-
1
-
-
0022996630
-
Phosphorylation of 3′-azido-3′-deoxythymidine and selective interaction of the 5′-triphosphate with human immunodeficiency virus reverse transciptase
-
Furman, P.A.; Fyfe, J.A.; St. Clair, M.H.; Weinhold, K.; Rideout, J.L.; Freeman, G.A.; Lehrman, S. N.; Bolognesi, D.P.; Broder, S.; Mitsuya, H.; Barry, D.W. Phosphorylation of 3′-azido-3′-deoxythymidine and selective interaction of the 5′-triphosphate with human immunodeficiency virus reverse transciptase. Proc. Natl. Acad. Sci. USA 1986, 83, 8333-8337.
-
(1986)
Proc. Natl. Acad. Sci. USA
, vol.83
, pp. 8333-8337
-
-
Furman, P.A.1
Fyfe, J.A.2
St. Clair, M.H.3
Weinhold, K.4
Rideout, J.L.5
Freeman, G.A.6
Lehrman, S.N.7
Bolognesi, D.P.8
Broder, S.9
Mitsuya, H.10
Barry, D.W.11
-
2
-
-
0023837875
-
-
Yarchoan, R.; Perno, C.F.; Thomas, R.V.; Klecker, R.W.; Allain, J.P.; Wills, R.J.; McAtee, N.; Leuther, M.; Collins, J.M.; Broder, S.; Fischl, M.A.; Dubinsky, R.; McNeeLy, M.C.; Mitsuya, H.; Lawley, T.J.; Safai, B.; Myers, C.E. Phase 1 studies of 2′,3′-dideoxycytidine in severe human immunodeficiency virus infection as a single agent and alternating with zidovudine (AZT). Lancet 1988, 1, 76-81.
-
Yarchoan, R.; Perno, C.F.; Thomas, R.V.; Klecker, R.W.; Allain, J.P.; Wills, R.J.; McAtee, N.; Leuther, M.; Collins, J.M.; Broder, S.; Fischl, M.A.; Dubinsky, R.; McNeeLy, M.C.; Mitsuya, H.; Lawley, T.J.; Safai, B.; Myers, C.E. Phase 1 studies of 2′,3′-dideoxycytidine in severe human immunodeficiency virus infection as a single agent and alternating with zidovudine (AZT). Lancet 1988, 1, 76-81.
-
-
-
-
3
-
-
0024349612
-
In vivo activity against HIV and favorable toxicity profile of 2′,3′- dideoxyinosine
-
Yarchoan, R.; Mitsuya, H.; Thomas, R.V.; Pluda, J.M.; Hartman, N.R.; Perno, C.F.; Marczyk, K.S.; Allain, J.P.; Johns, D.G.; Broder, S. In vivo activity against HIV and favorable toxicity profile of 2′,3′- dideoxyinosine. Science 1989, 245, 412-415.
-
(1989)
Science
, vol.245
, pp. 412-415
-
-
Yarchoan, R.1
Mitsuya, H.2
Thomas, R.V.3
Pluda, J.M.4
Hartman, N.R.5
Perno, C.F.6
Marczyk, K.S.7
Allain, J.P.8
Johns, D.G.9
Broder, S.10
-
4
-
-
0023196616
-
Potent and selective in vitro activity of 3′-deoxythymidin-2′-ene (3′-deoxy-2′, 3′-didehydrothymidine) against human immunodeficiency virus
-
Lin, T.S.; Schinazi, R.F.; Prusoff, W.H. Potent and selective in vitro activity of 3′-deoxythymidin-2′-ene (3′-deoxy-2′, 3′-didehydrothymidine) against human immunodeficiency virus. Biochem. Pharmacol. 1987, 36, 2713-2718.
-
(1987)
Biochem. Pharmacol
, vol.36
, pp. 2713-2718
-
-
Lin, T.S.1
Schinazi, R.F.2
Prusoff, W.H.3
-
5
-
-
7344264636
-
Activities of the four optical isomers of 2′,3′-dideoxy-3′-thiacytidine (BCH-189) against human immunodeficiency virus type 1 in human lymphocytes
-
Schinazi, R.F.; Chu, C.K.; Peck, A.; McMillan, A.; Mathis, R.; Cannon, D.; Jeong, L.S.; Beach, J.W.; Choi, W.B.; Yeola, S.; Liotta, D.C. Activities of the four optical isomers of 2′,3′-dideoxy-3′-thiacytidine (BCH-189) against human immunodeficiency virus type 1 in human lymphocytes. Antimicrob. Agents Chemother. 1992, 36, 672-676.
