-
1
-
-
0037244883
-
Selective synthesis and reactions of 6-substituted-2-β -galactosyl-1,2,4-triazines of potential anticancer activity
-
Mansour, A.K.; Eid, M.M.; Khahil, N.S.A.M. Selective synthesis and reactions of 6-substituted-2-β-galactosyl-1,2,4-triazines of potential anticancer activity. Nucleosides, Nucleotides & Nucleic Acids 2003, 22 (1), 21-44.
-
(2003)
Nucleosides, Nucleotides & Nucleic Acids
, vol.22
, Issue.1
, pp. 21-44
-
-
Mansour, A.K.1
Eid, M.M.2
Khahil, N.S.A.M.3
-
2
-
-
0026697262
-
Deoxycytidine deaminase - Resistant stereoisomer is the active form of (±)-2′,3′-dideoxy-3′-thiacytidine in the inhibitation of hepatitis B virus replication
-
Chang, C.N.; Doong, S.L.; Zhou, J.H.; Beach, J.W.; Jeong, L.S.; Chu, C.K.; Tsai, C.H.; Cheng, Y.C. Deoxycytidine deaminase - resistant stereoisomer is the active form of (±)-2′,3′-dideoxy-3′ -thiacytidine in the inhibitation of hepatitis B virus replication. J. Biol. Chem. 1992, 267, 13,938-13,942. Chem. Abstr. 1992, 117, 14,2910e.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 13938-13942
-
-
Chang, C.N.1
Doong, S.L.2
Zhou, J.H.3
Beach, J.W.4
Jeong, L.S.5
Chu, C.K.6
Tsai, C.H.7
Cheng, Y.C.8
-
3
-
-
0026697262
-
-
Chang, C.N.; Doong, S.L.; Zhou, J.H.; Beach, J.W.; Jeong, L.S.; Chu, C.K.; Tsai, C.H.; Cheng, Y.C. Deoxycytidine deaminase - resistant stereoisomer is the active form of (±)-2′,3′-dideoxy-3′ -thiacytidine in the inhibitation of hepatitis B virus replication. J. Biol. Chem. 1992, 267, 13,938-13,942. Chem. Abstr. 1992, 117, 14,2910e.
-
(1992)
Chem. Abstr.
, vol.117
-
-
-
4
-
-
34547773241
-
-
Purinyl- and pyrimidinyl-1,3-dioxolanes as anti-retrovirals. Eur. Pat. 337, 713, Oct 18, 1989
-
Belleau, B.; Dixit, D.; Nguyen-Ba, N.; Kraus, J.L. Purinyl- and pyrimidinyl-1,3-dioxolanes as anti-retrovirals. Eur. Pat. 337, 713, Oct 18, 1989. Chem. Abstr. 1990, 112 198359w.
-
(1990)
Chem. Abstr.
, vol.112
-
-
Belleau, B.1
Dixit, D.2
Nguyen-Ba, N.3
Kraus, J.L.4
-
5
-
-
0026469165
-
The anti-hepatitis B virus activities, cytotoxicities, and anabolic profiles of the (-) and (+) enantiomers of cis-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxothiolan-5-yl]-cytosine
-
Furman, P.A.; Davis, M.; Liotta, D.C.; Paff, M.; Frick, L.W.; Nelson, D.J.; Dornsife, R.E.; Wurster, J.A.; Wilson, L.J.; Fyfe, J.A.; Tuttle, J.V.; Miller, W.H.; Condreay, L.; Avereet, D.R.; Schinazi, R.F.; Painter, G.R.: The anti-hepatitis B virus activities, cytotoxicities, and anabolic profiles of the (-) and (+) enantiomers of cis-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxothiolan-5-yl]-cytosine. Antimicrob. Agents Chemother 1992, 36, 2686-2692. Chem. Abstr. 1993, 118, 93802f.
-
(1992)
Antimicrob. Agents Chemother.
