-
2
-
-
14944344464
-
New approaches toward anti-HIV chemotherapy
-
De Clercq, E. New approaches toward anti-HIV chemotherapy. J.Med. Chem., 2005, 48, 1297-313.
-
(2005)
J.Med. Chem
, vol.48
, pp. 1297-1313
-
-
De Clercq, E.1
-
3
-
-
70350708165
-
The history of antiretrovirals: Key discoveries overthe past 25 years
-
De Clercq, E. The history of antiretrovirals: key discoveries overthe past 25 years. Rev. Med. Virol., 2009, 19, 287-299.
-
(2009)
Rev. Med. Virol
, vol.19
, pp. 287-299
-
-
De Clercq, E.1
-
4
-
-
61449189645
-
Anti-HIV drugs: 25 compounds approved within 25years after the discovery of HIV
-
De Clercq, E. Anti-HIV drugs: 25 compounds approved within 25years after the discovery of HIV. Int. J. Antimicrob. Agents, 2009,33, 307-320.
-
(2009)
Int. J. Antimicrob. Agents
, vol.33
, pp. 307-320
-
-
De Clercq, E.1
-
5
-
-
77649202344
-
Highlights in the discovery of antiviral drugs: Apersonal retrospective
-
De Clercq, E. Highlights in the discovery of antiviral drugs: apersonal retrospective. J. Med. Chem., 2010, 53, 1438-1450.
-
(2010)
J. Med. Chem
, vol.53
, pp. 1438-1450
-
-
De Clercq, E.1
-
6
-
-
68449098788
-
Designed multiple ligands: An emerging anti-HIVdrug discovery paradigm
-
Zhan, P.; Liu, X. Designed multiple ligands: an emerging anti-HIVdrug discovery paradigm. Curr. Pharm. Des., 2009, 15, 1893-1917.
-
(2009)
Curr. Pharm. Des
, vol.15
, pp. 1893-1917
-
-
Zhan, P.1
Liu, X.2
-
7
-
-
0027996494
-
Design, synthesis, and biological evalua-tion of cosalane, a novel anti-HIV agent which inhibits multiplefeatures of virus reproduction
-
Cushman, M.; Golebiewski, W.M.; McMahon, J.B.; Buckheit, R.W.Jr.; Clanton, D.J.; Weislow, O.; Haugwitz, R.D.; Bader, J.P.; Graham, L.; Rice, W.G. Design, synthesis, and biological evalua-tion of cosalane, a novel anti-HIV agent which inhibits multiplefeatures of virus reproduction. J. Med. Chem., 1994, 37, 3040-3050.
-
(1994)
J. Med. Chem
, vol.37
, pp. 3040-3050
-
-
Cushman, M.1
Golebiewski, W.M.2
McMahon, J.B.3
Buckheit Jr., R.W.4
Clanton, D.J.5
Weislow, O.6
Haugwitz, R.D.7
Bader, J.P.8
Graham, L.9
Rice, W.G.10
-
8
-
-
33947397199
-
Aurin-tricarboxylic acid inhibits the early stage of vaccinia virus replica-tion by targeting both cellular and viral factors
-
Myskiw, C.; Deschambault, Y.; Jefferies, K.; He, R.; Cao, J. Aurin-tricarboxylic acid inhibits the early stage of vaccinia virus replica-tion by targeting both cellular and viral factors. J. Virol., 2007, 81,3027-3032.
-
(2007)
J. Virol
, vol.81
, pp. 3027-3032
-
-
Myskiw, C.1
Deschambault, Y.2
Jefferies, K.3
He, R.4
Cao, J.5
-
9
-
-
33646166978
-
Potential antivirals and antiviral strategies againstSARS coronavirus infections
-
De Clercq, E. Potential antivirals and antiviral strategies againstSARS coronavirus infections. Expert Rev. Anti. Infect. Ther., 2006,4, 291-302.
-
(2006)
Expert Rev. Anti. Infect. Ther
, vol.4
, pp. 291-302
-
-
De Clercq, E.1
-
10
-
-
20444486621
-
Structural analysis ofinhibition mechanisms of aurintricarboxylic acid on SARS-CoVpolymerase and other proteins
-
Yap, Y.; Zhang, X.; Andonov, A.; He, R. Structural analysis ofinhibition mechanisms of aurintricarboxylic acid on SARS-CoVpolymerase and other proteins. Comput. Biol. Chem., 2005, 29,212-219.
-
(2005)
Comput. Biol. Chem
, vol.29
, pp. 212-219
-
-
Yap, Y.1
Zhang, X.2
Andonov, A.3
He, R.4
-
11
-
-
3142661081
-
Po-tent and selective inhibition of SARS coronavirus replication byaurintricarboxylic acid
-
He, R.; Adonov, A.; Traykova-Adonova, M.; Cao, J.; Cutts, T.; Grudesky, E.; Deschambaul, Y.; Berry, J.; Drebot, M.; Li, X. Po-tent and selective inhibition of SARS coronavirus replication byaurintricarboxylic acid. Biochem. Biophys. Res. Commun., 2004,320, 1199-1203.
-
(2004)
Biochem. Biophys. Res. Commun
, vol.320
, pp. 1199-1203
-
-
He, R.1
Adonov, A.2
Traykova-Adonova, M.3
Cao, J.4
Cutts, T.5
Grudesky, E.6
Deschambaul, Y.7
Berry, J.8
Drebot, M.9
Li, X.10
-
12
-
-
58149476178
-
Aurintricar-boxylic acid inhibits influenza virus neuraminidase
-
Hung, H.C.; Tseng, C.P.; Yang, J.M.; Ju, Y.W.; Tseng, S.N.; Chen, Y.F.; Chao, Y.S.; Hsieh, H.P.; Shih, S.R.; Hsu, J.T. Aurintricar-boxylic acid inhibits influenza virus neuraminidase. Antiviral Res.,2009, 81, 123-131.
-
(2009)
Antiviral Res
, vol.81
, pp. 123-131
-
-
Hung, H.C.1
Tseng, C.P.2
Yang, J.M.3
Ju, Y.W.4
Tseng, S.N.5
Chen, Y.F.6
Chao, Y.S.7
Hsieh, H.P.8
Shih, S.R.9
Hsu, J.T.10
-
13
-
-
58149140518
-
Aurintricarboxylic acid upregulates the thrombomodulin expres-sion of endothelial cells and peripheral blood monocytes
-
Kim, H.K.; Kim, J.E.; Park, C.M.; Kim, Y.T.; Han, K.S.; Cho, H.I.Aurintricarboxylic acid upregulates the thrombomodulin expres-sion of endothelial cells and peripheral blood monocytes. BloodCoagul. Fibrinolysis., 2008, 19, 489-494.
