메뉴 건너뛰기




Volumn 13, Issue 6, 2003, Pages 773-786

Small molecule inhibitors of urokinase-type plasminogen activator

Author keywords

Benzo b thiophene carboxamidine; Guanidine; Naphthamidine; Plasminogen activator inhibitor 1 (PAI 1); Urokinase; Urokinase receptor; Urokinase type plasminogen activator (uPA); WX UK1

Indexed keywords

AMIDINE; AMINO ACID; ANGIOGENESIS INHIBITOR; ANTINEOPLASTIC AGENT; BENZOIC ACID DERIVATIVE; BENZOTHIOPHENE DERIVATIVE; BENZYLAMINE DERIVATIVE; CARBOLINE DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; CELL SURFACE RECEPTOR; CYCLOPEPTIDE; GROWTH FACTOR; GUANIDINE DERIVATIVE; HEPARIN; INDOLOAMIDINE DERIVATIVE; ISOTHIURONIUM DERIVATIVE; NAPHTHAMIDINE DERIVATIVE; PEPTOID; PHENYLPROPIONIC ACID DERIVATIVE; PLASMIN; PLASMINOGEN; PLASMINOGEN ACTIVATOR INHIBITOR; PLASMINOGEN ACTIVATOR INHIBITOR 1; RHODAMINE; SERINE PROTEINASE; UNCLASSIFIED DRUG; UNINDEXED DRUG; UROKINASE; UROKINASE RECEPTOR; WX UK 1; WX UK1;

EID: 0038647770     PISSN: 13543776     EISSN: None     Source Type: Journal    
DOI: 10.1517/13543776.13.6.773     Document Type: Review
Times cited : (14)

References (60)
  • 1
    • 0037724456 scopus 로고    scopus 로고
    • NO AUTHORS LISTED American Cancer Society Monograph
    • NO AUTHORS LISTED: Cancer Facts and Figures. American Cancer Society Monograph (2002):1-45.
    • (2002) Cancer Facts and Figures , pp. 1-45
  • 2
    • 0037192458 scopus 로고    scopus 로고
    • Matrix metalloprotease inhibitors and cancer: Trials and tribulations
    • COUSSENS, LM, FINGLETON B, MATRISIAN LM: Matrix metalloprotease inhibitors and cancer: trials and tribulations. Science (2002) 295:2387-2392.
    • (2002) Science , vol.295 , pp. 2387-2392
    • Coussens, L.M.1    Fingleton, B.2    Matrisian, L.M.3
  • 3
    • 0025240096 scopus 로고
    • 2-terminal amino acid sequence and glycosylation variants
    • 2-terminal amino acid sequence and glycosylation variants. J. Biol. Chem. (1990) 265(11 ):6453-6460.
    • (1990) J. Biol. Chem. , vol.265 , Issue.11 , pp. 6453-6460
    • Behrendt, N.1    Ronne, E.2    Ploug, M.3
  • 4
    • 0026892236 scopus 로고
    • Tumor-associated urokinase-type plasminogen activator: Biological and clinical significance
    • SCHMITT M, JANICKE F, MONIWA N et al.: Tumor-associated urokinase-type plasminogen activator: biological and clinical significance Biol. Chem. Hoppe Seyler (1992) 373(7):611-622.
    • (1992) Biol. Chem. Hoppe Seyler , vol.373 , Issue.7 , pp. 611-622
    • Schmitt, M.1    Janicke, F.2    Moniwa, N.3
  • 5
    • 0025527558 scopus 로고
    • Plasminogen activators and cancer
    • DUFFY MJ: Plasminogen activators and cancer. Blood Coagul. Fibrinolysis (1990) 1(6):681-687.
    • (1990) Blood Coagul. Fibrinolysis , vol.1 , Issue.6 , pp. 681-687
    • Duffy, M.J.1
  • 6
    • 0031406601 scopus 로고    scopus 로고
    • Urokinase in rheumatoid arthritis: Causal or coincidental?
    • BUSSO N, SO A: Urokinase in rheumatoid arthritis: causal or coincidental? Ann. Rheum. Dis. (1997) 56(12):705-706.
