Pharmacy / Pharmacology / Pharmaceutical Sciences / Medicinal Chemistry PDF
Q. What is the field of medical science that studies drugs and their precise interactions with the human body called? Answer: Pharmacology
Q. The biochemical study covering the processes of drug absorption, distribution, metabolism, and excretion is known as: Answer: Pharmacokinetics
Q. Which branch of science focuses on analyzing the specific mechanisms of drug actions and the resulting physiological effects on the body? Answer: Pharmacodynamics
Q. Chemical substances created by or derived from living organisms to destroy bacteria or halt their reproduction are called: Answer: Antibiotics
Q. Through which biological paths or secretions are drugs eliminated from the human body? Answer: All of the above (Kidneys, breast milk, saliva, sweat, and bile)
Q. From which of the following natural or artificial origins can therapeutic drugs be sourced? Answer: All of the above (Animals, plants, micro-organisms, and synthetic origin)
Q. Which clinical factors directly alter or impact the overall rate of drug absorption? Answer: All of the above (Route of administration, drug solubility, and the administration site)
Q. What is the term for introducing a liquid medication directly into a body orifice or cavity? Answer: Instillation
Q. The topical application of medication onto the skin, typically accompanied by surface friction or rubbing, is called: Answer: Inunction
Q. Through which specialized administrative route is Nitroglycerine typically given to a patient? Answer: By sublingual route
Q. When an injection introduces a therapeutic agent directly into the bone marrow cavity, the route is termed: Answer: Intramedullary
Q. Administering a medicinal solution directly into the spinal cavity describes which route? Answer: Intrathecal
Q. Which administrative route must a clinician use when delivering a diagnostic test dose of penicillin? Answer: Intradermal
Q. Injecting a drug past the primary layers of skin directly into the loose areolar tissue is known as: Answer: Subcutaneous administration
Q. To guarantee safe medication delivery, which components must a nurse verify within a written medical prescription? Answer: All of the above (Patient and drug names, dose and route, along with the date and physician’s signature)
Q. Identify the incorrect statement regarding the clinical administration of parenteral drugs: Answer: Parenteral route cannot be used in case of an unconscious patient.
Q. Choose the correct rule concerning patient care and proper drug administration: Answer: All of the above (Child doses are smaller, pregnancy/lactation must be evaluated for females, and the ‘five rights’ ensure patient safety)
Q. Medications specifically prescribed to alleviate or dull physical pain are classified as: Answer: Analgesics
Q. Which category of pharmaceutical agents is responsible for lowering an elevated body temperature during a fever? Answer: Antipyretics
Q. Which drug class is utilized to control, minimize, or treat convulsive seizures in an epileptic patient? Answer: Anticonvulsants
Q. Medical substances that are administered to neutralize or counteract the toxic impacts of a poison are called: Answer: Antidotes
Q. Which agents are designed to eradicate, destroy, and expel parasitic worms from the host body? Answer: Antihelminthics
Q. A localized or systemic drug used specifically to soothe or stop itching is an: Answer: Antipruritic
Q. Medications used to successfully manage, suppress, or prevent symptoms of nausea and vomiting are called: Answer: Antiemetics
Q. Which therapeutic agent is prescribed to elevate total hemoglobin levels within the bloodstream? Answer: Haematinics
Q. Which class of drugs acts directly on the kidneys to elevate total urine output? Answer: Diuretics
Q. Substances that expand blood vessel diameter to effectively lower systemic blood pressure are known as: Answer: Vasodilators
Q. Cardiotonic drugs are primarily administered to achieve which clinical outcome? Answer: Increase heart rate and cardiac muscle contractions
Q. Anxiolytic medications are strictly indicated for which of the following mental health uses? Answer: To relieve anxiety
Q. Mydriatic medications are topically applied to the eye in order to: Answer: Dilate the pupil of the eye
Q. Miotic eye drops are pharmaceutical agents designed to: Answer: Constrict the pupil of the eye
Q. Hypnotic agents are a class of medications primarily used to: Answer: Induce sleep
Q. A galactagogue is a specific substance administered to: Answer: Increase breast milk secretion
Q. Which essential fat-soluble vitamin is widely recognized as the anti-sterility vitamin? Answer: Vitamin E
Q. Which of the following is considered a key clinical advantage of using the Intravenous (I.V.) route? Answer: All of the above (Ideal for emergencies, allows large volume delivery, and provides immediate systemic response)
Q. When an injection is labeled as ‘Intra-articular’, the drug is being delivered directly into the: Answer: Joints
Q. What is an inherent therapeutic risk or disadvantage of using the Intravenous (I.V.) route? Answer: All of the above (Injected over-doses cannot be retrieved, demands specialized training, and presents infection risks)
Q. For an unconscious patient requiring immediate systemic medication, which route is preferred? Answer: Intravenous
Q. Which of the following issues represents a potential adverse complication of receiving clinical injections? Answer: All of the above (Infections, pyrogenic reactions, and localized tissue trauma)
Q. Injecting medications repeatedly into the exact same bodily location can trigger: Answer: All of the above (Skin induration with scar formation, nerve injuries, and blood vessel wall damage)
Q. Choosing the correct anatomical site for an injection depends heavily on which parameters? Answer: All of the above (Physician’s ordered route, total fluid volume, and unique chemical properties of the drug)
Q. In a clinical setting, an infusion labeled as 5% Glucose Saline signifies that: Answer: Each 100 ml contains 5 gms glucose and 0.9 gm sodium chloride.
