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Volumn 38, Issue 2, 2008, Pages 303-308

Convenient preparation of N-maleoyl amino acid succinimido esters using N-trifluoroacetoxysuccinimide

Author keywords

Heterobifunctional linker; Maleimide; N trifluoroacetoxysuccinimide; Succinimido ester

Indexed keywords

MALEIC ACID; N MALEOYL AMINO ACID N HYDROXYSUCCINIMIDO ESTER DERIVATIVE; N TRIFLUOROACETOXYSUCCINIMIDE; SUCCINIMIDE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 38349169662     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910701750151     Document Type: Article
Times cited : (13)

References (17)
  • 1
    • 0034999596 scopus 로고    scopus 로고
    • Effect of peptide-carrier coupling on peptide-specific immune responses
    • Kirkley, J.E.; Goldstein, A.L.; Naylor, P.H. Effect of peptide-carrier coupling on peptide-specific immune responses. Immunobiol. 2001, 203, 601-615.
    • (2001) Immunobiol , vol.203 , pp. 601-615
    • Kirkley, J.E.1    Goldstein, A.L.2    Naylor, P.H.3
  • 2
    • 0030811179 scopus 로고    scopus 로고
    • Bispecific rabbit Fab′-bovine serum albumin conjugate used in hemagglutination immunoassay for β-microseminoprotein
    • Yukawa, N.; Osawa, M.; Saito, T.; Hasegawa, T.; Matsuda, H.; Takahama, K.; Takeichi, S. Bispecific rabbit Fab′-bovine serum albumin conjugate used in hemagglutination immunoassay for β-microseminoprotein. J. Immunoassay 1997, 18, 215-233.
    • (1997) J. Immunoassay , vol.18 , pp. 215-233
    • Yukawa, N.1    Osawa, M.2    Saito, T.3    Hasegawa, T.4    Matsuda, H.5    Takahama, K.6    Takeichi, S.7
  • 4
    • 0037136489 scopus 로고    scopus 로고
    • A method for bioconjugation of carbohydrates using Diels-Alder cycloaddition
    • Pozsgay, V.; Vieira, N. E.; Yergey, A. A method for bioconjugation of carbohydrates using Diels-Alder cycloaddition. Org. Lett. 2002, 4, 3191-3194.
    • (2002) Org. Lett , vol.4 , pp. 3191-3194
    • Pozsgay, V.1    Vieira, N.E.2    Yergey, A.3
  • 5
    • 0037413342 scopus 로고    scopus 로고
    • Carbohydrate-centered maleimide clusters as a new type of templates for multivalent peptide assembling: Synthesis of multivalent HIV-1 gp41 peptides
    • Wang, L. X.; Ni, J. H.; Singh, S. Carbohydrate-centered maleimide clusters as a new type of templates for multivalent peptide assembling: Synthesis of multivalent HIV-1 gp41 peptides. Bioorg. Med. Chem. 2003, 11, 159-166.
    • (2003) Bioorg. Med. Chem , vol.11 , pp. 159-166
    • Wang, L.X.1    Ni, J.H.2    Singh, S.3
  • 7
    • 33646125185 scopus 로고    scopus 로고
    • Oriented immobillisation of engineered single-chain antibodies to develop biosensors for virus detection
    • Torrance, L.; Ziegler, A.; Pittman, H.; Paterson, M.; Toth, R.; Eggleston, I. Oriented immobillisation of engineered single-chain antibodies to develop biosensors for virus detection. J. Virol. Meth. 2006, 134, 164-170.
    • (2006) J. Virol. Meth , vol.134 , pp. 164-170
    • Torrance, L.1    Ziegler, A.2    Pittman, H.3    Paterson, M.4    Toth, R.5    Eggleston, I.6
  • 8
    • 10044258525 scopus 로고    scopus 로고
    • Integrated nanoparticle-biomolecule hybrid systems: Synthesis, properties, and applications
    • Katz, E.; Willner, I. Integrated nanoparticle-biomolecule hybrid systems: Synthesis, properties, and applications. Angew. Chem. Int. Ed. Engl. 2004, 43, 6042-6108.
    • (2004) Angew. Chem. Int. Ed. Engl , vol.43 , pp. 6042-6108
