mc-2 cmptd30-12-2019 3-1 SEC-B PDF
mc-2 cmptd30-12-2019 3-1 SEC-B PDF
mc-2 cmptd30-12-2019 3-1 SEC-B PDF
Course file
Faculty Name: D.Tirumala
Designation: Assistant professor
Batch: 2017-2021
Academic Year: 2019-20
Semester/Year: III/I
Course Name: Medicinal chemistry-II
Course Code/Regl: C331 /R17
S.No Course File Contents Check List (Yes/No) Remarks
13 CO Attainment Report NA
14 Action Taken Report
15 JNTUH old Question Paper/Question Bank Yes
16 Internal Test Question Papers (I, II & III Internal Yes
Question Papers/Sub/Obj/Key)
17 Assignment Questions Yes
18 Scheme of Evaluation Yes
19 Identification of Bright Students Yes
20 Identification of Weak Students Yes
21 Remedial Classes Time Table NA
22 Result Analysis NA
M1: Provide state of the art laboratories, information centre and learning environment for holistic
education.
M2: Adopt and implement best practices for learning and research.
M3: Collaborate with industry and society to identify problems, provide sustainable solutions and align
curriculum.
PEO-3- ATTITUDE
Pharmacy Graduates will practice ethical responsibilities towards their peers, employer’s, society and
world at large.
PROGRAM OUTCOMES
1. Pharmacy Knowledge: Possess knowledge and comprehension of the core and basic knowledge associated
with the profession of pharmacy, including biomedical sciences; pharmaceutical sciences; behavioral, social,
and administrative pharmacy sciences; and manufacturing practices.
2. Planning Abilities: Demonstrate effective planning abilities including time management, resource
management, delegation skills and organizational skills. Develop and implement plans and organize work to
meet deadlines.
3. Problem analysis: Utilize the principles of scientific enquiry, thinking analytically, clearly and critically, while
solving problems and making decisions during daily practice. Find, analyze, evaluate and apply information
systematically and shall make defensible decisions.
4. Modern tool usage: Learn, select, and apply appropriate methods and procedures, resources, and modern
pharmacy-related computing tools with an understanding of the limitations.
5. Leadership skills: Understand and consider the human reaction to change, motivation issues, leadership and
team-building when planning changes required for fulfillment of practice, professional and societal
responsibilities. Assume participatory roles as responsible citizens or leadership roles when appropriate to
facilitate improvement in health and well-being.
6. Professional Identity: Understand, analyze and communicate the value of their professional roles in society
(e.g. health care professionals, promoters of health, educators, managers, employers, employees).
7. Pharmaceutical Ethics: Honour personal values and apply ethical principles in professional and social
contexts. Demonstrate behavior that recognizes cultural and personal variability in values, communication
and lifestyles. Use ethical frameworks; apply ethical principles while making decisions and take responsibility
for the outcomes associated with the decisions.
8. Communication: Communicate effectively with the pharmacy community and with society at large, such as,
being able to comprehend and write effective reports, make effective presentations and documentation, and
give and receive clear instructions.
9. The Pharmacist and society: Apply reasoning informed by the contextual knowledge to assess societal,
health, safety and legal issues and the consequent responsibilities relevant to the professional pharmacy
practice.
10. Environment and sustainability: Understand the impact of the professional pharmacy solutions in societal
and environmental contexts, and demonstrate the knowledge of, and need for sustainable development.
11. Life-long learning: Recognize the need for, and have the preparation and ability to engage in independent
and life-long learning in the broadest context of technological change. Self-assess and use feedback
effectively from others to identify learning needs and to satisfy these needs on an ongoing basis.
