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4. Name the text boxes LName, FName, MInitial, ALine1, ALine2, City, and ZipCode. 5. Create the Combo box with the 50 states of the United States in it by clicking ComboBox in the Toolbox, and then clicking and dragging to position it in the artboard. Then click the Selection tool, select the combo box, right-click, and in the pop-up menu that appears choose Add ComboBoxItem. Do this 49 more times to add 49 ComboBoxItems, select each of them and change the Header in the Common Properties palette to each state name. (Do you really want to do that 50 times If not, see 21. We added the states using data binding to an XML file with the state names.) 6. Add a Submit button by double-clicking the Button tool in the Toolbox. Click the Selection tool, and click and drag to position the button where you want it. Then in the Common Properties palette change the Content property from Button to Submit. If you add a gradient to the LayoutRoot, your form should now look similar to the form in Figure 20.33, although feel free to make it look a lot better!



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If you use the Windows task manager, then you can examine the individual characteristics of the processes that are executing on a specific machine. For example, if you look at Figure 14-14 you will be able to see the name of each process on the machine, the percentage of the processor (CPU) that it is using, how much of the lifetime of the CPU it has used in total, and the amount of memory it is consuming. This information can be extremely useful in determining things such as memory leaks and performance bottlenecks.





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the C12-epimer of ( )-inophyllum B (3), and inophyllums G-1 (19) and G-2 (20) were novel compounds.9 All 11 natural products were evaluated for their inhibitory activity against HIV-1 RT. Among the most potent active compounds, inophyllum B (3), and inophyllum P (4), inhibited HIV-1 RT with IC50 values that were 38 nM and 130 nM, respectively, and both were active against HIV-1 in cell culture with EC50 values that were 1.4 mM and 1.6 mM, respectively. However, both inophyllum B (3) and inophyllum P (4) possessed the trans-C10,C11-dimethyl chromanone ring, which is different from the stereochemistry of the hydroxy group at the C12 position. The stereochemistry of the hydroxy group at the C12 position was not critical for antiviral activity, but the subsituents of carboxyl group at the C12 position lowered the activity signi cantly. For example, inophyllum C (11) and Inophyllum E (12) were much less active, whereas the closely related ( )-inophyllum D (18) and ( )-inophyllum A (17) possessing a cis-C10, C11 dimethylchromanol ring were less active. Furthermore, ( )-inophyllum P33 (soulattrolide, 16), a close structural resemblence to ( )-calanolide B (15), was found to be a potent inhibitor of HIV1 RT with an IC50 of 0.34 mM when HIV-RT was assessed for RNA-dependent DNA polymerase (RDDP). No appreciable activity was observed toward HIV-2 RT and avian myeloblastosis virus reverse transcriptase (AMVRT). The absolute con guration of ( )-inophyllum P as (10S, 11R, 12S) and other structurally related HIV-1 inhibitors, including ( )-inophyllum B (3), ( )-inophyllum P (4), ( )-calanolide A (1), ( )-calanolide B (2), ( )-calanolide B (15), ( )-cordatolide A (5), and ( )-cordatolide B (6) were also assigned.34 8.2.3 Anti-HIV-1 Activity of Cordatolides

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