Q. Before executing an injection procedure, a nurse must be competent in doing which of the following tasks? Answer: All of the above (Selecting matching equipment, choosing the site accurately, and preparing precise medication volumes)
Q. What is a practical advantage of choosing single-use plastic syringes over glass alternatives? Answer: All of the above (They are disposable and economical, highly shatter-resistant, and minimize air embolism risks)
Q. Which physical and clinical variables dictate the selection of specific syringes and needle sizes? Answer: All of the above (The prescribed route, solution viscosity, and total medication volume to be delivered)
Q. Which of the following anatomical structures is not considered a component of a standard medical syringe? Answer: Shaft
Q. When selecting an appropriate needle for patient care, which safety features should be verified? Answer: All of the above (A sharp hook-free bevel, using the smallest appropriate gauge, and ensuring a tight fit to the syringe hub)
Q. Which pharmacological fact is completely true regarding Paracetamol? Answer: All of the above (It possesses analgesic/antipyretic traits, has weak anti-inflammatory action, and is hepatotoxic in high doses)
Q. A fluid solution consisting of 5% Dextrose in Normal Saline (DNS) is categorized as a: Answer: Hypertonic fluid
Q. Which clinical statement regarding the properties of Aspirin (Acetylsalicylic acid) is incorrect? Answer: Aspirin increases platelet aggregation and helps in blood coagulation.
Q. What fact is clinically verified regarding a standard Normal Saline (NS) solution? Answer: All of the above (It consists of 0.9% sodium chloride, stands as an isotonic solution, and must be avoided in cases of CHF or pulmonary edema)
Q. Which of the following standard intravenous fluids is classified as an Isotonic solution? Answer: Both (a) and (c) (Ringer’s Lactate and 0.9% Normal Saline)
Q. Which of the following intravenous fluid concentrations is classified as a Hypotonic solution? Answer: All of the above (0.25% sodium chloride, 2.5% dextrose, and 0.45% sodium chloride solutions)
Q. What is the standard medical abbreviation used to represent the weight unit ‘grain’? Answer: gr
Q. Within the metrics framework, what is designated as the primary standard unit of mass or weight? Answer: Kilogram
Q. One kilogram (1 kg) converts roughly to how many pounds (lb)? Answer: 2.2 pounds
Q. What is the total mass of adrenaline present within a 100 ml flask of a 1:1000 concentration solution? Answer: 0.1 gm
Q. One fluid ounce (fl. oz.) is equivalent to approximately how many milliliters? Answer: 25 ml
Q. One regular avoirdupois ounce (oz) is equal to approximately how many grams? Answer: 30 grams
Q. One standard Imperial gallon is equivalent to which approximate volume in milliliters? Answer: 4000 ml
Q. One complete liquid gallon is comprised of how many fluid ounces? Answer: 160 fl. ounce
Q. What exact mass of raw sodium chloride is dissolved to prepare 1 liter of standard Isotonic Normal Saline? Answer: 9 gm
Q. In standardized medical liquid conversions, 1 pint is equivalent to: Answer: 500 ml
Q. One liquid pint is equal to how many fluid ounces? Answer: 20 oz
Q. A volume measuring a total of 5 pints is equivalent to: Answer: 2500 ml
Q. One standard domestic teaspoonful (tsp) provides a fluid volume equal to: Answer: 5 ml
Q. One standard domestic tablespoonful (tbsp) provides a fluid volume equal to: Answer: 15 ml
Q. A total volume of 1 liter of fluid is equivalent to: Answer: 2 pints
Q. Analgesic medications are specifically administered into a patient’s care plan to: Answer: Relieve pain
Q. A pure 5% Dextrose water intravenous solution is chemically categorized as: Answer: Isotonic solution
