Top200B MOA

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100 Terms

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acyclovir
Inhibits DNA synthesis and viral replication by competing with deoxyguanosine triphosphate for viral DNA polymerase and being incorporated into viral DNA
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amlodipine
Acts on vascular smooth muscle to produce peripheral arterial vasodilation by inhibiting calcium ions from entering select voltage-sensitive areas of vascular smooth muscle
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amoxicillin
Binds to penicillin-binding proteins (PBPs) which inhibits peptidoglycan synthesis in bacterial cell walls, thus inhibiting cell wall biosynthesis
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apixaban
Inhibits platelet activation and fibrin clot formation via direct, selective, and reversible inhibition of free and clot-bound factor Xa
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aspirin
Irreversibly inhibits cyclooxygenase-1 and 2 enzymes, via acetylation, which results in decreased formation of prostaglandin precursors Irreversibly inhibits formation of prostaglandin derivative, thromboxane A2, via acetylation of platelet cyclooxygenase, thus inhibiting platelet aggregation
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atenolol
Selectively blocks beta1-receptors
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atorvastatin
Inhibits 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase
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azithromycin
Inhibits RNA-dependent protein synthesis by binding to the 5S ribosomal subunit
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carvedilol
Nonselectively blocks beta-adrenoreceptors and alpha-adrenoreceptors
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cefazolin
Inhibits bacterial cell wall synthesis by binding to one or more of the penicillin-binding proteins (PBPs) which in turn inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls, thus inhibiting cell wall biosynthesis
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cefdinir
Binds to penicillin-binding proteins (PBPs) which inhibits peptidoglycan synthesis in bacterial cell walls, thus inhibiting cell wall biosynthesis
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cefepime
Inhibits bacterial cell wall synthesis by binding to one or more of the penicillin-binding proteins (PBPs) which in turn inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls, thus inhibiting cell wall biosynthesis
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ceftriaxone
Inhibits bacterial cell wall synthesis by binding to one or more of the penicillin-binding proteins (PBPs) which in turn inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls, thus inhibiting cell wall biosynthesis
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cephalexin
Binds to penicillin-binding proteins (PBPs) which inhibits peptidoglycan synthesis in bacterial cell walls, thus inhibiting cell wall biosynthesis
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chlorhexidine
The bactericidal effect is a result of the binding of this cationic molecule to negatively charged bacterial cell walls and extramicrobial complexes. At low concentrations, this causes an alteration of bacterial cell osmotic equilibrium and leakage of potassium and phosphorous resulting in a bacteriostatic effect At high concentrations, the cytoplasmic contents of the drug and bacterial cell precipitate and result in cell death.
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chlorthalidone
Sulfonamide-derived diuretic that inhibits sodium and chloride reabsorption in the distal convoluted tubule
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ciprofloxacin
Inhibits DNA-gyrase and promotes breakage of double-stranded DNA
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clindamycin
Binds to 5S ribosomal subunit resulting in inhibition of protein synthesis
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clonidine
Stimulates alpha2-adrenoceptors in the brain stem, thus activating an inhibitory neuron, resulting in reduced sympathetic outflow from the CNS
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clopidogrel
Irreversibly blocks the P2Y12 component of ADP receptors on the platelet surface
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dabigatran
Specific, reversible, direct thrombin inhibitor that inhibits both free and fibrin-bound thrombin
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daptomycin
Binds to components of the cell membrane of susceptible organisms and causes rapid depolarization, inhibiting intracellular synthesis of DNA, RNA, and protein
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darunavir
Binds to the site of HIV-1 protease activity and inhibits cleavage of viral Gag-Pol polyprotein precursors into individual functional proteins required for infectious HIV
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digoxin
Inhibits the sodium/potassium ATPase pump in myocardial cells leading to increased contractility Directly suppresses AV node conduction to increase effective refractory period and decrease conduction velocity
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diltiazem
Inhibits calcium ions from entering select voltage-sensitive areas of vascular smooth muscle and myocardium during depolarization
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docusate
Reduces surface tension of the oil-water interface of the stool resulting in enhanced incorporation of water and fat allowing for stool softening
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dopamine
Stimulates both adrenergic and dopaminergic receptors, lower doses are mainly dopaminergic stimulating and produce renal and mesenteric vasodilation, higher doses also are both dopaminergic and beta1-adrenergic stimulating and produce cardiac stimulation and renal vasodilation
