Half maximal effective concentration ( EC 50 ) is a measure of the concentration of a drug, antibody or toxicant which induces a biological response halfway between the baseline and maximum after a specified exposure time. More simply, EC 50 can be defined as the concentration required to obtain a 50% [...] effect and may be also written as [A] 50 . It is commonly used as a measure of a drug's potency , although the use of EC 50 is preferred over that of 'potency', which has been criticised for its vagueness. EC 50 is a measure of concentration, expressed in molar units (M), where 1 M is equivalent to 1 mol / L .
11-478: LT50 is the median Lethal Time (time until death) after exposure of an organism to a toxic substance or stressful condition. LT50 is commonly used in toxicology studies to quantify amount of a stressor necessary to kill an organism. LT50 can be used in conjunction with EC50 (median Exposure Concentration) for even more precise quantification. This toxicology -related article is a stub . You can help Misplaced Pages by expanding it . EC50 The EC 50 of
22-409: A graded dose response curve therefore represents the concentration of a compound where 50% of its maximal effect is observed. The EC 50 of a quantal dose response curve represents the concentration of a compound where 50% of the population exhibit a response, after a specified exposure duration. For clarification, a graded dose response curve shows the graded effect of the drug (y axis) over
33-462: Is 50% of E max is termed the half maximal effective concentration and is abbreviated EC 50 , or rarely [A] 50 . The term "potency" refers to the EC 50 value. The lower the EC 50 , the less the concentration of a drug is required to produce 50% of maximum effect and the higher the potency. The EC 10 and EC 90 concentrations to induce 10% and 90% maximal responses are defined similarly. There
44-433: Is a wide range of EC 50 values of drugs; they are typically anywhere from nM to mM. Hence, it is often more practical to refer to the logarithmically transformed p EC 50 values instead of EC 50 , where pEC 50 = − log 10 ( EC 50 ) {\displaystyle {\ce {pEC50}}=-\log _{10}({\ce {EC50}})} . A drug's potency
55-407: Is dependent on the drug's affinity and efficacy . Affinity describes how well a drug can bind to a receptor. Faster or stronger binding is represented by a higher affinity, or equivalently a lower dissociation constant. The EC 50 should not be confused with the affinity constant, K d . While the former reflects the drug concentration needed for a level of tissue response, the latter reflects
66-399: Is the EC 50 . The EC 50 is also related to IC 50 which is a measure of a compound's inhibition (50% inhibition). Biological responses to ligand concentrations typically follow a sigmoidal function. The inflection point at which the increase in response with increasing ligand concentration begins to slow is the EC 50 , which can be mathematically determined by derivation of
77-605: The best-fit line. While relying on a graph for estimation is more convenient, this typical method yields less accurate and precise results. The response or effect, E, is dependent on both the binding of the drug and the drug-bound receptor. The agonist that binds to the receptor and initiates the response is usually abbreviated A or D. At low agonist concentrations, [A], the response, E is immeasurably low but at higher [A], E becomes measurable. E increases with [A] until at sufficiently high [A], when E plateaus towards an asymptotic maximum attainable response, E max . The [A] at which E
88-425: The dose of the drug (x axis) in one or an average of subjects. A quantal dose response curve shows the percentage of subjects where a response is noted in an all-or-none manner (y axis) over the dose of the drug (x axis). For competition binding assays and functional antagonist assays IC 50 is the most common summary measure of the dose-response curve. For agonist/stimulator assays the most common summary measure
99-464: The drug concentration needed for an amount of receptor binding. Efficacy is the relationship between receptor occupancy and the ability to initiate a response at the molecular, cellular, tissue or system level. The EC 50 relates to the Hill equation , which is a function of the agonist concentration, [A]: where E is the observed response or effect above baseline, and n, the Hill coefficient reflects
110-400: The exposure time. Therefore, the EC 50 (and similar statistics) will be a function of exposure time. The exact shape of this time function will depend upon the stressor (e.g., the specific toxicant), its mechanism of action, the organism exposed, etc. This time dependency hampers the comparison of potency or toxicity between compounds and between different organisms. A drug will not have
121-461: The slope of the curve. The EC 50 represents the point of inflection of the Hill equation, beyond which increases of [A] have less impact on E. In dose response curves , the logarithm of [A] is often taken, turning the Hill equation into a sigmoidal logistic function . In this case, the EC 50 represents the rising section of the sigmoid curve. The effects of a stressor or drug generally depend on
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