structure of drugs Flashcards

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1
Q

why is a shape and chirality important for pharmacist

A

this is because our protiens are made up of amino acis and we are all chirals
dna is also chiral

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2
Q

history of thalidomide?

A

it was widely prescribed for morning sickness only outside of USA, however it was found to be serious teratogenic as it caused alot of defects in around 10,000 babies.
it was being sold as racemic mixture of the two enantiomers which is why the unwanted effects
and thus why it was unsafe for pregnant women.

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3
Q

what is the formula for ethane

A

ch3ch3

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4
Q

how many carbons in meth,eth,prop,but,pent,hex,hept,oct

A

1
2
3
4
5
6
7
8

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5
Q

what is the bond angle o=c=o

A

180degrees

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6
Q

bond angle in c-h-h-h-h

A

109.5

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7
Q

what are conformers

A

they used thermal energy to rotate single bonds in a molecule ususally explained by newmans projection

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8
Q

tricks for chrirocentre

A

ignore chs 3 groups at the end
ignore ch2 groups
ignore double-tripled bons

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9
Q

what is a chiral

A

this is when a carbon is bonded to 4 different groups

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10
Q

what are steroisomers

A

they have the same molecular formula but a different structure

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11
Q

what is a constitutional isomers

A

connected different and have have different carbons

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12
Q

what is a enantiomers?

A

they have a mirror image
and all of the chiroocentres must changes

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13
Q

what is a diastereomer?

A

the first chiro centre remains the same and the second one changes
this is when some of the chirocentres change but not all of them

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14
Q

what is a meso compound?

A

they have a line of symmetry
they are identical molecule and can never be enantiomers

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15
Q

what is cis /trans

A

cis = same side
trains = opposite side

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16
Q

e/z isomer

A

e= opposite side
z= same side
in e/z you can also use the CIP rule where the atomic number takes priority

17
Q
A