-
1
-
-
0032437454
-
The role of nonnucleoside reverse transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection
-
(a) De Clercq, E. The role of nonnucleoside reverse transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection. Antiviral Res. 1998, 38, 153-179.
-
(1998)
Antiviral Res.
, vol.38
, pp. 153-179
-
-
De Clercq, E.1
-
2
-
-
0029951587
-
Nonnucleoside anti-HIV-1 reverse transcriptase inhibitors (NNRTIs): A chemical survey from lead compounds to selected drugs for clinical trials
-
(b) Artico, M. Nonnucleoside anti-HIV-1 reverse transcriptase inhibitors (NNRTIs): a chemical survey from lead compounds to selected drugs for clinical trials. Farmaco 1996, 51, 305-331.
-
(1996)
Farmaco
, vol.51
, pp. 305-331
-
-
Artico, M.1
-
3
-
-
0027447592
-
Diarylsulphones, a new chemical class of nonnucleoside antiviral inhibitors of immunodeficiency virus type 1 reverse transcriptase
-
McMahon, J. B.; Gulakowski, R. J.; Weialow, O. S.; Shultz, R. J.; Narayanan, V. L.; Clanton, D. J.; Pedemonte, R.; Wassmundt, F. W.; Buckheit, R. W. Jr; Decker, W. D.; White, E. L.; Bader, J. P.; Boyd, M. R. Diarylsulphones, a new chemical class of nonnucleoside antiviral inhibitors of immunodeficiency virus type 1 reverse transcriptase. Antimicr. Agents Chemother. 1993, 37, 754-760.
-
(1993)
Antimicr. Agents Chemother.
, vol.37
, pp. 754-760
-
-
McMahon, J.B.1
Gulakowski, R.J.2
Weialow, O.S.3
Shultz, R.J.4
Narayanan, V.L.5
Clanton, D.J.6
Pedemonte, R.7
Wassmundt, F.W.8
Buckheit R.W., Jr.9
Decker, W.D.10
White, E.L.11
Bader, J.P.12
Boyd, M.R.13
-
4
-
-
0027195714
-
5-Chloro-3-(phenylsulfonyl)indole-2-carboxyamide: A novel nonnucleoside inhibitor of the HIV-1 reverse transcriptase
-
Williams, T. M.; Ciccarone, T. M.; MacTough, S. C.; Rooney, C. S.; Balani, S. K.; Condra, J. H.; Emini, E. A.; Goldman, M. E.; Greenlee, W. J.; Kauffman, L. R.; O'Brien, J. A.; Sardana, V. V.; Schleif, W. A.; Theoharides, A. D.; Anderson, P. S. 5-Chloro-3-(phenylsulfonyl)indole-2-carboxyamide: a novel nonnucleoside inhibitor of the HIV-1 reverse transcriptase. J. Med. Chem. 1993, 36, 1291-1294.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 1291-1294
-
-
Williams, T.M.1
Ciccarone, T.M.2
MacTough, S.C.3
Rooney, C.S.4
Balani, S.K.5
Condra, J.H.6
Emini, E.A.7
Goldman, M.E.8
Greenlee, W.J.9
Kauffman, L.R.10
O'Brien, J.A.11
Sardana, V.V.12
Schleif, W.A.13
Theoharides, A.D.14
Anderson, P.S.15
-
5
-
-
0028922354
-
Synthesis of pyrryl aryl sulfones targeted at the HIV-1 reverse transcriptase
-
Artico; M.; Silvestri, R.; Stefancich, G.; Massa, S.; R.; Pagnozzi, E.; Musiu, E.; Scintu, E.; Pinna, E.; Tinti, P.; La Colla, P. Synthesis of pyrryl aryl sulfones targeted at the HIV-1 reverse transcriptase. Arch. Pharm. (Weinheim) 1995, 328, 223-229.
-
(1995)
Arch. Pharm. (Weinheim)
, vol.328
, pp. 223-229
-
-
Artico, M.1
Silvestri, R.2
Stefancich, G.3
Massa, S.R.4
Pagnozzi, E.5
Musiu, E.6
Scintu, E.7
Pinna, E.8
Tinti, P.9
La Colla, P.10
-
6
-
-
0030045677
-
2-Sulfonyl-4-chloroanilino moiety: A potent pharmacophore for the anti-human immunodeficiency virus type 1 activity of pyrrolyl aryl sulfones
-
Artico, M.; Silvestri, R.; Massa, S.; Loi, A. G.; Corrias, S.; Piras, G.; La Colla, P. 2-Sulfonyl-4-chloroanilino Moiety: A Potent Pharmacophore for the Anti-Human Immunodeficiency Virus Type 1 Activity of Pyrrolyl Aryl Sulfones. J. Med. Chem. 1996, 39, 522-530.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 522-530
-
-
Artico, M.1
Silvestri, R.2
Massa, S.3
Loi, A.G.4
Corrias, S.5
Piras, G.6
La Colla, P.7
-
7
-
-
0022378015
-
A convenient synthesis of 3-acylindoles via Friedel-Crafts acylation of 1-(phenylsulfonyl)indole. A new route to pyridocarbazole-5, 11-quinones and ellipticine
-
Ketcha, D. M.; Gribble, G. W. A convenient synthesis of 3-acylindoles via Friedel-Crafts acylation of 1-(phenylsulfonyl)indole. A new route to pyridocarbazole-5, 11-quinones and ellipticine. J. Org. Chem. 1985, 26, 5451-5457.
