Search results for "dane"

showing 10 items of 116 documents

Synthetic studies of neoclerodane diterpenoids from Salvia splendens and evaluation of opioid receptor affinity

2008

Abstract Salvinorin A ( 1 ), a neoclerodane diterpene from the hallucinogenic mint Salvia divinorum , is the only known non-nitrogenous and specific κ-opioid agonist. Several structural congeners of 1 isolated from Salvia splendens ( 2 – 8 ) together with a series of semisynthetic derivatives ( 9 – 24 ), some of which possess a pyrazoline structural moiety ( 9 , 19 – 22 ), have been tested for affinity at human μ, δ, and κ opioid receptors. None of these compounds showed high affinity binding to these receptors. However, 10 showed modest affinity for κ receptors suggesting that other natural neoclerodanes from different Salvia species may possess opioid affinity.

AgonistbiologyChemistrymedicine.drug_classStereochemistryOrganic ChemistryPyrazolineSalviabiology.organism_classificationBiochemistryArticleSalvinorin Achemistry.chemical_compoundOpioid receptorClerodanes opioid receptors salviaDrug DiscoverySalvia divinorummedicineDiterpeneReceptor
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Arterial and mixed venous blood gas status during apnoea of intubation--proof of the Christiansen-Douglas-Haldane effect in vivo.

1989

The Christiansen-Douglas-Haldane effect, in short the Haldane effect, describes the dependence of the CO2 binding of blood on the degree of oxygenation of haemoglobin. Under the physiological conditions of an ‘open’ system between blood and alveoli the partial pressure of arterial C02 (PaCO2), must be less than that of mixed venous blood (P[Formula: see text]CO2). During the unphysiological conditions of a ‘closed’ system, e.g. hyperoxic apnoea, i.e. continuous oxygen uptake without CO2 delivery by the lungs, the Paco2 will not only approximate the P[Formula: see text]CO2 but will even exceed it. Without the Haldane effect, rapid adjustment of Paco2 to P[Formula: see text]CO2 would be expe…

Apneamedicine.medical_treatmentPartial PressureCritical Care and Intensive Care MedicinepCO2VeinsExcretionIn vivoHaldane effectmedicineIntubation IntratrachealIntubationHumansLungbusiness.industryApneaOxygenationArteriesCarbon DioxideHydrogen-Ion ConcentrationAnesthesiology and Pain Medicinemedicine.anatomical_structureAnesthesiaOxyhemoglobinsGasesmedicine.symptombusinessAnaesthesia and intensive care
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Cytotoxic labdane diterpenes and bisflavonoid atropisomers from leaves of Araucaria bidwillii

2017

Abstract Chemical investigation of a methanolic extract of leaves from Araucaria bidwillii (Araucariaceae) from Egypt afforded four new labdane diterpenoidal metabolites (1–4) together with one known diterpene, 7-oxocallitrisic acid (5), two triterpenoidal metabolites, 2-O-acetyl-11-keto-boswellic acid (6) and β-sitosterol-3-O-glucopyranoside (7), phloretic acid (8), and two methylated bisflavonoids, agathisflavone-4′,7,7″-trimethyl ether (9) and cupressuflavone-4′,7,7″-trimethyl ether (10). The new metabolites 1–4 were unambiguously identified by applying extensive 1D and 2D NMR spectroscopic studies as well as HRESIMS. The relative and absolute configurations of 1–4 were determined using …

Atropisomer010405 organic chemistryStereochemistryOrganic ChemistryEtherAraucaria bidwillii010402 general chemistryAntimicrobial01 natural sciencesBiochemistryfood.food0104 chemical sciencesLabdanechemistry.chemical_compoundfoodTermészettudományokchemistryDrug DiscoveryOrganic chemistryPhloretic acidDiterpeneKémiai tudományokTwo-dimensional nuclear magnetic resonance spectroscopyTetrahedron
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Effect of lindane on the blood of a freshwater fish

1991

Blood GlucosePollutantbiologyHealth Toxicology and MutagenesisGeneral MedicinePesticideAnguillaToxicologybiology.organism_classificationPollutionFisherychemistry.chemical_compoundCholesterolchemistryFresh waterFreshwater fishAnimalsEcotoxicologyPyruvatesLindaneHexachlorocyclohexaneBulletin of Environmental Contamination and Toxicology
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Changes in selected biochemical parameters in the brain of the fish, Anguilla anguilla (L.), exposed to lindane.

1991

Brain ChemistryHealth Toxicology and MutagenesisZoologyGeneral MedicineBiologyToxicologyAnguillaLipid MetabolismPollutionToxicologyLethal Dose 50chemistry.chemical_compoundchemistryFresh waterToxicityLactatesFish <Actinopterygii>EcotoxicologyAnimalsLindanePyruvatesGlycogenHexachlorocyclohexaneBulletin of environmental contamination and toxicology
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Complete 1H and 13C NMR assignments of clerodane diterpenoids of Salvia splendens.

