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Refinado por: Nome da Publicação: Bioorganic & Medicinal Chemistry remover
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Fragment-based lead discovery of indazole-based compounds as AXL kinase inhibitors
Fragment-based lead discovery of indazole-based compounds as AXL kinase inhibitors
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Fragment-based lead discovery of indazole-based compounds as AXL kinase inhibitors

Ng, Pearly Shuyi ; Foo, Klement ; Sim, Sandra ; Wang, Gang ; Huang, Chuhui ; Tan, Li Hong ; Poulsen, Anders ; Liu, Boping ; Tee, Doris Hui Ying ; Ahmad, Nur Huda Binte ; Wang, Sifang ; Ke, Zhiyuan ; Lee, May Ann ; Kwek, Zekui P. ; Joy, Joma ; Anantharajan, Jothi ; Baburajendran, Nithya ; Pendharkar, Vishal ; Manoharan, Vithya ; Vuddagiri, Susmitha ; Sangthongpitag, Kanda ; Hill, Jeffrey ; Keller, Thomas H. ; Hung, Alvin W.

Bioorganic & medicinal chemistry, 2021-11, Vol.49, p.116437, Article 116437 [Periódico revisado por pares]

England: Elsevier Ltd

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2
Design, synthesis, and biological evaluation of some novel indolizine derivatives as dual cyclooxygenase and lipoxygenase inhibitor for anti-inflammatory activity
Design, synthesis, and biological evaluation of some novel indolizine derivatives as dual cyclooxygenase and lipoxygenase inhibitor for anti-inflammatory activity
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Design, synthesis, and biological evaluation of some novel indolizine derivatives as dual cyclooxygenase and lipoxygenase inhibitor for anti-inflammatory activity

Shrivastava, Sushant K. ; Srivastava, Pavan ; Bandresh, Robin ; Tripathi, Prabhash Nath ; Tripathi, Avanish

Bioorganic & medicinal chemistry, 2017-08, Vol.25 (16), p.4424-4432 [Periódico revisado por pares]

England: Elsevier Ltd

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3
Design, synthesis, and biological activity of substituted 2-amino-5-oxo-5H-chromeno[2,3-b]pyridine-3-carboxylic acid derivatives as inhibitors of the inflammatory kinases TBK1 and IKKε for the treatment of obesity
Design, synthesis, and biological activity of substituted 2-amino-5-oxo-5H-chromeno[2,3-b]pyridine-3-carboxylic acid derivatives as inhibitors of the inflammatory kinases TBK1 and IKKε for the treatment of obesity
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Design, synthesis, and biological activity of substituted 2-amino-5-oxo-5H-chromeno[2,3-b]pyridine-3-carboxylic acid derivatives as inhibitors of the inflammatory kinases TBK1 and IKKε for the treatment of obesity

Beyett, Tyler S. ; Gan, Xinmin ; Reilly, Shannon M. ; Gomez, Andrew V. ; Chang, Louise ; Tesmer, John J.G. ; Saltiel, Alan R. ; Showalter, Hollis D.

Bioorganic & medicinal chemistry, 2018-11, Vol.26 (20), p.5443-5461 [Periódico revisado por pares]

England: Elsevier Ltd

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4
Tanshinones as selective and slow-binding inhibitors for SARS-CoV cysteine proteases
Tanshinones as selective and slow-binding inhibitors for SARS-CoV cysteine proteases
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Tanshinones as selective and slow-binding inhibitors for SARS-CoV cysteine proteases

Park, Ji-Young ; Kim, Jang Hoon ; Kim, Young Min ; Jeong, Hyung Jae ; Kim, Dae Wook ; Park, Ki Hun ; Kwon, Hyung-Jun ; Park, Su-Jin ; Lee, Woo Song ; Ryu, Young Bae

Bioorganic & medicinal chemistry, 2012-10, Vol.20 (19), p.5928-5935 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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5
N-(3,5-Dichloro-4-(2,4,6-trichlorophenoxy)phenyl)benzenesulfonamide: A new dual-target inhibitor of mitochondrial complex II and complex III via structural simplification
N-(3,5-Dichloro-4-(2,4,6-trichlorophenoxy)phenyl)benzenesulfonamide: A new dual-target inhibitor of mitochondrial complex II and complex III via structural simplification
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N-(3,5-Dichloro-4-(2,4,6-trichlorophenoxy)phenyl)benzenesulfonamide: A new dual-target inhibitor of mitochondrial complex II and complex III via structural simplification

Cheng, Hua ; Liu, Hong-Fu ; Yang, Lu ; Zhang, Rui ; Chen, Cheng ; Wu, Yuan ; Jiang, Wen