-
(1992)
Antimicrob. Agents Chemother
, vol.36
, pp. 672-676
-
-
Schinazi, R.F.1
Chu, C.K.2
Peck, A.3
McMillan, A.4
Mathis, R.5
Cannon, D.6
Jeong, L.S.7
Beach, J.W.8
Choi, W.B.9
Yeola, S.10
Liotta, D.C.11
-
6
-
-
0030982931
-
1592U89, a novel carbocyclic nucleoside analog with potent, selective anti-human immunodeficiency virus activity
-
Daluge, S.M.; Good, S.S.; Faletto, M.B.; Miller, W.H.; StClair, M.H.; Boone, L.R.; Tisdale, M.; Parry, N.R.; Reardon, J.E.; Dornsife, R.E.; Averett, D.R.; Krenitsky, T.A. 1592U89, a novel carbocyclic nucleoside analog with potent, selective anti-human immunodeficiency virus activity. Antimicrob. Agents Chemother. 1997, 41, 1082-1093.
-
(1997)
Antimicrob. Agents Chemother
, vol.41
, pp. 1082-1093
-
-
Daluge, S.M.1
Good, S.S.2
Faletto, M.B.3
Miller, W.H.4
StClair, M.H.5
Boone, L.R.6
Tisdale, M.7
Parry, N.R.8
Reardon, J.E.9
Dornsife, R.E.10
Averett, D.R.11
Krenitsky, T.A.12
-
7
-
-
0030782524
-
Synthesis, in vitro biological evaluation, and oral bioavailability of 9-[2-(phosphonomethoxy)propyl]adenine (PMPA) prodrugs
-
Arimilli, M.N.; Kim, C.U.; Dougherty, J.; Mulato, A.; Oliyai, R.; Shaw, J.P.; Cundy, K.C.; Bischofberger, N. Synthesis, in vitro biological evaluation, and oral bioavailability of 9-[2-(phosphonomethoxy)propyl]adenine (PMPA) prodrugs. Antiviral. Chem. Chemother. 1997, 8, 557-564.
-
(1997)
Antiviral. Chem. Chemother
, vol.8
, pp. 557-564
-
-
Arimilli, M.N.1
Kim, C.U.2
Dougherty, J.3
Mulato, A.4
Oliyai, R.5
Shaw, J.P.6
Cundy, K.C.7
Bischofberger, N.8
-
8
-
-
0028212546
-
Synthesis and biological evaluation of 2′,3′-dideoxy-L- pyrimidine nucleosides as potential antiviral agents against human immunodeficiency virus (HIV) and hepatitis B virus (HBV)
-
Lin, T.S.; Luo, M.Z.; Liu, M.C.; Pai, S.B.; Dutschman, G.E.; Cheng, Y.C. Synthesis and biological evaluation of 2′,3′-dideoxy-L- pyrimidine nucleosides as potential antiviral agents against human immunodeficiency virus (HIV) and hepatitis B virus (HBV). J. Med. Chem. 1994, 37, 798-803.
-
(1994)
J. Med. Chem
, vol.37
, pp. 798-803
-
-
Lin, T.S.1
Luo, M.Z.2
Liu, M.C.3
Pai, S.B.4
Dutschman, G.E.5
Cheng, Y.C.6
-
9
-
-
0028943355
-
Use of 2′-fluoro-5-methyl- β-L-araninofuranosyl uracil as a novel antiviral agent for hepatitis B virus and Epstein-Barr virus
-
Chu, C,K.; Ma, T.W.; Shanmuganthan, K.; Wang, C.G.; Xiang, Y.J.; Pai, S.B.; Yao, G.Q.; Sommadossi, J.P.; Cheng, Y.C. Use of 2′-fluoro-5-methyl- β-L-araninofuranosyl uracil as a novel antiviral agent for hepatitis B virus and Epstein-Barr virus. Antimicrob. Agents Chemother. 1995, 39, 979-981.
-
(1995)
Antimicrob. Agents Chemother
, vol.39
, pp. 979-981
-
-
Chu, C.K.1
Ma, T.W.2
Shanmuganthan, K.3
Wang, C.G.4
Xiang, Y.J.5
Pai, S.B.6
Yao, G.Q.7
Sommadossi, J.P.8
Cheng, Y.C.9
-
10
-
-
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, 13938-13942.
-
(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
-
11
-
-
34247870473
-
-
Belleau, B.; Dixit, D.; Ngueyn-Ba, N.; Karus, J.L. Purinyl- and pyrimidinyl-1,3-dioxolanes as antiretrovirals. Eur. Pat. 337, 713, Oct 18, 1989; Chem. Abstr. 1990, 112, 198359 w.
