about
Cuminaldehyde as the Major Component of Cuminum cyminum, a Natural Aldehyde with Inhibitory Effect on Alpha-Synuclein Fibrillation and CytotoxicityAnti-HIV-1 Activity Prediction of Novel Gp41 Inhibitors Using Structure-Based Virtual Screening and Molecular Dynamics Simulation.QSAR study of p56(lck) protein tyrosine kinase inhibitory activity of flavonoid derivatives using MLR and GA-PLS.QSAR study of anthranilic acid sulfonamides as inhibitors of methionine aminopeptidase-2 using LS-SVM and GRNN based on principal components.Effectiveness of budesonide-succinate-dextran conjugate as a novel prodrug of budesonide against acetic acid-induced colitis in rats.QSAR study of antimicrobial 3-hydroxypyridine-4-one and 3-hydroxypyran-4-one derivatives using different chemometric tools.QSAR study of PETT derivatives as potent HIV-1 reverse transcriptase inhibitors.Synthesis, antimicrobial evaluation and QSAR study of some 3-hydroxypyridine-4-one and 3-hydroxypyran-4-one derivatives.Design and biological evaluation of phenyl-substituted analogs of beta-phenylethylidenehydrazine.Computational evaluation of some indenopyrazole derivatives as anticancer compounds; application of QSAR and docking methodologies.The role of different sampling methods in improving biological activity prediction using deep belief network.QSAR analysis for some diaryl-substituted pyrazoles as CCR2 inhibitors by GA-stepwise MLR.Application of partial least squares and radial basis function neural networks in multivariate imaging analysis-quantitative structure activity relationship: study of cyclin dependent kinase 4 inhibitors.Validated QSAR analysis of some diaryl substituted pyrazoles as CCR2 inhibitors by various linear and nonlinear multivariate chemometrics methods.Application of PC-ANN and PC-LS-SVM in QSAR of CCR1 antagonist compounds: a comparative study.Elucidation of Molecular Mechanisms Behind the Self-Assembly Behavior of Chitosan Amphiphilic Derivatives Through Experiment and Molecular Modeling.Characterization of adenosine receptor in its native environment: insights from molecular dynamics simulations of palmitoylated/glycosylated, membrane-integrated human A(2B) adenosine receptor.Comparative studies on the inhibitory activities of selected benzoic acid derivatives against secretory phospholipase A2, a key enzyme involved in the inflammatory pathwayDeep neural network in QSAR studies using deep belief networkHomology modeling of human CCR5 and analysis of its binding properties through molecular docking and molecular dynamics simulationIron chelation afforded cardioprotection against H2O2-induced H9C2 cell injury: application of novel 3-hydroxy pyridine-4-one derivativesPreparation of budesonide-dextran conjugates using glutarate spacer as a colon-targeted drug delivery system: in vitro/in vivo evaluation in induced ulcerative colitisWound healing by topical application of antioxidant iron chelators: kojic acid and deferiproneExploring a model of a chemokine receptor/ligand complex in an explicit membrane environment by molecular dynamics simulation: the human CCR1 receptor
P50
Q28267154-03DEC213-14C0-4909-AE16-6FEA994B4E83Q39300262-6A295897-D4B3-4937-966F-F05509A5814BQ42108816-7FFBE2CC-49D8-4FD6-9943-37B4057AC9ABQ42944045-2EA0AB9B-9E80-4738-9D79-D8E6B9D2BE6CQ42952916-DDC7F574-273B-4EF1-9B77-2FFC1029F651Q43187867-F65C4235-84E2-471C-9DAD-13334FF6506CQ45943570-0E0D3292-E603-4862-8900-BEE1CE3DFE45Q46214339-99838A98-F940-488A-A784-9B4FB01F17B5Q46520159-25688E85-0E44-4799-9B51-794D349AC069Q46969486-A9580680-8CCE-4C90-90AD-A237122F4D5BQ50546343-AB22BA2A-A2AF-4108-B2E5-7ACFB994762BQ51629378-527DB070-D761-47E6-AB00-4063E5359F54Q51638430-03A430EB-CCA6-4293-B294-4B0D08191544Q51695767-2A56E25C-3109-40D4-9B69-EE44A97B06ACQ51720245-2BB596F3-64A9-485A-8128-74092CB86555Q51812830-B08F2946-3D8D-4DB8-A5E0-3BCE80B47952Q53437158-FF381B55-9D19-45B1-8482-1EEDA140F1E3Q57275084-6288901F-DDD6-45E3-ADD2-165125C06E71Q59405123-07CCC19D-AE0D-4FBC-A0CD-7058B94BD7D3Q82936190-1CE5A2EF-BADF-4DE4-A36A-4398842E0604Q83191013-440C07EB-2D9A-457D-BFE0-CA13488F65F8Q84131351-D4259629-A644-4121-BE5F-1DF1CDB3B9A8Q84202117-58B49F2E-4CEC-4F86-8E8B-CAA4133CDF80Q84937686-477F72DF-3334-4A12-8902-D529F8540598
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Afshin Fassihi
@ast
Afshin Fassihi
@en
Afshin Fassihi
@es
Afshin Fassihi
@nl
type
label
Afshin Fassihi
@ast
Afshin Fassihi
@en
Afshin Fassihi
@es
Afshin Fassihi
@nl
prefLabel
Afshin Fassihi
@ast
Afshin Fassihi
@en
Afshin Fassihi
@es
Afshin Fassihi
@nl
P106
P1153
54993358100
P31
P496
0000-0002-8042-5986