Search results for "Hexanol"

showing 10 items of 44 documents

CCDC 647577: Experimental Crystal Structure Determination

2007

Related Article: A.Valkonen, R.Kauppinen, E.Kolehmainen|2007|Acta Crystallogr.,Sect.E:Struct.Rep.Online|63|o2461|doi:10.1107/S1600536807016650

Space GroupCrystallographyCrystal Systemtrans-4-t-Butyl-1-methylcyclohexanol hemihydrateCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 615465: Experimental Crystal Structure Determination

2007

Related Article: H.Sopo, A.Vaisanen, R.Sillanpaa|2007|Polyhedron|26|184|doi:10.1016/j.poly.2006.08.006

Space GroupCrystallographyDioxo-bis(NN-bis(2-hydroxy-5-t-butyl-3-methylbenzyl)-4-amino-1-hexanol)-uranium toluene solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 916954: Experimental Crystal Structure Determination

2013

Related Article: Igor O. Koshevoy, Yuh-Chia Chang, Antti J. Karttunen, Julia R. Shakirova, Janne Jänis, Matti Haukka, Tapani Pakkanen, Pi-Tai Chou|2013|Chem.-Eur.J.|19|5104|doi:10.1002/chem.201204611

Space GroupCrystallographyoctakis(mu~2~-eta^2^-1-Ethynylcyclohexanol)-tetra-copper-tetra-gold heptane solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Development of antimigraine transdermal delivery systems of pizotifen malate.

2015

Abstract The aim of this study was to develop and evaluate a transdermal delivery system of pizotifen malate. Pizotifen is frequently used in the preventive treatment of migraine, but is also indicated in eating disorders. In the course of the project, the effects of chemical enhancers such as ethanol, 1,8-cineole, limonene, azone and different fatty acids (decanoic, decenoic, dodecanoic, linoleic and oleic acids) were determined, first using a pizotifen solution. Steady state flux, diffusion and partition parameters were estimated by fitting the Scheuplein equation to the data obtained. Among the chemical enhancers studied, decenoic acid showed the highest enhancement activity, which seeme…

SwineMigraine DisordersSkin AbsorptionPharmaceutical ScienceAbsorption (skin)PizotifenIn Vitro TechniquesAdministration Cutaneouschemistry.chemical_compoundDrug Delivery SystemsCyclohexenesmedicineOrganic chemistryAnimalsTransdermalDegree of unsaturationPizotylineEucalyptolIontophoresisEthanolTerpenesFatty AcidsAzepinesAnalgesics Non-NarcoticIontophoresisCyclohexanolsOleic acidchemistryMonoterpenesDecenoic AcidAzoneLimonenemedicine.drugInternational journal of pharmaceutics
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Standard partial molar volumes of alcohols in aqueous dodecyltrimethylammonium bromide solutions

1990

Density measurements of water-dodecyltrimethylammonium bromide (DTAB)-alcohol ternary systems as a function of alcohol and surfactant concentrations were carried out at 25°C. The alcohols were propanol (PrOH), 2-propanol (2-PrOH) and hexanol (HexOH). The apparent molar volume Vϕ,R of alcohols have been calculated and the standard (infinite dilution) partial molar volumes of alcohols V R at each surfactant concentration were obtained by means of a least squares fit of Vϕ,R vs. the alcohol concentration. The V R vs. surfactant concentration curves have been rationalized in terms of the partial molar volume of alcohol in the aqueous V f and the micellar V b phases and the distribution constant…

Ternary numeral systemChemistryButanolDistribution constantBiophysicsConcentration effectPartial molar propertyAlcoholBiochemistrychemistry.chemical_compoundMolar volumePhysical chemistryOrganic chemistryPhysical and Theoretical ChemistryMolecular BiologyHexanolJournal of Solution Chemistry
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An overview of the clinical efficacy of mirtazapine

2002

Mirtazapine is at least as effective as the tricyclic antidepressants and trazodone in a wide range of patient subgroups including in- and out-patients with moderate to severe depression. It also appears to be at least as effective as the serotonin and noradrenaline reuptake inhibitor venlafaxine in the treatment of severely depressed melancholic patients. When compared with the selective serotonin reuptake inhibitors (SSRIs), mirtazapine shows a significantly earlier onset of action. Further analysis of a study comparing mirtazapine with the SSRI paroxetine indicated that early improvement was a highly sensitive predictor of later stable response for both drugs. The positive predictive val…

Time FactorsMirtazapineVenlafaxine HydrochlorideMirtazapineVenlafaxineMianserinAntidepressive Agents TricyclicPharmacologymedicineHumansPharmacology (medical)chemistry.chemical_classificationClinical Trials as TopicDepressive DisorderAdrenergic Uptake Inhibitorsbusiness.industryVenlafaxine HydrochlorideTrazodoneCyclohexanolsParoxetineAntidepressive AgentsParoxetinePsychiatry and Mental healthTreatment OutcomeNeurologychemistryNeurology (clinical)SerotoninOnset of actionbusinessSelective Serotonin Reuptake Inhibitorsmedicine.drugTricyclicHuman Psychopharmacology: Clinical and Experimental
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Cytotoxic activity of secondary metabolites derived from Artemisia annua L. towards cancer cells in comparison to its designated active constituent a…

