-
1
-
-
84894094139
-
Development of novel potent orally bioavailable oseltamivir derivatives active against resistant influenza A
-
D. Schade, J. Kotthaus, L. Riebling, J. Kotthaus, H. Müller-Fielitz, W. Raasch, O. Koch, N. Seidel, M. Schmidtke, B. Clement, Development of novel potent orally bioavailable oseltamivir derivatives active against resistant influenza A, J. Med. Chem. 57 (2014) 759-769.
-
(2014)
J. Med. Chem.
, vol.57
, pp. 759-769
-
-
Schade, D.1
Kotthaus, J.2
Riebling, L.3
Kotthaus, J.4
Müller-Fielitz, H.5
Raasch, W.6
Koch, O.7
Seidel, N.8
Schmidtke, M.9
Clement, B.10
-
2
-
-
84929649290
-
Emergence of highly pathogenic avian influenza A (H5N1) virus PB1-F2 variants and their virulence in BALB/c mice
-
R.P. Kamal, A. Kumar, C. Davis, W.P. Tzeng, T. Nguyen, R.O. Donis, J.M. Kata, I.A. York, Emergence of highly pathogenic avian influenza A (H5N1) virus PB1-F2 variants and their virulence in BALB/c Mice, J. Virol. 89 (2015) 5835-5846.
-
(2015)
J. Virol.
, vol.89
, pp. 5835-5846
-
-
Kamal, R.P.1
Kumar, A.2
Davis, C.3
Tzeng, W.P.4
Nguyen, T.5
Donis, R.O.6
Kata, J.M.7
York, I.A.8
-
3
-
-
36949001617
-
Strategies of development of antiviral agents directed against influenza virus replication
-
H.P. Hsieh, J.T. Hsu, Strategies of development of antiviral agents directed against influenza virus replication, Curr. Pharm. Des. 13 (2007) 3531-3542.
-
(2007)
Curr. Pharm. Des.
, vol.13
, pp. 3531-3542
-
-
Hsieh, H.P.1
Hsu, J.T.2
-
4
-
-
84908389455
-
Discovery of N-substituted oseltamivir derivatives as potent and selective inhibitors of H5N1 influenza neuraminidase
-
Y.C. Xie, D.Q. Xu, B. Huang, X.L. Ma, W.B. Qi, F.Y. Shi, X.Y. Liu, Y.J. Zhang, W.F. Xu, Discovery of N-Substituted oseltamivir derivatives as potent and selective inhibitors of H5N1 influenza neuraminidase, J. Med. Chem. 57 (2014) 8445-8458.
-
(2014)
J. Med. Chem.
, vol.57
, pp. 8445-8458
-
-
Xie, Y.C.1
Xu, D.Q.2
Huang, B.3
Ma, X.L.4
Qi, W.B.5
Shi, F.Y.6
Liu, X.Y.7
Zhang, Y.J.8
Xu, W.F.9
-
5
-
-
84929027809
-
Influenza: The rational use of oseltamivir
-
H. Kelly, B.J. Cowling, Influenza: the rational use of oseltamivir, Lancet 385 (2015) 1700-1702.
-
(2015)
Lancet
, vol.385
, pp. 1700-1702
-
-
Kelly, H.1
Cowling, B.J.2
-
6
-
-
61849118968
-
Global transmission of oseltamivir-resistant influenza
-
A. Moscona, Global transmission of oseltamivir-resistant influenza, N. Engl. J. Med. 360 (2009) 953-956.
-
(2009)
N. Engl. J. Med.
, vol.360
, pp. 953-956
-
-
Moscona, A.1
-
8
-
-
84887926053
-
New 7-methylguanine derivatives targeting the influenza poly-merase PB2 cap-binding domain
-
S. Pautus, P. Sehr, J. Lewis, A. Fortunè, A. Wolkerstorfer, O. Szolar, D. Guilligay, T. Lunardi, J.L. Dècout, S. Cusack, New 7-methylguanine derivatives targeting the influenza poly-merase PB2 cap-binding domain, J. Med. Chem. 56 (2013) 8915-8930.
