Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Md Rimon Parves"'
1
Molecular dynamics-based insight of VEGFR-2 kinase domain: a combined study of pharmacophore modeling and molecular docking and dynamics
Autor: Md Rimon, Parves, Yasir Mohamed, Riza, Sanjida, Alam, Sadia, Jaman
Publikováno v: Journal of Molecular Modeling. 29
Inhibition of vascular endothelial growth factor receptor 2 (VEGFR-2) tyrosine kinase by small molecules has become a promising target in the treatment of cancer.In this study, we approached pharmacophore modeling coupled with a structure-based virtu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdbee8300710681ab99cd1839ad978fa
https://doi.org/10.1007/s00894-022-05427-x
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2
Exploring the potent inhibitors and binding modes of phospholipase A2 through in silico investigation
Autor: Shafi Mahmud, Nurul Absar, Zannati Ferdous Zaoti, Yasir Mohamed Riza, Sanjida Alam, Md. Rimon Parves, Suvendu Ray, Khaled Mahmud Sujon, Fahmida Alam Tithi
Publikováno v: Journal of Biomolecular Structure and Dynamics. 38:4221-4231
Snake venom of Naja naja comprises of several types of enzymes, and among them, water-soluble proteolytic enzyme, phospholipase A2 (PLA2), is noteworthy for its numerous adverse effects, such as cy...
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a96cd2a64e4627e725ef1de1fc422723
https://doi.org/10.1080/07391102.2019.1680440
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3
Designing potent inhibitors against the multidrug resistance P-glycoprotein
Autor: Mohammad A. Halim, Md. Rimon Parves, Sayo O. Fakayode, Md. Arif Khan, Lamiya Tabussum, Shafi Mahmud, Md. Ackas Ali, Md. Jahirul Islam, Sinthyia Ahmed
Publikováno v: Journal of biomolecular structuredynamics. 40(19)
The multidrug transporter P-glycoprotein is an ATP binding cassette (ABC) exporter responsible for resistance to tumor cells during chemotherapy. This study was designed with computational approaches aimed at identifying the best potent inhibitors of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::333e4b8d7eb1141f7b5692315d657492
https://pubmed.ncbi.nlm.nih.gov/34060432
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4
Inhibition of TNF-Alpha Using Plant-Derived Small Molecules for Treatment of Inflammation-Mediated Diseases
Autor: Nabila Rahman Jui, Yasir Mohamed Riza, M.M. Alam, Nurul Absar, Md. Iftekhar Alam Chowdhury, Khaled Mahmud Sujon, Mohammad Abu Raihan Uddin, Saiful Islam, Shafi Mahmud, Fahmida Alam Tithi, Md. Jahirul Islam, Md. Rimon Parves
Publikováno v: The 1st International Electronic Conference on Biomolecules: Natural and Bio-Inspired Therapeutics for Human Diseases.
Inhibition of tumor necrosis factor-alpha (TNF-α) has become a feasible target for alleviating inflammation-mediated diseases. Currently, techniques developed, such as anti-TNF antibody therapies, prove not to be nearly as beneficial enough to effec
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d636014bb8cc1bc7953aba8f0a085ac4
https://doi.org/10.3390/iecbm2020-08586
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5
Analysis of Ten Microsecond simulation data of SARS-CoV-2 dimeric main protease
Autor: Shafi Mahmud, Mirza Hasanuzzaman, Yasir Mohamed Riza, Md. Rimon Parves, Mohammad A. Halim, Sinthyia Ahmed, R. Islam, Bibi Ashiana Evy
The dimeric main protease of SARS-CoV-2, has become a crucial target for inhibiting/modulating its catalytic activity. However, understanding of its conformational change, and atomistic flexibility, is very much lucrative for designing/developing sma
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ad3f620f62984595bea18ed473c8269
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7
Prediction of Deleterious Non-synonymous SNPs of Human STK11 Gene by Combining Algorithms, Molecular Docking, and Molecular Dynamics Simulation
Autor: Mohammad A. Halim, Akib Mahmud Khan, Nayeem Hossain, Md. Rimon Parves, Md. Jahirul Islam
Publikováno v: Scientific Reports, Vol 9, Iss 1, Pp 1-16 (2019)
Scientific Reports
Serine-threonine kinase11 (STK11) is a tumor suppressor gene which plays a key role in regulating cell growth and apoptosis. It is widely known as a multitasking kinase and engaged in cell polarity, cell cycle arrest, chromatin remodeling, energy met
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66282af1f7bd9591a970b26e6b15ad9f
https://doi.org/10.1038/s41598-019-52308-0
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8
Quantum chemical calculation and binding modes of H1R; a combined study of molecular docking and DFT for suggesting therapeutically potent H1R antagonist
Autor: Yasir Mohamed Riza, Fahmida Alam Tithi, Sanjida Alam, Md. Rimon Parves
Histamine-1 receptor (H1R) belongs to the family of rhodopsin-like G-protein-coupled receptors expressed in cells that mediates allergies and other pathophysiological diseases. For alleviation of allergic symptoms, H1R antagonists are therapeutic dru
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dab3c8f55229b7fc18784859a30aac9e
https://europepmc.org/articles/PMC6389732/
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10
Assessment of structurally and functionally high-risk nsSNPs impacts on human bone morphogenetic protein receptor type IA (BMPR1A) by computational approach
Autor: Md. Abu Reza, Shafi Mahmud, Md. Jahirul Islam, Md. Rimon Parves, Fahmida Alam Tithi
Publikováno v: Computational biology and chemistry. 80
BMPR1A (BMP type 1 receptor) is a transmembrane cell-surface receptor also known as ALK3 (activin-like kinases-3) encodes for a type I serine/threonine kinase receptor and a member of the transforming growth-factor β–receptor (TGF-β) super family
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63f2c7eb26e645538c5f5518a2b0a81d
https://pubmed.ncbi.nlm.nih.gov/30884445
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