Search results for " Synthesis"

showing 10 items of 1625 documents

Herbicidal activity of phosphonic and phosphinic acid analogues of glutamic and aspartic acids

1992

Phosphonic and phosphinic acid analogues of glutamic and aspartic acids were synthesized and screened for herbicidal activity on Lepidium sativum L. Depending on the chemical structure, they exhibited significant or moderate herbicidal activity against L. sativum roots (with some representatives being equipotent with phosphinothricin), while their influence on shoot growth was negligible. Cucumis sativus L. appeared to be more tolerant to these analogues. The origin of this selectivity remains to be determined.

Lepidium sativumchemistry.chemical_compoundSativumGlufosinateChemistryStereochemistryChemical structureAspartic acidfood and beveragesBiological activityGlutamic acidApplied Microbiology and BiotechnologyChemical synthesisPesticide Science
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Synthesis and herbicidal activity of isoxazole-substituted 1-aminoethylphosphonates and 1-hydroxyethylphosphonates

1994

Isoxazole‐substituted 1‐aminoethyl‐ and 1‐hydroxyethyiphosphonates were synthesized by a multi‐step procedure and were screened for herbicidal activity against Lepidium sativum L. and Cucumis sativus L. All the synthesized compounds exhibited notable herbicidal activity.

Lepidium sativumchemistry.chemical_compoundbiologyChemistryStereochemistryBiological activityIsoxazolebiology.organism_classificationApplied Microbiology and BiotechnologyChemical synthesisCucurbitaceaeCucumisPesticide Science
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Stereoselective Total Synthesis and Absolute Configuration of the Natural Decanolides (−)-Microcarpalide and (+)-Lethaloxin. Identity of (+)-Lethalox…

2005

[reaction: see text] Convergent, stereoselective syntheses of the pharmacologically active, naturally occurring lactones (-)-microcarpalide and (+)-lethaloxin have been achieved from the commercially available, chiral reagents (R)-glycidol, (S,S)-tartaric acid, and d-ribose as the starting materials. These syntheses have further served to establish the hitherto unknown absolute configuration of (+)-lethaloxin and to show its identity with (+)-pinolidoxin.

LethaloxinChemistryStereochemistryOrganic ChemistryMolecular ConformationAbsolute configurationTotal synthesisStereoisomerismAlkenesKetonesPinolidoxinHeterocyclic Compounds 1-RingIdentity (mathematics)AlkanesStereoselectivityMicrocarpalideThe Journal of Organic Chemistry
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Catalytic Diastereo- and enantioselective vinylogous Mannich reaction of alkylidenepyrazolones to isatin-derived ketimines

2021

A valuable organocatalytic vinylogous Mannich reaction between alkylidenepyrazolones and isatin-derived ketimines has been successfully established. Squaramide organocatalyst, prepared from quinine, catalyzed the diastereo- and enantioselective vinylogous Mannich addition, affording a range of aminooxindole-pyrazolone adducts (24 examples) with excellent outcomes: up to 98% yield with complete diastereoselectivity and excellent enantioselectivity (up to 99% ee). Additionally, different synthetic transformations were performed with the chiral pyrazolone-oxindole adducts.

LetterChemistryIsatinOrganic ChemistrySquaramideEnantioselective synthesisBiochemistryCatalysisAdductReaccions químiqueschemistry.chemical_compoundCatàlisiYield (chemistry)Organic chemistryPhysical and Theoretical ChemistryMannich reactionQuímica orgànica
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ChemInform Abstract: Chemoenzymatic-Chemical Synthesis of a (2-3)-Sialyl T Threonine Building Block and Its Application to the Synthesis of the N-Ter…

2010

Protection of all functional groups of the carbohydrate portion of the chemoenzymatically synthesized sialyl T threonine ester 1 (R=R1 =H, R2 =tBu, Fmoc=9-fluorenylmethoxycarbonyl) and subsequent acidolysis of the tert-butyl ester afforded the building block 2 (R=Ac, R1 =Me, R2 =H). The latter is a useful tool in the solid-phase synthesis of the N-terminal sequence 3 of the leukemia-associated leukosialin.

LeukemiaStereochemistryChemistryBlock (permutation group theory)medicineSequence (biology)General MedicineThreonineLeukosialinCarbohydratemedicine.diseaseChemical synthesisChemInform
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Large-Scale Recombinant Production of the SARS-CoV-2 Proteome for High-Throughput and Structural Biology Applications

2021

The highly infectious disease COVID-19 caused by the Betacoronavirus SARS-CoV-2 poses a severe threat to humanity and demands the redirection of scientific efforts and criteria to organized research projects. The international COVID19-NMR consortium seeks to provide such new approaches by gathering scientific expertise worldwide. In particular, making available viral proteins and RNAs will pave the way to understanding the SARS-CoV-2 molecular components in detail. The research in COVID19-NMR and the resources provided through the consortium are fully disclosed to accelerate access and exploitation. NMR investigations of the viral molecular components are designated to provide the essential…