Q. Mixing 5% Dextrose directly into a Normal Saline solution creates a fluid that is: Answer: Hypertonic solution
Q. An intravenous solution containing Mannitol behaves inside the intravascular space as a: Answer: Hypertonic solution
Q. Which of the following clinical intravenous preparations is classified as a hypertonic solution? Answer: All of the above (5% dextrose in NS, 5% dextrose in ½ NS, and 5% dextrose in RL)
Q. Which of the following generic items is categorized as a functional antiemetic drug? Answer: All of the above (Metoclopramide, Domperidone, and Ondansetron)
Q. In what historical year was the original Poison Act enacted? Answer: 1919
Q. What is the clinical meaning of the pharmacy abbreviation ‘gtt’? Answer: A drop
Q. What is the standardized short symbol used to represent a gallon? Answer: gal
Q. The prescription abbreviation ‘Ung.’ indicates which type of drug preparation? Answer: Ointment
Q. Which of the following choices represents the correct pharmacy symbol for a powder form medicine? Answer: Pulv.
Q. The Latin prescription abbreviation ‘Mist.’ stands for which type of formulation? Answer: Mixture
Q. Which shorthand symbol represents plain water within a medical prescription layout? Answer: aq.
Q. The term ‘Lin.’ is a standard prescription abbreviation used to denote a: Answer: Liniment
Q. When a doctor writes the abbreviation ‘stat.’ on an order sheet, it means the drug must be given: Answer: At once
Q. The pharmacy abbreviation ‘prn.’ tells a clinician that the medicine should be administered: Answer: When required
Q. If a medical order displays the symbol ‘h.s.’, the nurse knows to administer the medication: Answer: At bed time
Q. The prescription shorthand ‘h.n.’ indicates that the medication must be given: Answer: Tonight
Q. What is the clinical definition of the Latin medical abbreviation ‘S.O.S.’? Answer: If necessary in emergency
Q. When a drug is marked with the symbol ‘a.c.’, it dictates that delivery should happen: Answer: Before meals
Q. The abbreviation ‘c.m.’ on a medical prescription stands for: Answer: Tomorrow morning
Q. What is the maximum recommended fluid volume that can be safely injected into a single Intramuscular (I.M.) site? Answer: 5 ml
Q. Which of the following items is a semi-synthetic or synthetic opioid, rather than a natural opium alkaloid? Answer: Pethidine
Q. Which of the following substances is classified as a natural opium alkaloid? Answer: Morphine
Q. For a patient experiencing excruciating visceral pain due to acute pancreatitis, which analgesic is preferred? Answer: Meperidine hydrochloride (Pethidine)
Q. Which of the following pain management options is classified as a synthetic opioid? Answer: All (Pethidine, Tramadol, and Methadone)
Q. Fentanyl belongs to which specific therapeutic drug class? Answer: Synthetic opioid analgesic
Q. What are the common physiological or psychological reactions caused by administering opioid (narcotic) analgesics? Answer: All of the above (Sedation/analgesia, euphoria/respiratory depression, and nausea/vomiting/constipation)
Q. Why is Morphine strictly contraindicated for a patient who has suffered an acute head injury? Answer: All of the above (It risks respiratory depression, raises intracranial pressure, and induces mental clouding/vomiting)
Q. Which statement regarding the clinical use and properties of Pethidine is accurate? Answer: All of the above are true (It is a synthetic morphine derivative, often preferred over morphine for specific pains, and manages visceral pain)
Q. Identify the incorrect statement regarding the narcotic painkiller Tramadol: Answer: It is a naturally occurring opium alkaloid.