    • (1997) Ann. Rheum. Dis. , vol.56 , Issue.12 , pp. 705-706
    • Busso, N.1    So, A.2
  • 7
    • 0030791995 scopus 로고    scopus 로고
    • Bone matrix degradation by the plasminigen activation system. Possible mechanism of bone destruction in arthritis
    • RONDAY HK, SMITS HH, QUAX PH et al.: Bone matrix degradation by the plasminigen activation system. Possible mechanism of bone destruction in arthritis. Br. J. Rheumatol. (1997) 36:9-15.
    • (1997) Br. J. Rheumatol. , vol.36 , pp. 9-15
    • Ronday, H.K.1    Smits, H.H.2    Quax, P.H.3
  • 8
    • 16944363984 scopus 로고    scopus 로고
    • Urokinase-generated plasmin activates matrix metalloproteinases during aneurysm formation
    • CARMELIET P, MOONS L, LIJNEN R et al.: Urokinase-generated plasmin activates matrix metalloproteinases during aneurysm formation. Nat. Genetics (1997) 17(4):439-444.
    • (1997) Nat. Genetics , vol.17 , Issue.4 , pp. 439-444
    • Carmeliet, P.1    Moons, L.2    Lijnen, R.3
  • 10
    • 0032826035 scopus 로고    scopus 로고
    • Inhibition of plasminogen activators or matrix metalloproteinases prevents cardiac rupture but impairs therapeutic angiogenesis and causes cardiac failure
    • HEYMANS S, LUTTUN A, NUYENS D: Inhibition of plasminogen activators or matrix metalloproteinases prevents cardiac rupture but impairs therapeutic angiogenesis and causes cardiac failure. Nat. Med. (1999) 5(10):1135-1142.
    • (1999) Nat. Med. , vol.5 , Issue.10 , pp. 1135-1142
    • Heymans, S.1    Luttun, A.2    Nuyens, D.3
  • 11
    • 0031733174 scopus 로고    scopus 로고
    • Multifunctional potential of the plasminogen activation system in tumor invasion and metastasis
    • (review)
    • REUNING U, MAGDOLEN V, WILHELM O et al.: Multifunctional potential of the plasminogen activation system in tumor invasion and metastasis (review). Int. J. Oncology (1998) 13(5):893-906.
    • (1998) Int. J. Oncology , vol.13 , Issue.5 , pp. 893-906
    • Reuning, U.1    Magdolen, V.2    Wilhelm, O.3
  • 12
    • 0031802807 scopus 로고    scopus 로고
    • Time and dose dependency of the suppression of pulmonary metastasis of rat mammary cancer by amiloride
    • EVANS DM, SLOAN-STAKLEFF K, ARVAN M, GUYTON DP: Time and dose dependency of the suppression of pulmonary metastasis of rat mammary cancer by amiloride. Clin. Exp. Metastasis (1998) 16:353-357.
    • (1998) Clin. Exp. Metastasis , vol.16 , pp. 353-357
    • Evans, D.M.1    Sloan-Stakleff, K.2    Arvan, M.3    Guyton, D.P.4
  • 13
    • 0032479554 scopus 로고    scopus 로고
    • The field bean protease inhibitor has the potential to suppress B16F10 melanoma cell lung metastasis in mice
    • BANERJI A, FERNANDES A, BANE S, AHIRE S: The field bean protease inhibitor has the potential to suppress B16F10 melanoma cell lung metastasis in mice. Cancer Lett. (1998) 129:15-20.
    • (1998) Cancer Lett. , vol.129 , pp. 15-20
    • Banerji, A.1    Fernandes, A.2    Bane, S.3    Ahire, S.4
  • 14
    • 0029642314 scopus 로고
    • Prevention of prostate-cancer metastasis in vivo by a novel synthetic inhibitor of urokinase-type plasminogen activator (uPA)
    • RABBANI SA, HARAKIDAS P, DAVIDSON DJ, HENKIN J, MAZAR AP: Prevention of prostate-cancer metastasis in vivo by a novel synthetic inhibitor of urokinase-type plasminogen activator (uPA). Int. J. Cancer (1995) 63(6):840-845.
