메뉴 건너뛰기




Volumn 57, Issue 17, 2014, Pages 7342-7354

Conjugation of a nonspecific antiviral sapogenin with a specific HIV fusion Inhibitor: A promising strategy for discovering new antiviral therapeutics

Author keywords

[No Author keywords available]

Indexed keywords

3BETA(PENT 4' YNOYLOXY)LUP 20(29) EN 28 OIC ACID; 3BETA(PENT 4' YNOYLOXY)OLEAN 12 EN 28 OIC ACID; 3BETA(PENT 4' YNOYLOXY)URS 12 EN 28 OIC ACID; ALLYL 3BETA(PENT 4' YNOYLOXY)LUP 20(29) EN 28 OATE; ALLYL 3BETA(PENT 4' YNOYLOXY)OLEAN 12 EN 28 OATE; ALLYL 3BETA(PENT 4' YNOYLOXY)URS 12 EN 28 OATE; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; ENFUVIRTIDE; PROP 2' YNYL 3BETA ACETOXYLUP 20(29) EN 28 OATE; PROP 2' YNYL 3BETA HYDROXYLUP 20(29) EN 28 OATE; PROP 2' YNYL 3BETA HYDROXYOLEAN 12 EN 28 OATE; PROP 2' YNYL 3BETA HYDROXYURS 12 EN 28 OATE; SAPOGENIN; UNCLASSIFIED DRUG; ZIDOVUDINE; ANTIVIRUS AGENT; GLYCOPROTEIN GP 41; HUMAN IMMUNODEFICIENCY VIRUS FUSION INHIBITOR; PEPTIDE FRAGMENT;

EID: 84907225755     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm500763m     Document Type: Article
Times cited : (40)

References (54)
  • 1
    • 77449151492 scopus 로고    scopus 로고
    • HIV-1 gp41 fusion intermediate: A target for HIV therapeutics
    • Pan, C.; Liu, S.; Jiang, S. HIV-1 gp41 fusion intermediate: a target for HIV therapeutics J. Formosan Med. Assoc. 2010, 109 (2) 94-105
    • (2010) J. Formosan Med. Assoc. , vol.109 , Issue.2 , pp. 94-105
    • Pan, C.1    Liu, S.2    Jiang, S.3
  • 2
    • 78349299437 scopus 로고    scopus 로고
    • Development of peptide and small-molecule HIV-1 fusion inhibitors that target gp41
    • Cai, L.; Jiang, S. Development of peptide and small-molecule HIV-1 fusion inhibitors that target gp41 ChemMedChem 2010, 5 (11) 1813-1824
    • (2010) ChemMedChem , vol.5 , Issue.11 , pp. 1813-1824
    • Cai, L.1    Jiang, S.2
  • 4
  • 6
    • 84857363079 scopus 로고    scopus 로고
    • Is there a future for antiviral fusion inhibitors?
    • Berkhout, B.; Eggink, D.; Sanders, R. W. Is there a future for antiviral fusion inhibitors? Curr. Opin. Virol. 2012, 2, 50-59
    • (2012) Curr. Opin. Virol. , vol.2 , pp. 50-59
    • Berkhout, B.1    Eggink, D.2    Sanders, R.W.3
  • 8
    • 0030970693 scopus 로고    scopus 로고
    • Core structure of gp41 from the HIV envelope glycoprotein
    • Chan, D. C.; Fass, D.; Berger, J. M.; Kim, P. S. Core structure of gp41 from the HIV envelope glycoprotein Cell 1997, 89, 263-273
    • (1997) Cell , vol.89 , pp. 263-273
    • Chan, D.C.1    Fass, D.2    Berger, J.M.3    Kim, P.S.4
  • 9
    • 0032577550 scopus 로고    scopus 로고
    • HIV entry and its inhibition
    • Chan, D. C.; Kim, P. S. HIV entry and its inhibition Cell 1998, 93, 681-684
    • (1998) Cell , vol.93 , pp. 681-684
    • Chan, D.C.1    Kim, P.S.2
  • 10
    • 0035900003 scopus 로고    scopus 로고
    • HIV-1 gp41 six-helix bundle formation occurs rapidly after the engagement of gp120 by CXCR4 in the HIV-1 Env-mediated fusion process
    • Gallo, S. A.; Puri, A.; Blumenthal, R. HIV-1 gp41 six-helix bundle formation occurs rapidly after the engagement of gp120 by CXCR4 in the HIV-1 Env-mediated fusion process Biochemistry (Moscow) 2001, 40, 12231-12236
    • (2001) Biochemistry (Moscow) , vol.40 , pp. 12231-12236
    • Gallo, S.A.1    Puri, A.2    Blumenthal, R.3
  • 11
    • 79956045703 scopus 로고    scopus 로고
