Cell Structure
Drug
Drug target at molecular level
Intermolecular binding force
Classification of drugs and Naming
100

What is the phospholipid bilayer made of?

The outer layer of the membrane is made up of phosphatidylcholine, whereas the inner layer is made up of phosphatidylethanolamine, phosphatidylserine, and phosphatidylinositol. Each phosphoglyceride molecule consists of a small polar head-group and two long, hydrophobic (water-hating) chains.

100

The definition of drug

Drugs are compounds that interact with a biological system to produce a biological response.

100

What are some main molecular targets for drugs?

Proteins (enzymes, receptors, and transport proteins) and nucleic acids (DNA and RNA).

100

Please compare the strength of different intermolecular bonds (ionic, hydrogen, van der Waals, dipole-dipole, ion-dipole)

ionic>ion-dipole>hydrogen>dipole-dipole>van der Waals

100

What are four main ways in which drugs might be classified or grouped?

Drugs can be classified by their pharmacological effect, their chemical structure, their effect on a target system, or their effect on a target structure.

200

How are the two layers of phospholipids arranged in the cell membrane?

In the cell membrane, the two layers of phospholipids are arranged such that the hydrophobic tails point toward each other and form a fatty, hydrophobic centre, while the ionic head-groups are placed at the inner and outer surfaces of the cell membrane.

200

The drugs are classified as good or bag drug based on which several aspects?

Positive effect

Side-effect

Manufaturing process(easy or difficult)

Addictivity

Tolerance


200

What is binding site and its typical form?

A specific area of the macromolecule where this takes place. The common form is a hollow or canyon on the surface of the macromolecule allowing the drug to sink into the body of the larger molecule.

200

What does hydrogen bond take place between and some requirements for it to occur?

A hydrogen bond takes place between an electronic-rich heteroatom and an e-deficient H.

The electronic-rich heteroatom must have a pair of lone pair of e-.

200

How can drugs be classified according to their pharmacological effect?

By pharmacological effect, Drugs can be classified
depending on the biological or pharmacological effect that they have.

300

What is the function of the nucleus?

The nucleus acts as the ‘control centre’ for the cell. The nucleus contains the genetic code—the DNA—which acts as the blueprint for the construction of all the cell’s proteins.

300

What is the principle of drugs?

Selective toxiscity

Only target to problem cells

300

Despite the binding groups, what will also play an important role in binding the drug to its target and through which type of interaction?

Carbon Skeleton

Through van der Waals interactions

300

How does the electron density of the heteroatom affect its strength as a HBA?

As the e- density of the heteroatom, its strength as a HBA increases. Thus all the factors that affect e- density of the HBA will also affect the ability of HBA

300

By chemical structure, many drugs which have a common skeleton are grouped together. What are some examples of this?

penicillins, barbiturates, opiates, steroids, and catecholamines.

400

How does the type of amino acid affect the degree to which a protein is embedded in the cell membrane structure?

Portions of protein that are embedded in the cell membrane have a large number of hydrophobic amino acids, whereas those portions that stick out from the surface have a large number of hydrophilic amino acids.

400

What is therapeutic index?

The therapeutic index is a measure of a drug’s beneficial effect at a low dose versus its harmful effects at higher dose.  

400

Please tell the difference between binding site, binding region and binding group.

The specific regions on the binding site where functional groups and carbon skeletons form intermolecular bonds with ‘visiting’ drugs are known as binding regions.

Functional groups present in the drug that form intermolecular bonds with the target binding site are binding groups.

400

How should the dipole moments be when dipole–dipole interactions are formed between a drug and a binding site?

The dipole moments should be parallel and in opposite-directions.

400

How can drugs be classified according to the target system?

By target system, drugs can be classified according to whether they affect a certain target system in the body.

500

What is glycoprotein?

Glycoprotein is a type of protein molecule that has had a carbohydrate attached to it.

500

What does a high TI represent?

A high therapeutic index indicates a large safety margin between beneficial and toxic doses.

500

What is pharmacodynamics?

The study of how drugs interact with their targets through binding interactions and produce a pharmacological effect.

500

What does it mean if the energy required to desolvate both the drug and the binding site is greater than the stabilization energy gained by the binding interactions?

The drug might be ineffective.

500

What are the names of clinically useful drugs?

Clinically useful drugs have a trade (or brand) name, as well as a recommended international non-proprietary name.

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