-
1
-
-
0031048319
-
Influenza neuraminidase inhibitors possessing a novel hydrophobic interaction in the enzyme active site: Design, synthesis, and structural analysis of carbocyclic sialic acid analogues with potent anti-influenza activity
-
Kim, C. U.; Lew, W.; Williams, M. A.; Liu, H.; Zhang, L.; Swaminathan, S.; Bischofberger, N.; Chen, M. S.; Mendel, D. B.; Tai, C. Y.; Laver, W. G.; Stevens, R. C. Influenza neuraminidase inhibitors possessing a novel hydrophobic interaction in the enzyme active site: design, synthesis, and structural analysis of carbocyclic sialic acid analogues with potent anti-influenza activity. J. Am. Chem. Soc. 1997, 119, 681-690.
-
(1997)
J. Am. Chem. Soc
, vol.119
, pp. 681-690
-
-
Kim, C.U.1
Lew, W.2
Williams, M.A.3
Liu, H.4
Zhang, L.5
Swaminathan, S.6
Bischofberger, N.7
Chen, M.S.8
Mendel, D.B.9
Tai, C.Y.10
Laver, W.G.11
Stevens, R.C.12
-
2
-
-
15444353753
-
Structure - activity relationship studies of novel carbocyclic influenza neuraminidase inhibitors
-
Kim, C. U.; Lew, W.; Williams, M. A.; Wu, H.; Zhang, L.; Chen, X.; Escarpe, P. A.; Mendel, D. B.; Laver, W. G.; Stevens, R. C. Structure - activity relationship studies of novel carbocyclic influenza neuraminidase inhibitors. J. Med. Chem. 1998, 41, 2451-2460.
-
(1998)
J. Med. Chem
, vol.41
, pp. 2451-2460
-
-
Kim, C.U.1
Lew, W.2
Williams, M.A.3
Wu, H.4
Zhang, L.5
Chen, X.6
Escarpe, P.A.7
Mendel, D.B.8
Laver, W.G.9
Stevens, R.C.10
-
3
-
-
0034084227
-
Discovery and development of GS 4104 (oseltamivir): An orally active influenza neuraminidase inhibitor
-
Lew, W.; Chen, X.; Kim, C. U. Discovery and development of GS 4104 (oseltamivir): an orally active influenza neuraminidase inhibitor. Curr. Med. Chem. 2000, 7, 663-672.
-
(2000)
Curr. Med. Chem
, vol.7
, pp. 663-672
-
-
Lew, W.1
Chen, X.2
Kim, C.U.3
-
4
-
-
0035096415
-
Oseltamivir: A review of its use in influenza
-
McClellan, K.; Perry, C. M. Oseltamivir: a review of its use in influenza. Drugs 2001, 61, 263-283.
-
(2001)
Drugs
, vol.61
, pp. 263-283
-
-
McClellan, K.1
Perry, C.M.2
-
5
-
-
0027287506
-
Rational design of potent sialidase-based inhibitors of influenza virus replication
-
von Itzstein, M.; Wu, W.-Y.; Kok, G. B.; Pegg, M. S.; Dyason, J. C.; Jin, B.; Phan, T. V.; Smythe, M. L.; White, H. F.; Oliver, S. W.; Colman, P. M.; Varghese, J. N.; Ryan, D. M.; Woods, J. M.; Bethell, R. C.; Hotham, V. J.; Cameron, J. M.; Penn, C. R. Rational design of potent sialidase-based inhibitors of influenza virus replication. Nature 1993, 363, 418-423.
-
(1993)
Nature
, vol.363
, pp. 418-423
-
-
von Itzstein, M.1
Wu, W.-Y.2
Kok, G.B.3
Pegg, M.S.4
Dyason, J.C.5
Jin, B.6
Phan, T.V.7
Smythe, M.L.8
White, H.F.9
Oliver, S.W.10
Colman, P.M.11
Varghese, J.N.12
Ryan, D.M.13
Woods, J.M.14
Bethell, R.C.15
Hotham, V.J.16
Cameron, J.M.17
Penn, C.R.18
-
6
-
-
0028325249
-
Molecular modeling studies on ligand binding to salidase from influenza virus and the mechanism of catalysis
-
Taylor, N. R.; von Itzstein, M. Molecular modeling studies on ligand binding to salidase from influenza virus and the mechanism of catalysis. J. Med. Chem. 1994, 37, 616-624.