-
Belleau, B.; Dixit, D.; Ngueyn-Ba, N.; Karus, J.L. Purinyl- and pyrimidinyl-1,3-dioxolanes as antiretrovirals. Eur. Pat. 337, 713, Oct 18, 1989; Chem. Abstr. 1990, 112, 198359 w.
-
-
-
-
12
-
-
0026469165
-
The antihepatitis 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 antihepatitis 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.
-
(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
-
13
-
-
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.
-
(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
-
14
-
-
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.
-
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.
-
-
-
-
15
-
-
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.
-
(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
-
16
-
-
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, 22414-22420.
-
(1992)
J. Biol. Chem
, vol.267
, pp. 22414-22420
-
-
Chang, C.N.1
Skalski, V.2
Zhou, J.H.3
Cheng, Y.C.4
-
17
-
-
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.
-
(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
-
18
-
-
0030045732
-
Inhibition of hepatitis B virus by a novel L-nucleoside, 2′-fluoro-5-methyl- β-L-arabinofuranosyluracil
-
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-arabinofuranosyluracil. Antimicrob. Agents Chemother. 1996, 40, 380-386.
-
(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
-
19
-
-
0030781982
-
Enzymatic properties of the unnatural β-L-enantiomers of 2′,3′-dideoxyadenosine 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′-dideoxyadenosine and 2′,3′-didehydro-2′, 3′-dideoxyadenosine. J. Med. Chem, 1997, 40, 3969-3973.
-
(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
-
-
0001536594
-
Stereoselective synthesis of α-ribonucleosides from 1-hydroxy sugars by using 2-fluoropyridinium tosylate
-
Mukaiyama, T.; Hashimoto, Y.; Hayashi, Y.; Shoda, S. Stereoselective synthesis of α-ribonucleosides from 1-hydroxy sugars by using 2-fluoropyridinium tosylate. Chem. Lett. 1984, 4, 557-560.
-
(1984)
Chem. Lett
, vol.4
, pp. 557-560
-
-
Mukaiyama, T.1
Hashimoto, Y.2
Hayashi, Y.3
Shoda, S.4
-
21
-
-
0016349990
-
Synthesis of 2,3-O- isopropylidene-5-O-trityl-β-D-ribofuranosyl chloride
-
Klein, R.S.; Ohrui, H.; Fox, J.J. Synthesis of 2,3-O- isopropylidene-5-O-trityl-β-D-ribofuranosyl chloride. J. Carbohydr. Nucleosides Nucleotides 1974, 1, 265-269.
-
(1974)
J. Carbohydr. Nucleosides Nucleotides
, vol.1
, pp. 265-269
-
-
Klein, R.S.1
Ohrui, H.2
Fox, J.J.3
-
22
-
-
0014288658
-
Syntheses with partially benzylated sugars. XII. 3,5-Di-O-benzyl-beta-D-ribofuranose and its use as an intermediate in the synthesis of partially substituted ribonucleosides
-
Haga, M.; Ness, R.K.; Fletcher, H.G. Syntheses with partially benzylated sugars. XII. 3,5-Di-O-benzyl-beta-D-ribofuranose and its use as an intermediate in the synthesis of partially substituted ribonucleosides. J. Org. Chem. 1968, 33, 1810-1815.
-
(1968)
J. Org. Chem
, vol.33
, pp. 1810-1815
-
-
Haga, M.1
Ness, R.K.2
Fletcher, H.G.3
-
23
-
-
0014288231
-
Syntheses with partially benzylated sugars. XI. Studies on the synthesis of anomeric 5,6-dimethyl-1- D-ribofuranosylbenzimidazoles (ribazoles). Comparison of the condensation of 2,3,5-tri-O-benzoyl-D-ribofuranosyl bromide and 2,3,5-tri-O-benzoyl-D-ribofuranosyl chloride with 5,6-dimethylbenzimidazole
-
Stevens, J.D.; Ness, R.K.; Fletcher, H.G. Syntheses with partially benzylated sugars. XI. Studies on the synthesis of anomeric 5,6-dimethyl-1- D-ribofuranosylbenzimidazoles (ribazoles). Comparison of the condensation of 2,3,5-tri-O-benzoyl-D-ribofuranosyl bromide and 2,3,5-tri-O-benzoyl-D-ribofuranosyl chloride with 5,6-dimethylbenzimidazole. J. Org. Chem. 1968, 33, 1806-1810.