    • (1995) Int. J. Cancer , vol.63 , Issue.6 , pp. 840-845
    • Rabbani, S.A.1    Harakidas, P.2    Davidson, D.J.3    Henkin, J.4    Mazar, A.P.5
  • 15
    • 0032411796 scopus 로고    scopus 로고
    • Inhibition of mammary tumor cell adhesion, migration, and invasion by the selective synthetic urokinase inhibitor B428
    • ALONSO DF, TEJERA AM, FARIAS EF, BAL DE KIER JOFFE E, GOMEZ DE: Inhibition of mammary tumor cell adhesion, migration, and invasion by the selective synthetic urokinase inhibitor B428. Anti-Cancer Res. (1998) 18:4499-4504.
    • (1998) Anti-Cancer Res. , vol.18 , pp. 4499-4504
    • Alonso, D.F.1    Tejera, A.M.2    Farias, E.F.3    Bal De Kier Joffe, E.4    Gomez, D.E.5
  • 16
    • 0029682495 scopus 로고    scopus 로고
    • Induction of primary cutaneous melanocytic neoplasms in urokinase-type plasminogen activator (uPA)-deficient and wild-type mice: Cellular blue nevi invade but do not progress to malignant melanoma in uPA-deficient animals
    • SHAPIRO RL, DUQUETTE JG, ROSES DF et al.: Induction of primary cutaneous melanocytic neoplasms in urokinase-type plasminogen activator (uPA)-deficient and wild-type mice: cellular blue nevi invade but do not progress to malignant melanoma in uPA-deficient animals. Cancer Res. (1996) 56(15):3597-3604.
    • (1996) Cancer Res. , vol.56 , Issue.15 , pp. 3597-3604
    • Shapiro, R.L.1    Duquette, J.G.2    Roses, D.F.3
  • 17
    • 0031890874 scopus 로고    scopus 로고
    • Inhibition of establishment of primary and micrometastatic tumors by a urokinase plasminogen activator receptor antagonist
    • IGNAR DM, ANDREWS JL, WITHERSPOON SM et al.: Inhibition of establishment of primary and micrometastatic tumors by a urokinase plasminogen activator receptor antagonist. Clin. Exp. Metastasis (1998) 16:9-20.
    • (1998) Clin. Exp. Metastasis , vol.16 , pp. 9-20
    • Ignar, D.M.1    Andrews, J.L.2    Witherspoon, S.M.3
  • 18
    • 0029834684 scopus 로고    scopus 로고
    • Overexpression of urokinase receptor in breast cancer cells results in increased tumor invasion, growth and metastasis
    • XING RH, RABBANI A: Overexpression of urokinase receptor in breast cancer cells results in increased tumor invasion, growth and metastasis. Int. J. Cancer (1996) 67:423-429.
    • (1996) Int. J. Cancer , vol.67 , pp. 423-429
    • Xing, R.H.1    Rabbani, A.2
  • 19
    • 0028919172 scopus 로고
    • Overexpression of plasminogen activator inhibitor 2 in human melanoma cells inhibits spontaneous metastasis in SCID/SCID mice
    • MUELLER BM, YU YB, LAUG WE: Overexpression of plasminogen activator inhibitor 2 in human melanoma cells inhibits spontaneous metastasis in SCID/SCID mice. Proc. Natl. Acad. Sci. USA (1995) 92:205-209.
    • (1995) Proc. Natl. Acad. Sci. USA , vol.92 , pp. 205-209
    • Mueller, B.M.1    Yu, Y.B.2    Laug, W.E.3
  • 20
    • 0028935381 scopus 로고
    • Plasminogen activator inhibitor-2: Prognostic relevance in 1012 patients with primary breast cancer
    • FOEKENS JA, BUESSECKER F, PETERS HA et al.: Plasminogen activator inhibitor-2: prognostic relevance in 1012 patients with primary breast cancer. Cancer Res. (1995) 55(7):1423-1427.
    • (1995) Cancer Res. , vol.55 , Issue.7 , pp. 1423-1427
    • Foekens, J.A.1    Buessecker, F.2    Peters, H.A.3
  • 21
    • 0031925511 scopus 로고    scopus 로고
    • Prognostic markers other than hormone receptors in breast cancer
    • FLEISHER M: Prognostic markers other than hormone receptors in breast cancer. J. Clin. Ligand Assay (1998) 21:41-46.