-
(1994)
J. Med. Chem
, vol.37
, pp. 616-624
-
-
Taylor, N.R.1
von Itzstein, M.2
-
7
-
-
0030044141
-
A study of the active site of influenza virus sialidase: An approach to the rational design of novel anti-influenza drugs
-
von Itzstein, M.; Dyason, J. C.; Oliver, S. W.; White, H. F.; Wu, W.-Y.; Kok, G. B.; Pegg, M. S. A study of the active site of influenza virus sialidase: an approach to the rational design of novel anti-influenza drugs. J. Med. Chem. 1996, 39, 388-391.
-
(1996)
J. Med. Chem
, vol.39
, pp. 388-391
-
-
von Itzstein, M.1
Dyason, J.C.2
Oliver, S.W.3
White, H.F.4
Wu, W.-Y.5
Kok, G.B.6
Pegg, M.S.7
-
8
-
-
0032710055
-
Zanamivir: A review of its use in influenza
-
Dunn, C. J.; Goa, K. L. Zanamivir: a review of its use in influenza. Drugs 1999, 58, 761-784.
-
(1999)
Drugs
, vol.58
, pp. 761-784
-
-
Dunn, C.J.1
Goa, K.L.2
-
9
-
-
25444501243
-
Neuraminidase inhibitors for influenza
-
Moscona, A. Neuraminidase inhibitors for influenza. N. Engl. J. Med. 2005, 353, 1363-1373.
-
(2005)
N. Engl. J. Med
, vol.353
, pp. 1363-1373
-
-
Moscona, A.1
-
10
-
-
33751517736
-
Antiviral agents actives against influenza A viruses
-
De Clercq, E. Antiviral agents actives against influenza A viruses. Nat. Rev. Drug Discovery 2006, 5, 1015-1025.
-
(2006)
Nat. Rev. Drug Discovery
, vol.5
, pp. 1015-1025
-
-
De Clercq, E.1
-
11
-
-
4644258940
-
Antiviral therapy for influenza
-
Schmidt, A. C. Antiviral therapy for influenza. Drugs 2004, 64, 2031-2046.
-
(2004)
Drugs
, vol.64
, pp. 2031-2046
-
-
Schmidt, A.C.1
-
12
-
-
0033897803
-
Resistance of influenza viruses to neuraminidase inhibitors - a review
-
McKimm-Breschkin, J. L. Resistance of influenza viruses to neuraminidase inhibitors - a review. Antiviral Res. 2000, 47, 1-17.
-
(2000)
Antiviral Res
, vol.47
, pp. 1-17
-
-
McKimm-Breschkin, J.L.1
-
13
-
-
0035190544
-
Comparison of the activities of zanamivir, oseltamivir, and RWJ-270201 against clinical isolates of influenza virus and neuraminidase inhibitor-resistant variants
-
Gubareva, L. V.; Webster, R. G.; Hayden, F. G. Comparison of the activities of zanamivir, oseltamivir, and RWJ-270201 against clinical isolates of influenza virus and neuraminidase inhibitor-resistant variants. Antimicrob. Agents Chemother. 2001, 48, 3403-3408.
-
(2001)
Antimicrob. Agents Chemother
, vol.48
, pp. 3403-3408
-
-
Gubareva, L.V.1
Webster, R.G.2
Hayden, F.G.3
-
14
-
-
29144528757
-
Oseltamivir resistance during treatment of influenza A (H5N1) infection
-
de Jong, M. D.; Tran, T. T.; Truong, H. K.; Vo, M.H.; Smith, G. J.; Nguyen, V. C.; Bach, V. C.; Phan, T. Q.; Do, Q. H.; Guan, Y.; Peiris, J. S.; Tran, T. H.; Farrar, J. Oseltamivir resistance during treatment of influenza A (H5N1) infection. N. Engl. J. Med. 2005, 353, 2667-2672.
-
(2005)
N. Engl. J. Med
, vol.353
, pp. 2667-2672
-
-
de Jong, M.D.1
Tran, T.T.2
Truong, H.K.3
Vo, M.H.4
Smith, G.J.5
Nguyen, V.C.6
Bach, V.C.7
Phan, T.Q.8
Do, Q.H.9
Guan, Y.10
Peiris, J.S.11
Tran, T.H.12
Farrar, J.13
-
15
-
-
29144433925
-
Oseltamivir resistance - disabling our influenza defenses
-
Anne Moscona, M. D. Oseltamivir resistance - disabling our influenza defenses. N. Engl. J. Med. 2005, 353, 2633-2636.
