## Abstract A series of 5β(1βphenylethyl)pyrimidines **2β10** (Table I) were designed and synthesized as potent and selective inhibitors of __Pneumocystis carinii (P. carinii), Toxoplasma gondii (T. gondii)__ and __Mycobacterium avium (M. avium)__ dihydrofolate reductases (DHFR). The structure of *
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7-Methyl Trimethoprim Analogues as Inhibitors of the Folate Metabolizing Enzymes.
β Scribed by Aleem Gangjee; Xin Lin; Sherry F. Queener
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 166 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
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