Search results for "QSPR"

showing 10 items of 14 documents

Polarity study of ionic liquids with the solvatochromic dye Nile Red: a QSPR approach using in silico VolSurf+ descriptors

2016

The in silico VolSurfþ descriptors, accounting for both cationic and anionic structural features of ionic liquids (ILs) were used to develop a Partial Least Squares (PLS) model able to establish a Quantitative Structure Property Relationship (QSPR) correlation with their solvatochromic dye Nile Red polarity. The PLS model allowed prediction of ENR values for 116 ILs providing an in silico ILs polarity database.

Quantitative structure–activity relationship010405 organic chemistryPolarity (physics)In silicoOrganic ChemistrySolvatochromismNile redIonic Liquids Polarity Nile Red QSPRSettore CHIM/06 - Chimica Organica010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesQuantitative Structure Property Relationshipchemistry.chemical_compoundchemistryComputational chemistryDrug DiscoveryIonic liquidPartial least squares regressionOrganic chemistryTetrahedron
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MADoSPRO: a new approach to molecular modelling studies on a series of DNA minor groove binders

2006

The aim of this work was devoted to develop a method to predict Delta G values for a series of minor groove binders. Starting from a matrix of docking dataset for 10 minor groove binders (known and not) to 20 DNA fragments, with various sequences, it was possible to analyze the interaction modes and to calculate the Delta G value for new derivatives through MADoSPRO procedure. The method allowed, through the QSPR analysis, to characterize the type of interactions in such complexes, that was demonstrated to be related to quantum chemical and electrostatic descriptors, in agreement with the information available in literature on the structural requirements of specific minor groove ligands. Mo…

Quantum chemicalPCAQuantitative structure–activity relationshipChemistryOrganic Chemistryminor groove bindersDNACombinatorial chemistryComputer Science Applicationschemistry.chemical_compoundDocking (molecular)antitumor agentQSPRDrug DiscoveryDNAMinor grooveQSAR & Combinatorial Science
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DNA minor groove binders: an overview on molecular modeling and QSAR approaches

2007

Molecular recognition of DNA by small molecules and proteins is a fundamental problem in structural biology and drug design. Understanding of recognition in both sequence-selective and sequence neutral ways at the level of successful prediction of binding modes and site selectivity will be instrumental for improvements in the design and synthesis of new molecules as potent and selective gene-regulatory drugs. Minor groove is the target of a large number of non-covalent binding agents. DNA binding with specific sequences, mostly AT, takes place by means of a combination of directed hydrogen bonding to base pair edges, van der Waals interactions with the minor groove walls and generalized ele…

Models MolecularPharmacologyDNA minor groove binders (mGBs) in silico techniques molecular modeling ab initio methods docking molecular dynamics simulations (MDS) QSAR QSPR.Molecular modelBase pairStereochemistryChemistryIn silicoOrganic ChemistryQuantitative Structure-Activity RelationshipDNAComputational biologyBiochemistrySmall moleculechemistry.chemical_compoundMolecular recognitionPharmaceutical PreparationsStructural biologyDocking (molecular)Drug DesignDrug DiscoveryNucleic Acid ConformationMolecular MedicineDNA
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Quantitative structure-property relationships approach of aroma compounds behaviour in polysaccharide gels

2010

International audience; Pectin and carrageenan are common used thickeners in fat free foods. The aim of this work was to study separately and to compare their respective effects on the aroma release, in order to investigate the nature of involved interactions. In this way, we studied the influence of the chemical structure of 13 aroma compounds on retention/release equilibrium between vapour phase and gels using QSPR tools. Six descriptors are involved in the best obtained QSPR equations, and three of them appeared to play a critical role in the behaviour of aroma compound. Our results put forward the role of polar effects on the retention of odorant molecules in both iota-carrageenan and p…

POLYSACCHARIDE[SPI.GPROC] Engineering Sciences [physics]/Chemical and Process EngineeringQSPR[SDV.IDA]Life Sciences [q-bio]/Food engineeringfood and beverages[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringODORANTS[SDV.IDA] Life Sciences [q-bio]/Food engineeringRETENTION-RELEASE
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Design of new DNA-interactive agents by molecular docking and QSPR approach

2010

The design of new series of pyrrolo-pyrimidine derivatives, further annelated with a third heterocycle of different size, which also present several chain shape moieties of variable length and with different physico-chemical character, is reported. In this contribution we showed that the combination of docking-based and QSPR-based methods could lead to good models for ligand-DNA interaction prediction. By means of these computational approaches on 360 proposed inhibitors, we were able to select the most promising candidates as DNA-interactive drugs potentially endowed with antitumor activity.

