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Drug mechanisms exam 6 Stats
Can you pick the Drug mechanisms exam 6
By
Dent2017
20m
96 Questions
15 Plays
15 Plays
15 Plays
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Avg Score
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Score
0/96
Timer
20:00
0
Plays Today
% Correct
Neutralizes acid
53.3%
Neutralizes acid
46.7%
Activates PPAR
46.7%
Block H2 receptor
40%
Inc. motility
40%
Binds opiate receptor
40%
Blocks muscarinic receptors
40%
Blocks Cl- channels in gut
40%
Decrease prostaglandin synth in gut
40%
Binds TNF
40%
Blocks H1 receptor
40%
Short-acting designer insulin
40%
Inhibits enzyme DPP-4
40%
Inhibits enzyme DPP-4
40%
Inhibits enzyme farensyl pyrophosphate synthetase
40%
Block H2 receptor
33.3%
Block H2 receptor
33.3%
Block H2 receptor
33.3%
Inhibits ATPase
33.3%
Neutralizes acid
33.3%
Neutralizes acid
33.3%
Becomes viscous in H+
33.3%
Prostaglandin analog
33.3%
Dopamine & serotonin agonist
33.3%
Acts direcly on motilin receptors
33.3%
Retains water
33.3%
Retains water
33.3%
Inc. motility
33.3%
Acts on PG receptor
33.3%
Activates guanylate cyclase
33.3%
Changes surface tension of gas pockets
33.3%
Metabolizes oligosaccharides to digestable sugars
33.3%
% Correct
Decrease prostaglandin synth in gut
33.3%
Decrease prostaglandin synth in gut
33.3%
Blocks H1 receptor
33.3%
Blocks H1 receptor
33.3%
Binds THC receptor
33.3%
Blocks DA receptor
33.3%
Blocks 5HT receptor
33.3%
Binds specific receptor on beta cell (Incretin analog)
33.3%
Causes formation of abnormal ATP
33.3%
Inhibits enzyme farensyl pyrophosphate synthetase
33.3%
Inhibits enzyme farensyl pyrophosphate synthetase
33.3%
Inhibits enzyme farensyl pyrophosphate synthetase
33.3%
Inhibits ATPase
26.7%
Inhibits ATPase
26.7%
Inc. mucous production
26.7%
Blocks opiate receptor in gut
26.7%
Emulsifies colon contents
26.7%
Retains water
26.7%
Retains water
26.7%
Binds opiate receptor
26.7%
Binds opiate receptor
26.7%
Binds opiate receptor
26.7%
Decrease prostaglandin synth in gut
26.7%
Binds receptor to induce lipocortin
26.7%
Blocks H1 receptor
26.7%
Blocks 5HT receptor
26.7%
Short-acting designer insulin
26.7%
Short-acting designer insulin
26.7%
Blocks K+ channel on beta cells
26.7%
Inhibits enzyme DPP-4
26.7%
Activates a protein kinase
26.7%
Activates PPAR
26.7%
% Correct
Inhibits Na+-Glu cotransporter (SGLT2)
26.7%
Inhibits Na+-Glu cotransporter (SGLT2)
26.7%
Causes formation of abnormal ATP
26.7%
Inhibits enzyme farensyl pyrophosphate synthetase
26.7%
Sensitizes parathyroid Ca++ receptors
26.7%
Vitamin D analog
26.7%
Blocks RANKL receptor
26.7%
Inc. motility
20%
Inc. motility
20%
Long-acting designer insulin
20%
Long-acting designer insulin
20%
Int-acting designer insulin
20%
Blocks K+ channel on beta cells
20%
Blocks K+ channel on beta cells
20%
Blocks K+ channel on beta cells
20%
Blocks K+ channel on beta cells
20%
Blocks K+ channel on beta cells
20%
Blocks different site on K+ channel
20%
Blocks different site on K+ channel
20%
Binds specific receptor on beta cell (Incretin analog)
20%
Inhibits enzyme alpha-glucosidase
20%
Inhibits enzyme alpha-glucosidase
20%
Inhibits Na+-Glu cotransporter (SGLT2)
20%
Activates estrogen receptors in bone (Inhibits osteoclasts)
20%
Vitamin D2
20%
Short-acting designer insulin
13.3%
Binds specific receptor on beta cell (Incretin analog)
13.3%
Binds specific receptor on beta cell (Incretin analog)
13.3%
Inhibits enzyme DPP-4
13.3%
Activates amylin receptors
13.3%
Stimulates osteoblasts (long term = osteoclasts)
13.3%
Binds to & inhibits osteoclasts
13.3%
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Last Updated: Feb 16, 2017
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