

1、单选题:
The target is ______ with a specific function in the body, and the drug exerts its efficacy by combining with it.
选项:
A: organ
B: organization
C: biomacromolecule
D: cell
答案: 【 biomacromolecule】
2、单选题:
Which of the following is not a requirement for an effective drug?
选项:
A: Interact with target
B: Binding to plasma proteins
C: Maintain an appropriate concentration at the target
D: Have enough time to interact with the target
答案: 【 Binding to plasma proteins】
3、单选题:
Which of the following does not fall into the category of drug-receptor interaction theory?
选项:
A: Lipinski rule
B: Lock and key theory
C: Molecular recognition
D: Induced fit theory
答案: 【 Lipinski rule】
1、单选题:
What are the two classifications of structure-based drug design?
选项:
A: Direct drug design, indirect drug design
B: Fragment drug design, drug property design
C: Direct drug design, fragment drug design
D: Direct drug design,drug property design
答案: 【 Direct drug design, indirect drug design】
2、单选题:
Indirect drug design is based on the design of the three-dimensional structure of ____.
选项:
A: Receptor
B: Protein
C: Compound
D: Ligand
答案: 【 Ligand】
3、单选题:
What are the ways to discover lead compounds?
选项:
A: Screening approach
B: Structure-based drug design
C: Property-based drug design
D: All of the above
答案: 【 All of the above】
1、单选题:
How many years does it take to discover modern innovative drugs?
选项:
A: 2-3 years
B: 5-8 years
C: 12-15 years
D: 20-30 years
答案: 【 12-15 years】
2、单选题:
Modern innovative drug discovery is a research process from genes to drugs. It has gone through three stages, which of the following is not?
选项:
A: Discovery of new targets
B: Discovery of lead compounds
C: Drug development
D: Consistency evaluation
答案: 【 Consistency evaluation】
3、单选题:
The main methods of drug design include ().
选项:
A: Drug design based on the interaction between the target and the drug
B: Computer aided drug design
C: Drug design based on early ADME/T evaluation
D: All of them
答案: 【 All of them】
1、单选题:
The concept of structural biology inspired by the structure of the target promoted the discovery of ______, which is the First of Class drug of Puri series antihypertensive drugs and the prototype of drug design based on ______. .
选项:
A: Enalapril, ligand pharmacophore
B: Captopril, structure
C: Enalapril, structure
D: Captopril, ligand pharmacophore
答案: 【 Captopril, structure】
2、单选题:
__________ is the main way of early drug discovery.
选项:
A: High-throughput screening
B: Random screening
C: Target-based screening
D: Pharmacophore model screening
答案: 【 Random screening】
3、单选题:
Modern drug design ideas based on the research of disease mechanisms, gene defects and other signal pathways discovered by _____ as the core reflect the new progress and new trends in the contemporary drug discovery field.
选项:
A: Random screening
B: Combinatorial chemistry
C: Target
D: High-throughput screening
答案: 【 Target】
1、单选题:
Modern innovative drug discovery is a research process from genes to drugs. It has gone through three stages, which of the following is not?
选项:
A: Discovery of new targets
B: Discovery of lead compounds
C: Drug development
D: Consistency evaluation
答案: 【 Consistency evaluation】
2、单选题:
How many years does it take to discover modern innovative drugs?
选项:
A: 2-3 years
B: 5-8 years
C: 12-15 years
D: 20-30 years
答案: 【 12-15 years】
3、单选题:
The concept of structural biology inspired by the structure of the target promoted the discovery of ______, which is the First of Class drug of Puri series antihypertensive drugs and the prototype of drug design based on ______.
选项:
A: Enalapril, ligand pharmacophore
B: Captopril structure
C: Enalapril, structure
D: Captopril, ligand pharmacophore
答案: 【 Captopril structure】
4、单选题:
The main methods of drug design include ()
选项:
A: Drug design based on the interaction between the target and the drug
B: Computer aided drug design
C: Drug design based on early ADME/T evaluation
D: All of them
答案: 【 All of them】
5、单选题:
Modern drug design ideas based on the research of disease mechanisms, gene defects and other signal pathways discovered by _____ as the core reflect the new progress and new trends in the contemporary drug discovery field.
选项:
A: Random screening
B: Combinatorial chemistry
C: High-throughput screening
D: Target
答案: 【 Target】
6、单选题:
_________ is the main way of classic drug discovery.
选项:
A: High-throughput screening
B: Random screening
C: Target-based screening
D: Pharmacophore model screening
答案: 【 Random screening】
7、单选题:
The target is ______ with a specific function in the body, and the drug exerts its efficacy by combining with it.