Q. Which pharmaceutical agent is utilized as the specific clinical antidote to reverse a Morphine overdose? Answer: Naloxone
Q. Which of the following formulations belongs to the natural Penicillin group? Answer: All of the above (Benzyl penicillin–G, Procaine penicillin–G, and Benzathine penicillin)
Q. Which specific natural penicillin variation provides the longest duration of therapeutic action? Answer: Benzathine penicillin (Penidura)
Q. Which broad-spectrum penicillin variant maintains high efficacy when delivered via both oral and parenteral pathways? Answer: Amoxicillin
Q. Which administrative routes are considered part of the enteral route category? Answer: All (Oral, Sublingual, and Rectal)
Q. Which of the following antimicrobial medications exert a direct bactericidal (bacteria-killing) action? Answer: Gentamycin and Penicillin
Q. Which statements accurately describe the clinical properties and risks of Penicillins? Answer: All of the above are true (They are cell-wall synthesis inhibiting bactericidals, neurotoxic in massive doses, and susceptible to penicillinase destruction)
Q. Which of the following choices belongs to the first-generation Cephalosporin family? Answer: Cefadroxil
Pharmaceutical Sciences / Medicinal Chemistry
Q1: Medicinal chemistry is a science of which roots are interlinked with? Answer: Chemistry and Biology
Q2: Morphine was isolated from opium by? Answer: Sertuner
Q3: Aspirin was introduced by ______ in 1889. Answer: Dreser’s
Q4: First hormone epinephrine was synthesized in which year? Answer: 1904
Q5: Who is the founder of modern medicine? Answer: Hippocrates
Q6: Identification of a new chemical entity as a potential therapeutic agent (From Hit to Lead) is known as? Answer: Drug discovery
Q7: The process of bringing a new pharmaceutical drug to the market after the lead compound has been identified is known as? Answer: Drug development
Q8: Natural products, derivatives, or synthetic substances with good binding ability in drug discovery are known as? Answer: Hit
Q9: A compound with good activity and selectivity during drug discovery screening is known as? Answer: Lead
Q10: The main goals of pre-clinical studies are? Answer: To determine the safe dose for first-in-man study and assess a product’s safety profile.
Q11: IND stands for? Answer: Investigational New Drug
Q12: Human micro-dosing studies are conducted in which clinical phase? Answer: Phase 0
Q13: MTD stands for? Answer: Maximum Tolerated Dose
Q14: Single ascending dose studies are done in? Answer: Phase Ia
Q15: NDA stands for? Answer: New Drug Application
Q16: Phase IV trial is also known as? Answer: Post Marketing Surveillance
Q17: How many people are selected for Phase I trial? Answer: 20–50 people
Q18: How many people are selected for Phase II trial? Answer: 20–300 people
Q19: How many people are selected for Phase III trial? Answer: 300–3000 people
Q20: Which one of the following will be checked under Phase IV surveillance? Answer: The whole market will be under surveillance
Q21: Precision Medicine is an emerging approach depending on? Answer: Genomic study of an individual
Q22: How many main families of GPCRs are there? Answer: 6
Q23: Which reaction is catalyzed by adenylate cyclase? Answer: Conversion of ATP to cyclic AMP
Q24: Oxadiazole ring contains? Answer: 2 Nitrogen and 1 Oxygen atoms
Q25: The heteroaromatic radical is called? Answer: Naphthyl
Q26: Name of the given aromatic ring. Answer: 1-Ethyl-2-methyl naphthalene
Q27: Name of the given aromatic ring. Answer: Azepane
Q28: Which statement best describes pharmacodynamics? Answer: The study of how a drug interacts with its target binding site at the molecular level.
Q29: Which statement best describes pharmacokinetics? Answer: The study of how drugs reach their target in the body and how drug levels are affected by ADME.
Q30: What are soft drugs? Answer: Chemical drugs which are already found in the body.
