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Volumn 9, Issue 6, 2005, Pages 1267-1282

The therapeutic potential of CXCR4 antagonists in the treatment of HIV infection, cancer metastasis and rheumatoid arthritis

Author keywords

Cancer cell progression; Cancer metastasis; Chemokine receptor; HIV infection; Low molecular weight CXCR4 antagonist; Rheumatoid arthritis (RA); T140; T22

Indexed keywords

1,1' [1,4 PHENYLENEBIS(METHYLENE)]BIS(1,4,8,11 TETRAAZACYCLOTETRADECANE); ALPHA N ACETYLNONA DEXTRO ARGININE AMIDE; AMD 070; AMD 3465; AMD 3645; AMD 8665; CHEMOKINE RECEPTOR AFFECTING AGENT; CHEMOKINE RECEPTOR ANTAGONIST; CHEMOKINE RECEPTOR CXCR4; COLLAGEN; DEXAMETHASONE; ENFUVIRTIDE; FC 131; FC 151; FC 341; FC 351; FLUDARABINE; KRH 1636; N (6 AMINOHEXYL)GLYCYL N (3 GUANIDINOPROPYL)GLYCYL N (3 GUANIDINOPROPYL)GLYCYL N BENZYLGLYCYL N (3 GUANIDINOPROPYL)GLYCYL DEXTRO LYSYL DEXTRO LYSYL DEXTRO ARGINYL DEXTRO PROLINAMIDE; POLYLACTIC ACID; POLYPEPTIDE; POLYPHEMUSIN 2; PROTEINASE INHIBITOR; RNA DIRECTED DNA POLYMERASE INHIBITOR; STROMAL CELL DERIVED FACTOR 1; T 140; T 140 DERIVATIVE; T 22; TACHYPLESIN; UNCLASSIFIED DRUG; UNINDEXED DRUG; VINCRISTINE;

EID: 28944452573     PISSN: 14728222     EISSN: None     Source Type: Journal    
DOI: 10.1517/14728222.9.6.1267     Document Type: Review
Times cited : (62)

References (92)
  • 1
    • 0028324454 scopus 로고
    • Molecular cloning and structure of a pre-B-cell growth-stimulating factor
    • NAGASAWA T, KIKUTANI H, KISHIMOTO T: Molecular cloning and structure of a pre-B-cell growth-stimulating factor. Proc. Natl. Acad. Sci. USA (1994) 91:2305-2309.
    • (1994) Proc. Natl. Acad. Sci. USA , vol.91 , pp. 2305-2309
    • Nagasawa, T.1    Kikutani, H.2    Kishimoto, T.3
  • 2
    • 0029775576 scopus 로고    scopus 로고
    • The lymphocyte chemoattractant SDF-1 is a ligand for LESTR/fusin and blocks HIV-1 entry
    • BLEUL CC, FARZAN M, CHOE H et al.: The lymphocyte chemoattractant SDF-1 is a ligand for LESTR/fusin and blocks HIV-1 entry. Nature (1996) 382:829-833.
    • (1996) Nature , vol.382 , pp. 829-833
    • Bleul, C.C.1    Farzan, M.2    Choe, H.3
  • 3
    • 16044370087 scopus 로고    scopus 로고
    • The CXC chemokine SDF-1 is the ligand for LESTR/fusin and prevents infection by T-cell-line-adapted HIV-1
    • OBERLIN E, AMARA A, BACHELERIE F et al.: The CXC chemokine SDF-1 is the ligand for LESTR/fusin and prevents infection by T-cell-line-adapted HIV-1. Nature (1996) 382:833-835.
    • (1996) Nature , vol.382 , pp. 833-835
    • Oberlin, E.1    Amara, A.2    Bachelerie, F.3
  • 4
    • 0027165675 scopus 로고
    • Signal sequence trap: A cloning strategy for secreted proteins and Type I membrane proteins
    • TASHIRO K, TADA H, HEILKER R, SHIROZU M, NAKANO T, HONJO T: Signal sequence trap: a cloning strategy for secreted proteins and Type I membrane proteins. Science (1993) 261:600-603.
    • (1993) Science , vol.261 , pp. 600-603
    • Tashiro, K.1    Tada, H.2    Heilker, R.3    Shirozu, M.4    Nakano, T.5    Honjo, T.6
  • 5
    • 0030002637 scopus 로고    scopus 로고
    • HIV-1 entry co-factor: Functional cDNA cloning of a seven-transmembrane, G protein-coupled receptor
    • FENG Y, BRODER CC, KENNEDY PE, BERGER EA: HIV-1 entry co-factor: Functional cDNA cloning of a seven-transmembrane, G protein-coupled receptor. Science (1996) 272:872-877.
    • (1996) Science , vol.272 , pp. 872-877
    • Feng, Y.1    Broder, C.C.2    Kennedy, P.E.3    Berger, E.A.4
  • 6
    • 0035282432 scopus 로고    scopus 로고
    • Involvement of chemokine receptors in breast cancer metastasis
    • MÜLLER A, HOMEY B, SOTO H et al.: Involvement of chemokine receptors in breast cancer metastasis. Nature (2001) 410:50-56.
    • (2001) Nature , vol.410 , pp. 50-56
    • Müller, A.1    Homey, B.2    Soto, H.3
  • 7
    • 0033818476 scopus 로고    scopus 로고
    • Expression of stromal cell-derived factor 1 and CXCR4 ligand receptor system in pancreatic cancer: A possible role for tumor progression
    • KOSHIBA T, HOSOTANI R, MIYAMOTO Y et al.: Expression of stromal cell-derived factor 1 and CXCR4 ligand receptor system in pancreatic cancer: a possible role for tumor progression. Clin. Cancer Res. (2000) 6:3530-3535.
    • (2000) Clin. Cancer Res. , vol.6 , pp. 3530-3535
    • Koshiba, T.1    Hosotani, R.2    Miyamoto, Y.3
  • 8
    • 2942692286 scopus 로고    scopus 로고
    • CXCR4 antagonist inhibits stromal cell-derived factor 1-induced migration and invasion of human pancreatic cancer
    • MORI T, DOI R, KOIZUMI K et al.: CXCR4 antagonist inhibits stromal cell-derived factor 1-induced migration and invasion of human pancreatic cancer. Mol. Cancer Ther. (2004) 3:29-37.
