메뉴 건너뛰기




Volumn 62, Issue 1, 2003, Pages 1-10

Tri(propylene glycol) glycerolate diacrylate cross-linked polystyrene: A new resin support for solid-phase peptide synthesis

Author keywords

Glycerol support; Hydroxyl resin; Solid phase peptide synthesis; Tri(propylene glycol) glycerolate diacrylate cross linked polystyrene support

Indexed keywords

ACRYLIC ACID RESIN; ALANINE; ARGININE; CALMODULIN BINDING PROTEIN; COPOLYMER; HYDROXYL GROUP; LYSINE; PEPTIDE DERIVATIVE; POLYPEPTIDE; POLYSTYRENE DERIVATIVE; PROPANEDIOL DERIVATIVE; RESIN; TRI(PROPYLENE GLYCOL) GLYCEROLATE DIACRYLATE; UNCLASSIFIED DRUG;

EID: 0037495849     PISSN: 1397002X     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-3011.2003.00057.x     Document Type: Article
Times cited : (7)

References (25)
  • 1
    • 20744456789 scopus 로고
    • Solid Phase Peptide Synthesis: The synthesis of a tetra peptide
    • Merrield, R.B. (1963) Solid Phase Peptide Synthesis: The synthesis of a tetra peptide. J. Am. Chem. Soc. 85, 2149-2154.
    • (1963) J. Am. Chem. Soc. , vol.85 , pp. 2149-2154
    • Merrield, R.B.1
  • 2
    • 0026419319 scopus 로고
    • Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery
    • Houghten, R.A., Pinilla, C., Blondelle, S.E., Appel, J.R., Dooley, C.T. & Cuvervo, J.H. (1991) Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery. Nature 354, 84-86.
    • (1991) Nature , vol.354 , pp. 84-86
    • Houghten, R.A.1    Pinilla, C.2    Blondelle, S.E.3    Appel, J.R.4    Dooley, C.T.5    Cuvervo, J.H.6
  • 3
    • 0028318863 scopus 로고
    • Application of combinatorial technologies to drug discovery. 2. Combinatorial organic synthesis, library screening strategies, and future directions
    • Gordon, E.M., Barret, R.W., Dower, W.J., Foder, S.P.A. & Gallop, M.A. (1994) Application of combinatorial technologies to drug discovery. 2. Combinatorial organic synthesis, library screening strategies, and future directions. J. Med. Chem. 37, 1385-1401.
    • (1994) J. Med. Chem. , vol.37 , pp. 1385-1401
    • Gordon, E.M.1    Barret, R.W.2    Dower, W.J.3    Foder, S.P.A.4    Gallop, M.A.5
  • 4
    • 7044263277 scopus 로고    scopus 로고
    • Synthesis and applications of small molecule libraries
    • Thompson, L.A. & Ellnan, J.A. (1996) Synthesis and applications of small molecule libraries. Chem. Rev. 96, 555-600.
    • (1996) Chem. Rev. , vol.96 , pp. 555-600
    • Thompson, L.A.1    Ellnan, J.A.2
  • 6
    • 0033624589 scopus 로고    scopus 로고
    • An activated O → N acyl transfer auxiliary: Efficient amide-backbone substitution of hindered difficult peptides
    • Miranda, L.P., Meuterrmans, W.D.F., Smythe, M.L. & Alewood, P.F. (2000) An activated O → N acyl transfer auxiliary: efcient amide-backbone substitution of hindered difcult peptides. J. Org. Chem. 65, 5460-5468.
    • (2000) J. Org. Chem. , vol.65 , pp. 5460-5468
    • Miranda, L.P.1    Meuterrmans, W.D.F.2    Smythe, M.L.3    Alewood, P.F.4
  • 7
    • 37049102463 scopus 로고
    • Peptide synthesis. Part 1. Preparation and use of polar supports based on poly(dimethylacrylamide)
    • Arshady, R., Atherton, E., Clive, D.L.J. & Sheppard, R.C. (1981) Peptide synthesis. Part 1. Preparation and use of polar supports based on poly(dimethylacrylamide). J. Chem. Soc. Perkin Trans. 1, 529-537.
    • (1981) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 529-537
    • Arshady, R.1    Atherton, E.2    Clive, D.L.J.3    Sheppard, R.C.4
  • 8
    • 0000975803 scopus 로고
    • Poly(ethylene glycol)s grafted onto crosslinked polystyrenes, 2, Multidetachably anchored polymer systems for the synthesis of solubilized peptides
    • Hellermann, H., Lucas, H.W., Maul, J., Pillai, V.N.R. & Mutter, M. (1983) Poly(ethylene glycol)s grafted onto crosslinked polystyrenes, 2, Multidetachably anchored polymer systems for the synthesis of solubilized peptides. Makromol. Chem. 184, 2603-2617.