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doxycycline
Inhibits protein synthesis by binding with the 3S ribosomal subunit
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dutasteride
Selectively inhibits 5α-reductase, resulting in inhibition of the conversion of testosterone to dihydrotestosterone and markedly suppressed serum dihydrotestosterone levels
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emtricitabine, tenofovir, and efavirenz (combination)
Non-nucleoside reverse transcriptase inhibitor of HIV-1, thereby blocking the RNA-dependent and DNA-dependent DNA polymerase resulting in inhibition of viral replication Nucleoside reverse transcriptase inhibitor, which interferes with HIV viral RNA dependent DNA polymerase resulting in inhibition of viral replication Nucleotide reverse transcriptase inhibitor, interferes with the HIV viral RNA dependent DNA polymerase resulting in inhibition of viral replication
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enalapril
Inhibits angiotensin converting enzyme, preventing the conversion of angiotensin I to angiotensin II
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enoxaparin
Strong inhibitor of factor Xa
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epinephrine
Stimulates alpha-, beta1-, and beta2-adrenergic receptors resulting in relaxation of smooth muscle of the bronchial tree, cardiac stimulation (increasing myocardial oxygen consumption), and dilation of skeletal muscle vasculature; Small doses can cause vasodilation via beta2-vascular receptors; large doses may produce constriction of skeletal and vascular smooth muscle
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ertapenem
Inhibits bacterial cell wall synthesis by binding to one or more of the penicillin-binding proteins; which in turn inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls, thus inhibiting cell wall biosynthesis
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esomeprazole
Suppresses gastric acid secretion by inhibition of the H+/K+-ATPase in the gastric parietal cell
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estradiol
Responsible for the development and maintenance of the female reproductive system and secondary sexual characteristics Modulate the pituitary secretion of gonadotropins, luteinizing hormone, and follicle-stimulating hormone through a negative feedback system
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ethinyl estradiol and etonogestrel (combination)
Combination hormonal contraceptives inhibit ovulation via a negative feedback mechanism on the hypothalamus, which alters the normal pattern of gonadotropin secretion of a follicle-stimulating hormone (FSH) and luteinizing hormone by the anterior pituitary
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ezetimibe
Inhibits absorption of cholesterol at the brush border of the small intestine via the sterol transporter, Niemann-Pick C1-Like1 (NPC1L1)
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famotidine
Competitively inhibits histamine at H2 receptors of the gastric parietal cells, which inhibits gastric acid secretion
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fenofibrate and derivatives
Agonist for the nuclear transcription factor peroxisome proliferator-activated receptor-alpha (PPAR-alpha), downregulates apoprotein C-III (an inhibitor of lipoprotein lipase) and upregulates the synthesis of apolipoprotein A-I, fatty acid transport protein, and lipoprotein lipase resulting in an increase in VLDL catabolism, fatty acid oxidation, and elimination of triglyceride-rich particles
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finasteride
Selectively inhibits 5α-reductase, resulting in inhibition of the conversion of testosterone to dihydrotestosterone and markedly suppressed serum dihydrotestosterone levels
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fluconazole
Interferes with fungal cytochrome P450 activity (lanosterol 14-α-demethylase), and decreases ergosterol synthesis which inhibits cell membrane formation
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furosemide
Inhibits reabsorption of sodium and chloride in the ascending loop of Henle and proximal and distal renal tubules, interfering with the chloride-binding cotransport system, thus causing increased excretion of water, sodium, chloride, magnesium, and calcium
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gentamicin
Interferes with bacterial protein synthesis by binding to 30S ribosomal subunit resulting in a defective bacterial cell membrane
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Group: Oral Contraceptives
Combination hormonal contraceptives inhibit ovulation via a negative feedback mechanism on the hypothalamus, which alters the normal pattern of gonadotropin secretion of a follicle-stimulating hormone (FSH) and luteinizing hormone by the anterior pituitary
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heparin
Potentiates the action of antithrombin III and thereby inactivates thrombin (as well as other coagulation factors IXa, Xa, XIa, XIIa, and plasmin) and prevents the conversion of fibrinogen to fibrin; also stimulates release of lipoprotein lipase (lipoprotein lipase hydrolyzes triglycerides to glycerol and free fatty acids)
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hydralazine
Direct vasodilation of arterioles
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hydrochlorothiazide
Inhibits sodium reabsorption in the distal tubules causing increased excretion of sodium and water as well as potassium and hydrogen ions
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imipenem and cilastatin (combination)
Inhibits bacterial cell wall synthesis
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isosorbide mononitrate