, vol.36
, pp. 2686-2692
-
-
Furman, P.A.1
Davis, M.2
Liotta, D.C.3
Paff, M.4
Frick, L.W.5
Nelson, D.J.6
Dornsife, R.E.7
Wurster, J.A.8
Wilson, L.J.9
Fyfe, J.A.10
Tuttle, J.V.11
Miller, W.H.12
Condreay, L.13
Avereet, D.R.14
Schinazi, R.F.15
Painter, G.R.16
-
6
-
-
0026469165
-
-
Furman, P.A.; Davis, M.; Liotta, D.C.; Paff, M.; Frick, L.W.; Nelson, D.J.; Dornsife, R.E.; Wurster, J.A.; Wilson, L.J.; Fyfe, J.A.; Tuttle, J.V.; Miller, W.H.; Condreay, L.; Avereet, D.R.; Schinazi, R.F.; Painter, G.R.: The anti-hepatitis B virus activities, cytotoxicities, and anabolic profiles of the (-) and (+) enantiomers of cis-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxothiolan-5-yl]-cytosine. Antimicrob. Agents Chemother 1992, 36, 2686-2692. Chem. Abstr. 1993, 118, 93802f.
-
(1993)
Chem. Abstr.
, vol.118
-
-
-
7
-
-
0027981440
-
Pure nucleoside enantiomers of β-2′,3′-dideoxycytidine analogs are selective inhibitors of hepatitis B virus in vitro
-
Schinazi, R.F.; Gosselin, G.; Faraj, A.; Korba, B.E.; Liotta, D.C.; Chu, C.K.; Mathe, C.; Imbach, J.; Sommadossi, J. Pure nucleoside enantiomers of β-2′,3′-dideoxycytidine analogs are selective inhibitors of hepatitis B virus in vitro. Antimicrob. Agents Chemother 1994, 38, 2172-2174. Chem. Abstr. 1994, 121, 200749e.
-
(1994)
Antimicrob. Agents Chemother.
, vol.38
, pp. 2172-2174
-
-
Schinazi, R.F.1
Gosselin, G.2
Faraj, A.3
Korba, B.E.4
Liotta, D.C.5
Chu, C.K.6
Mathe, C.7
Imbach, J.8
Sommadossi, J.9
-
8
-
-
0027981440
-
-
Schinazi, R.F.; Gosselin, G.; Faraj, A.; Korba, B.E.; Liotta, D.C.; Chu, C.K.; Mathe, C.; Imbach, J.; Sommadossi, J. Pure nucleoside enantiomers of β-2′,3′-dideoxycytidine analogs are selective inhibitors of hepatitis B virus in vitro. Antimicrob. Agents Chemother 1994, 38, 2172-2174. Chem. Abstr. 1994, 121, 200749e.
-
(1994)
Chem. Abstr.
, vol.121
-
-
-
9
-
-
0026507919
-
(-)-2′-Deoxy-3′-thiacytidine is a potent, highly selective inhibitor of human immunodeficiency virus type 1 and type 2 replication in vitro
-
Coates, J., A.V.; Cammack, N.; Jenkinson, H.J.; Jowett, A.J.; Jowett, M.I.; Pearson, B.A.; Penn, C.R.; Rouse, P.L.; Viner, K.C.; Cameron, J.M. (-)-2′-Deoxy-3′-thiacytidine is a potent, highly selective inhibitor of human immunodeficiency virus type 1 and type 2 replication in vitro. Antimicrob. Agents Chemother 1992, 36, 733-739. Chem. Abstr. 1992, 116, 211044u.
-
(1992)
Antimicrob. Agents Chemother.
, vol.36
, pp. 733-739
-
-
Coates, J.A.V.1
Cammack, N.2
Jenkinson, H.J.3
Jowett, A.J.4
Jowett, M.I.5
Pearson, B.A.6
Penn, C.R.7
Rouse, P.L.8
Viner, K.C.9
Cameron, J.M.10
-
10
-
-
0026507919
-
-
Coates, J., A.V.; Cammack, N.; Jenkinson, H.J.; Jowett, A.J.; Jowett, M.I.; Pearson, B.A.; Penn, C.R.; Rouse, P.L.; Viner, K.C.; Cameron, J.M. (-)-2′-Deoxy-3′-thiacytidine is a potent, highly selective inhibitor of human immunodeficiency virus type 1 and type 2 replication in vitro. Antimicrob. Agents Chemother 1992, 36, 733-739. Chem. Abstr. 1992, 116, 211044u.
-
(1992)
Chem. Abstr.
