5. The belonging of drugs to the group of nitrogenous bases is proved with? A. Marki`s reagent B. Reactant Bouchard-Wagner C. Tollens' reagent D. Fehling's reagent.
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5. The belonging of drugs to the group of nitrogenous bases is proved with?
A. Marki`s reagent
B. Reactant Bouchard-Wagner
C. Tollens' reagent
D. Fehling's reagent.
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- Define the following terms:a. alkylating agentb. base analoguec. nonalkylating agentd. intercalating agente. ethidium bromideThe structures of two antiviral drugs are shown below. Draw the structures of the natural compounds they mimic and briefly describe in your own words the mechanism of action of these drugs. Br- `NH НО N' HO-P Но- HO Но. он (a) Foscarnet (b) BrivudineThe Xanthoproteic test involves what type of reaction? O Elimination reaction Pericyclic reaction O Electrophilic aromatic substitution Nucleophilic aromatic substitution
- 3. Based on the name of the following hypothetical drug salts, which of the following statements is correct for the parent drugs (in their unionized forms)? A. Catodium potassium B. Dogodium tartarate C. Hungaryon acetate D. Cureitall hydrobromide E. Eddyolone triethyamine A) A and E are acidic B) B and C are acidic C) A and E are basic D) C and D are basic E) D and E are acidic1. Prepare 200 mL of an isotonic aqueous solution of thimerosal (MW 404.84; L iso 3.4). The concentration of this antiinfective drug is 1:5000. a. Calculate the E value. b. Adjust the Isotonicity of the solution using NaCl.Last edit was seconds ago I text Calibri BIUA 12 E - E E E 1 4. 4. Chloramphenicol: a. Where does this drug bind? b. How does it inhibit protein synthesis? li
- 84) An antimicrobial is described as preventing alanine-alanine bridge formation. This means it6. What is a racemic mixture? Discuss the advantages and disadvantages of using single isomers of drugs instead of racemic mixtures.2. i. Calculate the Log-P values of the following drugs. ii. Are these compounds hydrophilic or lipophilic? NH2 N. CI Он OH Cefaclor Ibuprofen provide the complete steps of soultion not only numbers with complete steps and show works. what is the information needed I get the question like that the question want to calculate log p of drugs.
- Define the followings drug? 13. Alkaloid 14. Pro drug 15. Inotropic drugs.In the design of H2 antagonists, the polar guanidine group of compound A was proposed to interact with the antagonist binding region by two hydrogen bonds. This compelled researchers to derivatize compound B from compound A. HN EN Chain Extension Rigidification ZI compound A What drug design strategy has been used here? Simplification H₂N NH Substituent variation HN NH₂ HN NH N compound B4. On a TLC plate containing silica gel, which compound will have the largest Rf value when ethyl acetate is used as the mobile phase? Circle your answer for credit. Compound A CH3 cor CH3 H₂C COOH Compound B H.C. 0 CH,