-
(2013)
J. Med. Chem.
, vol.56
, pp. 8915-8930
-
-
Pautus, S.1
Sehr, P.2
Lewis, J.3
Fortunè, A.4
Wolkerstorfer, A.5
Szolar, O.6
Guilligay, D.7
Lunardi, T.8
Dècout, J.L.9
Cusack, S.10
-
9
-
-
79956103650
-
CL-385319 inhibits H5N1 avian influenza A virus infection by blocking viral entry
-
S.W. Liu, R.M. Li, R.T. Zhang, C.C.S. Chan, B.M. Xi, Z.B. Zhu, J. Yang, V.K.M. Poon, J. Zhou, M. Chen, J. Münch, F. Kirchhoff, S. Pleschka, T. Haarmann, U. Dietrich, C.G. Pan, L.Y. Du, S.B. Jiang, B.J. Zheng, CL-385319 inhibits H5N1 avian influenza A virus infection by blocking viral entry, Eur. J. Pharmacol. 660 (2011) 460-467.
-
(2011)
Eur. J. Pharmacol.
, vol.660
, pp. 460-467
-
-
Liu, S.W.1
Li, R.M.2
Zhang, R.T.3
Chan, C.C.S.4
Xi, B.M.5
Zhu, Z.B.6
Yang, J.7
Poon, V.K.M.8
Zhou, J.9
Chen, M.10
Münch, J.11
Kirchhoff, F.12
Pleschka, S.13
Haarmann, T.14
Dietrich, U.15
Pan, C.G.16
Du, L.Y.17
Jiang, S.B.18
Zheng, B.J.19
-
10
-
-
84895064488
-
Emerging antiviral strategies to interfere with influenza virus entry
-
E. Vanderlinden, L. Naesens, Emerging antiviral strategies to interfere with influenza virus entry, Med. Res. Rev. 34 (2014) 301-339.
-
(2014)
Med. Res. Rev.
, vol.34
, pp. 301-339
-
-
Vanderlinden, E.1
Naesens, L.2
-
11
-
-
67349218766
-
An overview of influenza haemagglutinin and neuraminidase
-
J. Skehel, An overview of influenza haemagglutinin and neuraminidase, Biologicals 37 (2009) 177-178.
-
(2009)
Biologicals
, vol.37
, pp. 177-178
-
-
Skehel, J.1
-
12
-
-
84903835090
-
Functionalization, cyclization and antiviral activity of secotriterpenoids
-
V.V. Grishko, N.V. Galaiko, I.A. Tolmacheva, I.I. Kucherov, V.F. Eremin, E.I. Boreko, O.V. Savinova, P.A. Slepukhin, Functionalization, cyclization and antiviral activity of secotriterpenoids, Eur. J. Med. Chem. 83 (2014) 601-608.
-
(2014)
Eur. J. Med. Chem.
, vol.83
, pp. 601-608
-
-
Grishko, V.V.1
Galaiko, N.V.2
Tolmacheva, I.A.3
Kucherov, I.I.4
Eremin, V.F.5
Boreko, E.I.6
Savinova, O.V.7
Slepukhin, P.A.8
-
13
-
-
84911388077
-
Antitumor and antiviral activity of pentacyclic triterpenes
-
R. Paduch, M. Kandefer-Szerszen, Antitumor and antiviral activity of pentacyclic triterpenes, Mini-Rev. Org. Chem. 11 (2014) 262-268.
-
(2014)
Mini-Rev. Org. Chem.
, vol.11
, pp. 262-268
-
-
Paduch, R.1
Kandefer-Szerszen, M.2
-
14
-
-
84907225755
-
Conjugation of a nonspecific antiviral sapogenin with a specific HIV fusion inhibitor: A promising strategy for discovering new antiviral therapeutics
-
C. Wang, L. Lu, H.Y. Na, X.P. Li, Q. Wang, X.F. Jiang, X.F. Xu, F. Yu, T.H. Zhang, J.L. Li, Conjugation of a nonspecific antiviral sapogenin with a specific HIV fusion inhibitor: a promising strategy for discovering new antiviral therapeutics, J. Med. Chem. 54 (2014) 7342-7354.
