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Volumn 43, Issue 35, 2004, Pages 4644-4646

Simple synthesis of nodulation-factor analogues exhibiting high affinity towards a specific binding protein

Author keywords

Aromatic substitution; Glycolipids; Lipid analogues; Nitrogen fixation; Oligosaccharides

Indexed keywords

AROMATIC COMPOUNDS; BIOTECHNOLOGY; LIPIDS; POLYSACCHARIDES; SYNTHESIS (CHEMICAL);

EID: 5344254615     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200460275     Document Type: Article
Times cited : (16)

References (26)
  • 5
    • 0025361205 scopus 로고
    • P. Lerouge, P. Roche, C. Faucher, F. Maillet, G. Truchet, J.-C. Promé, J. Dénarié, Nature 1990, 344, 781; G. Truchet, P. Roche, P. Lerouge, J. Vasse, S. Camut, F. de Billy, J.-C. Promé, J. Dénarié, Nature 1991, 351, 670; P. Roche, F. Debellé, F. Maillet, P. Lerouge, C. Faucher, G. Truchet, J. Dénarié, J.-C. Promé, Cell 1991, 67, 1131.
    • (1990) Nature , vol.344 , pp. 781
    • Lerouge, P.1    Roche, P.2    Faucher, C.3    Maillet, F.4    Truchet, G.5    Promé, J.-C.6    Dénarié, J.7
  • 6
    • 0006341523 scopus 로고
    • P. Lerouge, P. Roche, C. Faucher, F. Maillet, G. Truchet, J.-C. Promé, J. Dénarié, Nature 1990, 344, 781; G. Truchet, P. Roche, P. Lerouge, J. Vasse, S. Camut, F. de Billy, J.-C. Promé, J. Dénarié, Nature 1991, 351, 670; P. Roche, F. Debellé, F. Maillet, P. Lerouge, C. Faucher, G. Truchet, J. Dénarié, J.-C. Promé, Cell 1991, 67, 1131.
    • (1991) Nature , vol.351 , pp. 670
    • Truchet, G.1    Roche, P.2    Lerouge, P.3    Vasse, J.4    Camut, S.5    De Billy, F.6    Promé, J.-C.7    Dénarié, J.8
  • 7
    • 0026350534 scopus 로고
    • P. Lerouge, P. Roche, C. Faucher, F. Maillet, G. Truchet, J.-C. Promé, J. Dénarié, Nature 1990, 344, 781; G. Truchet, P. Roche, P. Lerouge, J. Vasse, S. Camut, F. de Billy, J.-C. Promé, J. Dénarié, Nature 1991, 351, 670; P. Roche, F. Debellé, F. Maillet, P. Lerouge, C. Faucher, G. Truchet, J. Dénarié, J.-C. Promé, Cell 1991, 67, 1131.
    • (1991) Cell , vol.67 , pp. 1131
    • Roche, P.1    Debellé, F.2    Maillet, F.3    Lerouge, P.4    Faucher, C.5    Truchet, G.6    Dénarié, J.7    Promé, J.-C.8
  • 13
    • 0142240337 scopus 로고    scopus 로고
    • By using a genetic approach, two genes involved in the perception of Nod factors and encoding transmembrane-receptor-like serine/threonine kinases with extracellular domains containing modules potentially involved in the oligosaccharide binging (LysM motifs) were recently identified: E. Limpens, C. Franken, P. Smit, J. Willemse, T. Bisseling, R. Geurts, Science 2003, 302, 630; S. Radutoiu, L. H. Madsen, E. B. Madsen, H. H. Felle, Y. Umehara, M. Gronlund, S. Sato, Y. Nakamura, S. Tabata, N. Sandal, J. Stougaard, Nature 2003, 425, 585; E. B. Madsen, L. H. Madsen, S. Radutoiu, M. Olbryt, M. Rakwalska, K. Szczyglowski, S. Sato, S. Kaneko, S. Tabata, N. Sandal, J. Stougaard, Nature 2003, 425, 637.
    • (2003) Science , vol.302 , pp. 630
    • Limpens, E.1    Franken, C.2    Smit, P.3    Willemse, J.4    Bisseling, T.5    Geurts, R.6
  • 14
    • 0142041483 scopus 로고    scopus 로고