-
(2005)
N. Engl. J. Med
, vol.353
, pp. 2633-2636
-
-
Anne Moscona, M.D.1
-
16
-
-
27144468290
-
Isolation of drug-resistant H5N1 virus
-
Le, Q. M; Kiso, M.; Someya, K.; Sakai, Y. T.; Nguyen, T. H.; Nguyen, K. H.; Pham, N. D.; Ngyen, H. H.; Yamada, S.; Muramoto, Y.; Horimoto, T.; Takada, A.; Goto, H.; Suzuki, T.; Suzuki, Y.; Kawaoka, Y. Isolation of drug-resistant H5N1 virus. Nature 2005, 437, 1108.
-
(2005)
Nature
, vol.437
, pp. 1108
-
-
Le, Q.M.1
Kiso, M.2
Someya, K.3
Sakai, Y.T.4
Nguyen, T.H.5
Nguyen, K.H.6
Pham, N.D.7
Ngyen, H.H.8
Yamada, S.9
Muramoto, Y.10
Horimoto, T.11
Takada, A.12
Goto, H.13
Suzuki, T.14
Suzuki, Y.15
Kawaoka, Y.16
-
17
-
-
34848839869
-
Synthesis of tamiflu and its phosphonate congeners possessing potent anti-influenza activity
-
Shie, J.-J.; Fang, J.-M.; Wang, S.-Y.; Tsai, K.-C.; Cheng, E. Y.-S.; Yang, A.-S.; Hsiao, S.-C.; Su, C.-Y.; Wong, C.-H. Synthesis of tamiflu and its phosphonate congeners possessing potent anti-influenza activity. J. Am. Chem. Soc. 2007, 129, 11892-11893.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 11892-11893
-
-
Shie, J.-J.1
Fang, J.-M.2
Wang, S.-Y.3
Tsai, K.-C.4
Cheng, E.Y.-S.5
Yang, A.-S.6
Hsiao, S.-C.7
Su, C.-Y.8
Wong, C.-H.9
-
18
-
-
53549123019
-
A concise and flexible synthesis of the potent anti-influenza agents tamiflu and tamiphosphor
-
Shie, J.-J.; Fang, J.-M.; Wong, C.-H. A concise and flexible synthesis of the potent anti-influenza agents tamiflu and tamiphosphor. Angew. Chem., Int. Ed. 2008, 47, 5788-5791.
-
(2008)
Angew. Chem., Int. Ed
, vol.47
, pp. 5788-5791
-
-
Shie, J.-J.1
Fang, J.-M.2
Wong, C.-H.3
-
19
-
-
46249111790
-
Crystal structures of oseltamivir-resistant influenza virus neuraminidase mutants
-
Collins, P. J.; Haire, L. F.; Lin, Y. P.; Liu, J.; Russell, R. J.; Walker, P. A.; Skehel, J. J.; Martin, S. R.; Hay, A. J.; Gamblin, S. J. Crystal structures of oseltamivir-resistant influenza virus neuraminidase mutants. Nature 2008, 453, 1108-1261.
-
(2008)
Nature
, vol.453
, pp. 1108-1261
-
-
Collins, P.J.1
Haire, L.F.2
Lin, Y.P.3
Liu, J.4
Russell, R.J.5
Walker, P.A.6
Skehel, J.J.7
Martin, S.R.8
Hay, A.J.9
Gamblin, S.J.10
-
20
-
-
62149120632
-
Infections with oseltamivir-resistant influenza A (H1N1) virus in the United States
-
Dharan, N. J.; Gubareva, L. V.; Meyer, J. J.; Okomo-Adhiambo, M.; McClinton, R. C.; Marshall, S. A.; George, K.; Epperson, S.; Brammer, L.; Klimov, A. I.; Bresee, J. S.; Fry, A. M. Infections with oseltamivir-resistant influenza A (H1N1) virus in the United States. JAMA, J. Am. Med. Assoc. 2009, 301, 1034-1041.