4. SYLLABUS COPY:
UNIT- I 10 Hours
Antihistaminic agents: Histamine, receptors and their distribution in the humanbody
H1–antagonists: Diphenhydramine hydrochloride*, Dimenhydrinate, Doxylamines
succinate, Clemastine fumarate, Diphenylphyraline hydrochloride, Tripelenamine
hydrochloride, Chlorcyclizine hydrochloride, Meclizine hydrochloride, Buclizine
hydrochloride, Chlorpheniramine maleate, Triprolidine hydrochloride*, Phenidamine
tartarate, Promethazine hydrochloride*, Trimeprazine tartrate, Cyproheptadine
hydrochloride, Azatidine maleate, Astemizole, Loratadine, Cetirizine, Levocetrazine
Cromolyn sodium
H2-antagonists: Cimetidine*, Famotidine, Ranitidin.
Gastric Proton pump inhibitors: Omeprazole, Lansoprazole, Rabeprazole,
Pantoprazole Anti-neoplastic agents:
Alkylating agents: Meclorethamine*, Cyclophosphamide, Melphalan,
Chlorambucil, Busulfan, Thiotepa
Antimetabolites: Mercaptopurine*, Thioguanine, Fluorouracil, Floxuridine, Cytarabine,
Methotrexate*, Azathioprine
Antibiotics: Dactinomycin, Daunorubicin, Doxorubicin, Bleomycin
Plant products: Etoposide, Vinblastin sulphate, Vincristin sulphate
Miscellaneous: Cisplatin, Mitotane.
UNIT – II 10 Hours
Anti-anginal:
Vasodilators: Amyl nitrite, Nitroglycerin*, Pentaerythritol tetranitrate, Isosorbide
dinitrite*, Dipyridamole.
Calcium channel blockers: Verapamil, Bepridil hydrochloride, Diltiazem hydrochloride,
Nifedipine, Amlodipine, Felodipine, Nicardipine, Nimodipine.
Diuretics:
Carbonic anhydrase inhibitors: Acetazolamide*, Methazolamide, Dichlorphenamide.
Thiazides: Chlorthiazide*, Hydrochlorothiazide, Hydroflumethiazide, Cyclothiazide,
Loop diuretics: Furosemide*, Bumetanide, Ethacrynic acid.
Potassium sparing Diuretics: Spironolactone, Triamterene, Amiloride.
Osmotic Diuretics: Mannitol
Anti-hypertensive Agents: Timolol, Captopril, Lisinopril, Enalapril, Benazepril hydrochloride, Quinapril
UNIT - IV 08 Hours
Drugs acting on Endocrine system
Nomenclature, Stereochemistry and metabolism of steroids
Sex hormones: Testosterone, Nandralone, Progestrones, Oestriol, Oestradiol,
Oestrione, Diethyl stilbestrol.
Drugs for erectile dysfunction: Sildenafil, Tadalafil.
Oral contraceptives: Mifepristone, Norgestril, Levonorgestrol
Corticosteroids: Cortisone, Hydrocortisone, Prednisolone, Betamethasone, Dexamethasone
Thyroid and antithyroid drugs: L-Thyroxine, L-Thyronine, Propylthiouracil, Methimazole.
UNIT – V 07 Hours
Antidiabetic agents:
Insulin and its preparations
Sulfonyl ureas: Tolbutamide*, Chlorpropamide, Glipizide, Glimepiride.
Biguanides: Metformin.
Thiazolidinediones: Pioglitazone, Rosiglitazone.
Meglitinides: Repaglinide, Nateglinide.
Glucosidase inhibitors: Acarbose, Voglibose.
Local Anesthetics: SAR of Local anesthetics
Benzoic Acid derivatives; Cocaine, Hexylcaine, Meprylcaine, Cyclomethycaine,
Piperocaine. Amino Benzoic acid derivatives: Benzocaine*, Butamben, Procaine*,
Butacaine, Propoxycaine, Tetracaine, Benoxinate.
Lidocaine/Anilide derivatives: Lignocaine, Mepivacaine, Prilocaine, Etidocaine.
