Lecture 1 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
Q

Chemical name

A

Atomic or molecular structure of the drug

26
Q

Generic

A

official name

27
Q

Brand

A

(proprietary or trademark or trade) name

28
Q

Prototype Drug

A

A drug that typifies the most important characteristics of the group of drugs

29
Q

-cilllin

A

penicillins (antibiotics)

30
Q

-olol

A

B-blockers

31
Q

-mab

A

monoclonal antibodies
(-mumab= fully humanized)
(-zumab= antigen binding region from a mouse antibody)
(-ximab= chimeric with human and mouse parts)
(-omab= entirely mouse)

32
Q

Indications

A

What shows that the drug is for treatment

33
Q

Contraindications

A

Should not use due to potential harmful effects

34
Q

Black box

A

Should not give this drug to those in the black box group

35
Q
A