Q31: Addition of a non-polar group ______ partition coefficient. Answer: Improves
Q32: Gentamicin and streptokinase can be given by which route? Answer: Parenterally
Q33: What is the distance between a hydrogen bond? Answer: 2.5–3.2 Å
Q34: What is the angle of a hydrogen bond? Answer: 130°–180°
Q35: What is the strength of a hydrogen bond? Answer: 1–7 kcal/mol
Q36: p-Nitrophenol contains which type of hydrogen bond? Answer: Intermolecular hydrogen bond
Q37: Which factor related to protein-drug binding is not related to drugs? Answer: Number of binding sites on the binding agent
Q38: Which factor related to protein-drug binding is not related to drug interactions with the binding site? Answer: Inter-subject variation
Q39: Which of the following is a drug interaction factor for protein-drug binding? Answer: Competition between drugs for the binding site
Q40: Only unbound or free drug is capable of being eliminated. Answer: True
Q41: Plasma proteins bind with drugs by the formation of? Answer: All of the above
Q42: The most significant protein involved in drug binding is? Answer: Albumin
Q43: The most abundant plasma protein is? Answer: Albumin (Human Serum Albumin)
Q44: Chelating agent Dimercaprol is used in the treatment of? Answer: Arsenic poisoning
Q45: Which chelating agent is used as an antidote in lead and vanadium poisoning? Answer: Disodium EDTA
Q46: Absorption of tetracycline is reduced in the presence of milk because of? Answer: Chelation
Q47: Functional groups of the same valence and ring equivalents are known as? Answer: Classical Bioisosteres
Q48: Bioisosteres have? Answer: Same physical, chemical, and similar biological properties
Q49: R(−)-Epinephrine shows 3-point interaction with the receptor, while S(+)-Epinephrine shows 2-point interaction. Answer: True
Q50: (+)-Warfarin is ______ times more potent than (−)-Warfarin. Answer: 5
Q51: (+)-Sotalol is a beta blocker while (−)-Sotalol is? Answer: Antiarrhythmic
Q52: D-Penicillamine is antiarthritic while L-Penicillamine is? Answer: Toxic
Q53: D-Asparagine has a sweet taste while L-Asparagine has? Answer: Tasteless
Q54: Biotransformation of drugs is defined as the conversion from one physical form to another. Answer: False
Q55: Drug biotransformation is a detoxification process. Answer: True
Q56: Phase I reactions are also known as synthetic reactions. Answer: True
Q57: Phase I reactions are detoxification pathways. Answer: True
Q58: Phase II reactions are detoxification pathways. Answer: True
Q59: Which of the following is not a Phase I reaction? Answer: Sulphide reactions
Q60: Which statement best describes Phase I metabolism? Answer: Reactions which add a polar functional group to a drug.
Q61: Which statement best describes Phase II metabolism? Answer: Reactions which add a polar molecule to a functional group already present on a drug or one of its metabolites.
Q62: Which of the following is not a characteristic of moieties transferred in Phase II reactions? Answer: Strong non-polar groups are attached.
Q63: Which enzyme is not involved in catalyzing Phase I metabolic reactions? Answer: Glucuronyl transferase
Q64: Which of the following is not a Phase I metabolic transformation? Answer: Conjugation to alcohols
Q65: What is the major end product of oxidation of aromatic carbon atoms? Answer: Arenols
Q66: Which of the following is not a common nitrogen-containing functional group undergoing reduction? Answer: Nitrite compounds
Q67: Hydrolysis of Aspirin yields? Answer: Salicylic acid and CH₃COOH
Q68: Which enzyme is important in Phase II reactions? Answer: Transferase
Q69: Which group is least susceptible to cytochrome P450 enzymes? Answer: Quaternary carbon atoms
Q70: Alkenes and aromatic groups are metabolized to diols by? Answer: Cytochrome P450 enzymes and epoxide hydrolase
Q71: Solubility of a drug in polar and non-polar solvents depends upon? Answer: All of the above
Q72: Drug diffusion across a membrane is higher when? Answer: Partition coefficient is high
Q73: Diazepam metabolized into Hydroxydiazepam is an example of? Answer: Oxidation at the carbon alpha to carbonyl and imino group
Q74: Which reaction is most common in drugs having ester or amide functional groups? Answer: Hydrolysis
Q122: The given reaction is an example of? Answer: Oxidation of Alicyclic carbon
Q123: Desulphuration of the given drug results in? Answer: Hydrolysis
Q124: By glycine conjugation, Benzoic acid forms? Answer: Hippuric acid
Q125: Enzymes are divided into which two categories? Answer: Microsomal and Non-microsoma
1: Aspirin was introduced by ________ in 1889. Answer: Dreser’s
Q2: First hormone epinephrine was synthesized in which year? Answer: 1904
Q3: Who is the founder of modern medicine? Answer: Hippocrates
Q4: Identification of a new chemical entity as a potential therapeutic agent (From Hit to Lead) is known as? Answer: Drug Discovery
Q5: The process of bringing a new pharmaceutical drug to the market after the lead compound has been identified is known as? Answer: Drug Development
Q6: Natural products, derivatives, or synthetic substances with good binding ability in drug discovery are known as? Answer: Hit
Q7: A compound with good activity and selectivity during drug discovery screening is known as? Answer: Lead
Q8: What are the main goals of pre-clinical studies? Answer: To determine the safe dose for first-in-man study and assess a product’s safety profile.