Bioorganic & medicinal chemistry, 2020-03, Vol.28 (5), p.115299, Article 115299 [Periódico revisado por pares]

England

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6
Design, synthesis, and biological evaluation of novel N-Benzyl piperidine derivatives as potent HDAC/AChE inhibitors for Alzheimer’s disease
Design, synthesis, and biological evaluation of novel N-Benzyl piperidine derivatives as potent HDAC/AChE inhibitors for Alzheimer’s disease
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Design, synthesis, and biological evaluation of novel N-Benzyl piperidine derivatives as potent HDAC/AChE inhibitors for Alzheimer’s disease

Qin, Pengxia ; Ran, Yingying ; Xie, Fei ; Liu, Yujing ; Wei, Chao ; Luan, Xiaoyi ; Wu, Jingde

Bioorganic & medicinal chemistry, 2023-02, Vol.80, p.117178-117178, Article 117178 [Periódico revisado por pares]

England: Elsevier Ltd

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7
Sulfonamides incorporating 1,3,5-triazine moieties selectively and potently inhibit carbonic anhydrase transmembrane isoforms IX, XII and XIV over cytosolic isoforms I and II: Solution and X-ray crystallographic studies
Sulfonamides incorporating 1,3,5-triazine moieties selectively and potently inhibit carbonic anhydrase transmembrane isoforms IX, XII and XIV over cytosolic isoforms I and II: Solution and X-ray crystallographic studies
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Sulfonamides incorporating 1,3,5-triazine moieties selectively and potently inhibit carbonic anhydrase transmembrane isoforms IX, XII and XIV over cytosolic isoforms I and II: Solution and X-ray crystallographic studies

Carta, Fabrizio ; Garaj, Vladimir ; Maresca, Alfonso ; Wagner, Jason ; Avvaru, Balendu Sankara ; Robbins, Arthur H. ; Scozzafava, Andrea ; McKenna, Robert ; Supuran, Claudiu T.

Bioorganic & medicinal chemistry, 2011-05, Vol.19 (10), p.3105-3119 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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8
Novel pyrazoline derivatives as bi-inhibitor of COX-2 and B-Raf in treating cervical carcinoma
Novel pyrazoline derivatives as bi-inhibitor of COX-2 and B-Raf in treating cervical carcinoma
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Novel pyrazoline derivatives as bi-inhibitor of COX-2 and B-Raf in treating cervical carcinoma

Yu, Minmin ; Yang, Hui ; Wu, Kaihua ; Ji, Ying ; Ju, Lili ; Lu, Xiaoyuan

Bioorganic & medicinal chemistry, 2014-08, Vol.22 (15), p.4109-4118 [Periódico revisado por pares]

England: Elsevier Ltd

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9
The discovery of 2,5-isomers of triazole-pyrrolopyrimidine as selective Janus kinase 2 (JAK2) inhibitors versus JAK1 and JAK3
The discovery of 2,5-isomers of triazole-pyrrolopyrimidine as selective Janus kinase 2 (JAK2) inhibitors versus JAK1 and JAK3
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The discovery of 2,5-isomers of triazole-pyrrolopyrimidine as selective Janus kinase 2 (JAK2) inhibitors versus JAK1 and JAK3

Lee, Sun-Mi ; Yoon, Kyoung Bin ; Lee, Hyo Jeong ; Kim, Jiwon ; Chung, You Kyoung ; Cho, Won-Jea ; Mukai, Chisato ; Choi, Sun ; Kang, Keon Wook ; Han, Sun-Young ; Ko, Hyojin ; Kim, Yong-Chul

Bioorganic & medicinal chemistry, 2016-11, Vol.24 (21), p.5036-5046 [Periódico revisado por pares]

England: Elsevier Ltd

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10
Discovery of a potent inhibitor of MELK that inhibits expression of the anti-apoptotic protein Mcl-1 and TNBC cell growth
Discovery of a potent inhibitor of MELK that inhibits expression of the anti-apoptotic protein Mcl-1 and TNBC cell growth
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Discovery of a potent inhibitor of MELK that inhibits expression of the anti-apoptotic protein Mcl-1 and TNBC cell growth

Edupuganti, Ramakrishna ; Taliaferro, Juliana M. ; Wang, Qiantao ; Xie, Xuemei ; Cho, Eun Jeong ; Vidhu, Fnu ; Ren, Pengyu ; Anslyn, Eric V. ; Bartholomeusz, Chandra ; Dalby, Kevin N.

Bioorganic & medicinal chemistry, 2017-05, Vol.25 (9), p.2609-2616 [Periódico revisado por pares]

England: Elsevier Ltd

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