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DRUG RECEPTOR INTERACTIONS
DRUG RECEPTOR INTERACTIONS

... - a drug that has both affinity and high intrinsic activity. ...
Environmental pathology lec.1
Environmental pathology lec.1

... of lung cancer in non-smokers exposed to second-hand smoke is 1.3 times greater than in individuals not exposed to environmental smoke. Effects of Alcohol Adverse alcohol effects are due to: Acute alcohol injury including hepatic steatosis (fatty change), gastritis and ulceration, and the depression ...
estrogens & androgens
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... densitometry, corresponds to the lowest 10%. Her comorbidities include hypertension; diabetes mellitus, type 2; and congestive heart failure (CHE). The attending physician suggests that if this patient had received long-term treatment with a drug affecting calcium metabolism her fracture could have ...
Benedict`S Soln(Qualitative)
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... Bioaccumulation potential: Toxicity: Quantitative data on the ecological effect of this product are not available. Adverse ecological effects cannot be excluded in the event of improper handling or disposal. Do not allow to enter drinking water supplies, waste water, or soil! The following applies t ...
Pharm Test 1
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Power Point Presentation
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Aquatic Communities: Habitats
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PEC/PNEC approach - Deltares Public Wiki

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estrogens and androgens
estrogens and androgens

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5-Mechanism of drug action2015-10-14 05:152.0 MB

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Definition of the word `Drug`: Drugs are chemicals that prevent

... steric interactions between specific chemical groups of the drug. These sites are termed receptors.  Types of Receptors: There are several types of receptors. G-protein coupled receptors, ion-gated channels, enzyme-linked receptors, intracellular receptors.  Receptor definition is changing … DNA a ...
AZ compound details for MRC Asset Sharing Sept 2016
AZ compound details for MRC Asset Sharing Sept 2016

... somnolence, and headache. These were transient, mild, and related to peak plasma concentrations. In patients dosed for up to 28 days, AZD7325 was generally well tolerated with the most frequent adverse events being dizziness, headache, and somnolence although one grand mal convulsion was also report ...
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Toxicodynamics



Toxicodynamics, termed pharmacodynamics in pharmacology, describes the dynamic interactions of a toxicant with a biological target and its biological effects. A biological target, also known as the site of action, can be binding proteins, ion channels, DNA, or a variety of other receptors. When a toxicant enters an organism, it can interact with these receptors and produce structural or functional alterations. The mechanism of action of the toxicant, as determined by a toxicant’s chemical properties, will determine what receptors are targeted and the overall toxic effect at the cellular level and organismal level.Toxicants have been grouped together according to their chemical properties by way of quantitative structure-activity relationships (QSARs), which allows prediction of toxic action based on these properties. endocrine disrupting chemicals (EDCs) and carcinogens are examples of classes of toxicants that can act as QSARs. EDCs mimic or block transcriptional activation normally caused by natural steroid hormones. These types of chemicals can act on androgen receptors, estrogen receptors and thyroid hormone receptors. This mechanism can include such toxicants as dichlorodiphenyltrichloroethane (DDE) and polychlorinated biphenyls (PCBs). Another class of chemicals, carcinogens, are substances that cause cancer and can be classified as genotoxic or nongenotoxic carcinogens. These categories include toxicants such as polycyclic aromatic hydrocarbon (PAHs) and carbon tetrachloride (CCl4). The process of toxicodynamics can be useful for application in environmental risk assessment by implementing toxicokinetic-toxicodynamic (TKTD) models. TKTD models include phenomenas such as time-varying exposure, carry-over toxicity, organism recovery time, effects of mixtures, and extrapolation to untested chemicals and species. Due to their advantages, these types of models may be more applicable for risk assessment than traditional modeling approaches.
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