-
(2009)
JAMA, J. Am. Med. Assoc
, vol.301
, pp. 1034-1041
-
-
Dharan, N.J.1
Gubareva, L.V.2
Meyer, J.J.3
Okomo-Adhiambo, M.4
McClinton, R.C.5
Marshall, S.A.6
George, K.7
Epperson, S.8
Brammer, L.9
Klimov, A.I.10
Bresee, J.S.11
Fry, A.M.12
-
21
-
-
62149112223
-
The evolution of influenza resistance and treatment
-
Weinstock, D.M.; Zuccotti, G. The evolution of influenza resistance and treatment. JAMA, J. Am. Med. Soc. 2009, 301, 1066-1069.
-
(2009)
JAMA, J. Am. Med. Soc
, vol.301
, pp. 1066-1069
-
-
Weinstock, D.M.1
Zuccotti, G.2
-
22
-
-
0032710063
-
Synthesis and influenza virus sialidase inhibitory activity of analogues of 4-guanidino-Neu5Ac2en (zanamivir) modified in the glycerol sidechain
-
Andrews, D. M.; Cherry, P. C.; Humber, D. C.; Jones, P. S.; Keeling, S. P.; Martin, P. F.; Shawa, C. D.; Swanson, S. Synthesis and influenza virus sialidase inhibitory activity of analogues of 4-guanidino-Neu5Ac2en (zanamivir) modified in the glycerol sidechain. Eur. J. Med. Chem. 1999, 34, 563-574.
-
(1999)
Eur. J. Med. Chem
, vol.34
, pp. 563-574
-
-
Andrews, D.M.1
Cherry, P.C.2
Humber, D.C.3
Jones, P.S.4
Keeling, S.P.5
Martin, P.F.6
Shawa, C.D.7
Swanson, S.8
-
23
-
-
0037025439
-
Synthesis and anti-influenza virus activity of 7-O-alkylated derivatives related zanamivir
-
Honda, T.; Masuda, T.; Yoshida, S.; Arai, M.; Kaneko, S.; Yamashita, M. Synthesis and anti-influenza virus activity of 7-O-alkylated derivatives related zanamivir. Bioorg. Med. Chem. Lett. 2002, 12, 1925-1928.
-
(2002)
Bioorg. Med. Chem. Lett
, vol.12
, pp. 1925-1928
-
-
Honda, T.1
Masuda, T.2
Yoshida, S.3
Arai, M.4
Kaneko, S.5
Yamashita, M.6
-
24
-
-
0020629047
-
Structure of the influenza virus glycoprotein antigen neuraminidase at 2.9 Å resolution
-
Varghese, J. N.; Laver, W. G.; Colman, P. M. Structure of the influenza virus glycoprotein antigen neuraminidase at 2.9 Å resolution. Nature 1983, 303, 35-40.
-
(1983)
Nature
, vol.303
, pp. 35-40
-
-
Varghese, J.N.1
Laver, W.G.2
Colman, P.M.3
-
25
-
-
0020633096
-
Structure of the catalytic and antigenic sites in the influenza virus neuraminidase
-
Colman, P. M.; Varghese, J. N.; Laver, W. G. Structure of the catalytic and antigenic sites in the influenza virus neuraminidase. Nature 1983, 303, 41-44.
-
(1983)
Nature
, vol.303
, pp. 41-44
-
-
Colman, P.M.1
Varghese, J.N.2
Laver, W.G.3
-
26
-
-
9644275467
-
-
Macdonald, S. J. F.; Watson, K. G.; Cameron, R.; Chalmers, D. K.; Demaine, D. A.; Fenton, R. J.; Gower, D.; Hamblin, J. N.; Hamilton, S.; Hart, G. J.; Inglis, G. G. A.; Jin, B.; Jones, H. T.; McConnell, D. B.; Mason, A. M.; Nguyen, V.; Owens, I. J.; Parry, N.; Reece, P. A.; Shanahan, S. E.; Smith, D.; Wu, W.-Y.; Tucker, S. P. Potent and long-acting dimeric inhibitors of influenza virus neuraminidase are effective at a once-weekly dosing regimen. Antimicrob. Agents Chemother. 2004, 48, 4542-4549.