-
(2008)
BloodCoagul. Fibrinolysis
, vol.19
, pp. 489-494
-
-
Kim, H.K.1
Kim, J.E.2
Park, C.M.3
Kim, Y.T.4
Han, K.S.5
Cho, H.I.6
-
14
-
-
33745145464
-
Biological evaluation, chelation,and molecular modeling studies of novel metal-chelating inhibitorsof NF-kappaB-DNA binding: Structure activity relationships
-
Sharma, R.K.; Chopra, S.; Sharma, S.D.; Pande, V.; Ramos, M.J.; Meguro, K.; Inoue, J.; Otsuka, M. Biological evaluation, chelation,and molecular modeling studies of novel metal-chelating inhibitorsof NF-kappaB-DNA binding: structure activity relationships. J.Med. Chem., 2006, 49, 3595-3601.
-
(2006)
J.Med. Chem
, vol.49
, pp. 3595-3601
-
-
Sharma, R.K.1
Chopra, S.2
Sharma, S.D.3
Pande, V.4
Ramos, M.J.5
Meguro, K.6
Inoue, J.7
Otsuka, M.8
-
15
-
-
0033930849
-
Aurine tricarboxylic acid, a potent metal-chelating inhibitor of NFkappaB-DNA binding
-
Sharma, R.K.; Garg, B.S.; Kurosaki, H.; Goto, M.; Otsuka, M.; Yamamoto, T.; Inoue, J. Aurine tricarboxylic acid, a potent metal-chelating inhibitor of NFkappaB-DNA binding. Bioorg. Med.Chem., 2000, 8, 1819-1823.
-
(2000)
Bioorg. Med.Chem
, vol.8
, pp. 1819-1823
-
-
Sharma, R.K.1
Garg, B.S.2
Kurosaki, H.3
Goto, M.4
Otsuka, M.5
Yamamoto, T.6
Inoue, J.7
-
16
-
-
4344630688
-
Induction ofapoptosis by benzamide and its inhibition by aurin tricarboxylicacid (ATA) in Chinese hamster V79 cells
-
Ghosh, U.; Pandit, B.; Dutta, J.; Bhattacharyya, N.P. Induction ofapoptosis by benzamide and its inhibition by aurin tricarboxylicacid (ATA) in Chinese hamster V79 cells. Mutat. Res., 2004, 554,121-129.
-
(2004)
Mutat. Res
, vol.554
, pp. 121-129
-
-
Ghosh, U.1
Pandit, B.2
Dutta, J.3
Bhattacharyya, N.P.4
-
17
-
-
1842846611
-
Inhibition of cytokine-induced JAK-STAT signalling pathways byan endonuclease inhibitor aurintricarboxylic acid
-
Chen, C.W.; Chao, Y.; Chang, Y.H.; Hsu, M.J.; Lin, W.W.Inhibition of cytokine-induced JAK-STAT signalling pathways byan endonuclease inhibitor aurintricarboxylic acid. Br. J. Pharma-col., 2002, 137, 1011-1020.
-
(2002)
Br. J. Pharma-col
, vol.137
, pp. 1011-1020
-
-
Chen, C.W.1
Chao, Y.2
Chang, Y.H.3
Hsu, M.J.4
Lin, W.W.5
-
18
-
-
5444255232
-
Novel shift of Jak/Stat signalling characterizes the pro-tective effect of aurintricarboxylic acid (ATA) from tumor necrosisfactor-alpha toxicity in human B lymphocytes
-
Marchisio, M.; Grimley, P.M.; Di Baldassarre, A.; Santavenere, E.; Miscia, S. Novel shift of Jak/Stat signalling characterizes the pro-tective effect of aurintricarboxylic acid (ATA) from tumor necrosisfactor-alpha toxicity in human B lymphocytes. Int. J. Immunopa-thol. Pharmacol., 2004, 17, 5-14.
-
(2004)
Int. J. Immunopa-thol. Pharmacol
, vol.17
, pp. 5-14
-
-
Marchisio, M.1
Grimley, P.M.2
Di Baldassarre, A.3
Santavenere, E.4
Miscia, S.5
-
19
-
-
0032923499
-
Aurintricarboxylic acidinhibits apoptosis and supports proliferation in a haemopoieticgrowth-factor dependent myeloid cell line
-
Andrew, D.J.; Hay, A.W.; Evans, S.W. Aurintricarboxylic acidinhibits apoptosis and supports proliferation in a haemopoieticgrowth-factor dependent myeloid cell line. Immunopharmacology,1999, 41, 1-10.
-
(1999)
Immunopharmacology
, vol.41
, pp. 1-10
-
-
Andrew, D.J.1
Hay, A.W.2
Evans, S.W.3
-
20
-
-
0034114537
-
Pharmacokinetics, biliary excretion, and tissue distribution of novelanti-HIV agents, cosalane and dihydrocosalane, in Sprague-Dawleyrats
-
Kuchimanchi, K.R.; Udata, C.; Johnston, T.P.; Mitra, A.K.Pharmacokinetics, biliary excretion, and tissue distribution of novelanti-HIV agents, cosalane and dihydrocosalane, in Sprague-Dawleyrats. Drug Metab. Dispos., 2000, 28, 403-408.
-
(2000)
Drug Metab. Dispos
, vol.28
, pp. 403-408
-
-
Kuchimanchi, K.R.1
Udata, C.2
Johnston, T.P.3
Mitra, A.K.4
-
21
-
-
0033822279
-
Transport of cosalane-a highlylipophilic novel anti-HIV agent-across caco-2 cell monolayers. J
-
Pal, D.; Udata, C.; Mitra, A.K. Transport of cosalane-a highlylipophilic novel anti-HIV agent-across caco-2 cell monolayers. J.Pharm. Sci., 2000, 89, 826-833.
-
(2000)
Pharm. Sci
, vol.89
, pp. 826-833
-
-
Pal, D.1
Udata, C.2
Mitra, A.K.3
-
22
-
-
0030033216
-
Correlation of anti-ing normal alkenyl and phosphodiester chains as cholestane re-placements
-
Keyes, R.F.; Golebiewski, W.M.; Cushman, M. Correlation of anti-ing normal alkenyl and phosphodiester chains as cholestane re-placements. J. Med. Chem., 1996, 39, 508-514.