Miscellaneous: Phenacaine, Diperodon, Dibucaine.*
5. Personal Timetable
Period 1 2 3 4 5 6 7
Wed MC-II
Thurs
Fri
Sat
6.CALENDER OF EVENTS
15 16 17 18 19 20 21
Commencement
of Instruction
22 23 24 25 26 27 28
Bonalu
29 30 31 - - - -
July’2019
Aug’2019 - - - 1 2 3 4
5 6 7 8 9 10 11
12 13 14 15 16 17 18
Bakrid Independence
Day
19 20 21 22 23 24 25
Krishnastami
26 27 28 29 30 31 -
Orientation
day
Sep’2019 - - - - - - 1
2 3 4 5 6 7 8
Vinayakachavithi Teachers Day
9 10 11 12 13 14 15
Moharam Nimajjanam Ist Mid Term Examination
16 17 18 19 20 21 22
23 24 25 26 27 28 29
Pharmacist Bathukamma
day
celebrations
30 - - - - - -
Oct’2019 - 1 2 3 4 5 6
Gandhi Bathukamma
Jayanthi Celebrations
7 8 9 10 13
11 12
Dussehra Holidays
14 15 16 17 18 19 20
21 22 23 24 25 26 27
28 29 30 31 - - -
- - - - 1 2 3
4 5 6 7 8 9 10
11 12 13 14 15 16 17
Gurunanak Dravyaka
Jayanthi
18 19 20 21 22 24
23
IInd Mid Term Examination
Nov’2019
UNIT-3
24 1 Anti arrhythmic agents 11-9-2019 11-9-2019
25 2 First internal exam 16-9-2019 16-9-2019
26 2 Moa ,structure, uses of Anti arrhythmic agents 23-9-2019 23-9-2019
UNIT-5
35 1 Insulin and its preparations,sulfonyl ureas 30-10-2019 30-10-2019
36 2
Biguanidines,Thaizolinediones, Metaglitinides 4-11-2019 4-11-2019
8.COURSE NOTES
9. STUDENT LIST:
NO OF PERCENTAGE
CLASES
S.No HTNO NO OF CLASES CONDUCTEED ATTENDED
1 17FA1R0001 57 36 63.2
57
2 17FA1R0003 33 57.9
57
3 17Z51R0043 46 80.7
57
4 17Z51R0044 49 86.0
57
5 17Z51R0045 43 75.4
57
6 17Z51R0046 40 70.2
57
7 17Z51R0047 33 57.9
57
8 17Z51R0048 52 91.2
57
9 17Z51R0049 37 64.9
57
10 17Z51R0050 51 89.5
57
11 17Z51R0051 43 75.4
57
12 17Z51R0052 33 57.9
57
13 17Z51R0053 38 66.7
57
14 17Z51R0054 36 63.2
57
15 17Z51R0055 52 91.2
57
16 17Z51R0056 38 66.7
57
17 17Z51R0057 47 82.5
57
18 17Z51R0058 43 75.4
57
19 17Z51R0059 40 70.2
57
20 17Z51R0060 43 75.4
57
21 17Z51R0061 37 64.9
57
22 17Z51R0062 46 80.7
57
23 17Z51R0063 37 64.9
57
24 17Z51R0064 52 91.2
57
25 17Z51R0065 37 64.9
57
26 17Z51R0067 15 26.3
57
27 17Z51R0068 42 73.7
57
28 17Z51R0069 41 71.9
57
29 17Z51R0070 49 86.0
57
30 17Z51R0071 32 56.1
57
31 17Z51R0072 48 84.2
57
32 17Z51R0073 56 98.2
57
33 17Z51R0074 34 59.6
57
34 17Z51R0075 40 70.2
57
35 17Z51R0076 38 66.7
57
36 17Z51R0077 37 64.9
57
37 17Z51R0078 41 71.9
57
38 17Z51R0079 45 78.9
57
39 17Z51R0080 46 80.7
57
40 17Z51R0081 52 91.2
57
41 17Z51R0082 50 87.7
57
42 17Z51R0083 45 78.9
57
43 17Z51R0084 49 86.0
57
44 17Z51R0085 34 59.6
57
44 17FA1R0001 48 84.2
BOTTA
8 17Z51R0048 SUPRIYA 10 6.5 5 22 9 5.5 5 20 21 5 5 5
C.N.B.S.