    • (1983) Makromol. Chem. , vol.184 , pp. 2603-2617
    • Hellermann, H.1    Lucas, H.W.2    Maul, J.3    Pillai, V.N.R.4    Mutter, M.5
  • 9
    • 0028458901 scopus 로고
    • Preparation and application of polyethyleneglycolpolystyrene graft resin supports for solid-phase peptide synthesis
    • Zalipsky, S., Chang, J.L., Albericio, F. & Barany, G. (1994) Preparation and application of polyethyleneglycolpolystyrene graft resin supports for solid-phase peptide synthesis. React. Polym. 22, 243-258.
    • (1994) React. Polym. , vol.22 , pp. 243-258
    • Zalipsky, S.1    Chang, J.L.2    Albericio, F.3    Barany, G.4
  • 10
    • 0026704473 scopus 로고
    • PEGA: A flow stable polyethyleneglycol dimethylacrylamide copolymer for solid phase synthesis
    • Meldal, M. (1992) PEGA: a flow stable polyethyleneglycol dimethylacrylamide copolymer for solid phase synthesis. Tetrahedron Lett. 33, 3077-3080.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 3077-3080
    • Meldal, M.1
  • 11
    • 0029778868 scopus 로고    scopus 로고
    • CLEAR: A novel family of highly cross-linked polymeric supports for solid-phase peptide synthesis
    • Kempe, M. & Barany, G. (1996) CLEAR: a novel family of highly cross-linked polymeric supports for solid-phase peptide synthesis. J. Am. Chem. Soc. 118, 7083-7093.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 7083-7093
    • Kempe, M.1    Barany, G.2
  • 12
    • 0030593595 scopus 로고    scopus 로고
    • POEPOP and POEPS: Inert polyethylene glycol cross linked polymeric supports for solid synthesis
    • Renil, M. & Meldal, M. (1996) POEPOP and POEPS: inert polyethylene glycol cross linked polymeric supports for solid synthesis. Tetrahedron Lett. 37, 6185-6188.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 6185-6188
    • Renil, M.1    Meldal, M.2
  • 13
    • 0033575063 scopus 로고    scopus 로고
    • SPOCC: A resin for solid-phase organic chemistry and enzymatic reactions on solid phase
    • Rademann, J., Grotli, M., Meldal, M. & Bock, K. (1999) SPOCC: a resin for solid-phase organic chemistry and enzymatic reactions on solid phase. J. Am. Chem. Soc. 121, 5459-5466.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 5459-5466
    • Rademann, J.1    Grotli, M.2    Meldal, M.3    Bock, K.4
  • 14
    • 0034700653 scopus 로고    scopus 로고
    • HYDRA: A novel hydroxy and amine functionalised resin synthesised by reductive amination of PEG aldehyde and polyamine
    • Groth, T.; Grotli, M.; Lubell, W.D.; Miranda, L.P. and Meldal, M. (2000) HYDRA: a novel hydroxy and amine functionalised resin synthesised by reductive amination of PEG aldehyde and polyamine. J. Chem. Soc. Perkin Trans. 1, 4258-4264.
    • (2000) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 4258-4264
    • Groth, T.1    Grotli, M.2    Lubell, W.D.3    Miranda, L.P.4    Meldal, M.5
  • 15
    • 0242660258 scopus 로고    scopus 로고
    • EXPO 3000 a new expandable polymer for synthesis and enzymatic assays
    • Tornoe, C.M.; Meldal, M. (2002) EXPO 3000 a new expandable polymer for synthesis and enzymatic assays. Tetrahedron Lett. 43, 6409-6411.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 6409-6411
    • Tornoe, C.M.1    Meldal, M.2
  • 16
    • 0034910117 scopus 로고    scopus 로고
    • Syntheses, characterization and application of CLPSER as a novel polymer support for polypeptide syntheses
    • Leena, S. & Kumar, K.S. (2001) Syntheses, characterization and application of CLPSER as a novel polymer support for polypeptide syntheses. J. Peptide Res. 58, 117-128.
    • (2001) J. Peptide Res. , vol.58 , pp. 117-128
    • Leena, S.1    Kumar, K.S.2
  • 17
    • 0036134126 scopus 로고    scopus 로고
    • Solid phase peptide synthesis on JandaJel™ resin
    • Moss, A.J., Dickerson, J.T. & Janda K.D. (2002) Solid phase peptide synthesis on JandaJel™ resin. Tetrahedron Lett. 43, 37-40.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 37-40