-
Macdonald, S. J. F.; Watson, K. G.; Cameron, R.; Chalmers, D. K.; Demaine, D. A.; Fenton, R. J.; Gower, D.; Hamblin, J. N.; Hamilton, S.; Hart, G. J.; Inglis, G. G. A.; Jin, B.; Jones, H. T.; McConnell, D. B.; Mason, A. M.; Nguyen, V.; Owens, I. J.; Parry, N.; Reece, P. A.; Shanahan, S. E.; Smith, D.; Wu, W.-Y.; Tucker, S. P. Potent and long-acting dimeric inhibitors of influenza virus neuraminidase are effective at a once-weekly dosing regimen. Antimicrob. Agents Chemother. 2004, 48, 4542-4549.
-
-
-
-
27
-
-
10744221268
-
Highly potent and long-acting trimeric and tetrameric inhibitors of influenza virus neuraminidase
-
Watson, K. G.; Cameron, R.; Fenton, R. J.; Gower, D.; Hamilton, S.; Jin, B.; Krippner, G. Y.; Luttick, A.; McConnell, D.; Macdonald, S. J. F.; Mason, A. M.; Nguyen, V.; Tucker, S. P.; Wu, W.-Y. Highly potent and long-acting trimeric and tetrameric inhibitors of influenza virus neuraminidase. Bioorg. Med. Chem. Lett. 2004, 14, 1589-1592.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 1589-1592
-
-
Watson, K.G.1
Cameron, R.2
Fenton, R.J.3
Gower, D.4
Hamilton, S.5
Jin, B.6
Krippner, G.Y.7
Luttick, A.8
McConnell, D.9
Macdonald, S.J.F.10
Mason, A.M.11
Nguyen, V.12
Tucker, S.P.13
Wu, W.-Y.14
-
28
-
-
20944450978
-
-
Macdonald, S. J.; Cameron, R.; Demaine, D. A.; Fenton, R. J.; Foster, G.; Gower, D.; Hamblin, J. N.; Hamilton, S.; Hart, G. J.; Hill, A. P.; Inglis, G. G. A.; Jin, B.; Jones, H. T.; McConnell, D. B.; McKimm-Breschkin, J.; Mills, G.; Nguyen, V.; Owens, I. J.; Parry, N.; Shanahan, S. E.; Smith, D.; Watson, K. G.; Wu, W. Y.; Tucker, S. P. Dimeric zanamivir conjugates with various linking groups are potent, long-lasting inhibitors of influenza neuraminidase including H5N1 avian influenza. J. Med. Chem. 2005, 48, 2964-2971.
-
Macdonald, S. J.; Cameron, R.; Demaine, D. A.; Fenton, R. J.; Foster, G.; Gower, D.; Hamblin, J. N.; Hamilton, S.; Hart, G. J.; Hill, A. P.; Inglis, G. G. A.; Jin, B.; Jones, H. T.; McConnell, D. B.; McKimm-Breschkin, J.; Mills, G.; Nguyen, V.; Owens, I. J.; Parry, N.; Shanahan, S. E.; Smith, D.; Watson, K. G.; Wu, W. Y.; Tucker, S. P. Dimeric zanamivir conjugates with various linking groups are potent, long-lasting inhibitors of influenza neuraminidase including H5N1 avian influenza. J. Med. Chem. 2005, 48, 2964-2971.
-
-
-
-
29
-
-
59749091876
-
CS-8958, a prodrug of the new neuraminidase inhibitor R-125489, shows long-acting anti-influenza virus activity
-
Yamashita, M.; Tomozawa, T.; Kakuta, M.; Tokumitsu, A.; Nasu, H.; Kubo, S. CS-8958, a prodrug of the new neuraminidase inhibitor R-125489, shows long-acting anti-influenza virus activity. Antimicrob. Agents Chemother. 2009, 53, 186-192.
-
(2009)
Antimicrob. Agents Chemother
, vol.53
, pp. 186-192
-
-
Yamashita, M.1
Tomozawa, T.2
Kakuta, M.3
Tokumitsu, A.4
Nasu, H.5
Kubo, S.6
-
30
-
-
3142767850
-
Synthesis and anti-influenza evaluation of polyvalent salidase inhibitors bearing 4-guanidino-Neu5Ac2en derivatives
-
Masuda, T.; Yoshida, S.; Arai, M.; Kanedo, S.; Yamashita, M.; Honda, T. Synthesis and anti-influenza evaluation of polyvalent salidase inhibitors bearing 4-guanidino-Neu5Ac2en derivatives. Chem. Pharm. Bull. 2003, 51, 1386-1398.
