MCQ pharmacognosy and phytochemistry with answers

Multiple Choice Questions /MCQ of pharmacognosy and phytochemistry of B.pharma / GPAT with answers. Here we provide mcq for GPAT preparing student and for any competitive exams related to pharmacy. For any kind of pharmacy related mcq, please visit us.

pharmacognosy MCQs with answers

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1. The number of double bones in polyene, antibiotic, amphotericin B is

  • (a) 4
  • (b) 5
  • (c) 7
  • (d) 6

Answer- (c) 7

2. Norfloxacin, quinolone derivative

  • (a) is only effective against Proteus SPS.
  • (b) possess a broad spectrum of activity
  • (c) is only effective against gram-positive microorganisms
  • (d) None of the above

Answer-(b) possess a broad spectrum of activity

3. Cycloserine is stereochemically related to amino acid

  • (a) L-alanine
  • (b) D-serine
  • (c) D-alanine
  • (d) D-phenylalanine

Answer-(b) D-serine

4. Identify the odd one regarding rifampin

  • (a) Rifampin possesses the macrocyclic ring
  • (b) It is moisture sensitive
  • (c) Its metabolic product, deacetyl rifampin is also active
  • (d) Resistance toward rifampicin is not developed readily

Answer- (d) Resistance toward rifampicin is not developed readily

5. The absolute stereochemistry of penicillins is designated as

  • (a) 3S: 5R: 6R
  • (c) 3S5S: 6S
  • (b) 3R: 5R: 6R
  • (d) 3S: 5R: 6S

Answer-(a) 3S: 5R: 6R

6. Benizyl penicillin is not suitable for oral administration because

  • (a) it is metabolized rapidly
  • (b) its absorption is poor in the GIT tract
  • (c) it is degraded in the stomach
  • (d) it contains the allyl group at the C-6 position

Answer-(c) it is degraded in the stomach

7. The ampicillin is stable in acidic solution because

  • (a) it contains amino groups at a position
  • (b) it has broad-spectrum activity
  • (c) it contains an allyl group at a position
  • (d) it is the basic drug

Answer- (a) it contains amino groups at a position

8. The stability of enzyme penicillinase is increased by

  • (a) causing the steric hindrance at the a-carbon of the acyl group
  • (b) placing an electron-withdrawing group at the a-carbon of the acyl group
  • (c) placing an electron-donating group
  • (d) None of the above

Answer- (a) causing the steric hindrance at the a-carbon of the acyl group

9. Which one of these is acid as well as penicillinase-resistant?

  • (a) Dicloxacillin
  • (b) Carbenicillin
  • (c) Melhicillin
  • (d) Amoxicillin

Answer-(a) Dicloxacillin

10. The spectrum of activity of penicillin can be increased by

  • (a) placing an electron-withdrawing group at the a-carbon atom of the acyl group
  • (b) placing a polar group at a-carbon of an acyl group
  • (c) causing a steric hindrance at a-carbon of an acyl group
  • (d) None of the above

Answer-(b) placing a polar group at a-carbon of an acyl group

11. Which one of these is a-acylureido substituted penicillin?

  • (a) Ampicillin
  • (b) Amoxicillin
  • (c) Mezlocillin
  • (d) Cloxacillin

Answer-(c) Mezlocillin

12. Which one of these penicillin does not possess a broad spectrum of activity?

  • (a)
  • (b) Piperacillin
  • (c) Amoxicillin
  • (d) Nafcillin

Answer-(c) Amoxicillin

13. Dicloxacillin is named as

  • (a) 3-(0-Chlorophenyl)-5-methyl-4-isoxazolyl penicillin
  • (b) 3-(2, 6-Dichlorophenyl)-5-methyl-4-isoxazolyl penicillin
  • (c) 5-Methyl-(3-phenyl-4-isoxazolyl) penicillin
  • (d) 3-(2,5-Dichlorophenyl)-5-methyl-4-isoxazolyl penicillin

