Common Molecules Flashcards

1
Q

What is meant by carboxylation?

A

Addition of –COO group

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2
Q

What is meant by decarboxylation?

A

Removal of –COO group

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3
Q
A

Acetaldehyde

formed from breakdown of ETOH

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4
Q
A

Acetoacetate

formed during ketogenesis

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5
Q
A

Acetone

formed during ketogenesis

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6
Q
A

Acetyl CoA

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7
Q
A

Acetylcholine

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8
Q
A

Adenine

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9
Q
A

Adenosine

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10
Q
A

ATP

Adenosine Triphosphate

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11
Q
A

Amylose

alpha-1,4 glycosidic

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12
Q
A

Beta-Hydroxybutyrate

formed during ketogenesis

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13
Q
A

Beta Lactam

ABx

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14
Q
A

cAMP

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15
Q
A

Cytidine

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16
Q
A

Cytosine

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17
Q

ID the molecule shown

Which is the anomeric carbon?

A

D-Glucose

we know this because the OH is on the right in the fisher projection

Carbonyl carbon

this is the carbon that is attacked intramolecularly by carbon 5

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18
Q

ID the molecule shown

Which carbon is the anomeric carbon?

A

D-glucose

we know it’s D-glucose because the highest numbered carbon (upper left corner) is R.

Carbon 1 is the anomeric carbon

the carbon that has 2 oxygens attached to it (right-most carbon) You can prove this by viewing D-glucose in fisher projection form and performing an intramolecular nucleophillic attack.

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19
Q
A

Epinephrine

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20
Q
A

Fructose

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21
Q
A

Furan

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22
Q
A

Furanose ring

comparison group for sugar naming (Aldofuranose/ Ketofuranose)

“<strong>F</strong>uran, <strong>F</strong>ive” because it’s a 5-membered ring

23
Q

ID the molecule shown

Which carbon tells alpha vs. beta?

Which carbon tells D/L?

A

Alpha-D-Galactose

the 4th carbon is emphasized because this is the differential between glucose and galactose. Glucose has an equatorial OH, while Galactose has an axial OH.

Alpha/Beta is determined by carbon 1 (anomeric carbon)

it’s always good to “B Up”

D/L is determined by carbon 5, the penultimate carbon

Figure out chirality of the stereocenter. (R in this case)

24
Q
A

Beta-D-Glucose

we know it’s D-glucose because the highest numbered carbon is R.

we know it’s Beta because the OH on carbon 1 (anomeric carbon) is up, and “It’s always good to B UP” because Beta sugars are more stable than Alpha sugars.

25
**Alpha-D-Glucose** we know it's D-glucose because the highest numbered carbon is R. we know it's alpha because the OH on carbon 1 (anomeric carbon) is down.
26
# ID the molecule shown Also, what bonds are pointed to below?
**Glycogen** alpha-1,4 and alpha 1,6
27
**Guanine**
28
**Guanosine**
29
**Hemiacetal** Anomeric carbon has 2 oxygens attached
30
**Hydroquinone** No direct function in humans, it's derivatives are seen in coenzyme Q of the Electron transport chain
31
**Malonly CoA**
32
**Maltose** Glucose + Glucose
33
What is the molecule on the left and right?
Left = **pyruvate** Right = **acetyl coA** PDC complex
34
**Prostaglandin**
35
**Pyranose** useful for naming sugars
36
**Pyridine**
37
**Quinone** ETC enzymes derive from this
38
**Sucrose** Glucose + Fructose
39
**Thymidine**
40
**Thymine**
41
**Ubiquinone** ETC co-factor
42
**Uracil**
43
**Uridine**
44
**Vitamin A** Retinol most notably produces pigment in the retina of the eye
45
**Vitamin B12** Riboflavin helps convert carbohydrates into ATP
46
**Vitamin B3** Niacin is for metabolism and helping to make some sex/stress hormones
47
**Vitamin B5** Pantothenic Acid is needed to synthesize CoA
48
**Vitamin B7** Biotin is important for metabolic pathways
49
Cellulose 2 glucose sub-units connected via beta-1,4 glycosidic bonds
50
Cytidine 5' monophosphate
51
Lactose Galactose + Glucose Beta-1,4 Glycosidic bond
52
Lactose Galactose + Glucose Beta-1,4 Glycosidic bond
53
ID the molecule shown below
**Porphyrin Ring** made up of several pyrrole subunits, this ring constitutes most of the molecular weight of hemoglobin molecules
54
ID the following molecule
Phosphatidylcholine