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Identification of novel small-molecule inhibitors of α-methylacyl-CoA racemase (AMACR; P504S) and structure-activity relationships
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Identification of novel small-molecule inhibitors of α-methylacyl-CoA racemase (AMACR; P504S) and structure-activity relationships

Petrova, Yoana ; Wadda, Katty ; Nathubhai, Amit ; Jevglevskis, Maksims ; Mitchell, Paul ; James, Tony ; Threadgill, Michael ; Woodman, Tim ; Lloyd, Matthew

Bioorganic Chemistry, 2019-11, Vol.92, Article 103264 [Periódico revisado por pares]

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Identification of novel small-molecule inhibitors of α-methylacyl-CoA racemase (AMACR; P504S) and structure-activity relationships
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Artigo
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Identification of novel small-molecule inhibitors of α-methylacyl-CoA racemase (AMACR; P504S) and structure-activity relationships

Petrova, Yoana D. ; Wadda, Katty ; Nathubhai, Amit ; Yevglevskis, Maksims ; Mitchell, Paul J. ; James, Tony D. ; Threadgill, Michael D. ; Woodman, Timothy J. ; Lloyd, Matthew D.

Bioorganic chemistry, 2019-11, Vol.92, p.103264, Article 103264 [Periódico revisado por pares]

United States: Elsevier Inc

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Novel 2-arylthiopropanoyl-CoA inhibitors of α-methylacyl-CoA racemase 1A (AMACR; P504S) as potential anti-prostate cancer agents
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Artigo
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Novel 2-arylthiopropanoyl-CoA inhibitors of α-methylacyl-CoA racemase 1A (AMACR; P504S) as potential anti-prostate cancer agents

Yevglevskis, Maksims ; Nathubhai, Amit ; Wadda, Katty ; Lee, Guat L. ; Al-Rawi, Suzanne ; Jiao, Tingying ; Mitchell, Paul J. ; James, Tony D. ; Threadgill, Michael D. ; Woodman, Timothy J. ; Lloyd, Matthew D.

Bioorganic chemistry, 2019-11, Vol.92, p.103263, Article 103263 [Periódico revisado por pares]

United States: Elsevier Inc

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Design, synthesis, and biological evaluation of novel indanone-based hybrids as multifunctional cholinesterase inhibitors for Alzheimer's disease
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Artigo
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Design, synthesis, and biological evaluation of novel indanone-based hybrids as multifunctional cholinesterase inhibitors for Alzheimer's disease

Shahrivar-Gargari, Mohammad ; Hamzeh-Mivehroud, Maryam ; Hemmati, Salar ; Shahbazi Mojarrad, Javid ; Notash, Behrouz ; Tüylü Küçükkılınç, Tuba ; Ayazgök, Beyza ; Dastmalchi, Siavoush

Journal of molecular structure, 2021-04, Vol.1229, p.129787, Article 129787 [Periódico revisado por pares]

Elsevier B.V

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Characterization of nimbidiol as a potent intestinal disaccharidase and glucoamylase inhibitor present in Azadirachta indica (neem) useful for the treatment of diabetes
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Characterization of nimbidiol as a potent intestinal disaccharidase and glucoamylase inhibitor present in Azadirachta indica (neem) useful for the treatment of diabetes

Mukherjee, Abhishek ; Sengupta, Subhabrata

Journal of enzyme inhibition and medicinal chemistry, 2013-10, Vol.28 (5), p.900-910 [Periódico revisado por pares]

England: Informa Healthcare

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The Relevance of Glutathione Reductase Inhibition by Fluoxetine to Human Health and Disease: Insights Derived from a Combined Kinetic and Docking Study
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The Relevance of Glutathione Reductase Inhibition by Fluoxetine to Human Health and Disease: Insights Derived from a Combined Kinetic and Docking Study

Dalmizrak, Ozlem ; Teralı, Kerem ; Asuquo, Evelyn Bright ; Ogus, Izzet Hamdi ; Ozer, Nazmi

The Protein Journal, 2019-10, Vol.38 (5), p.515-524 [Periódico revisado por pares]

New York: Springer US

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Synthesis and in vitro evaluation of botryllazine B analogues as a new class of inhibitor against human aldose reductase
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Synthesis and in vitro evaluation of botryllazine B analogues as a new class of inhibitor against human aldose reductase

Saito, Ryota ; Tokita, Mai ; Uda, Keisuke ; Ishikawa, Chikako ; Satoh, Mitsutoshi

Tetrahedron, 2009-04, Vol.65 (15), p.3019-3026 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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A Kunitz trypsin inhibitor of Entada scandens seeds: Another member with single disulfide bridge
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A Kunitz trypsin inhibitor of Entada scandens seeds: Another member with single disulfide bridge

Lingaraju, M.H. ; Gowda, Lalitha R.

Biochimica et biophysica acta. Proteins and proteomics, 2008-05, Vol.1784 (5), p.850-855 [Periódico revisado por pares]

Elsevier B.V

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Oleuropein potently inhibits mammalian target of rapamycin: possible involvement of tandem anomeric hyperconjugation–Michael reaction
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Oleuropein potently inhibits mammalian target of rapamycin: possible involvement of tandem anomeric hyperconjugation–Michael reaction

Taha, Mutasem O. ; Khanfar, Mohammad A.

Medicinal chemistry research, 2015-02, Vol.24 (2), p.616-623 [Periódico revisado por pares]

Boston: Springer US

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10
Kinetic and inhibition studies for the aerobic cometabolism of 1,1,1-trichloroethane, 1,1-dichloroethylene, and 1,1-dichloroethane by a butane-grown mixed culture
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Kinetic and inhibition studies for the aerobic cometabolism of 1,1,1-trichloroethane, 1,1-dichloroethylene, and 1,1-dichloroethane by a butane-grown mixed culture

Kim, Young ; Arp, Daniel J. ; Semprini, Lewis

Biotechnology and bioengineering, 2002-12, Vol.80 (5), p.498-508 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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