Answer-(b) 3-(2, 6-Dichlorophenyl)-5-methyl-4-isoxazolyl penicillin

14. The IUPAC name of ampicillin is

  • (a) 6-[D-a-Aminophenyl acetamido] penicillanic acid
  • (b) 6-[L-a-Aminophenyl acetamido] acid
  • (c) 6-[D-a-amhiophenyl benzamido] penicillanic acid
  • (d) None of the above

Answer-(a) 6-[D-a-Aminophenyl acetamido] penicillanic acid

15. The penicillins are named as

  • (a) 4-Thia-1-azabicyclo (3, 2, 1) heptanes
  • (b) 4-Thia-1-azacyclo (3, 2, 0) heptanes
  • (c) 4-Thia-1-azabicyclo (3, 2, 1) heptanes
  • (d) 4-Thia-1-azabicyclo (2, 2, 0) heptanes
  • Answer-(b) 4-Thia-1-azacyclo (3, 2, 0) heptanes

16. Which one of these is a 1-oxopenam derivative?

  • (a) Clavanic acid
  • (b) Thienamycin
  • (c) Cefradoxine
  • (d) Nafcillin

Answer-(a) Clavanic acid

17. Which is a 2-carbapenem derivative?

  • (a) Clavulanate potassium
  • (b) Thienamycin
  • (c) Sulbactam
  • (d) All of the above

Answer-(b) Thienamycin

18. The cephalosporin is designated as

  • (a) 4-Thia-1-azabicyclo [4, 2, 0] oct-2-ene
  • (b) 4-Thia-1-azabicyclo [4, 2, 1] oct-2-ene
  • (c) 4-Thia-1-azabicyclo [4, 3, 1] oct-2-ene
  • (d) 4-Thia-1-azabicyclo [3, 3, 1] oct-2-ene

Answer-(a) 4-Thia-1-azabicyclo [4, 2, 0] oct-2-ene

19. Streptomycin on hydrolysis gives

  • (a) Streptidine + L-Streptose + L-glucosamine
  • (b) L-streptose + L-glucosamine
  • (c) Streptidine + L-Streptose + N-methyl-L-glucosemine
  • (d) None of the above

Answer- (c) Streptidine + L-Streptose + N-methyl-L-glucosemine

20. Oxytetracycline is a derivative of

  • (a) Hydronapthacene
  • (b) Octahydronapthacene
  • (c) Hexahydronapthacene
  • (d) Decahydronapthacene

Answer- (b) Octahydronapthacene

21. The tetracycline is

  • (a) acidic in nature
  • (b) neutral in nature
  • (c) basic in nature
  • (d) amphoteric in nature

Answer- (a) acidic in nature

22. Epitetracycline is formed due to epimerization which takes place at

  • (a) C-4 in acidic PH
  • (b) C-2 in acidic PH
  • (c) C-10 in acidic PH
  • (d) C-11a in acidic PH

Answer-(a) C-4 in acidic PH

23. Anhydrotetracyclines are formed by the attack of strong acid/base on tetracycline possessing

  • (a) 3-hydroxyl group
  • (b) 4-hydroxyl group
  • (c) 11-hydroxyl group
  • (d) 6-hydroxyl group

Answer- (d) 6-hydroxyl group

24. The dimethylamino group at 4-position in tetracycline has

  • (a) a-orientation
  • (b) B-orientation
  • (c) a- or B-orientation depending on individual tetracycline
  • (d) none of the above

Answer-(a) a-orientation

25. In which tetracycline, the amide group at 2-position is substituted

  • (a) Demeclocycline
  • (b) Doxycycline
  • (c) Minocycline
  • (d) Rolitetracycline

Answer-(d) Rolitetracycline

26. IUPAC name of tetracycline is

  • (a) 4-dimethyulamino-1, 4, 4a, 5, 5a, 6, 12a-octa napthacene
  • (b) 4-dimethylamino-1, 4, 4a, 5, 5a, 6, 12a-octahydro 3, 6, 10, 12, 12a – pentahydroxy – 6 -methyl-1, 11-dioxo – 2 naphthacene carbonamide
  • (c) 4-Amino-1, 4, 4a, 5, 5a, 6, 12a-oct a hydro-3, 6, 10, 12, 12a-pentahydromy-6-methyl 1, 11-dioxo-2-naphthacene carbonamide
  • (d) None of the above