-
(2014)
J. Med. Chem.
, vol.54
, pp. 7342-7354
-
-
Wang, C.1
Lu, L.2
Na, H.Y.3
Li, X.P.4
Wang, Q.5
Jiang, X.F.6
Xu, X.F.7
Yu, F.8
Zhang, T.H.9
Li, J.L.10
-
15
-
-
84879063655
-
Development of oleanane-type triterpenes as a new class of HCV entry inhibitors
-
F. Yu, Q. Wang, Z. Zhang, Y. Peng, Y. Qiu, Y. Shi, Y. Zheng, S. Xiao, H. Wang, X. Huang, L. Zhu, K. Chen, C. Zhao, C. Zhang, M. Yu, D. Sun, L. Zhang, D. Zhou, Development of oleanane-type triterpenes as a new class of HCV entry inhibitors, J. Med. Chem. 56 (2013) 4300-4319.
-
(2013)
J. Med. Chem.
, vol.56
, pp. 4300-4319
-
-
Yu, F.1
Wang, Q.2
Zhang, Z.3
Peng, Y.4
Qiu, Y.5
Shi, Y.6
Zheng, Y.7
Xiao, S.8
Wang, H.9
Huang, X.10
Zhu, L.11
Chen, K.12
Zhao, C.13
Zhang, C.14
Yu, M.15
Sun, D.16
Zhang, L.17
Zhou, D.18
-
16
-
-
84875202040
-
New betulinic acid derivatives for bevirimat-resistant human immunodeficiency vrus type-1
-
Z. Dang, P. Ho, L. Zhu, K.D. Qian, K.H. Lee, L. Huang, C.H. Chen, New betulinic acid derivatives for bevirimat-resistant human immunodeficiency vrus type-1, J. Med. Chem. 56 (2013) 2029-2037.
-
(2013)
J. Med. Chem.
, vol.56
, pp. 2029-2037
-
-
Dang, Z.1
Ho, P.2
Zhu, L.3
Qian, K.D.4
Lee, K.H.5
Huang, L.6
Chen, C.H.7
-
17
-
-
84896703583
-
Co-administration of betulinic acid and methamphetamine causes toxicity to dopaminergic and serotonergic nerve terminals in the striatum of late adolescent rats
-
B. Killinger, M. Shah, A. Moszczynska, Co-administration of betulinic acid and methamphetamine causes toxicity to dopaminergic and serotonergic nerve terminals in the striatum of late adolescent rats, J. Neurochem. 128 (2014) 764-775.
-
(2014)
J. Neurochem.
, vol.128
, pp. 764-775
-
-
Killinger, B.1
Shah, M.2
Moszczynska, A.3
-
18
-
-
84896536482
-
Development of bivalent oleanane-type triterpenes as potent HCV entry inhibitors
-
F. Yu, Y.Y. Peng, Q. Wang, Y.Y. Shi, L.L. Si, H. Wang, Y.X. Zheng, E. Lee, S.L. Xiao, M.R. Yu, Development of bivalent oleanane-type triterpenes as potent HCV entry inhibitors, Eur. J. Med. Chem. 77 (2014) 258-268.
-
(2014)
Eur. J. Med. Chem.
, vol.77
, pp. 258-268
-
-
Yu, F.1
Peng, Y.Y.2
Wang, Q.3
Shi, Y.Y.4
Si, L.L.5
Wang, H.6
Zheng, Y.X.7
Lee, E.8
Xiao, S.L.9
Yu, M.R.10
-
19
-
-
84899932631
-
Synthesis and anti-HCV entry activity studies of bcyclodextrin-pentacyclic triterpene conjugates
-
S.L. Xiao, Q. Wang, L.L. Si, Y.Y. Shi, H. Wang, F. Yu, Y.M. Zhang, Y.B. Li, Y.X. Zheng, L. Zhang, Synthesis and anti-HCV entry activity studies of bcyclodextrin-pentacyclic triterpene conjugates, Chem Med chem 9 (2014) 1060-1070.
-
(2014)
Chem Med Chem
, vol.9
, pp. 1060-1070
-
-
Xiao, S.L.1
Wang, Q.2
Si, L.L.3
Shi, Y.Y.4
Wang, H.5
Yu, F.6
Zhang, Y.M.7
Li, Y.B.8
Zheng, Y.X.9
Zhang, L.10
-
20
-
-
67349169731
-
Glycyrrhizin inhibits influenza A virus uptake into the cell
-
A. Wolkerstorfer, H. Kurz, N. Bachhofner, O.H.J. Szolar, Glycyrrhizin inhibits influenza A virus uptake into the cell, Antivir. Res. 83 (2009) 171-178.
-
(2009)
Antivir. Res.
