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This paper may be consulted for a comprehensive bibliography of our past work on DHFR inhibitors as potential drugs against opportunistic infections
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1542640568
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note
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22 However, only the synthesis of this compound was described in the patent, and no data on binding to either Pc or Ma were disclosed.
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31
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1542745821
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U.S. Patent 5,763,450 (9 June 1998), assigned to Hoffmann-La Roche, Inc., Nutley, NJ.
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Guerry, P.; Jolidon, S.; Masciadri, R.; Salder, H.; Then, R. U.S. Patent 5,763,450 (9 June 1998), assigned to Hoffmann-La Roche, Inc., Nutley, NJ.
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1542535709
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We are grateful to Dr. Melanie Cushion, Dept. of the VA Medical Center, University of Cincinnati, for kindly performing these assays.
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We are grateful to Dr. Melanie Cushion, Dept. of the VA Medical Center, University of Cincinnati, for kindly performing these assays.
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35
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1542535710
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note
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13.
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36
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1542640569
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note
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14 reported that 2,4-diamino-5-[3′,4′-dimethoxy-5′-(5- carboxypentyloxy)]pyrimidine, a structural analogue of 6, had nearly the same activity as TMP against S. aureus, but was 300-fold less active than TMP against E. coli organisms in culture even though it had 50-fold greater affinity for E. coli DHFR in a cell-free assay.
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