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1
Nocathiacin I analogues: synthesis, in vitro and in vivo biological activity of novel semi-synthetic thiazolyl peptide antibiotics
Nocathiacin I analogues: synthesis, in vitro and in vivo biological activity of novel semi-synthetic thiazolyl peptide antibiotics
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Nocathiacin I analogues: synthesis, in vitro and in vivo biological activity of novel semi-synthetic thiazolyl peptide antibiotics

Naidu, B. Narasimhulu ; Sorenson, Margaret E. ; Zhang, Yunhui ; Kim, Oak K. ; Matiskella, John D. ; Wichtowski, John A. ; Connolly, Timothy P. ; Li, Wenying ; Lam, Kin S. ; Bronson, Joanne J. ; Pucci, Michael J. ; Clark, Junius M. ; Ueda, Yasutsugu

Bioorganic & medicinal chemistry letters, 2004-11, Vol.14 (22), p.5573-5577 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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2
Phosphinic acid-based MMP-13 inhibitors that spare MMP-1 and MMP-3
Phosphinic acid-based MMP-13 inhibitors that spare MMP-1 and MMP-3
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Phosphinic acid-based MMP-13 inhibitors that spare MMP-1 and MMP-3

Reiter, Lawrence A. ; Mitchell, Peter G. ; Martinelli, Gary J. ; Lopresti-Morrow, Lori L. ; Yocum, Sue A. ; Eskra, James D.

Bioorganic & medicinal chemistry letters, 2003-07, Vol.13 (14), p.2331-2336 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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3
Synthesis and biological activity of piperazine-Based dual MMP-13 and TNF-α converting enzyme inhibitors
Synthesis and biological activity of piperazine-Based dual MMP-13 and TNF-α converting enzyme inhibitors
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Synthesis and biological activity of piperazine-Based dual MMP-13 and TNF-α converting enzyme inhibitors

Letavic, Michael A. ; Barberia, John T. ; Carty, Thomas J. ; Hardink, Joel R. ; Liras, Jennifer ; Lopresti-Morrow, Lori L. ; Mitchell, Peter G. ; Noe, Mark C. ; Reeves, Lisa M. ; Snow, Sheri L. ; Stam, Ethan J. ; Sweeney, Francis J. ; Vaughn, Marcie L. ; Yu, Chul H.

Bioorganic & medicinal chemistry letters, 2003-10, Vol.13 (19), p.3243-3246 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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4
N-substituted 4-(5-indolyl)benzoic acids. Synthesis and evaluation of steroid 5α-reductase type I and II inhibitory activity
N-substituted 4-(5-indolyl)benzoic acids. Synthesis and evaluation of steroid 5α-reductase type I and II inhibitory activity
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N-substituted 4-(5-indolyl)benzoic acids. Synthesis and evaluation of steroid 5α-reductase type I and II inhibitory activity

Baston, Eckhard ; Hartmann, Rolf W.

Bioorganic & medicinal chemistry letters, 1999-06, Vol.9 (11), p.1601-1606 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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5
Structure-activity studies related to ABT-594, a potent nonopioid analgesic agent: Effect of pyridine and azetidine ring substitutions on nicotinic acetylcholine receptor binding affinity and analgesic activity in mice
Structure-activity studies related to ABT-594, a potent nonopioid analgesic agent: Effect of pyridine and azetidine ring substitutions on nicotinic acetylcholine receptor binding affinity and analgesic activity in mice
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Structure-activity studies related to ABT-594, a potent nonopioid analgesic agent: Effect of pyridine and azetidine ring substitutions on nicotinic acetylcholine receptor binding affinity and analgesic activity in mice

Holladay, Mark W. ; Bai, Hao ; Li, Yihong ; Lin, Nan-Horng ; Daanen, Jerome F. ; Ryther, Keith B. ; Wasicak, James T. ; Kincaid, John F. ; He, Yun ; Hettinger, Anne-Marie ; Huang, Peggy ; Anderson, David J. ; Bannon, Anthony W. ; Buckley, Michael J. ; Campbell, Jeffrey E. ; Donnelly-Roberts, Diana L. ; Gunther, Karen L. ; Kim, David J.B. ; Kuntzweiler, Theresa A. ; Sullivan, James P. ; Decker, Michael W. ; Arneric, Stephen P.

