Translation for 'potency' from English to Portuguese

potency

potência {f}med.quím.

• It is one of the most potent AAS to have ever been synthesized, with 120 to 300 times the oral anabolic potency and 60 to 70 times the androgenic potency of the reference AAS methyltestosterone in castrated male rats, although the same level of potency has not been observed in studies in humans.
• EE was estimated to have 241-fold the potency of estradiol valerate in terms of suppression follicle-stimulating hormone (FSH) levels, 2,918-fold the potency in terms of increased PZP levels, and 779-fold the potency in terms of increased SHBG levels.
• Furethidine is a 4-phenylpiperidine derivative that is related to the clinically used opioid analgesic drug pethidine (meperidine), but with around 25x higher potency.
• The table above shows the potency of PDE2 inhibitors including EHNA.
• Chlorpromazine is classified as a low-potency typical antipsychotic.

• Clocortolone is an upper-mid potency topical corticosteroid formulation. It is rated at a class 4 potency on a scale of 1 (highest potency) to 7 (lowest potency).
• The protein nitrogen unit (PNU) measures the potency of the compounds used in allergy skin tests, and is equivalent to 0.01 microgram (µg) of phosphotungstic acid-precipitable protein nitrogen.
• In general, methyl quaternization is optimal for potency but, opposing this rule, the trimethyl derivatives of gallamine are of lower potency than gallamine.
• To reduce the risk of adverse events, high-potency glucocorticoid should not be applied on the face, intertriginous areas, areas with thin layers of skin (e.g. ...
• It is a derivative of an older drug viminol, which has been modified to improve potency and metabolic stability.

• When evaluating the phosphoramidate ester substituent (R3) the 1-naphthyl ester has the greatest potency but it is also cytotoxic so it is not a viable substituent.
• The curve toward the left represents a higher potency (potency arrow does not indicate direction of increase) since lower concentrations are needed for a given response.
• In studies on mice, it was found to be approximately 40% the potency of LSD, compared to the 60% increase in potency seen with ETH-LAD and roughly equivalent potency in AL-LAD and PRO-LAD.
• Oral potency may be less than parenteral potency because significant amounts (up to 50% in some cases) may not reach the circulation.
• Potency is the amount of agonist needed to elicit a desired response.

• A series of 3-benzazepine derivatives, such as Lorcaserin (Figure 6) have been evaluated for their potency and selectivity for the 5-HT2C receptors.
• Agents that are part of this class of duocarmycins have the potency in the low picomolar range.
• Compared to amphetamine, tranylcypromine shows low potency as a dopamine releasing agent, with even weaker potency for norepinephrine and serotonin release.