, vol.116
-
-
-
11
-
-
0026058540
-
Inhibition of the replication of hepatitis B virus in vitro by 2′,3′-dideoxy-3′-thiacytidine and related analog
-
Doong, S.L.; Tsai, C.H.; Schinazi, R.F.; Liotta, D.C.; Cheng, Y.C. Inhibition of the replication of hepatitis B virus in vitro by 2′,3′-dideoxy-3′-thiacytidine and related analog. Proc. Natl. Acad. Sci. USA 1991, 88, 8495-8499. Chem. Abstr. 1991, 115, 269987z.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 8495-8499
-
-
Doong, S.L.1
Tsai, C.H.2
Schinazi, R.F.3
Liotta, D.C.4
Cheng, Y.C.5
-
12
-
-
0026058540
-
-
Doong, S.L.; Tsai, C.H.; Schinazi, R.F.; Liotta, D.C.; Cheng, Y.C. Inhibition of the replication of hepatitis B virus in vitro by 2′,3′-dideoxy-3′-thiacytidine and related analog. Proc. Natl. Acad. Sci. USA 1991, 88, 8495-8499. Chem. Abstr. 1991, 115, 269987z.
-
(1991)
Chem. Abstr.
, vol.115
-
-
-
13
-
-
0026563976
-
Biochemical pharmacology of the (+)- and (-)-2′,3′ -dideoxy-3′-thiacytidine as antihepatitis B virus agents
-
Chang, C.N.; Skalski, V.; Zhou, J.H.; Cheng, Y.C. Biochemical pharmacology of the (+)- and (-)-2′,3′-dideoxy-3′ -thiacytidine as antihepatitis B virus agents. J. Biol. Chem. 1992, 267, 22,414-22,420. Chem. Abstr. 1992, 117, 225781q.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 22414-22420
-
-
Chang, C.N.1
Skalski, V.2
Zhou, J.H.3
Cheng, Y.C.4
-
14
-
-
0026563976
-
-
Chang, C.N.; Skalski, V.; Zhou, J.H.; Cheng, Y.C. Biochemical pharmacology of the (+)- and (-)-2′,3′-dideoxy-3′ -thiacytidine as antihepatitis B virus agents. J. Biol. Chem. 1992, 267, 22,414-22,420. Chem. Abstr. 1992, 117, 225781q.
-
(1992)
Chem. Abstr.
, vol.117
-
-
-
15
-
-
0028982940
-
Anticancer activity of β-L-dioxolanecytidine, a novel nucleoside analog with the unnatural L configuration
-
Grove, K.L.; Guo, X.; Liu, S.H.; Gao, Z.; Chu, C.K.; Cheng, Y.C. Anticancer activity of β-L-dioxolanecytidine, a novel nucleoside analog with the unnatural L configuration. Cancer Res. 1995, 55, 3008-3011. Chem. Abstr. 1995, 123, 132205p.
-
(1995)
Cancer Res.
, vol.55
, pp. 3008-3011
-
-
Grove, K.L.1
Guo, X.2
Liu, S.H.3
Gao, Z.4
Chu, C.K.5
Cheng, Y.C.6
-
16
-
-
0028982940
-
-
Grove, K.L.; Guo, X.; Liu, S.H.; Gao, Z.; Chu, C.K.; Cheng, Y.C. Anticancer activity of β-L-dioxolanecytidine, a novel nucleoside analog with the unnatural L configuration. Cancer Res. 1995, 55, 3008-3011. Chem. Abstr. 1995, 123, 132205p.
-
(1995)
Chem. Abstr.
, vol.123
-
-
-
17
-
-
0030045732
-
Inhibition of hepatitis B virus by a novel L-nucleoside, 2′-fluoro-5-methyl-β-L-arabinofuranosyl uracil
-
Pai, S.B.; Liu, S.H.; Zhu, Y.L.; Chu, C.K.; Cheng, Y.C. Inhibition of hepatitis B virus by a novel L-nucleoside, 2′-fluoro-5-methyl-β -L-arabinofuranosyl uracil. Antimicrob. Agents Chemother 1996, 40, 380-386. Chem. Abstr. 1996, 124, 219475w.
-
(1996)
Antimicrob. Agents Chemother.
