Please write NEATLY and
CLEARLY.
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Please write NEATLY and CLEARLY. (7.4 pts.) In Figure 3 of Section 4 “Designing the Drug...
7. (4 pts.) In Figure 3 of Section 4 “Designing the Drug
Thalidomide”, two possible hydrolysis products are shown. Provide
the mechanism to generate compound 4. The first step of the
mechanism with the curved arrow pushing is done for you.
O + H-OH2 -N: Н. 0:0:- -NH2 N- 4 -ОН о о
In Figure 3 of Section 4 “Designing the Drug Thalidomide”, two
possible hydrolysis products are shown. Provide the mechanism to
generate compound 4. The first step of the mechanism with the
curved arrow pushing is done for you.
I' + H-OH2 -N: -NH, N 4 ОН о о
Please write NEATLY and
CLEARLY. Make arrows very obvious.
2. [2.5 pts.) Shown below is the general mechanism for the interconversion of the enantiomers of thalidomide. Draw the appropriate curved arrow pushing for each step of the mechanism. H-OH ÖH2 + H-SHz H N -0+ H-OH2 -N 0:0 H
Provide the mechanism to generate compound 4. The first step of the mechanism with the curved arrow pushing is done for you. -NH2 H O + H-OH2 4 -ОН 0:0:- H
Provide the mechanism to generate compound 4. The first step of the mechanism with the curved arrow pushing is done for you. -NH2 H O + H-OH2 4 -ОН 0:0:- H
8. (3 pts.) In the section “designing the drug thalidomide”,
you learned that researchers create various analogs to determine
which structural features are necessary for biological activity and
which are responsible for side effects. the analogs were created
using the molecule shown below. using the information found in
table 3, draw the corresponding analogs #7, 8, and 11.
8. (3 pts.) In the section Designing the Drug Thalidomide" you learned that researchers create various analogs to determine which structural features...
please answer question 9
8 (3 pts.) In the section Designing the Drug Thalidomide", you learned that researchers create various analogs to determine which structural features are necessary for biological activity and which are responsible for side effects. The analogs were created using the molecule shown below. Using the information found in Table 3. draw the corresponding analogs #78, and 11 o N IHz NH2 IC 50.= 150 km Analog #7 "NH2 'NH2 OCHS KTOCH2CH3 "OCH₂ CH3 IC 5o =...
8. In the section "Designing the Drug Thalidomide", you
learned that researchers create various analogues to determine
which structural features are necessary for biological activity and
which are responsible for side effects. The analogues were created
using the molecule shown below. Using the information found in
Tabkw 3, sraw the corresponding analogs #7, 8, and 11.
9. Thalidomide is known to be an inhibitor of TBF-a. TNF-a is
a protein mediator, and when to much of this mediator is present,...
4. (1 pt.) This question is in reference to Table 1 found in Section 3 "Scientific Results in Support of Thalidome Victims". Based on the results, what can you conclude about the teratogenicity of the racemic mixture versus RA enantiomers of thalidomide? 5. (1 pt.) This question is in reference to Table 2 found in Section 3 "Scientific Results in Support of Thalidomide Victims". What can you conclude about the inversion rate for the two enantiomers? Table 1: Teratogenicity of...
8) (11 pts) a) Write out thc 3-step arrow pushing mechanism showing how cthyl propanoate is hydrolyzed in the presence of I mole equivalent NaOH to form sodium propanoate and ethanol. b) H/HO also serve to hydrolyze an ester; brielly explain why NaOH HO is generally preferable. 10) (8 pts) Fill in the missing reagents in cach of the following reductions. More than one step may be required. For + racinho HO + NaOH e come to Na + HO...