    • (2004) Mol. Cancer Ther. , vol.3 , pp. 29-37
    • Mori, T.1    Doi, R.2    Koizumi, K.3
  • 9
    • 0035976899 scopus 로고    scopus 로고
    • Expression of functional chemokine receptors CXCR3 and CXCR4 on human melanoma cells
    • ROBLEDO MM, BARTOLOME RA, LONGO N et al.: Expression of functional chemokine receptors CXCR3 and CXCR4 on human melanoma cells. J. Biol. Chem. (2001) 276:45098-45105.
    • (2001) J. Biol. Chem. , vol.276 , pp. 45098-45105
    • Robledo, M.M.1    Bartolome, R.A.2    Longo, N.3
  • 10
    • 2942654586 scopus 로고    scopus 로고
    • A single treatment with microcapsules containing a CXCR4 antagonist suppresses pulmonary metastasis of murine melanoma
    • TAKENAGA M, TAMAMURA H, HIRAMATSU K et al.: A single treatment with microcapsules containing a CXCR4 antagonist suppresses pulmonary metastasis of murine melanoma. Biochem. Biophys. Res. Commun. (2004) 320:226-231
    • (2004) Biochem. Biophys. Res. Commun. , vol.320 , pp. 226-231
    • Takenaga, M.1    Tamamura, H.2    Hiramatsu, K.3
  • 12
    • 18544373080 scopus 로고    scopus 로고
    • CXCR4/CXCL12 expression and signaling in kidney cancer
    • SCHRADER AJ, LECHNER O, TEMPLIN M et al.: CXCR4/CXCL12 expression and signaling in kidney cancer. Br. J. Cancer (2002) 86:1250-1256.
    • (2002) Br. J. Cancer , vol.86 , pp. 1250-1256
    • Schrader, A.J.1    Lechner, O.2    Templin, M.3
  • 13
    • 0035887626 scopus 로고    scopus 로고
    • A possible role for CXCR4 and its ligand, the CXC chemokine stromal cell-derived factor-1, in the development of bone marrow metastases in neuroblastoma
    • GEMINDER H, SAGI-ASSIF O, GOLDBERG L et al.: A possible role for CXCR4 and its ligand, the CXC chemokine stromal cell-derived factor-1, in the development of bone marrow metastases in neuroblastoma. J. Immunol. (2001) 167: 4747-4757.
    • (2001) J. Immunol. , vol.167 , pp. 4747-4757
    • Geminder, H.1    Sagi-Assif, O.2    Goldberg, L.3
  • 14
    • 0036606772 scopus 로고    scopus 로고
    • CXCR4 neutralization, a novel therapeutic approach for non-Hodgkids lymphoma
    • BERTOLINI F, DELL'AGNOLA C, MANCUSO P et al.: CXCR4 neutralization, a novel therapeutic approach for non-Hodgkids lymphoma. Cancer Res. (2002) 62:3106-3112.
    • (2002) Cancer Res. , vol.62 , pp. 3106-3112
    • Bertolini, F.1    Dell'Agnola, C.2    Mancuso, P.3
  • 15
    • 0036830045 scopus 로고    scopus 로고
    • Regulation of cellular proliferation, cytoskeletal function, and signal transduction through CXCR4 and c-Kit in small cell lung cancer cells
    • KIJIMA T, MAULIK G, MA PC et al.: Regulation of cellular proliferation, cytoskeletal function, and signal transduction through CXCR4 and c-Kit in small cell lung cancer cells. Cancer Res. (2002) 62:6304-6311.
    • (2002) Cancer Res. , vol.62 , pp. 6304-6311
    • Kijima, T.1    Maulik, G.2    Ma, P.C.3
  • 16
    • 0345687920 scopus 로고    scopus 로고
    • Functional expression of CXCR4 (CD184) on small-cell lung cancer cells mediates migration, integrin activation, and adhesion to stromal cells
    • BURGER M, GLODEK A, HARTMANN T et al.: Functional expression of CXCR4 (CD184) on small-cell lung cancer cells mediates migration, integrin activation, and adhesion to stromal cells. Oncogene (2003) 22:8093-8101.
    • (2003) Oncogene , vol.22 , pp. 8093-8101
    • Burger, M.1    Glodek, A.2    Hartmann, T.3
  • 18
    • 0037108923 scopus 로고    scopus 로고
    • Multiple actions of the chemokine CXCL12 on epithelial tumor cells in human ovarian cancer
    • SCOTTON CJ, WILSON JL, SCOTT K et al.: Multiple actions of the chemokine CXCL12 on epithelial tumor cells in human ovarian cancer. Cancer Res. (2002) 62:5930-5938.
    • (2002) Cancer Res. , vol.62 , pp. 5930-5938
    • Scotton, C.J.1    Wilson, J.L.2    Scott, K.3
  • 19
    • 0035863789 scopus 로고    scopus 로고
    • Chemokine stromal cell-derived factor-1α modulates VLA-4 integrin-mediated multiple myeloma cell adhesion to CS-1/fibronectin and VCAM-1
    • SANZ-RODRIGUEZ F, HIDALGO A, TEIXIDO J: Chemokine stromal cell-derived factor-1α modulates VLA-4 integrin-mediated multiple myeloma cell adhesion to CS-1/fibronectin and VCAM-1. Blood (2001) 97:346-351.
    • (2001) Blood , vol.97 , pp. 346-351
    • Sanz-Rodriguez, F.1    Hidalgo, A.2    Teixido, J.3
  • 20
    • 20144388592 scopus 로고    scopus 로고
    • Elevated serum levels of SDF-1α are associated with increased osteoclast activity and osteolytic bone disease in multiple myeloma patients
    • ZANNETTINO ACW, FARRUGIA AN, KORTESIDIS A et al.: Elevated serum levels of SDF-1α are associated with increased osteoclast activity and osteolytic bone disease in multiple myeloma patients Cancer Res. (2005) 65:1700-1709.
    • (2005) Cancer Res. , vol.65 , pp. 1700-1709
    • Zannettino, A.C.W.1    Farrugia, A.N.2    Kortesidis, A.3
  • 21
    • 0036464610 scopus 로고    scopus 로고
    • Distinctive features of 'nurselike' cells that differentiate in the context of chronic lymphocytic leukemia
    • TSUKADA N, BURGER JA, ZVAIFLER NJ, KIPPS TJ et al.: Distinctive features of 'nurselike' cells that differentiate in the context of chronic lymphocytic leukemia. Blood (2002) 99:1030-1037.