, vol.83
, pp. 171-178
-
-
Wolkerstorfer, A.1
Kurz, H.2
Bachhofner, N.3
Szolar, O.H.J.4
-
21
-
-
84918496682
-
Discovery of pentacyclic triterpenoids as potential entry inhibitors of influenza viruses
-
M.R. Yu, L.L. Si, Y.F. Wang, Y.M. Wu, F. Yu, P.X. Jiao, Y.Y. Shi, H. Wang, S.L. Xiao, G. Fu, K. Tian, Y.T. Wang, Z.H. Guo, X.S. Ye, L.H. Zhang, D.M. Zhou, Discovery of pentacyclic triterpenoids as potential entry inhibitors of influenza viruses, J. Med. Chem. 57 (2014) 10058-10071.
-
(2014)
J. Med. Chem.
, vol.57
, pp. 10058-10071
-
-
Yu, M.R.1
Si, L.L.2
Wang, Y.F.3
Wu, Y.M.4
Yu, F.5
Jiao, P.X.6
Shi, Y.Y.7
Wang, H.8
Xiao, S.L.9
Fu, G.10
Tian, K.11
Wang, Y.T.12
Guo, Z.H.13
Ye, X.S.14
Zhang, L.H.15
Zhou, D.M.16
-
22
-
-
72249102363
-
Discovery of the first series of small molecule H5N1 entry inhibitors
-
G.P. Song, S. Yang, W. Zhang, Y.L. Cao, P. Wang, N. Ding, Z.H. Zhang, Y. Guo, Y.X. Li, Discovery of the first series of small molecule H5N1 entry inhibitors, J. Med. Chem. 52 (2009) 7368-7371.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 7368-7371
-
-
Song, G.P.1
Yang, S.2
Zhang, W.3
Cao, Y.L.4
Wang, P.5
Ding, N.6
Zhang, Z.H.7
Guo, Y.8
Li, Y.X.9
-
23
-
-
84861594223
-
Structure-activity relationships of saponin derivatives: A series of entry inhibitors for highly pathogenic H5N1 influenza virus
-
N. Ding, Q. Chen, W. Zhang, S.M. Ren, Y. Guo, Y.X. Li, Structure-activity relationships of saponin derivatives: a series of entry inhibitors for highly pathogenic H5N1 influenza virus, Eur. J. Med. Chem. 53 (2012) 316-326.
-
(2012)
Eur. J. Med. Chem.
, vol.53
, pp. 316-326
-
-
Ding, N.1
Chen, Q.2
Zhang, W.3
Ren, S.M.4
Guo, Y.5
Li, Y.X.6
-
24
-
-
84923563089
-
Structure-activity relationships of 3-O-β-chacotriosyl ursolic acid derivatives as novel H5N1 entry inhibitors
-
G.P. Song, X.T. Shen, S.M. Li, Y.B. Li, Y.P. Liu, Y.S. Zheng, R.H. Lin, J.H. Fan, H.M. Ye, S.W. Liu, Structure-activity relationships of 3-O-β-chacotriosyl ursolic acid derivatives as novel H5N1 entry inhibitors, Eur. J. Med. Chem. 93 (2015) 431-442.
-
(2015)
Eur. J. Med. Chem.
, vol.93
, pp. 431-442
-
-
Song, G.P.1
Shen, X.T.2
Li, S.M.3
Li, Y.B.4
Liu, Y.P.5
Zheng, Y.S.6
Lin, R.H.7
Fan, J.H.8
Ye, H.M.9
Liu, S.W.10
-
25
-
-
45749110639
-
Naturally occurring pentacyclic triterpenes as inhibitors of glycogen phosphorylase: Synthesis, structure-activity relationships, and X-ray crystallographic studies
-
X.A. Wen, H.B. Sun, J. Liu, K.G. Cheng, P. Zhang, L.Y. Zhang, J. Hao, L.Y. Zhang, P.Z. Ni, S.E. Zographos, D.D. Leonidas, K.M. Alexacou, T. Gimisis, J.M. Hayes, N.G. Oikonomakos, Naturally occurring pentacyclic triterpenes as inhibitors of glycogen phosphorylase: synthesis, structure-activity relationships, and X-ray crystallographic studies, J. Med. Chem. 51 (2008) 3540-3554.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 3540-3554
-
-
Wen, X.A.1
Sun, H.B.2
Liu, J.3
Cheng, K.G.4
Zhang, P.5
Zhang, L.Y.6
Hao, J.7
Zhang, L.Y.8
Ni, P.Z.9
Zographos, S.E.10
Leonidas, D.D.11
Alexacou, K.M.12
Gimisis, T.13
Hayes, J.M.14
Oikonomakos, N.G.15
-
26
-
-
69249235734
-
Oleanane-type triterpene oligoglycosides with pancreatic lipase inhibitory activity from the pericarps of sapindus rarak
-
T. Morikawa, Y.Y. Xie, Y. Asao, M. Okamoto, C. Yamashita, O. Muraoka, H. Matsuda, Y. Pongpiriyadacha, D. Yuan, M. Yoshikawa, Oleanane-type triterpene oligoglycosides with pancreatic lipase inhibitory activity from the pericarps of Sapindus rarak, Phytochemistry 70 (2009) 1166-1172.