-
(1996)
J. Med. Chem
, vol.39
, pp. 508-514
-
-
Keyes, R.F.1
Golebiewski, W.M.2
Cushman, M.3
-
23
-
-
0030272456
-
Exploration of theeffects of linker chain modifications on anti-HIV activities in a se-ries of cosalane analogues
-
Golebiewski, W.M.; Keyes, R.F.; Cushman, M. Exploration of theeffects of linker chain modifications on anti-HIV activities in a se-ries of cosalane analogues. Bioorg. Med. Chem., 1996, 4, 1637-1648.
-
(1996)
Bioorg. Med. Chem
, vol.4
, pp. 1637-1648
-
-
Golebiewski, W.M.1
Keyes, R.F.2
Cushman, M.3
-
24
-
-
0032770434
-
Disposition of cosalane, a novelanti-HIV agent, in isolated perfused rat livers
-
Udata, C.; Mitra, A.K.; Badr, M.Z. Disposition of cosalane, a novelanti-HIV agent, in isolated perfused rat livers. Drug Metab. Dis-pos., 1999, 27, 947-950.
-
(1999)
Drug Metab. Dis-pos
, vol.27
, pp. 947-950
-
-
Udata, C.1
Mitra, A.K.2
Badr, M.Z.3
-
25
-
-
78650003024
-
The next ten stories on antiviral drug discovery (partE): Advents, Advances, and Adventures
-
Oct20. DOI 10.1002/med.20179
-
De Clercq, E. The next ten stories on antiviral drug discovery (partE): Advents, Advances, and Adventures. Med. Res. Rev., 2009 Oct20. DOI 10.1002/med.20179.
-
(2009)
Med. Res. Rev
-
-
De Clercq, E.1
-
27
-
-
37249090226
-
Targeting HIV attachment and entry for therapy
-
Strizki, J. Targeting HIV attachment and entry for therapy. AdvPharmacol., 2008, 56, 93-120.
-
(2008)
AdvPharmacol
, vol.56
, pp. 93-120
-
-
Strizki, J.1
-
28
-
-
0032492726
-
Synthesis of a cosalane analog with an extended polyanionic phar-macophore conferring enhanced potency as an anti-HIV agent
-
Cushman, M.; Insaf, S.; Ruell, J.A.; Schaeffer, C.A.; Rice, W.G.Synthesis of a cosalane analog with an extended polyanionic phar-macophore conferring enhanced potency as an anti-HIV agent.Bioorg. Med. Chem. Lett., 1998, 8, 833-836.
-
(1998)
Bioorg. Med. Chem. Lett
, vol.8
, pp. 833-836
-
-
Cushman, M.1
Insaf, S.2
Ruell, J.A.3
Schaeffer, C.A.4
Rice, W.G.5
-
29
-
-
0033587023
-
Extension of the polyan-ionic cosalane pharmacophore as a strategy for increasing anti-HIVpotency
-
Cushman, M.; Insaf, S.; Paul, G.; Ruell, J.A.; De Clercq, E.; Schols, D.; Pannecouque, C.; Witvrouw, M.; Schaeffer, C.A.; Turpin, J.A.; Williamson, K.; Rice, W.G. Extension of the polyan-ionic cosalane pharmacophore as a strategy for increasing anti-HIVpotency. J. Med. Chem., 1999, 42, 1767-1777.
-
(1999)
J. Med. Chem
, vol.42
, pp. 1767-1777
-
-
Cushman, M.1
Insaf, S.2
Paul, G.3
Ruell, J.A.4
De Clercq, E.5
Schols, D.6
Pannecouque, C.7
Witvrouw, M.8
Schaeffer, C.A.9
Turpin, J.A.10
Williamson, K.11
Rice, W.G.12
-
30
-
-
0033812685
-
Identificationof optimal anion spacing for anti-HIV activity in a series ofcosalane tetracarboxylates
-
Paul, G.C.; De Clercq, E.; Pannecouque, C.; Witvrouw, M.; Loftus, T.L.; Turpin, J.A.; Buckheit, R.W.Jr.; Cushman, M. Identificationof optimal anion spacing for anti-HIV activity in a series ofcosalane tetracarboxylates. Bioorg. Med. Chem. Lett., 2000, 10,2149-2152.
-
(2000)
Bioorg. Med. Chem. Lett
, vol.10
, pp. 2149-2152
-
-
Paul, G.C.1
De Clercq, E.2
Pannecouque, C.3
Witvrouw, M.4
Loftus, T.L.5
Turpin, J.A.6
Buckheit Jr., R.W.7
Cushman, M.8
-
31
-
-
0034694347
-
Anti-HIVactivity of a series of cosalane amino acid conjugates
-
Santhosh, K.C.; De Clercq, E.; Pannecouque, C.; Witvrouw, M.; Loftus, T.L.; Turpin, J.A.; Buckheit, R.W.; Cushman, M. Anti-HIVactivity of a series of cosalane amino acid conjugates. Bioorg. Med.Chem. Lett., 2000, 10, 2505-2508.
-
(2000)
Bioorg. Med.Chem. Lett
, vol.10
, pp. 2505-2508
-
-
Santhosh, K.C.1
de Clercq, E.2
Pannecouque, C.3
Witvrouw, M.4
Loftus, T.L.5
Turpin, J.A.6
Buckheit, R.W.7
Cushman, M.8
-
32
-
-
0035283023
-
Correlation of Anti-HIV Activity With Anion Spacingin a Series of Cosalane Analogues With Extended Polycarboxylatepharmacophores
-
Santhosh, K.C.; Paul, G.C.; De Clercq, E.; Pannecouque, C.; Witvrouw, M.; Loftus, T.L.; Turpin, J.A.; Buckheit, R.W.Jr.; Cushman, M.Correlation of anti-HIV activity with anion spacingin a series of cosalane analogues with extended polycarboxylatepharmacophores. J. Med. Chem., 2001, 44, 703-714.
-
(2001)
J. Med. Chem
, vol.44
, pp. 703-714
-
-
Santhosh, K.C.1
Paul, G.C.2
de Clercq, E.3
Pannecouque, C.4
Witvrouw, M.5
Loftus, T.L.6
Turpin, J.A.7
Buckheit Jr., R.W.8
Cushman, M.9
-
33
-
-
0037074101
-
Intestinal absorptionand biodistribution of cosalane and its amino acid conjugates:Novel anti-HIV agents
-
Kuchimanchi, K.R.; Gandhi, M.D.; Sheta, R.R.; Johnston, T.P.; Santhosh, K.C.; Cushman, M.; Mitra, A.K. Intestinal absorptionand biodistribution of cosalane and its amino acid conjugates:novel anti-HIV agents. Int. J. Pharm., 2002, 231, 197-211.
