-
1
-
-
46749104685
-
Improving non-nucleoside reverse transcriptase inhibitors for first-line treatment of HIV infection: The development pipeline and recent clinical data
-
Sweeney, Z. K.; Klumpp, K. Improving non-nucleoside reverse transcriptase inhibitors for first-line treatment of HIV infection: the development pipeline and recent clinical data Curr. Opin. Drug Discovery Dev. 2008, 11, 458-470
-
(2008)
Curr. Opin. Drug Discovery Dev.
, vol.11
, pp. 458-470
-
-
Sweeney, Z.K.1
Klumpp, K.2
-
2
-
-
78651070324
-
An overview on HIV-1 reverse transcriptase inhibitors
-
Ravichandran, S.; Veerasamy, R.; Raman, S.; Krishnan, P. N.; Agrawal, R. K. An overview on HIV-1 reverse transcriptase inhibitors Dig. J. Nanomater. Biosci. 2008, 3, 171-187
-
(2008)
Dig. J. Nanomater. Biosci.
, vol.3
, pp. 171-187
-
-
Ravichandran, S.1
Veerasamy, R.2
Raman, S.3
Krishnan, P.N.4
Agrawal, R.K.5
-
3
-
-
15444380338
-
From 4,5,6,7-tetrahydro-5-methylimidazo[4,5,1- jk ](1,4)benzodiazepin-2(1 H)-one (TIBO) to Etravirine (TMC125): Fifteen years of research on non-nucleoside inhibitors of HIV-1 reverse transcriptase
-
De Corte, B. L. From 4,5,6,7-tetrahydro-5-methylimidazo[4,5,1- jk ](1,4)benzodiazepin-2(1 H)-one (TIBO) to Etravirine (TMC125): fifteen years of research on non-nucleoside inhibitors of HIV-1 reverse transcriptase J. Med. Chem. 2005, 48, 1689-1696
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1689-1696
-
-
De Corte, B.L.1
-
4
-
-
0037317499
-
Non-nucleoside reverse transcriptase inhibitors-an overview
-
Bell, C.; Matthews, G. V.; Nelson, M. R. Non-nucleoside reverse transcriptase inhibitors-an overview Int. J. STD AIDS 2003, 14, 71-77
-
(2003)
Int. J. STD AIDS
, vol.14
, pp. 71-77
-
-
Bell, C.1
Matthews, G.V.2
Nelson, M.R.3
-
5
-
-
8744243260
-
Design of non-nucleoside inhibitors of HIV-1 reverse transcriptase with improved drug resistance properties. 1
-
DOI 10.1021/jm040071z
-
Hopkins, A. L.; Ren, J.; Milton, J.; Hazen, R. J.; Chan, J. H.; Stuart, D. I.; Stammers, D. K. Design of non-nucleoside inhibitors of HIV-1 reverse transcriptase with improved drug resistance properties. 1 J. Med. Chem. 2004, 47, 5912-5922 (Pubitemid 39517015)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.24
, pp. 5912-5922
-
-
Hopkins, A.L.1
Ren, J.2
Milton, J.3
Hazen, R.J.4
Chan, J.H.5
Stuart, D.I.6
Stammers, D.K.7
-
6
-
-
2342620790
-
Roles of conformational and positional adaptability in structure-based design of TMC125-R165335 (Etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-type and drug-resistant HIV-1 variants
-
Das, K.; Clark, A. D.; Lewi, J. P. J.; Heeres, J.; De Jonge, M. R.; Koymans, L. M. H.; Vinkers, H. M.; Daeyaert, F.; Ludovici, D. W.; Kukla, M. J.; De Corte, B.; Kavash, R. W.; Ho, C. Y.; Ye, H.; Lichtenstein, M. A.; Andries, K.; Pauwels, R.; De Béthune, M.-P.; Boyer, P. L.; Clark, P.; Hughes, S. H.; Janssen, P. A. J.; Arnold, E. Roles of conformational and positional adaptability in structure-based design of TMC125-R165335 (Etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-type and drug-resistant HIV-1 variants J. Med. Chem. 2004, 47, 2550-2560
-
(2004)
J. Med. Chem.
, vol.47
, pp. 2550-2560
-
-
Das, K.1
Clark, A.D.2
Lewi, J.P.J.3
Heeres, J.4
De Jonge, M.R.5
Koymans, L.M.H.6
Vinkers, H.M.7
Daeyaert, F.8
Ludovici, D.W.9
Kukla, M.J.10
De Corte, B.11
Kavash, R.W.12
Ho, C.Y.13
Ye, H.14
Lichtenstein, M.A.15
Andries, K.16
Pauwels, R.17
De Béthune, M.-P.18
Boyer, P.L.19
Clark, P.20
Hughes, S.H.21
Janssen, P.A.J.22
Arnold, E.23
more..