VEDA
SAMHIT
9 17Z51R0049 H 8 4 5 17 7 0 5 12 14.5 5 5 5
CHALLA
VENKATA
DHARAN
10 17Z51R0050 I 6 2.5 5 14 8 2.5 5 16 15 5 5 5
D
AISWAR
11 17Z51R0051 YA 10 4.5 5 20 10 3 5 18 19 5 5 5
DEVARS
HETTY
12 17Z51R0052 SHREYA 7 3 5 15 7.5 3.5 5 16 15.5 5 5 5
DWARAM
PUDI
HARSHIT
13 17Z51R0053 A 7.5 3 5 16 9 4 5 18 17 5 5 5
GUNDAM
MOUNIK
14 17Z51R0054 A 4 5 5 14 6.5 3.5 5 15 14.5 5 5 5
J
SUCHITH
15 17Z51R0055 A 6 3.5 5 15 8 2 5 15 15 5 5 5
KANKAN
ALA
16 17Z51R0056 RAGHU 9.5 4 5 19 6 4 5 15 17 5 5 5
KHALED
A
17 17Z51R0057 AFROZE 8 4.5 5 18 8 3.5 5 17 17.5 5 5 5
KONDA
18 17Z51R0058 AKHILA 10 6.5 5 22 10 3.5 5 19 20.5 5 5 5
KOTHAP
ALLI
19 17Z51R0059 SNEHA 8 3 5 16 9 3.5 5 17 16.5 5 5 5
KRUTHI
20 17Z51R0060 T 6.5 4.5 5 16 8 3 5 16 16 5 5 5
KUNCHE
21 17Z51R0061 PU ANIL 7.5 2.5 5 15 9 3 5 17 16 5 5 5
LACHUB
UKTHA
22 17Z51R0062 LEKHA 9 3.5 5 18 7.5 5 5 18 18 5 5 5
M
MRUDUL
A
GAYATH
23 17Z51R0063 RI 6 2.5 5 14 6 4 5 15 14.5 5 5 5
MADHIR
EDDY
SRIJA
24 17Z51R0064 REDDY 10 6.5 5 22 10 3.5 5 19 20.5 5 5 5
MANDAL
APARTHI
AKHILES
25 17Z51R0065 H 7 4.5 5 17 8 3 5 16 16.5 5 5 5
MOHAM
MED
SAMREE
N
26 17Z51R0067 BEGUM 9 5.5 5 20 10 6.5 5 22 21 5 5 5
MOKA
PRISCILL
27 17Z51R0068 A 7 5 5 17 10 7.5 5 23 20 5 5 5
NUTHUL
APATI
28 17Z51R0069 VARSHA 9 6 5 20 10 8 5 23 21.5 5 5 5
P
29 17Z51R0070 SWAPNA 6.5 5.5 5 17 8 8.5 5 22 19.5 5 5 5
PAILLA
MADHUR
30 17Z51R0071 I 10 5 5 20 10 8 5 23 21.5 5 5 5
POOJITH
A
31 17Z51R0072 PINJALA 10 9 5 24 10 8.5 5 24 24 5 5 5
R POOJA
32 17Z51R0073 SREE 5 4.5 5 15 10 7 5 22 18.5 5 5 5
RIMSHA
TAHREE
33 17Z51R0074 M 7.5 4 5 17 8 6 5 19 18 5 5 5
SANGAM
34 17Z51R0075 NANDINI 7.5 4 5 17 6.5 7 5 19 18 5 5 5
SHARIYA
35 17Z51R0076 FIRDOSE 6.5 0.5 5 12 8 7.5 5 21 16.5 5 5 5
SINGARA
JU
36 17Z51R0077 JAHNAVI 6.5 4 5 16 9 8.5 5 23 19.5 5 5 5
TANDALE
37 17Z51R0078 VISHAL 9 5 5 19 10 8.5 5 24 21.5 5 5 5
UPPALA
38 17Z51R0079 POOJA 9 6.5 5 21 9.5 8.5 5 23 22 5 5 5
VANAPAL
LI
39 17Z51R0080 SINDHU 10 8 5 23 10 9 5 24 23.5 5 5 5
VOOKAN
TI
40 17Z51R0081 SWATHI 9.5 8.5 5 23 10 8.5 5 24 23.5 5 5 5
VUNNAV
41 17Z51R0082 A 10 6 5 21 10 7.5 5 23 22 5 5 5
PRATHYU
SHA
YELLU
LAKSHMI
NARASI
MHA
42 17Z51R0083 REDDY 7.5 5.5 5 18 10 8 5 23 20.5 5 5 5
ADEPU
43 17Z51R0084 SOWMYA 9 6 5 20 7 8 5 10 15 5 5 5
SAMA
44 17Z51R0085 KEERTHI 7.5 5 5 18 10 4.5 5 20 19 5 5 5
PART-B (50MARKS)
2.
a) What is drug metabolism? write the factors affecting drug metabolism.
b) Write a note on bioisosterism. (5+5)
OR
3.