-
(2002)
Int. J. Pharm
, vol.231
, pp. 197-211
-
-
Kuchimanchi, K.R.1
Gandhi, M.D.2
Sheta, R.R.3
Johnston, T.P.4
Santhosh, K.C.5
Cushman, M.6
Mitra, A.K.7
-
34
-
-
0034806573
-
Synthesis and anti-HIV activity of cosalane ana-logues incorporating two dichlorodisalicylmethane pharmacophorefragments
-
Casimiro-Garcia, A.; De Clercq, E.; Pannecouque, C.; Witvrouw, M.; Loftus, T.L.; Turpin, J.A.; Buckheit, R.W.Jr.; Fanwick, P.E.; Cushman, M. Synthesis and anti-HIV activity of cosalane ana-logues incorporating two dichlorodisalicylmethane pharmacophorefragments. Bioorg. Med. Chem., 2001, 9, 2827-2841.
-
(2001)
Bioorg. Med. Chem
, vol.9
, pp. 2827-2841
-
-
Casimiro-Garcia, A.1
de Clercq, E.2
Pannecouque, C.3
Witvrouw, M.4
Loftus, T.L.5
Turpin, J.A.6
Buckheit Jr., R.W.7
Fanwick, P.E.8
Cushman, M.9
-
35
-
-
0034048588
-
Synthesis and anti-HIV activity of cosalane analogues incorporat-ing nitrogen in the linker chain
-
Casimiro-Garcia, A.; De Clercq, E.; Pannecouque, C.; Witvrouw, M.; Stup, T.L.; Turpin, J.A.; Buckheit, R.W.Jr.; Cushman, M.Synthesis and anti-HIV activity of cosalane analogues incorporat-ing nitrogen in the linker chain. Bioorg. Med. Chem., 2000, 8, 191-200.
-
(2000)
Bioorg. Med. Chem
, vol.8
, pp. 191-200
-
-
Casimiro-Garcia, A.1
de Clercq, E.2
Pannecouque, C.3
Witvrouw, M.4
Stup, T.L.5
Turpin, J.A.6
Buckheit Jr., R.W.7
Cushman, M.8
-
36
-
-
2342595186
-
Nonnucleoside inhibitors of HIV-1reverse transcriptase: From the biology of reverse transcription tomolecular design
-
Tronchet, J.M.; Seman, M. Nonnucleoside inhibitors of HIV-1reverse transcriptase: from the biology of reverse transcription tomolecular design. Curr. Top Med. Chem., 2003, 3, 1496-1511.
-
(2003)
Curr. Top Med. Chem
, vol.3
, pp. 1496-1511
-
-
Tronchet, J.M.1
Seman, M.2
-
37
-
-
48949117560
-
The current status of theNNRTI family of antiretrovirals used in the HAART regimeagainst HIV infection
-
Martins, S.; Ramos, M.J.; Fernandes, P.A. The current status of theNNRTI family of antiretrovirals used in the HAART regimeagainst HIV infection. Curr. Med. Chem., 2008, 15, 1083-1095.
-
(2008)
Curr. Med. Chem
, vol.15
, pp. 1083-1095
-
-
Martins, S.1
Ramos, M.J.2
Fernandes, P.A.3
-
38
-
-
33845462923
-
HIV-1 RT nonnucleoside inhibitorsand their interaction with RT for antiviral drug development. In-fect. Disord
-
Zhou, Z.; Lin, X.; Madura, J.D. HIV-1 RT nonnucleoside inhibitorsand their interaction with RT for antiviral drug development. In-fect. Disord. Drug Targets, 2006, 6, 391-413.
-
(2006)
Drug Targets
, vol.6
, pp. 391-413
-
-
Zhou, Z.1
Lin, X.2
Madura, J.D.3
-
39
-
-
54449084056
-
Etravirine for the treat-ment of HIV infection
-
Seminari, E.; Castagna, A.; Lazzarin, A. Etravirine for the treat-ment of HIV infection. Expert. Rev. Anti. Infect. Ther., 2008, 6,427-433.
-
(2008)
Expert. Rev. Anti. Infect. Ther
, vol.6
, pp. 427-433
-
-
Seminari, E.1
Castagna, A.2
Lazzarin, A.3
-
40
-
-
55449092395
-
Emerging resistance profiles of newly approved antiret-roviral drugs
-
Daar, E.S. Emerging resistance profiles of newly approved antiret-roviral drugs. Top HIV Med., 2008, 16, 110-116.
-
(2008)
Top HIV Med
, vol.16
, pp. 110-116
-
-
Daar, E.S.1
-
41
-
-
70349395798
-
Recent advances in the discovery anddevelopment of novel HIV-1 NNRTI platforms: 2006-2008 update
-
Zhan, P.; Liu, X.; Li, Z. Recent advances in the discovery anddevelopment of novel HIV-1 NNRTI platforms: 2006-2008 update.Curr. Med. Chem., 2009, 16, 2876-89.
-
(2009)
Curr. Med. Chem.
, vol.16
, pp. 2876-2889
-
-
Zhan, P.1
Liu, X.2
Li, Z.3
-
42
-
-
70450184400
-
Design strategies of novel NNRTIsto overcome drug resistance
-
Zhan, P.; Liu, X.; Li, Z.; Pannecouque, C.; De Clercq, E. Design strategies of novel NNRTIsto overcome drug resistance. Curr. Med. Chem., 2009, 16, 3903-3917.
-
(2009)
Curr. Med. Chem
, vol.16
, pp. 3903-3917
-
-
Zhan, P.1
Liu, X.2
Li, Z.3
Pannecouque, C.4
De Clercq, E.5
-
43
-
-
68149109726
-
Sulfanyltria-zole/tetrazoles: A promising class of HIV-1 NNRTIs
-
Zhan, P.; Li, Z.; Liu, X.; De Clercq, E. Sulfanyltria-zole/tetrazoles: a promising class of HIV-1 NNRTIs. Mini. Rev.Med. Chem., 2009, 9, 1014-1023.
