID 20491108 DOI: 10.1002/Anie.201001200 |
0.668 |
|
2009 |
Keck GE, Poudel YB, Welch DS, Kraft MB, Truong AP, Stephens JC, Kedei N, Lewin NE, Blumberg PM. Substitution on the A-ring confers to bryopyran analogues the unique biological activity characteristic of bryostatins and distinct from that of the phorbol esters. Organic Letters. 11: 593-6. PMID 19113896 DOI: 10.1021/Ol8027253 |
0.724 |
|
2006 |
Keck GE, Welch DS, Poudel YB. Synthetic Studies Toward Bryostatin 1: Preparation of a C(1)-C(16) Fragment by Pyran Annulation. Tetrahedron Letters. 47: 8267-8270. PMID 17404602 DOI: 10.1016/J.Tetlet.2006.09.094 |
0.78 |
|
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