메뉴 건너뛰기




Volumn 385, Issue 11, 2004, Pages 1035-1039

Design of inhibitors against HIV, HTLV-I, and Plasmodium falciparum aspartic proteases

Author keywords

AIDS; Allophenylnorstatine; Antiviral activity; HTLV I; Malaria; Protease inhibitors

Indexed keywords

3 AMINO 2 HYDROXY 4 PHENYLBUTYRIC ACID; AMINO ACID; ASPARTIC PROTEINASE; ASPARTIC PROTEINASE INHIBITOR; CATHEPSIN D; GAG PROTEIN; JE 2147; KNI 10006; KNI 10007; KNI 10026; KNI 10159; KNI 10160; KNI 10161; KNI 10162; KNI 1269; KNI 1689; KNI 727; KNI 764; KNI 840; KYNOSTATIN 272; PLASMEPSIN II; PROTEIN P19; PROTEINASE INHIBITOR; SM 319777; UNCLASSIFIED DRUG;

EID: 10044264132     PISSN: 14316730     EISSN: None     Source Type: Journal    
DOI: 10.1515/BC.2004.134     Document Type: Short Survey
Times cited : (40)

References (22)
  • 2
    • 0038324472 scopus 로고    scopus 로고
    • Inhibitors of the Plasmodium falciparum parasite aspartic protease plasmepsin II as potential antimalarial agents
    • Boss, C., Richard-Bildstein, S., Weller, T., Fischli, W., Meyerm S., and Binkert, C. (2003). Inhibitors of the Plasmodium falciparum parasite aspartic protease plasmepsin II as potential antimalarial agents. Curr. Med. Chem. 10, 883-907.
    • (2003) Curr. Med. Chem. , vol.10 , pp. 883-907
    • Boss, C.1    Richard-Bildstein, S.2    Weller, T.3    Fischli, W.4    Meyerm, S.5    Binkert, C.6
  • 3
    • 0035521154 scopus 로고    scopus 로고
    • Aspartic proteases of Plasmodium falciparum and other parasitic protozoa as drug targets
    • Coombs, G.H., Goldberg, D.E., Klemba, M., Berry, C., Kay, J., and Mottram, J. (2001). Aspartic proteases of Plasmodium falciparum and other parasitic protozoa as drug targets. Trends Parasitol. 17, 532-537.
    • (2001) Trends Parasitol. , vol.17 , pp. 532-537
    • Coombs, G.H.1    Goldberg, D.E.2    Klemba, M.3    Berry, C.4    Kay, J.5    Mottram, J.6
  • 4
    • 10044243071 scopus 로고    scopus 로고
    • Protease inhibitors: Design and new features
    • Hamada, Y., and Kiso, Y. (2003). Protease inhibitors: design and new features. Kagaku To Seibutsu 41, 796-803.
    • (2003) Kagaku To Seibutsu , vol.41 , pp. 796-803
    • Hamada, Y.1    Kiso, Y.2
  • 5
    • 10044270288 scopus 로고    scopus 로고
    • Design and synthesis of dipeptide-type HIV-1 protease inhibitors with high antiviral activity
    • M. Ueki, ed. (Osaka, Japan: The Japanese Peptide Society)
    • Kimura, T., Hidaka, K., Abdel-Rahman, H.M., Matsumoto, H., Tanaka, Y., Matsui, Y., Hayashi, Y., and Kiso, Y. (2004). Design and synthesis of dipeptide-type HIV-1 protease inhibitors with high antiviral activity. In: Peptide Science 2003, M. Ueki, ed. (Osaka, Japan: The Japanese Peptide Society), pp. 241-244.
    • (2004) Peptide Science 2003 , pp. 241-244
    • Kimura, T.1    Hidaka, K.2    Abdel-Rahman, H.M.3    Matsumoto, H.4    Tanaka, Y.5    Matsui, Y.6    Hayashi, Y.7    Kiso, Y.8
  • 6
    • 33746893200 scopus 로고    scopus 로고
    • Dipeptide-type inhibitors targeting plasmepsins from Plasmodium faliciparum
    • M. Ueki, ed. (Osaka, Japan: The Japanese Peptide Society)
    • Kiso, A., Hidaka, K., Tsuchiya, Y., Kimura, T., Hayashi, Y., Nezami, A., Liu, J., Goldberg, D.E., Freire, E., and Kiso, Y. (2004a). Dipeptide-type inhibitors targeting plasmepsins from Plasmodium faliciparum. In: Peptide Science 2003, M. Ueki, ed. (Osaka, Japan: The Japanese Peptide Society), pp. 235-238.