    • By using a genetic approach, two genes involved in the perception of Nod factors and encoding transmembrane-receptor-like serine/threonine kinases with extracellular domains containing modules potentially involved in the oligosaccharide binging (LysM motifs) were recently identified: E. Limpens, C. Franken, P. Smit, J. Willemse, T. Bisseling, R. Geurts, Science 2003, 302, 630; S. Radutoiu, L. H. Madsen, E. B. Madsen, H. H. Felle, Y. Umehara, M. Gronlund, S. Sato, Y. Nakamura, S. Tabata, N. Sandal, J. Stougaard, Nature 2003, 425, 585; E. B. Madsen, L. H. Madsen, S. Radutoiu, M. Olbryt, M. Rakwalska, K. Szczyglowski, S. Sato, S. Kaneko, S. Tabata, N. Sandal, J. Stougaard, Nature 2003, 425, 637.
    • (2003) Nature , vol.425 , pp. 585
    • Radutoiu, S.1    Madsen, L.H.2    Madsen, E.B.3    Felle, H.H.4    Umehara, Y.5    Gronlund, M.6    Sato, S.7    Nakamura, Y.8    Tabata, S.9    Sandal, N.10    Stougaard, J.11
  • 15
    • 0142104972 scopus 로고    scopus 로고
    • By using a genetic approach, two genes involved in the perception of Nod factors and encoding transmembrane-receptor-like serine/threonine kinases with extracellular domains containing modules potentially involved in the oligosaccharide binging (LysM motifs) were recently identified: E. Limpens, C. Franken, P. Smit, J. Willemse, T. Bisseling, R. Geurts, Science 2003, 302, 630; S. Radutoiu, L. H. Madsen, E. B. Madsen, H. H. Felle, Y. Umehara, M. Gronlund, S. Sato, Y. Nakamura, S. Tabata, N. Sandal, J. Stougaard, Nature 2003, 425, 585; E. B. Madsen, L. H. Madsen, S. Radutoiu, M. Olbryt, M. Rakwalska, K. Szczyglowski, S. Sato, S. Kaneko, S. Tabata, N. Sandal, J. Stougaard, Nature 2003, 425, 637.
    • (2003) Nature , vol.425 , pp. 637
    • Madsen, E.B.1    Madsen, L.H.2    Radutoiu, S.3    Olbryt, M.4    Rakwalska, M.5    Szczyglowski, K.6    Sato, S.7    Kaneko, S.8    Tabata, S.9    Sandal, N.10    Stougaard, J.11
  • 16
    • 0001235009 scopus 로고
    • Synthesis of Nod factors from monomers: K. C. Nicolaou, N. J. Bockovich, D. R. Carcanague, C. W. Hummel, L. F. Even, J. Am. Chem. Soc. 1992, 114, 8701; S. Ikeshita, A. Sakamoto, Y. Nakahara, Y. Nakahara, T. Ogawa, Tetrahedron Lett. 1994, 35, 3123; L. X. Wang, C. Li, Q. W. Wang, Y. Z. Hui, J. Chem. Soc. Perkin Trans. 1 1994, 621; J. S. Debenham, R. Rodebaugh, B. Fraser-Reid, J. Org. Chem. 1996, 61, 6478.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 8701
    • Nicolaou, K.C.1    Bockovich, N.J.2    Carcanague, D.R.3    Hummel, C.W.4    Even, L.F.5
  • 17
    • 0028318566 scopus 로고
    • Synthesis of Nod factors from monomers: K. C. Nicolaou, N. J. Bockovich, D. R. Carcanague, C. W. Hummel, L. F. Even, J. Am. Chem. Soc. 1992, 114, 8701; S. Ikeshita, A. Sakamoto, Y. Nakahara, Y. Nakahara, T. Ogawa, Tetrahedron Lett. 1994, 35, 3123; L. X. Wang, C. Li, Q. W. Wang, Y. Z. Hui, J. Chem. Soc. Perkin Trans. 1 1994, 621; J. S. Debenham, R. Rodebaugh, B. Fraser-Reid, J. Org. Chem. 1996, 61, 6478.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 3123
    • Ikeshita, S.1    Sakamoto, A.2    Nakahara, Y.3    Nakahara, Y.4    Ogawa, T.5
  • 18
    • 37049072364 scopus 로고
    • Synthesis of Nod factors from monomers: K. C. Nicolaou, N. J. Bockovich, D. R. Carcanague, C. W. Hummel, L. F. Even, J. Am. Chem. Soc. 1992, 114, 8701; S. Ikeshita, A. Sakamoto, Y. Nakahara, Y. Nakahara, T. Ogawa, Tetrahedron Lett. 1994, 35, 3123; L. X. Wang, C. Li, Q. W. Wang, Y. Z. Hui, J. Chem. Soc. Perkin Trans. 1 1994, 621; J. S. Debenham, R. Rodebaugh, B. Fraser-Reid, J. Org. Chem. 1996, 61, 6478.