, vol.40
, pp. 380-386
-
-
Pai, S.B.1
Liu, S.H.2
Zhu, Y.L.3
Chu, C.K.4
Cheng, Y.C.5
-
18
-
-
0030045732
-
-
Pai, S.B.; Liu, S.H.; Zhu, Y.L.; Chu, C.K.; Cheng, Y.C. Inhibition of hepatitis B virus by a novel L-nucleoside, 2′-fluoro-5-methyl-β -L-arabinofuranosyl uracil. Antimicrob. Agents Chemother 1996, 40, 380-386. Chem. Abstr. 1996, 124, 219475w.
-
(1996)
Chem. Abstr.
, vol.124
-
-
-
19
-
-
0030781982
-
Enzymatic properties of the unnatural β-L-enantiomers of 2′,3′-dideoxyadeno-sine and 2′,3′-didehydro-2′ ,3′-dideoxyadenosine
-
Pelicano, H.; Pierra, C.; Eriksson, S.; Gosselin, G.; Imbach, J.L.; Maury, G. Enzymatic properties of the unnatural β-L-enantiomers of 2′,3′-dideoxyadeno-sine and 2′,3′-didehydro-2′ ,3′-dideoxyadenosine. J. Med. Chem. 1997, 40, 3969-3973. Chem. Abstr. 1998, 128, 18411f.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 3969-3973
-
-
Pelicano, H.1
Pierra, C.2
Eriksson, S.3
Gosselin, G.4
Imbach, J.L.5
Maury, G.6
-
20
-
-
0030781982
-
-
Pelicano, H.; Pierra, C.; Eriksson, S.; Gosselin, G.; Imbach, J.L.; Maury, G. Enzymatic properties of the unnatural β-L-enantiomers of 2′,3′-dideoxyadeno-sine and 2′,3′-didehydro-2′ ,3′-dideoxyadenosine. J. Med. Chem. 1997, 40, 3969-3973. Chem. Abstr. 1998, 128, 18411f.
-
(1998)
Chem. Abstr.
, vol.128
-
-
-
21
-
-
84955852276
-
Nucleoside derivatives of 1,2,4-triazine. Reaction of some derivatives of 1,2,4-triazine with tetra O-acetyle-α-D-glucopyranosyl bromide
-
Mansour, A.K.; Ibrahim, Y.A.; Eid, M.M. Nucleoside derivatives of 1,2,4-triazine. Reaction of some derivatives of 1,2,4-triazine with tetra O-acetyle-α-D-glucopyranosyl bromide. Z. Naturforsch 1976, 31b, 505-508.
-
(1976)
Z. Naturforsch
, vol.31 B
, pp. 505-508
-
-
Mansour, A.K.1
Ibrahim, Y.A.2
Eid, M.M.3
-
22
-
-
0012737104
-
A.L.N-Glucosyl derivatives of some 1,2,4-triazines, with tetra-O-acetyl-α-D-glucopyranosyl bromide
-
Mansour, A.K.; Ibrahim, Y.A.; Eid, M.M.; Abdel-Hady, S. A.L.N-Glucosyl derivatives of some 1,2,4-triazines, with tetra-O-acetyl-α -D-glucopyranosyl bromide. J. Carbohydrates. Nucleosides. Nucleotides 1981, 8 (2), 81-99.
-
(1981)
J. Carbohydrates. Nucleosides. Nucleotides
, vol.8
, Issue.2
, pp. 81-99
-
-
Mansour, A.K.1
Ibrahim, Y.A.2
Eid, M.M.3
Abdel-Hady, S.4
-
23
-
-
0012652067
-
Facile approach for the selective glycosidation of cyclic asymmetric amides and thioamides
-
Ibrahim, Y.A. Facile approach for the selective glycosidation of cyclic asymmetric amides and thioamides. Carbohydrate Leters 1996, 1, 425-432.
-
(1996)
Carbohydrate Leters
, vol.1
, pp. 425-432
-
-
Ibrahim, Y.A.1
-
24
-
-
0030512101
-
Synthesis and structure of 2-deoxyribosyl-6-azauracil derivatives
-
Ibrahim, Y.A. Synthesis and structure of 2-deoxyribosyl-6-azauracil derivatives. Carbohydrate Letters 1996, 2, 189-195.
