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Refinado por: Nome da Publicação: Bioorganic & Medicinal Chemistry remover
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Avermectins and flea control : Structure-activity relationships and the selection of selamectin for development as an endectocide for companion animals
Avermectins and flea control : Structure-activity relationships and the selection of selamectin for development as an endectocide for companion animals
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Avermectins and flea control : Structure-activity relationships and the selection of selamectin for development as an endectocide for companion animals

BANKS, B. J ; BISHOP, B. F ; EVANS, N. A ; GIBSON, S. P ; GOUDIE, A. C ; GRATION, K. A. F ; PACEY, M. S ; PERRY, D. A ; WITTY, M. J

Bioorganic & medicinal chemistry, 2000-08, Vol.8 (8), p.2017-2025 [Periódico revisado por pares]

Oxford: Elsevier Science

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2
Discovery and optimization of pyridazinone non-nucleoside inhibitors of HIV-1 reverse transcriptase
Discovery and optimization of pyridazinone non-nucleoside inhibitors of HIV-1 reverse transcriptase
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Discovery and optimization of pyridazinone non-nucleoside inhibitors of HIV-1 reverse transcriptase

Sweeney, Zachary K. ; Dunn, James P. ; Li, Yu ; Heilek, Gabrielle ; Dunten, Pete ; Elworthy, Todd R. ; Han, Xiaochun ; Harris, Seth F. ; Hirschfeld, Donald R. ; Hogg, J. Heather ; Huber, Walter ; Kaiser, Ann C. ; Kertesz, Denis J. ; Kim, Woongki ; Mirzadegan, Taraneh ; Roepel, Michael G. ; Saito, Y. David ; Silva, Tania M.P.C. ; Swallow, Steven ; Tracy, Jahari L. ; Villasenor, Armando ; Vora, Harit ; Zhou, Amy S. ; Klumpp, Klaus

Bioorganic & medicinal chemistry, 2008-08, Vol.18 (15), p.4352-4354 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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3
Design, synthesis and biological evaluation of 2,4-disubstituted oxazole derivatives as potential PDE4 inhibitors
Design, synthesis and biological evaluation of 2,4-disubstituted oxazole derivatives as potential PDE4 inhibitors
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Design, synthesis and biological evaluation of 2,4-disubstituted oxazole derivatives as potential PDE4 inhibitors

Li, Ya-Sheng ; Hu, De-Kun ; Zhao, Dong-Sheng ; Liu, Xing-Yu ; Jin, Hong-Wei ; Song, Gao-Peng ; Cui, Zi-Ning ; Zhang, Lian-Hui

Bioorganic & medicinal chemistry, 2017-03, Vol.25 (6), p.1852-1859 [Periódico revisado por pares]

England: Elsevier Ltd

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4
N-Alkyl-5H-pyrido[4,3-b]indol-1-amines and derivatives as novel urotensin-II receptor antagonists
N-Alkyl-5H-pyrido[4,3-b]indol-1-amines and derivatives as novel urotensin-II receptor antagonists
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N-Alkyl-5H-pyrido[4,3-b]indol-1-amines and derivatives as novel urotensin-II receptor antagonists

YONGHUI WANG ; ZINING WU ; GUIDA, Brian F ; LAWRENCE, Sarah K ; NEEB, Michael J ; RIVERO, Ralph A ; DOUGLAS, Stephen A ; JIAN JIN

Bioorganic & medicinal chemistry, 2008-09, Vol.18 (18), p.4936-4939 [Periódico revisado por pares]

Oxford: Elsevier

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5
Structure–activity relationship of 2,2-dimethyl-2H-chromene based arylsulfonamide analogs of 3,4-dimethoxy-N-[(2,2-dimethyl-2H-chromen-6-yl)methyl]-N-phenylbenzenesulfonamide, a novel small molecule hypoxia inducible factor-1 (HIF-1) pathway inhibitor and anti-cancer agent
Structure–activity relationship of 2,2-dimethyl-2H-chromene based arylsulfonamide analogs of 3,4-dimethoxy-N-[(2,2-dimethyl-2H-chromen-6-yl)methyl]-N-phenylbenzenesulfonamide, a novel small molecule hypoxia inducible factor-1 (HIF-1) pathway inhibitor and anti-cancer agent
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Structure–activity relationship of 2,2-dimethyl-2H-chromene based arylsulfonamide analogs of 3,4-dimethoxy-N-[(2,2-dimethyl-2H-chromen-6-yl)methyl]-N-phenylbenzenesulfonamide, a novel small molecule hypoxia inducible factor-1 (HIF-1) pathway inhibitor and anti-cancer agent

Mun, Jiyoung ; Jabbar, Adnan Abdul ; Devi, Narra Sarojini ; Liu, Yuan ; Van Meir, Erwin G. ; Goodman, Mark M.