    • (2002) Blood , vol.99 , pp. 1030-1037
    • Tsukada, N.1    Burger, J.A.2    Zvaifler, N.J.3    Kipps, T.J.4
  • 22
    • 23944488816 scopus 로고    scopus 로고
    • Small peptide inhibitors of the CXCR4 chemokine receptor (CD184) antagonize the activation, migration and antiapoptotic responses of CXCL12 in chronic lymphocytic leukemia B cells
    • BURGER M, HARTMANN T, KROME M et al.: Small peptide inhibitors of the CXCR4 chemokine receptor (CD184) antagonize the activation, migration and antiapoptotic responses of CXCL12 in chronic lymphocytic leukemia B cells. Blood (2005) 106:1824-1830.
    • (2005) Blood , vol.106 , pp. 1824-1830
    • Burger, M.1    Hartmann, T.2    Krome, M.3
  • 23
    • 0038103869 scopus 로고    scopus 로고
    • Effects of inhibitors of the chemokine receptor CXCR4 on acute lymphoblastic leukemia cells in vitro
    • JUAREZ J, BRADSTOCK KF, GOTTLIEB DJ, BENDALL LJ: Effects of inhibitors of the chemokine receptor CXCR4 on acute lymphoblastic leukemia cells in vitro. Leukemia (2003) 17:1294-1300.
    • (2003) Leukemia , vol.17 , pp. 1294-1300
    • Juarez, J.1    Bradstock, K.F.2    Gottlieb, D.J.3    Bendall, L.J.4
  • 24
    • 0344823964 scopus 로고    scopus 로고
    • A small-molecule antagonist of CXCR4 inhibits intracranial growth of primary brain tumors
    • RUBIN JB, KUNG AL, KLEIN RS et al.: A small-molecule antagonist of CXCR4 inhibits intracranial growth of primary brain tumors. Proc. Natl. Acad. Sci. USA (2003) 100:13513-13518.
    • (2003) Proc. Natl. Acad. Sci. USA , vol.100 , pp. 13513-13518
    • Rubin, J.B.1    Kung, A.L.2    Klein, R.S.3
  • 25
    • 0142102523 scopus 로고    scopus 로고
    • T140 analogs as CXCR4 antagonists identified as anti-metastatic agents in the treatment of breast cancer
    • TAMAMURA H, HORI A, KANZAKI N et al.: T140 analogs as CXCR4 antagonists identified as anti-metastatic agents in the treatment of breast cancer. FEBS Lett. (2003) 550:79-83.
    • (2003) FEBS Lett. , vol.550 , pp. 79-83
    • Tamamura, H.1    Hori, A.2    Kanzaki, N.3
  • 26
    • 19944433306 scopus 로고    scopus 로고
    • Chemokine receptor expression in EBV-associated lymphoproliferation in Hu/SCID mice: Implications for CXCL12/CXCR4 axis in lymphoma generation
    • PIOVAN E, TOSELLO V, INDRACCOLO S et al.: Chemokine receptor expression in EBV-associated lymphoproliferation in Hu/SCID mice: Implications for CXCL12/CXCR4 axis in lymphoma generation. Blood (2005) 105:931-939.
    • (2005) Blood , vol.105 , pp. 931-939
    • Piovan, E.1    Tosello, V.2    Indraccolo, S.3
  • 27
    • 0034544508 scopus 로고    scopus 로고
    • Stromal cell-derived factor-1-CXC chemokine receptor 4 interactions play a central role in CD4+ T cell accumulation in rheumatoid arthritis synovium
    • NANKI T, HAYASHIDA K, EL-GABALAWY HS et al.: Stromal cell-derived factor-1-CXC chemokine receptor 4 interactions play a central role in CD4+ T cell accumulation in rheumatoid arthritis synovium. J. Immunol. (2000) 165:6590-6598.
    • (2000) J. Immunol. , vol.165 , pp. 6590-6598
    • Nanki, T.1    Hayashida, K.2    El-Gabalawy, H.S.3
  • 28
    • 15844419153 scopus 로고    scopus 로고
    • Identification of a major co-receptor for primary isolates of HIV-1
    • DENG H, LIU R, ELLMEIER W et al.: Identification of a major co-receptor for primary isolates of HIV-1. Nature (1996) 381:661-666.
    • (1996) Nature , vol.381 , pp. 661-666
    • Deng, H.1    Liu, R.2    Ellmeier, W.3
  • 29
    • 15844389650 scopus 로고    scopus 로고
    • HIV-1 entry into CD4+ cells is mediated by the chemokine receptor CC-CKR-5
    • DRAGIC T, LITWIN V, ALLAWAY GP et al.: HIV-1 entry into CD4+ cells is mediated by the chemokine receptor CC-CKR-5. Nature (1996) 381:667-673.
    • (1996) Nature , vol.381 , pp. 667-673
    • Dragic, T.1    Litwin, V.2    Allaway, G.P.3
  • 30
    • 0030018156 scopus 로고    scopus 로고
    • A RANTES, MIP-1α, MIP-1β receptor as a fusion cofactor for macrophage-tropic HIV-1
    • ALKHATIB G, COMBADIERE C, BRODER CC et al.: A RANTES, MIP-1α, MIP-1β receptor as a fusion cofactor for macrophage-tropic HIV-1. Science (1996) 272:1955-1958.
    • (1996) Science , vol.272 , pp. 1955-1958
    • Alkhatib, G.1    Combadiere, C.2    Broder, C.C.3
  • 31
    • 0005014748 scopus 로고    scopus 로고
    • The β-chemokine receptors CCR3 and CCR5 facilitate infection by primary HIV-1 isolates
    • CHOE H, FARZAN M, SUN Y et al.: The β-chemokine receptors CCR3 and CCR5 facilitate infection by primary HIV-1 isolates. Cell (1996) 85:1135-1148.
    • (1996) Cell , vol.85 , pp. 1135-1148
    • Choe, H.1    Farzan, M.2    Sun, Y.3
  • 32
    • 0030604727 scopus 로고    scopus 로고
    • A dual-tropic primary HIV-1 isolate that uses fusin and the β-chemokine receptors CKR-5, CKR-3, and CKR-2b as fusion cofactors
    • DORANZ BJ, RUCKER J, YI Y et al.: A dual-tropic primary HIV-1 isolate that uses fusin and the β-chemokine receptors CKR-5, CKR-3, and CKR-2b as fusion cofactors. Cell (1996) 85:1149-1158.