-
(1968)
J. Org. Chem
, vol.33
, pp. 1806-1810
-
-
Stevens, J.D.1
Ness, R.K.2
Fletcher, H.G.3
-
24
-
-
31544480090
-
Synthesis of novel α-L-arabinopyranosides of β-lactams with potential antimicrobial activity
-
Khalil, N.S.A.M. Synthesis of novel α-L-arabinopyranosides of β-lactams with potential antimicrobial activity. Nucleosides Nucleotides Nucleic Acids 2005, 24, 1277-1287.
-
(2005)
Nucleosides Nucleotides Nucleic Acids
, vol.24
, pp. 1277-1287
-
-
Khalil, N.S.A.M.1
-
25
-
-
0141788618
-
Synthesis of some new 2-α-L-arabinopyranosyl-1,2,4-triazines as potential antitumor chemotherapeutics
-
Mansour, A.K.; Eid, M.M.; Khalil, N.S.A.M. Synthesis of some new 2-α-L-arabinopyranosyl-1,2,4-triazines as potential antitumor chemotherapeutics. Nucleosides Nucleotides Nucleic Acids 2003, 22, 1805-1823.
-
(2003)
Nucleosides Nucleotides Nucleic Acids
, vol.22
, pp. 1805-1823
-
-
Mansour, A.K.1
Eid, M.M.2
Khalil, N.S.A.M.3
-
26
-
-
33947481778
-
Antiviral chemotherapy. I. The activity of pyridine and quinoline derivatives against neurovaccina in mice
-
Jones, D.H.; Slack, R.; Squires, S.; Wooldridge, K.R.H. Antiviral chemotherapy. I. The activity of pyridine and quinoline derivatives against neurovaccina in mice. J. Med. Chem. 1965, 8, 676-680.
-
(1965)
J. Med. Chem
, vol.8
, pp. 676-680
-
-
Jones, D.H.1
Slack, R.2
Squires, S.3
Wooldridge, K.R.H.4
-
27
-
-
0021689408
-
Synthesis and antibacterial activity of 1-(2,4-dichlorobenzoyl)-4-substituted thiosemicarbazides, 1,2,4-triazoles and their methyl derivatives
-
Goswami, B.N.; Kataky, J.C.S.; Baruah, J.N. Synthesis and antibacterial activity of 1-(2,4-dichlorobenzoyl)-4-substituted thiosemicarbazides, 1,2,4-triazoles and their methyl derivatives. J. Heterocycl. Chem. 1984, 21, 1225-1229.
-
(1984)
J. Heterocycl. Chem
, vol.21
, pp. 1225-1229
-
-
Goswami, B.N.1
Kataky, J.C.S.2
Baruah, J.N.3
-
28
-
-
0000365179
-
Synthesis of 4-(5-nitro-2-furfurylidene)amino-3-mercapto-5-(substituted)-1,2,4-triazoles as possible antibacterial agents
-
Holla, B.S.; Kalluraya, B.; Sridhar, K.R. Synthesis of 4-(5-nitro-2-furfurylidene)amino-3-mercapto-5-(substituted)-1,2,4-triazoles as possible antibacterial agents. Curr. Sci. 1987, 56, 236-238.
-
(1987)
Curr. Sci
, vol.56
, pp. 236-238
-
-
Holla, B.S.1
Kalluraya, B.2
Sridhar, K.R.3
-
29
-
-
0030504902
-
Synthesis, characterisation and antifungal activity of some N-bridged heterocycles derived from 3-(3-bromo-4-methoxyphenyl)-4-amino-5-mercapto-1,2,4-triazole
-
Holla, B.S.; Poojary, K.N.; Kalluraya, B.; Gowda, P.V. Synthesis, characterisation and antifungal activity of some N-bridged heterocycles derived from 3-(3-bromo-4-methoxyphenyl)-4-amino-5-mercapto-1,2,4-triazole. Farmaco 1996, 51, 793-799.
-
(1996)
Farmaco
, vol.51
, pp. 793-799
-
-
Holla, B.S.1
Poojary, K.N.2
Kalluraya, B.3
Gowda, P.V.4
-
30
-
-
0346522832
-
Synthesis and biological activity of certain 5-mercapto-3-(3-pyridyl)-4H-1,2,4-triazole derivatives
-
Abdou, N.A.; Amin, F.M. Synthesis and biological activity of certain 5-mercapto-3-(3-pyridyl)-4H-1,2,4-triazole derivatives. Mansoura J. Pharm. Sci. 1990, 6, 25-29.