-
7
-
-
38149000209
-
Novel indole-3-sulfonamides as potent HIV non-nucleoside reverse transcriptase inhibitors (NNRTIs)
-
Zhao, Z.; Wolkenberg, S. E.; Lu, M.; Munshi, V.; Moyer, G.; Feng, M.; Carella, A. V.; Ecto, L. T.; Gabryelski, L. J.; Lai, M.-T.; Prasad, S. G.; Yan, Y.; McGaughey, G. B.; Miller, M. D.; Lindsley, C. W.; Hartman, G. D.; Vacca, J. P.; Williams, T. M. Novel indole-3-sulfonamides as potent HIV non-nucleoside reverse transcriptase inhibitors (NNRTIs) Bioorg. Med. Chem. 2008, 18, 554-559
-
(2008)
Bioorg. Med. Chem.
, vol.18
, pp. 554-559
-
-
Zhao, Z.1
Wolkenberg, S.E.2
Lu, M.3
Munshi, V.4
Moyer, G.5
Feng, M.6
Carella, A.V.7
Ecto, L.T.8
Gabryelski, L.J.9
Lai, M.-T.10
Prasad, S.G.11
Yan, Y.12
McGaughey, G.B.13
Miller, M.D.14
Lindsley, C.W.15
Hartman, G.D.16
Vacca, J.P.17
Williams, T.M.18
-
8
-
-
0027195714
-
5-Chloro-3-(phenylsulfonyl)indole-2-carboxamide: A novel, non-nucleoside inhibitor of 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. 5-Chloro-3-(phenylsulfonyl)indole-2-carboxamide: a novel, non-nucleoside inhibitor of 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
-
9
-
-
34948862163
-
Indolyl aryl sulfones as HIV-1 non-nucleoside reverse transcriptase inhibitors: Role of two halogen atoms at the indole ring in developing new analogues with improved antiviral activity
-
La Regina, G.; Coluccia, A.; Piscitelli, F.; Bergamini, A.; Sinistro, A.; Cavazza, A.; Maga, G.; Samuele, A.; Zanoli, S.; Novellino, E.; Artico, M.; Silvestri, R. Indolyl aryl sulfones as HIV-1 non-nucleoside reverse transcriptase inhibitors: role of two halogen atoms at the indole ring in developing new analogues with improved antiviral activity J. Med. Chem. 2007, 50, 5034-5038
-
(2007)
J. Med. Chem.
, vol.50
, pp. 5034-5038
-
-
La Regina, G.1
Coluccia, A.2
Piscitelli, F.3
Bergamini, A.4
Sinistro, A.5
Cavazza, A.6
Maga, G.7
Samuele, A.8
Zanoli, S.9
Novellino, E.10
Artico, M.11
Silvestri, R.12
-
10
-
-
43049106403
-
Novel HIV-1 reverse transcriptase inhibitors
-
Jochmans, D. Novel HIV-1 reverse transcriptase inhibitors Virus Res. 2008, 134, 171-185
-
(2008)
Virus Res.
, vol.134
, pp. 171-185
-
-
Jochmans, D.1
-
11
-
-
0034640387
-
Binding of the second generation non-nucleoside inhibitor S-1153 to HIV-1 reverse transcriptase involves extensive main chain hydrogen bonding
-
Ren, J.; Nichols, C.; Bird, L. E.; Fujiwara, T.; Sugimoto, H.; Stuart, D. I.; Stammers, D. K. Binding of the second generation non-nucleoside inhibitor S-1153 to HIV-1 reverse transcriptase involves extensive main chain hydrogen bonding J. Biol. Chem. 2000, 275, 14316-14320
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 14316-14320
-
-
Ren, J.1
Nichols, C.2
Bird, L.E.3
Fujiwara, T.4
Sugimoto, H.5
Stuart, D.I.6
Stammers, D.K.7
-
12
-
-
0034435564
-
Structural basis for the resilience of efavirenz (DMP-266) to drug resistance mutations in HIV-1 reverse transcriptase
-
Ren, J.; Milton, J.; Weaver, K. L.; Short, S. A.; Stuart, D. I.; Stammers, D. K. Structural basis for the resilience of efavirenz (DMP-266) to drug resistance mutations in HIV-1 reverse transcriptase Struct. Fold. Des. 2000, 8, 1089-1094
-
(2000)
Struct. Fold. Des.