    • (1996) Cell , vol.85 , pp. 1149-1158
    • Doranz, B.J.1    Rucker, J.2    Yi, Y.3
  • 33
    • 2342591450 scopus 로고    scopus 로고
    • The significance of cancer cell expression of the chemokine receptor CXCR4
    • BALKWILL F: The significance of cancer cell expression of the chemokine receptor CXCR4. Semin. Cancer Biol. (2004) 14:171-179.
    • (2004) Semin. Cancer Biol. , vol.14 , pp. 171-179
    • Balkwill, F.1
  • 34
    • 0032577550 scopus 로고    scopus 로고
    • HIV entry and its inhibition
    • CHAN DC, KIM PS: 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
  • 35
    • 0002052695 scopus 로고    scopus 로고
    • Drug development. A. Discovery and development of antiretroviral therapeutics for HIV infection
    • Merigan TC, Bartlett JG, Bolognesi D (Eds), Williams & Wilkins, Baltimore
    • MITSUYA H, ERICKSON J: Drug development. A. Discovery and development of antiretroviral therapeutics for HIV infection. In: Textbook of AIDS Medicine. Merigan TC, Bartlett JG, Bolognesi D (Eds), Williams & Wilkins, Baltimore (1999):751-780.
    • (1999) Textbook of AIDS Medicine , pp. 751-780
    • Mitsuya, H.1    Erickson, J.2
  • 36
    • 18744416007 scopus 로고    scopus 로고
    • Highly active antiretroviral therapy: Current state of the art, new agents and their pharmacological interactions useful for improving therapeutic outcome
    • BARBARO G, SCOZZAFAVA A, MASTROLORENZO A, SUPURAN CT: Highly active antiretroviral therapy: current state of the art, new agents and their pharmacological interactions useful for improving therapeutic outcome. Curr. Pharm. Des. (2005) 11:1805-1843.
    • (2005) Curr. Pharm. Des. , vol.11 , pp. 1805-1843
    • Barbaro, G.1    Scozzafava, A.2    Mastrolorenzo, A.3    Supuran, C.T.4
  • 37
    • 27844544370 scopus 로고    scopus 로고
    • Development of anti-HIV agents targeting dynamic supramolecular mechanism: Entry and fusion inhibitors based on CXCR4/CCR5 antagonists and gp41-C34-remodeling peptides
    • In press
    • TAMAMURA H, OTAKA A, FUJII N: Development of anti-HIV agents targeting dynamic supramolecular mechanism: entry and fusion inhibitors based on CXCR4/ CCR5 antagonists and gp41-C34-remodeling peptides. Curr. HIV Res. In press.
    • Curr. HIV Res.
    • Tamamura, H.1    Otaka, A.2    Fujii, N.3
  • 38
    • 0023700978 scopus 로고
    • Tachyplesin, a class of antimicrobial peptide from the hemocytes of the horseshoe crab (Tachypleus tridentatus)
    • NAKAMURA T, FURUNAKA H, MIYATA T et al.: Tachyplesin, a class of antimicrobial peptide from the hemocytes of the horseshoe crab (Tachypleus tridentatus). J. Biol. Chem. (1988) 263:16709-16713.
    • (1988) J. Biol. Chem. , vol.263 , pp. 16709-16713
    • Nakamura, T.1    Furunaka, H.2    Miyata, T.3
  • 39
    • 0024741960 scopus 로고
    • Antimicrobial peptides, isolated from horseshoe crab hemocytes, tachyplesin II, and polyphemusins I and II: Chemical structures and biological activity
    • MIYATA T, TOKUNAGA F, YONEYA T et al.: Antimicrobial peptides, isolated from horseshoe crab hemocytes, tachyplesin II, and polyphemusins I and II: chemical structures and biological activity J. Biochem. (1989) 106:663-668.
    • (1989) J. Biochem. , vol.106 , pp. 663-668
    • Miyata, T.1    Tokunaga, F.2    Yoneya, T.3
  • 40
    • 0027094178 scopus 로고
    • A novel anti-HIV synthetic peptide, T-22 ([Tyr5,12, Lys7]-polyphemusin II)
    • MASUDA M, NAKASHIMA H, UEDA T et al.: A novel anti-HIV synthetic peptide, T-22 ([Tyr5,12, Lys7]-polyphemusin II). Biochem. Biophys. Res. Commun. (1992) 189:845-850.
    • (1992) Biochem. Biophys. Res. Commun. , vol.189 , pp. 845-850
    • Masuda, M.1    Nakashima, H.2    Ueda, T.3
  • 41
    • 0026625277 scopus 로고
    • Anti-human immunodeficiency virus activity of a novel synthetic peptide, T22 ([Tyr-5,12, Lys-7] polyphemusin II): A possible inhibitor of virus-cell fusion
    • NAKASHIMA H, MASUDA M, MURAKAMI T et al.: Anti-human immunodeficiency virus activity of a novel synthetic peptide, T22 ([Tyr-5,12, Lys-7] polyphemusin II): a possible inhibitor of virus-cell fusion. Antimicrob. Agents Chemother. (1992) 36:1249-1255.
    • (1992) Antimicrob. Agents Chemother. , vol.36 , pp. 1249-1255
    • Nakashima, H.1    Masuda, M.2    Murakami, T.3
  • 42
    • 0032583575 scopus 로고    scopus 로고
    • A low molecular weight inhibitor against the chemokine receptor CXCR4: A strong anti-HIV peptide T140
    • TAMAMURA H, XU Y, HATTORI T et al.: A low molecular weight inhibitor against the chemokine receptor CXCR4: a strong anti-HIV peptide T140. Biochem. Biophys. Res. Commun. (1998) 253:877-882.
    • (1998) Biochem. Biophys. Res. Commun. , vol.253 , pp. 877-882
    • Tamamura, H.1    Xu, Y.2    Hattori, T.3
  • 43
    • 0030780377 scopus 로고    scopus 로고
    • A small molecule CXCR4 inhibitor that blocks T cell line-tropic HIV-1 infection
    • MURAKAMI T, NAKAJIMA T, KOYANAGI Y et al.: A small molecule CXCR4 inhibitor that blocks T cell line-tropic HIV-1 infection. J. Exp. Med. (1997) 186:1389-1393.
    • (1997) J. Exp. Med. , vol.186 , pp. 1389-1393
    • Murakami, T.1    Nakajima, T.2    Koyanagi, Y.3
  • 44
    • 0033586442 scopus 로고    scopus 로고
    • Marked increase in anti-HIV activity, as well as inhibitory activity against HIV entry mediated by CXCR4, linked to enhancement of the binding ability of tachyplesin analogs to CXCR4
    • XU Y, TAMAMURA H, ARAKAKI R et al.: Marked increase in anti-HIV activity, as well as inhibitory activity against HIV entry mediated by CXCR4, linked to enhancement of the binding ability of tachyplesin analogs to CXCR4. AIDS Res. Hum. Retroviruses (1999) 15:419-427.