    • (1998) J. Clin. Ligand Assay , vol.21 , pp. 41-46
    • Fleisher, M.1
  • 22
    • 0031029405 scopus 로고    scopus 로고
    • Plasminogen activator inhibitor Type 1 in cytosolic tumor extracts predicts prognosis in low-risk breast cancer patients
    • GRONDAHL-HANSEN J, CHRISTENSEN IJ, BRIAND P et al.: Plasminogen activator inhibitor Type 1 in cytosolic tumor extracts predicts prognosis in low-risk breast cancer patients. Clin. Cancer Res. (1997) 3(2):233-239.
    • (1997) Clin. Cancer Res. , vol.3 , Issue.2 , pp. 233-239
    • Grondahl-Hansen, J.1    Christensen, I.J.2    Briand, P.3
  • 23
    • 0031902286 scopus 로고    scopus 로고
    • Absence of host plasminogen activator inhibitor 1 prevents cancer invasion and vascularization
    • BAJOU K, NOEL A, GERARD RD et al.: Absence of host plasminogen activator inhibitor 1 prevents cancer invasion and vascularization. Nat. Med. (1998) 4(8):923-928.
    • (1998) Nat. Med. , vol.4 , Issue.8 , pp. 923-928
    • Bajou, K.1    Noel, A.2    Gerard, R.D.3
  • 24
    • 2642705008 scopus 로고    scopus 로고
    • Prognostic impact of urokinase-type plasminogen activator (PA), PA inhibitor type-1, and tissue-type PA antigen levels in node-negative breast cancer: A prospective study on multicenter basis
    • KIM SJ, SHIBA E, KOBAYASHI T et al.: Prognostic impact of urokinase-type plasminogen activator (PA), PA inhibitor type-1, and tissue-type PA antigen levels in node-negative breast cancer: a prospective study on multicenter basis. Clin. Cancer Res. (1998) 4(1):177-182.
    • (1998) Clin. Cancer Res. , vol.4 , Issue.1 , pp. 177-182
    • Kim, S.J.1    Shiba, E.2    Kobayashi, T.3
  • 25
    • 15144342245 scopus 로고    scopus 로고
    • Prognostic impact of tumor biological factors on survival in nodenegative breast cancer
    • HARBECK N, DETTMAR P, THOMSSEN C et al.: Prognostic impact of tumor biological factors on survival in nodenegative breast cancer. Anti-Cancer Res. (1998) 18:2187-2198.
    • (1998) Anti-Cancer Res. , vol.18 , pp. 2187-2198
    • Harbeck, N.1    Dettmar, P.2    Thomssen, C.3
  • 26
    • 0034014726 scopus 로고    scopus 로고
    • Plasminogen activator inhibitor 1 may promote tumour growth through inhibition of apoptosis
    • KWAAN HC, WANG J, SVOBODA K, DECLERCK PJ: Plasminogen activator inhibitor 1 may promote tumour growth through inhibition of apoptosis. Br. J. Cancer (2000) 82:1702-1706.
    • (2000) Br. J. Cancer , vol.82 , pp. 1702-1706
    • Kwaan, H.C.1    Wang, J.2    Svoboda, K.3    Declerck, P.J.4
  • 27
    • 0002606253 scopus 로고    scopus 로고
    • The urokinase plasminogen activator system in cancer: Implications for tumor angiogenesis and metastasis
    • MAZAR A, HENKIN J, GOLDFARB RH: The urokinase plasminogen activator system in cancer: implications for tumor angiogenesis and metastasis. Angiogenesis (1999) 3:15-32.
    • (1999) Angiogenesis , vol.3 , pp. 15-32
    • Mazar, A.1    Henkin, J.2    Goldfarb, R.H.3
  • 28
    • 0027223048 scopus 로고
    • High levels of urokinase-type plasminogen activator and its inhibitor PAI-1 in cytosolic extracts of breast carcinomas are associated with poor prognosis
    • GRONDAHL-HANSEN J, CHRISTENSEN IJ, ROSENQUIST C et al.: High levels of urokinase-type plasminogen activator and its inhibitor PAI-1 in cytosolic extracts of breast carcinomas are associated with poor prognosis. Cancer Res. (1993) 53(11):2513-2521.