, vol.8
, pp. 1089-1094
-
-
Ren, J.1
Milton, J.2
Weaver, K.L.3
Short, S.A.4
Stuart, D.I.5
Stammers, D.K.6
-
14
-
-
33845553875
-
Generation and reactions of 3-lithio-1-(phenylsulfonyl)indole
-
Saulnier, M. G.; Gribble, G. W. Generation and reactions 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
-
-
0028215732
-
Preparation and reactions of 1-(tert -butyldimethylsilyl)-3-lithioindole. Regioselective synthesis of 3-substituted indoles
-
Amat, M.; Hadida, S.; Sathyanarayana, S.; Bosch, J. Preparation and reactions of 1-(tert -butyldimethylsilyl)-3-lithioindole. Regioselective synthesis of 3-substituted indoles J. Org. Chem. 1994, 59, 10-11
-
(1994)
J. Org. Chem.
, vol.59
, pp. 10-11
-
-
Amat, M.1
Hadida, S.2
Sathyanarayana, S.3
Bosch, J.4
-
16
-
-
0001031256
-
Halogen-magnesium exchange reaction of iodoindole derivatives
-
Kondo, Y.; Yoshida, A.; Sato, S.; Sakamoto, T. Halogen-magnesium exchange reaction of iodoindole derivatives Heterocycles 1996, 42, 105-108
-
(1996)
Heterocycles
, vol.42
, pp. 105-108
-
-
Kondo, Y.1
Yoshida, A.2
Sato, S.3
Sakamoto, T.4
-
17
-
-
0009488238
-
Synthesis of novel phosphorus heterocycles:1,3-dihydro-2,l- benzoxaphosphole l-oxides
-
Miles, J. A.; Grabiak, R. C.; Cummins, C. Synthesis of novel phosphorus heterocycles:1,3-dihydro-2,l-benzoxaphosphole l-oxides J. Org. Chem. 1982, 47, 1677-1682
-
(1982)
J. Org. Chem.
, vol.47
, pp. 1677-1682
-
-
Miles, J.A.1
Grabiak, R.C.2
Cummins, C.3
-
18
-
-
0002016039
-
Synthesis and NMR spectroscopic investigation of phenylphosphoryl derivatives
-
Duddeck, H.; Lecht, R. Synthesis and NMR spectroscopic investigation of phenylphosphoryl derivatives Phosphorus Sulfur 1987, 29, 169-178
-
(1987)
Phosphorus Sulfur
, vol.29
, pp. 169-178
-
-
Duddeck, H.1
Lecht, R.2
-
19
-
-
37049071784
-
Influence of ortho methyl and isopropyl substituents on the reactivity of N - T -butyl P -arylphosphonamidic chlorides with isopropylamine and t -butylamine: Steric acceleration of metaphosphonimidate formation by an elimination addition mechanism; Contrasting behaviour of N, N -dimethyl P -arylphosphonamidic chlorides
-
Freeman, S.; Harger, M. J. P. Influence of ortho methyl and isopropyl substituents on the reactivity of N-t -butyl P -arylphosphonamidic chlorides with isopropylamine and t -butylamine: steric acceleration of metaphosphonimidate formation by an elimination addition mechanism; contrasting behaviour of N, N -dimethyl P -arylphosphonamidic chlorides J. Chem. Soc., Perkin Trans. 1 1987, 1399-1406
-
(1987)
J. Chem. Soc., Perkin Trans. 1
, pp. 1399-1406
-
-
Freeman, S.1
Harger, M.J.P.2
-
20
-
-
62549146633
-
Synthesis and antiviral evaluation of thieno[3,4- d ]pyrimidine C-nucleoside analogues of 2′,3′-dideoxy- and 2′,3′- dideoxy-2′,3′-didehydro-adenosine and -inosine
-
Hamann, M.; Pierra, C.; Sommadossi, J.P.; Musiu, C.; Vargiu, L.; Liuzzi, M.; Storer, R.; Gosselin, G. Synthesis and antiviral evaluation of thieno[3,4- d ]pyrimidine C-nucleoside analogues of 2′,3′-dideoxy- and 2′,3′-dideoxy-2′,3′-didehydro-adenosine and -inosine Bioorg. Med. Chem. 2009, 17, 2321-2326
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 2321-2326
-
-
Hamann, M.1
Pierra, C.2
Sommadossi, J.P.3
Musiu, C.4
Vargiu, L.5
Liuzzi, M.6
Storer, R.7
Gosselin, G.8
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