    • Insights into the mechanism of HIV-1 envelope induced membrane fusion as revealed by its inhibitory peptides
    • Ashkenazi, A.; Shai, Y. Insights into the mechanism of HIV-1 envelope induced membrane fusion as revealed by its inhibitory peptides Eur. Biophys. J. 2011, 40 (4) 349-357
    • (2011) Eur. Biophys. J. , vol.40 , Issue.4 , pp. 349-357
    • Ashkenazi, A.1    Shai, Y.2
  • 13
    • 0036223198 scopus 로고    scopus 로고
    • Peptide and non-peptide HIV fusion inhibitors
    • Jiang, S.; Zhao, Q.; Debnath, A. K. Peptide and non-peptide HIV fusion inhibitors Curr. Pharm. Des. 2002, 8, 563-580
    • (2002) Curr. Pharm. Des. , vol.8 , pp. 563-580
    • Jiang, S.1    Zhao, Q.2    Debnath, A.K.3
  • 14
    • 0027959493 scopus 로고
    • Peptides corresponding to a predictive alpha-helical domain of human immunodeficiency virus type 1 gp41 are potent inhibitors of virus infection
    • Wild, C. T.; Shugars, D. C.; Greenwell, T. K.; McDanal, C. B.; Matthews, T. J. Peptides corresponding to a predictive alpha-helical domain of human immunodeficiency virus type 1 gp41 are potent inhibitors of virus infection Proc. Natl. Acad. Sci. U. S. A. 1994, 91, 9770-9774
    • (1994) Proc. Natl. Acad. Sci. U. S. A. , vol.91 , pp. 9770-9774
    • Wild, C.T.1    Shugars, D.C.2    Greenwell, T.K.3    McDanal, C.B.4    Matthews, T.J.5
  • 16
    • 57649155175 scopus 로고    scopus 로고
    • Rationally designed anti-HIV peptides containing multifunctional domains as molecule probes for studying the mechanisms of action of the first and second generation HIV fusion inhibitors
    • Qi, Z.; Shi, W.; Xue, N.; Pan, C.; Jing, W.; Liu, K.; Jiang, S. Rationally designed anti-HIV peptides containing multifunctional domains as molecule probes for studying the mechanisms of action of the first and second generation HIV fusion inhibitors J. Biol. Chem. 2008, 283 (44) 30376-30384
    • (2008) J. Biol. Chem. , vol.283 , Issue.44 , pp. 30376-30384
    • Qi, Z.1    Shi, W.2    Xue, N.3    Pan, C.4    Jing, W.5    Liu, K.6    Jiang, S.7
  • 17
    • 34248155890 scopus 로고    scopus 로고
    • HIV gp41 C-terminal heptad repeat contains multifunctional domains. Relation to mechanisims of action of anti-HIV peptides
    • Liu, S.; Jing, W.; Cheung, B.; Lu, H.; Sun, J.; Yan, X.; Niu, J.; Farmar, J.; Wu, S.; Jiang, S. HIV gp41 C-terminal heptad repeat contains multifunctional domains. Relation to mechanisims of action of anti-HIV peptides J. Biol. Chem. 2007, 282 (13) 9612-9620
    • (2007) J. Biol. Chem. , vol.282 , Issue.13 , pp. 9612-9620
    • Liu, S.1    Jing, W.2    Cheung, B.3    Lu, H.4    Sun, J.5    Yan, X.6    Niu, J.7    Farmar, J.8    Wu, S.9    Jiang, S.10
  • 21
    • 80052059686 scopus 로고    scopus 로고
    • The saponins: Polar isoprenoids with important and diverse biological activities
    • Osbourn, A.; Gossb, R. J. M.; Field, R. A. The saponins: polar isoprenoids with important and diverse biological activities Nat. Prod. Rep. 2011, 28, 1261-1268
    • (2011) Nat. Prod. Rep. , vol.28 , pp. 1261-1268
    • Osbourn, A.1    Gossb, R.J.M.2    Field, R.A.3
  • 22
    • 33748539751 scopus 로고    scopus 로고
    • Anti-AIDS agents 69. Moronic acid and other triterpene derivatives as novel potent anti-HIV agents
