Macromolecules Flashcards

1
Q

Why do drugs work

A

Biosynthesis of dna protein
Drugs enter world of chemicals
Drugs have specific effect

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2
Q

Main drug targets

A

Carbohydrates
Lipids
Proteins
Nucleic acids

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3
Q

Macromolecules

A

Carbohydrates
Lipids
Proteins
Nucleic acid

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4
Q

Size of drug

A

Smaller than molecular target

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5
Q

Macromolecules

A

Large organic molecules
Made of monomoers
Eg carbs/lipids/proteins/Nucleic acids

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6
Q

Carbohydrates

A

Quick short term energy
Monomer=monosaccharide
E.g. monosac/ disac/ polysac

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7
Q

Examples of monosaccharides

A

Single molecule sugars
Glucose /galactose
Deoxyribose
Ribose
Fructose
Ribose

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8
Q

Disaccharides

A

Two sugar unit

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9
Q

Polysaccharide

A

Many units
Starch
Glycogen
Cellulose

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10
Q

Glycogen

A

Made in liver
Energy storage in animals

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11
Q

Starch

A

Energy storage in plants

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12
Q

Lipids

A

Fats that do not mix in water
Eg
Fats
Phospholipids
Oils
Waxes
Steeoid hormones
Triglycerides

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13
Q

Six functions if lipids

A

Long term energy storage
Insulation
Cushion and protect organs
Protection against water koss
Chemical messengers(hormones)
Major component of cell membranes (phospholipids)

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14
Q

Triglycerides

A

Glycerol and 3 fatty acids
Hydrophobic

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15
Q

Amino acids

A

Building blocks for proteins
With chiral centre

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16
Q

Which amino acids can humans use

A

L natural amino acids

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17
Q

Amino acids

A

Amine group
Carboxylic group

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18
Q

Different types of amino acids

A

Aromatic
Hydrophobic (non-polar)
Hydroxyl/sulfur containing
Hydrophilic (acidic/basic)

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19
Q

Proteins

A

Monomer of 20 amino acids bonded by peptide bonds
Shape of protein determines function

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20
Q

Intermolecular forces

A

Hydrophobic interactions
Disulphide bridges
Hydrophobic interactions
Hydrophillic
Ionic bonding

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21
Q

Function of protein

A

Storage
Transport
Regulatory
Movement
Structural membrane hair/nails
Enzymes: cellular reactions

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22
Q

Nucleic acids

A

Store generic info composed if nucleotides
Rna- helps make protein
Dna- stores genetic information

23
Q

Drug interactions

A

Process of binding at the biding site on target

24
Q

Intermolecular bonding

A

Drug and macromolecule,
Interactions can be broken and reformed generating an equilibrium between bound and unbound drug

25
Describe strength & interaction of drug
Strong enough to have an effect but weak enough for drug to come away
26
Binding groups
Functional groups
27
Ionic bonds
Strongest if intermolecular bonds Between groups of opposite charges Non-directional- further drug, weaker interaction Hydrophbic binding site
28
Hydrogen bonds
Occur between electron rich heteroatom Electron deficient hydrogen
29
Strength of H bonds
Depends on how strong donor and acceptor are
30
Good H acceptors
Electronegative and have a lone pair
31
Strong Hbas
Po3 Co2
32
Strength ofVan der waals interactions
Very weak
33
Neutral van der waals
Non polar Electronic distribution never even or symmetrical
34
Mechanism of van dee waals
Transient areas of high and low electron densities leading to temporary dipoles
35
Dipole dipole interaction
Drug and macromolecules have dipoles and bond Have arrows
36
Role of water and hydrophobic interaction
Drugs and molecular target both need to be displace solvent water before binding
37
Repulsive interaction
Prevent molecules merging with each other Charges repel
38
Three broad isomers
Constitutional Conformational Configuration-stereoisomers
39
Constitutional isomers
Same formula different connectivity
40
Conformational isomee
Differ only by rotation about a single bond Interconvert freely at all but extremely low temps
41
Configuration
Stereoisomers Same connectivity but cannot be interconverted through single bond rotation Bond breaking and bond formation are required for interconversion
42
Enantiomers
Molecules that have identical binds between atoms but are non superimposable mirror images Eg hands
43
Properties of enantiomers
Non chiral environment, identical physical properties Cannot be separated simple distillation/ recrystallisation/ chromatography Impossible to distinguish spectroscopy
44
How would you identify enantiomers
Optical Chiral reagents
45
Different enantiomers will have different
Rates if reaction Solubilites in chiral solvents Different spectra in chiral solvents Binding to enzymes Physio effects
46
Ways of telling enantiomers apart
Polarises light Polarimetry
47
Clockwise
R
48
Anticlockwise
S
49
Double bond isomer
Geometric isomer
50
Geometric same side
Z isomer
51
Cis isomer
Same side of double bond
52
Trans isomer
Different side of double bond
53
Opposite side
E isomer
54
Effect of asymmetry on bio systems
Enantiomers interconvert in body preventing use if a single enantiomer for treatment if morning sickness Eg thalidomide Limonene