Bioorganic & medicinal chemistry letters, 1998-10, Vol.8 (19), p.2797-2802 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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6
DNA alkylation properties of the duocarmycins: (+)-duocarmycin A, epi-(+)-duocarmycin A, ent-(−)-duocarmycin A and epi,ent-(−)-duocarmycin A
DNA alkylation properties of the duocarmycins: (+)-duocarmycin A, epi-(+)-duocarmycin A, ent-(−)-duocarmycin A and epi,ent-(−)-duocarmycin A
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DNA alkylation properties of the duocarmycins: (+)-duocarmycin A, epi-(+)-duocarmycin A, ent-(−)-duocarmycin A and epi,ent-(−)-duocarmycin A

Boger, Dale L. ; Yun, Weiya ; Terashima, Shiro ; Fukuda, Yasumichi ; Nakatani, Kazuhiko ; Kitos, Paul A. ; Jin, Qing

Bioorganic & medicinal chemistry letters, 1992, Vol.2 (7), p.759-765 [Periódico revisado por pares]

OXFORD: Elsevier Ltd

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7
Synthesis, stereochemical assignment and biological activity of a novel series of C-4″ modified aza-Macrolides
Synthesis, stereochemical assignment and biological activity of a novel series of C-4″ modified aza-Macrolides
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Synthesis, stereochemical assignment and biological activity of a novel series of C-4″ modified aza-Macrolides

Bronk, Brian S ; Letavic, Michael A ; Bertsche, Camilla D ; George, David M ; Hayashi, Shigeru F ; Kamicker, Barbara J ; Kolosko, Nicole L ; Norcia, Laura J ; Rushing, Margaret A ; Santoro, Sheryl L ; Yang, Bingwei V

Bioorganic & medicinal chemistry letters, 2003-06, Vol.13 (12), p.1955-1958 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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8
N ε-carboxymethyllysine formation by direct addition of glyoxal to lysine during the Maillard reaction
N ε-carboxymethyllysine formation by direct addition of glyoxal to lysine during the Maillard reaction
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N ε-carboxymethyllysine formation by direct addition of glyoxal to lysine during the Maillard reaction

Al-Abed, Yousef ; Bucala, Richard

Bioorganic & medicinal chemistry letters, 1995, Vol.5 (18), p.2161-2162 [Periódico revisado por pares]

Elsevier Ltd

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9
The synthesis of novel 8a-aza-8a-homoerythromycin derivatives via the beckmann rearrangement of (9z)-erythromycin a oxime
The synthesis of novel 8a-aza-8a-homoerythromycin derivatives via the beckmann rearrangement of (9z)-erythromycin a oxime
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The synthesis of novel 8a-aza-8a-homoerythromycin derivatives via the beckmann rearrangement of (9z)-erythromycin a oxime

Wilkening, Robert R. ; Ratcliffe, Ronald W. ; Doss, George A. ; Bartizal, Kenneth F. ; Graham, Amy C. ; Herbert, Charmaine M.

Bioorganic & medicinal chemistry letters, 1993, Vol.3 (6), p.1287-1292 [Periódico revisado por pares]

Elsevier Ltd

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10
A depsipeptide fungal metabolite inhibitor of cholesteryl ester transfer protein
A depsipeptide fungal metabolite inhibitor of cholesteryl ester transfer protein
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A depsipeptide fungal metabolite inhibitor of cholesteryl ester transfer protein

HEGDE, V. R ; PING DAI ; PATEL, M ; DAS, P. R ; WANG, S ; PUAR, M. S

Bioorganic & medicinal chemistry letters, 1998-06, Vol.8 (11), p.1277-1280 [Periódico revisado por pares]

Oxford: Elsevier

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