    • Yu, D.; Sakurai, Y.; Chen, C. H.; Chang, F. R.; Huang, L.; Kashiwada, Y.; Lee, K. H. Anti-AIDS agents 69. Moronic acid and other triterpene derivatives as novel potent anti-HIV agents J. Med. Chem. 2006, 49, 5462-5469
    • (2006) J. Med. Chem. , vol.49 , pp. 5462-5469
    • Yu, D.1    Sakurai, Y.2    Chen, C.H.3    Chang, F.R.4    Huang, L.5    Kashiwada, Y.6    Lee, K.H.7
  • 24
    • 79952900480 scopus 로고    scopus 로고
    • Molecular activities, biosynthesis and evolution of triterpenoid saponins
    • Augustin, J. M.; Kuzina, V.; Andersen, S. B.; Bak, S. Molecular activities, biosynthesis and evolution of triterpenoid saponins Phytochemistry 2011, 72, 435-457
    • (2011) Phytochemistry , vol.72 , pp. 435-457
    • Augustin, J.M.1    Kuzina, V.2    Andersen, S.B.3    Bak, S.4
  • 25
    • 81855185501 scopus 로고    scopus 로고
    • Structure-function relationship of the saponins from the roots of Platycodon grandiflorum for hemolytic and adjuvant activity
    • Sun, H. X.; Chen, L. Q.; Wang, J. J.; Wang, K. W.; Zhou, J. Y. Structure-function relationship of the saponins from the roots of Platycodon grandiflorum for hemolytic and adjuvant activity Int. Immunopharmacol. 2011, 11, 2047-2056
    • (2011) Int. Immunopharmacol. , vol.11 , pp. 2047-2056
    • Sun, H.X.1    Chen, L.Q.2    Wang, J.J.3    Wang, K.W.4    Zhou, J.Y.5
  • 26
    • 84861594223 scopus 로고    scopus 로고
    • Structure-activity relationships of saponin derivatives: A series of entry inhibitors for highly pathogenic H5N1 influenza virus
    • Ding, N.; Chen, Q.; Zhang, W.; Ren, S. M.; Guo, Y.; Li, Y. X. Structure-activity relationships of saponin derivatives: a series of entry inhibitors for highly pathogenic H5N1 influenza virus Eur. J. Med. Chem. 2012, 53, 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
  • 27
    • 0034924823 scopus 로고    scopus 로고
    • Mechanism of viral membrane fusion and its inhibition
    • Eckert, D. M.; Kim, P. S. Mechanism of viral membrane fusion and its inhibition Annu. Rev. Biochem. 2001, 70, 777-810
    • (2001) Annu. Rev. Biochem. , vol.70 , pp. 777-810
    • Eckert, D.M.1    Kim, P.S.2
  • 28
    • 49549112472 scopus 로고    scopus 로고
    • Novel anti-HIV peptides containing multiple copies of artificially designed heptad repeat motifs
    • Shi, W.; Qi, Z.; Pan, C.; Xue, N.; Debnath, A. K.; Qie, J.; Jiang, S.; Liu, K. Novel anti-HIV peptides containing multiple copies of artificially designed heptad repeat motifs Biochem. Biophys. Res. Commun. 2008, 374, 767-772
    • (2008) Biochem. Biophys. Res. Commun. , vol.374 , pp. 767-772
    • Shi, W.1    Qi, Z.2    Pan, C.3    Xue, N.4    Debnath, A.K.5    Qie, J.6    Jiang, S.7    Liu, K.8
  • 29
    • 84875704905 scopus 로고    scopus 로고
    • Design, synthesis, and biological evaluation of highly potent small molecule-peptide conjugates as new HIV-1 fusion inhibitors
    • Wang, C.; Shi, W.; Cai, L.; Lu, L.; Wang, Q.; Zhang, T.; Li, J.; Zhang, Z.; Wang, K.; Xu, L.; Jiang, X.; Jiang, S.; Liu, K. Design, synthesis, and biological evaluation of highly potent small molecule-peptide conjugates as new HIV-1 fusion inhibitors J. Med. Chem. 2013, 56 (6) 2527-2539
    • (2013) J. Med. Chem. , vol.56 , Issue.6 , pp. 2527-2539
    • Wang, C.1    Shi, W.2    Cai, L.3    Lu, L.4    Wang, Q.5    Zhang, T.6    Li, J.7    Zhang, Z.8    Wang, K.9    Xu, L.10    Jiang, X.11    Jiang, S.12    Liu, K.13
  • 31