-
(2003)
Chem. Pharm. Bull
, vol.51
, pp. 1386-1398
-
-
Masuda, T.1
Yoshida, S.2
Arai, M.3
Kanedo, S.4
Yamashita, M.5
Honda, T.6
-
31
-
-
11944260641
-
Photosensitizers of the porphyrin and phthalocyanine series for photodynamic therapy
-
Bonnett, R. Photosensitizers of the porphyrin and phthalocyanine series for photodynamic therapy. Chem. Soc. Rev. 1995, 24, 19-33.
-
(1995)
Chem. Soc. Rev
, vol.24
, pp. 19-33
-
-
Bonnett, R.1
-
33
-
-
16244383546
-
Mechanism in photodynamic therapy: Part one - photosensitizers, photochemistry and cellular localization
-
Castano, A. P.; Demidova, T. N.; Hambline, M. R. Mechanism in photodynamic therapy: part one - photosensitizers, photochemistry and cellular localization. Photodiagn. Photodynam. Ther. 2004, 1, 279-293.
-
(2004)
Photodiagn. Photodynam. Ther
, vol.1
, pp. 279-293
-
-
Castano, A.P.1
Demidova, T.N.2
Hambline, M.R.3
-
34
-
-
3042779537
-
Photodynamic therapy: A new anti-microbial approach to infectious disease?
-
Hamblin, M. R.; Hasan, T. Photodynamic therapy: a new anti-microbial approach to infectious disease?. Photochem. Photobiol. Sci. 2004, 3, 436-450.
-
(2004)
Photochem. Photobiol. Sci
, vol.3
, pp. 436-450
-
-
Hamblin, M.R.1
Hasan, T.2
-
35
-
-
30344462349
-
The potential for photodynamic therapy in the treatment of localized infections
-
O'Riordan, K.; Akilov, O. E.; Hasan, T. The potential for photodynamic therapy in the treatment of localized infections. Photodiagn. Photodynam. Ther. 2005, 2, 247-262.
-
(2005)
Photodiagn. Photodynam. Ther
, vol.2
, pp. 247-262
-
-
O'Riordan, K.1
Akilov, O.E.2
Hasan, T.3
-
36
-
-
14744297285
-
Antibody-targeted photolysis of bacteria in vivo
-
Berthiaume, F.; Reiken, S.; Toner, M.; Tompkins, R.; Yarmush, M. Antibody-targeted photolysis of bacteria in vivo. Biotechnology 1994, 12, 703-706.
-
(1994)
Biotechnology
, vol.12
, pp. 703-706
-
-
Berthiaume, F.1
Reiken, S.2
Toner, M.3
Tompkins, R.4
Yarmush, M.5
-
37
-
-
3042818896
-
Photoinactivation of Viruses
-
Wainwright, M. Photoinactivation of Viruses. Photochem. Photobiol. Sci. 2004, 3, 406-411.
-
(2004)
Photochem. Photobiol. Sci
, vol.3
, pp. 406-411
-
-
Wainwright, M.1
-
38
-
-
0026526708
-
Clinical effects of photodynamic therapy on recurrent laryngeal papillomas
-
Abramson, A. L.; Shikowitz, M. J.; Mullooly, V. M.; Steinberg, B. M.; Amella, C. A.; Rothstein, H. R. Clinical effects of photodynamic therapy on recurrent laryngeal papillomas. Arch. Otolaryngol. Head Neck Surg. 1992, 118, 25-29.
-
(1992)
Arch. Otolaryngol. Head Neck Surg
, vol.118
, pp. 25-29
-
-
Abramson, A.L.1
Shikowitz, M.J.2
Mullooly, V.M.3
Steinberg, B.M.4
Amella, C.A.5
Rothstein, H.R.6
-
39
-
-
0031776126
-
Efficacy of DHE photodynamic therapy for respiratory papillomatosis: Immediate and long-term results
-
Shikowitz, M, J.; Abramson, A. L.; Freeman, K.; Steinberg, B. M.; Nouri, M. Efficacy of DHE photodynamic therapy for respiratory papillomatosis: immediate and long-term results. Laryngoscope 1998, 108, 962-967.