Bioorganic & medicinal chemistry, 2012-07, Vol.20 (14), p.4590-4597 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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6
Discovery of novel indane derivatives as liver-selective thyroid hormone receptor β (TRβ) agonists for the treatment of dyslipidemia
Discovery of novel indane derivatives as liver-selective thyroid hormone receptor β (TRβ) agonists for the treatment of dyslipidemia
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Discovery of novel indane derivatives as liver-selective thyroid hormone receptor β (TRβ) agonists for the treatment of dyslipidemia

Shiohara, Hiroaki ; Nakamura, Tetsuya ; Kikuchi, Norihiko ; Ozawa, Tomonaga ; Nagano, Ryuichi ; Matsuzawa, Akane ; Ohnota, Hideki ; Miyamoto, Takahide ; Ichikawa, Kazuo ; Hashizume, Kiyoshi

Bioorganic & medicinal chemistry, 2012-06, Vol.20 (11), p.3622-3634 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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7
Polycyclic aromatic compounds as anticancer agents: structure–activity relationships of chrysene and pyrene derivatives
Polycyclic aromatic compounds as anticancer agents: structure–activity relationships of chrysene and pyrene derivatives
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Polycyclic aromatic compounds as anticancer agents: structure–activity relationships of chrysene and pyrene derivatives

Banik, Bimal K ; Becker, Frederick F

Bioorganic & medicinal chemistry, 2001-03, Vol.9 (3), p.593-605 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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8
Structure-Activity relationship of 1-(Furan-2ylmethyl)Pyrrolidine-Based Stimulation-2 (ST2) inhibitors for treating graft versus host disease
Structure-Activity relationship of 1-(Furan-2ylmethyl)Pyrrolidine-Based Stimulation-2 (ST2) inhibitors for treating graft versus host disease
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Structure-Activity relationship of 1-(Furan-2ylmethyl)Pyrrolidine-Based Stimulation-2 (ST2) inhibitors for treating graft versus host disease

Yuan, Xinrui ; Jiang, Hua ; Fu, Denggang ; Robida, Aaron ; Rajanayake, Krishani ; Yuan, Hebao ; Wen, Bo ; Sun, Duxin ; Watch, Brennan T. ; Chinnaswamy, Krishnapriya ; Stuckey, Jeanne A. ; Paczesny, Sophie ; Rech, Jason C. ; Yang, Chao-Yie

Bioorganic & medicinal chemistry, 2022-10, Vol.71, p.116942-116942, Article 116942 [Periódico revisado por pares]

Elsevier Ltd

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9
Synthesis, anticonvulsant activity, and neuropathic pain-attenuating activity of N-benzyl 2-amino-2-(hetero)aromatic acetamides
Synthesis, anticonvulsant activity, and neuropathic pain-attenuating activity of N-benzyl 2-amino-2-(hetero)aromatic acetamides
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Synthesis, anticonvulsant activity, and neuropathic pain-attenuating activity of N-benzyl 2-amino-2-(hetero)aromatic acetamides

Baruah, Pranjal K. ; Dinsmore, Jason ; King, Amber M. ; Salomé, Christophe ; De Ryck, Marc ; Kaminski, Rafal ; Provins, Laurent ; Kohn, Harold

Bioorganic & medicinal chemistry, 2012-06, Vol.20 (11), p.3551-3564 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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10
Potent, nonpeptide inhibitors of human mast cell tryptase. Synthesis and biological evaluation of novel spirocyclic piperidine amide derivatives
Potent, nonpeptide inhibitors of human mast cell tryptase. Synthesis and biological evaluation of novel spirocyclic piperidine amide derivatives
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Potent, nonpeptide inhibitors of human mast cell tryptase. Synthesis and biological evaluation of novel spirocyclic piperidine amide derivatives

Costanzo, Michael J. ; Yabut, Stephen C. ; Zhang, Han-Cheng ; White, Kimberley B. ; de Garavilla, Lawrence ; Wang, Yuanping ; Minor, Lisa K. ; Tounge, Brett A. ; Barnakov, Alexander N. ; Lewandowski, Frank ; Milligan, Cynthia ; Spurlino, John C. ; Abraham, William M. ; Boswell-Smith, Victoria ; Page, Clive P. ; Maryanoff, Bruce E.

Bioorganic & medicinal chemistry, 2008-03, Vol.18 (6), p.2114-2121 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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