    • (1999) AIDS Res. Hum. Retroviruses , vol.15 , pp. 419-427
    • Xu, Y.1    Tamamura, H.2    Arakaki, R.3
  • 45
    • 0032815929 scopus 로고    scopus 로고
    • Inhibitory mechanism of the CXCR4 antagonist T22 against human immunodeficiency virus Type 1 infection
    • MURAKAMI T, ZHANG T.-Y., KOYANAGI Y et al.: Inhibitory mechanism of the CXCR4 antagonist T22 against human immunodeficiency virus Type 1 infection. J. Virol. (1999) 73:7489-7496.
    • (1999) J. Virol. , vol.73 , pp. 7489-7496
    • Murakami, T.1    Zhang, T.-Y.2    Koyanagi, Y.3
  • 46
    • 0035847678 scopus 로고    scopus 로고
    • Conformational study of a highly specific CXCR4 inhibitor, T140, disclosing the close proximity of its intrinsic pharmacophores associated with strong anti-HIV activity
    • and 2409
    • TAMAMURA H, SUGIOKA M, ODAGAKI Y et al.: Conformational study of a highly specific CXCR4 inhibitor, T140, disclosing the close proximity of its intrinsic pharmacophores associated with strong anti-HIV activity. Bioorg. Med. Chem. Lett. (2001) 11:359-362 and 2409.
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , pp. 359-362
    • Tamamura, H.1    Sugioka, M.2    Odagaki, Y.3
  • 47
    • 0034606466 scopus 로고    scopus 로고
    • Pharmacophore identification of a specific CXCR4 inhibitor, T140, leads to development of effective anti-HIV agents with very high selectivity indexes
    • TAMAMURA H, OMAGARI A, OISHI S et al.: Pharmacophore identification of a specific CXCR4 inhibitor, T140, leads to development of effective anti-HIV agents with very high selectivity indexes. Bioorg. Med. Chem. Lett. (2000) 10:2633-2637.
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 2633-2637
    • Tamamura, H.1    Omagari, A.2    Oishi, S.3
  • 48
    • 0035939252 scopus 로고    scopus 로고
    • Development of specific CXCR4 inhibitors possessing high selectivity indexes as well as complete stability in serum based on an anti-HIV peptide T140
    • TAMAMURA H, OMAGARI A, HIRAMATSU K et al.: Development of specific CXCR4 inhibitors possessing high selectivity indexes as well as complete stability in serum based on an anti-HIV peptide T140. Bioorg. Med. Chem. Lett. (2001) 11:1897-1902.
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , pp. 1897-1902
    • Tamamura, H.1    Omagari, A.2    Hiramatsu, K.3
  • 49
    • 0142096799 scopus 로고    scopus 로고
    • Synthesis of potent CXCR4 inhibitors possessing low cytotoxicity and improved biostability based on T140 derivatives
    • TAMAMURA H, HIRAMATSU K, KUSANO S et al.: Synthesis of potent CXCR4 inhibitors possessing low cytotoxicity and improved biostability based on T140 derivatives. Org. Biomol. Chem. (2003) 1:3656-3662.
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 3656-3662
    • Tamamura, H.1    Hiramatsu, K.2    Kusano, S.3
  • 50
    • 0345412742 scopus 로고    scopus 로고
    • Enhancement of the T140-based pharmacophores leads to the development of more potent and biostable CXCR4 antagonists
    • TAMAMURA H, HIRAMATSU K, MIZUMOTO M et al.: Enhancement of the T140-based pharmacophores leads to the development of more potent and biostable CXCR4 antagonists. Org. Biomol. Chem. (2003) 1:3663-3669.
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 3663-3669
    • Tamamura, H.1    Hiramatsu, K.2    Mizumoto, M.3
  • 51
    • 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 CT, SHUGARS DC, GREENWELL TK et al.: 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. USA. (1994) 91:9770-9774.
    • (1994) Proc. Natl. Acad. Sci. USA , vol.91 , pp. 9770-9774
    • Wild, C.T.1    Shugars, D.C.2    Greenwell, T.K.3
  • 52
    • 0034928930 scopus 로고    scopus 로고
    • Biological and genetic characterization of a human immunodeficiency virus strain resistant to CXCR4 antagonist T134
    • KANBARA K, SATO S, TANUMA J et al.: Biological and genetic characterization of a human immunodeficiency virus strain resistant to CXCR4 antagonist T134. AIDS Res. Hum. Retroviruses (2001) 17:615-622.
    • (2001) AIDS Res. Hum. Retroviruses , vol.17 , pp. 615-622
    • Kanbara, K.1    Sato, S.2    Tanuma, J.3
  • 53
    • 0037115647 scopus 로고    scopus 로고
    • Expression of CXC chemokine receptor-4 enhances the pulmonary metastatic potential of murine B16 melanoma cells
    • MURAKAMI T, MAKI W, CARDONES AR et al.: Expression of CXC chemokine receptor-4 enhances the pulmonary metastatic potential of murine B16 melanoma cells. Cancer Res. (2002) 62:7328-7334.
    • (2002) Cancer Res. , vol.62 , pp. 7328-7334
    • Murakami, T.1    Maki, W.2    Cardones, A.R.3
  • 54
    • 0003154770 scopus 로고
    • Small cell lung cancer
    • 4th Edn. VTJ De Vita, S Hellmann, SA Rosenberg (Eds), JB Lippincott: Philadelphia
    • IHDE D, PASS H, GLASTEIN: Small cell lung cancer. In: Cancer. Principles and Practice of Oncology. 4th Edn. VTJ De Vita, S Hellmann, SA Rosenberg (Eds), JB Lippincott: Philadelphia (1993):591-687.
    • (1993) Cancer: Principles and Practice of Oncology , pp. 591-687
    • Ihde, D.1    Pass, H.2    Glastein3
  • 55
    • 21744433347 scopus 로고    scopus 로고
    • CXCR4 chemokine receptor and integrin signaling co-operate in mediating adhesion and chemoresistance in small cell lung cancer (SCLC) cells
    • HARTMANN TN, BURGER JA, GLODEK A, FUJII N, BURGER M: CXCR4 chemokine receptor and integrin signaling co-operate in mediating adhesion and chemoresistance in small cell lung cancer (SCLC) cells. Oncogene (2005) 24:4462-4471.