-
(1998)
Laryngoscope
, vol.108
, pp. 962-967
-
-
Shikowitz, M.J.1
Abramson, A.L.2
Freeman, K.3
Steinberg, B.M.4
Nouri, M.5
-
40
-
-
13444262220
-
Clinical trial of photodynamic therapy with meso-tetra (hydroxyphenul) chlorin for respiratory papillomatosis
-
Shikowitz, M. J.; Abramson, A. L.; Steinberg, B. M.; DeVoti, J.; Bonagura, V. R.; Mullooly, V.; Nouri, M.; Ronn, A. M.; Inglis, A.; McClay, J.; Kathrine Freeman, K. Clinical trial of photodynamic therapy with meso-tetra (hydroxyphenul) chlorin for respiratory papillomatosis. Arch. Otolaryngol. Head Neck Surg. 2005, 131, 99-105.
-
(2005)
Arch. Otolaryngol. Head Neck Surg
, vol.131
, pp. 99-105
-
-
Shikowitz, M.J.1
Abramson, A.L.2
Steinberg, B.M.3
DeVoti, J.4
Bonagura, V.R.5
Mullooly, V.6
Nouri, M.7
Ronn, A.M.8
Inglis, A.9
McClay, J.10
Kathrine Freeman, K.11
-
41
-
-
37049084551
-
-
Chandler, M.; Bamford, M. J.; Conroy, R.; Lamont, B.; Patel, B.; Patel, V. K.; Steeples, I. P.; Storer, R.; Weir, N. G.; Wright, M.; Williamson, C. J. Synthesis of the potent influenza neuraminidase inhibitor 4-guanidino Neu5Ac2en. X-Ray molecular structure of 5-acetamido-4-amino-2,6-anhydro-3,4,5-trideoxy-D- erythro-L-gluconononic acid. J. Chem. Soc., Perkin Trans. 1995, 1, 1173-1180.
-
Chandler, M.; Bamford, M. J.; Conroy, R.; Lamont, B.; Patel, B.; Patel, V. K.; Steeples, I. P.; Storer, R.; Weir, N. G.; Wright, M.; Williamson, C. J. Synthesis of the potent influenza neuraminidase inhibitor 4-guanidino Neu5Ac2en. X-Ray molecular structure of 5-acetamido-4-amino-2,6-anhydro-3,4,5-trideoxy-D- erythro-L-gluconononic acid. J. Chem. Soc., Perkin Trans. 1995, 1, 1173-1180.
-
-
-
-
42
-
-
26944484395
-
One-bead-one-inhibitor-one-substrate screening of neuraminidase activity
-
Ying, L.; Gervay-Hague, J. One-bead-one-inhibitor-one-substrate screening of neuraminidase activity. ChemBioChem 2005, 6, 1857-1865.
-
(2005)
ChemBioChem
, vol.6
, pp. 1857-1865
-
-
Ying, L.1
Gervay-Hague, J.2
-
43
-
-
0037099395
-
A stepwise Huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
-
Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. Angew. Chem., Int. Ed. 2002, 41, 2596-2599.
-
(2002)
Angew. Chem., Int. Ed
, vol.41
, pp. 2596-2599
-
-
Rostovtsev, V.V.1
Green, L.G.2
Fokin, V.V.3
Sharpless, K.B.4
-
44
-
-
33744966628
-
A new solvent system for efficient synthesis of 1,2,3-triazoles
-
Lee, B.-Y.; Parka, S. R.; Jeon, H. B.; Kim, K. S. A new solvent system for efficient synthesis of 1,2,3-triazoles. Tetrahedron Lett. 2006, 47, 5105-5109.
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 5105-5109
-
-
Lee, B.-Y.1
Parka, S.R.2
Jeon, H.B.3
Kim, K.S.4
-
45
-
-
0000358206
-
Carbohydrate - protein interactions: Basis of glycobiology
-
Lee, Y. C.; Lee, R. T. Carbohydrate - protein interactions: basis of glycobiology. Acc. Chem. Res. 1995, 28, 321-327.
-
(1995)
Acc. Chem. Res
, vol.28
, pp. 321-327
-
-
Lee, Y.C.1
Lee, R.T.2
-
46
-
-
0032476812
-
Polyvalent interactions in biological systems: Implications for design and use of multivalent ligands and inhibitors
-
Mammen, M.; Choi, S. K.; Whitesides, G. M. Polyvalent interactions in biological systems: implications for design and use of multivalent ligands and inhibitors. Angew. Chem., Int. Ed. 1998, 37, 2755-2794.
