Rational Design and Simple Chemistry Yield a Superior, Neuroprotective HDAC6 Inhibitor, Tubastatin A
Butler, Kyle V., Kalin, Jay, Brochier, Camille, Vistoli, Guilio, Langley, Brett, Kozikowski, Alan P.·2010·Journal of the American Chemical Society
Cited by (902)
Items 801–900 of 902
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- BindingDB Entry 50007194: Highly fluorescent and HDAC6 selective scriptaid analogues.BindingDB · 2021 · UC San Diego
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- BindingDB Entry 50012231: PTG-0861: A novel HDAC6-selective inhibitor as a therapeutic strategy in acute myeloid leukaemia.BindingDB · 2022 · UC San Diego
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- BindingDB Entry 50000059: Design, Multicomponent Synthesis, and Anticancer Activity of a Focused Histone Deacetylase (HDAC) Inhibitor Library with Peptoid-Based Cap Groups.BindingDB · 2019 · UC San Diego
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- BindingDB Entry 50022156: Contilisant+Tubastatin A Hybrids: Polyfunctionalized Indole Derivatives as New HDAC Inhibitor-Based Multitarget Small Molecules with In Vitro and In Vivo Activity in Neurodegenerative Diseases.BindingDB · 2025 · UC San Diego
- BindingDB Entry 50047055: Design, Synthesis, and Pharmacological Evaluation of Novel N-Acylhydrazone Derivatives as Potent Histone Deacetylase 6/8 Dual Inhibitors.BindingDB · 2017 · UC San Diego
- BindingDB Entry 50007718: Discovery of Novel Janus Kinase (JAK) and Histone Deacetylase (HDAC) Dual Inhibitors for the Treatment of Hematological Malignancies.BindingDB · 2021 · UC San Diego
- BindingDB Entry 50032567: Inhibitors selective for HDAC6 in enzymes and cells.BindingDB · 2011 · UC San Diego
- BindingDB Entry 50013057: Novel quinolone-based potent and selective HDAC6 inhibitors: Synthesis, molecular modeling studies and biological investigation.BindingDB · 2022 · UC San Diego
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- BindingDB Entry 50007910: Discovery of a New Isoxazole-3-hydroxamate-Based Histone Deacetylase 6 Inhibitor SS-208 with Antitumor Activity in Syngeneic Melanoma Mouse Models.BindingDB · 2021 · UC San Diego
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- BindingDB Entry 50009674: Novel Benzohydroxamate-Based Potent and Selective Histone Deacetylase 6 (HDAC6) Inhibitors Bearing a Pentaheterocyclic Scaffold: Design, Synthesis, and Biological Evaluation.BindingDB · 2021 · UC San Diego
- BindingDB Entry 50005915: Synthesis and structure-activity relationship of 3-hydroxypyridine-2-thione-based histone deacetylase inhibitors.BindingDB · 2020 · UC San Diego
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- BindingDB Entry 50044729: The antileishmanial activity of isoforms 6- and 8-selective histone deacetylase inhibitors.BindingDB · 2016 · UC San Diego
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- BindingDB Entry 50010615: Structural and in Vivo Characterization of Tubastatin A, a Widely Used Histone Deacetylase 6 Inhibitor.BindingDB · 2021 · UC San Diego
- BindingDB Entry 50021935: Re-exploration of tetrahydro-β-carboline scaffold: Discovery of selective histone deacetylase 6 inhibitors with neurite outgrowth-promoting and neuroprotective activities.BindingDB · 2025 · UC San Diego
- BindingDB Entry 50002898: The structural requirements of histone deacetylase inhibitors: C4-modified SAHA analogs display dual HDAC6/HDAC8 selectivity.BindingDB · 2020 · UC San Diego
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- BindingDB Entry 50045731: Design and synthesis of orally bioavailable aminopyrrolidinone histone deacetylase 6 inhibitors.BindingDB · 2016 · UC San Diego
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- BindingDB Entry 50040017: Design, synthesis, modeling, biological evaluation and photoaffinity labeling studies of novel series of photoreactive benzamide probes for histone deacetylase 2.BindingDB · 2013 · UC San Diego
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- BindingDB Entry 50022374: Tetrahydro-β-carboline derivatives as potent histone deacetylase 6 inhibitors with broad-spectrum antiproliferative activity.BindingDB · 2025 · UC San Diego
- BindingDB Entry 50015248: Discovery of Novel Histone Deacetylase 6 (HDAC6) Inhibitors with Enhanced Antitumor Immunity of Anti-PD-L1 Immunotherapy in Melanoma.BindingDB · 2023 · UC San Diego
- BindingDB Entry 50033283: Discovery of histone deacetylase 8 selective inhibitors.BindingDB · 2011 · UC San Diego
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- BindingDB Entry 50040629: Novel histone deacetylase 8 ligands without a zinc chelating group: exploring an 'upside-down' binding pose.BindingDB · 2013 · UC San Diego
- BindingDB Entry 50000899: Marbostat-100 Defines a New Class of Potent and Selective Antiinflammatory and Antirheumatic Histone Deacetylase 6 Inhibitors.BindingDB · 2020 · UC San Diego
- BindingDB Entry 50042784: 3-Hydroxypyridin-2-thione as novel zinc binding group for selective histone deacetylase inhibition.BindingDB · 2013 · UC San Diego
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- Targeting the catalytic and ZnF-UBP domains of HDAC6 differentially controls NLRP3 inflammasome priming and assembly in paclitaxel-induced peripheral neuropathyHaoran Ying, Ruizhu Yue, Jin Zhang, Xing Guo, Jinsong Li, Wenyu Mo, Yue Hao · 2026 · Pharmacological Research
- Structure-activity relationship and target identification of marine anthranilamides as anti-inflammatory agentsYue Zhou, Guifeng Ji, Ya Chen, Liangzhou Li, Xiangyu Wang, Ahmed Naseer, Xuanyi Xue, Jichen Yang, Tao Lu, Lujie Wang et al. · 2026 · European Journal of Medicinal Chemistry