Übersetzung für 'antagonists' von Englisch nach Deutsch

antagonists

Widersacher {pl}

Antagonisten {pl}

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calcium antagonists

Calciumantagonisten {pl}pharm.

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dopamine antagonists

Dopamin-Antagonisten {pl}pharm.

hormone antagonists

Hormonantagonisten {pl}pharm.

receptor antagonists

Rezeptorantagonisten {pl}pharm.

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folic acid antagonists

Folsäureantagonisten {pl}chem.

H2-receptor antagonists

H2-Rezeptorantagonisten {pl}pharm.

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angiotensin II receptor antagonists

Angiotensin-II-Rezeptor-Antagonisten {pl}pharm.

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N-methyl-D-aspartate antagonists <NMDA antagonists>

N-Methyl-D-Aspartat-Antagonisten {pl} <NMDA-Antagonisten>pharm.

• Alpha-blockers, also known as α-blockers or α-adrenoreceptor antagonists, are a class of pharmacological agents that act as antagonists on α-adrenergic receptors (α-adrenoceptors).
• Examples include histamine receptor agonists and histamine receptor antagonists (or antihistamines).
• Chemicals that deactivate the NMDA receptor are called antagonists.
• Hence, anticholinergics, antihistamines, dopamine antagonists, serotonin antagonists, and cannabinoids are used as antiemetics.
• It became clear years later that aldosterone antagonists inhibit a specific receptor protein.

• Doxazosin is usually added to other antihypertensive therapy such as calcium channel antagonists, diuretics, beta-adrenoreceptor antagonists, angiotensin-converting enzyme inhibitors and angiotensin-2 receptor blockers.
• Conversely, coadministration of NMDA-antagonists with alpha-2 adrenergic antagonists, like yohimbine, could theoretically potentiate NAN.
• H2-receptor antagonists are sometimes used in addition to H1-antagonists to treat urticaria, but there is limited evidence for their efficacy.
• Derivative of willardiine have been developed as synthetic kainate and AMPA receptor antagonists ("See:" #Synthesis for specifics on development of antagonists).
• Silent antagonists are competitive receptor antagonists that have zero intrinsic activity for activating a receptor.

• Even though small molecule antagonists and NTD antagonist targeting AF2 surface differ in binding sites, they both inhibit AR function by disrupting AF2 function.