Lecture 1- Intro Flashcards

1
Q

What is MOA

A

Mechanism of Action: a cell signaling system or process that is impacted by a drug through its interaction with a specific target molecule

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2
Q

Drug (ligand)

A

substance that causes change in biological function through its chemical actions

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3
Q

Receptor

A

Macromolecule (target molecule) in membrane or inside cell that binds with a drug molecule

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4
Q

MOA

A

process by which a drug functions to produce a pharmacological effect
Drug–> ligand–> receptor–> response (pharm effect)

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5
Q

What are the two mechanisms of a drug molecule?

A

Agonist: activator
Antagonist: inhibitor-when binds to a receptor

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6
Q

Appropriate requirements for drug response

A

Size
Electrical charge
Shape
Atomic composition

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7
Q

1 used nonselective cyclooxygenase (COX) inhibitor

A

aspirin (acetacylic acid: agonist/inhibitor)

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8
Q

What are the 3 major types of chemical forces/bonds

A

covalent (strong)
electrostatic (ionic)
hydrophobic (weak)

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9
Q

Drug selectivity

A

degree to which a drug acts on a given site relative to other sites

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10
Q

3 types of drug selectivity

A

Relatively nonselective drugs: affect many different tissues or organs (atroprine)

Relatively selective drugs: affect targeted areas (NSAIDs ie aspirin/ibuprofen)

Highly selective drugs: affect a single organ or system (digoxin/sleep aids)

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11
Q

Poisons

A

Drugs that have almost exclusively harmful effects (ie Warfarin for blood thinner and rat poison)

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12
Q

Drugs that can be synthesized within the body

A

Hormones

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13
Q

Toxins

A

Poisons of biological origin, synthesized by plants or animals

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14
Q

Inorganic poisons

A

Poisons such as lead or arsenic

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15
Q

Chiral

A

4 unique attachments to a molecule, and make up more than half of all useful drugs

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16
Q

Racemic mixtures

A

S & R isomers within drug with one usually being active and the other inactive
(enantomiers)

17
Q

Pharmacodynamics

A

Study of magnitude and variation of drug responses.

18
Q

What does pharmacodynamics involve?

A

receptor binding
post-receptor effects
chemical interactions

19
Q

Biodisposition

A

Processes of metabolism and excretion

20
Q

Different drug actions of Pharmacokinetics

A

Movement of drugs in body, absorption, distribution, metabolism, elimination

21
Q

Patient related factors influencing PK

A

age, race, individual physiology, weight, etc.

22
Q

PK-PD relationship

A

PK: Dose–> Concentration vs. Time
PD: Effect vs. Concentration
Dose–> Effect vs. Time

23
Q

Half-life

A

Time for 50% of drug to be eliminated from body

24
Q

What is off-label drug use?

A

When the indication, dose, or form of a drug is not FDA approved to treat an illness or symptoms

25
Chemical name
Atomic or molecular structure of the drug
26
Generic
official name
27
Brand
(proprietary or trademark or trade) name
28
Prototype Drug
A drug that typifies the most important characteristics of the group of drugs
29
-cilllin
penicillins (antibiotics)
30
-olol
B-blockers
31
-mab
monoclonal antibodies (-mumab= fully humanized) (-zumab= antigen binding region from a mouse antibody) (-ximab= chimeric with human and mouse parts) (-omab= entirely mouse)
32
Indications
What shows that the drug is for treatment
33
Contraindications
Should not use due to potential harmful effects
34
Black box
Should not give this drug to those in the black box group