    • (1993) Cancer Res. , vol.53 , Issue.11 , pp. 2513-2521
    • Grondahl-Hansen, J.1    Christensen, I.J.2    Rosenquist, C.3
  • 29
    • 0030815119 scopus 로고    scopus 로고
    • Inhibition of metastasis of intraocular melanomas by adenoviral gene transfer of plasminogen activator inhibitor Type 1 (PAI-1) in an athymic mouse model
    • MA D, GERARD RD, LI XY, ALIZADEH H, NIEDERKORN JY: Inhibition of metastasis of intraocular melanomas by adenoviral gene transfer of plasminogen activator inhibitor Type 1 (PAI-1) in an athymic mouse model. Blood (1997) 90:2738-2746.
    • (1997) Blood , vol.90 , pp. 2738-2746
    • Ma, D.1    Gerard, R.D.2    Li, X.Y.3    Alizadeh, H.4    Niederkorn, J.Y.5
  • 30
    • 0028821827 scopus 로고
    • Expression of plasminogen activator inhibitor Type 1 in human prostate carcinoma cells inhibits primary tumor growth, tumor-associated angiogenesis and metastasis to lung and liver in athymic mouse model
    • SOFF GA, SANDEROWITZ J, GATELY S et al.: Expression of plasminogen activator inhibitor Type 1 in human prostate carcinoma cells inhibits primary tumor growth, tumor-associated angiogenesis and metastasis to lung and liver in athymic mouse model. J. Clin. Invest. (1995) 96(6):2593-2600.
    • (1995) J. Clin. Invest. , vol.96 , Issue.6 , pp. 2593-2600
    • Soff, G.A.1    Sanderowitz, J.2    Gately, S.3
  • 32
    • 0000124642 scopus 로고    scopus 로고
    • Plasminogen activator inhibitor-1 represses integrin and vitronectin-mediated cell migration independently of its function as an inhibitor of plasminogen activation
    • KJOLLER L, KANSE SM, KIRKEGAARD T et al.: Plasminogen activator inhibitor-1 represses integrin and vitronectin-mediated cell migration independently of its function as an inhibitor of plasminogen activation. Exp. Cell Res. (1997) 232:420-429.
    • (1997) Exp. Cell Res. , vol.232 , pp. 420-429
    • Kjoller, L.1    Kanse, S.M.2    Kirkegaard, T.3
  • 33
    • 0035823504 scopus 로고    scopus 로고
    • Plasminogen activator inhibitor-1 regulates tumor growth and angiogenesis
    • MCMAHON GA, PETITCLERC E, STEFANSSON S et al.: Plasminogen activator inhibitor-1 regulates tumor growth and angiogenesis. J. Biol. Chem. (2001) 276(36):33964-33968.
    • (2001) J. Biol. Chem. , vol.276 , Issue.36 , pp. 33964-33968
    • Mcmahon, G.A.1    Petitclerc, E.2    Stefansson, S.3
  • 34
    • 0037146737 scopus 로고    scopus 로고
    • Both uPA inhibition and vitronectin binding by plasminogen activator inhibitor 1 regulates HT1080 fibrosarcoma cell metastasis
    • PRAUS M, COLLEN D, GERARD RD: Both uPA inhibition and vitronectin binding by plasminogen activator inhibitor 1 regulates HT1080 fibrosarcoma cell metastasis. Int. J. Cancer (2002) 102:584-591.
    • (2002) Int. J. Cancer , vol.102 , pp. 584-591
    • Praus, M.1    Collen, D.2    Gerard, R.D.3
  • 35
    • 0026793887 scopus 로고
    • Heparin binding to the urokinase kringle domain
    • STEPHENS RW, BOKMAN AM, MYOHANEN HT et al.: Heparin binding to the urokinase kringle domain. Biochemistry (1992) 31(33):7572-7579.
    • (1992) Biochemistry , vol.31 , Issue.33 , pp. 7572-7579
    • Stephens, R.W.1    Bokman, A.M.2    Myohanen, H.T.3
  • 36
    • 0028292224 scopus 로고
    • Solution structure of the amino-terminal fragment of urokinase-type plasminogen activator
    • HANSEN AP, PETROS AM, MEADOWS RP et al.: Solution structure of the amino-terminal fragment of urokinase-type plasminogen activator. Biochemistry (1994) 33(16):4847-4864.
    • (1994) Biochemistry , vol.33 , Issue.16 , pp. 4847-4864
    • Hansen, A.P.1    Petros, A.M.2    Meadows, R.P.3
  • 37
    • 0027335769 scopus 로고
    • 1H]-NMR characterization of the urokinase kringle module. Structural, but not functional, relatedness to homologous domains
    • 1H]-NMR characterization of the urokinase kringle module. Structural, but not functional, relatedness to homologous domains. J. Biol. Chem. (1993) 268(19):13858-13868.
