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- Topic: Pharmaceutical chemistry. Biosynthesis of secondary metabolites. 1. Circle the biosynthetic units of crosanthin O and name them .COOH HO Figure. Structure of Crosanthin O (from Gardenia jasminoides fruits)me (1).docx BIU A A- are they different? 3. What are three ways that 2-deoxystreptamine (2-DOS) aminoglycosides can inhibit protein synthesis? 4. Chloramphenicol: a. Where does this drug bind? b. How does it inhibit protein synthesis?Diagnosis of covid-19 What are some future diagnostic approaches? word limit-250only recognised websites (who,fda etc) must be used as references. Reference from punblised scientific journal/articles should be used. [Please mention the references along with answer. Otherwise it'll be of no use in my assignment.]
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- 252F%252Fbbniagaraccc.sin.suny.edu%252Fwebapps signment Saved He One of the uses of diazepam is as an antiepileptic that can be administered by slow IV infusion at a rate of 0.5 mg/min for 1 hour. If the infusion solution consists of 6 ml and there are 15 drops per milliliter of solution, how many drops per minute should be administered? drops per minuteRNSG 1301 Pharmacology 3. The half- life of a medication is 60 minutes. What does this mean?Be sure to answer all parts. Give the amino acid sequence of an octapeptide that contains the amino acids Lys, Pro, Tyr, Ile (2 equiv) , Gln, Trp, Phe, and forms the following fragments when partially hydrolyzed with HCl: Lys–Ile-Phe-Pro, Phe-Pro-Gln-Tyr, and Trp-Ile-Lys.
- Need help with the following question. I would appreciate it if you could explain your work.true or false 6. Nucleotides are more acidic than nucleosides and nitrogenous bases.7. Similar to aromatic amino acids, the sugar-phosphate backbone also absorbs a wavelength of 260 to 280 nm.8. Cyclic adenosine monophosphate relays the primary signal to the target mechanism inside the cell.9. Adenine has higher UV absorbing capacity compared to thymine.10. Adenine and guanine are more soluble in aqueous solutions compared to adenosine and guanosineThese are option to choose and fill. 1.a.very acidicb.neutralc.very basic 2.a.asparagine and glutamineb.arginine and lysinec.phenylalanine and tyrosine 3.a.neutralb.negatively chargedc.aromaticd.positively charged 4.a.negatively charged phosphatesb.positively charged phosphatesc.aromatic nucleotidesd.neutral phosphoric acid groups 5.a.lose their aromatic side chainsb.lose their positive chargec.lose their negative charged.increase their positive chargee.increase their negative charge 6.a.more attraction to the phosphatesb.no attraction to the phosphatesc.no attraction to the aromatic groups 7.a.not as unfavorable becauseb.even less favorable becausec.comparatively favorable even though 8.a.carry negative chargesb.carry positive chargesc.are neutral