Prostaglandins
Thromboxanes
Prostacyclin
Leukotrienes
All of the above
Prostanoids; prostanoids
Prostanoids; leukotrienes
Leukotrienes; prostanoids
Leukotrienes; leukotrienes
COX 1
COX 2
LOX
COX 3
PGD
PGI2
PGE1
PGF
Gastrointestinal inflammation
Asthma
Fever
Pain
Isomerase
Transferase
Endoperoxide
Reductase
Medulla
Pituitary
Amygdala
Hypothalamus
COX-1
COX-2
COX-3
COX-1 and COX-2
COX-1 and COX-3
All of the above
Phosphorylation
Peroxidation
Hydration
Acetylation
Glutathione
Acetylcysteine
Acetyliminoquinone
Aniline
Glucuronide
Aniline
Glutathione
Hydroxyamid
Carbon bond
Bezylidene bond
Sulfur bond
All of the above
Z propionic acid, Ibuprofen
Cis-indolic acid, piroxicam
6MNA, Naproxen
None of the above
Ibuprofen
Ketoprofen
Naproxen
Ketololac
They are carboxylic acid anti-inflammatories
They are non-carboxylic acid anti-inflammatories
They are N-arylanthranillic acid anti-inflammatories
They are not heteroarylpropionic acid anti-inflammatories
Cationic
Anionic
Fluorinated
Chelated
Vioxx
Celebrex
Bextra
Prexige
Carboxylic acid
Sulfone
Thiol
P-chlorobenzoyl
All of the above
Celebrex, carboxylic acid
Prexige, sulfone
Prexige,carboxylic acid
Vioxx, sulfonamide
Vioxx, sulfone
Effective in the treatment of arthritic disorders
Typically used along with a NSAID or steroid in combination
Exhibit activity in standard assays for antiarthritic drugs
They have a very slow onset of action
Aurothioglucose
Sodium aurothiomalate
Methotrexate
Auranofin
Auranofin
Aurothiomalate
Aurothioglucose
None of the above
Dihyroorotic acid → uridine concurrent with ubiquinone (-OH) → ubiquinone (=O)
Dihyroorotic acid → uridine concurrent with ubiquinone (=O) → ubiquinone (-OH)
Uridine → dihyroorotic acid concurrent with ubiquinone (=O) → ubiquinone (-OH)
Uridine → dihyroorotic acid concurrent with ubiquinone (-OH) → ubiquinone (=O)
Adenine
Guanine
Thymine
Uracil
Disodium urate
Monosodium glutamate
Monosodium urate
Uric acid crystal deposits in toes
Xanthine and Uric Acid
Uric Acid and hypoxanthine
Xanthine and adenine
4.Adenine and Uric Acid
Increase
Decrease
No change
Hydrogen
Methyl
Glucoronide
Benzene ring
Imidazole ring
Enol functionality
Methyl substituent
π; π
Ï€; Ï„
τ; π
Ï„; Ï„
Kellin
Chromene
Benzofuan
Benzene
4 or 5 carbons in length, a 5 membered ring, branched, saturated or unsaturated
2 or 3 carbons in length, a 5 membered ring, branched, saturated or unsaturated
4 or 5 carbons in length, some ring structure, branched, saturated or unsaturated
2 or 3 carbons in length, some ring structure, branched, saturated or unsaturated
I-A, II-B, III-C
I-C, II-B, III-A
I-B, II-C, III-A
I-C, II- A, III-B
Pheniramine, 1st generation, acidic
Doxylamine, 2nd generation, basic
Certirizine, 2nd generation, acidic
Certirazine, 2nd generation, amphoteric
Certirizine, 1st generation, basic
Methyl group
Tertiary nitrogen group
Aniline group
Butyl group
Ethanolamine ether
Ethylenediamines
Ring halogenated alkyl amines
CH3
CH2OH
CH3CH3
CO2H
None of the above
H1
H2
H3
H4
H5
Loratadine
Terfenadine
Ceterizin
Fexofenadine
Ketotifen
Non-polar, non-basic
Non-polar, basic
Polar, non-basic
Polar, basic
Potency
Decreased bascity
Selectivity
The O
CH2 adjacent to the sulfur on the right
The purine ring to the left of the sulfur
The lone pair off of the sulfur
I-A, II-B, III-C
I-B, II-C, III-A
I-C, II-A, III-B
I-C, II-B, II-A
Alcohol dehydrogenase
COMT
MOA
Phosphodiesterase
Methyl
Ethyl
Hydrogen
Benzyl
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