a) Discuss the prodrug approach in drug design giving suitable examples.
b) Explain the importance of stereochemistry of drugs on biological activities.
(5+5)
4.
a) Define and classify local anesthetics. Outline the synthesis of procaine.
b) Write the chemical structure, nomenclacture, mode of action and uses of any one antipsychotic
drug. (6+4)
OR
5.
a) Write the definition of anti-epileptics and its chemical classification.
b) Write the chemical structure, nomenclature, synthesis and uses of Ethosuximide.
(3+7)
6.
a) Discuss the SAR of muscarinic agonists .
b) Outline the synthesis of Carbachol. (6+4)
OR
7.
a) What are anti cholinesterases? Give the classification with suitable examples. Write the
mechanism of action of anti cholinesterases.
b) Outline the synthesis of Pyridostigmine. (6+4)
8.
a) Write the chemical classification of NSAIDS with suitable examples.
b) Discuss the synthesis, mechanism of action and stereochemical aspects of Ibuprofen.
(3+7)
OR
9.
a) Outline the synthesis of Meperidine.
b) Write a brief account on types of pain and inflammation. (4+6)
10.
a) Discuss the SAR of Benzothiadiazine diuretics.
b) Write the synthesis of procinamide. (6+4)
OR
11.
a) Discuss the mechanism of action and synthesis of Isosorbide dinitrate.
b) Write the steps involved in synthesis of Enalapril. (6+4)
1. a) Define the term bio-isosterism. Discuss how bio-isosterism affects biological activity of drug
molecules with the help of suitable examples.
b) Describe a method for the synthesis of Phenobarbitone and mention its mechanism of action and
uses. Label each reactant and the reaction conditions required for the synthesis. [16]
2. a) Classify Local anesthetic agents with one example with chemical structure for each class. Give
the mode of action and uses of local anesthetic agents.
b) Give the synthesis, mechanism of action and uses of carbachol and dicyclomine. Label each
reactant and the reaction conditions required for synthesis. [16]
4. a) Classify anti-epileptic agents with one example with chemical structure for each class. Give the
mode of action and uses of anti-epileptic agents.
b) Describe a method for the synthesis of Phenytoin and salbutamol. Label each reactant and the
reaction conditions required for the synthesis. [16]
5. a) Classify adrenergic agents with one example with chemical structure for each class. Give the
mode of action and uses of adrenergic agents.
