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from the latex of Calophyllum teysmanni var inophyllolide17 A total of 14 analogs were synthesized and tested by the NCI primary anti-HIV evaluation using XTT assay, whereas no compounds exhibited anti-HIV activity superior to the two natural lead products (1 and 15) Some structure activity requirements were apparent from the relative anti-HIV potencies of the various analogs Reduction of the 7,8ole nic bond indicated only a slight change in potency, and a hetero atom is required at C12, for activity such as ( )-12-oxo-calanolide B and ( )-12-oxocalanolide A still showed antiviral activity Zembower et al27 prepared a series of racemic structural analogs of ( )-calanolide A focused on the modi cation of the trans-10,11-dimethyldihydropyran-12-ol ring (ring C) and evaluated their anti-HIV activity using a CEM-SS cytoprotection assay.

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In this example, you step through a custom installation. Office lets you specify where you want to install the files notice that it is at the bottom of the screen, as shown in Figure 2-5. You can use the default subdirectory, which is usually C:\Program Files\Microsoft Office\, or click the Browse button to change the default location.

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Introduction of the extra methyl group into either the C10 or C11 position resulted in only two chiral centers with lowering of the activity relative to ( )calanolide A Substitution of the C10-methyl group with an isopropyl chain led to loss of activity Analogs containing a cis-relationship between the C10 and C11 alkyl groups were completely devoid of the potency except for the synthetic intermediate in which the C12-hydroxyl group in the ketone form possessed activity less potent than that of calanolide A with either the C10-C11-cis- or C10-C11-trans-relationship It is interesting that these two ketones represent the rst derivatives in the calanolide series to exhibit anti-HIV activity while not containing a C12-hydroxyl group and including a cis-relationship between the C10- and C11-methyl groups Some structural modi cations of racemic calanolide A have been studied by us.

# apt-get install samba samba-common smbclient swat # /etc/init.d/samba start # /etc/init.d/smb-client start

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The use of XML-based encryption in SOAP permits secure communication and access control to be implemented by encrypting any element in the SOAP envelope. The W3C XML Encryption WG (XENC) defines the mechanisms of XML encryption in the SOAP messages. In SOAP communication, encryption can be done at the SOAP sender node or at any of the intermediaries in the message path.

Kone Inc. realized that it must implement and manage a global-standard IT environment. But the company also realized that its business is about escalators and elevators, not IT, so it decided to pursue IT outsourcing. Kone had had an experience with IT outsourcing before, when it outsourced its mainframe operations to Computer Science Corp. But this time the scope of outsourcing was much larger, so the company solicited proposals and nally decided to partner with two global IT providers, SAP AG from Germany and Hewlett-Packard (HP) from the United States. As described in 8, SAP is the world s largest ERP provider, and almost all the 72 modules of SAP R/3 software (including a data warehouse) were deployed at Kone. The SAP environment is deployed in 16 countries, where 4,300 users, in all functional areas, work in this highly integrated product. HP was hired to provide and manage the hardware on which SAP is run. The decision to use two vendors was not easy. IBM and Oracle each could have provided both the

58 Removal of C11-methyl or methyl groups at both C11 and C6 positions maintains the basic stereochemistry of ( )-calanolide A as well as evaluates their antiHIV activity ( )-C11-demethyl calanolide A and ( )-calanolide A exhibited similar potencies, whereas the 6,6,11-demethyl calanolide A also had diminished activity The primary biological indicated that two methyl groups in the C6 position might be necessary for antiviral activity Recently Sharma et al59,60 envisaged that replacement of the coumarin ring oxygen atom (at position C1) of calanolide A with the nitrogen atom lead to dipyranogsuinolinone with a calanolide skeleton, namely, aza-calanolide A The EC50 value of ( ) aza-calanolide A (012 mM) is much lower than that of the natural product ( )-calanolide A (027 mM) The IC50 value for ( )-aza-calanolide A and ( )-calanolide A are 15 mM and 23 mM, respectively.

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