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1-benzyl-2-phenylbenzimidazole (BPB), a benzimidazole derivative, induces cell apoptosis in human chondrosarcoma through intrinsic and extrinsic pathways
1-benzyl-2-phenylbenzimidazole (BPB), a benzimidazole derivative, induces cell apoptosis in human chondrosarcoma through intrinsic and extrinsic pathways
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1-benzyl-2-phenylbenzimidazole (BPB), a benzimidazole derivative, induces cell apoptosis in human chondrosarcoma through intrinsic and extrinsic pathways

Liu, Ju-Fang ; Huang, Yuan-Li ; Yang, Wei-Hung ; Chang, Chih-Shiang ; Tang, Chih-Hsin

International journal of molecular sciences, 2012-12, Vol.13 (12), p.16472-16488 [Periódico revisado por pares]

Switzerland: MDPI AG

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2
1-Deoxynojirimycin Alleviates Insulin Resistance via Activation of Insulin Signaling PI3K/AKT Pathway in Skeletal Muscle of db/db Mice
1-Deoxynojirimycin Alleviates Insulin Resistance via Activation of Insulin Signaling PI3K/AKT Pathway in Skeletal Muscle of db/db Mice
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1-Deoxynojirimycin Alleviates Insulin Resistance via Activation of Insulin Signaling PI3K/AKT Pathway in Skeletal Muscle of db/db Mice

Liu, Qingpu ; Li, Xuan ; Li, Cunyu ; Zheng, Yunfeng ; Peng, Guoping

Molecules (Basel, Switzerland), 2015-12, Vol.20 (12), p.21700-21714 [Periódico revisado por pares]

Switzerland: MDPI AG

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3
10-Alkoxy-anthracenyl-isoxazole analogs have sub-micromolar activity against a Glioblastoma multiforme cell line
10-Alkoxy-anthracenyl-isoxazole analogs have sub-micromolar activity against a Glioblastoma multiforme cell line
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10-Alkoxy-anthracenyl-isoxazole analogs have sub-micromolar activity against a Glioblastoma multiforme cell line

Duncan, Nathan S. ; Campbell, Michael J. ; Backos, Donald S. ; Li, Chun ; Rider, Kevin C. ; Stump, Sascha ; Weaver, Matthew J. ; Gajewski, Mariusz P. ; Beall, Howard D. ; Reigan, Philip ; Natale, Nicholas R.

Bioorganic & medicinal chemistry, 2022-09, Vol.69, p.116911-116911, Article 116911 [Periódico revisado por pares]

Elsevier Ltd

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4
10-N-heterocylic aryl-isoxazole-amides (AIMs) have robust anti-tumor activity against breast and brain cancer cell lines and useful fluorescence properties
10-N-heterocylic aryl-isoxazole-amides (AIMs) have robust anti-tumor activity against breast and brain cancer cell lines and useful fluorescence properties
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10-N-heterocylic aryl-isoxazole-amides (AIMs) have robust anti-tumor activity against breast and brain cancer cell lines and useful fluorescence properties

Weaver, Matthew J. ; Stump, Sascha ; Campbell, Michael J. ; Backos, Donald S. ; Li, Chun ; Reigan, Philip ; Adams, Earle ; Beall, Howard D. ; Natale, Nicholas R.

Bioorganic & medicinal chemistry, 2020-11, Vol.28 (22), p.115781-115781, Article 115781 [Periódico revisado por pares]

England: Elsevier Ltd

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5
[12] Relationships of human immunodeficiency virus protease with eukaryotic aspartic proteases
[12] Relationships of human immunodeficiency virus protease with eukaryotic aspartic proteases
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[12] Relationships of human immunodeficiency virus protease with eukaryotic aspartic proteases

Lin, Xin-li ; Lin, Ying-zhang ; Tang, Jordan

Methods in Enzymology, 1994, Vol.241, p.195-224 [Periódico revisado por pares]