-
(1985)
J. Org. Chem.
, vol.26
, pp. 5451-5457
-
-
Ketcha, D.M.1
Gribble, G.W.2
-
9
-
-
12444281523
-
-
Indole derivatives as inhibitors of HIV reverse transcriptase. PCT Int. Appl. WO 94 19, 321
-
Williams, T. M.; Ciccarone, T. M.; Saari, W. S.; Wai, J. S.; Greenlee, W. J.; Balani, S. K.; Goldman, M. E.; Hoffman, J. M. Jr; Lumma, W. C. Jr; et al. Indole derivatives as inhibitors of HIV reverse transcriptase. PCT Int. Appl. WO 94 19, 321; Chem. Abstr. 1994, 121, 255644x.
-
(1994)
Chem. Abstr.
, vol.121
-
-
Williams, T.M.1
Ciccarone, T.M.2
Saari, W.S.3
Wai, J.S.4
Greenlee, W.J.5
Balani, S.K.6
Goldman, M.E.7
Hoffman J.M., Jr.8
Lumma W.C., Jr.9
-
10
-
-
0031899273
-
Synthesis and biological evaluation of 5H-indolo[3,2-b] [1,5]-benzothiazepine derivatives, designed as conformationally constrained analogues of human immunodeficiency virus type 1 reverse transcriptase inhibitor L-737,126
-
Silvestri, R.; Artico, M.; Bruno, B.; Massa, S.; Novellino, E.; Greco, G.; Marongiu, M. E.; Pani, A.; De Montis, A.; La Colla, P. Synthesis and biological evaluation of 5H-indolo[3,2-b] [1,5]- benzothiazepine derivatives, designed as conformationally constrained analogues of human immunodeficiency virus type 1 reverse transcriptase inhibitor L-737,126. Antiviral Chem. Chemother. 1998, 9, 139-148.
-
(1998)
Antiviral Chem. Chemother.
, vol.9
, pp. 139-148
-
-
Silvestri, R.1
Artico, M.2
Bruno, B.3
Massa, S.4
Novellino, E.5
Greco, G.6
Marongiu, M.E.7
Pani, A.8
De Montis, A.9
La Colla, P.10
-
11
-
-
0036987892
-
Discovery of second generation quinazolinone non-nucleoside reverse transcriptase inhibitors of HIV-1
-
Corbett, J. M.; Rodgers, J. D. Discovery of second generation quinazolinone non-nucleoside reverse transcriptase inhibitors of HIV-1, Progress in Med. Chem. 2002, 40, 63-105.
-
(2002)
Progress in Med. Chem.
, vol.40
, pp. 63-105
-
-
Corbett, J.M.1
Rodgers, J.D.2
-
13
-
-
33947086466
-
Syntheses with N-protected 2-lithioindoles
-
Sundberg, R. J.; Russel, H. F. Syntheses with N-protected 2-lithioindoles. J. Org. Chem. 1983, 38, 3324-3330.
-
(1983)
J. Org. Chem.
, vol.38
, pp. 3324-3330
-
-
Sundberg, R.J.1
Russel, H.F.2
-
14
-
-
33845553875
-
Generation and reaction of 3-lithio-1-(phenylsulfonyl) indole
-
Saulnier, M. G.; Gribble, G. W. Generation and reaction of 3-lithio-1-(phenylsulfonyl) indole. J. Org. Chem. 1982, 47, 757-761.
-
(1982)
J. Org. Chem.
, vol.47
, pp. 757-761
-
-
Saulnier, M.G.1
Gribble, G.W.2
-
15
-
-
0001074332
-
Synthesis of carbazole alkaloids hyellazole and 6-chlorohyellazole
-
Kano, S.; Sugino, E.; Shibuya, S.; Hibino, S. Synthesis of carbazole alkaloids hyellazole and 6-chlorohyellazole. J. Org. Chem. 1981, 46, 3856-3859.
-
(1981)
J. Org. Chem.
, vol.46
, pp. 3856-3859
-
-
Kano, S.1
Sugino, E.2
Shibuya, S.3
Hibino, S.4
-
16
-
-
0023687234
-
A rapid and automated tetrazolium-based colorimetric assay for the detection of anti HIV compounds
-
Pauwels, R.; Balzarini, J.; Baba, M.; Snoeck, R.; Schols, D.; Hederwijn, P.; Desmyster, J.; De Clercq, E. A rapid and automated tetrazolium-based colorimetric assay for the detection of anti HIV compounds. J. Virol. Methods 1988, 20, 309-321.
-
(1988)
J. Virol. Methods
, vol.20
, pp. 309-321
-
-
Pauwels, R.1
Balzarini, J.2
Baba, M.3
Snoeck, R.4
Schols, D.5
Hederwijn, P.6
Desmyster, J.7
De Clercq, E.8
-
17
-
-
0026540533
-
HIV-1 reverse transcriptase inhibition by a dipyridodiazepinone derivative BI-RG-587
-
Tramontano, E.; Cheng, Y.-C. HIV-1 reverse transcriptase inhibition by a dipyridodiazepinone derivative BI-RG-587. Biochem. Pharmacol. 1992, 43, 1371-1376.
-
(1992)
Biochem. Pharmacol.
, vol.43
, pp. 1371-1376
-
-
Tramontano, E.1
Cheng, Y.-C.2
|