选项:
A: organ
B: organization
C: biomacromolecule
D: cell
答案: 【 biomacromolecule】
8、单选题:
Which of the following is not a requirement for an effective drug?
选项:
A: Interact with target
B: Binding to plasma proteins
C: Maintain an appropriate concentration at the target
D: Have enough time to interact with the target
答案: 【 Binding to plasma proteins】
9、单选题:
Which of the following does not fall into the category of drug-receptor interaction theory?
选项:
A: Lipinski rule
B: Lock and key theory
C: Molecular recognition
D: Induced fit theory
答案: 【 Lipinski rule】
10、单选题:
What are the two classifications of structure-based drug design?
选项:
A: Direct drug design, indirect drug design
B: Fragment drug design, drug property design
C: Direct drug design, fragment drug design
D: Direct drug design, drug property design
答案: 【 Direct drug design, indirect drug design】
11、单选题:
Indirect drug design is based on the design of the three-dimensional structure of ____.
选项:
A: Receptor
B: Protein
C: Compound
D: Ligand
答案: 【 Ligand】
12、单选题:
What are the ways to discover lead compounds?
选项:
A: Screening approach
B: Structure-based drug design
C: Property-based drug design
D: All of them
答案: 【 All of them】
1、单选题:
The following cases that are not targeted drug discovery are
选项:
A: Discovering gefitinib through EGFR overexpression mechanism
B: Discovered acetylsalicylic acid by relieving toothache
C: Gefitinib was discovered through EGFR activating mutation mechanism
D: Sofosbuvir was discovered through NS5B mechanism
答案: 【 Discovered acetylsalicylic acid by relieving toothache】
2、单选题:
The discovery and verification methods of drug targets do not include
选项:
A: Forward recognition method
B: Phenotypic observation
C: Reverse identification method
D: Clinical Trials
答案: 【 Phenotypic observation】
3、单选题:
Which of the following methods is not a classic drug discovery model?
选项:
A: Mouse writhing model
B: Rat forced swimming model
C: Mouse water maze model
D: HERG gene expression model
答案: 【 HERG gene expression model】
1、单选题:
Muscarinic acetylcholine receptors belong to
选项:
A: Ligand-gated ion channel receptor
B: G protein coupled receptor
C: Nuclear receptor
D: Receptor tyrosine kinase
答案: 【 G protein coupled receptor】
2、单选题:
The substrate of monoamine oxidase B is
选项:
A: Serotonin
B: Norepinephrine
C: Dopamine
D: Glutamate
答案: 【 Dopamine】
3、单选题:
Clenbuterol is also known as Clenbuterol, which belongs to β2 adrenergic receptor
选项:
A: Agonist
B: Antagonist
C: Inverse agonist
D: Allosteric modulator
答案: 【 Agonist】
1、单选题:
The following are not suitable as drug targets:
选项:
A: Histamine receptor
B: Dihydrofolate reductase
C: Tumor necrosis factor
D: All of the above can be used as drug targets
答案: 【 All of the above can be used as drug targets】
2、单选题:
The following statement about the target is incorrect:
选项:
A: Target theory is the foundation of modern drug discovery
B: Target theory is based on the discovery of drugs through phenotypes
C: Cytokines can also become targets of drug action
D: The druggability of the target is the key to the verification of the target
答案: 【 Target theory is based on the discovery of drugs through phenotypes】
3、单选题:
The research hypothesis of the second-generation anti-tumor drug imatinib is
选项:
A: Philadelphia chromosome aberration and BCR-ABL fusion gene expression
B: Tumor angiogenesis
C: EGFR level overexpression
D: p53 tumor suppressor gene inactivation
答案: 【 Philadelphia chromosome aberration and BCR-ABL fusion gene expression】
1、单选题:
Regarding the druggability statement, the following statement is correct
选项:
A: GPCR-like membrane protein receptors belong to the target type with lower Druggability
B: Refers to whether the target is druggable
C: The druggability of existing drug targets is low
D: High druggability without drug market targets
答案: 【 Refers to whether the target is druggable】
2、单选题:
For the requirements of drug targets, what is incorrect is
选项:
A: The signal pathway where the drug target is located must have a critical impact on the disease
B: The drug target must have a key role in the function of the signal pathway
C: The drug target must have a pocket in the structure to bind the drug
D: The drug target is a simplification of the relationship between disease and drug
答案: 【 The drug target must have a pocket in the structure to bind the drug】
3、单选题:
The following antihypertensive drugs that are not in the same signaling pathway as other options are
选项:
A: Valsartan
B: Aliskiren
C: Enalapril
D: Nifedipine
答案: 【 Nifedipine】
1、单选题:
Which of the following scientists proposed the idea of side chain that is the prototype of modern drug target theory?