Answer-(b) 4-dimethylamino-1, 4, 4a, 5, 5a, 6, 12a-octahydro 3, 6, 10, 12, 12a – pentahydroxy – 6 -methyl-1, 11-dioxo – 2 naphthacene carbonamide

27. Tetracyclines medicinal chemistry question at C-4 between pH4 and 8 to give

  • (a) Isotetracyclines
  • (b) Epitetracyclines
  • (c) Nor tetracyclines
  • (d) none of the above

Answer-(b) Epitetracyclines

28. Morphine and heroin differ from each other in respect of

  • (a) Methyl group on Nitrogen
  • (b) Acetylgioup at C, and C
  • (c) Absence of double bond between C, and C
  • (d) Absence of D ring

Answer-(b) Acetylgioup at C, and C

29. 3- Etherification of morphine molecule causes

  • (a) Morphine antagonism
  • (b) No change in activity
  • (c) Decrease in analgesic and addiction.
  • (d) Increase in analgesic and addiction

Answer- (c) Decrease in analgesic and addiction.

30. D-a-Aminobenzylpenicillin is a chemical name for

  • (a) Amoxicillin
  • (b) Ampicillin
  • (c) Azlocillin
  • (d) None of the above

Answer- (b) Ampicillin

31. C17 a, Bunsaturated lactone ring is a common feature in

  • (a) Digitalis and squil glycosides
  • (b) Digitalis and strophanthus glycosides.
  • (c) Digitalis and semna glycosides
  • (d) Digitalis and amygdalin

Answer- (b) Digitalis and strophanthus glycosides.

32. Chemical name of Amoxicillin is

  • (a) 6-[D-(-) a – amino p-hydroxy phenyl acetamido] pencillanic acid
  • (b) 4-[D-(-) a-amino p-hydroxy phenyl acetamido] pencillanic acid
  • (c) B-Hydroxy analogue of Benzylpenicillin
  • (d) a-Carboxy benzylpenicillin

Answer-(b) 4-[D-(-) a-amino p-hydroxy phenyl acetamido] pencillanic acid

33. Acidity of Ascorbic acid is due to the presence of

  • (a) free carboxylic acid
  • (b) a number of hydroxyl groups
  • (c) enolic groups
  • (d) None of the above

Answer- (c) enolic groups

34. Vitamin D, is

  • (a) 22,23-dihydro-5, 6-cisergocalciferol
  • (b) 5, 6-cis- cholecaliciferol
  • (c) 7-dehydrocholesterol
  • (d) 21, 24-dihydro-5, 6- cis ergocalciferol

Answer- (a) 22,23-dihydro-5, 6-cisergocalciferol

35. Erythromycin is a macrolide antibiotic due to specific chemical features. Identify it

  • (a) Large size lactone ring
  • (b) Ketone group
  • (c) Glycosidically linked amino sugar
  • (d) Double bond

Answer- (a) Large size lactone ring

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36. The optimum pH for the stability of erythromycin is

  • (a) 4-5
  • (b) 6.5 to 7.5
  • (c) 9
  • (d) 11

Answer- (b) 6.5 to 7.5

37. Which antibiotic contains a sulfur atom?

  • (a) Erythromycin
  • (b) Lincomycin
  • (c) Tobramycin
  • (d) Kanamycin

Answer- (b) Lincomycin

38. Commercial bacitracin is a mixture of

  • (a) F (major amount) and the smaller amount of A, B, D, E, and F
  • (b) B (major amount) and a smaller amount of A, B, D, E, and F
  • (c) A (major amount) and a smaller amount of B, D, E, and F
  • (d) D (major amount) and a smaller amount of A, B, E, and F

Answer- (c) A (major amount) and a smaller amount of B, D, E, and F

39. Polymyxin B sulfate is frequently combined with bacitracin for topical application because

  • (a) it is only effective in presence of bacitracin
  • (b) the activity of polymyxim B is increased due to the synergistic effect caused by bacitracin
  • (c) the spectrum of activity is increased as polymyxin B sulfate is only effective against the negative organism
  • (d) the toxicity of polymyxin is decreased

