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Results: 1-11 |
Results: 11
Enhancement of the bioavailability of oral uridine by coadministration of 5-(phenylthio) acyclouridine, a uridine phosphorylase inhibitor: implications for uridine rescue regimens in chemotherapy
Authors: Al Safarjalani, ON Zhou, XJ Naguib, FNM Shi, JX Schinazi, RF el Kouni, MH
Citation: On. Al Safarjalani et al., Enhancement of the bioavailability of oral uridine by coadministration of 5-(phenylthio) acyclouridine, a uridine phosphorylase inhibitor: implications for uridine rescue regimens in chemotherapy, CANC CHEMOT, 48(5), 2001, pp. 389-397
Modulation of the pharmacokinetics of endogenous plasma uridine by 5-(phenylthio) acyclouridine, a uridine phosphorylase inhibitor: implications for chemotherapy
Authors: Al Safarjalani, ON Zhou, XJ Naguib, FNM Goudgaon, NM Schinazi, RF el Kouni, MH
Citation: On. Al Safarjalani et al., Modulation of the pharmacokinetics of endogenous plasma uridine by 5-(phenylthio) acyclouridine, a uridine phosphorylase inhibitor: implications for chemotherapy, CANC CHEMOT, 48(2), 2001, pp. 145-150
Effect of 5-(phenylselenenyl)acyclouridine, an inhibitor of uridine phosphorylase, on plasma concentration of uridine released from 2 ',3 ',5 '-tri-O-acetyluridine, a prodrug of uridine: relevance to uridine rescue in chemotherapy
Authors: Ashour, OM Naguib, FNM Goudgaon, NM Schinazi, RF el Kouni, MH
Citation: Om. Ashour et al., Effect of 5-(phenylselenenyl)acyclouridine, an inhibitor of uridine phosphorylase, on plasma concentration of uridine released from 2 ',3 ',5 '-tri-O-acetyluridine, a prodrug of uridine: relevance to uridine rescue in chemotherapy, CANC CHEMOT, 46(3), 2000, pp. 235-240
Modulation of plasma uridine concentration by 5-(phenylselenenyl)acyclouridine, an inhibitor of uridine phosphorylase: relevance to chemotherapy
Authors: Ashour, OM Al Safarjalani, ON Naguib, FNM Goudgaon, NM Schinazi, RF el Kouni, MH
Citation: Om. Ashour et al., Modulation of plasma uridine concentration by 5-(phenylselenenyl)acyclouridine, an inhibitor of uridine phosphorylase: relevance to chemotherapy, CANC CHEMOT, 45(5), 2000, pp. 351-361
5-phenylthioacyclouridine: A potent and specific inhibitor of uridine phosphorylase
Authors: el Kouni, MH Goudgaon, NM Rafeeq, M Al Safarjalani, ON Schinazi, RF Naguib, FNM
Citation: Mh. El Kouni et al., 5-phenylthioacyclouridine: A potent and specific inhibitor of uridine phosphorylase, BIOCH PHARM, 60(6), 2000, pp. 851-856
Effect of administration of 5-(phenylselenenyl)acyclouridine, an inhibitorof uridine phosphorylase, on the anti-tumor efficacy of 5-fluoro-2 '-deoxyuridine against murine colon tumor C26-10
Authors: Ashour, OM Naguib, FNM Goudgaon, NM Schinazi, RF el Kouni, MH
Citation: Om. Ashour et al., Effect of administration of 5-(phenylselenenyl)acyclouridine, an inhibitorof uridine phosphorylase, on the anti-tumor efficacy of 5-fluoro-2 '-deoxyuridine against murine colon tumor C26-10, BIOCH PHARM, 60(5), 2000, pp. 687-692
Modulation of 5-fluorouracil host toxicity by 5-(benzyloxybenzyl)barbituric acid acyclonucleoside, a uridine phosphorylase inhibitor, and 2 ',3 ',5 '-tri-O-acetyluridine, a prodrug of uridine
Authors: Ashour, OM Naguib, FNM Panzica, RP Al Safarjalani, ON el Kouni, MH
Citation: Om. Ashour et al., Modulation of 5-fluorouracil host toxicity by 5-(benzyloxybenzyl)barbituric acid acyclonucleoside, a uridine phosphorylase inhibitor, and 2 ',3 ',5 '-tri-O-acetyluridine, a prodrug of uridine, BIOCH PHARM, 60(3), 2000, pp. 427-431
Uridine phosphorylase inhibitors: Chemical modification of benzyloxybenzyl-barbituric acid and its effects on UrdPase inhibition
Authors: Guerin, DJ Mazeas, D Musale, MS Naguib, FNM Al Safarjalani, ON el Kouni, MH Panzica, RP
Citation: Dj. Guerin et al., Uridine phosphorylase inhibitors: Chemical modification of benzyloxybenzyl-barbituric acid and its effects on UrdPase inhibition, BIOORG MED, 9(11), 1999, pp. 1477-1480
Insertional tagging of at least two loci associated with resistance to adenine arabinoside in Toxoplasma gondii, and cloning of the adenosine kinase locus
Authors: Sullivan, WJ Chiang, CW Wilson, CM Naguib, FNM el Kouni, MH Donald, RGK Roos, DS
Citation: Wj. Sullivan et al., Insertional tagging of at least two loci associated with resistance to adenine arabinoside in Toxoplasma gondii, and cloning of the adenosine kinase locus, MOL BIOCH P, 103(1), 1999, pp. 1-14
Metabolism and selective toxicity of 6-nitrobenzylthioinosine in Toxoplasma gondii
Authors: el Kouni, MH Guarcello, V al Safarjalani, ON Naguib, FNM
Citation: Mh. El Kouni et al., Metabolism and selective toxicity of 6-nitrobenzylthioinosine in Toxoplasma gondii, ANTIM AG CH, 43(10), 1999, pp. 2437-2443
The adenosine transporter of Toxoplasma gondii - Identification by insertional mutagenesis, cloning, and recombinant expression
Authors: Chiang, CW Carter, N Sullivan, WJ Donald, RGK Roos, DS Naguib, FNM el Kouni, MH Ullman, B Wilson, CM
Citation: Cw. Chiang et al., The adenosine transporter of Toxoplasma gondii - Identification by insertional mutagenesis, cloning, and recombinant expression, J BIOL CHEM, 274(49), 1999, pp. 35255-35261
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