메뉴 건너뛰기




Volumn 67, Issue 11, 2009, Pages 1977-1984

A fully automated two-step synthesis of an 18F-labelled tyrosine kinase inhibitor for EGFR kinase activity imaging in tumors

Author keywords

Click chemistry; Epidermal growth factor receptor; Fluorine 18; Molecular imaging

Indexed keywords

AUTOMATED SYNTHESIS; CLICK CHEMISTRY; DIPOLAR CYCLOADDITIONS; EPIDERMAL GROWTH FACTOR RECEPTOR; EPIDERMAL GROWTH FACTOR RECEPTORS; FLUORINE-18; KINASE ACTIVITY; MOLECULAR IMAGING; MULTI-STEP; OVER-EXPRESSION; PET IMAGES; QUINAZOLINES; TUMOR XENOGRAFTS; TWO-STEP SYNTHESIS; TYROSINE KINASE; TYROSINE KINASE INHIBITOR;

EID: 69549123869     PISSN: 09698043     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apradiso.2009.07.018     Document Type: Article
Times cited : (28)

References (15)
  • 1
    • 33845935326 scopus 로고    scopus 로고
    • Evaluation of radiolabeled ML04, a putative irreversible inhibitor of epidermal growth factor receptor, as a bioprobe for PET imaging of EGFR-overexpressing tumors
    • Abourbeh G., Dissoki S., Jacobson O., Litchi A., Daniel R.B., Laki D., Levitzki A., and Mishani E. Evaluation of radiolabeled ML04, a putative irreversible inhibitor of epidermal growth factor receptor, as a bioprobe for PET imaging of EGFR-overexpressing tumors. Nucl. Med. Biol. 34 1 (2007) 55-70
    • (2007) Nucl. Med. Biol. , vol.34 , Issue.1 , pp. 55-70
    • Abourbeh, G.1    Dissoki, S.2    Jacobson, O.3    Litchi, A.4    Daniel, R.B.5    Laki, D.6    Levitzki, A.7    Mishani, E.8
  • 2
    • 33748093767 scopus 로고    scopus 로고
    • Linking oncogenic pathways with therapeutic opportunities
    • Bild A.H., Potti A., and Nevins J.R. Linking oncogenic pathways with therapeutic opportunities. Nat. Rev. Cancer 6 (2006) 735-741
    • (2006) Nat. Rev. Cancer , vol.6 , pp. 735-741
    • Bild, A.H.1    Potti, A.2    Nevins, J.R.3
  • 3
    • 69549128406 scopus 로고    scopus 로고
    • Considine, J.L, Daigneault, S, Chew, W, Iera, S, Duncan, S.M, Ren, J, 2004. A large-scale synthesis of 4-amino-2-butenoyl chlorides, useful as intermediates in preparation of, dimethylaminocrotonylamido]quinoline derivatives. PCT Int. Appl. WO 2004066919 A2
    • Considine, J.L., Daigneault, S., Chew, W., Iera, S., Duncan, S.M., Ren, J., 2004. A large-scale synthesis of 4-amino-2-butenoyl chlorides, useful as intermediates in preparation of [(dimethylaminocrotonyl)amido]quinoline derivatives. PCT Int. Appl. WO 2004066919 A2.
  • 4
    • 0035856890 scopus 로고    scopus 로고
    • An intramolecular [2+3] cycloaddition route to fused 5-heterosubstituted tetrazoles
    • Demko Z.P., and Sharpless K.B. An intramolecular [2+3] cycloaddition route to fused 5-heterosubstituted tetrazoles. Org. Lett. 3 25 (2001) 4091-4094
    • (2001) Org. Lett. , vol.3 , Issue.25 , pp. 4091-4094
    • Demko, Z.P.1    Sharpless, K.B.2
  • 5
    • 34548217626 scopus 로고    scopus 로고
    • The effect of the [18F]-PEG group on tracer qualification of [4-(phenylamino)-quinazolin-6-yl]-amide moiety-An EGFR putative irreversible inhibitor