-
(2009)
Mini. Rev.Med. Chem
, vol.9
, pp. 1014-1023
-
-
Zhan, P.1
Li, Z.2
Liu, X.3
de Clercq, E.4
-
44
-
-
0029783936
-
Synthesis and biologi-cal evaluation of certain alkenyldiarylmethanes as anti-HIV-1agents which act as non-nucleoside reverse transcriptase inhibitors
-
Cushman, M.; Golebiewski, W.M.; Graham, L.; Turpin, J.A.; Rice, W.G.; Fliakas-Boltz, V.; Buckheit, R.W.Jr. Synthesis and biologi-cal evaluation of certain alkenyldiarylmethanes as anti-HIV-1agents which act as non-nucleoside reverse transcriptase inhibitors.J. Med. Chem., 1996, 39, 3217-3227.
-
(1996)
J. Med. Chem
, vol.39
, pp. 3217-3227
-
-
Cushman, M.1
Golebiewski, W.M.2
Graham, L.3
Turpin, J.A.4
Rice, W.G.5
Fliakas-Boltz, V.6
Buckheit Jr., R.W.7
-
45
-
-
0032482316
-
New alkenyldiarylmethanes with enhanced potencies asanti-HIV agents which act as non-nucleoside reverse transcriptaseinhibitors
-
Cushman, M.; Casimiro-Garcia, A.; Hejchman, E.; Ruell, J.A.; Huang, M.; Schaeffer, C.A.; Williamson, K.; Rice, W.G.; Buckheit, R.W.Jr. New alkenyldiarylmethanes with enhanced potencies asanti-HIV agents which act as non-nucleoside reverse transcriptaseinhibitors. J. Med. Chem., 1998, 41, 2076-2089.
-
(1998)
J. Med. Chem
, vol.41
, pp. 2076-2089
-
-
Cushman, M.1
Casimiro-Garcia, A.2
Hejchman, E.3
Ruell, J.A.4
Huang, M.5
Schaeffer, C.A.6
Williamson, K.7
Rice, W.G.8
Buckheit Jr., R.W.9
-
46
-
-
0032548456
-
Synthesis of a non-nucleoside reverse transcriptase inhibitor in thealkenyldiarylmethane (ADAM) series with optimized potency andtherapeutic index
-
Cushman, M.; Casimiro-Garcia, A.; Williamson, K.; Rice, W.G.Synthesis of a non-nucleoside reverse transcriptase inhibitor in thealkenyldiarylmethane (ADAM) series with optimized potency andtherapeutic index. Bioorg. Med. Chem. Lett., 1998, 8, 195-198.
-
(1998)
Bioorg. Med. Chem. Lett
, vol.8
, pp. 195-198
-
-
Cushman, M.1
Casimiro-Garcia, A.2
Williamson, K.3
Rice, W.G.4
-
47
-
-
0032744956
-
Novel modifications inthe alkenyldiarylmethane (ADAM) series of non-nucleoside re-verse transcriptase inhibitors
-
Casimiro-Garcia, A.; Micklatcher, M.; Turpin, J.A.; Stup, T.L.; Watson, K.; Buckheit, R.W.; Cushman, M. Novel modifications inthe alkenyldiarylmethane (ADAM) series of non-nucleoside re-verse transcriptase inhibitors. J. Med. Chem., 1999, 42, 4861-4874.
-
(1999)
J. Med. Chem
, vol.42
, pp. 4861-4874
-
-
Casimiro-Garcia, A.1
Micklatcher, M.2
Turpin, J.A.3
Stup, T.L.4
Watson, K.5
Buckheit, R.W.6
Cushman, M.7
-
48
-
-
0035935730
-
The Biological Effects of Structural Variation At Themeta Position of the Aromatic Rings and At the End of The Alkenylchain In The Alkenyldiarylmethane Series of Non-nucleoside Reversetranscriptase Inhibitors
-
Xu, G.; Micklatcher, M.; Silvestri, M.A.; Hartman, T.L.; Burrier, J.; Osterling, M.C.; Wargo, H.; Turpin, J.A.; Buckheit, R.W.Jr.; Cushman, M. The biological effects of structural variation at themeta position of the aromatic rings and at the end of the alkenylchain in the alkenyldiarylmethane series of non-nucleoside reversetranscriptase inhibitors. J. Med. Chem., 2001, 44, 4092-4113.
-
(2001)
J. Med. Chem
, vol.44
, pp. 4092-4113
-
-
Xu, G.1
Micklatcher, M.2
Silvestri, M.A.3
Hartman, T.L.4
Burrier, J.5
Osterling, M.C.6
Wargo, H.7
Turpin, J.A.8
Buckheit Jr., R.W.9
Cushman, M.10
-
49
-
-
0035823172
-
Solid-phase synthesis of the alkenyldiarylmethane(ADAM) series of non-nucleoside HIV-1 reverse transcriptase in-hibitors
-
Xu, G.; Loftus, T.L.; Wargo, H.; Turpin, J.A.; Buckheit, R.W.Jr.; Cushman, M. Solid-phase synthesis of the alkenyldiarylmethane(ADAM) series of non-nucleoside HIV-1 reverse transcriptase in-hibitors. J. Org. Chem., 2001, 66, 5958-5964.
-
(2001)
J. Org. Chem
, vol.66
, pp. 5958-5964
-
-
Xu, G.1
Loftus, T.L.2
Wargo, H.3
Turpin, J.A.4
Buckheit Jr., R.W.5
Cushman, M.6
-
50
-
-
0036132217
-
Synthesis of alkenyldiarylmethane (ADAM) non-nucleoside HIV-1 reverse transcriptase inhibitors with non-identical aromatic rings
-
Xu, G.; Hartman, T.L.; Wargo, H.; Turpin, J.A.; Buckheit, R.W.; Cushman, M. Synthesis of alkenyldiarylmethane (ADAM) non-nucleoside HIV-1 reverse transcriptase inhibitors with non-identical aromatic rings. Bioorg. Med. Chem., 2002, 10, 283-290.
-
(2002)
Bioorg. Med. Chem
, vol.10
, pp. 283-290
-
-
Xu, G.1
Hartman, T.L.2
Wargo, H.3
Turpin, J.A.4
Buckheit, R.W.5
Cushman, M.6
-
51
-
-
2542513226
-
Design, synthesis, anti-HIV activities, and metabolicstabilities of alkenyldiarylmethane (ADAM) non-nucleoside re-verse transcriptase inhibitors
-
Silvestri, M.A.; Nagarajan, M.; De Clercq, E.; Pannecouque, C.; Cushman, M. Design, synthesis, anti-HIV activities, and metabolicstabilities of alkenyldiarylmethane (ADAM) non-nucleoside re-verse transcriptase inhibitors. J. Med. Chem., 2004, 47, 3149-3162.