    • (2004) Peptide Science 2003 , pp. 235-238
    • Kiso, A.1    Hidaka, K.2    Tsuchiya, Y.3    Kimura, T.4    Hayashi, Y.5    Nezami, A.6    Liu, J.7    Goldberg, D.E.8    Freire, E.9    Kiso, Y.10
  • 7
    • 8644243887 scopus 로고    scopus 로고
    • Search for substrate-based inhibitors fitting the S2′ space of malarial aspartic protease plasmepsin II
    • in press
    • Kiso, A., Hidaka, K., Kimura, T., Hayashi, Y., Nezami, A., Freire, E., and Kiso, Y. (2004b). Search for substrate-based inhibitors fitting the S2′ space of malarial aspartic protease plasmepsin II. J. Peptide Sci., in press.
    • (2004) J. Peptide Sci.
    • Kiso, A.1    Hidaka, K.2    Kimura, T.3    Hayashi, Y.4    Nezami, A.5    Freire, E.6    Kiso, Y.7
  • 8
    • 0029943637 scopus 로고    scopus 로고
    • Design and synthesis of substrate-based peptidomimetic human immunodeficiency virus protease inhibitors containing the hydroxymethylcarbonyl isostere
    • Kiso, Y. (1996). Design and synthesis of substrate-based peptidomimetic human immunodeficiency virus protease inhibitors containing the hydroxymethylcarbonyl isostere. Biopolymers 40, 235-244.
    • (1996) Biopolymers , vol.40 , pp. 235-244
    • Kiso, Y.1
  • 9
    • 0033003998 scopus 로고    scopus 로고
    • Small dipeptide-based HIV protease inhibitors containing the hydroxymethylcarbonyl isostere as an ideal transition-state mimic
    • Kiso, Y., Matsumoto, H., Mizumoto, S., Kimura, T., Fujiwara, Y., and Akaji, K. (1999). Small dipeptide-based HIV protease inhibitors containing the hydroxymethylcarbonyl isostere as an ideal transition-state mimic. Biopolymers 51, 59-68.
    • (1999) Biopolymers , vol.51 , pp. 59-68
    • Kiso, Y.1    Matsumoto, H.2    Mizumoto, S.3    Kimura, T.4    Fujiwara, Y.5    Akaji, K.6
  • 10
    • 0038309409 scopus 로고    scopus 로고
    • Effect of nucleoside-based antiretroviral chemotherapy on human T cell leukemia/lymphotropic virus type 1 (HTLV-I) infection in vitro
    • Macchi, B., Balestrieri, E., and Mastino, A. (2003). Effect of nucleoside-based antiretroviral chemotherapy on human T cell leukemia/lymphotropic virus type 1 (HTLV-I) infection in vitro. J. Antimicrob. Chemother. 51, 1327-1330.
    • (2003) J. Antimicrob. Chemother. , vol.51 , pp. 1327-1330
    • Macchi, B.1    Balestrieri, E.2    Mastino, A.3
  • 11
    • 10044298970 scopus 로고    scopus 로고
    • Identification of peptidomimetic HTLV-I protease inhibitors containing allophenylnorstatine as a transition-state isostere
    • E. Benedetti and C. Pedone, eds. (Naples, Italy: Edizioni Ziino)
    • Maegawa, H., Kimura, T., Arii, Y., Matsui, Y., Hayashi, Y., and Kiso, Y. (2002). Identification of peptidomimetic HTLV-I protease inhibitors containing allophenylnorstatine as a transition-state isostere. In: Peptides 2002, E. Benedetti and C. Pedone, eds. (Naples, Italy: Edizioni Ziino), pp. 548-549.
    • (2002) Peptides 2002 , pp. 548-549
    • Maegawa, H.1    Kimura, T.2    Arii, Y.3    Matsui, Y.4    Hayashi, Y.5    Kiso, Y.6
  • 12
    • 7044254904 scopus 로고    scopus 로고
    • Identification of peptidomimetic HTLV-I protease inhibitors containing allophenylnorstatine as the transition-state mimic
    • in press
    • Maegawa, H., Kimura, T., Arii, Y., Matsui, Y., Kasai, S., Hayashi, Y., and Kiso, Y. (2004). Identification of peptidomimetic HTLV-I protease inhibitors containing allophenylnorstatine as the transition-state mimic. Bioorg. Med. Chem. Lett., in press.