Answer- (c) the spectrum of activity is increased as polymyxin B sulfate is only effective against the negative organism

40. The chloramphenicol is named as

  • (a) 2,3-Dichloro-N [a-hydroxy-methyl) B-hydroxy-p-nitrophenyl acetamide
  • (b) 2,2-Dichloro-N [B-hydroxymethyl B-hydroxy-p-nitrophenyl acetamide
  • (c) 1,2-Dichloro-N-[a-hydroxy methyl] B-hydroxy-p-nitrophenyl acetamide
  • (d) 1,2-Dichloro-N [a-hydroxy methyl] B-hydroxy-p-nitrophenyl benzamide

Answer- (a) 2,3-Dichloro-N [a-hydroxy-methyl) B-hydroxy-p-nitrophenyl acetamide

41. Four isomers of chloramphenicol are possible due to the presence of two asymmetric carbon atoms. Identify the

  • (a) L- thero isomers biologically active isomer
  • (b) L-threo isomer
  • (c) D- Erythro isomer
  • (d) D- Erythro isomer

Answer- (a) L- thero isomers biologically active isomer

42. Chloramphenicol on hydrolysis in presence of acid gives

  • (a) 1-(p-nitrophenyl)-1-aminopropan-1, 3-diol and dichloroacetic acid
  • (b) 1-(p-nitrophenyl)-2-aminopropan-1, 3-diol and dichloroacetic acid
  • (c) 1-(p-nitrophenyl)-2-aminopropan-1, 3-diol and chloroacetic acid
  • (d) 1-(p-nitrophenyl) – 1-aminopropan-1, 2-diol and dichloroacetic acid

Answer- (b) 1-(p-nitrophenyl)-2-aminopropan-1, 3-diol and dichloroacetic acid

43. Which antibiotic is beneficial in Rocky Mountain spotted fever?

  • (a) Lincomycin
  • (b) Chloramphenicol
  • (c) Polymyxin B Sulphate
  • (d) Novobiocin

Answer- (c) Polymyxin B Sulphate

44. The actinomycins used in cancer therapy contain the same chromophoric moiety. Identify it

  • (a) 2-Phenoxazone-1, 9-dicarboxylic acid
  • (b) 3-Phenaxazone-1, 9- dicarboxylic acid
  • (c) 3 – Phenoxazone – 1, 8- dicarbo-xylic acid
  • (d) none of the above

Answer- (b) 3-Phenaxazone-1, 9- dicarboxylic acid

45. Daunorubicin contain

  • (a) Anthraquinone
  • (b) Macrolide ring
  • (d) Anthra cyclone

Answer- (d) Anthra cyclone

46. Which enzyme is effective in the treatment of acute lymphocytic leukemia?

  • (a) Lyase
  • (b) Asparaginase
  • (c) Adenyl cyclase
  • (d) Xanthine oxidase

Answer- (b) Asparaginase

47. Picrotoxin is analeptic agent. It acts by

  • (a) inhibiting the enzyme MAO
  • (b) interfering in the GABA activity
  • (c) interfering in the serotonin
  • (d) none of the above

Answer- (b) interfering in the GABA activity

48. Pseudoephedrine is a

  • (a) Erythro isomer
  • (b) Threo isomer
  • (c) Mero isomer
  • (d) Racemic mixture

Answer- (b) Threo isomer

49. Pregnenolone, an intermediate in the synthesis of steroids on oppeneur oxidation gives

  • (a) Progesterone
  • (b) 9a-Flurocortisol
  • (c) Triamcinolone
  • (d) a-Methyl prednisolone

