Design potential selective inhibitors for human leukocyte common antigen-related (PTP-LAR) with fragment replace approach. Issue 18 (11th December 2020)
- Record Type:
- Journal Article
- Title:
- Design potential selective inhibitors for human leukocyte common antigen-related (PTP-LAR) with fragment replace approach. Issue 18 (11th December 2020)
- Main Title:
- Design potential selective inhibitors for human leukocyte common antigen-related (PTP-LAR) with fragment replace approach
- Authors:
- Wu, Jing-Wei
Zhang, Huan
Li, Wei-Ya
Tang, Xue
Li, Hong-Lian
Lu, Xin-Hua
Zheng, Zhi-Hui
Ma, Ying
Wang, Run-Ling - Abstract:
- Abstract: The overexpression of PTP-LAR could cause the insulin resistance, so PTP-LAR might be a promising target for treating diabetes. In this study, we applied the computer modeling methods with fragment replace approach to screen the fragment database by targeting PTP domain and site B with the aim to discover potent and selective PTP-LAR inhibitors. A series of novel 4-thiazolidone derivatives were gained. The results of their ADMET predictions indicated that these new compounds might become drug candidates. The series of these derivatives were synthesized. Subsequently, their PTP-LAR inhibitory activities were assayed. The compound7d showed highly selectivity for PTP-LAR (10.41 μM) over its close homolog PTP1B (IC50 =44.40 μM), SHP2 (IC50 >122.81 μM) and CDC25B (IC50 >122.81 μM) and docking and molecular dynamics simulation were applied to propose the most likely binding mode of compound7d with PTP-LAR. Thus, our findings reported here may pave a way for discovering potential selective PTP-LAR inhibitors. Abbreviations: PTP-LAR Human leukocyte common antigen-related PTP Protein Tyrosine Phosphatase IR insulin receptor PTP1B Protein tyrosine phosphatase-1B LRP Lung resistance protein ADMET absorption, distribution, metabolism, excretion, toxicity PPB plasma protein binding BBB blood brain barrier penetration CYP450 cytochrome P450 HIA human intestinal absorption TLC thin-layer chromatography UV Ultra Violet NMR nuclear magnetic resonance TMS tetramethylsilane MS massAbstract: The overexpression of PTP-LAR could cause the insulin resistance, so PTP-LAR might be a promising target for treating diabetes. In this study, we applied the computer modeling methods with fragment replace approach to screen the fragment database by targeting PTP domain and site B with the aim to discover potent and selective PTP-LAR inhibitors. A series of novel 4-thiazolidone derivatives were gained. The results of their ADMET predictions indicated that these new compounds might become drug candidates. The series of these derivatives were synthesized. Subsequently, their PTP-LAR inhibitory activities were assayed. The compound7d showed highly selectivity for PTP-LAR (10.41 μM) over its close homolog PTP1B (IC50 =44.40 μM), SHP2 (IC50 >122.81 μM) and CDC25B (IC50 >122.81 μM) and docking and molecular dynamics simulation were applied to propose the most likely binding mode of compound7d with PTP-LAR. Thus, our findings reported here may pave a way for discovering potential selective PTP-LAR inhibitors. Abbreviations: PTP-LAR Human leukocyte common antigen-related PTP Protein Tyrosine Phosphatase IR insulin receptor PTP1B Protein tyrosine phosphatase-1B LRP Lung resistance protein ADMET absorption, distribution, metabolism, excretion, toxicity PPB plasma protein binding BBB blood brain barrier penetration CYP450 cytochrome P450 HIA human intestinal absorption TLC thin-layer chromatography UV Ultra Violet NMR nuclear magnetic resonance TMS tetramethylsilane MS mass spectrometry ANM anisotropic network mode PDB Protein Data Bank DMF N, N-Dimethylformamide pNPP para-nitrophenyl phosphate DTT dithiothreitol MD molecular dynamic RMSD root-mean-square deviation RMSF root-mean-square fluctuation SPC single-point charge PME Particle Mesh Ewald MM-PBSA molecular mechanics Poisson Boltzmann surface area H bond, hydrogen bond VDW Van der Waals Communicated by Ramaswamy H. Sarma … (more)
- Is Part Of:
- Journal of biomolecular structure & dynamics. Volume 38:Issue 18(2020)
- Journal:
- Journal of biomolecular structure & dynamics
- Issue:
- Volume 38:Issue 18(2020)
- Issue Display:
- Volume 38, Issue 18 (2020)
- Year:
- 2020
- Volume:
- 38
- Issue:
- 18
- Issue Sort Value:
- 2020-0038-0018-0000
- Page Start:
- 5338
- Page End:
- 5348
- Publication Date:
- 2020-12-11
- Subjects:
- PTP-LAR -- fragment replace -- synthesis -- docking -- molecular dynamics
Biomolecules -- Periodicals
Molecular structure -- Periodicals
Molecular Biology -- Periodicals
Biomechanics -- Periodicals
572 - Journal URLs:
- http://www.tandfonline.com/loi/tbsd20 ↗
http://www.tandfonline.com/ ↗ - DOI:
- 10.1080/07391102.2019.1699862 ↗
- Languages:
- English
- ISSNs:
- 0739-1102
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4953.850000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 14610.xml