    • Dissoki S., Aviv Y., Laky D., Abourbeh G., Levitzki A., and Mishani E. The effect of the [18F]-PEG group on tracer qualification of [4-(phenylamino)-quinazolin-6-yl]-amide moiety-An EGFR putative irreversible inhibitor. Appl. Radiat. Isot. 65 10 (2007) 1140-1151
    • (2007) Appl. Radiat. Isot. , vol.65 , Issue.10 , pp. 1140-1151
    • Dissoki, S.1    Aviv, Y.2    Laky, D.3    Abourbeh, G.4    Levitzki, A.5    Mishani, E.6
  • 8
    • 0037429659 scopus 로고    scopus 로고
    • Mechanism of action of erbB tyrosine kinase inhibitors
    • Fry D.W. Mechanism of action of erbB tyrosine kinase inhibitors. Exp. Cell Res. 284 1 (2003) 131-139
    • (2003) Exp. Cell Res. , vol.284 , Issue.1 , pp. 131-139
    • Fry, D.W.1
  • 9
    • 34347338806 scopus 로고    scopus 로고
    • 18F]fluoroethylazide for positron emission tomography
    • 18F]fluoroethylazide for positron emission tomography. Bioconj. Chem. 18 3 (2007) 989-993
    • (2007) Bioconj. Chem. , vol.18 , Issue.3 , pp. 989-993
    • Glaser, M.1    Årstad, E.2
  • 10
    • 36849012163 scopus 로고    scopus 로고
    • 18F]-labeling of RGD peptides and microPET imaging of tumor integrin αvβ3 expression
    • 18F]-labeling of RGD peptides and microPET imaging of tumor integrin αvβ3 expression. Bioconj. Chem. 18 6 (2007) 1987-1994
    • (2007) Bioconj. Chem. , vol.18 , Issue.6 , pp. 1987-1994
    • Li, Z.-B.1    Wu, Z.2    Chen, K.3    Chin, F.T.4    Chen, X.5
  • 11
    • 33645467137 scopus 로고    scopus 로고
    • An iterative route to decorated ethylene glycol-based linkers
    • Lu G., Lam S., and Burgess K. An iterative route to decorated ethylene glycol-based linkers. Chem. Commun. 15 (2006) 1652-1654
    • (2006) Chem. Commun. , vol.15 , pp. 1652-1654
    • Lu, G.1    Lam, S.2    Burgess, K.3
  • 12
    • 0037106273 scopus 로고    scopus 로고
    • Targeting the epidermal growth factor receptor for cancer therapy
    • Mendelsohn J. Targeting the epidermal growth factor receptor for cancer therapy. J. Clin. Oncol. 20 Suppl. 18 (2002) S1-S13
    • (2002) J. Clin. Oncol. , vol.20 , Issue.SUPPL. 18
    • Mendelsohn, J.1
  • 14
    • 13344262678 scopus 로고    scopus 로고
    • Tyrosine kinase inhibitors. 9. synthesis and evaluation of fused tricyclic quinazoline analogs as ATP site inhibitors of the tyrosine kinase activity of the epidermal growth factor receptor
    • Rewcastle G.W., Palmer B.D., Bridges A.J., Showalter H.D.H., Sun L., Nelson J., McMichael A., Kraker A.J., Fry D.W., and Denny W.A. Tyrosine kinase inhibitors. 9. synthesis and evaluation of fused tricyclic quinazoline analogs as ATP site inhibitors of the tyrosine kinase activity of the epidermal growth factor receptor. J. Med. Chem. 39 4 (1996) 918-928
    • (1996) J. Med. Chem. , vol.39 , Issue.4 , pp. 918-928
    • Rewcastle, G.W.1    Palmer, B.D.2    Bridges, A.J.3    Showalter, H.D.H.4    Sun, L.5    Nelson, J.6    McMichael, A.7    Kraker, A.J.8    Fry, D.W.9    Denny, W.A.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.