Life sciences; biologySARS-COV-2; COVID-19; protein production; structural biology NMR[SDV.BIO]Life Sciences [q-bio]/BiotechnologyBiochemistry Genetics and Molecular Biology (miscellaneous)BiochemistryAccessory proteinsNMR spectroscopyddc:570[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]Molecular Biosciencesddc:610Nonstructural proteinsMolecular BiologyOriginal Research[SDV.BBM.BS]Life Sciences [q-bio]/Biochemistry Molecular Biology/Structural Biology [q-bio.BM]SARS-CoV-2Intrinsically disordered regionnonstructural proteinsCOVID-19structural proteinsCell-free protein synthesisintrinsically disordered regioncell-free protein synthesisaccessory proteins[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/VirologyStructural proteins
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Synthesis of tritium labeled (�)-1-[2(triphenylmethoxy)ethyl]-3-piperidinecarboxylic acid: a possible compound to determine the efficacy of potential…

2000

(±)-1-[2-(Triphenyl[ 3 H]methoxy)ethyl]-3-piperidinecarboxylic acid ([ 3 H]SNAP-5114) with a specific activity of 40 Ci/mmol was prepared in a two step synthesis starting from ethyl (2-(4-hydroxyphenyl)bis(4-methoxyphenyl)methoxy)-ethyl)piperidine-3-carboxylate and [ 3 H]methyliodide with subsequent hydrolysis of the resulting ester with lithium hydroxide to yield the desired [ 3 H]SNAP-5114.

LigandStereochemistryOrganic ChemistryEtherBiochemistryChemical synthesisMedicinal chemistryLithium hydroxideAnalytical Chemistrychemistry.chemical_compoundHydrolysischemistryYield (chemistry)Drug DiscoveryRadiology Nuclear Medicine and imagingTritiumSpecific activitySpectroscopyJournal of Labelled Compounds and Radiopharmaceuticals
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Cognitive factors in the evaluation of synthetic speech

1998

Abstract This paper illustrates the importance of various cognitive factors involved in perceiving and comprehending synthetic speech. It includes findings drawn from the relative psychological and psycholinguistic literature together with experimental results obtained at the Fondazione Ugo Bordoni laboratory. Overall, it is shown that listening to and comprehending synthetic voices is more difficult than with a natural voice. However, and more importantly, this difficulty can and does decrease with the subjects' exposure to said synthetic voices. Furthermore, greater workload demands are associated with synthetic speech and subjects listening to synthetic passages are required to pay more …

Linguistics and LanguageCommunicationSpeech recognitionmedia_common.quotation_subjectCognitionWorkloadSpeech processingLanguage and LinguisticsPsycholinguisticsComputer Science ApplicationsText to speech synthesisModeling and SimulationPerceptionNatural (music)Active listeningComputer Vision and Pattern RecognitionPsychologySoftwareCognitive psychologymedia_commonSpeech Communication
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The synthesis and effect of fluorinated chalcone derivatives on nitric oxide production

2002

Abstract Dimethoxy- and trimethoxychalcone derivatives, with various patterns of fluorination, were synthesized and evaluated for their influence on nitric oxide production. Some of them, chalcones 1 , 5 , 7 , 10 , 11 and 17 , inhibited NO production with an IC 50 in the submicromolar range; 17 is especially noteworthy because of its potency (IC 50 30 nM). These effects were not the consequence of a direct inhibitory action on enzyme activity but the inhibition of enzyme expression.

LipopolysaccharidesChalconeHydrocarbons FluorinatedClinical BiochemistryNitric Oxide Synthase Type IIPharmaceutical ScienceEtherNitric OxideBiochemistryChemical synthesisCell LineNitric oxideInhibitory Concentration 50MiceStructure-Activity Relationshipchemistry.chemical_compoundChalconeDrug DiscoveryAnimalsOrganic chemistryMolecular BiologyNitriteschemistry.chemical_classificationbiologyChemistryMacrophagesAnti-Inflammatory Agents Non-SteroidalOrganic ChemistryHaloketoneCombinatorial chemistryEnzyme assayEnzymeEnzyme Inductionbiology.proteinMolecular MedicineNitric Oxide SynthaseEnoneBioorganic & Medicinal Chemistry Letters
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Solid-phase synthesis and inhibitory effects of some pyrido[1,2-c]pyrimidine derivatives on leukocyte formations and experimental inflammation.

2001

A number of pyrido[1,2-c]pyrimidines bearing a nitrogen, oxygen, or sulfur functionality at C-1 were synthesized on solid-phase using the iminophosphorane methodology and tested for their effects on leukocyte functions in vitro and antiinflammatory activity. Compound 5c was found to be a strong scavenger of superoxide anion and an inhibitor of chemiluminescence induced by 12-O-tetradecanoylphorbol 13-acetate in human neutrophils. These pyrido[1,2-c]pyrimidines inhibited the generation of PGE(2) by COX-2 in RAW 264.7 macrophages stimulated with lipopolysaccharide. Compounds 7, 5f, 6, and 8 inhibited enzyme activity, whereas the remaining compounds also acted on the induction phase. In additi…

LipopolysaccharidesLipopolysaccharideNeutrophilsChemical synthesisDinoprostoneNeutrophil Activationchemistry.chemical_compoundMiceStructure-Activity RelationshipDrug DiscoveryAnimalsEdemaHumansCells CulturedbiologyPancreatic ElastaseSuperoxideMacrophagesAnti-Inflammatory Agents Non-SteroidalMembrane ProteinsBiological activityFree Radical ScavengersIn vitroEnzyme assayCarrageenanIsoenzymesPyrimidineschemistryEicosanoidBiochemistryCyclooxygenase 2Prostaglandin-Endoperoxide SynthasesLuminescent Measurementsbiology.proteinMolecular MedicineTetradecanoylphorbol AcetateJournal of medicinal chemistry
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