    • (1993) J. Biol. Chem. , vol.268 , Issue.19 , pp. 13858-13868
    • Bokman, A.M.1    Jimenez-Barbero, J.2    Llinas, M.3
  • 38
    • 0028181436 scopus 로고
    • Solution structure of the kringle domain from urokinase-type plasminogen activator
    • LI X, BOKMAN AM, LLINAS M, SMITH RA, DOBSON CM: Solution structure of the kringle domain from urokinase-type plasminogen activator. J. Mol. Biol. (1994) 235(5):1548-1559.
    • (1994) J. Mol. Biol. , vol.235 , Issue.5 , pp. 1548-1559
    • Li, X.1    Bokman, A.M.2    Llinas, M.3    Smith, R.A.4    Dobson, C.M.5
  • 39
    • 0037687339 scopus 로고    scopus 로고
    • Anti-angiogenic activity of the recombinant kringle domain of urokinase and its specific entry into endothelial cells
    • KIM KS, HONG YK, JOE YA et al.: Anti-angiogenic activity of the recombinant kringle domain of urokinase and its specific entry into endothelial cells. J. Biol. Chem. (2003) 278(13):11449-11456.
    • (2003) J. Biol. Chem. , vol.278 , Issue.13 , pp. 11449-11456
    • Kim, K.S.1    Hong, Y.K.2    Joe, Y.A.3
  • 40
    • 0023223148 scopus 로고
    • The receptor-binding sequence of urokinase. A biological function for the growth-factor module of proteases
    • APPELLA E, ROBINSON EA, ULLRICH SJ et al.: The receptor-binding sequence of urokinase. A biological function for the growth-factor module of proteases. J. Biol. Chem. (1987) 262(10):4437-4440.
    • (1987) J. Biol. Chem. , vol.262 , Issue.10 , pp. 4437-4440
    • Appella, E.1    Robinson, E.A.2    Ullrich, S.J.3
  • 41
    • 9344234400 scopus 로고    scopus 로고
    • Systematic mutational analysis of the receptor-binding region of the human urokinase-type plasminogen activator
    • MAGDOLEN V, RETTENBERGER P, KOPPITZ M et al.: Systematic mutational analysis of the receptor-binding region of the human urokinase-type plasminogen activator. Eur. J. Biochem. (1996) 237(3):743-751.
    • (1996) Eur. J. Biochem. , vol.237 , Issue.3 , pp. 743-751
    • Magdolen, V.1    Rettenberger, P.2    Koppitz, M.3
  • 42
    • 0037038308 scopus 로고    scopus 로고
    • Synthesis, solution structure and biological evaluation of urokinase-type plasminogen activator (uPA)-derived receptor binding domain mimetics
    • SCHMIEDEBERG N, SCHMITT M, ROLZ C et al.: Synthesis, solution structure and biological evaluation of urokinase-type plasminogen activator (uPA)-derived receptor binding domain mimetics. J. Med. Chem. (2002) 45(23):4984-4994.
    • (2002) J. Med. Chem. , vol.45 , Issue.23 , pp. 4984-4994
    • Schmiedeberg, N.1    Schmitt, M.2    Rolz, C.3
  • 43
    • 0029645121 scopus 로고
    • The crystal structure of the catalytic domain of human urokinase-type plasminogen activator
    • SPRAGGON G, PHILLIPS C, NOWAK UK et al.: The crystal structure of the catalytic domain of human urokinase-type plasminogen activator. Structure (1995) 3(7):681-691.
    • (1995) Structure , vol.3 , Issue.7 , pp. 681-691
    • Spraggon, G.1    Phillips, C.2    Nowak, U.K.3
  • 44
    • 0034629461 scopus 로고    scopus 로고
    • Re-engineering of human urokinase provides a system for structure-based drug design at high resolution and reveals a novel structural subsite
    • NIENABER V, WANG J, DAVIDSON D, HENKIN J: Re-engineering of human urokinase provides a system for structure-based drug design at high resolution and reveals a novel structural subsite. J. Biol. Chem. (2000) 275(10):7239-7248.
