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You are tasked to evaluate an antihypertensive drug for its oral bioavailability. Which physicochemical parameters are important to determine if a drug is feasible for oral administration? List and briefly describe optimal ranges for these parameters. Then evaluate the following structure and the provided information from SwissADME to determine if this structure has beneficial ADME properties for oral administration. Structure of antihypertensive drug Physicochemical properties Formula C17H18N2O6 Molecular weight 346.33 g/mol Num. heavy atoms 25 Num. arom. heavy atoms 6 Fraction Csp3 0.29 Num. rotatable bonds 6 Num. H-bond acceptors 6 Num. H-bond donors 1 Molar Refractivity 94.52 TPSA 110.45 Ų Log Po/w (XLOGP3) 2.20 Log S (ESOL) -3.15 Solubility 2.42e-01 mg/ml ; 7.00e-04 mol/l Class Soluble P-gp substrate No CYP3A4 inhibitor No Provide as much information as possible.

You are tasked to analyze a tablet formulation of a pharmaceutical drug using LC-MS. Explain in detail how this analytical method works (both LC and MS), how a sample containing multiple compounds can be analyzed, what the advantages of LC-MS over other analytical techniques are, and how you would validate (i.e. describing the validation parameters) a LC-MS method. Provide as much detail as possible and feel free to draw chromatograms and MS spectra to illustrate the interpretation of results.

Which of the following distinguish biopharmaceutical agents from small molecular weight drugs?

Which of the following are advantages of solid phase extraction compared to liquid-liquid extraction?

What regulation provides the framework for the conduct of a non-clinical labortaory study?

Match the respective definition with the specific antibody. 

Drugs that behave like morphine but also have antagonist activity are known as:

Arrange the functional groups in order of increasing difference in electronegativity.

You can upload the log-dose response curve here.

What is the mechanism of antibacterial action for sulfonamide antibiotics?