-
(2004)
J. Med. Chem
, vol.47
, pp. 3149-3162
-
-
Silvestri, M.A.1
Nagarajan, M.2
De Clercq, E.3
Pannecouque, C.4
Cushman, M.5
-
52
-
-
24944473828
-
Synthesis, anti-HIVactivity, and metabolic stability of new alkenyldiarylmethane HIV-1 non-nucleoside reverse transcriptase inhibitors
-
Deng, B.L.; Hartman, T.L.; Buckheit, R.W.Jr.; Pannecouque, C.; De Clercq, E.; Fanwick, P.E.; Cushman, M. Synthesis, anti-HIVactivity, and metabolic stability of new alkenyldiarylmethane HIV-1 non-nucleoside reverse transcriptase inhibitors. J. Med. Chem.,2005, 48, 6140-6155.
-
(2005)
J. Med. Chem
, vol.48
, pp. 6140-6155
-
-
Deng, B.L.1
Hartman, T.L.2
Buckheit Jr., R.W.3
Pannecouque, C.4
de Clercq, E.5
Fanwick, P.E.6
Cushman, M.7
-
53
-
-
33747593758
-
Replacement of the metabolically la-bile methyl esters in the alkenyldiarylmethane series of non-nucleoside reverse transcriptase inhibitors with isoxazolone, isoxa-zole, oxazolone, or cyano substituents
-
Deng, B.L.; Hartman, T.L.; Buckheit, R.W.Jr.; Pannecouque, C.; De Clercq, E.; Cushman, M. Replacement of the metabolically la-bile methyl esters in the alkenyldiarylmethane series of non-nucleoside reverse transcriptase inhibitors with isoxazolone, isoxa-zole, oxazolone, or cyano substituents. J. Med. Chem., 2006, 49,5316-5323.
-
(2006)
J. Med. Chem
, vol.49
, pp. 5316-5323
-
-
Deng, B.L.1
Hartman, T.L.2
Buckheit Jr., R.W.3
Pannecouque, C.4
de Clercq, E.5
Cushman, M.6
-
54
-
-
34447514125
-
Synthesis and anti-HIV activity of new metabolically stable alken-yldiarylmethane non-nucleoside reverse transcriptase inhibitors in-corporating N-methoxy imidoyl halide and 1,2,4-oxadiazole sys-tems
-
Sakamoto, T.; Cullen, M.D.; Hartman, T.L.; Watson, K.M.; Buck-heit, R.W.; Pannecouque, C.; De Clercq, E.; Cushman, M. Synthesis and anti-HIV activity of new metabolically stable alken-yldiarylmethane non-nucleoside reverse transcriptase inhibitors in-corporating N-methoxy imidoyl halide and 1,2,4-oxadiazole sys-tems. J. Med. Chem., 2007, 50, 3314-3321.
-
(2007)
J. Med. Chem
, vol.50
, pp. 3314-3321
-
-
Sakamoto, T.1
Cullen, M.D.2
Hartman, T.L.3
Watson, K.M.4
Buck-Heit, R.W.5
Pannecouque, C.6
De Clercq, E.7
Cushman, M.8
-
55
-
-
34948889252
-
Synthesisand biological evaluation of alkenyldiarylmethane HIV-1 non-nucleoside reverse transcriptase inhibitors that possess increasedhydrolytic stability
-
Cullen, M.D.; Deng, B.L.; Hartman, T.L.; Watson, K.M.; Buckheit, R.W.Jr.; Pannecouque, C.; De Clercq, E.; Cushman, M. Synthesisand biological evaluation of alkenyldiarylmethane HIV-1 non-nucleoside reverse transcriptase inhibitors that possess increasedhydrolytic stability. J. Med. Chem., 2007, 50, 4854-4867.
-
(2007)
J. Med. Chem
, vol.50
, pp. 4854-4867
-
-
Cullen, M.D.1
Deng, B.L.2
Hartman, T.L.3
Watson, K.M.4
Buckheit Jr., R.W.5
Pannecouque, C.6
De Clercq, E.7
Cushman, M.8
-
56
-
-
60549090996
-
Synthesisof alkenyldiarylmethanes (ADAMs) containing benzo [d]isoxazoleand oxazolidin-2-one rings, a new series of potent non-nucleosideHIV-1 reverse transcriptase inhibitors
-
Deng, B.L.; Zhao, Y.; Hartman, T.L.; Watson, K.; Buckheit, R.W.Jr.; Pannecouque, C.; De Clercq, E.; Cushman, M. Synthesisof alkenyldiarylmethanes (ADAMs) containing benzo [d]isoxazoleand oxazolidin-2-one rings, a new series of potent non-nucleosideHIV-1 reverse transcriptase inhibitors. Eur. J. Med. Chem., 2009,44, 1210-1214.
-
(2009)
Eur. J. Med. Chem
, vol.44
, pp. 1210-1214
-
-
Deng, B.L.1
Zhao, Y.2
Hartman, T.L.3
Watson, K.4
Buckheit Jr., R.W.5
Pannecouque, C.6
De Clercq, E.7
Cushman, M.8
-
57
-
-
32944470419
-
Synthesis and anti-HIV activity of new alkenyldiarylmethane(ADAM) non-nucleoside reverse transcriptase inhibitors (NNRTIs)incorporating benzoxazolone and benzisoxazole rings
-
Deng, B.L.; Cullen, M.D.; Zhou, Z.; Hartman, T.L.; Buckheit, R.W.Jr.; Pannecouque, C.; De Clercq, E.; Fanwick, P.E.; Cushman, M. Synthesis and anti-HIV activity of new alkenyldiarylmethane(ADAM) non-nucleoside reverse transcriptase inhibitors (NNRTIs)incorporating benzoxazolone and benzisoxazole rings. Bioorg MedChem., 2006, 14, 2366-2374.
-
(2006)
Bioorg MedChem
, vol.14
, pp. 2366-2374
-
-
Deng, B.L.1
Cullen, M.D.2
Zhou, Z.3
Hartman, T.L.4
Buckheit Jr., R.W.5
Pannecouque, C.6
de Clercq, E.7
Fanwick, P.E.8
Cushman, M.9
-
58
-
-
70350066155
-
Crystallographic study of a novel sub-nanomolar inhibitor provides insight on the binding interactions of alkenyldiarylmethanes with human immunodeficiency virus-1 re-verse transcriptase
-
Cullen, M.D.; Ho, W.C.; Bauman, J.D.; Das, K.; Arnold, E.; Hart-man, T.L.; Watson, K.M.; Buckheit, R.W.; Pannecouque, C.; DeClercq, E.; Cushman, M. Crystallographic study of a novel sub-nanomolar inhibitor provides insight on the binding interactions of alkenyldiarylmethanes with human immunodeficiency virus-1 re-verse transcriptase. J. Med. Chem., 2009, 52, 6467-6473.
