Search Results - "Pissurlenkar, Raghuvir R.S"
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Identification of novel potential anti-diabetic candidates targeting human pancreatic [alpha]-amylase and human [alpha]-glycosidase: an exhaustive structure-based screening
Published in Canadian journal of chemistry (01-05-2022)“…Diabetes is a major health issue that has reached alarming levels, affecting nearly half a billion people worldwide. It is a serious and long-term medical…”
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Identification of novel potential anti-diabetic candidates targeting human pancreatic α-amylase and human α-glycosidase: an exhaustive structure-based screening
Published in Canadian journal of chemistry (01-05-2022)“…Diabetes is a major health issue that has reached alarming levels, affecting nearly half a billion people worldwide. It is a serious and long-term medical…”
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Synthesis, in-silico studies, and biological evaluation of some novel 3-thiazolyl-indoles as CDK2–inhibitors
Published in Results in Chemistry (01-12-2023)“…The essential enzyme cyclin-dependent kinase 2 (CDK2) is a promising target for anticancer drug development due to its pivotal role in regulating the cell…”
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Extracting structural requirements for activity of GPR119 agonists: a hologram quantitative structure activity relationship (HQSAR) study
Published in Canadian journal of chemistry (01-07-2014)“…GPR119 is a potential target for the treatment of diabetes mellitus. GPR119 agonists minimize the side-effects observed with sulphonyl ureas and glucagon-like…”
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Identification of new checkpoint kinase-1 (Chk1) inhibitors by docking, 3D-QSAR, and pharmacophore-modeling methods
Published in Canadian journal of chemistry (01-08-2012)“…Inhibition of checkpoint kinase-1 (Chk1) by small molecules is of great therapeutic interest in the field of oncology and for understanding cell-cycle…”
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Comprehensive computational study in the identification of novel potential cholesterol lowering agents targeting proprotein convertase subtilisin/kexin type 9
Published in Journal of biomolecular structure & dynamics (12-06-2024)“…The enzymatic target proprotein convertase subtilisin/kexin type 9 (PCSK9) is critically involved in the regulation of the lipoprotein metabolism leading to…”
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Synthesis, biological screening and in silico studies of new N-phenyl-4-(1,3-diaryl-1H-pyrazol-4-yl)thiazol-2-amine derivatives as potential antifungal and antitubercular agents
Published in European journal of medicinal chemistry (05-10-2023)“…A new series of N-aryl-4-(1,3-diaryl-1H-pyrazol-4-yl)thiazol-2-amine, (8a-x) have been synthesized by a cyclo-condensation reaction of…”
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Synthesis, antidiabetic activity and in silico studies of benzo[b]thiophene based small molecule α-amylase inhibitors
Published in Journal of molecular structure (15-09-2024)“…•Benzo[b]thiophene based small molecule α-amylase inhibitors.•Significant antidiabetic activity with IC50 ranging from 5.37 to 29.89 μM.•Compound 3b more…”
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Solvent-free synthesis, biological evaluation and in silico studies of novel 2-amino-7-(bis(2-hydroxyethyl)amino)-4H-chromene-3-carbonitrile derivatives as potential a-amylase inhibitors
Published in Journal of molecular structure (05-04-2024)“…•Solvent free multicomponent protocol for novel 2-amino-4H-chromene derivatives.•Structure determination by IR, mass, 1H & 13C NMR spectroscopy and elemental…”
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Curcumin and kaempferol prevent lysozyme fibril formation by modulating aggregation kinetic parameters
Published in Biochimica et biophysica acta (01-03-2014)“…Interaction of small molecule inhibitors with protein aggregates has been studied extensively, but how these inhibitors modulate aggregation kinetic parameters…”
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The reorganization of conformations, stability and aggregation of serum albumin isomers through the interaction of glycopeptide antibiotic teicoplanin: A thermodynamic and spectroscopy study
Published in International journal of biological macromolecules (15-11-2020)“…The drugs-protein binding study is of growing importance for drug-repurposing against amyloidosis. In this work, we study the binding of teicoplanin (TPN), a…”
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New thiazolyl-isoxazole derivatives as potential anti-infective agents: design, synthesis, in vitro and in silico antimicrobial efficacy
Published in Journal of biomolecular structure & dynamics (23-01-2024)“…Antimicrobial resistance threatens the efficacious prevention and treatment of infectious diseases caused by microorganisms. To combat microbial infections,…”
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An Efficient Synthesis, Antimicrobial Evaluation and In Silico Studies of 1,2,3‐Triazolyl‐isoxazolyl‐ethanol Derivatives
Published in ChemistrySelect (Weinheim) (05-02-2024)“…A series of 2‐(1‐substituted benzyl‐1H‐1,2,3‐triazol‐4‐yl)‐1‐(5‐arylisoxazol‐3‐yl)ethanol (8 a–p) have been designed and efficiently synthesized. The structure…”
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Physical basis for the ofloxacin-induced acceleration of lysozyme aggregation and polymorphism in amyloid fibrils
Published in Archives of biochemistry and biophysics (15-02-2016)“…Aggregation of globular proteins is an intractable problem which generally originates from partially folded structures. The partially folded structures first…”
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The cocrystal of 3-((4-(3-isocyanobenzyl) piperazine-1-yl) methyl) benzonitrile with 5-hydroxy isophthalic acid prevents protofibril formation of serum albumin
Published in Journal of biomolecular structure & dynamics (02-01-2022)“…The formation of amyloid-like fibrils is a central problem in biophysical chemistry and medicine. Fibril formation and their deposition in various tissues and…”
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Synthesis and studies of covalently linked meso-furyl boron-dipyrromethene-ferrocene conjugates
Published in Journal of organometallic chemistry (2012)“…Four meso-furyl BODIPY-ferrocene conjugates 1– 4 in which one or more ferrocene groups were connected directly to BODIPY core or meso-furyl group were…”
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Synthesis, anticancer evaluation and in silico studies of novel N‐substituted arylidenethiazolidine‐2,4‐dione derivatives as adenosine monophosphate‐activated protein kinase activators
Published in Journal of heterocyclic chemistry (01-05-2024)“…Design and development of AMP‐activated protein kinase (AMPK) activator emerged as a potential therapeutic approach for various types of cancers. In this…”
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Effects of hesperidin, a flavanone glycoside interaction on the conformation, stability, and aggregation of lysozyme: multispectroscopic and molecular dynamic simulation studies?
Published in Journal of biomolecular structure & dynamics (02-09-2015)“…Hesperidin (HESP), a flavanone glycoside, shows high antioxidant properties and posses ability to go through the blood-brain barrier. Therefore, it could be a…”
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Design, Synthesis and Antidiabetic Activity of Biphenylcarbonitrile‐Thiazolidinedione Conjugates as Potential α‐Amylase Inhibitors
Published in ChemistrySelect (Weinheim) (05-03-2021)“…The α‐amylase inhibition has been considered as an effective therapeutic approach against chronic Type 2 Diabetes mellitus (DM). In the present study, a series…”
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Effects of 2-amino-8-hydroxyquinoline interaction on the conformation of physiological isomers of human serum albumin
Published in European biophysics journal (01-05-2015)“…The methods of synthetic chemistry create small molecules rapidly for screening, and ligand–protein interaction studies provide information on how a potential…”
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