2006

Unambiguous and complete assignments of 1H and 13C NMR chemical shifts for five clerodane diterpenes, four of them isolated from Salvia splendens (salviarin, splendidin and splenolides A and B) and one obtained by acetylation of splenolide A, are presented. The assignments are based on 2D shift-correlated [1H,1H–COSY, 1H,13C-gHSQC–1J(C,H) and 1H,13C-gHMBC-nJ(C,H) (n = 2 and 3)] and nuclear Overhauser effect (NOE) experiments. The conformation of the rings of these compounds is supported by the 3J(H,H) values and NOE results. Copyright © 2006 John Wiley & Sons, Ltd.

Carbon IsotopesMagnetic Resonance SpectroscopybiologyStereochemistryChemistryChemical shiftAcetylationGeneral ChemistryNuclear Overhauser effectCarbon-13 NMRSalviabiology.organism_classificationDiterpenes ClerodaneUnambiguous and complete assignments of 1H and 13C NMR chemical shifts for five clerodane diterpenes four of them isolated from Salvia splendens (salviarin splendidin and splenolides A and B) and one obtained by acetylation of splenolide A are presented. The assignments are based on 2D shiftcorrelated [1H1H–COSY 1H13C-gHSQC–1J(CH) and 1H13C-gHMBC-nJ(CH) (n = 2 and 3)] and nuclear Overhauser effect (NOE) experiments. The conformation of the rings of these compounds is supported by the 3J(HH) values and NOE results. Copyright  2006 John Wiley & Sons LtdClerodane DiterpenesProton NMRGeneral Materials ScienceSalviaHydrogenMagnetic resonance in chemistry : MRC
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The Measurement of the CO2 Hb Binding Curve of Human Hemoglobin by 13C-NMR Spectrometry

1980

It is well known that under physiological conditions CO2 binds to the four terminal amino groups of hemoglobin (Hb) (Kilmartin and Rossi-Bernardi, 1971). The carbamino compounds which are formed by this reaction are involved in the Haldane effect.

ChemistryHaldane effectStereochemistryHemoglobinCarbon-13 NMRMass spectrometry
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Mercury and chlorinated hydrocarbons in zoobenthos of Lake Päijänne, Finland

1979

The average amounts of mercury, PCBs, and sigma DDT (primarily DDE), found in macrozoobenthos, on the wet basis, in Lake Päijänne, Finland, for the time period 1972-1974, were 79 ng/g, 29 ng/g, and 8 ng/g, respectively. Lindane was found in negligible amounts in only 2% of the samples examined; aldrin was present in 10% of the samples; no dieldrin was detected. Mercury and PCB concentrations varied regionally in the lake. PCB and sigma DDT concentrations were greater in the predatory bottom animals than in the herbivores or detritus feeders, and the amounts of chlorinated hydrocarbons were greater in profundal animals than in littoral animals. No significant correlation was apparent between…

ChemistryHealth Toxicology and MutagenesisDetritivorechemistry.chemical_elementFresh WaterMercuryGeneral MedicineToxicologyInvertebratesPolychlorinated BiphenylsPollutionDDTMercury (element)chemistry.chemical_compoundDieldrinEnvironmental chemistryHydrocarbons ChlorinatedLittoral zoneAnimalsEcotoxicologyAldrinProfundal zoneLindaneFinlandArchives of Environmental Contamination and Toxicology
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Hyperoxic Intubation Apnoea: An In Vivo Model for the Proof of the Christiansen-Douglas-Haldane Effect

1989

The Christiansen-Douglas-Haldane effect (HALDANE effect) describes the different CO2 binding capacity of haemoglobin on its degree of oxygenation and was first demonstrated in vitro in 1914 (Christiansen, Douglas and Haldane, 1914).

ChemistryIn vivoHaldane effectAnesthesiamedicine.medical_treatmentmedicineIntubationMixed venous blood
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Labdane Diterpenes from Stachys plumosa

2000

Three new labdane diterpenoids were isolated from the aerial parts of Stachys plumosa. The first two (1, 2) were the dextrorotatory enantiomers of the known 6-deoxyandalusol and 13-epijabugodiol. Structures were determined using NMR and MS techniques. The absolute stereochemistry of the third compound (3) was not experimentally proved.

Chromatography GasMagnetic Resonance SpectroscopyOptical RotationStereochemistryPharmaceutical ScienceGas Chromatography-Mass SpectrometryAnalytical ChemistryDextrorotatoryLabdanechemistry.chemical_compoundBalkan peninsulaDrug DiscoveryOrganic chemistryPharmacologyLamiaceaePlant StemsChemistryOrganic ChemistryAbsolute configurationStachys plumosaTerpenoidPlant LeavesItalyComplementary and alternative medicineChromatography GelMolecular MedicineSpectrophotometry UltravioletEpimerDiterpenesDiterpeneJournal of Natural Products
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