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The metabolism of formycin B in Leishmaniadonovani
Authors:Donald J Nelson  Stephen W Lafon  Thomas E Jones  Thomas Spector  Randolph L Berens  JJoseph Marr
Institution:1. Wellcome Research Laboratories Burroughs Wellcome Co. Research Triangle Park, NC 27709 USA;2. St. Louis University School of Medicine St. Louis, MO 63104 USA
Abstract:Formycin B, a pyrazolo(4,3-d)pyrimidine C-nucleoside, inhibited the growth of Leishmaniadonovani promastigotes in culture with an ED90 of 0.2 μg/ml. Promastigotes incubated for 24 hrs with Formycin B at 10 μg/ml were found to convert it to the ribonucleotide, formycin B 5′-monophosphate. The parasites were also capable of aminating formycin B 5′-monophosphate as evidenced by the appearance of formycin A di- and triphosphate. The RNA contained the formycin A moiety in 3′,5′-polynucleotide linkage. Succino-AMP synthetase from these parasites was able to use formycin B 5′-monophosphate as an alternate-substrate with a K'm of 26 μM and a V'm of about 1% the V'm IMP. Formycin B 5′-monophosphate was also a substrate for mammalian succino-AMP synthetase with a Vm' of 40% the Vm' of IMP.
Keywords:HPPR  allopurinol ribonucleoside  HPPR-MP  allopurinol ribonucleoside 5′-monophosphate  APPR-MP  4-aminopyrazolo(3  4-d)pyrimidine 5′-ribonucleotide  FormB-MP  formycin B 5′-monophosphate  FormA-MP  formycin A 5′-monophosphate  FormA-DP  formycin A 5′-diphosphate  FormA-TP  formycin A 5′-triphosphate  HPLC  high performance liquid chromatography  dCF  2′-deoxycoformycin  succino-AMP  adenylosuccinate
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