-
(1996)
Carbohydrate Letters
, vol.2
, pp. 189-195
-
-
Ibrahim, Y.A.1
-
25
-
-
0032740988
-
Selective synthesis and structure of 6-arylvinyl-2-and 4,glucosyl-1,2,4-triazines of expected interesting biological activity
-
Mansour, A.J.; Ibrahim, Y.A.; Khalil, N.S.A.M. Selective synthesis and structure of 6-arylvinyl-2-and 4,glucosyl-1,2,4-triazines of expected interesting biological activity. Nucleosides & Nucleotides 1999, 18 (10), 2265-2283.
-
(1999)
Nucleosides & Nucleotides
, vol.18
, Issue.10
, pp. 2265-2283
-
-
Mansour, A.J.1
Ibrahim, Y.A.2
Khalil, N.S.A.M.3
-
26
-
-
0025232567
-
Reaction of some 1,2,4-triazines with acetobromoglucose
-
Eid, M.M.; Abdelhady, S.A.; Ali, H.A.W. Reaction of some 1,2,4-triazines with acetobromoglucose. Arch. Pharm. 1990, 323 (4), 243-245.
-
(1990)
Arch. Pharm.
, vol.323
, Issue.4
, pp. 243-245
-
-
Eid, M.M.1
Abdelhady, S.A.2
Ali, H.A.W.3
-
27
-
-
84864577120
-
Synthesen sticktoffhaltiger heterocyclen, XXVII. Über 1.2.4-triazine, I. Darstellung einiger neuer s-triazolo [3.2-c]-as-triazine
-
Dornow, A.; Menzel, H.; Marx, P. Synthesen sticktoffhaltiger heterocyclen, XXVII. Über 1.2.4-triazine, I. Darstellung einiger neuer s-triazolo [3.2-c]-as-triazine. Chem. Ber. 1964, 97, 2173-2178.
-
(1964)
Chem. Ber.
, vol.97
, pp. 2173-2178
-
-
Dornow, A.1
Menzel, H.2
Marx, P.3
-
28
-
-
0141696265
-
Synthesis of 6-(p-Halobenzyl)-1,2,4-triazine-3,5(2H, 4H)-dithiones having potential antimicrobial activity
-
Ahmad, R.; Ajaz, S. Synthesis of 6-(p-Halobenzyl)-1,2,4-triazine-3,5(2H, 4H)-dithiones having potential antimicrobial activity. J. Chem. Soc. Pak. 1985, 7 (4), 315-320.
-
(1985)
J. Chem. Soc. Pak.
, vol.7
, Issue.4
, pp. 315-320
-
-
Ahmad, R.1
Ajaz, S.2
-
29
-
-
0141807664
-
Synthesis and structure of as-triazinoquinolines, II
-
Badawy, M.A.; Abdel-Hady, S.A.L.; Eid, M.M.; Ibrahim, Y.A. Synthesis and structure of as-triazinoquinolines, II. Chem. Ber. 1984, 117, 1083-188.
-
(1984)
Chem. Ber.
, vol.117
, pp. 1083-1188
-
-
Badawy, M.A.1
Abdel-Hady, S.A.L.2
Eid, M.M.3
Ibrahim, Y.A.4
-
30
-
-
0023831659
-
Synthesis, reactions and biological evaluation of some 1,2,3-triazine derivatives
-
Mansour, A.K.; Eid, M.M.; Hassan, R.A.; Haemers, A.; Pattyn, S.R.; Vanden Berghe, D.A.; Van. Hoof, L. Synthesis, reactions and biological evaluation of some 1,2,3-triazine derivatives. J. Heterocycl. Chem. 1988, 25, 279-283.
-
(1988)
J. Heterocycl. Chem.
, vol.25
, pp. 279-283
-
-
Mansour, A.K.1
Eid, M.M.2
Hassan, R.A.3
Haemers, A.4
Pattyn, S.R.5
Vanden Berghe, D.A.6
Van Hoof, L.7
-
31
-
-
12444316822
-
-
Longman group Limited
-
Furniss, B.S.; Hannaford, A.J.; Rogers, V.; Smith, P.W.G.; Tatchell, A.R. Vogel's Textbook of Practical Organic Chemistry; Longman group Limited, 1978; Vol. 4, 458pp.
-
(1978)
Vogel's Textbook of Practical Organic Chemistry
, vol.4
-
-
Furniss, B.S.1
Hannaford, A.J.2
Rogers, V.3
Smith, P.W.G.4
Tatchell, A.R.5
|