Answer- (a) Progesterone

50. Testosterone can be commercially synthesized from

  • (a) Sarsasapogenin
  • (b) Mexogenin
  • (c) Qubagenin
  • (d) Halotensin

Answer- (a) Sarsasapogenin

51. Erythromycin is an antibiotic. It belongs to the class of

  • (a) Blactam
  • (b) Aminoglycoside
  • (c) Macrolide
  • (d) Peptide

Answer- (c) Macrolide

52. The 5p pregnane nucleus is said to have a

  • (a) trans- anti trans c – anti-trans
  • (b) cis-anti trans anti trans
  • (c) cis- syn-trans- syn – trans
  • (d) trans- anti – cis – anti- cis

Answer- (b) cis-anti trans anti trans

53. D-Fructose on simple reduction gives

  • (a) only mannitol
  • (b) only sorbitol
  • (c) L-fructose
  • (d) the mixture of mannitol and sorbitol

Answer- (d) the mixture of mannitol and sorbitol

54. The ‘Hemiacetal’ form of aldosterone is between

  • (a) C-11, B-hydroxyl and C-20 carbonyl
  • (b) C-11, B-hydroxyl and C-21 carbonyl
  • (c) C-11, B-hydroxyl and C – 18 carbonyl
  • (d) C-21 hydroxyl and C-20 carbonyl

Answer- (c) C-11, B-hydroxyl and C – 18 carbonyl

55. The active ergot alkaloid differs from the inactive one only differ in

  • (a) functional group at 1-position
  • (b) configuration at position 8 of the molecule
  • (c) saturation between positions 9 and 10
  • (d) Solubility in water

Answer- (b) configuration at position 8 of the molecule

56. Which is a prototype drug in cholinergic blocker?

  • (a) Atropine
  • (b) Cocaine
  • (c) Hyoscyamine
  • (d) Homatropine

Answer- (a) Atropine

57. Which one of these is an amino alcohol ester, used as a cholinergic blocker?

  • (a) Ipratropium bromide
  • (b) Ethopropazine hydrochloride
  • (c) Cyclopentolate hydrochloride

Answer- (c) Cyclopentolate hydrochloride

58. IUPAC name for papaverine is

  • (a) 4,5-dimethoxy – 1 – veratryl isoquinoline
  • (b) 3,4-dimethoxy – 1 – veratryl isoquinoline
  • (c) 6,7-dimethoxy – 1 – veratryl isoquinoline
  • (d) 5,6-dimethoxy – I – veratryl isoquinoline

Answer- (c) 6,7-dimethoxy – 1 – veratryl isoquinoline

59. The curare-like activity is a common property of all ‘onium’ compounds. The activity decreases in the following order

  • (a) (CH₂)₂N+> (CH₂), St> (CH₂), P+
  • (b) (CH₂),S*> (CH₂), N*> (CH₂), P+
  • (c) (CH,),N>(CH,), P* > (CH,), S*
  • (d) (CH,) P*>(CH,),S*>(CH,),N*

Answer- (a) (CH₂)₂N+> (CH₂), St> (CH₂), P+

60. Tubocurarine chloride is

  • (a) (+)-Tubocurarine chloride
  • (b) (-)- Tubocurarine chloride
  • (c) meso-tubocurarine chloride
  • (d) recemic-tubocurarine chloride

Answer- (a) (+)-Tubocurarine chloride

61. B-sitosterol is beneficial in the treatment of hyperlipoproteinemias. It differs from cholesterol in one aspect. Identify it

  • (a) B-sitosterol contains an ethyl group at the C-24 position
  • (b) B-sitosterol does not contain a double bond
  • (c) Methyl group at C-19 position is not present
  • (d) Hydroxy group is esterified

Answer-(a) B-sitosterol contains an ethyl group at the C-24 position

62. Liothyronine is

  • (a) O-[4-hydroxy-3, 5- diiodophenyl) 3, 5 – diiodo – 2 – tyrosine
  • (b) 0-[4-hydroxy-3- iodophenyl) 3,5-diiodo – L – tyrosine
  • (c) O-[4-hydroxy-3- iodophenyl) 3, 5-diiodo – D – tyrosine
  • (d) O-[4-hydroxy – 2- iodophenyl) 3, 5- diiodo – D – tyrosine

Answer- (b) 0-[4-hydroxy-3- iodophenyl) 3,5-diiodo – L – tyrosin

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