b) Describe a method for the synthesis of bethanecol and Pralidoxime. Label each reactant and the
reaction conditions required for the synthesis. [16]
6. a) Classify anti-psychotic agents with one example with chemical structure for each class. Give the
mode of action and uses of anti-psychotic agents.
b) Give the synthesis, mechanism of action and uses of Halothane and haloperidol. Label each
reactant and the reaction conditions required for the synthesis. [16]
7. a) Classify general anesthetics with one example with chemical structure for each class. Give the
mode of action and uses of general anesthetics.
b) Give the synthesis, mechanism of action and uses of procaine and succinyl choline. Label each
reactant and the reaction conditions required for the synthesis. [16]
8. Write a note on
a) Effect of hydrogen bonding on biological activity of drugs.
b) Synthesis, mode of action and uses of lignocaine.
c) Conjugation reactions in drug metabolism.
d) soft- drug and pro-dug approach in drug design. [16]
Code No:226AA
JAWAHARLAL NEHRU TECHNOLOGICAL UNIVERSITY HYDERABAD
B.Pharmacy III Year II Semester Examinations, December – 2018
MEDICINAL CHEMISTRY – I
Time : 3 hours Max.Marks :
75
Note : This question paper contains two parts A and B
Part A is compulsory which carries 25 marks. Answer all questions in part A
Part B consists of 5 units. Answer any one full question from each unit. Each question
carries 10 marks and may have a,b,c as sub questions.
PART – A (25 Marks)
1.a) Define bio isosterism. (2)
b) Give the role of solubility in drug action. (3)
c) classify anti – epileptics with examples. (2)
d) Write the structures of diazepam, imipramine, and ethosuximide. (3)
e) Define anti choline esterase inhibitors with examples. (2)
f) Classfiy adrenergic drugs. (3)
g) Draw any two structures of COX-2 inhibitors. (2)
h) Write the various types of pain. (3)
i) classify antihypertensives. (2)
j) write the structures of Enalaprill, acetazolamide and isosorbide. (3)
PART - B
(50 Marks)
2. Explain in detail about phase -2 metabolic reaction with examples. (10)
OR
3. Explain in detail about partition coefficient. (10)
4. Explain in detail about neurotransmitters. (10)
OR
5. Classify sedatives and hypnotics.Write the synthesis of imipramine and phenobarbitone. (10)
6. Classify cholinergic drugs with examples and give there structures. (10)
OR
7. Write the synthesis of ephedrine and amphetamine. (10)
8. Explain in detail about the bio synthesis of prostaglandin E1. (10)
OR
9. Classify NSAIDS. Write the SAR of Opiod analgesics. (10)
10. Write short notes on nitrates. (10)
OR
11. Classify diuritics. Write the synthesis of actazolamide and hydrochlorthiazide. (10)
Code No:216AA
JAWAHARLAL NEHRU TECHNOLOGICAL UNIVERSITY HYDERABAD
B.Pharmacy III Year II Semester Examinations, October – 2016
MEDICINAL CHEMISTRY – I
Time : 3 hours Max.Marks : 75
Note : This question paper contains two parts A and B
Part A is compulsory which carries 25 marks. Answer all questions in part A
Part B consists of 5 units. Answer any one full question from each unit. Each question
carries 10 marks and may have a,b,c as sub questions.
PART – A
(25 Marks)
1.a) Write about partition –coefficient for biological activity.
b) define metabolism. Write the different metabolic reactions.
c) write the structure and mode of action of alprazolam.
d) give the structure and mechanism of action of thiopental sodium.
e) classify adrenergic blockers and give the significance of adrenergic blockade.
f) Write the structure and mechanism of action of any one neuro muscular blocker.
PART - B
(50 Marks)
2.a) Explain bio isosterism and steric features of drugs.
b) Discuss the soft drug approach with examples.