Q9: IND stands for? Answer: Investigational New Drug
Q10: Human micro-dosing studies are conducted in which clinical phase? Answer: Phase 0
Q11: MTD stands for? Answer: Maximum Tolerated Dose
Q12: Single ascending dose studies are done in? Answer: Phase Ia
Q13: NDA stands for? Answer: New Drug Application
Q14: Phase IV trial is also known as? Answer: Post Marketing Surveillance
Q15: How many people are selected for Phase I trial? Answer: 20–50 people
Q16: How many people are selected for Phase II trial? Answer: 20–300 people
Q17: How many people are selected for Phase III trial? Answer: 300–3000 people
Q18: What is checked under Phase IV surveillance? Answer: The whole market will be under surveillance.
Q19: Precision Medicine is an emerging approach based on? Answer: Genomic study of an individual
Q20: How many main families of GPCRs are there? Answer: 6
Q21: Which reaction is catalyzed by adenylate cyclase? Answer: Conversion of ATP to cyclic AMP
Q22: Oxadiazole ring contains? Answer: 2 Nitrogen and 1 Oxygen
Q23: The heteroaromatic radical is called? Answer: Naphthyl
Q24: Name of the given aromatic ring. Answer: 1-Ethyl-2-methyl naphthalene
Q25: Name of the given aromatic ring. Answer: Azepane
Q26: What best describes pharmacodynamics? Answer: The study of how a drug interacts with its target binding site at the molecular level.
Q27: What best describes pharmacokinetics? Answer: The study of how drugs reach their target in the body and how drug levels are affected by various factors.
Q28: What are soft drugs? Answer: Chemical drugs which are already found in the body.
Q29: The most important physicochemical properties affecting drug action are? Answer: All of the above
Q30: In QSAR, the letter “Q” stands for? Answer: Quantitative
Q31: Dimercaprol is a chelating agent used in the treatment of? Answer: Arsenic poisoning
Q32: Non-polar compounds are dispersed by? Answer: By interacting with lipid
Q33: pKa is a parameter that indicates? Answer: All of the above
Q34: 85% of drugs are ionized at which pH? Answer: 1.5–8
Q35: Bioisosterism is the process of? Answer: Replacement with a similar valence group
Q36: A drug like phenytoin and barbiturate with pKa greater than 7 is? Answer: Unionised at pH 6
Q37: A drug with pKa 7 that remains unionised at all pH is? Answer: Very weak acidic
Q38: Dissolution and pKa help in drug? Answer: Dissociation and solubility
Q39: Bioisosteres are similar in their? Answer: Both physical and chemical characteristics
Q40: Which of the following is not a bivalent? Answer: SH
Q41: A molecule having three chiral carbon centers has? Answer: 9 sets of enantiomers
Q42: 3D structure elucidation is done by? Answer: NMR
Q43: Which is the odd one regarding drug-receptor interaction? Answer: Dipole-induced dipole interaction
Q44: Which of the following is the fastest receptor? Answer: GPCR
Q45: Which of the following is not an optical isomer? Answer: Enantiomers
Q46: Enantiomer having higher affinity to a receptor is called? Answer: Eudismic
Q47: Hydrogen bonding occurring between molecules is called? Answer: Intermolecular hydrogen bonding
Q48: Which compound is capable of forming a ring structure with metal atoms? Answer: Chelates
Q49: Which condition is necessary for dissolution of a solute in a solvent? Answer: Solute-solvent interaction should equal or exceed solute-solute and solvent-solvent interaction.