-
(1998)
Angew. Chem., Int. Ed
, vol.37
, pp. 2755-2794
-
-
Mammen, M.1
Choi, S.K.2
Whitesides, G.M.3
-
47
-
-
0036462602
-
The cluster glycoside effect
-
Lundquist, J. J.; Toone, E. J. The cluster glycoside effect. Chem. Rev. 2002, 102, 555-578.
-
(2002)
Chem. Rev
, vol.102
, pp. 555-578
-
-
Lundquist, J.J.1
Toone, E.J.2
-
48
-
-
33744780166
-
Roles of neuraminidase in the initial stage of influenza virus infection
-
Ohuchi, M.; Asaoka, N.; Sakoi, T.; Ohuchi, R. Roles of neuraminidase in the initial stage of influenza virus infection. Microb. Infect. 2006, 8, 1287-1293.
-
(2006)
Microb. Infect
, vol.8
, pp. 1287-1293
-
-
Ohuchi, M.1
Asaoka, N.2
Sakoi, T.3
Ohuchi, R.4
-
49
-
-
56949102614
-
Origins and evolution of "controlled" drug delivery systems
-
Hoffman, A. S Origins and evolution of "controlled" drug delivery systems. J. Controlled Release 2008, 132, 153-163.
-
(2008)
J. Controlled Release
, vol.132
, pp. 153-163
-
-
Hoffman, A.S.1
-
50
-
-
64249112661
-
Current constructs and targets in clinical development for antibody-based cancer therapy
-
Deckert, P. M. Current constructs and targets in clinical development for antibody-based cancer therapy. Curr. Drug Targets 2009, 10, 158-175.
-
(2009)
Curr. Drug Targets
, vol.10
, pp. 158-175
-
-
Deckert, P.M.1
-
51
-
-
34247884233
-
An efficient F-18 labeling method for PET study: Huisgen 1,3-dipolar cycloaddition of bioactive substances and F-18-labeled compounds
-
Sirion, U.; Kim, H. J.; Lee, J. H.; Seo, J. W.; Lee, B. S.; Lee, S. J.; Oh, S. J.; Chi, D. Y. An efficient F-18 labeling method for PET study: Huisgen 1,3-dipolar cycloaddition of bioactive substances and F-18-labeled compounds. Tetrahedron Lett. 2007, 48, 3953-3957.
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 3953-3957
-
-
Sirion, U.1
Kim, H.J.2
Lee, J.H.3
Seo, J.W.4
Lee, B.S.5
Lee, S.J.6
Oh, S.J.7
Chi, D.Y.8
-
52
-
-
34249685481
-
Synthesis and evaluation of homo-bivalent GnRHR ligands
-
Bonger, K. M.; van den Berg, R. J. B. H. N.; Heitman, L. H.; Ijzerman, A. P.; Oosterom, J.; Timmers, C. M.; Overkleeft, H. S.; van der Marel, G. A. Synthesis and evaluation of homo-bivalent GnRHR ligands. Bioorg. Med. Chem. 2007, 15, 4841-4856.
-
(2007)
Bioorg. Med. Chem
, vol.15
, pp. 4841-4856
-
-
Bonger, K.M.1
van den Berg, R.J.B.H.N.2
Heitman, L.H.3
Ijzerman, A.P.4
Oosterom, J.5
Timmers, C.M.6
Overkleeft, H.S.7
van der Marel, G.A.8
-
53
-
-
33745158157
-
A simple method of estimating fifty percent endpoints
-
Reed, L. J.; Muench, H. A simple method of estimating fifty percent endpoints. Am. J. Hyg. 1938, 27, 493-497.
-
(1938)
Am. J. Hyg
, vol.27
, pp. 493-497
-
-
Reed, L.J.1
Muench, H.2
-
54
-
-
0004221581
-
-
Academic Press: San Diego, CA
-
Burleson, F. G.; Chambers, T. M.; Wiedbrauk, D. L. Virology, a Laboratory Manual; Academic Press: San Diego, CA, 1992.
-
(1992)
Virology, a Laboratory Manual
-
-
Burleson, F.G.1
Chambers, T.M.2
Wiedbrauk, D.L.3
|