Antitumor activitylcsh:QD241-441Quantitative structure–activity relationshipchemistry.chemical_compoundlcsh:Organic chemistryChemistryOrganic ChemistryDNA-interactive agents molecular docking QSPRComputational biologyVariable lengthCombinatorial chemistrySettore CHIM/08 - Chimica FarmaceuticaDNA
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Prediction of ionic liquid's heat capacity by means of their in silico principal properties

2016

The in silico principal properties (PPs) of ionic liquids (ILs), derived by means of the VolSurf+ approach, were used to develop a Partial Least Squares (PLS) model able to find a quantitative correlation among IL descriptors (accounting for both cationic and anionic structural features) and heat capacity values, providing affordable predictions validated by experimental Cp measurements for an external set of ILs. In silico predictions allowed the selection of a limited number of structurally different ILs with similar Cp values, providing the possibility to select an optimal IL according to efficiency, as well as to environmental and economic sustainability. The present general procedure, …

Quantitative structure–activity relationshipHeat capacity010405 organic chemistryGeneral Chemical EngineeringIn silicoPrincipal (computer security)Chemistry (all)General ChemistrySettore CHIM/06 - Chimica Organica010402 general chemistry01 natural sciencesHeat capacityQuantitative correlation0104 chemical sciencesIonic liquidschemistry.chemical_compoundEconomic sustainabilitychemistryIonic liquids; QSPR; Heat capacityQSPRPartial least squares regressionIonic liquidChemical Engineering (all)Biological systemMathematics
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Study of relationships between the structure of aroma compounds and their retention-release between vapour phase and dairy gels

2010

An integrated approach physicochemistry and structures activity relationships has been carried out to study the aroma compounds retention-release phenomenon in a fat free dairy gel added with pectin. This study aimed to identify the molecular properties that govern this phenomenon assuming that modifying the structure leads automatically to a change in the retention-release of aroma compounds. For this purpose, we have determined the partition coefficients of 28 aroma compounds in water, in pectin gels and in dairy gels supplemented or not supplemented with pectin, at equilibrium conditions using the PRV method (Phase Ratio Variation). Then, we have performed a structure-retention relations…

Qsar/qsprAroma compoundComposé d’arômeCoefficient de partagePartition coefficientPectinHeadspaceRetention-releasePrvStructure-activity/structure-property relationships[SDV.AEN] Life Sciences [q-bio]/Food and NutritionRétention-libérationPectineDairy gelGel laitierRelations structure-activité/structure-propriété
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Flavor Release from i-Carrageenan Matrix: A Quantitative Structure-Property Relationships Approach

2006

International audience; We carried out a QSPR (quantitative structure-property relationships) approach to evaluate the influence of the chemical structure of aqueous matrixes over the partition coefficient between the gas phase and the matrix. The determination of the partition coefficient of flavor ingredients was performed by headspace analysis at equilibrium for both saline solution and -carrageenan gel. Starting from an initial list of 90 descriptors, we selected 10 descriptors to perform equation generation by the GFA (genetic function approximation) method available in the Cerius2 package. The best obtained equations involve only five descriptors, which encode electronic properties of…

HEADSPACE ANALYSISQSARQSPRi-CARRAGEENANAROMA RELEASE[SDV.IDA]Life Sciences [q-bio]/Food engineering[SDV.IDA] Life Sciences [q-bio]/Food engineeringPARTITION COEFFICIENTGENETIC FUNCTION APPROXIMATIONINTERACTION
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Exemples de QSAR sur des coefficients de partage

2005

National audience

IOTA-CARAGEENAN[SPI.GPROC] Engineering Sciences [physics]/Chemical and Process EngineeringQSARQSPRAROMA RELEASE[SDV.IDA]Life Sciences [q-bio]/Food engineering[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process Engineering[SDV.IDA] Life Sciences [q-bio]/Food engineeringPARTITION COEFFICIENTINTERACTIONHEADSCAPE ANALYSISGELSComputingMilieux_MISCELLANEOUS
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Study on the mechanism of action of antitumor photochemotherapic agents by means of docking and QSPR analysis

2008

photochemotherapic agentQSPRdockingSettore CHIM/08 - Chimica Farmaceutica
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