-
(2009)
Phytochemistry
, vol.70
, pp. 1166-1172
-
-
Morikawa, T.1
Xie, Y.Y.2
Asao, Y.3
Okamoto, M.4
Yamashita, C.5
Muraoka, O.6
Matsuda, H.7
Pongpiriyadacha, Y.8
Yuan, D.9
Yoshikawa, M.10
-
27
-
-
84906504562
-
Sulfamates of methyl triterpenoates are effective and competitive inhibitors of carbonicanhydrase II
-
S. Schwarz, S. Sommerwerk, S.D. Lucas, L. Heller, R. Csuk, Sulfamates of methyl triterpenoates are effective and competitive inhibitors of carbonicanhydrase II, Eur. J. Med. Chem. 86 (2014) 95-102.
-
(2014)
Eur. J. Med. Chem.
, vol.86
, pp. 95-102
-
-
Schwarz, S.1
Sommerwerk, S.2
Lucas, S.D.3
Heller, L.4
Csuk, R.5
-
28
-
-
84929206646
-
Discovery of 3-O-β-chacotriosyl oleanane-type triterpenes as H5N1 entry inhibitors
-
G.P. Song, X.T. Shen, S.M. Li, H.Z. Si, Y.B. Li, H.Y. Luan, J.H. Fan, Q.Q. Liang, S.W. Liu, Discovery of 3-O-β-chacotriosyl oleanane-type triterpenes as H5N1 entry inhibitors, RSC Adv. 5 (2015) 39145-39154.
-
(2015)
RSC Adv.
, vol.5
, pp. 39145-39154
-
-
Song, G.P.1
Shen, X.T.2
Li, S.M.3
Si, H.Z.4
Li, Y.B.5
Luan, H.Y.6
Fan, J.H.7
Liang, Q.Q.8
Liu, S.W.9
-
29
-
-
84877079384
-
Synthesis and antitumor activities of naturally occurring oleanolic acid triterpenoid saponins and their derivatives
-
Q.C. Liu, H.C. Liu, L. Zhang, T.T. Guo, P. Wang, M.Y. Geng, Y.X. Li, Synthesis and antitumor activities of naturally occurring oleanolic acid triterpenoid saponins and their derivatives, Eur. J. Med. Chem. 64 (2013) 1-15.
-
(2013)
Eur. J. Med. Chem.
, vol.64
, pp. 1-15
-
-
Liu, Q.C.1
Liu, H.C.2
Zhang, L.3
Guo, T.T.4
Wang, P.5
Geng, M.Y.6
Li, Y.X.7
-
30
-
-
17344371121
-
Inhibition of influenza A virus replication by compounds interfering with the fusogenic function of the viral hemagglutinin
-
S.J. Plotch, B. O'Hara, J. Morin, O. Palant, J. LaRocque, J.D. Bloom, S.A. Lang, M.J. DiGrandi, M. Bradley, R. Nilakantan, Y. Gluzman, Inhibition of influenza A virus replication by compounds interfering with the fusogenic function of the viral hemagglutinin, J. Virol. 73 (1999) 140-151.
-
(1999)
J. Virol.
, vol.73
, pp. 140-151
-
-
Plotch, S.J.1
O'Hara, B.2
Morin, J.3
Palant, O.4
LaRocque, J.5
Bloom, J.D.6
Lang, S.A.7
DiGrandi, M.J.8
Bradley, M.9
Nilakantan, R.10
Gluzman, Y.11
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