Q50: Addition of a polar group in a drug increases its interaction with? Answer: Water
Q51: Methyl Prednisolone is water insoluble, but which of its salts is water soluble? Answer: Sodium
Q52: Phenobarbitone is water insoluble, but which of its salts is water soluble? Answer: Sodium
Q53: Which ester of Chloramphenicol is prepared to mask its bitter taste? Answer: Palmitate
Q54: Generally, drugs are absorbed in which form? Answer: Unionized form
Q55: Most weakly acidic drugs (pKa < 2) are absorbed from? Answer: Stomach
Q56: Most weakly basic drugs (pKa > 8) are absorbed from? Answer: Intestine
Q57: Absorption of neutral drugs (pKa 6–8) is independent of pH. Answer: True
Q58: Which form of barbituric acid has CNS activity? Answer: 3
Q59: Addition of a non-polar group ________ partition coefficient. Answer: Improves
Q60: Gentamicin and Streptokinase can be given by which route? Answer: Parenterally
Q61: The distance between a hydrogen bond is? Answer: 2.5–3.2 Å
Q62: The angle of a hydrogen bond is? Answer: 130°–180°
Q63: The strength of a hydrogen bond is? Answer: 1–7 kcal/mol
Q64: p-Nitrophenol contains which type of hydrogen bond? Answer: Intermolecular hydrogen bond
Q65: Which factor related to protein-drug binding is not related to drugs? Answer: Number of binding sites on the binding agent
Q66: Which factor related to protein-drug binding is not related to drug interactions with the binding site? Answer: Inter-subject variation
Q67: Which of the following is a drug interaction factor for protein-drug binding? Answer: Competition between drugs for the binding site
Q68: Only unbound or free drug is capable of being eliminated. Answer: True
Q69: Plasma proteins bind with drugs by the formation of? Answer: All of the above
Q70: The most significant protein involved in drug binding is? Answer: Albumin
Q71: The most abundant plasma protein is? Answer: Albumin (Human Serum Albumin)
Q72: Dimercaprol is used in the treatment of? Answer: Arsenic poisoning
Q73: Which chelating agent is used as an antidote in lead and vanadium poisoning? Answer: Disodium EDTA
Q74: Absorption of Tetracycline is reduced in the presence of milk because of? Answer: Chelation
Q75: Functional groups of the same valence and ring equivalents are known as? Answer: Classical Bioisosteres
Q76: Bioisosteres have? Answer: Same physical, chemical, and similar biological properties
Q77: R(-)-Epinephrine shows 3-point interaction with the receptor while S(+)-Epinephrine shows 2-point interaction. Answer: True
Q78: (+)-Warfarin is _____ times more potent than (−)-Warfarin. Answer: 5
Q79: (+)-Sotalol is a beta blocker while (−)-Sotalol is? Answer: Antiarrhythmic
Q80: D-Penicillamine is antiarthritic while L-Penicillamine is? Answer: Toxic
Q81: D-Asparagine has a sweet taste while L-Asparagine has? Answer: Tasteless
Q82: Biotransformation of drugs is defined as the conversion from one physical form to another. Answer: False
Q83: Drug biotransformation is a detoxification process. Answer: True
Q84: Phase I reactions are also known as synthetic reactions. Answer: True
Q85: Phase I reactions are detoxification pathways. Answer: True
Q86: Phase II reactions are detoxification pathways. Answer: True
Q87: Which of the following is not a Phase I reaction? Answer: Sulphide reactions
Q88: Which statement best describes Phase I metabolism? Answer: Reactions which add a polar functional group to a drug.
Q89: Which statement best describes Phase II metabolism? Answer: Reactions which add a polar molecule to a functional group already present on a drug or one of its metabolites.
Q90: Which of the following is not a characteristic of moieties transferred in Phase II reactions? Answer: Strong non-polar groups are attached.
Q91: Which enzyme is not involved in catalyzing Phase I metabolic reactions? Answer: Glucuronyl transferase
Q92: Which of the following is not a Phase I metabolic transformation? Answer: Conjugation to alcohols
Q93: What is the major end product of oxidation of aromatic carbon atoms? Answer: Arenols
Q94: Which of the following is not a common nitrogen-containing functional group undergoing reduction? Answer: Nitrite compounds
Q95: Hydrolysis of Aspirin yields? Answer: Salicylic acid and CH₃COOH
Q96: Which enzyme is important in Phase II reactions? Answer: Transferase
Q97: Which group is least susceptible to cytochrome P450 enzymes? Answer: Quaternary carbon atoms
Q98: Alkenes and aromatic groups are metabolized to diols by? Answer: Cytochrome P450 enzymes and epoxide hydrolase
Q99: Solubility of a drug in polar and non-polar solvents depends upon? Answer: All of the above
Q100: Drug diffusion across a membrane is higher when? Answer: Higher partition coefficient
Q101: Diazepam is metabolized into Hydroxydiazepam by which type of reaction? Answer: Oxidation at the carbon alpha to carbonyl and imino group
Q102: Which reaction is most common in drugs having ester or amide functional groups? Answer: Hydrolysis