    • (2005) Oncogene , vol.24 , pp. 4462-4471
    • Hartmann, T.N.1    Burger, J.A.2    Glodek, A.3    Fujii, N.4    Burger, M.5
  • 56
    • 3042593906 scopus 로고    scopus 로고
    • Identification of a CXCR4 antagonist, a T140 analog, as an anti-rheumatoid arthritis agent
    • TAMAMURA H, FUJISAWA M, HIRAMATSU K et al.: Identification of a CXCR4 antagonist, a T140 analog, as an anti-rheumatoid arthritis agent. FEBS Lett. (2004) 569:99-104.
    • (2004) FEBS Lett. , vol.569 , pp. 99-104
    • Tamamura, H.1    Fujisawa, M.2    Hiramatsu, K.3
  • 57
    • 0037025357 scopus 로고    scopus 로고
    • A point mutation that confers constitutive activity to CXCR4 reveals T140 is an inverse agonist and AMD3100 and ALX40-4C are weak partial agonists
    • ZHANG W, NAVENOT JM, HARIBABU B et al.: A point mutation that confers constitutive activity to CXCR4 reveals T140 is an inverse agonist and AMD3100 and ALX40-4C are weak partial agonists. J. Biol. Chem. (2002) 277:24515-24521.
    • (2002) J. Biol. Chem. , vol.277 , pp. 24515-24521
    • Zhang, W.1    Navenot, J.M.2    Haribabu, B.3
  • 58
    • 0344012474 scopus 로고    scopus 로고
    • Lipid bilayer simulations of CXCR4 with inverse agonists and weak partial agonists
    • TRENT JO, WANG Z, MURRAY JL et al.: Lipid bilayer simulations of CXCR4 with inverse agonists and weak partial agonists. J. Biol. Chem. (2003) 278:47136-47144.
    • (2003) J. Biol. Chem. , vol.278 , pp. 47136-47144
    • Trent, J.O.1    Wang, Z.2    Murray, J.L.3
  • 59
    • 1842584928 scopus 로고    scopus 로고
    • Stromal cell-derived factor 1-mediated CXCR4 signaling in fat and human cortical neural progenitor cells
    • PENG H, HUANG Y, ROSE J et al.: Stromal cell-derived factor 1-mediated CXCR4 signaling in fat and human cortical neural progenitor cells. J. Neurosci. Res. (2004) 76:35-50.
    • (2004) J. Neurosci. Res. , vol.76 , pp. 35-50
    • Peng, H.1    Huang, Y.2    Rose, J.3
  • 60
    • 4644219817 scopus 로고    scopus 로고
    • Germinal center dark and light zone organization is mediated by CXCR4 and CXCR5
    • ALLEN CDC, ANSEL KM, LOW C et al.: Germinal center dark and light zone organization is mediated by CXCR4 and CXCR5. Nat. Immunol. (2004) 5:943-952.
    • (2004) Nat. Immunol. , vol.5 , pp. 943-952
    • Allen, C.D.C.1    Ansel, K.M.2    Low, C.3
  • 61
    • 0028860743 scopus 로고
    • Structure-activity relationships of cyclic pentapeptide endothelin A receptor antagonists
    • FUKAMI T, NAGASE T, FUJITA K et al.: Structure-activity relationships of cyclic pentapeptide endothelin A receptor antagonists. J. Med. Chem. (1995) 38:4309-4324.
    • (1995) J. Med. Chem. , vol.38 , pp. 4309-4324
    • Fukami, T.1    Nagase, T.2    Fujita, K.3
  • 63
    • 0029837395 scopus 로고    scopus 로고
    • Rediscovering an endothelin antagonist (BQ-123): A self-deconvoluting cyclic pentapeptide library
    • SPATOLA AF, CROZET Y, DEWIT D, YANAGISAWA M. Rediscovering an endothelin antagonist (BQ-123): A self-deconvoluting cyclic pentapeptide library. J. Med. Chem. (1996) 39:3842-3846.
    • (1996) J. Med. Chem. , vol.39 , pp. 3842-3846
    • Spatola, A.F.1    Crozet, Y.2    Dewit, D.3    Yanagisawa, M.4
  • 65
    • 0033000078 scopus 로고    scopus 로고
    • Cyclic pentapeptides of chiral sequence DLDDL as scaffold for antagonism of G-protein coupled receptors: Synthesis, activity and conformational analysis by NMR and molecular dynamics of ITF 1565 a substance P inhibitor
    • PORCELLI M, CASU M, LAI A et al.: Cyclic pentapeptides of chiral sequence DLDDL as scaffold for antagonism of G-protein coupled receptors: synthesis, activity and conformational analysis by NMR and molecular dynamics of ITF 1565 a substance P inhibitor. Biopolymers (1999) 50:211-219.
    • (1999) Biopolymers , vol.50 , pp. 211-219
    • Porcelli, M.1    Casu, M.2    Lai, A.3
  • 67
    • 10744227507 scopus 로고    scopus 로고
    • Molecular-size reduction of a potent CXCR4-chemokine antagonist using orthogonal combination of conformation-and sequence-based libraries
    • FUJII N, OISHI S, HIRAMATSU K et al.: Molecular-size reduction of a potent CXCR4-chemokine antagonist using orthogonal combination of conformation-and sequence-based libraries. Angew. Chem. Int. Ed. Engl. (2003) 42:3251-3253.
    • (2003) Angew. Chem. Int. Ed. Engl. , vol.42 , pp. 3251-3253
    • Fujii, N.1    Oishi, S.2    Hiramatsu, K.3
  • 69
    • 33751158672 scopus 로고
    • SN2' reactions of peptide aziridines. A cuprate-based approach to (E)-alkene isosteres
    • WIPF P, FRITCH PC: SN2' reactions of peptide aziridines. A cuprate-based approach to (E)-alkene isosteres. J. Org. Chem. (1994) 59:4875-4886.
    • (1994) J. Org. Chem. , vol.59 , pp. 4875-4886
    • Wipf, P.1    Fritch, P.C.2
  • 70
    • 37049074279 scopus 로고
    • N2' ring opening of aziridines bearing an α,β-unsaturated ester group with organocopper reagents. A new stereoselective synthetic route to (E)-alkene dipeptide isosteres
    • N2' ring opening of aziridines bearing an α,β-unsaturated ester group with organocopper reagents. A new stereoselective synthetic route to (E)-alkene dipeptide isosteres. J. Chem. Soc. (1995):1359-1371.