2010

Artemisia annua L. (sweet wormwood, qinhao) has traditionally been used in Chinese medicine. The isolation of artemisinin from Artemisia annua and its worldwide accepted application in malaria therapy is one of the showcase success stories of phytomedicine during the past decades. Artemisinin-type compounds are also active towards other protozoal or viral diseases as well as cancer cells in vitro and in vivo. Nowadays, Artemisia annua tea is used as a self-reliant treatment in developing countries. The unsupervised use of Artemisia annua tea has been criticized to foster the development of artemisinin resistance in malaria and cancer due to insufficient artemisinin amounts in the plant as c…

Trypanosoma brucei bruceiArtemisia annuaPharmaceutical ScienceArtemisia annuaPharmacologyHeLachemistry.chemical_compoundPhytomedicineParasitic Sensitivity TestsScopoletinparasitic diseasesDrug DiscoverymedicineHumansArtemisininOligonucleotide Array Sequence AnalysisPharmacologyScopoletinEucalyptolDose-Response Relationship DrugMolecular StructurebiologyPlant Extractsfood and beveragesCyclohexanolsbiology.organism_classificationAntineoplastic Agents PhytogenicTrypanocidal AgentsArtemisininsBioactive compoundEucalyptolComplementary and alternative medicinechemistryDrug Resistance NeoplasmCancer cellMonoterpenesMolecular MedicineDrug Screening Assays AntitumorHeLa Cellsmedicine.drugPhytomedicine
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Enthalpies of Mixing of Some Primary Hydrogenated and Fluorinated Alcohols and Sodium Dodecanoate Aqueous Solutions

1993

Abstract The enthalpies of transfer from water to the surfactant solutions ΔH(W → W + S) of some hydrogenated and fiuorinated alkanols and of sodium dodecanoate NaL were determined. In the premicellar region the measurements were carried out as functions of both the additive and the surfactant concentrations in order to evaluate the interaction parameters between the additive and the surfactant molecules. It is shown that in this region, pair, triplet, and quadruplet interaction parameters between unlike solute molecules contribute to ΔH(W → W + S). Within the large uncertainty with which these parameters are determined because of the very narrow surfactant and alcohol concentration interva…

chemistry.chemical_classificationAqueous solutionDistribution constantEnthalpyConcentration effectSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsPropanolchemistry.chemical_compoundColloid and Surface ChemistrychemistryPulmonary surfactantPhysical chemistryOrganic chemistryAlkylHexanolJournal of Colloid and Interface Science
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Enantioselective Protonation of the Lithium Transient Enolate of2-Methyltetralone with 2-Sulfinyl Alcohols

2005

A new catalytic cycle for the enantioselective protonation of cyclic ketone enolates with sulfinyl alcohols has been developed. An enol trifluoroacetate that can be easily obtained from the corresponding ketone is used for the first time as an enolate precursor of a cyclic ketone enolate. In this method, the achiral alcohol plays two roles: it is involved, as is usual in catalytic asymmetric protonation reactions, in the turnover of the chiral proton source and also in the generation of a transient enolate through the reaction of its corresponding alkoxide with the enol trifluoroacetate precursor. Stereoselectivity is highly dependent on the structure of the achiral alcohol. High levels of …

chemistry.chemical_classificationKetoneOrganic ChemistryEnantioselective synthesisCyclohexanolProtonationMedicinal chemistryEnolchemistry.chemical_compoundchemistryCatalytic cycleAlkoxideOrganic chemistryStereoselectivityPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Über die synthese von oligophenylenes mit einer o-verknüpfung. 10. Mitteilung

1960

Es werden zwei Wege zur Darstellung von Oligophenylenen mit einer o-Winkelung beschrieben. Als Ausgangssubstanzen dienen der Mono-enolather des Cyclohexandion (1,2) bzw. Cyclohexenoxyd. Die Darstellung des Mono-enolathylathers des Cyclohexandion (1,2) wird beschrieben. Durch Oxydation nach OPPENAUER mit Chinon als Wasserstoffacceptor konnen die als Zwischenprodukte der Oligophenylene erhaltenen Cyclohexanolderivate in 90%iger Ausbeute in die benotigten Ketone ubergefuhrt werden. Folgende o-gewinkelten Oligophenylene wurden synthetisiert : o-Terphenyl; 2o2-Quater-phenyl ; 32, 43-Dimethyl-2o2-quaterphenyl ; 3o2-Quinquiphenyl ; 12, 23-Dimethyl-3o2-quinquiphenyl ; 12, 23, 42, 53-Tetramethyl-3o2…

chemistry.chemical_classificationchemistry.chemical_compoundKetonechemistryYield (chemistry)Polymer chemistryMelting pointCyclohexanolOppenauer oxidationAcceptorQuinoneDie Makromolekulare Chemie
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