    • (1994) J. Chem. Soc. Perkin Trans. 1 , pp. 621
    • Wang, L.X.1    Li, C.2    Wang, Q.W.3    Hui, Y.Z.4
  • 19
    • 0029842852 scopus 로고    scopus 로고
    • Synthesis of Nod factors from monomers: K. C. Nicolaou, N. J. Bockovich, D. R. Carcanague, C. W. Hummel, L. F. Even, J. Am. Chem. Soc. 1992, 114, 8701; S. Ikeshita, A. Sakamoto, Y. Nakahara, Y. Nakahara, T. Ogawa, Tetrahedron Lett. 1994, 35, 3123; L. X. Wang, C. Li, Q. W. Wang, Y. Z. Hui, J. Chem. Soc. Perkin Trans. 1 1994, 621; J. S. Debenham, R. Rodebaugh, B. Fraser-Reid, J. Org. Chem. 1996, 61, 6478.
    • (1996) J. Org. Chem. , vol.61 , pp. 6478
    • Debenham, J.S.1    Rodebaugh, R.2    Fraser-Reid, B.3
  • 20
    • 0023730523 scopus 로고
    • Some examples of aromatic derivatives designed to resemble unsaturated lipids: D. W. Snyder, P. R. Bernstein, Prostaglandins 1988, 35, 903; R. C. Larock, N. H. Lee, J. Org. Chem. 1991, 56, 6253; H. Hashizume, H. Ito, K. Yamada, H. Nagashima, M. Kanao, H. Tomoda, T. Sunazuka, H. Kumagai, S. Omura, Chem. Pharm. Bull. 1994, 42, 512; J. P. F. C. Rossi, J. M. Delfino, A. J. Caride, H. N. Fernández, Biochemistry 1995, 34, 3802.
    • (1988) Prostaglandins , vol.35 , pp. 903
    • Snyder, D.W.1    Bernstein, P.R.2
  • 21
    • 0000913447 scopus 로고
    • Some examples of aromatic derivatives designed to resemble unsaturated lipids: D. W. Snyder, P. R. Bernstein, Prostaglandins 1988, 35, 903; R. C. Larock, N. H. Lee, J. Org. Chem. 1991, 56, 6253; H. Hashizume, H. Ito, K. Yamada, H. Nagashima, M. Kanao, H. Tomoda, T. Sunazuka, H. Kumagai, S. Omura, Chem. Pharm. Bull. 1994, 42, 512; J. P. F. C. Rossi, J. M. Delfino, A. J. Caride, H. N. Fernández, Biochemistry 1995, 34, 3802.
    • (1991) J. Org. Chem. , vol.56 , pp. 6253
    • Larock, R.C.1    Lee, N.H.2
  • 22
    • 0028390681 scopus 로고
    • Some examples of aromatic derivatives designed to resemble unsaturated lipids: D. W. Snyder, P. R. Bernstein, Prostaglandins 1988, 35, 903; R. C. Larock, N. H. Lee, J. Org. Chem. 1991, 56, 6253; H. Hashizume, H. Ito, K. Yamada, H. Nagashima, M. Kanao, H. Tomoda, T. Sunazuka, H. Kumagai, S. Omura, Chem. Pharm. Bull. 1994, 42, 512; J. P. F. C. Rossi, J. M. Delfino, A. J. Caride, H. N. Fernández, Biochemistry 1995, 34, 3802.
    • (1994) Chem. Pharm. Bull. , vol.42 , pp. 512
    • Hashizume, H.1    Ito, H.2    Yamada, K.3    Nagashima, H.4    Kanao, M.5    Tomoda, H.6    Sunazuka, T.7    Kumagai, H.8    Omura, S.9
  • 23
    • 0028953747 scopus 로고
    • Some examples of aromatic derivatives designed to resemble unsaturated lipids: D. W. Snyder, P. R. Bernstein, Prostaglandins 1988, 35, 903; R. C. Larock, N. H. Lee, J. Org. Chem. 1991, 56, 6253; H. Hashizume, H. Ito, K. Yamada, H. Nagashima, M. Kanao, H. Tomoda, T. Sunazuka, H. Kumagai, S. Omura, Chem. Pharm. Bull. 1994, 42, 512; J. P. F. C. Rossi, J. M. Delfino, A. J. Caride, H. N. Fernández, Biochemistry 1995, 34, 3802.
    • (1995) Biochemistry , vol.34 , pp. 3802
    • Rossi, J.P.F.C.1    Delfino, J.M.2    Caride, A.J.3    Fernández, H.N.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.