    • (2000) J. Biol. Chem. , vol.275 , Issue.10 , pp. 7239-7248
    • Nienaber, V.1    Wang, J.2    Davidson, D.3    Henkin, J.4
  • 45
    • 0034657792 scopus 로고    scopus 로고
    • Structure-directed discovery of potent non-peptidic inhibitors of human urokinase that access a novel binding subsite
    • NIENABER VL, DAVIDSON D, EDALJI R et al.: Structure-directed discovery of potent non-peptidic inhibitors of human urokinase that access a novel binding subsite. Structure (2000) 8(5):553-563.
    • (2000) Structure , vol.8 , Issue.5 , pp. 553-563
    • Nienaber, V.L.1    Davidson, D.2    Edalji, R.3
  • 47
    • 0034636986 scopus 로고    scopus 로고
    • Crystals of the urokinase-type plasminogen activator variant β c-uPA in complex with small molecule inhibitors open the way towards structure-based drug design
    • ZESLAWSKA E, SCHWEINITZ A, KARCHER A et al.: Crystals of the urokinase-type plasminogen activator variant β c-uPA in complex with small molecule inhibitors open the way towards structure-based drug design. J. Mol. Biol. (2000) 301:465-475.
    • (2000) J. Mol. Biol. , vol.301 , pp. 465-475
    • Zeslawska, E.1    Schweinitz, A.2    Karcher, A.3
  • 48
    • 0028277928 scopus 로고
    • High-affinity urokinase receptor antagonists identified with bacteriophage peptide display
    • GOODSON RJ, DOYLE MV, KAUFMAN SE, ROSENBERG S: High-affinity urokinase receptor antagonists identified with bacteriophage peptide display. Proc. Nat. Acad. Sci. USA (1994) 91(15):7129-7133.
    • (1994) Proc. Nat. Acad. Sci. USA , vol.91 , Issue.15 , pp. 7129-7133
    • Goodson, R.J.1    Doyle, M.V.2    Kaufman, S.E.3    Rosenberg, S.4
  • 49
    • 0035833983 scopus 로고    scopus 로고
    • Peptide derived antagonists of the urokinase receptor
    • PLOUG M, OSTERGAARD S, GARDSVOLL H et al.: Peptide derived antagonists of the urokinase receptor. Biochemistry (2001) 40(40):12157-12168.
    • (2001) Biochemistry , vol.40 , Issue.40 , pp. 12157-12168
    • Ploug, M.1    Ostergaard, S.2    Gardsvoll, H.3
  • 50
    • 17944377395 scopus 로고    scopus 로고
    • Cyclo19,31[D-Cys19]-uPA 19-31 is a potent competitive antagonist of the interaction of urokinase-type plasminogen activator with its receptor (CD87)
    • MAGDOLEN V, BURGLE M, DE PRADA NA et al.: Cyclo19,31[D-Cys19]-uPA 19-31 is a potent competitive antagonist of the interaction of urokinase-type plasminogen activator with its receptor (CD87). Biol. Chem. (2001) 382(8):1197-205.
    • (2001) Biol. Chem. , vol.382 , Issue.8 , pp. 1197-1205
    • Magdolen, V.1    Burgle, M.2    De Prada, N.A.3
  • 51
    • 0030878999 scopus 로고    scopus 로고
    • Optimal subsite occupancy and design of a selective inhibitor of urokinase
    • KE SH, COOMBS GS, TACHIAS K, COREY DR, MADISON EL: Optimal subsite occupancy and design of a selective inhibitor of urokinase. J. Biol. Chem. (1997) 272(33):20456-20462.