-
(1990)
Mansoura J. Pharm. Sci
, vol.6
, pp. 25-29
-
-
Abdou, N.A.1
Amin, F.M.2
-
31
-
-
0026323886
-
-
Mishra, R.K.; Tewari, R.K.; Srivastava, S.K.; Bahel, S.C. Synthesis and antifungal activity of some 1,4-disubstitued-thiosemicarbazides, 2,5-disubstituted-1,3,4-thiadiazoles and 3,4-disubstituted-5-mercapto-1,2,4- triazoles. J. Indian Chem. Soc. 1991, 68, 110-112.
-
Mishra, R.K.; Tewari, R.K.; Srivastava, S.K.; Bahel, S.C. Synthesis and antifungal activity of some 1,4-disubstitued-thiosemicarbazides, 2,5-disubstituted-1,3,4-thiadiazoles and 3,4-disubstituted-5-mercapto-1,2,4- triazoles. J. Indian Chem. Soc. 1991, 68, 110-112.
-
-
-
-
32
-
-
0026730087
-
Novel 1,2,4-oxadiazoles and 1,2,4-thiadiazoles as dual 5-lipoxygenase and cyclooxygenase inhibitors
-
Unangst, P.C.; Shurum, G.P.; Connor, D.T.; Dyer, R.D.; Schrier, D.J. Novel 1,2,4-oxadiazoles and 1,2,4-thiadiazoles as dual 5-lipoxygenase and cyclooxygenase inhibitors. J. Med. Chem. 1992, 35, 3691-3698.
-
(1992)
J. Med. Chem
, vol.35
, pp. 3691-3698
-
-
Unangst, P.C.1
Shurum, G.P.2
Connor, D.T.3
Dyer, R.D.4
Schrier, D.J.5
-
33
-
-
0027221539
-
-
Mullican, M.D.; Wilson, M.W.; Connor, D.T.; Kostlan, C.R.; Schrier, D.J.; Dyer, R.D. Design of 5-(3,5-di-tert-butyl-4-hydroxyphenyl)-1,3,4- thiadiazoles, -1,3,4-oxadiazoles, and -1,2,4-triazoles as orally active, nonulcerogenic antiinflammatory agents. J. Med. Chem. 1993, 36, 1090-1099.
-
Mullican, M.D.; Wilson, M.W.; Connor, D.T.; Kostlan, C.R.; Schrier, D.J.; Dyer, R.D. Design of 5-(3,5-di-tert-butyl-4-hydroxyphenyl)-1,3,4- thiadiazoles, -1,3,4-oxadiazoles, and -1,2,4-triazoles as orally active, nonulcerogenic antiinflammatory agents. J. Med. Chem. 1993, 36, 1090-1099.
-
-
-
-
34
-
-
0017832138
-
Medicinal applications of indole derivatives
-
Sugden, J.K.; Yoloye, T.O. Medicinal applications of indole derivatives. Pharm. Acta Helv. 1978, 53, 65-92.
-
(1978)
Pharm. Acta Helv
, vol.53
, pp. 65-92
-
-
Sugden, J.K.1
Yoloye, T.O.2
-
35
-
-
0016294444
-
-
Shams El-Dine, Sh. A.; Hazzaa, A.A.B. Synthesis of compounds with potential fungicidal activity. Pharmazie 1974, 29, 761-763.
-
Shams El-Dine, Sh. A.; Hazzaa, A.A.B. Synthesis of compounds with potential fungicidal activity. Pharmazie 1974, 29, 761-763.
-
-
-
-
36
-
-
34247858199
-
-
Misato, T.; Ko, K.; Honma, Y.; Konno, K.; Taniyama, E. 1,3,4-thiadiazole derivatives as fungicides. Jpn. Kokai Tokkyo Koho 77 25,028, 1977. Chem. Abstr. 1977, 87, 147054 a.
-
Misato, T.; Ko, K.; Honma, Y.; Konno, K.; Taniyama, E. 1,3,4-thiadiazole derivatives as fungicides. Jpn. Kokai Tokkyo Koho 77 25,028, 1977. Chem. Abstr. 1977, 87, 147054 a.
-
-
-
-
37
-
-
0347748059
-
Synthesis and biological activities of some Mannich bases of 5-(2-furyl)-1,2,4-triazole-3- thiones
-
Cansiz, A.; Servi, S.; Koparir, M.; Altintas, M.; Digrak, M. Synthesis and biological activities of some Mannich bases of 5-(2-furyl)-1,2,4-triazole-3- thiones. J. Chem. Soc. Pak. 2001, 23, 237-240.
