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Results: 1-14 |
Results: 14
METABOLISM AND SELECTIVE TOXICITY OF 6-NITROBENZYLTHIOINOSINE IN TOXOPLASMA-GONDII
Authors: ELKOUNI MH GUARCELLO V ALSAFARJALANI ON NAGUIB FNM
Citation: Mh. Elkouni et al., METABOLISM AND SELECTIVE TOXICITY OF 6-NITROBENZYLTHIOINOSINE IN TOXOPLASMA-GONDII, The FASEB journal, 12(4), 1998, pp. 733-733
ANTITUMOR-ACTIVITY AND PHARMACOKINETICS FOLLOWING ORAL-ADMINISTRATIONOF NATURAL PRODUCT DNA TOPOISOMERASE-I INHIBITORS 10-HYDROXYCAMPTOTHECIN AND CAMPTOTHECIN IN SCID MICE BEARING HUMAN BREAST-CANCER XENOGRAFTS
Authors: ZHANG RW CAI QY LINDSEY JR LI YF CHAMBLESS B NAGUIB FNM
Citation: Rw. Zhang et al., ANTITUMOR-ACTIVITY AND PHARMACOKINETICS FOLLOWING ORAL-ADMINISTRATIONOF NATURAL PRODUCT DNA TOPOISOMERASE-I INHIBITORS 10-HYDROXYCAMPTOTHECIN AND CAMPTOTHECIN IN SCID MICE BEARING HUMAN BREAST-CANCER XENOGRAFTS, International journal of oncology, 10(6), 1997, pp. 1147-1156
5-(M-BENZYLOXYBENZYL)BARBITURIC ACID ACYCLONUCLEOSIDE, A URIDINE PHOSPHORYLASE INHIBITOR, AND 2',3',5'-TRI-O-ACETYLURIDINE, A PRODRUG OF URIDINE, AS MODULATORS OF PLASMA URIDINE CONCENTRATION - IMPLICATIONS FOR CHEMOTHERAPY
Authors: ASHOUR OM NAGUIB FNM ELKOUNI MH
Citation: Om. Ashour et al., 5-(M-BENZYLOXYBENZYL)BARBITURIC ACID ACYCLONUCLEOSIDE, A URIDINE PHOSPHORYLASE INHIBITOR, AND 2',3',5'-TRI-O-ACETYLURIDINE, A PRODRUG OF URIDINE, AS MODULATORS OF PLASMA URIDINE CONCENTRATION - IMPLICATIONS FOR CHEMOTHERAPY, Biochemical pharmacology, 51(12), 1996, pp. 1601-1611
EFFECTS OF MODIFICATIONS IN THE PENTOSE MOIETY AND CONFORMATIONAL-CHANGES ON THE BINDING OF NUCLEOSIDE LIGANDS TO URIDINE PHOSPHORYLASE FROM TOXOPLASMA-GONDII
Authors: ELKOUNI MH NAGUIB FNM PANZICA RP OTTER BA CHU SH GOSSELIN G CHU CK SCHINAZI RF SHEALY YF GOUDGAON N OZEROV AA UEDA T ILTZSCH MH
Citation: Mh. Elkouni et al., EFFECTS OF MODIFICATIONS IN THE PENTOSE MOIETY AND CONFORMATIONAL-CHANGES ON THE BINDING OF NUCLEOSIDE LIGANDS TO URIDINE PHOSPHORYLASE FROM TOXOPLASMA-GONDII, Biochemical pharmacology, 51(12), 1996, pp. 1687-1700
SYNTHESIS OF [4-(HYDROXY)TETRAHYDROFURAN-2-YL]NUCLEOSIDES AS A NOVEL CLASS OF URIDINE PHOSPHORYLASE INHIBITORS
Authors: YANG TF KOTRA LP TENG Q NAGUIB FNM SOMMADOSSI JP ELKOUNI M CHU CK
Citation: Tf. Yang et al., SYNTHESIS OF [4-(HYDROXY)TETRAHYDROFURAN-2-YL]NUCLEOSIDES AS A NOVEL CLASS OF URIDINE PHOSPHORYLASE INHIBITORS, Tetrahedron letters, 36(7), 1995, pp. 983-986
ENHANCEMENT OF 5-FLUORO-2'-DEOXYURIDINE ANTITUMOR EFFICACY BY THE URIDINE PHOSPHORYLASE INHIBITOR 5-(BENZYLOXYBENZYL)BARBITURIC ACID ACYCLONUCLEOSIDE
Authors: ASHOUR OM NAGUIB FNM KHALIFA MMA ABDELRAHEEM MH PANZICA RP ELKOUNI MH
Citation: Om. Ashour et al., ENHANCEMENT OF 5-FLUORO-2'-DEOXYURIDINE ANTITUMOR EFFICACY BY THE URIDINE PHOSPHORYLASE INHIBITOR 5-(BENZYLOXYBENZYL)BARBITURIC ACID ACYCLONUCLEOSIDE, Cancer research, 55(5), 1995, pp. 1092-1098
STRUCTURE-ACTIVITY-RELATIONSHIPS FOR THE BINDING OF LIGANDS TO XANTHINE OR GUANINE PHOSPHORIBOSYL TRANSFERASE FROM TOXOPLASMA-GONDII