-
(2009)
J. Med. Chem
, vol.52
, pp. 6467-6473
-
-
Cullen, M.D.1
Ho, W.C.2
Bauman, J.D.3
Das, K.4
Arnold, E.5
Hart-Man, T.L.6
Watson, K.M.7
Buckheit, R.W.8
Pannecouque, C.9
Declercq, E.10
Cushman, M.11
-
59
-
-
0030992580
-
Tetrahydron-aphthalene lignan compounds as potent anti-HIV type 1 agents
-
Hara, H.; Fujihashi, T.; Sakata, T.; Kaji, A.; Kaji, H. Tetrahydron-aphthalene lignan compounds as potent anti-HIV type 1 agents.AIDS Res. Hum. Retroviruses, 1997, 13, 695-705.
-
(1997)
AIDS Res. Hum. Retroviruses
, vol.13
, pp. 695-705
-
-
Hara, H.1
Fujihashi, T.2
Sakata, T.3
Kaji, A.4
Kaji, H.5
-
60
-
-
0035821597
-
2-Amino-6-arylsulfonylbenzo-nitriles as non-nucleoside reverse transcriptase inhibitors of HIV-1
-
Chan, J.H.; Hong, J.S.; Hunter, RN. 3rd.; Orr, G.F.; Cowan, J.R.; Sherman, D.B.; Sparks, S.M.; Reitter, B.E.; Andrews, CW 3rd.;Hazen, R.J.; St Clair, M.; Boone, L.R.; Ferris, R.G.; Creech, K.L.; Roberts, G.B.; Short, S.A.; Weaver, K.; Ott, R.J.; Ren, J.; Hopkins, A.; Stuart, D.I.; Stammers, D.K. 2-Amino-6-arylsulfonylbenzo-nitriles as non-nucleoside reverse transcriptase inhibitors of HIV-1.J. Med. Chem., 2001, 44, 1866-1882.
-
(2001)
J. Med. Chem
, vol.44
, pp. 1866-1882
-
-
Chan, J.H.1
Hong, J.S.2
Hunter, R.N.3
Orr, G.F.4
Cowan, J.R.5
Sherman, D.B.6
Sparks, S.M.7
Reitter, B.E.8
Andrews, C.W.9
Hazen, R.J.10
Clair St., M.11
Boone, L.R.12
Ferris, R.G.13
Creech, K.L.14
Roberts, G.B.15
Short, S.A.16
Weaver, K.17
Ott, R.J.18
Ren, J.19
Hopkins, A.20
Stuart, D.I.21
Stammers, D.K.22
more..
-
61
-
-
64349086788
-
Novel indazole non-nucleoside reverse transcriptase inhibitorsusing molecular hybridization based on crystallographic overlays
-
Jones, L.H.; Allan.; Barba, O.; Burt, C.; Corbau, R.; Dupont, T.; Kno chel, T.; Irving, S.; Middleton, D.S.; Mowbray, C.E.; Perros, M.; Ringrose, H.; Swain, N.A.; Webster, R.; Westby, M.; Phillips, C. Novel indazole non-nucleoside reverse transcriptase inhibitorsusing molecular hybridization based on crystallographic overlays.J. Med. Chem., 2009, 52, 1219-1223.
-
(2009)
J. Med. Chem
, vol.52
, pp. 1219-1223
-
-
Jones, L.H.1
Allan Barba, O.2
Burt, C.3
Corbau, R.4
Dupont, T.5
Kno Chel, T.6
Irving, S.7
Middleton, D.S.8
Mowbray, C.E.9
Perros, M.10
Ringrose, H.11
Swain, N.A.12
Webster, R.13
Westby, M.14
Phillips, C.15
-
62
-
-
0029041267
-
Benzophenone Derivatives: A Novel Series of Potent Andselective Inhibitors of Human Immunodeficiency Virus Type 1 Re-verse Transcriptase
-
Wyatt, P.G.; Bethell, R.C.; Cammack, N.; Charon, D.; Dodic, N.; Dumaitre, B.; Evans, D.N.; Green, D.V.; Hopewell, P.L.; Humber, D.C.; et al. Benzophenone derivatives: a novel series of potent andselective inhibitors of human immunodeficiency virus type 1 re-verse transcriptase. J. Med. Chem. 1995, 38, 1657-1665.
-
(1995)
J. Med. Chem
, vol.38
, pp. 1657-1665
-
-
Wyatt, P.G.1
Bethell, R.C.2
Cammack, N.3
Charon, D.4
Dodic, N.5
Dumaitre, B.6
Evans, D.N.7
Green, D.V.8
Hopewell, P.L.9
Humber, D.C.10
-
63
-
-
43049147306
-
The design and synthesis of diaryl ether second generationHIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs)with enhanced potency versus key clinical mutations
-
Tucker, T.J.; Saggar, S.; Sisko, J.T.; Tynebor, R.M.; Williams, T.M.; Felock, P.J.; Flynn, J.A.; Lai, M.T.; Liang, Y.; McGaughey, G.; Liu, M.; Miller, M.; Moyer, G.; Munshi, V.; Perlow-Poehnelt, R.; Prasad, S.; Sanchez, R.; Torrent, M.; Vacca, J.P.; Wan, B.L.; Yan, Y. The design and synthesis of diaryl ether second generationHIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs)with enhanced potency versus key clinical mutations. Bioorg. Med.Chem. Lett., 2008, 18, 2959-2966.
-
(2008)
Bioorg. Med.Chem. Lett
, vol.18
, pp. 2959-2966
-
-
Tucker, T.J.1
Saggar, S.2
Sisko, J.T.3
Tynebor, R.M.4
Williams, T.M.5
Felock, P.J.6
Flynn, J.A.7
Lai, M.T.8
Liang, Y.9
McGaughey, G.10
Liu, M.11
Miller, M.12
Moyer, G.13
Munshi, V.14
Perlow-Poehnelt, R.15
Prasad, S.16
Sanchez, R.17
Torrent, M.18
Vacca, J.P.19
Wan, B.L.20
Yan, Y.21
more..