-
(2001)
J. Chem. Soc. Pak
, vol.23
, pp. 237-240
-
-
Cansiz, A.1
Servi, S.2
Koparir, M.3
Altintas, M.4
Digrak, M.5
-
38
-
-
0023007148
-
Substituted 1,3,4-thiadiazoles with anticonvulsant activity. 2. Aminoalkyl derivatives
-
Stillings, M.R.;Welbourn, A.P.;Walter, D.S. Substituted 1,3,4-thiadiazoles with anticonvulsant activity. 2. Aminoalkyl derivatives. J. Med. Chem. 1986, 29, 2280-2284.
-
(1986)
J. Med. Chem
, vol.29
, pp. 2280-2284
-
-
Stillings, M.R.1
Welbourn, A.P.2
Walter, D.S.3
-
39
-
-
0023892787
-
2,4-Dihydro-3H-1,2,4-triazole-3-thiones as potential antidepressant agents
-
Kane, J.M.; Dudley, M.W.; Sorensen, S.M.; Miller, F.P. 2,4-Dihydro-3H-1,2,4-triazole-3-thiones as potential antidepressant agents. J. Med. Chem. 1988, 31, 1253-1258.
-
(1988)
J. Med. Chem
, vol.31
, pp. 1253-1258
-
-
Kane, J.M.1
Dudley, M.W.2
Sorensen, S.M.3
Miller, F.P.4
-
40
-
-
0015044957
-
Synthesis of some s-triazoles with potential analgesic and antiinflammatory activities
-
George, T.; Mehta, D.V.; Tahilramani R.; David, J.; Talwalker, P.K. Synthesis of some s-triazoles with potential analgesic and antiinflammatory activities. J. Med. Chem. 1971, 14, 335-338.
-
(1971)
J. Med. Chem
, vol.14
, pp. 335-338
-
-
George, T.1
Mehta, D.V.2
Tahilramani, R.3
David, J.4
Talwalker, P.K.5
-
41
-
-
24444446864
-
Synthesis of fungicidal 1,2,4-triazoles and related compounds
-
Srivastava, U.; Khan, R.H.; Bahel, S.C. Synthesis of fungicidal 1,2,4-triazoles and related compounds. Bokin Bobai. 1979, 7, T414-T417.
-
(1979)
Bokin Bobai
, vol.7
-
-
Srivastava, U.1
Khan, R.H.2
Bahel, S.C.3
-
42
-
-
0018723389
-
Cyanoalkylation of 4-amino-1,2,4-triazol-3- thione
-
Rudnicka, W.; Osmailowska, Z. Cyanoalkylation of 4-amino-1,2,4-triazol-3- thione. Acta Pol. Pharm. 1979, 36, 411-419.
-
(1979)
Acta Pol. Pharm
, vol.36
, pp. 411-419
-
-
Rudnicka, W.1
Osmailowska, Z.2
-
43
-
-
0005121851
-
-
Shu-Qing, K.; Sun-Yung, T.; Hung-Shan, T.; Ki, C. Wei Sheng Wu Hsueh Pao 1980, 20, 208-212.
-
(1980)
Wei Sheng Wu Hsueh Pao
, vol.20
, pp. 208-212
-
-
Shu-Qing, K.1
Sun-Yung, T.2
Hung-Shan, T.3
Ki, C.4
-
44
-
-
0018754766
-
Synthesis of some new bis(1,2,4-triazol-3-yl) disulfides, sulfides and sulfones as potential pestcides
-
Singh, H.; Yadav, L.D.S.; Bhattacharya, B.K. Synthesis of some new bis(1,2,4-triazol-3-yl) disulfides, sulfides and sulfones as potential pestcides. J. Indian Chem. Soc. 1979, 56, 1013-1016.
-
(1979)
J. Indian Chem. Soc
, vol.56
, pp. 1013-1016
-
-
Singh, H.1
Yadav, L.D.S.2
Bhattacharya, B.K.3
-
45
-
-
0017826148
-
Novel anxiolytic agents derived from alpha.-amino-.alpha.-phenyl-o- tolyl-4H-triazoles and -imidazoles
-
Gall, M.; Lahti, R.A.; Rudzik, A.D.; Duchamp, D.J.; Chidester, C.; Scahill, T. Novel anxiolytic agents derived from alpha.-amino-.alpha.-phenyl-o- tolyl-4H-triazoles and -imidazoles. J. Med. Chem. 1978, 21, 542-548.
