BPS 313 Lecture Notes - Lecture 50: Lactam, Covalent Bond, Ketone

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turquoisebear962

12 Sep 2016

School

URI

Department

Biomedical and Pharmaceutical Sciences

Course

BPS 313

Professor

Deyu Li

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Document Summary

Hydrogen bond donor: identify the binding interactions that might be possible at the specified positions of the following drug: = ionic interactions: identify the binding interactions that might be possible at the specified positions of the following drug. = hydrogen bond donor: identify the binding interactions that might be possible at the specified positions of the following drug. Page reference: 232: extension, simplification, rigidification, conformational blocking, in the development of the antifungal agent, nevirapine, structure (ii) was found to bind more strongly to the target enzyme than the lead compound (i). Page reference: 232-234: the molecular weight, the stereochemistry, the pharmacophore, the hydrophobic character, there are three general methods by which molecules can be simplified. Page reference: 212: pharmacodynamics, pharmacokinetics, structure-activity relationships, pharmacological activity, identify which of the bonding interactions shown below are possible for the functional groups highlighted. Page reference: 214-216, 218: ionic bonding and h-bond acceptor = the carboxylate group (a) b.

Related Questions

Need help with biology questions:

1. To increase the excretion of an acidic drug, what would you do to the urine?

	A.	Make it more basic
	B.	None of the above
	C.	Make it neutral
	D.	Make it more acidic

2. G-Protein coupled receptors directly act on which of the following secondary messenger molecules:

	A.	cAMP
	B.	ATP
	C.	ADP
	D.	GTP
	E.	None of the above or more than one of the above

3. Drug A and Drug B both produce the same level of biological/physiological response. Drug A produces this effect with 100 mg/kg dose. Drug B produces this effect with 50 mg/kg dose. Which of the following is true?:

	A.	Drug B is more efficacious than Drug A. Both drugs are equally potent.
	B.	Drug A is more efficacious than Drug B. Both drugs are equally potent.
	C.	Drug A and B are equally efficacious. Drug A is more potent than Drug B.
	D.	Drug A and B are equally efficacious. Drug B is more potent than Drug A.

4. The stomach has a ______ pH, whereas the small intestines have a _______ pH. The colon has an approximately ___________ pH.

	A.	High; low; neutral
	B.	Low; high; neutral
	C.	Low; neutral; neutral
	D.	None of the above

5. Which receptor is most likely to reduce norepinephrine levels when activated?

	A.	alpha 2 adrenergic
	B.	alpha 1 adrenergic
	C.	dopamine D1 receptors

6. Which of the following statements are FALSE?

	A.	If the Vd of a drug is between 60 and 80 L the drug has likely distributed to the total body water of a 200 kg man.
	B.	In the enterohepatic system the activity of bacteria to remove conjugates from a drug in the gut will decrease the clearance of the drug.
	C.	Lipid drugs are more likely to be reabsorbed by the kidney from the urine.
	D.	A weak basic drug (pKa = 6) will be mostly ionized in urine of a pH= 3 and only the non- ionized drug will be eliminated.
	E.	The major conjugate in Phase 2 metabolism is glucuronide.

7. Isoproterenol (Î²-agonist) is a vasodilator that increases HR. What happens to systolic and diastolic pressures upon IV administration of isoproterenol?

	A.	â systolic; â diastolic
	B.	â systolic; â diastolic
	C.	â systolic; â diastolic
	D.	â systolic; â diastolic
	E.	None of the above

8. If you want to increase the blood concentration of a drug A, you can perform which of the following procedures:

	A.	Inhibit Drug A metabolism with Drug B
	B.	Enhance Drug A reabsorption from renal proximal tubule by changing ionization of Drug A with Drug B
	C.	Allow competition of Drug B with Drug A for active renal secretion processes
	D.	Increase the binding of Drug A to serum albumin
	E.	All of the above

9. Which of the following describes Phase I metabolism?

	A.	Inactive products are always produced in this phase.
	B.	Large molecules such as glucuronic acid are conjugated to drugs in this phase.
	C.	This phase may produce active metabolites from prodrugs.
	D.	This phase only occurs in the liver.

10. Which of the following is NOT an enzyme involved in the biosynthesis of biogenic amines?

	A.	Phenylethanolamine N-methyl Transferase
	B.	Dopamine Î²-hydroxylase
	C.	Tyrosine dehydroxylase
	D.	DOPA decarboxylase
	E.	All of the above

11. Why would an antibiotic at the same concentration be more active against bacteria in water than in serum or plasma? (Activity is measured in a test tube)

	A.	activity of the antibiotic is increased in water.
	B.	due to drug-protein interaction in serum
	C.	the antibiotic is more stable in water
	D.	all of the above
	E.	none of the above

12. Ion channels are targets for drugs. Which drug class targets Na+ channels?

	A.	Benzodiazepines
	B.	Beta blockers
	C.	Local anesthetics
	D.	Antihypertensive drugs (cardiac and smooth muscle)
	E.	Glibenclimide (diabetic drug)

13. _________________ not metabolized by catechol-O-methyltransferase (COMT).

	A.	Dopamine
	B.	Epinephrine
	C.	Phenylephrine
	D.	Norepinephrine
	E.	All of the above are metabolized by COMT.

The type of macromolecule found in highest concentration on a weight basis in a HeLa cell is

protein.

lipid.

polysaccharide.

nucleic acid.

water

Co and Zn ions are required by humans in

microgram amounts.

gram or near gram amounts.

kilogram amounts.

d. milligram amounts.

Which description best characterizes the length of a hydrogen bond between water molecules?

About the same length as the calculated van der Waals distance for two water molecules.

About the same length as a covalent O----H bond.

Shorter than a covalent O---H bond.

Longer than a covalent O---H bond, but shorter than the calculated van der Waals distance between water molecules.

Which of the following statements about water is not true?

Water will hydrogen bond into highly ordered structures or "cages" around non-polar molecules.

The electron-rich oxygen atom of one water molecule can interact with an electron-poor hydrogen on another water molecule to form a hydrogen bond.

Water is a key player in the energetics of the hydrophobic effect.

In an ice crystal water molecules pack into open lattices consisting of five-membered oxygen rings.

At 25 degrees celsius liquid water is about 85% as hydrogen bonded as the water in ice, with each molecule in an average of 3.4 hydrogen bonds.

Which of the following is the strongest?

Ionic interactions

Permanent dipole - permanent dipole interactions

London dispersion forces

Co-linear hydrogen bonds

Which of the following is the best explanation for the hydrophobic effect?

It is caused by the attraction of hydrophobic groups for each other.

It is an entropic effect caused by the tendency of hydrophobic groups to increase their entropy by associating with other hydrophobic groups.

It is an entropic effect, caused by the tendency of water molecules to increase their entropy by excluding hydrophobic groups, which they must otherwise surround with highly ordered structures.

It is caused by the attraction of water for hydrophobic groups.

It is an entropic effect, caused by the tendency of water molecules to increase their entropy by forming highly ordered structures around the hydrophobic groups.

Which of the following is NOT defined as a buffer? (pKa PIPES-H⁺ = 6.76; pKa MOPS-H⁺ = 7.15; pKa HEPES-H⁺ = 7.47)

0.15 M MOPS, pH 6.50

0.05 M HEPES-H⁺ / 0.04 M HEPES

0.20 M PIPES, pH 7.97

0.01 M HEPES, pH 7.30

BPS 313 Lecture Notes - Lecture 50: Lactam, Covalent Bond, Ketone

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