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Mechanistic basis of differential cellular responses of phosphatidylinositol 3,4-bisphosphate- and phosphatidylinositol 3,4,5-trisphosphate-binding pleckstrin homology domainsMicroplate-based characterization of protein-phosphoinositide binding interactions using a synthetic biotinylated headgroup analogue.Alkyl Cinnamates Induce Protein Kinase C Translocation and Anticancer Activity against Breast Cancer Cells through Induction of the Mitochondrial Pathway of Apoptosis.Nitrobenzofurazan derivatives of N'-hydroxyamidines as potent inhibitors of indoleamine-2,3-dioxygenase 1.Development of diacyltetrol lipids as activators for the C1 domain of protein kinase C.Mechanistic insights into the phosphatidylinositol binding properties of the pleckstrin homology domain of lamellipodin.Fused Heterocyclic Compounds as Potent Indoleamine-2,3-dioxygenase 1 Inhibitors.3-Amino-4-aminoximidofurazan derivatives: small molecules possessing antimicrobial and antibiofilm activity against Staphylococcus aureus and Pseudomonas aeruginosa.Insights into the inhibitory mechanism of triazole-based small molecules on phosphatidylinositol-4,5-bisphosphate binding pleckstrin homology domain.Real-time cell assays of phospholipase A(2)s using fluorogenic phospholipids.Danazol has potential to cause PKC translocation, cell cycle dysregulation, and apoptosis in breast cancer cells.Azidophosphonate Chemistry as a Route for a Novel Class of Vesicle-Forming Phosphonolipids.Membrane Interaction and Protein Kinase C-C1 Domain Binding Properties of 4-Hydroxy-3-(hydroxymethyl) Phenyl Ester Analogues.Phosphate bioisostere containing amphiphiles: a novel class of squaramide-based lipids.Synthesis and protein kinase C (PKC)-C1 domain binding properties of diacyltetrol based anionic lipids.Structural and functional consequences of mutating a proteobacteria-specific surface residue in the catalytic domain of Escherichia coli GluRS.Alkyl cinnamates as regulator for the C1 domain of protein kinase C isoforms.Elucidating the interaction of γ-hydroxymethyl-γ-butyrolactone substituents with model membranes and protein kinase C-C1 domains.Ring-Opening of Indoles: An Unconventional Route for the Transformation of Indoles to 1 H-Pyrazoles Using Lewis AcidDiphenylethylenediamine-Based Potent Anionophores: Transmembrane Chloride Ion Transport and Apoptosis Inducing ActivitiesEffects of ortho substituent groups of protocatechualdehyde derivatives on binding to the C1 domain of novel protein kinase CTransition Metal, Azide, and Oxidant-Free Homo- and Heterocoupling of Ambiphilic Tosylhydrazones to the Regioselective Triazoles and PyrazolesSynthesis and evaluation of oxindoles as promising inhibitors of the immunosuppressive enzyme indoleamine 2,3-dioxygenase 1Tuning the solubility of ionophores: glutathione-mediated transport of chloride ions across hydrophobic membranes4,5-Disubstituted 1,2,3-triazoles: Effective Inhibition of Indoleamine 2,3-Dioxygenase 1 Enzyme Regulates T cell Activity and Mitigates Tumor GrowthpH-Regulated anion transport activities of bis(iminourea) derivatives across the cell and vesicle membraneA stimuli-responsive anticancer drug delivery system with inherent antibacterial activitiesSunlight-Mediated Thiol-Ene/Yne Click Reaction: Synthesis and DNA Transfection Efficiency of New Cationic Lipids
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description
researcher
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wetenschapper
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հետազոտող
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name
Debasis Manna
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Debasis Manna
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Debasis Manna
@es
Debasis Manna
@nl
type
label
Debasis Manna
@ast
Debasis Manna
@en
Debasis Manna
@es
Debasis Manna
@nl
prefLabel
Debasis Manna
@ast
Debasis Manna
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Debasis Manna
@es
Debasis Manna
@nl
P106
P1153
22985917500
P31
P496
0000-0002-6920-9000