    • Katz, E.1    Willner, I.2
  • 9
    • 0016849770 scopus 로고
    • Preparation and some properties of maleimido acids and maleoyl derivatives of peptides
    • Keller, O.; Rudinger, J. Preparation and some properties of maleimido acids and maleoyl derivatives of peptides. Helv. Chim. Acta 1975, 58, 531-540.
    • (1975) Helv. Chim. Acta , vol.58 , pp. 531-540
    • Keller, O.1    Rudinger, J.2
  • 10
    • 0016754770 scopus 로고
    • Alkylating derivatives of amino acids and peptides-synthesis of N-maleoyl amino acids, (1-(N-maleoylglycyl)cysteinyl)oxytocin, and (1-(N-maleoyl-11- aminoundecanoyl)-cysteinly)oxytocin-effects on vasopressin-stimulated water loss from isolated toad baldder
    • Rich, D. H.; Gesellchen, P. D.; Tong, A.; Cheung, A.; Buckner, C. K. Alkylating derivatives of amino acids and peptides-synthesis of N-maleoyl amino acids, (1-(N-maleoylglycyl)cysteinyl)oxytocin, and (1-(N-maleoyl-11- aminoundecanoyl)-cysteinly)oxytocin-effects on vasopressin-stimulated water loss from isolated toad baldder. J. Med. Chem. 1975, 18, 1004-1010.
    • (1975) J. Med. Chem , vol.18 , pp. 1004-1010
    • Rich, D.H.1    Gesellchen, P.D.2    Tong, A.3    Cheung, A.4    Buckner, C.K.5
  • 12
    • 0025917377 scopus 로고
    • Facile synthesis of reagents containing a terminal maleimido ligand linked to an active ester
    • Nielsen, O.; Buchardt, O. Facile synthesis of reagents containing a terminal maleimido ligand linked to an active ester. Synthesis 1991, 819-821.
    • (1991) Synthesis , pp. 819-821
    • Nielsen, O.1    Buchardt, O.2
  • 13
    • 25444510985 scopus 로고
    • Synthesis of pentafluorophenyl-4-(N- maleimidomethyl) cyclohexane-1-carboxylate (FMCC)
    • Adamczyk, M.; Johnson, D. Synthesis of pentafluorophenyl-4-(N- maleimidomethyl) cyclohexane-1-carboxylate (FMCC). Org. Prep. Proced. Int. 1993, 25, 592-594.
    • (1993) Org. Prep. Proced. Int , vol.25 , pp. 592-594
    • Adamczyk, M.1    Johnson, D.2
  • 14
    • 0013816716 scopus 로고
    • Trifluoroacetate method of peptide synthesis I. Synthesis and use of trifluoroacetate reagents
    • Sakakibara, S.; Inukai, N. Trifluoroacetate method of peptide synthesis I. Synthesis and use of trifluoroacetate reagents. Bull. Chem. Soc. Jpn. 1965, 38, 1979-1984.
    • (1965) Bull. Chem. Soc. Jpn , vol.38 , pp. 1979-1984
    • Sakakibara, S.1    Inukai, N.2
  • 16
    • 0037152297 scopus 로고    scopus 로고
    • TFA-NHS as bifunctional protecting agent: Simulaneous protection and activation of amino carboxylic acids
    • Rao, T. S.; Nampalli, S.; Sekher, P.; Kumar, S. TFA-NHS as bifunctional protecting agent: simulaneous protection and activation of amino carboxylic acids. Tetrahedron Lett. 2002, 43, 7793-7795.
    • (2002) Tetrahedron Lett , vol.43 , pp. 7793-7795
    • Rao, T.S.1    Nampalli, S.2    Sekher, P.3    Kumar, S.4
  • 17
    • 85008103987 scopus 로고
    • Preparation and characterization of hetero-bifunctional cross-linking reagents for protein modifications
    • Kitagawa, T.; Shimozono, T.; Aikawa, T.; Yoshida, T.; Nishimura, H. Preparation and characterization of hetero-bifunctional cross-linking reagents for protein modifications. Chem. Pharm. Bull. 1981, 29, 1130-1135.
    • (1981) Chem. Pharm. Bull , vol.29 , pp. 1130-1135
    • Kitagawa, T.1    Shimozono, T.2    Aikawa, T.3    Yoshida, T.4    Nishimura, H.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.