메뉴 건너뛰기




Volumn 13, Issue 6, 2003, Pages 737-749

The 2-oxindole chemotype and patent activity inspired by the SU5416 franchise

Author keywords

Indolones; Kinase inhibitors; Oxindole; Semaxinib; SU11248; SU5416; SU6668

Indexed keywords

2,4 DIMETHYL 5 (2 OXO 1H INDOL 3 YLMETHYLENE) 3 PYRROLEPROPIONIC ACID; ANGIOGENESIS INHIBITOR; AROMATASE INHIBITOR; BENZENE DERIVATIVE; CAMPTOTHECIN DERIVATIVE; CYCLIN DEPENDENT KINASE INHIBITOR; CYCLODEXTRIN DERIVATIVE; EPIDERMAL GROWTH FACTOR RECEPTOR; ESTRADIOL; ESTRAMUSTINE PHOSPHATE; EXEMESTANE; FLUOROPYRIMIDINE DERIVATIVE; FLUOROURACIL; GEFITINIB; HUMAN ALBUMIN; HYDRAZINE DERIVATIVE; LOMETREXOL; OXINDOLE; PEPTIDE DERIVATIVE; PLATELET DERIVED GROWTH FACTOR RECEPTOR; PROTEIN FARNESYLTRANSFERASE INHIBITOR; PROTEIN TYROSINE KINASE INHIBITOR; QUINAZOLINE DERIVATIVE; SEMAXANIB; SOMATOMEDIN C RECEPTOR; SU 4312; SU 4932; SUNITINIB; UNCLASSIFIED DRUG; VASCULOTROPIN INHIBITOR; VASCULOTROPIN RECEPTOR 2;

EID: 0037971531     PISSN: 13543776     EISSN: None     Source Type: Journal    
DOI: 10.1517/13543776.13.6.737     Document Type: Review
Times cited : (10)