    • 0028176540 scopus 로고
    • Anti-AIDS agents, 11. Betulinic acid and platanic acid as anti-HIV principles from Syzigium claviflorum, and the anti-HIV activity of structurally related triterpenoids
    • Fujioka, T.; Kashiwada, Y.; Kilkuskie, R. E.; Cosentino, L. M.; Ballas, L. M.; Jiang, J. B.; Janzen, W. P.; Chen, I. S.; Lee, K. H. Anti-AIDS agents, 11. Betulinic acid and platanic acid as anti-HIV principles from Syzigium claviflorum, and the anti-HIV activity of structurally related triterpenoids J. Nat. Prod. 1994, 57, 243-247
    • (1994) J. Nat. Prod. , vol.57 , pp. 243-247
    • Fujioka, T.1    Kashiwada, Y.2    Kilkuskie, R.E.3    Cosentino, L.M.4    Ballas, L.M.5    Jiang, J.B.6    Janzen, W.P.7    Chen, I.S.8    Lee, K.H.9
  • 32
    • 84866879469 scopus 로고    scopus 로고
    • Anti-AIDS agents 90. Novel C-28 modified bevirimat analogues as potent HIV maturation inhibitors
    • Qian, K.; Bori, I. D.; Chen, C. H.; Huang, L.; Lee, K. H. Anti-AIDS agents 90. Novel C-28 modified bevirimat analogues as potent HIV maturation inhibitors J. Med. Chem. 2012, 55, 8128-8136
    • (2012) J. Med. Chem. , vol.55 , pp. 8128-8136
    • Qian, K.1    Bori, I.D.2    Chen, C.H.3    Huang, L.4    Lee, K.H.5
  • 33
    • 84875202040 scopus 로고    scopus 로고
    • New betulinic acid derivatives for bevirimat-resistant human immunodeficiency virus type-1
    • Dang, Z.; Ho, P.; Zhu, L.; Qian, K.; Lee, K. H.; Huang, L.; Chen, C. H. New betulinic acid derivatives for bevirimat-resistant human immunodeficiency virus type-1 J. Med. Chem. 2012, 56, 2029
    • (2012) J. Med. Chem. , vol.56 , pp. 2029
    • Dang, Z.1    Ho, P.2    Zhu, L.3    Qian, K.4    Lee, K.H.5    Huang, L.6    Chen, C.H.7
  • 34
    • 11844249942 scopus 로고    scopus 로고
    • Betulinic acid derivatives as HIV-1 antivirals
    • Aiken, C.; Chen, C. H. Betulinic acid derivatives as HIV-1 antivirals Trends Mol. Med. 2005, 11, 31-36
    • (2005) Trends Mol. Med. , vol.11 , pp. 31-36
    • Aiken, C.1    Chen, C.H.2
  • 35
    • 77951105934 scopus 로고    scopus 로고
    • Anti-AIDS agents 81. Design, synthesis, and structure-activity relationship study of betulinic acid and moronic acid derivatives as potent HIV maturation inhibitors
    • Qian, K.; Kuo, R.; Chen, C. H.; Huang, L.; Morris-Natschke, S. L.; Lee, K. H. Anti-AIDS agents 81. Design, synthesis, and structure-activity relationship study of betulinic acid and moronic acid derivatives as potent HIV maturation inhibitors J. Med. Chem. 2010, 53, 3133-3141
    • (2010) J. Med. Chem. , vol.53 , pp. 3133-3141
    • Qian, K.1    Kuo, R.2    Chen, C.H.3    Huang, L.4    Morris-Natschke, S.L.5    Lee, K.H.6
  • 36
    • 84864418445 scopus 로고    scopus 로고
    • Synthesis of betulinic acid derivatives as entry inhibitors against HIV-1 and bevirimat-resistant HIV-1 variants
    • Dang, Z.; Qian, K.; Ho, P.; Zhu, L.; Lee, K. H.; Huang, L.; Chen, C. H. Synthesis of betulinic acid derivatives as entry inhibitors against HIV-1 and bevirimat-resistant HIV-1 variants Bioorg. Med. Chem. Lett. 2012, 22, 5190-5194
    • (2012) Bioorg. Med. Chem. Lett. , vol.22 , pp. 5190-5194
    • Dang, Z.1    Qian, K.2    Ho, P.3    Zhu, L.4    Lee, K.H.5    Huang, L.6    Chen, C.H.7
  • 37
    • 33748539751 scopus 로고    scopus 로고
    • Anti-AIDS agents 69. Moronic acid and other triterpene derivatives as novel potent anti-HIV agents
