Search results for "DISCOVERY"

showing 10 items of 4119 documents

Novel examples of the N-methyl effect on cyclisations of N-Boc derivatives of amino alcohols. A theoretical study

2004

New examples of the N-methyl effect on the cyclisation of N-tert-butoxycarbonyl derivatives of amino alcohols are reported. Ab initio studies for the displacement step with formation of the five-membered heterocycle indicate that the increase of the nucleophile character of the carbonyl oxygen of the carbamate group with the N-methyl substitution is responsible for the acceleration of the cyclisation step.

CarbamateNucleophileStereochemistryChemistrymedicine.medical_treatmentOrganic ChemistryDrug DiscoveryThorpe–Ingold effectAb initiomedicineBiochemistryTetrahedron
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Effect of electron-withdrawing substituents on the electrophilicity of carbonyl carbons

2005

Indexación: Scopus The substituent effects on the carbonyl carbon atom for a series of twelve substituted phenyl acetates have been rationalized using a global electrophilicity index. This index is linearly correlated with the experimental reaction rate coefficients. We found that, in contrast to the proposed interpretation based on experimental 13C NMR chemical shifts and ground state destabilization calculations, the electrophilicity of carbonyl compounds increases due to the effect promoted by electron-withdrawing groups in these systems. https://www.sciencedirect.com/science/article/pii/S0040402004018046?via%3Dihub

Carbon atomChemistryChemical shiftOrganic ChemistrySubstituentcarbonyl derivativecarbonylCarbon-13 NMRcarbon nuclear magnetic resonancePhotochemistryDFT calculationsBiochemistryMedicinal chemistryParrReaction rateElectron-withdrawing effectschemistry.chemical_compoundElectronegativityDrug DiscoveryElectrophilePolar effectChemical Reactivityphenylacetic acid derivativeElectrophilicityGround state
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Calix[4]arenes with alkylidene bridges, synthesis and conformational properties

1994

Abstract Calix[4]arenes with one or two alkylidene bridges were synthesized by “2+2” fragment condensation. As predicted by molecular mechanics calculations aliphatic residues at the bridging carbon atom(s) prefer the equatorial position.

Carbon atomChemistryStereochemistryOrganic ChemistryDrug DiscoveryCondensationBiochemistryTetrahedron Letters
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Eine einfache Synthese für N-[3-[3-(1-Piperidinylmethyl)-phenoxy]propyl]hydrazincarbothioamid

1985

Synthese par reaction one pot de l'amino-3″ propoxy-3' benzyl-1 piperidine avec CS 2 , l'iodomethane et l'hydrazine

Carbon disulfidechemistry.chemical_compoundchemistryOne pot reactionDrug DiscoveryPharmaceutical ScienceAliphatic compoundMedicinal chemistryArchiv der Pharmazie
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Functionalization of Metal and Carbon Nanoparticles with Potential in Cancer Theranostics

2021

Cancer theranostics is a new concept of medical approach that attempts to combine in a unique nanoplatform diagnosis, monitoring and therapy so as to provide eradication of a solid tumor in a non-invasive fashion. There are many available solutions to tackle cancer using theranostic agents such as photothermal therapy (PTT) and photodynamic therapy (PDT) under the guidance of imaging techniques (e.g., magnetic resonance—MRI, photoacoustic—PA or computed tomography—CT imaging). Additionally, there are several potential theranostic nanoplatforms able to combine diagnosis and therapy at once, such as gold nanoparticles (GNPs), graphene oxide (GO), superparamagnetic iron oxide nanoparticles (SP…

Carbon nanoparticlesMaterials scienceCancer therapySuperparamagnetic iron oxide nanoparticlesCarbon NanoparticlesMetal NanoparticlesPharmaceutical ScienceNanotechnologyReviewTheranostic NanomedicineAnalytical Chemistrylaw.inventionQD241-441BiopolymersCancer MedicinelawCell Line TumorNeoplasmsDiagnosisDrug DiscoverymedicineCarbon dotsHumansPhysical and Theoretical ChemistryConjugationGraphenePrecision medicineOrganic ChemistryCancerPhotothermal therapyTheranosticsmedicine.diseaseCarbonSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoChemistry (miscellaneous)Colloidal goldMolecular MedicineSurface modificationGraphiteGrapheneMolecules
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Mass Transport Analysis of Bicarbonate Buffer: Effect of the CO2–H2CO3 Hydration–Dehydration Kinetics in the Fluid Boundary Layer and the Apparent Ef…

2019

The main buffering system influencing ionizable drug dissolution in the human intestinal fluid is bicarbonate-based; however, it is rarely used in routine pharmaceutical practice due to the volatility of dissolved CO2. The typical pharmaceutical buffers used fail to capture the unique aspects of the hydration-dehydration kinetics of the bicarbonate-CO2 system. In particular, CO2 is involved in a reversible interconversion with carbonic acid (H2CO3), which is the actual conjugate acid of the system, as follows CO2 + H2O ⇌ H2CO3. In contrast to ionization reactions, this interconversion does not equilibrate very rapidly compared to the diffusional processes through a typical fluid diffusion b…

Carbonic acidChemistryved/biologyBicarbonateved/biology.organism_classification_rank.speciesPharmaceutical ScienceThermodynamics02 engineering and technology021001 nanoscience & nanotechnology030226 pharmacology & pharmacyDiffusion layerReaction rate03 medical and health scienceschemistry.chemical_compound0302 clinical medicineDehydration reactionDrug DiscoveryMolecular MedicineDissolution testing0210 nano-technologyDissolutionConjugate acidMolecular Pharmaceutics
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Highly efficient separation of amines by electrokinetic chromatography using resorcarene-octacarboxylic acids as pseudo-stationary phases