    • Moss, A.J.1    Dickerson, J.T.2    Janda, K.D.3
  • 18
    • 0028318322 scopus 로고
    • Gel-phase peptide synthesis on a new high capacity tetraethyleneglycol diacrylate cross linked polystyrene support: Synthesis of pardaxin (16-33)
    • Renil, M., Nagaraj, R. & Pillai, V.N.R. (1994) Gel-phase peptide synthesis on a new high capacity tetraethyleneglycol diacrylate cross linked polystyrene support: synthesis of pardaxin (16-33). Tetrahedron 50, 6681-6688.
    • (1994) Tetrahedron , vol.50 , pp. 6681-6688
    • Renil, M.1    Nagaraj, R.2    Pillai, V.N.R.3
  • 19
    • 0342804257 scopus 로고    scopus 로고
    • Synthesis of acyl carrier protein fragment 65-74 on a crossed D sign exible cross-linked polystyrene support: Comparison with Merrield
    • Arunan, C. & Pillai, V.N.R. (2000) Synthesis of acyl carrier protein fragment 65-74 on a crossed D sign exible cross-linked polystyrene support: comparison with Merrield. Tetrahedron 56, 3005-3011.
    • (2000) Tetrahedron , vol.56 , pp. 3005-3011
    • Arunan, C.1    Pillai, V.N.R.2
  • 20
    • 12944291588 scopus 로고    scopus 로고
    • Synthesis, characterization, and application of butanediol dimethacrylate cross-linked polystyrene: A flexible support for gel phase peptide synthesis
    • Roice, M., Kumar, K.S. & Pillai, V.N.R. (1999) Synthesis, characterization, and application of butanediol dimethacrylate cross-linked polystyrene: a flexible support for gel phase peptide synthesis. Macromolecules 32, 8807-8815.
    • (1999) Macromolecules , vol.32 , pp. 8807-8815
    • Roice, M.1    Kumar, K.S.2    Pillai, V.N.R.3
  • 21
    • 0035136841 scopus 로고    scopus 로고
    • Synthesis of immunodominant peptide region of HCV viral pathogens using PS-BDODMA resin. A single peptide derived from the conserved domain E2/NS1 was highly effective in detecting anti HCV antibodies
    • Kumar, K.S.; Roice, M.; Sasikumar, P.G.; Podurai, C.D.; Sugunan, V.S.; Pillai, V.N.R. & Das, M.R. (2001) Synthesis of immunodominant peptide region of HCV viral pathogens using PS-BDODMA resin. A single peptide derived from the conserved domain E2/NS1 was highly effective in detecting anti HCV antibodies. J. Peptide Res. 57, 140-150.
    • (2001) J. Peptide Res. , vol.57 , pp. 140-150
    • Kumar, K.S.1    Roice, M.2    Sasikumar, P.G.3    Podurai, C.D.4    Sugunan, V.S.5    Pillai, V.N.R.6    Das, M.R.7
  • 22
    • 0025265014 scopus 로고
    • An efficient method for anchoring Fmoc-amino acids to hydroxyl-functionalized solid supports
    • Blankemeyer-Menge, B., Nimitz, M. & Frank, R. (1990) An efficient method for anchoring Fmoc-amino acids to hydroxyl-functionalized solid supports. Tetrahedron Lett. 31, 1701-1704.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 1701-1704
    • Blankemeyer-Menge, B.1    Nimitz, M.2    Frank, R.3
  • 24
    • 0014772602 scopus 로고
    • Colour test for the detection of free terminal amino groups in the solid-phase synthesis of peptides
    • Kaiser, E., Colescott, R.C., Bossinger, C.D. & Cook, P.I. (1970) Colour test for the detection of free terminal amino groups in the solid-phase synthesis of peptides. Anal. Biochem. 34, 595-598.
    • (1970) Anal. Biochem. , vol.34 , pp. 595-598
    • Kaiser, E.1    Colescott, R.C.2    Bossinger, C.D.3    Cook, P.I.4
  • 25
    • 0025103048 scopus 로고
    • A cleavage method which minimizes side reactions following Fmoc-solid phase peptide synthesis
    • King, D.S., Fields, C.G. & Fields, G.B. (1990) A cleavage method which minimizes side reactions following Fmoc-solid phase peptide synthesis. Int. J. Peptide Prot. Res. 36, 255-266.
    • (1990) Int. J. Peptide Prot. Res. , vol.36 , pp. 255-266
    • King, D.S.1    Fields, C.G.2    Fields, G.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.