    • Yu, D. L.; Sakurai, Y.; Chen, C. H.; Chang, F. R.; Huang, L.; Kashiwada, Y.; Lee, K. H. Anti-AIDS agents 69. Moronic acid and other triterpene derivatives as novel potent anti-HIV agents J. Med. Chem. 2006, 49, 5462-5469
    • (2006) J. Med. Chem. , vol.49 , pp. 5462-5469
    • Yu, D.L.1    Sakurai, Y.2    Chen, C.H.3    Chang, F.R.4    Huang, L.5    Kashiwada, Y.6    Lee, K.H.7
  • 39
    • 77949796395 scopus 로고    scopus 로고
    • Copper-catalyzed azide-alkyne cycloaddition (CuAAC) and beyond: New reactivity of copper(I) acetylides
    • Hein, J. E.; Fokin, V. V. Copper-catalyzed azide-alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper(I) acetylides Chem. Soc. Rev. 2010, 39, 1302-1315
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 1302-1315
    • Hein, J.E.1    Fokin, V.V.2
  • 40
    • 72449154666 scopus 로고    scopus 로고
    • Analysis and optimization of copper-catalyzed azide-alkyne cycloaddition for bioconjugation
    • Hong, V.; Presolski, S. I.; Ma, C.; Finn, M. G. Analysis and optimization of copper-catalyzed azide-alkyne cycloaddition for bioconjugation Angew. Chem. Int, Ed. 2009, 48, 9879-9883
    • (2009) Angew. Chem. Int, Ed. , vol.48 , pp. 9879-9883
    • Hong, V.1    Presolski, S.I.2    Ma, C.3    Finn, M.G.4
  • 41
    • 0026749942 scopus 로고
    • Hydroxyl radical mediated damage to proteins, with special reference to the crystallins
    • Guptasarma, P.; Balasubramanian, D. Hydroxyl radical mediated damage to proteins, with special reference to the crystallins Biochemistry 1992, 31, 4296-4303
    • (1992) Biochemistry , vol.31 , pp. 4296-4303
    • Guptasarma, P.1    Balasubramanian, D.2
  • 42
    • 84865335285 scopus 로고    scopus 로고
    • HIV-1 variants with a single-point mutation in the gp41 pocket region exhibiting different susceptibility to HIV fusion inhibitors with pocket- or membrane-binding domain
    • Lu, L.; Tong, P.; Yu, X.; Pan, C.; Zou, P.; Chen, Y.; Jiang, S. HIV-1 variants with a single-point mutation in the gp41 pocket region exhibiting different susceptibility to HIV fusion inhibitors with pocket- or membrane-binding domain Biochim. Biophys. Acta, Biomembr. 2012, 1818 (12) 2950-2957
    • (2012) Biochim. Biophys. Acta, Biomembr. , vol.1818 , Issue.12 , pp. 2950-2957
    • Lu, L.1    Tong, P.2    Yu, X.3    Pan, C.4    Zou, P.5    Chen, Y.6    Jiang, S.7
  • 43
    • 33845399649 scopus 로고    scopus 로고
    • A broad antiviral neutral glycolipid, fattiviracin FV-8, is a membrane fluidity modulator
    • Harada, S.; Yokomizo, K.; Monde, K.; Maeda, Y.; Yusa, K. A broad antiviral neutral glycolipid, fattiviracin FV-8, is a membrane fluidity modulator Cell. Microbiol. 2007, 9, 196-203
    • (2007) Cell. Microbiol. , vol.9 , pp. 196-203
    • Harada, S.1    Yokomizo, K.2    Monde, K.3    Maeda, Y.4    Yusa, K.5
  • 44
    • 28044459176 scopus 로고    scopus 로고
    • The broad anti-viral agent glycyrrhizin directly modulates the fluidity of plasma membrane and HIV-1 envelope
    • Harada, S. The broad anti-viral agent glycyrrhizin directly modulates the fluidity of plasma membrane and HIV-1 envelope Biochem. J. 2005, 392, 191-199
    • (2005) Biochem. J. , vol.392 , pp. 191-199
    • Harada, S.1
  • 45
    • 84868297922 scopus 로고    scopus 로고