1998

Abstract Resorcarene-octacarboxylic acids, macrocyclic molecules built up by four alkylidene-bridged resorcinol units, were synthesized and used as pseudostationary phases in electrokinetic chromatography (EKC). Resorcarenes provide a stable structure and good solubility in electrolytes even with organic modifiers. The high electrophoretic mobility of the resorcarene-octacarboxylic acids introduced here as pseudostationary phases is based on the eight partly deprotonated carboxylic groups. This offers a broad migration time window, which is the main parameter for the resolution of peaks. From three compounds with different alkyl chain lengths (C 1 , C 5 , C 11 ), the C 11 -resorcarene-octa-…

Carboxylic acidClinical BiochemistryKineticsCarboxylic AcidsResorcinolElectrochemistryHigh-performance liquid chromatographyBiochemistryMicellar electrokinetic chromatographyAnalytical ChemistryHomologous serieschemistry.chemical_compoundElectrokinetic phenomenaColumn chromatographyDrug DiscoveryElectrochemistryAminesDerivatizationMolecular BiologyAlkylchemistry.chemical_classificationPharmacologyChromatographyChromatographyElutionHydrophilic interaction chromatographyOrganic ChemistryResorcinolsGeneral MedicineCapacity factorKineticschemistryChromatography columnBiomedical Chromatography
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Cytotoxicity of oleanolic and ursolic acid derivatives toward hepatocellular carcinoma and evaluation of NF-κB involvement.

2019

Oleanolic and ursolic acids are two ubiquitous isomeric triterpene phytochemicals known for their anticancer activity. A set of derivatives of the two compounds with a modified oxidation state and lipophylicity at C-3 and C-28 positions, were prepared and tested as anticancer agents versus the lines HepG2, Hep3B and HA22T/VGH of hepatocarcinoma, a strongly aggressive tumor that is not responsive toward the standard therapies. New derivatives containing a three carbons side chain on the C-3 position were synthetized in both stereoisomeric forms by the Barbier-Grignard procedure and three of them were found to be active toward all of the three targets. The implication of the transcriptional n…

Carcinoma HepatocellularApoptosis01 natural sciencesBiochemistrychemistry.chemical_compoundUrsolic acid Oleanolic acid HepG2 Hep3B HA22T/VGH Antitumor activity NF−κBUrsolic acidTriterpeneOleaDrug DiscoverymedicineTumor Cells CulturedHumansSettore BIO/15 - Biologia FarmaceuticaOleanolic AcidCytotoxicityMolecular BiologyCell Proliferationchemistry.chemical_classification010405 organic chemistryPlant ExtractsOrganic ChemistryLiver NeoplasmsNF-kappa BNF-κBSettore CHIM/06 - Chimica Organicamedicine.diseaseAntineoplastic Agents Phytogenicdigestive system diseasesTriterpenes0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryMechanism of actionHepatocellular carcinomaMalusSettore BIO/14 - FarmacologiaCancer researchmedicine.symptomBioorganic chemistry
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Cardioprotective effects of phytopigments via multiple signaling pathways.

2021

Abstract Background Cardiovascular diseases (CVDs) are among the deadliest non-communicable diseases, and millions of dollars are spent every year to combat CVDs. Unfortunately, the multifactorial etiology of CVDs complicates the development of efficient therapeutics. Interestingly, phytopigments show significant pleiotropic cardioprotective effects both in vitro and in vivo. Purpose This review gives an overview of the cardioprotective effects of phytopigments based on in vitro and in vivo studies as well as clinical trials. Methods A literature-based survey was performed to collect the available data on cardioprotective activities of phytopigments via electronic search engines such as Pub…

Cardiotonic AgentsPharmaceutical ScienceAnthraquinonesXanthophyllsBioinformaticsstatAntioxidantsAnthocyaninsDrug DiscoveryMedicineAnimalsHumansClinical efficacyProtein kinase BPharmacologyFlavonoidsbusiness.industryNF-kappa BAMPKCarotenoidsClinical trialComplementary and alternative medicineCardiotoxicitiesCardiac hypertrophyMolecular MedicineSignal transductionbusinessSignal TransductionPhytomedicine : international journal of phytotherapy and phytopharmacology
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New cytostatic agents obtained by molecular topology

1996

Abstract Four new cytostatic compounds have been obtained by computer aided selection based on Molecular Connectivity, a topological approach to molecular structural study. Three of them, namely tetracycline, doxycycline and piromidic acid are well known antibiotic agents, and the fourth, carminic acid, is an innocuous colorant. Although no previous report of activity was found, on the used cell lines, for any of the selected compounds, carminic acid may be considered a new lead one since no structure-related cytostatic molecules have been reported in the literature. These results are interesting for two reasons: First, new potential low-toxicity anticancer drugs show to be a possible thera…

Carminic acidOrganic ChemistryClinical BiochemistryCytostatic agentsPharmaceutical ScienceComputational biologyPharmacologyPiromidic acidBiochemistrychemistry.chemical_compoundAntibiotic AgentschemistryDrug DiscoverymedicineMolecular MedicineMolecular topologyMolecular Biologymedicine.drugBioorganic & Medicinal Chemistry Letters
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