-
(1978)
J. Med. Chem
, vol.21
, pp. 542-548
-
-
Gall, M.1
Lahti, R.A.2
Rudzik, A.D.3
Duchamp, D.J.4
Chidester, C.5
Scahill, T.6
-
46
-
-
0015424606
-
Design, synthesis, and broad spectrum antiviral activity of 1-β-D- ribofuranosyl-1,2,4-triazole-3-carboxamide and related nucleosides
-
Witkowski, J.T.; Robins, R.K.; Sidwell, R.W.; Simon, L.N. Design, synthesis, and broad spectrum antiviral activity of 1-β-D- ribofuranosyl-1,2,4-triazole-3-carboxamide and related nucleosides. J. Med. Chem. 1972, 15, 1150-1154.
-
(1972)
J. Med. Chem
, vol.15
, pp. 1150-1154
-
-
Witkowski, J.T.1
Robins, R.K.2
Sidwell, R.W.3
Simon, L.N.4
-
47
-
-
10644273795
-
-
Smith, R.A, Kirkpatrick, W, eds, Academic Press, London
-
Smith, R.A.; Kirkpatrick, W., eds. The pharmacology of ribavirin, Academic Press, London, 1980, pp. 133-156,
-
(1980)
The pharmacology of ribavirin
, pp. 133-156
-
-
-
48
-
-
0002703721
-
-
Sidwell, R.W, ed, Academic Press, Orlando, FL
-
Sidwell, R.W., ed. In vitro and in vivo Inhibition of DNA Viruses by Ribavirin, Academic Press, Orlando, FL, 1984, pp. 19-32.
-
(1984)
In vitro and in vivo Inhibition of DNA Viruses by Ribavirin
, pp. 19-32
-
-
-
49
-
-
0003802153
-
-
Smith, R.A, Knight, V, Smith, J.A.D, eds, Academic Press, Orlando, FL
-
Smith, R.A.; Knight, V.; Smith, J.A.D., eds. Clinical Applications of Ribavirin, Academic Press, Orlando, FL, 1984, pp. 222.
-
(1984)
Clinical Applications of Ribavirin
, pp. 222
-
-
-
50
-
-
33746210056
-
Efficient synthesis, structure, and antimicrobial activity of some novel N- and S-β-D-glucosides of 5-pyridin-3-yl-1,2,4-triazoles
-
Khalil, N.S.A.M. Efficient synthesis, structure, and antimicrobial activity of some novel N- and S-β-D-glucosides of 5-pyridin-3-yl-1,2,4-triazoles. Carbohydr. Res. 2006, 341, 2187-2199.
-
(2006)
Carbohydr. Res
, vol.341
, pp. 2187-2199
-
-
Khalil, N.S.A.M.1
-
51
-
-
31544466526
-
Synthesis of some new 1,3/ or 1,4-bis(glucopyranosyl-1,2,4-triazol-5-ylthio)propanes/or butanes as potential antimicrobial agents
-
Abbas, A.A.; Khalil, N.S.A.M. Synthesis of some new 1,3/ or 1,4-bis(glucopyranosyl-1,2,4-triazol-5-ylthio)propanes/or butanes as potential antimicrobial agents. Nucleosides Nucleotides Nucleic Acids 2005, 24, 1353-1372.
-
(2005)
Nucleosides Nucleotides Nucleic Acids
, vol.24
, pp. 1353-1372
-
-
Abbas, A.A.1
Khalil, N.S.A.M.2
-
52
-
-
10644254401
-
-
Khalil, N.S.A.M.; Mansour, A.K.; Eid, M.M. Synthesis of some novel 6-benzyl(or substituted benzyl)-2-β-D-glucopyranosyl-1,2,4- triazolo[4,3-b][1,2,4]triazines as potential antimicrobial chemotherapeutics. Nucleosides Nucleotides Nucleic Acids 2004, 23, 1889-1910.
-
Khalil, N.S.A.M.; Mansour, A.K.; Eid, M.M. Synthesis of some novel 6-benzyl(or substituted benzyl)-2-β-D-glucopyranosyl-1,2,4- triazolo[4,3-b][1,2,4]triazines as potential antimicrobial chemotherapeutics. Nucleosides Nucleotides Nucleic Acids 2004, 23, 1889-1910.
-
-
-
-
53
-
-
15944369211
-
-
Khalil, N.S.A.M. Synthesis of some novel N-ribosyl-1,2,4-triazin- 6(1H)-/ones or thiones as potential antibacterial and antifungal chemotherapeutics. Nucleosides Nucleotides Nucleic Acids 2005, 24, 111-120.
