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2285 - BP601T Medicinal Chemistry - Iii - 72 - (30-04-24 07 - 33 - 39 - 910 Am)

The document is an examination paper for the B.Pharm. (Semester–VI) course in Medicinal Chemistry–III, consisting of multiple-choice questions and descriptive questions. It covers various topics related to medicinal chemistry, including classifications, structure-activity relationships (SAR), and synthesis of different drugs. Candidates are instructed to answer all questions and illustrate their answers with sketches where necessary.

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Abhishek Bhonde
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0% found this document useful (0 votes)
23 views3 pages

2285 - BP601T Medicinal Chemistry - Iii - 72 - (30-04-24 07 - 33 - 39 - 910 Am)

The document is an examination paper for the B.Pharm. (Semester–VI) course in Medicinal Chemistry–III, consisting of multiple-choice questions and descriptive questions. It covers various topics related to medicinal chemistry, including classifications, structure-activity relationships (SAR), and synthesis of different drugs. Candidates are instructed to answer all questions and illustrate their answers with sketches where necessary.

Uploaded by

Abhishek Bhonde
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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AF-2285

Faculty of Pharmacy Technology

a il
B.Pharm. (Semester–VI) (New) Examination

m
GE
MEDICINAL CHEMISTRY–III

l
ai
RE
BP601T

Em
Time : Three Hours] [Maximum Marks : 75

AR INSTRUCTIONS TO CANDIDATES

EG
(i) Answer all questions.

R
(ii) Illustrate your answer wherever necessary with the help of neat sketches.

AR
(iii) Use pen of Blue/Black ink/refill only for writing the answer book.
1. (1) Oxytetracycine is obtained from : 20
(a) Streptomyces rimosus (b) Streptomyces aureofaciens
(c) Streptomyces kanamyeliticus (d) Streptomyces rimosus
(2) The following drug is radical curative in vivax malaria.
(a) Quinine (b) Primaquine

(3)
(c) Mefluquine
Penicilin G is example of ______. a il
(d) Chloroquine

(a) Aminopenicillins E m
(b) Penicillinase resistant
(c) Carboxy penicillins
E G (d) Natural penicillins
(4) R
What is target for clavulanic acid ?
R
(c) Lactamase
A
(a) The transpeptidase enzyme (b) Penicillin acylase
(d) L-alaracemase
(5) Which is naturally occuring antimalaria drug ?
(a) Artemisinin (b) Mefloquine
(c) Quinacrine (d) Mepacrine
(6) Choose the azole antifungal drug which is used only topically :
(a) Ketoconazole (b) Fluconazole
(c) Ifraconazole (d) Econozole
(7) Remdesivir have structural similarity with :
(a) Adenosine monophosphate
(b) Adenosine diphosphate
a il a il
m
(c) Adenosine triphosphate
E E m
(8) E G
(d) Guanine monophosphate
The following anthelmentics are found to be safe in pregnancy : E G
R R
(a) Thiabendazole (b) Piperozine
R R
A
(c) Albendazole (d) A
Pyrantel pamolate

LV–23622 1 (Contd.)
(9) The quinolones class of UTI was evolved by ______ of nalidixic acid.
(a) Chlorination (b) Methylation
(c) Fluorination (d) Acetylation

a il
(10) Drug of choice for malaria in pregnancy is ______.
m
GE
(a) Quinine (b) Chloroquine

l
ai
RE
(c) Pyrimethamine (d) Primaquine

Em
AR
(11) Identify the metabolite of prontosil responsible for its antibacterial activiy :
(a) Sulphacetamide (b) Probenec

EG
(c) PABA (d) Sulphanilamide

R
(12) In QSAR, study of medicinal chemistry Q stands for

AR
(a) Qualitative (b) Quantitaive
(c) Both (d) Quantum
(13) Which of the following is non competitive inhibitor of the enzyme reverse transcriptase in
HIV ?
(a) Lamivudine (b) Nevirapine
(c) Ritonavir (d) Tenofovir

a il
(14) Benzyl pencillinn is chemical name for which of following penicillin ?
m
GE
(a) Penicillin-F (b) Penicillin-G

RE
(c) Penicillin-V (d) Phenethean

AR
(15) Chloroquine can be synthesized by reaction of 4- diethylamino-1-methylbuty lamine with ?
(a)  -naphthol (b) 4, 7-dichloroquinoline
(c)  -naphthol (d) None of the above
(16) Aminoglycosides works by irreversible binding to the ______
(a) 30 S (b) 50 S
(c) Both (d) None of above
(17) Sulphonamides do not have adverse drug interaction with :
(a) Oral coagulants (b) Sulphon ylureas
(c) Hydantoin anticoagulants (d) Dihydrofolate reductase inhibitors

il
(18) A combination of medications which are applied to treat tuberculosis is :
a a il
(a)
m
1-thia-4-azabicyclo [3,2.1] heptane
E E m
(b)
G
4-thia-1-azabicyclo [3.2] heptane
E E G
(c)
R R 4-thia-1-azabicyclo [3.2.0] heptane
R R
A
(d) 1-thia-4-azabicyclo [1,2.3] heptane
A

LV–23622 2 (Contd.)
(19) Basic Nucleus of cephalosporins and penicillins is ______
(a) Lactone (b)  -lactam ring
(c) Thiazole

ail
(d) Lactum ring
(20) Chloramphenecol has two asymmetric centers. What is the configuration and optical activity of

E m
the active form of the antibiotics ?
G

l
(a) D-threo (–) (b) L-threo, (+)

ai
R E

Em
(c) D-erythro, (–) (d) L-erythro, (+)
2. A R
Solve any two : 20

EG
(1) Classify  -Lactam antibiotics, explain SAR of penicillin in detail with application.

R
(2) Classify antitubercular drugs in detail; explain SAR of any one class and synthesis of Isoniazide.

AR
(3) What are quinolones ? Classify them with their SAR and synthesis of nitrofurantoin in detail.
3. Solve any seven : 35
(1) Classify antifungal agents in detail.
(2) Classify anti-protozoal agents and synthesis of metronidazole.
(3) Classify antimalarials with SAR of any two drugs.
(4) il
What is QSAR ? Write details about parameters used in QSAR study.
a
(5) m
What is combinatorial chemistry ? Give its applications.
E
(6)
G
Write about folate reductase inhibitors in detail.
E
(7)
R
What is prodrug ? Give its applications in detail.
R
(8)
A
Write synthesis of para amino salicylic acid.
(9) Write SAR and synthesis of acyclovir.

a il a il
E m E m
E G E G
R R R R
A A

LV–23622 3 25

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