Search results for "Bioinformatic"

showing 10 items of 1651 documents

Use of Specific Chemical Reagents for Detection of Modified Nucleotides in RNA

2011

International audience; Naturally occurring cellular RNAs contain an impressive number of chemically distinct modified residues which appear posttranscriptionally, as a result of specific action of the corresponding RNA modification enzymes. Over 100 different chemical modifications have been identified and characterized up to now. Identification of the chemical nature and exact position of these modifications is typically based on 2D-TLC analysis of nucleotide digests, on HPLC coupled with mass spectrometry, or on the use of primer extension by reverse transcriptase. However, many modified nucleotides are silent in reverse transcription, since the presence of additional chemical groups fre…

chemistry.chemical_classification0303 health scienceslcsh:QH426-470030302 biochemistry & molecular biologyRNA[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biologyReview ArticleBiologyMass spectrometryBioinformaticsBiochemistryReverse transcriptasePrimer extensionlcsh:Biochemistry03 medical and health scienceslcsh:GeneticsEnzymechemistryBiochemistryReagentReactivity (chemistry)Nucleotidelcsh:QD415-436Molecular Biology030304 developmental biologyJournal of Nucleic Acids
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Therapeutic use of omega-3 fatty acids in bipolar disorder

2011

Bipolar disorder (BD) is a severe, chronic affective disorder, associated with significant disability, morbidity and premature mortality. Omega-3 polyunsaturated fatty acids (PUFAs) play several important roles in brain development and functioning. Evidence from animal models of dietary omega-3 (n-3) PUFA deficiency suggest that these fatty acids are relevant to promote brain development and to regulate behavioral and neurochemical aspects related to mood disorders, such as stress responses, depression and aggression, as well as dopaminergic content and function. Preclinical and clinical evidence suggests roles for PUFAs in BD. n-3 PUFAs seem to be an effective adjunctive treatment for unip…

chemistry.chemical_classificationBipolar Disordermedicine.drug_classBrain-Derived Neurotrophic FactorGeneral NeuroscienceDopaminergicMood stabilizerBioinformaticsmedicine.diseaseNeuroprotectionNeuroprotective AgentsNeurochemicalMood disorderschemistryFatty Acids Omega-3Adjunctive treatmentmedicineAnimalsHumansPharmacology (medical)Neurology (clinical)Bipolar disorderPsychologyClinical psychologyPolyunsaturated fatty acidExpert Review of Neurotherapeutics
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Chlorido(dimethyl sulfoxide)(pyridine-2-thiolato N-oxide-κ2S,O)platinum(II)

2008

The asymmetric unit of the title compound, [Pt(C5H4NOS)Cl(C2H6OS)], contains two independent complex molecules having similar geometries. Each PtII atom is four-coordinated in a distorted square-planar geometry by S and O atoms of one pyridine N-oxide ligand, the S atom of one dimethyl sulfoxide molecule and one terminal Cl− ion. The molecules are linked into a three-dimensional framework by C—H...O and C—H...Cl hydrogen bonds.

chemistry.chemical_classificationChemistryHydrogen bondLigandDimethyl sulfoxideOxidechemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsBioinformaticsMedicinal chemistryIonlcsh:Chemistrychemistry.chemical_compoundlcsh:QD1-999PyridineThiolGeneral Materials SciencePlatinumActa Crystallographica Section E
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N-[3-(5-Oxo-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-2-ylamino)phenyl]furan-3-carboxamide

2010

In the title compound, C26H20N2O3, the two aromatic rings of the tricyclic unit are oriented at a dihedral angle of 54.53 (9)°. The crystal structure displays intermolecular N—H...O hydrogen bonding.

chemistry.chemical_classificationChemistrymedicine.drug_classHydrogen bondCarboxamideAromaticityGeneral ChemistryCrystal structureDihedral angleCondensed Matter PhysicsBioinformaticsMedicinal chemistryOrganic Paperslcsh:Chemistrychemistry.chemical_compoundlcsh:QD1-999FuranmedicineGeneral Materials ScienceTricyclicActa Crystallographica Section E
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N-(2-Benzoyl-4-chlorophenyl)-4-chlorobenzenesulfonamide

2008

The title compound, C19H13Cl2NO3S, is an N-arylsulfonyl derivative of 2-amino-5-chlorobenzophenone. The compound is biologically active and shows potential to be utilized as an inhibitor of CCR2 and CCR9 receptor functions. In the crystal structure, there is an intramolecular N—H...O hydrogen bond between the amide and carbonyl groups. The benzoyl and 4-chlorophenyl groups form intramolecular and intermolecular face-to-face contacts, with a dihedral angle of 10.6 (1)° between their mean planes in both cases, and centroid–centroid separations of 4.00 (1) and 4.25 (1) Å for the intra- and intermolecular interactions, respectively.

chemistry.chemical_classificationCrystallographyHydrogen bondGeneral ChemistryCrystal structureDihedral angleCondensed Matter PhysicsBioinformaticsOrganic PapersMedicinal chemistrySulfonamidechemistry.chemical_compoundchemistryQD901-999AmideBenzophenoneGeneral Materials ScienceBenzeneDerivative (chemistry)Acta Crystallographica Section E Structure Reports Online
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1-{2-[4-(4-Nitrophenyl)piperazin-1-yl]ethyl}-4-aza-1-azoniabicyclo[2.2.2]octane iodide