    • (1995) J. Chem. Soc. , pp. 1359-1371
    • Fujii, N.1    Nakai, K.2    Tamamura, H.3
  • 71
    • 0029157638 scopus 로고
    • Allylsilanes in organic synthesis; stereoselective synthesis of transalkene peptide isosteres
    • DALY MJ, WARD RA, THOMPSON DF, PROCTER G.: Allylsilanes in organic synthesis; stereoselective synthesis of transalkene peptide isosteres. Tetrahedron Lett. (1995) 36:7545-7548.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 7545-7548
    • Daly, M.J.1    Ward, R.A.2    Thompson, D.F.3    Procter, G.4
  • 72
    • 18344368807 scopus 로고    scopus 로고
    • Synthesis and evaluation of pseudopeptide analogues of a specific CXCR4 inhibitor, T140: The insertion of an (E)-alkene dipeptide isostere into the βII'-turn moiety
    • TAMAMURA H, HIRAMATSU K, MIYAMOTO K et al.: Synthesis and evaluation of pseudopeptide analogues of a specific CXCR4 inhibitor, T140: the insertion of an (E)-alkene dipeptide isostere into the βII'-turn moiety. Bioorg. Med. Chem. Lett. (2002) 12:923-928.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 923-928
    • Tamamura, H.1    Hiramatsu, K.2    Miyamoto, K.3
  • 73
    • 0344519605 scopus 로고    scopus 로고
    • Reduction of peptide character of HIV protease inhibitors that exhibit nanomolar potency against multi-drug resistant HIV-1 strains
    • TAMAMURA H, KOH Y, UEDA S et al.: Reduction of peptide character of HIV protease inhibitors that exhibit nanomolar potency against multi-drug resistant HIV-1 strains. J. Med. Chem. (2003) 46:1764-1768.
    • (2003) J. Med. Chem. , vol.46 , pp. 1764-1768
    • Tamamura, H.1    Koh, Y.2    Ueda, S.3
  • 74
    • 0000596010 scopus 로고    scopus 로고
    • Regiospecific ring-opening reactions of aziridines bearing an αβ-unsaturated ester group with trifluoroacetic acid or methanesulfonic acid: Application to the stereoselective synthesis of (E)-alkene dipeptide isosteres
    • TAMAMURA H, YAMASHITA M, MURAMATSU H et al.: Regiospecific ring-opening reactions of aziridines bearing an αβ-unsaturated ester group with trifluoroacetic acid or methanesulfonic acid: Application to the stereoselective synthesis of (E)-alkene dipeptide isosteres. Chem. Commun. (1997) 2327-2328.
    • (1997) Chem. Commun. , pp. 2327-2328
    • Tamamura, H.1    Yamashita, M.2    Muramatsu, H.3
  • 75
    • 33746385828 scopus 로고    scopus 로고
    • Regiospecific ring-opening reactions of β-aziridinyl α,β-enoates with acids: Application to the stereoselective synthesis of a couple of diastereoisomeric (E)-alkene dipeptide isosteres from a single β-aziridinyl α,β-enoate and to the convenient preparation of amino alcohols bearing α,β-unsaturated ester groups
    • TAMAMURA H, YAMASHITA M, NAKAJIMA Y et al.: Regiospecific ring-opening reactions of β-aziridinyl α,β-enoates with acids: application to the stereoselective synthesis of a couple of diastereoisomeric (E)-alkene dipeptide isosteres from a single β-aziridinyl α,β-enoate and to the convenient preparation of amino alcohols bearing α,β-unsaturated ester groups. J. Chem. Soc. (1999) 2983-2996.
    • (1999) J. Chem. Soc. , pp. 2983-2996
    • Tamamura, H.1    Yamashita, M.2    Nakajima, Y.3
  • 76
    • 0034740849 scopus 로고    scopus 로고
    • Stereoselective synthesis of a set of two functionalized (E)-alkene dipeptide isosteres of L-amino acid-L-Glu and L-amino acid-D-Glu
    • OISHI S, TAMAMURA H, YAMASHITA M et al.: Stereoselective synthesis of a set of two functionalized (E)-alkene dipeptide isosteres of L-amino acid-L-Glu and L-amino acid-D-Glu. J. Chem. Soc., Perkin Trans. 1(2001) 2445-2451.
    • (2001) J. Chem. Soc., Perkin Trans. 1 , pp. 2445-2451
    • Oishi, S.1    Tamamura, H.2    Yamashita, M.3
  • 77
    • 19944431731 scopus 로고    scopus 로고
    • Stereoselective synthesis of [L-Arg, L/D-3-(2-naphthyl)alanine]-type (E)-alkene dipeptide isosteres and its application to the synthesis and biological evaluation of pseudopeptide analogs of the CXCR4 antagonist FC131
    • TAMAMURA H, HIRAMATSU K, UEDA S et al.: Stereoselective synthesis of [L-Arg, L/D-3-(2-naphthyl)alanine]-type (E)-alkene dipeptide isosteres and its application to the synthesis and biological evaluation of pseudopeptide analogs of the CXCR4 antagonist FC131. J. Med. Chem. (2005) 48:380-391.
    • (2005) J. Med. Chem. , vol.48 , pp. 380-391
    • Tamamura, H.1    Hiramatsu, K.2    Ueda, S.3
  • 78
    • 20944452022 scopus 로고    scopus 로고
    • Identification of novel low molecular weight CXCR4 antagonists by structural tuning of cyclic tetrapeptide-scaffolds
    • TAMAMURA H, ARAKI T, UEDA S et al.: Identification of novel low molecular weight CXCR4 antagonists by structural tuning of cyclic tetrapeptide-scaffolds. J. Med. Chem. (2005) 48:3280-3289.
    • (2005) J. Med. Chem. , vol.48 , pp. 3280-3289
    • Tamamura, H.1    Araki, T.2    Ueda, S.3
  • 79
    • 0034899714 scopus 로고    scopus 로고
    • Small molecule antagonists of chemokine receptors as emerging anti-HIV agents
    • MASTROLORENZO A, SCOZZAFAVA A, SUPURAN CT: Small molecule antagonists of chemokine receptors as emerging anti-HIV agents. Expert Opin. Ther. Pat. (2001) 11:1245-1252.