United States: Elsevier Science & Technology

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6
1,2,4-Thiadiazole: A novel Cathepsin B inhibitor
1,2,4-Thiadiazole: A novel Cathepsin B inhibitor
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1,2,4-Thiadiazole: A novel Cathepsin B inhibitor

Leung-Toung, Regis ; Wodzinska, Jolanta ; Li, Wanren ; Lowrie, Jayme ; Kukreja, Rahul ; Desilets, Denis ; Karimian, Khashayar ; Tam, Tim Fat

Bioorganic & medicinal chemistry, 2003-12, Vol.11 (24), p.5529-5537 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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7
1,25-Dihydroxyvitamin D3 and 20-Hydroxyvitamin D3 Upregulate LAIR-1 and Attenuate Collagen Induced Arthritis
1,25-Dihydroxyvitamin D3 and 20-Hydroxyvitamin D3 Upregulate LAIR-1 and Attenuate Collagen Induced Arthritis
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1,25-Dihydroxyvitamin D3 and 20-Hydroxyvitamin D3 Upregulate LAIR-1 and Attenuate Collagen Induced Arthritis

Myers, Linda K ; Winstead, Michael ; Kee, John D ; Park, Jeoungeun J ; Zhang, Sicheng ; Li, Wei ; Yi, Ae-Kyung ; Stuart, John M ; Rosloniec, Edward F ; Brand, David D ; Tuckey, Robert C ; Slominski, Andrzej T ; Postlethwaite, Arnold E ; Kang, Andrew H

International journal of molecular sciences, 2021-12, Vol.22 (24), p.13342 [Periódico revisado por pares]

Switzerland: MDPI AG

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8
1,2,5-Thiadiazolidin-3-one 1,1 Dioxide: A Powerful Scaffold for Probing the S′ Subsites of (Chymo)trypsin-Like Serine Proteases
1,2,5-Thiadiazolidin-3-one 1,1 Dioxide: A Powerful Scaffold for Probing the S′ Subsites of (Chymo)trypsin-Like Serine Proteases
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1,2,5-Thiadiazolidin-3-one 1,1 Dioxide: A Powerful Scaffold for Probing the S′ Subsites of (Chymo)trypsin-Like Serine Proteases

Groutas, William C. ; Epp, Jeffrey B. ; Kuang, Rongze ; Ruan, Sumei ; Chong, Lee S. ; Venkataraman, Radhika ; Tu, Juan ; He, Shu ; Yu, Hongyi ; Fu, Qinghong ; Li, Yue He ; Truong, Tien M. ; Vu, Nga T.

Archives of biochemistry and biophysics, 2001-01, Vol.385 (1), p.162-169 [Periódico revisado por pares]

United States: Elsevier Inc

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9
129/Sv mice--a model system for studying germ cell biology and testicular cancer
129/Sv mice--a model system for studying germ cell biology and testicular cancer
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129/Sv mice--a model system for studying germ cell biology and testicular cancer

Jiang, L I ; Nadeau, J H

Mammalian genome, 2001-02, Vol.12 (2), p.89-94 [Periódico revisado por pares]

United States: Springer Nature B.V

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10
14-3-3 adaptor proteins recruit AID to 5′-AGCT-3′-rich switch regions for class switch recombination
14-3-3 adaptor proteins recruit AID to 5′-AGCT-3′-rich switch regions for class switch recombination
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14-3-3 adaptor proteins recruit AID to 5′-AGCT-3′-rich switch regions for class switch recombination

Pone, Egest J ; Mai, Thach ; White, Clayton A ; Li, Zenggang ; Yates, John ; Zhang, Jinsong ; Park, Seok-Rae ; Casali, Paolo ; Thomas, Lisa M ; Otto, Markus ; Fulop, Zsolt ; Wu, Guikai ; Xu, Zhenming ; Steinacker, Petra ; Herron, Bruce ; Al-Qahtani, Ahmed ; Fu, Haian ; Zan, Hong

Nature structural & molecular biology, 2010-09, Vol.17 (99), p.1124-1135 [Periódico revisado por pares]

United States: Nature Publishing Group

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