2012

The title compound, C18H28N5O2+·I−, was observed as a main product in an intended 1:1 reaction between 4-iodonitrobenzene and 1,4-diazabicyclo[2.2.2]octane (DABCO). In the reaction, DABCO undergoes a ring opening to yield a quaternary salt of DABCO and 1-ethyl-4-(4-nitrophenyl)piperazine with an iodide anion. The crystal structure determination was carried out as no crystal structure had been previously reported in the investigations describing the corresponding reaction with 4-chloronitrobenze. Indeed, the crystal structure of the title compound confirms the molecular composition proposed earlier for the analogous chloride salt. The cation conformation is similar to the …

chemistry.chemical_classificationCrystallographyIodideGeneral ChemistryDABCOCrystal structureCondensed Matter PhysicsBioinformaticsRing (chemistry)Organic PapersMedicinal chemistryChloridechemistry.chemical_compoundPiperazinechemistryQD901-999NitromedicineGeneral Materials Scienceta116Octanemedicine.drugActa Crystallographica Section E Structure Reports Online
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Detoxication Strategy of Epoxide Hydrolase—The Basis for a Novel Threshold for Definable Genotoxic Carcinogens

2004

From our recent work on the three-dimensional structure of epoxide hydrolases we theoretically deduced the likelihood of a two-step catalytic mechanism that we and others have subsequently experimentally confirmed. Analysis of the rate of the two steps by us and by others show that the first step—responsible for removal of the reactive epoxide from the system—works extraordinarily fast (typically three orders of magnitude faster than the second step), sucking up the epoxide like a sponge. Regeneration of the free enzyme (the second step of the catalytic mechanism) is slow. This becomes a toxicological problem only at doses of the epoxide that titrate the enzyme out. Our genotoxicity work s…

chemistry.chemical_classificationDNA damagelcsh:RM1-950Epoxide10050 Institute of Pharmacology and Toxicology610 Medicine & healthArticlesBiologymedicine.disease_causeBioinformaticsCombinatorial chemistryDetoxicationchemistry.chemical_compoundEnzymelcsh:Therapeutics. PharmacologychemistryEpoxide Hydrolasesmedicine570 Life sciences; biologyEpoxide hydrolaseCarcinogenGenotoxicity
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(Z)-Ethyl 2-oxo-3-(1,2-dihydroquinolin-2-ylidene)propanoate

2010

Both independent molecules in the asymmetric unit of the tautomeric title compound, C14H13NO3, a synthetic product obtained from 2-lithiomethylquinoline and diethyl oxalate, crystallize in the enaminone form with a Z configuration around the double bond. Intramolecular N—H...O hydrogen bonds occur, generating an S(6) graph-set motif. In the crystal, weak intermolecular C—H...O and π–π stacking interactions [centroid–centroid distances = 3.7020 (14)–3.7429 (13)Å] define a three-dimensional supramolecular network.

chemistry.chemical_classificationDouble bondHydrogen bondChemistryStackingGeneral ChemistryCondensed Matter PhysicsBioinformaticsOrganic PapersMedicinal chemistryTautomerlcsh:ChemistryCrystallcsh:QD1-999General Materials ScienceDiethyl oxalateActa Crystallographica Section E Structure Reports Online
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(1S,2R,4S)-1-[(Benzyl­amino)­meth­yl]-4-(prop-1-en-2-yl)cyclo­hexane-1,2-diol

2010

The title compound, C17H25NO2, was synthesized by epoxidation of the double bond of (S)-perillyl alcohol [(S)-4-isopropenyl-1-cyclohexenylmethanol], followed by the oxirane ring-opening by benzylamine using [Ca(CF3CO2)2] as catalyst under solvent-free condition at 313 K. The molecular conformation is stabilized by an intramolecular O—H...N hydrogen bond. In the crystal, molecules are linked by intermolecular N—H...O hydrogen bonds, forming chains parallel to the a axis, which are further connected by O—H...O hydrogen bonds into sheets parallel to (010). The absolute configuration of the molecule is known from the synthetic procedure.

chemistry.chemical_classificationDouble bondHydrogen bondDiolAbsolute configurationAlcoholGeneral ChemistryCondensed Matter PhysicsBioinformaticsMedicinal chemistryOrganic PapersCatalysisHexaneCrystallcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999General Materials ScienceActa Crystallographica Section E: Structure Reports Online
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Tribenzylammonium chloride

2014

Single crystals of the title salt, C21H21NH+·Cl−, were isolated as a side product from the reaction involving [(C6H5CH2)3NH]2[HPO4] and Sn(CH3)3Cl in ethanol. Both the cation and the anion are situated on a threefold rotation axis. The central N atom in the cation has a slightly distorted tetrahedral environment, with angles ranging from 107.7 to 111.16 (10)°. In the crystal, the tribenzylammonium cations and chloride anions are linked through N—H...Cl and C—H...Cl hydrogen bonds, leading to the formation of infinite chains along [001]. The crystal studied was a merohedral twin.

chemistry.chemical_classificationEthanolCrystallographyHydrogen bondSalt (chemistry)General ChemistryCondensed Matter PhysicsBioinformaticsChlorideOrganic PapersIonCrystalchemistry.chemical_compoundCrystallographychemistryQD901-999AtommedicineGeneral Materials ScienceAmmonium chloridemedicine.drugActa Crystallographica Section E
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