    • (2004) Bioorg. Med. Chem. Lett.
    • Maegawa, H.1    Kimura, T.2    Arii, Y.3    Matsui, Y.4    Kasai, S.5    Hayashi, Y.6    Kiso, Y.7
  • 14
    • 0347931880 scopus 로고    scopus 로고
    • Structure-activity and structure-metabolism relationships of HIV protease inhibitors containing the 3-hydroxy-2-methylbenzoyl-allophenylnorstatine structure
    • Mimoto, T., Terashima, K., Nojima, S., Takaku, H., Nakayama, M., Shintani, M., Yamaoka, T., and Hayashi, H. (2004). Structure-activity and structure-metabolism relationships of HIV protease inhibitors containing the 3-hydroxy-2-methylbenzoyl-allophenylnorstatine structure. Bioorg. Med. Chem. 12, 281-293.
    • (2004) Bioorg. Med. Chem. , vol.12 , pp. 281-293
    • Mimoto, T.1    Terashima, K.2    Nojima, S.3    Takaku, H.4    Nakayama, M.5    Shintani, M.6    Yamaoka, T.7    Hayashi, H.8
  • 15
    • 0037133223 scopus 로고    scopus 로고
    • Identification and characterization of allophenylnorstatine-based inhibitors of plasmepsin II, an antimalarial target
    • Nezami, A., Laque, I., Kimura, T., Kiso, Y., and Freire, E. (2002). Identification and characterization of allophenylnorstatine-based inhibitors of plasmepsin II, an antimalarial target. Biochemistry 41 2273-2280.
    • (2002) Biochemistry , vol.41 , pp. 2273-2280
    • Nezami, A.1    Laque, I.2    Kimura, T.3    Kiso, Y.4    Freire, E.5
  • 16
    • 0037780064 scopus 로고    scopus 로고
    • High-affinity inhibition of a family of Plasmodium falciparum proteases by a designed adaptive inhibitor
    • Nezami, A., Kimura, T., Hidaka, K., Kiso., A., Liu, J., Kiso, Y., Goldberg, D.E., and Freire, E. (2003). High-affinity inhibition of a family of Plasmodium falciparum proteases by a designed adaptive inhibitor. Biochemistry 42, 8459-8464.
    • (2003) Biochemistry , vol.42 , pp. 8459-8464
    • Nezami, A.1    Kimura, T.2    Hidaka, K.3    Kiso, A.4    Liu, J.5    Kiso, Y.6    Goldberg, D.E.7    Freire, E.8
  • 17
    • 0037046143 scopus 로고    scopus 로고
    • Anisotropic dynamics of the JE-2147-HIV protease complex: Drug resistance and thermodynamic binding mode examined in a 1.09 Å structure
    • Reiling, K.K., Endres, N.F., Dauber, D.S., Craik, C.S., and Stroud, R.M. (2002). Anisotropic dynamics of the JE-2147-HIV protease complex: drug resistance and thermodynamic binding mode examined in a 1.09 Å structure. Biochemistry 41, 4582-4594.
    • (2002) Biochemistry , vol.41 , pp. 4582-4594
    • Reiling, K.K.1    Endres, N.F.2    Dauber, D.S.3    Craik, C.S.4    Stroud, R.M.5
  • 19
    • 10044273549 scopus 로고    scopus 로고
    • UNAIDS and World Health Organization Report
    • UNAIDS and World Health Organization Report (2003). http://www.unaids.org.
    • (2003)
  • 21
    • 0035876257 scopus 로고    scopus 로고
    • The binding energetics of first and second-generation HIV-1 protease inhibitors: Implications for drug design
    • Velazquez-Campoy, A., Kiso, Y., and Freire, E. (2001). The binding energetics of first and second-generation HIV-1 protease inhibitors: implications for drug design. Arch. Biochem. Biophys. 390 169-175.
    • (2001) Arch. Biochem. Biophys. , vol.390 , pp. 169-175
    • Velazquez-Campoy, A.1    Kiso, Y.2    Freire, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.