Search results for "TOXICITY"

showing 10 items of 2261 documents

Filtration and ingestion rates of brachionus calyciflorus after exposure to endosulfan and diazinon

1992

Abstract 1. Rotifers Brachionus calyciflorus were exposed to endosulfan and diazinon to determine the effect on nitration and ingestion rates. 2. The experiments were carried out with the algae Nannochloris oculata in a density of 5 × 105 cell/ml. 3. Rates of filtration and ingestion were decreased significantly at sublethal concentrations of pesticide tested after 5 hr exposure. 4. The effective concentration at which filtration and ingestion rates were reduced to 50% of those in controls ( ec 50) were calculated for both toxicants.

PharmacologyDiazinonImmunologyPesticideBiologybiology.organism_classificationlaw.inventionToxicologychemistry.chemical_compoundchemistryAlgaelawToxicityBrachionus calyciflorusIngestionFood scienceFiltrationEndosulfanComparative Biochemistry and Physiology Part C: Comparative Pharmacology
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Steroidal saponins from Dioscorea preussii.

2014

Abstract Three new steroidal saponins, named diospreussinosides A–C (1–3), along with two known ones (4, 5) were isolated from rhizomes of Dioscorea preussii. Their structures were elucidated mainly by 1D and 2D NMR spectroscopic analysis and mass spectrometry as (25S)-17α,25-dihydroxyspirost-5-en-3β-yl-O-α- l -rhamnopyranosyl-(1 → 4)-α- l -rhamnopyranosyl-(1 → 4)-β- d -glucopyranoside (1), (25S)-17α,25-dihydroxyspirost-5-en-3β-yl-O-α- l -rhamnopyranosyl-(1 → 4)-α- l -rhamnopyranosyl-(1 → 4)-[α- l -rhamnopyranosyl-(1 → 2)]-β- d -glucopyranoside (2), and (24S,25R)-17α,24,25-trihydroxyspirost-5-en-3β-yl-O-α- l -rhamnopyranosyl-(1 → 4)-α- l -rhamnopyranosyl-(1 → 4)-[α- l -rhamnopyranosyl-(1 → …

PharmacologyDioscorea preussiiMolecular StructureStereochemistryChemistryDioscoreaPhytosterolsGeneral MedicineSaponinsMass spectrometryHCT116 CellsRhizomeDihydroxylationCarcinoma CellDrug DiscoveryHumansDrug Screening Assays AntitumorCytotoxicityTwo-dimensional nuclear magnetic resonance spectroscopyHT29 CellsHuman colonFitoterapia
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INFLUENCE OF α-6-DEOXY-5-OXYTETRACYCLINE ON SOME PHARMA-COLOGICAL CHARACTERISTICS OF DAUNOMYCIN

1973

(1) Treatment with doxycyline substantially reduces the acute toxicity of daunomycin to the mouse. Treatment with doxycycline alters the distribution of daunomycin amongst the body tissues of the mouse. The ability of the isolated kidney to bind the daunomycin is enhanced by pretreatment with doxycycline. This observation is in agreement with the phenomenon noted in vivo with the same organ. (2) The antineoplastic activity of daunomycin, tested in vivo in mice bearing Sarcoma 180 is not modified by treatment with doxycyctine, nor does doxycycline modify the inhibition of DNA synthesis in isolated Sarcoma 180 cells by daunomycin. (3) The experiments carried out on isolated cell, namely: (a) …

PharmacologyDoxycyclineDNA synthesisOxytetracyclinePharmacologyBiologyAcute toxicitychemistry.chemical_compoundchemistryIn vivoDrug DiscoverymedicineDistribution (pharmacology)ThymidineReceptormedicine.drugThe Journal of Antibiotics
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An LD50model for predicting psychotropic drug toxicity using biopartitioning micellar chromatography

2001

The LD50 determination is the main way to measure the acute toxicity of all types of substances. At the present time, however, there is increasing opposition to the use of living animals in research and testing activities from animal rights groups as well as some scientists. Nevertheless, the need to have a tool for estimating the potential toxicity of new compounds for human consumption has encouraged the development of alternative methods. Under adequate conditions, the partitioning in micellar liquid chromatography can describe the drug biopartitioning. We have named this chromatographic system biopartitioning micellar chromatography (BMC). In this paper, an LD50 QRAR model developed for…

PharmacologyDrugAlternative methodsChromatographyChemistrymedia_common.quotation_subjectClinical BiochemistryGeneral MedicinePharmacologyBiochemistryAcute toxicityAnalytical ChemistryPsychotropic drugMicellar liquid chromatographyDrug DiscoveryToxicityMolecular Biologymedia_commonPotential toxicityBiomedical Chromatography
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Cytotoxicity of main anthraquinone aglycons towards drug sensitive and multi drug resistant T leukaemia cancer cells

2016

PharmacologyDrugChemistrymedia_common.quotation_subjectOrganic ChemistryPharmaceutical ScienceAnthraquinoneAnalytical Chemistrychemistry.chemical_compoundComplementary and alternative medicineDrug DiscoveryCancer cellCancer researchMolecular MedicineMulti drug resistantCytotoxicitymedia_commonPlanta Medica
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Oxidized respiratory molecules induced in vivo by nitrite in Pontodrilus littoralis (oligochaeta)

1992

Abstract 1. The in vivo effect of nitrite has been investigated in Pontodrilus littoralis. 2. Exposure of the animals at nitrite concentrations (0.05–0.1%) produced methaemoglobin and hemichromes. 3. Disappearance of oxidized forms was obtained when normal rearing conditions were restored. 4. Longer exposure to higher nitrite concentrations produced irreversible oxidized forms.