-
64
-
-
0034615103
-
1-[2-(Diphenylmethoxy)ethyl]-2-methyl-5-nitroimida-zole: A potent lead for the design of novel NNRTIs
-
Silvestri, R.; Artico, M.; Massa, S.; Marceddu, T.; De Montis, F.;La Colla, P. 1-[2-(Diphenylmethoxy)ethyl]-2-methyl-5-nitroimida-zole: a potent lead for the design of novel NNRTIs. Bioorg. Med.Chem. Lett., 2000, 10, 253-256.
-
(2000)
Bioorg. Med.Chem. Lett
, vol.10
, pp. 253-256
-
-
Silvestri, R.1
Artico, M.2
Massa, S.3
Marceddu, T.4
De Montis, F.5
La Colla, P.6
-
65
-
-
36749018204
-
Privileged structures: Auseful concept for the rational design of new lead drug candidates
-
Duarte, C.D.; Barreiro, E.J.; Fraga, C.A. Privileged structures: auseful concept for the rational design of new lead drug candidates.Mini. Rev. Med. Chem., 2007, 7, 1108-1119.
-
(2007)
Mini. Rev. Med. Chem
, vol.7
, pp. 1108-1119
-
-
Duarte, C.D.1
Barreiro, E.J.2
Fraga, C.A.3
-
66
-
-
4243159924
-
Privileged structures: Applications in drug discovery
-
DeSimone, R.W.; Currie, K.S.; Mitchell, S.A.; Darrow, J.W.; Pip-pin, D.A. Privileged structures: applications in drug discovery.Comb. Chem. High Throughput Screen, 2004, 7, 473-494.
-
(2004)
Comb. Chem. High Throughput Screen
, vol.7
, pp. 473-494
-
-
Desimone, R.W.1
Currie, K.S.2
Mitchell, S.A.3
Darrow, J.W.4
Pip-Pin, D.A.5
-
67
-
-
63749103205
-
Fragment-based ligand discovery
-
Fischer, M.; Hubbard, R.E. Fragment-based ligand discovery. Mol.Interv., 2009, 9, 22-30.
-
(2009)
Mol.Interv
, vol.9
, pp. 22-30
-
-
Fischer, M.1
Hubbard, R.E.2
-
68
-
-
34547484265
-
Molecular hybridization: A useful tool in the de-sign of new drug prototypes
-
Viegas-Junior, C.; Danuello, A.; da Silva Bolzani, V.; Barreiro, E.J.; Fraga, C.A. Molecular hybridization: a useful tool in the de-sign of new drug prototypes. Curr. Med. Chem., 2007, 14, 1829-1852.
-
(2007)
Curr. Med. Chem
, vol.14
, pp. 1829-1852
-
-
Viegas-Junior, C.1
Danuello, A.2
da Silva Bolzani, V.3
Barreiro, E.J.4
Fraga, C.A.5
-
69
-
-
33646493006
-
Scaffold-hopping potential of ligand-based similarity concepts
-
Renner, S.; Schneider, G. Scaffold-hopping potential of ligand-based similarity concepts. ChemMedChem, 2006, 1, 181-185.
-
(2006)
ChemMedChem
, vol.1
, pp. 181-185
-
-
Renner, S.1
Schneider, G.2
-
70
-
-
0036285753
-
Synthesis of Substituted Diarylmethylenepiperidines(DAMPs), a Novel Class of Anti-HIV Agents
-
Xu, G.; Kannan, A.; Hartman, T.L.; Wargo, H.; Watson, K.; Turpin, J.A.; Buckheit, R.W.Jr.; Johnson, A.A.; Pommier, Y.; Cushman, M.Synthesis of substituted diarylmethylenepiperidines(DAMPs), a novel class of anti-HIV agents. Bioorg. Med. Chem.,2002, 10, 2807-2816.
-
(2002)
Bioorg. Med. Chem
, vol.10
, pp. 2807-2816
-
-
Xu, G.1
Kannan, A.2
Hartman, T.L.3
Wargo, H.4
Watson, K.5
Turpin, J.A.6
Buckheit Jr., R.W.7
Johnson, A.A.8
Pommier, Y.9
Cushman, M.10
-
71
-
-
38949192887
-
Investigation of The Alkenyldiarylmethane Non-nucleoside Reverse Transcriptase Inhibitors As Potential CAMP Phos-phodiesterase-4B2 Inhibitors
-
Cullen, M.D.; Cheung, Y.F.; Houslay, M.D.; Hartman, T.L.; Wat-son, K.M.; Buckheit, R.W.Jr.; Pannecouque, C.; De Clercq, E.; Cushman, M. Investigation of the alkenyldiarylmethane non-nucleoside reverse transcriptase inhibitors as potential cAMP phos-phodiesterase-4B2 inhibitors. Bioorg. Med. Chem. Lett., 2008, 18,1530-1533.
-
(2008)
Bioorg. Med. Chem. Lett
, vol.18
, pp. 1530-1533
-
-
Cullen, M.D.1
Cheung, Y.F.2
Houslay, M.D.3
Hartman, T.L.4
Wat-Son, K.M.5
Buckheit Jr., R.W.6
Pannecouque, C.7
De Clercq, E.8
Cushman, M.9
-
72
-
-
38349013226
-
Inhibition of tubulin polymerization by select alkenyldi-arylmethanes
-
Cullen, M.D.; Sarkar, T.; Hamel, E.; Hartman, T.L.; Watson, K.M.; Buckheit, R.W.Jr.; Pannecouque, C.; De Clercq, E.; Cushman, M.Inhibition of tubulin polymerization by select alkenyldi-arylmethanes. Bioorg. Med. Chem. Lett., 2008, 18, 469-473.
-
(2008)
Bioorg. Med. Chem. Lett
, vol.18
, pp. 469-473
-
-
Cullen, M.D.1
Sarkar, T.2
Hamel, E.3
Hartman, T.L.4
Watson, K.M.5
Buckheit Jr., R.W.6
Pannecouque, C.7
De Clercq, E.8
Cushman, M.9
-
73
-
-
0035825335
-
Inhibition of RANTES/CCR1-mediated chemo-taxis by cosalane and related compounds
-
Howard OM, Dong HF, Oppenheim JJ, Insaf S, Santhosh KC., Paul G., Cushman M. Inhibition of RANTES/CCR1-mediated chemo-taxis by cosalane and related compounds. Bioorg. Med. Chem.Lett., 2001, 11, 59-62.
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(2001)
Bioorg. Med. Chem.Lett
, vol.11
, pp. 59-62
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Howard, O.M.1
Dong, H.F.2
Oppenheim, J.J.3
Insaf, S.4
Santhosh, K.C.5
Paul, G.6
Cushman, M.7
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