    • (2001) Expert Opin. Ther. Pat. , vol.11 , pp. 1245-1252
    • Mastrolorenzo, A.1    Scozzafava, A.2    Supuran, C.T.3
  • 81
    • 0030830661 scopus 로고    scopus 로고
    • Inhibition of T-tropic HIV strains by selective antagonization of the chemokine receptor CXCR4
    • SCHOLS D, STRUYF S, VAN DAMME J, ESTE JA, HENSON G, DE CLERCQ E: Inhibition of T-tropic HIV strains by selective antagonization of the chemokine receptor CXCR4. J. Exp. Med. (1997) 186:1383-1388.
    • (1997) J. Exp. Med. , vol.186 , pp. 1383-1388
    • Schols, D.1    Struyf, S.2    Van Damme, J.3    Este, J.A.4    Henson, G.5    De Clercq, E.6
  • 82
    • 0030773515 scopus 로고    scopus 로고
    • A small-molecule inhibitor directed against the chemokine receptor CXCR4 prevents its use as an HIV-1 coreceptor
    • DORANZ BJ, GROVIT-FERBAS K, SHARRON MP et al.: A small-molecule inhibitor directed against the chemokine receptor CXCR4 prevents its use as an HIV-1 coreceptor. J. Exp. Med. (1997) 186:1395-1400.
    • (1997) J. Exp. Med. , vol.186 , pp. 1395-1400
    • Doranz, B.J.1    Grovit-Ferbas, K.2    Sharron, M.P.3
  • 83
    • 0036846898 scopus 로고    scopus 로고
    • New anti-HIV agents and targets
    • DE CLERCQ E: New anti-HIV agents and targets. Med. Res. Rev. (2002) 22:531-565.
    • (2002) Med. Res. Rev. , vol.22 , pp. 531-565
    • De Clercq, E.1
  • 84
    • 3042595910 scopus 로고    scopus 로고
    • Small-molecule antagonists of CCR5 and CXCR4: A promising new class of anti-HIV-1 drugs
    • SEIBERT C, SAKMAR TP. Small-molecule antagonists of CCR5 and CXCR4: A promising new class of anti-HIV-1 drugs. Curr. Pharm. Design 2004) 10:2041-2062.
    • (2004) Curr. Pharm. Design , vol.10 , pp. 2041-2062
    • Seibert, C.1    Sakmar, T.P.2
  • 85
    • 27844585259 scopus 로고    scopus 로고
    • Virus resistance to the CXCR4 inhibitor AMD070 develops slowly and does not induce a co-receptor switch
    • VERMEIRE K, HATSE S, PRINCEN K et al.: Virus resistance to the CXCR4 inhibitor AMD070 develops slowly and does not induce a co-receptor switch. Antiviral Res. (2004) 62: A42-A43.
    • (2004) Antiviral Res. , vol.62
    • Vermeire, K.1    Hatse, S.2    Princen, K.3
  • 86
    • 0347360255 scopus 로고    scopus 로고
    • New bicyclam-GalCer analogue conjugates: Synthesis and in vitro anti-HIV activity
    • DAOUDI J-M, GREINER J, AUBERTIN A-M, VIERLING P: New bicyclam-GalCer analogue conjugates: synthesis and in vitro anti-HIV activity. Bioorg. Med. Chem. Lett. (2004) 14:495-498.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 495-498
    • Daoudi, J.-M.1    Greiner, J.2    Aubertin, A.-M.3    Vierling, P.4
  • 87
    • 0037388121 scopus 로고    scopus 로고
    • A duodenally absorbable CXC chemokine receptor 4 antagonist, KRH-1636, exhibits a potent and selective anti-HIV-1 activity
    • ICHIYAMA K, YOKOYAMA-KUMAKURA S, TANAKA Y et al.: A duodenally absorbable CXC chemokine receptor 4 antagonist, KRH-1636, exhibits a potent and selective anti-HIV-1 activity. Proc. Natl. Acad. Sci. USA. (2003) 100:4185-4190.
    • (2003) Proc. Natl. Acad. Sci. USA. , vol.100 , pp. 4185-4190
    • Ichiyama, K.1    Yokoyama-Kumakura, S.2    Tanaka, Y.3
  • 88
    • 0036027903 scopus 로고    scopus 로고
    • Anti-HIV activity of a novel aminoglycoside-arginine conjugate
    • CABRERA C, GUTIERREZ A, BARRETINA J et al.: Anti-HIV activity of a novel aminoglycoside-arginine conjugate. Antiviral Res. (2002) 53:1-8.
    • (2002) Antiviral Res. , vol.53 , pp. 1-8
    • Cabrera, C.1    Gutierrez, A.2    Barretina, J.3
  • 89
    • 0034192188 scopus 로고    scopus 로고
    • Anti-human immunodeficiency virus activity of novel aminoglycoside-arginine conjugates at early stages of infection
    • CABRERA C, GUTIERREZ A, BLANCO J et al.: Anti-human immunodeficiency virus activity of novel aminoglycoside-arginine conjugates at early stages of infection. AIDS Res. Hum. Retroviruses (2000) 16:627-634.
    • (2000) AIDS Res. Hum. Retroviruses , vol.16 , pp. 627-634
    • Cabrera, C.1    Gutierrez, A.2    Blanco, J.3
  • 90
    • 0033971512 scopus 로고    scopus 로고
    • A second target for the peptoid Tat/transactivation response element inhibitor CGP64222: Inhibition of human immunodeficiency virus replication by blocking CXC-chemokine receptor 4-mediated virus entry
    • DAELEMANS D, SCHOLS D, WITVROUW M et al.: A second target for the peptoid Tat/transactivation response element inhibitor CGP64222: Inhibition of human immunodeficiency virus replication by blocking CXC-chemokine receptor 4-mediated virus entry. Mol. Pharmacol. (2000) 57:116-124.
    • (2000) Mol. Pharmacol. , vol.57 , pp. 116-124
    • Daelemans, D.1    Schols, D.2    Witvrouw, M.3
  • 91
    • 14444282418 scopus 로고    scopus 로고
    • Inhibition of in vitro and in vivo HIV replication by a distamycin analogue that interferes with chemokine receptor function: A candidate for chemotherapeutic and microbicidal application
    • HOWARD OMZ, OPPENHEIM JJ, HOLLINGSHEAD MG et al.: Inhibition of in vitro and in vivo HIV replication by a distamycin analogue that interferes with chemokine receptor function: a candidate for chemotherapeutic and microbicidal application. J. Med. Chem. (1998) 41:2184-2193.
    • (1998) J. Med. Chem. , vol.41 , pp. 2184-2193
    • Howard, O.M.Z.1    Oppenheim, J.J.2    Hollingshead, M.G.3


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