PharmacologyHemeproteinImmunologychemistry.chemical_elementNitrogenMethemoglobinchemistry.chemical_compoundBiochemistrychemistryIn vivoToxicityHemoglobinRespiratory systemNitriteComparative Biochemistry and Physiology Part C: Comparative Pharmacology
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Modulation of the pharmacokinetics, therapeutic and adverse effects of NSAIDs by Chinese herbal medicines.

2014

Concomitant use of NSAIDs and Chinese herbal medicines (CHMs) is frequent, yet summarized information on their interactions is lacking.A systematic review of literature in four evidence-based English databases was performed. Articles which reported CHMs altering the pharmacokinetics, therapeutic and adverse effects of NSAIDs were identified and summarized. Such interactions may lead to beneficial, detrimental or no change in outcomes. The current review covers four therapeutic effects of NSAIDs, including: i) anti-inflammatory; ii) analgesic; iii) antiplatelet, cardiovascular and cerebrovascular; and iv) anticancer effects and four adverse effects of NSAIDs, including: i) gastrointestinal u…

PharmacologyHerb-drug interactionsbusiness.industryAnalgesicTherapeutic effectAnti-Inflammatory Agents Non-SteroidalHerb-Drug InteractionsGeneral MedicinePharmacologyToxicologyRisk Assessmentdigestive system diseasesNephrotoxicityPharmacokineticsMedicineAnimalsHumansGastrointestinal ulcerbusinessAdverse effectDrugs Chinese HerbalExpert opinion on drug metabolismtoxicology
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A3- and A2B-nitrocorroles: synthesis and antiviral activity evaluation against human cytomegalovirus infection

2020

Human cytomegalovirus (hCMV) is responsible for several pathologies impacting immunocompromised patients and can trigger life-threatening infection. Several antivirals are available and are used in the clinic, but hCMV resistant strains have appeared and patients have encountered therapeutic failure. Hence, there is a constant need for new best in class or first in class antiviral molecules. We have previously shown that nitrocorroles could be used as a potent anti-hCMV agent without acute toxicity in mice. They therefore represent an excellent platform to perform structure–activity relationship (SAR) studies and to increase efficiency or reduce toxicity. We have generated original A2B- and…

PharmacologyHuman cytomegalovirus0303 health sciences010405 organic chemistrybusiness.industryOrganic ChemistryPharmaceutical Sciencemedicine.disease01 natural sciencesBiochemistryAcute toxicity0104 chemical sciences03 medical and health sciencesDrug DiscoveryToxicityCancer researchMolecular MedicineMedicineTherapeutic failurebusiness030304 developmental biologyRSC Medicinal Chemistry
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Indole alkaloids from the coprophilous fungus Aphanoascus fulvescens

2019

Abstract The Ascomycete fungus Aphanoascus fulvescens isolated from goose dung was investigated for its secondary metabolites, yielding five new indole alkaloids okaramines V–Z (1–5) and eleven known derivatives (6–16). Their structures were determined by 1D, 2D NMR spectra and HRMS data. Compounds 6, 8, 11 and 12 showed significant to moderate cytotoxicity against the mouse lymphoma cell line L5178Y with IC50 values ranging from 4.0 to 14.7 μM. Preliminary structure-activity relationships are discussed.

PharmacologyIndole testbiology010405 organic chemistryChemistryStereochemistryMouse LymphomaGeneral MedicineFungusAphanoascus fulvescensbiology.organism_classification01 natural sciences0104 chemical sciences010404 medicinal & biomolecular chemistryGoosebiology.animalDrug DiscoveryIc50 valuesCytotoxicityTwo-dimensional nuclear magnetic resonance spectroscopyFitoterapia
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Pharmacological evaluation of the dichloromethanol extract fromInula crithmoides L.

1995

The pharmacological effect of the dichloromethanol extract of Inula crithmoides L. was analysed in in vitro and in vivo models. The extract dose-dependently decreased arterial blood pressure and furthermore it showed low acute toxicity, CNS depressor activity and analgesic and antiinflammatory effects. Preincubation of the guinea-pig ileum and rat duodenum (100 μg/mL) produced a significant reduction in the contractile effects of histamine and acetylcholine and a concentration-related inhibition of the effects of serotonin. Following further fractionation the methylene chloride/acetone (50/50) fraction caused a significant decrease in motor activity and significantly reduced the threshold o…

PharmacologyInulabiologyAnalgesicBiological activityPharmacologybiology.organism_classificationAcute toxicitychemistry.chemical_compoundchemistryIn vivoAnesthesiaToxicitymedicineHistamineAcetylcholinemedicine.drugPhytotherapy Research
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