-
Khalil, N.S.A.M. Synthesis of some novel N-ribosyl-1,2,4-triazin- 6(1H)-/ones or thiones as potential antibacterial and antifungal chemotherapeutics. Nucleosides Nucleotides Nucleic Acids 2005, 24, 111-120.
-
-
-
-
54
-
-
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.; Khalil, 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, 21-44.
-
(2003)
Nucleosides Nucleotides Nucleic Acids
, vol.22
, pp. 21-44
-
-
Mansour, A.K.1
Eid, M.M.2
Khalil, N.S.A.M.3
-
55
-
-
0141788616
-
-
Mansour, A.K.; Eid, M.M.; Khalil, N.S.A.M. Synthesis of some N-galactosides of 3-aryl-5-benzyl (or substituted benzyl)-1,2,4-triazin- 6(1H)-/ones or thiones of expected biological activity. Nucleosides Nucleotides Nucleic Acids 2003, 22, 1825-1833.
-
Mansour, A.K.; Eid, M.M.; Khalil, N.S.A.M. Synthesis of some N-galactosides of 3-aryl-5-benzyl (or substituted benzyl)-1,2,4-triazin- 6(1H)-/ones or thiones of expected biological activity. Nucleosides Nucleotides Nucleic Acids 2003, 22, 1825-1833.
-
-
-
-
56
-
-
3342912990
-
Synthesis and reactions of some new heterocyclic carbohydrazides and related compounds as potential anticancer agents
-
Mansour, A.K.; Eid, M.M.; Khalil, N.S.A.M. Synthesis and reactions of some new heterocyclic carbohydrazides and related compounds as potential anticancer agents. Molecules 2003, 8, 744-755.
-
(2003)
Molecules
, vol.8
, pp. 744-755
-
-
Mansour, A.K.1
Eid, M.M.2
Khalil, N.S.A.M.3
-
57
-
-
0032740988
-
Selective synthesis and structure of 6-arylvinyl-2- and 4- glucosyl-1,2,4-triazines of expected interesting biological activity
-
Mansour, A.K.; 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, 2265-2283.
-
(1999)
Nucleosides Nucleotides
, vol.18
, pp. 2265-2283
-
-
Mansour, A.K.1
Ibrahim, Y.A.2
Khalil, N.S.A.M.3
-
58
-
-
0016351762
-
-
Niedballa, U.; Vorbr̈uggen. H. A general synthesis of N-glycosides. I. Synthesis of pyrimidine nucleosides. J. Org. Chem. 1974, 39, 3654-3660; and references cited therein.
-
Niedballa, U.; Vorbr̈uggen. H. A general synthesis of N-glycosides. I. Synthesis of pyrimidine nucleosides. J. Org. Chem. 1974, 39, 3654-3660; and references cited therein.
-
-
-
-
59
-
-
0015820488
-
Synthesis of nucleosides. VIII. NMR and CD spectra of pyrimidine nucleosides and their 2-thio analogs
-
Cleve, G.; Hoyer, G.A.; Schulz, G.; Vorbr̈uggen, H. Synthesis of nucleosides. VIII. NMR and CD spectra of pyrimidine nucleosides and their 2-thio analogs. Chem. Ber. 1973, 106, 3062-3072.
-
(1973)
Chem. Ber
, vol.106
, pp. 3062-3072
-
-
Cleve, G.1
Hoyer, G.A.2
Schulz, G.3
Vorbr̈uggen, H.4
-
61
-
-
84982335830
-
-
Walter, W.; Maerten, G. Structure of thioamides and their derivatives. I. Configuration studies of substituted thioformamides and formamides by N.M.R. spectroscopy. Justus Liebigs Ann. Chem. 1968, 712, 58-66.
-
Walter, W.; Maerten, G. Structure of thioamides and their derivatives. I. Configuration studies of substituted thioformamides and formamides by N.M.R. spectroscopy. Justus Liebigs Ann. Chem. 1968, 712, 58-66.
-
-
-
-
62
-
-
0003905534
-
-
Furniss, B.S, Hannaford, A.J, Smith, P.W.G, Tatchell, A.R, eds, Longman Group UK, Ltd, England, 5th ed, pp
-
Furniss, B.S.; Hannaford, A.J.; Smith, P.W.G.; Tatchell, A.R.; eds. Vogel's Textbook of Practical Organic Chemistry, Longman Group UK, Ltd., England, 1989, 5th ed., pp. 648.
-
(1989)
Vogel's Textbook of Practical Organic Chemistry
, pp. 648
-
-
|