OR
3.a) Discuss in detail about phase-2 reactions with examples.
b) Explain in brief about solubility and lipophilicity in bio activity of drugs
4.a) Define anxiolytics. Write the synthesis and mechanism of action of diazepam.
b) classify general anesthetic agents. Give the physiochemical and sterio chemical aspects of
procaine.
OR
5.a) Define and classify antidepressants. Write the synthesis of fluoxetine.
b) Write the SAR and metabolism of local anesthetics.
6.a) Classify anti cholinesterases with examples and write the synthesis of pyridostigmine.
b) Write the SAR and general meachanism of action of anticholinergics.
OR
7.a) write the metabolism and therapeutic uses of ephedrine.
b) Give the synthesis and mechanism of action of ipratropium bromide.
8.a) Discuss the bio synthesis of prostaglandin E1.
b) Classify NSAIDS and give the synthesis of meloxicam
Code No:226AA
Time : 3 hours JAWAHARLAL NEHRU TECHNOLOGICAL UNIVERSITY HYDERABAD
Note : This B.Pharmacy III Year II Semester Examinations, December – 2018
question paper contains two parts A and B MEDICINAL CHEMISTRY – I Max.Marks :
Part A is compulsory which carries 75
25 marks. Answer all questions in part A
Part B consists of 5 units. Answer any one full question from each unit. Each question
carries 10 marks and may have a,b,c as sub questions.
PART – A
(25 Marks)
1.a) Define bio isosterism. (2)
b) Give the role of solubility in drug action (3)
c) classify anti – epileptics with examples. (2)
d) Write the structures of diazepam, imipramine, and ethosuximide. (3)
e) Define anti choline esterase inhibitors with examples. (2)
f) Classfiy adrenergic drugs. (3)
g) Draw any two structures of COX-2 inhibitors. (2)
h) Write the various types of pain. (3)
i) classify antihypertensives. (2)
j) write the structures of Enalaprill, acetazolamide and isosorbide. (3)
PART - B
(50 Marks)
2. Explain in detail about phase -2 metabolic reaction with examples. (10)
OR
3. Explain in detail about partition coefficient. (10)
4. Explain in detail about neurotransmitters. (10)
OR
5. Classify sedatives and hypnotics.Write the synthesis of imipramine and phenobarbitone. (10)
6. Classify cholinergic drugs with examples and give there structures. (10)
OR
Year/Sem
Batch: 2017-21 Academic Year: 2019-20 III/I/A&B
/Section
Course Maximum
R17 10
Code/Regl: Marks:
Max. CO
Q. No Question KL
Marks No
Note: Internal splitting of questions depends on the subject. Each question may be subdivided into
maximum of two sub questions
CO- Course Outcome (1to5); KL- Blooms knowledge Level (K1, K2, K3, K4, K5, K6)
K1 – Remember K2 – Understand K3 – Apply K4 – Analyze K5 – Evaluate K6 – Create
B. Pharmacy III- Year I-Sem, Sec-A & B I-Mid Term Exam, September-2019 Medicinal
Chemistry- II - OBJECTIVE EXAM
Name: ______________________________ Hall Ticket No.________________
Answer All Questions. All Questions Carry Equal Marks. Time: 20 Min. Marks: 10
c) Chlorambucil d) Doxorubicin
c) Amylnitrite d) Dipyridamole
c) Lidocaine d) Adenosine
c) Acetazolamide d) Vaptans
c) Conivaptan d) Furosemide
c) Labetalol d) Atenolol
8. Fluorouracil is an ( )
a) Purine analogue b) Pyrimidine analogue
9. The fallowing drug is an 1,4 -Dihydro pyridine derivative used as calcium channel blocker ( )
a) Verapamil b) Bepridil
c) Diltiazem d) Nimodipine
10.