Authors: NAGUIB FNM ILTZSCH MH ELKOUNI MM PANZICA RP ELKOUNI MH
Citation: Fnm. Naguib et al., STRUCTURE-ACTIVITY-RELATIONSHIPS FOR THE BINDING OF LIGANDS TO XANTHINE OR GUANINE PHOSPHORIBOSYL TRANSFERASE FROM TOXOPLASMA-GONDII, Biochemical pharmacology, 50(10), 1995, pp. 1685-1693
O-(5',16)-METHANOCYTIDINE - SYNTHESIS, CONFORMATIONAL PROPERTIES AND DEAMINATION BY CYTIDINE DEAMINASE
Authors: MEGATI S EALICK SE NAGUIB FNM ELKOUNI MH KLEIN RS OTTER BA
Citation: S. Megati et al., O-(5',16)-METHANOCYTIDINE - SYNTHESIS, CONFORMATIONAL PROPERTIES AND DEAMINATION BY CYTIDINE DEAMINASE, Nucleosides & nucleotides, 13(10), 1994, pp. 2151-2168
POTENTIATION OF 5-FLUOROURACIL EFFICACY BY THE DIHYDROURACIL DEHYDROGENASE INHIBITOR, 5-BENZYLOXYBENZYLURACIL
Authors: NAGUIB FNM HAO SN ELKOUNI MH
Citation: Fnm. Naguib et al., POTENTIATION OF 5-FLUOROURACIL EFFICACY BY THE DIHYDROURACIL DEHYDROGENASE INHIBITOR, 5-BENZYLOXYBENZYLURACIL, Cancer research, 54(19), 1994, pp. 5166-5170
PHENYLSELENENYL-SUBSTITUTED AND PHENYLTHIO-SUBSTITUTED PYRIMIDINES ASINHIBITORS OF DIHYDROURACIL DEHYDROGENASE AND URIDINE PHOSPHORYLASE
Authors: GOUDGAON NM NAGUIB FNM ELKOUNI MH SCHINAZI RF
Citation: Nm. Goudgaon et al., PHENYLSELENENYL-SUBSTITUTED AND PHENYLTHIO-SUBSTITUTED PYRIMIDINES ASINHIBITORS OF DIHYDROURACIL DEHYDROGENASE AND URIDINE PHOSPHORYLASE, Journal of medicinal chemistry, 36(26), 1993, pp. 4250-4254
SYNTHESIS OF A NEW CLASS OF URIDINE PHOSPHORYLASE INHIBITORS
Authors: LEVESQUE DL WANG EC WEI DC TZENG CC PANZICA RP NAGUIB FNM ELKOUNI MH
Citation: Dl. Levesque et al., SYNTHESIS OF A NEW CLASS OF URIDINE PHOSPHORYLASE INHIBITORS, Journal of heterocyclic chemistry, 30(5), 1993, pp. 1399-1404
DIFFERENCES IN ACTIVITIES AND SUBSTRATE-SPECIFICITY OF HUMAN AND MURINE PYRIMIDINE NUCLEOSIDE PHOSPHORYLASES - IMPLICATIONS FOR CHEMOTHERAPY WITH 5-FLUOROPYRIMIDINES (VOL 53, PG 3687, 1993)
Authors: ELKOUNI MH ELKOUNI MM NAGUIB FNM
Citation: Mh. Elkouni et al., DIFFERENCES IN ACTIVITIES AND SUBSTRATE-SPECIFICITY OF HUMAN AND MURINE PYRIMIDINE NUCLEOSIDE PHOSPHORYLASES - IMPLICATIONS FOR CHEMOTHERAPY WITH 5-FLUOROPYRIMIDINES (VOL 53, PG 3687, 1993), Cancer research, 53(19), 1993, pp. 4738-4738
DIFFERENCES IN ACTIVITIES AND SUBSTRATE-SPECIFICITY OF HUMAN AND MURINE PYRIMIDINE NUCLEOSIDE PHOSPHORYLASES - IMPLICATIONS FOR CHEMOTHERAPY WITH 5-FLUOROPYRIMIDINES
Authors: ELKOUNI MH ELKOUNI MM NAGUIB FNM
Citation: Mh. Elkouni et al., DIFFERENCES IN ACTIVITIES AND SUBSTRATE-SPECIFICITY OF HUMAN AND MURINE PYRIMIDINE NUCLEOSIDE PHOSPHORYLASES - IMPLICATIONS FOR CHEMOTHERAPY WITH 5-FLUOROPYRIMIDINES, Cancer research, 53(16), 1993, pp. 3687-3693
5-BENZYLBARBITURIC ACID-DERIVATIVES, POTENT AND SPECIFIC INHIBITORS OF URIDINE PHOSPHORYLASE
Authors: NAGUIB FNM LEVESQUE DL WANG EC PANZICA RP ELKOUNI MH
Citation: Fnm. Naguib et al., 5-BENZYLBARBITURIC ACID-DERIVATIVES, POTENT AND SPECIFIC INHIBITORS OF URIDINE PHOSPHORYLASE, Biochemical pharmacology, 46(7), 1993, pp. 1273-1283
Risultati: 1-14 |