Activates cGMP leading to dephosphorylation of myosin light chains and smooth muscle relaxation
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lansoprazole
Suppresses gastric acid secretion by inhibition of the H+/K+-ATPase in the gastric parietal cell
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levofloxacin
Inhibits DNA-gyrase and promotes breakage of double-stranded DNA
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levothyroxine
Synthetic form of thyroxine (T4), which is converted to active thyroid hormone
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linezolid
Inhibits bacterial protein synthesis by binding to bacterial 23s ribosomal RNA
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liothyronine
Active (T3) thyroid hormone
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lisinopril
Inhibits angiotensin converting enzyme, preventing the conversion of angiotensin I to angiotensin II
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losartan
Antagonizes angiotensin receptors, blocking the vasoconstrictor and aldosterone secreting effects of angiotensin II
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meropenem
Inhibits bacterial cell wall synthesis
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metoprolol
Selectively blocks beta1-receptors
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metronidazole
Interacts with DNA to cause a loss of helical DNA structure and strand breakage resulting in inhibition of protein synthesis and cell death
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minocycline
Inhibits protein synthesis by binding with the 30S ribosomal subunit
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mupirocin
Binds to bacterial isoleucyl transfer-RNA synthetase resulting in the inhibition of protein synthesis
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nifedipine
Acts on vascular smooth muscle to produce peripheral arterial vasodilation by inhibiting calcium ions from entering select voltage-sensitive areas of vascular smooth muscle
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nitrofurantoin
Inactivates or alters bacterial ribosomal proteins leading to inhibition of protein synthesis, aerobic energy metabolism, DNA, RNA, and cell wall synthesis
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nitroglycerin
Activates cGMP leading to dephosphorylation of myosin light chains and smooth muscle relaxation
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norepinephrine
Stimulates beta1-adrenergic receptors and alpha-adrenergic receptors causing increased contractility and heart rate as well as vasoconstriction, thereby increasing systemic blood pressure and coronary blood flow
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norethindrone
Suppresses ovulation, thickens cervical mucus, alters follicle-stimulating hormone (FSH) and luteinizing hormone (LH) concentrations, slows the movement of ovum through the fallopian tubes, and alters the endometrium
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omega-3 fatty acids
Reduction in hepatic production of VLDL and a reduction in the hepatic synthesis of triglycerides
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omeprazole
Suppresses gastric acid secretion by inhibition of the H+/K+-ATPase in the gastric parietal cell
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ondansetron
Selective 5-HT3-receptor antagonist
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oseltamivir
Inhibits influenza virus neuraminidase
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oxybutynin
Direct antispasmodic effect on smooth muscle and inhibits the action of acetylcholine
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pantoprazole
Suppresses gastric acid secretion by inhibition of the H+/K+-ATPase in the gastric parietal cell
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penicillin v potassium
Interferes with bacterial cell wall synthesis during active multiplication, causing cell wall death and resultant bactericidal activity against susceptible bacteria
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phentermine
secondary to CNS effects, including stimulation of the hypothalamus to release norepinephrine
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piperacillin and tazobactam (combination)
Interferes with bacterial cell wall synthesis during active multiplication, causing cell wall death and resultant bactericidal activity against susceptible bacteria
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polyethylene glycol
osmotic agent, causes water retention in the stool
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pravastatin
Inhibits 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase
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promethazine
Blocks postsynaptic mesolimbic dopaminergic receptors in the brain; exhibits a strong alpha-adrenergic blocking effect and depresses the release of hypothalamic and hypophyseal hormones; competes with histamine for the H1-receptor
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propranolol
Nonselective beta-adrenergic blocker; competitively blocks response to beta1- and beta2-adrenergic receptors
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rivaroxaban
Inhibits platelet activation and fibrin clot formation via direct, selective and reversible inhibition of free and clot-bound factor Xa
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rosuvastatin
Inhibits 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase
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sacubitril and valsartan (combination)
Prodrug that inhibits neprilysin, leading to increased levels of natriuretic peptides that induces vasodilation and natriuresis Produces direct antagonism of the angiotensin II (AT2) receptors.