选项:
A: Gerhard Domagk who invented Prontosil
B: Paul Janssen who invented haloperidol and fentanyl
C: Paul Ehrlich who invented Ars vannamei
D: James Black who invented propranolol and cimetidine
答案: 【 Paul Ehrlich who invented Ars vannamei】
2、单选题:
Which of the following technologies is not a target structural biology research technology?
选项:
A: Cryo-EM technology
B: NMR technology
C: X-ray single crystal diffraction technique
D: Computer tomography
答案: 【 Computer tomography】
3、单选题:
The following are not drug targets:
选项:
A: Dopamine receptor
B: Serotonin reuptake transporter
C: Amoeba
D: Tetrahydropteroate synthase
答案: 【 Amoeba】
1、单选题:
Which of the following scientists proposed the idea of side chain that is the prototype of modern drug target theory?
选项:
A: Gerhard Domagk who invented Prontosil
B: Paul Janssen who invented haloperidol and fentanyl
C: Paul Ehrlich who invented Ars vannamei
D: James Black who invented propranolol and cimetidine
答案: 【 Paul Ehrlich who invented Ars vannamei】
2、单选题:
Which of the following technologies is not a target structural biology research technology?
选项:
A: Cryo-EM technology
B: NMR technology
C: X-ray single crystal diffraction technique
D: Computer tomography
答案: 【 Computer tomography】
3、单选题:
The following are not drug targets
选项:
A: Dopamine receptor
B: Serotonin reuptake transporter
C: Amoeba
D: Tetrahydropteroate synthase
答案: 【 Amoeba】
4、单选题:
The following are not suitable as drug targets
选项:
A: Histamine receptor
B: Dihydrofolate reductase
C: Tumor necrosis factor
D: All of the above can be used as drug targets
答案: 【 All of the above can be used as drug targets】
5、单选题:
The following statement about the target is incorrect.
选项:
A: Target theory is the foundation of modern drug discovery
B: Target theory is based on the discovery of drugs through phenotypes
C: Cytokines can also be targets of drug action
D: The druggability of the target is the key to the verification of the target
答案: 【 Target theory is based on the discovery of drugs through phenotypes】
6、单选题:
The research hypothesis of the second-generation anti-tumor drug imatinib is
选项:
A: Philadelphia chromosome aberration and BCR-ABL fusion gene expression
B: Tumor angiogenesis
C: EGFR level overexpression
D: Inactivation of p53 tumor suppressor gene
答案: 【 Philadelphia chromosome aberration and BCR-ABL fusion gene expression】
7、单选题:
Muscarinic acetylcholine receptors belong to
选项:
A: Ligand-gated ion channel receptor
B: G protein coupled receptor
C: Nuclear receptor
D: Receptor tyrosine kinase
答案: 【 G protein coupled receptor】
8、单选题:
The substrate of monoamine oxidase B is
选项:
A: Serotonin
B: Norepinephrine
C: Dopamine
D: Glutamate
答案: 【 Dopamine】
9、单选题:
Clenbuterol, a wheezing drug that belongs to β2 adrenergic receptor, also known as clenbuterol
选项:
A: Agonist
B: Antagonist
C: Inverse agonist
D: Allosteric modulator
答案: 【 Agonist】
10、单选题:
Regarding the druggability statement, which statement is correct:
选项:
A: GPCR-like membrane protein receptors belong to the target type with lower Druggability
B: Refers to whether the target is druggable
C: Low druggability of listed drugs targets
D: High druggability without listed drugs targets
答案: 【 Refers to whether the target is druggable】
11、单选题:
For the requirements of drug targets, what is incorrect is:
选项:
A: The signal pathway where the drug target is located must have a critical impact on the disease
B: The drug target must have a key role in the function of the signal pathway
C: The drug target must have a pocket in the structure to bind the drug
D: The drug target is a simplification of the relationship between disease and drug
答案: 【 The drug target must have a pocket in the structure to bind the drug】
12、单选题:
The following antihypertensive drugs that are not in the same signaling pathway as other options are:
选项:
A: Valsartan
B: Aliskiren
C: Enalapril
D: Nifedipine
答案: 【 Nifedipine】
13、单选题:
The following cases that are not targeted drug discovery are:
选项:
A: Discovering gefitinib through EGFR overexpression mechanism
B: Discovered acetylsalicylic acid by relieving toothache
C: Gefitinib was discovered through EGFR
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