    • (1997) J. Biol. Chem. , vol.272 , Issue.33 , pp. 20456-20462
    • Ke, S.H.1    Coombs, G.S.2    Tachias, K.3    Corey, D.R.4    Madison, E.L.5
  • 53
    • 0037025461 scopus 로고    scopus 로고
    • 4-Aminoarylguanidine and 4-aminobenzamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors
    • SPENCER JR, MCGEE D, ALLEN D et al.: 4-Aminoarylguanidine and 4-aminobenzamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors. Bioorg. Med. Chem. Lett. (2002) 12(15):2023-2026.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , Issue.15 , pp. 2023-2026
    • Spencer, J.R.1    Mcgee, D.2    Allen, D.3
  • 54
    • 0037025460 scopus 로고    scopus 로고
    • 2-(2-Hydroxy-3-alkoxyphenyl)-1H-benzimidazole-5-carboxamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors
    • MACKMAN RL, HUI HC, BREITENBUCHER JG et al.: 2-(2-Hydroxy-3-alkoxyphenyl)-1H-benzimidazole-5-carboxamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors. Bioorg. Med. Chem. Lett. (2002) 12(15):2019-2022.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , Issue.15 , pp. 2019-2022
    • Mackman, R.L.1    Hui, H.C.2    Breitenbucher, J.G.3
  • 55
    • 0035832101 scopus 로고    scopus 로고
    • Synthesis of thiophene-2-carboxamidines containing 2-aminothiazoles and their biological evaluation as urokinase inhibitors
    • WILSON KJ, ILLIG CR, SUBASINGHE N et al.: Synthesis of thiophene-2-carboxamidines containing 2-aminothiazoles and their biological evaluation as urokinase inhibitors. Bioorg. Med. Chem. Lett. (2001) 11(7):915-918.
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , Issue.7 , pp. 915-918
    • Wilson, K.J.1    Illig, C.R.2    Subasinghe, N.3
  • 56
    • 18244395613 scopus 로고    scopus 로고
    • Design and synthesis of 4,5-disubstituted-thiophene-2-amidines as potent urokinase inhibitors
    • RUDOLPH MJ, ILLIG CR, SUBASINGHE NL et al.: Design and synthesis of 4,5-disubstituted-thiophene-2-amidines as potent urokinase inhibitors. Bioorg. Med. Chem. Lett. (2002) 12(3):491-495.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , Issue.3 , pp. 491-495
    • Rudolph, M.J.1    Illig, C.R.2    Subasinghe, N.L.3
  • 57
    • 0027314501 scopus 로고
    • Inhibition of urokinase by 4-substituted benzo[b]thiophene-2-carboxamidines: An important new class of selective synthetic urokinase inhibitor
    • TOWLE MJ, LEE A, MADUAKOR EC, SCHWARTZ CE, BRIDGES AJ, LITTLEFIELD BA: Inhibition of urokinase by 4-substituted benzo[b]thiophene-2-carboxamidines: an important new class of selective synthetic urokinase inhibitor. Cancer Res. (1993) 53(11):2553-2559.
    • (1993) Cancer Res. , vol.53 , Issue.11 , pp. 2553-2559
    • Towle, M.J.1    Lee, A.2    Maduakor, E.C.3    Schwartz, C.E.4    Bridges, A.J.5    Littlefield, B.A.6
  • 58
    • 0035207827 scopus 로고    scopus 로고
    • Selective urokinase inhibitors based on substituted aryl guanidines
    • NO AUTHORS LISTED
    • NO AUTHORS LISTED: Selective urokinase inhibitors based on substituted aryl guanidines. Exp. Opin. Ther. Patents (2001) 11(12):1975-1977.
    • (2001) Exp. Opin. Ther. Patents , vol.11 , Issue.12 , pp. 1975-1977
  • 59
    • 0037147792 scopus 로고    scopus 로고
    • Selective urokinase-type plasminogen activator (uPA) inhibitors. Part 2: (3-substituted-5-halo-2-pyridinyl)guanidines
    • BARBER CG, DICKINSON RP: Selective urokinase-type plasminogen activator (uPA) inhibitors. Part 2: (3-substituted-5-halo-2-pyridinyl)guanidines. Bioorg. Med. Chem. Lett. (2002) 12(2):185-187.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , Issue.2 , pp. 185-187
    • Barber, C.G.1    Dickinson, R.P.2
  • 60
    • 0037147798 scopus 로고    scopus 로고
    • Selective urokinase-type plasminogen activator (uPA) inhibitors. Part 1: 2-pyridinylguanidines
    • BARBER CG, DICKINSON RP, HORNE VA: Selective urokinase-type plasminogen activator (uPA) inhibitors. Part 1: 2-pyridinylguanidines. Bioorg. Med. Chem. Letters (2002) 12(2):181-184
    • (2002) Bioorg. Med. Chem. Letters , vol.12 , Issue.2 , pp. 181-184
    • Barber, C.G.1    Dickinson, R.P.2    Horne, V.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.