Sodium nitroprusside is a ( )
a) Vasodilator b) Diuretic
1. A
2. D
3. A
4. B
5. C
6. D
7. A
8. B
9. D
10. A
11. H2 antagonists
13. Angiotensin
14. ACE
16. H+K+ATPase
17. Na+
19. Aldosterone
20. H2
Biochemistry (sec-A)
Year/Sem
Batch: 2017-21 Academic Year: 2019-20 III/I/A&B
/Section
Course Maximum
R17 10
Code/Regl: Marks:
Note: Internal splitting of questions depends on the subject. Each question may be subdivided into
maximum of two sub questions
CO- Course Outcome (1to5); KL- Blooms knowledge Level (K1, K2, K3, K4, K5, K6)
K1 – Remember K2 – Understand K3 – Apply K4 – Analyze K5 – Evaluate K6 – Create
B. Pharmacy III- Year I-Sem, Sec-A & B II-Mid Term Exam, November-2019 Medicinal
Chemistry- II - OBJECTIVE EXAM
Name: ______________________________ Hall Ticket No.________________
Answer All Questions. All Questions Carry Equal Marks. Time: 20 Min. Marks: 10
a) Benzocaine b) Procaine
c) Cocaine d) Lidocaine
c) Acarbose d) Glipizide
10.
Drugs used in graves disease ( )
a) Thyroxin b) Levothyronin
c) T4 d) Propylthiouracil
KEYS
1. D
2. B
3. C
4. C
5. B
6. D
7. C
8. B
9. C
10. D
11.Cholesterol
13.Homo
14. 7.5-9.5
17.HMG CoA-reductase
18. Coumarin
19. Na
Unit-1
1. Write the sar ,moa,uses ,synthesis of cimentidine,triprolidine hydrochloride,promethazine
hydrochloride
2. Give the sar ofalkylating agents.,antimetabolites
3. Write a short notes onhistamine receptors and their distribution in the body
4. Define proton pump inhibitors and give any two drug structures along with moa and uses
5. a) Classify anti cancer agents
b). Mention any two plant product antineoplastic agents structures&cisplatin structure
Unit-II
1. Write a note on diuretics with example, write the synthesis of acetazolamide,furosemide
2. Classify diuretics,write the structure of verapamil,nifedipine,reserpine,minoxidil
3. a).enumerate vasodilators ,give the structure of diltiazim
b).Give the sar ,m.o.a structure and uses of amolodipine,hydrochlorthaizide
4. Write down the m.o.a and s.a.r of loop diuretics
5. Write down the m.o.a and s.a.r,uses of carbonic anhydrase inhibitors
Unit-III
1. Define and classify a note on antihyperlipedemic agents with structure
2. Classiify anticoagulants ,write the structure and uses of clofibrate
3. Give an acouunt on statins including moa ,write the structure of lovastatin,lidocaine,amilodarone
4. Classify antiarrythmic agents and give the synthesis and s.a.r of disopyramide phosphate
5. Write the moa and uses ,synthesis of warfarin
6. What is congestive heart failure ,classification,general m.o.a of cardiac glycosides
Unit-IV
1. Explain the nomenclature and chemistry,metabolism of steroids
2. Write a note on oral contraceptives with examples
3. Clasify thyroid and antithyroid drugs with examples ,and give the structure and m.o.a of
methimazole,propylthiouracil
4. Give the detailed account on corticosteroids along with structure of any two drugs .
5. Write down the structure and uses of cortisone ,nandralone,
Unit-V
1. Write a note on hypoglycemic agents,and synthesis of tolbutamide
2. Give the structure of metformin,mention the drugs used in pancreatic malfunctioning
3. Write a short notes on anti diabetic agents,and give the structure of pioglitazone,rosiglitazone
4. Describe the structure, m.o.a and uses of ailpha glucoside inhibitors
5. Give the sar of local anesthetic agents
6. Write the m.o.a ,uses,synthesis of benzocaine,procaine,dibucaine