    • Sphingopeptides: Dihydrosphingosine-based fusion inhibitors against wild-type and enfuvirtide-resistant HIV-1
    • Ashkenazi, A.; Viard, M.; Unger, L.; Blumenthal, R.; Shai, Y. Sphingopeptides: dihydrosphingosine-based fusion inhibitors against wild-type and enfuvirtide-resistant HIV-1 FASEB J. 2012, 26, 4628-4636
    • (2012) FASEB J. , vol.26 , pp. 4628-4636
    • Ashkenazi, A.1    Viard, M.2    Unger, L.3    Blumenthal, R.4    Shai, Y.5
  • 47
    • 33846173312 scopus 로고    scopus 로고
    • HIV entry inhibitors targeting gp41: From polypeptides to small-molecule compounds
    • Liu, S.; Wu, S.; Jiang, S. HIV entry inhibitors targeting gp41: from polypeptides to small-molecule compounds Curr. Pharm. Des. 2007, 13 (2) 143-162
    • (2007) Curr. Pharm. Des. , vol.13 , Issue.2 , pp. 143-162
    • Liu, S.1    Wu, S.2    Jiang, S.3
  • 49
    • 84880519156 scopus 로고    scopus 로고
    • Oral delivery of therapeutic proteins and peptides: A review on recent developments
    • Gupta, S.; Jain, A.; Chakraborty, M.; Sahni, J. K.; Ali, J.; Dang, S. Oral delivery of therapeutic proteins and peptides: a review on recent developments Drug Delivery 2013, 20, 237-246
    • (2013) Drug Delivery , vol.20 , pp. 237-246
    • Gupta, S.1    Jain, A.2    Chakraborty, M.3    Sahni, J.K.4    Ali, J.5    Dang, S.6
  • 51
    • 35948978102 scopus 로고    scopus 로고
    • Demonstrating the C-terminal boundary of the HIV-1 fusion conformation in a dynamic ongoing fusion process and implication for fusion inhibition
    • Wexler-Cohen, Y.; Shai, Y. Demonstrating the C-terminal boundary of the HIV-1 fusion conformation in a dynamic ongoing fusion process and implication for fusion inhibition FASEB J. 2007, 21 (13) 3677-3684
    • (2007) FASEB J. , vol.21 , Issue.13 , pp. 3677-3684
    • Wexler-Cohen, Y.1    Shai, Y.2
  • 52
    • 84870562697 scopus 로고    scopus 로고
    • A bivalent recombinant protein inactivates HIV-1 by targeting the gp41 prehairpin fusion intermediate induced by CD4 D1D2 domains
    • Lu, L.; Pan, C.; Li, Y.; Lu, H.; Wu, H.; Jiang, S. A bivalent recombinant protein inactivates HIV-1 by targeting the gp41 prehairpin fusion intermediate induced by CD4 D1D2 domains Retrovirology 2012, 9, 104
    • (2012) Retrovirology , vol.9 , pp. 104
    • Lu, L.1    Pan, C.2    Li, Y.3    Lu, H.4    Wu, H.5    Jiang, S.6
  • 53
    • 33748794547 scopus 로고    scopus 로고
    • Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies
    • Chou, T. C. Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies Pharmacol. Rev. 2006, 58, 621-681
    • (2006) Pharmacol. Rev. , vol.58 , pp. 621-681
    • Chou, T.C.1
  • 54
    • 84886265114 scopus 로고    scopus 로고
    • An engineered HIV-1 gp41 trimeric coiled coil with increased stability and anti-HIV-1 activity: Implication for developing anti-HIV microbicides
    • Tong, P.; Lu, Z.; Chen, X.; Wang, Q.; Yu, F.; Zou, P.; Yu, X.; Li, Y.; Lu, L.; Chen, Y. H.; Jiang, S. B. An engineered HIV-1 gp41 trimeric coiled coil with increased stability and anti-HIV-1 activity: implication for developing anti-HIV microbicides J. Antimicrob. Chemother. 2013, 68, 2533-2544
    • (2013) J. Antimicrob. Chemother. , vol.68 , pp. 2533-2544
    • Tong, P.1    Lu, Z.2    Chen, X.3    Wang, Q.4    Yu, F.5    Zou, P.6    Yu, X.7    Li, Y.8    Lu, L.9    Chen, Y.H.10    Jiang, S.B.11


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.