References (14)
  • 1
    • 0034693811 scopus 로고    scopus 로고
    • Development of inhibitors for protein tyrosine kinases
    • AL-OBEIDI FA, LAM KS: Development of inhibitors for protein tyrosine kinases. Oncogene (2000) 19:5690-5701.
    • (2000) Oncogene , vol.19 , pp. 5690-5701
    • Al-Obeidi, F.A.1    Lam, K.S.2
  • 2
    • 0001854511 scopus 로고    scopus 로고
    • Protein tyrosine kinase inhibitors as therapeutic agents
    • LEVITZKI A: Protein tyrosine kinase inhibitors as therapeutic agents. Bioorg. Chem. Biol. Signal Transduction (2001) 211:1-15.
    • (2001) Bioorg. Chem. Biol. Signal Transduction , vol.211 , pp. 1-15
    • Levitzki, A.1
  • 3
    • 0035117012 scopus 로고    scopus 로고
    • Protein kinase inhibitors: Emerging pharmacophores 1997-2000
    • DUMAS J: Protein kinase inhibitors: emerging pharmacophores 1997-2000. Exp. Opin. Ther. Patents (2001) 11(3):405-429.
    • (2001) Exp. Opin. Ther. Patents , vol.11 , Issue.3 , pp. 405-429
    • Dumas, J.1
  • 4
    • 0037706003 scopus 로고    scopus 로고
    • Sugen acquisition would add three anticancer agents to P&U pipeline
    • NO AUTHORS LISTED Scrip (17 June)
    • NO AUTHORS LISTED: Sugen acquisition would add three anticancer agents to P&U pipeline. Scrip (17 June 1999).
    • (1999)
  • 5
    • 4243833544 scopus 로고    scopus 로고
    • Pharmacia drops lead angiogenesis product
    • NO AUTHORS LISTED: Scrip (12 February)
    • NO AUTHORS LISTED: Pharmacia drops lead angiogenesis product. Scrip (12 February 2002).
    • (2002)
  • 6
    • 0036086863 scopus 로고    scopus 로고
    • Pharmacia's SU5416 not effective
    • NO AUTHORS LISTED
    • NO AUTHORS LISTED: Pharmacia's SU5416 not effective. Exp. Rev. Anticancer Ther. (2002) 2(1):5-8.
    • (2002) Exp. Rev. Anticancer Ther. , vol.2 , Issue.1 , pp. 5-8
  • 7
    • 0032474915 scopus 로고    scopus 로고
    • Synthesis and biological evaluations of 3-substituted indolin-2-ones: A novel class of tyrosine kinase inhibitors that exhibit selectivity toward particular receptor tyrosine kinases
    • SUN L, TRAN N, TANGF, APP H, HIRTH P et al.: Synthesis and biological evaluations of 3-substituted indolin-2-ones: a novel class of tyrosine kinase inhibitors that exhibit selectivity toward particular receptor tyrosine kinases. J. Med. Chem. (1998) 41(14):2588-2603.
    • (1998) J. Med. Chem. , vol.41 , Issue.14 , pp. 2588-2603
    • Sun, L.1    Tran, N.2    Tangf, A.3    App, H.4    Hirth, P.5
  • 8
    • 19244370071 scopus 로고    scopus 로고
    • Design, synthesis, and evaluations of substituted 3-[(3- or 4-carboxyethylpyrrol-2-yl)methylidenyl]indolin-2-ones as inhibitors of VEGF, FGF and PDGF receptor tyrosine kinases
    • SUN L, TRAN N, LIANG C,TANGF, RICE A et al.: Design, synthesis, and evaluations of substituted 3-[(3- or 4-carboxyethylpyrrol-2-yl)methylidenyl]indolin-2-ones as inhibitors of VEGF, FGF and PDGF receptor tyrosine kinases. J. Med Chem. (1999) 42(25):5120.
    • (1999) J. Med. Chem. , vol.42 , Issue.25 , pp. 5120
    • Sun, L.1    Tran, N.2    Liang, C.3    Tangf, A.4    Rice, A.5
  • 9
    • 0035012816 scopus 로고    scopus 로고
    • Simultaneous determination of SU5416 and its phase I and phase II metabolites in rat and dog plasma by LC/MS/MS
    • ZHAO YP, YANG CY, HAZNEDAR J, ANTONIAN L: Simultaneous determination of SU5416 and its phase I and phase II metabolites in rat and dog plasma by LC/MS/MS. J. Pharm. Biomed. Anal. (2001) 25:821-832.
    • (2001) J. Pharm. Biomed. Anal. , vol.25 , pp. 821-832
    • Zhao, Y.P.1    Yang, C.Y.2    Haznedar, J.3    Antonian, L.4
  • 10
    • 12244301581 scopus 로고    scopus 로고
    • In vivo antitumor activity of SU11248, a novel tyrosine kinase inhibitor targeting vascular endothelial growth factor and platelet-derived growth factor receptors: Determination of a pharmacokinetic/pharmacodynamic relationship
    • MENDEL DB, LAIRD AD, XIN XH, LOUIE SG, CHRISTENSEN JG et al.: In vivo antitumor activity of SU11248, a novel tyrosine kinase inhibitor targeting vascular endothelial growth factor and platelet-derived growth factor receptors: determination of a pharmacokinetic/pharmacodynamic relationship. Clin. Cancer Res. (2003) 9:327-337.
    • (2003) Clin. Cancer Res. , vol.9 , pp. 327-337
    • Mendel, D.B.1    Laird, A.D.2    Xin, X.H.3    Louie, S.G.4    Christensen, J.G.5
  • 12
    • 17144460676 scopus 로고    scopus 로고
    • The discovery of potent cRaf1 kinase inhibitors
    • LACKEY K, CORY M, DAVIS R et al.: The discovery of potent cRaf1 kinase inhibitors. Bioorg. Med. Chem. Lett. (2000) 10(3):223-226.
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , Issue.3 , pp. 223-226
    • Lackey, K.1    Cory, M.2    Davis, R.3
  • 13
    • 0035818942 scopus 로고    scopus 로고
    • Oxindole-based inhibitors of cyclin-dependent kinase 2 (Cdk2): Design, synthesis, enzymatic activities, and X-ray crystallographic analysis
    • BRAMSON HN, CORONA J, DAVIS ST et al.: Oxindole-based inhibitors of cyclin-dependent kinase 2 (Cdk2): design, synthesis, enzymatic activities, and X-ray crystallographic analysis. J. Med. Chem. (2001) 44(25):4339-4358.
    • (2001) J. Med. Chem. , vol.44 , Issue.25 , pp. 4339-4358
    • Bramson, H.N.1    Corona, J.2    Davis, S.T.3
  • 14
    • 0035412371 scopus 로고    scopus 로고
    • Stable remission after administration of the receptor tyrosine kinase inhibitor SU5416 in a patient with refractory acute myeloid leukemia
    • MESTERS RM, PADRO T, BIEKER R, STEINS M, KREUTER M et al.: Stable remission after administration of the receptor tyrosine kinase inhibitor SU5416 in a patient with refractory acute myeloid leukemia. Blood (2001) 98:241-243.
    • (2001) Blood , vol.98 , pp. 241-243
    • Mesters, R.M.1    Padro, T.2    Bieker, R.3    Steins, M.4    Kreuter, M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.