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sildenafil
Inhibits phosphodiesterase type 5 (PDE-5), causing increased levels of cGMP, resulting in smooth muscle relaxation and increased blood flow
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simvastatin
Inhibits 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase
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sofosbuvir and ledipasvir (combination)
Ledipasvir inhibits the HCV NS5A protein necessary for viral replication sofosbuvir inhibits NS5B RNA-dependent RNA polymerase
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solifenacin
Inhibits muscarinic receptors resulting in decreased urinary bladder contraction, increased residual urine volume, and decreased detrusor muscle pressure
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spironolactone
Competes with aldosterone for receptor sites in the distal renal tubules, increasing sodium chloride and water excretion while conserving potassium and hydrogen ions Blocks the effect of aldosterone on arteriolar smooth muscle
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sulfamethoxazole and trimethoprim (combination)
Interferes with bacterial folic acid synthesis Inhibits bacterial folic acid metabolism
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tadalafil
Inhibits phosphodiesterase type 5 (PDE-5), causing increased levels of cGMP, resulting in smooth muscle relaxation and increased blood flow
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tamsulosin
Antagonist of alpha1A-adrenoreceptors leading to relaxation of smooth muscle in the bladder and prostate
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tenofovir alafenamide and emtricitabine (combination)
Each drug interferes with HIV viral RNA dependent DNA polymerase activities resulting in inhibition of viral replication
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testosterone
Principle endogenous androgen responsible for growth and development of male sex organs and maintaining secondary sex characteristics
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ticagrelor
Reversibly and noncompetitively binds the adenosine diphosphate (ADP) P2Y12 receptor on the platelet surface which prevents ADP-mediated activation of the GPIIb/IIIa receptor complex thereby reducing platelet aggregation
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triamterene
Blocks epithelial sodium channels in the late distal convoluted tubule and collecting duct which inhibits sodium reabsorption from the lumen. This effectively reduces intracellular sodium, decreasing the function of Na+/K+ ATPase, leading to potassium retention and decreased calcium, magnesium, and hydrogen excretion
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valacyclovir
Inhibits DNA synthesis and viral replication by competing with deoxyguanosine triphosphate for viral DNA polymerase and being incorporated into viral DNA
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vancomycin
Inhibits bacterial cell wall synthesis by blocking glycopeptide polymerization through binding tightly to D-alanyl-D-alanine portion of cell wall precursor
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vasopressin
stimulates a family of arginine vasopressin (AVP) receptors, oxytocin receptors, and purinergic receptors stimulates the AVPR1a (or V1) receptor and increases systemic vascular resistance and mean arterial blood pressure. stimulates the AVPR2 (or V2) receptor is then cyclic adenosine monophosphate (cAMP) increases which in turn increases water permeability at the renal tubule resulting in decreased urine volume and increased osmolality also causes smooth muscle contraction in the GI tract by stimulating muscular V1 receptors and release of prolactin and ACTH via AVPR1b (or V3) receptors
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verapamil
Inhibits calcium ions from entering select voltage-sensitive areas of vascular smooth muscle and myocardium during depolarization
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warfarin
Inhibits subunit 1 of the multi-unit VKOR complex, leading to depletion of factors II, VII, IX, and X, as well as proteins C and S.