메뉴 건너뛰기




Volumn 15, Issue PART B., 1996, Pages 671-679

An Approach Toward the Semiquantitation of Molecular Recognition Phenomena in Noncovalent Molecularly Imprinted Polymer Systems: Consequences for Molecularly Imprinted Polymer Design

(1)  Nicholls, Ian A a  

a NONE

Author keywords

[No Author keywords available]

Indexed keywords


EID: 77956867449     PISSN: 15692558     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S1569-2558(08)60145-9     Document Type: Article
Times cited : (11)

References (28)
  • 1
    • 77956823380 scopus 로고
    • Molecular imprinting-a versatile technique for the preparation of separation materials of predetermined selectivity
    • Street G. (Ed), Chapman-Hall, London in press
    • Andersson L.I., Nicholls I.A., and Mosbach K. Molecular imprinting-a versatile technique for the preparation of separation materials of predetermined selectivity. In: Street G. (Ed). Separations in Biotechnology (1993), Chapman-Hall, London in press
    • (1993) Separations in Biotechnology
    • Andersson, L.I.1    Nicholls, I.A.2    Mosbach, K.3
  • 2
    • 77956811306 scopus 로고    scopus 로고
    • Andersson, L.I., Nicholls, I.A., & Mosbach, K. (1996). Molecular imprinting. In: this
    • Andersson, L.I., Nicholls, I.A., & Mosbach, K. (1996). Molecular imprinting. In: this volume.
  • 3
    • 0021745755 scopus 로고
    • Functional group contributions to drug receptor interactions
    • Andrews P.R., Craik D.J., and Martin J.L. Functional group contributions to drug receptor interactions. J. Med. Chem. 27 (1984) 1648-1657
    • (1984) J. Med. Chem. , vol.27 , pp. 1648-1657
    • Andrews, P.R.1    Craik, D.J.2    Martin, J.L.3
  • 4
    • 0025916753 scopus 로고
    • Molecular recognition in aqueous solution: An estimate of the intrinsic binding energy of an amide-hydroxyl hydrogen bond
    • Cox J.P., Nicholls L.I.A., and Williams D.H. Molecular recognition in aqueous solution: An estimate of the intrinsic binding energy of an amide-hydroxyl hydrogen bond. J. Chem. Soc., Chem. Commun. (1991) 1295-1297
    • (1991) J. Chem. Soc., Chem. Commun. , pp. 1295-1297
    • Cox, J.P.1    Nicholls, L.I.A.2    Williams, D.H.3
  • 5
    • 0026331366 scopus 로고
    • Direct enantioseparation of ß-adrenergic blockers using a chiral stationary phase prepared by molecular imprinting
    • Fischer L., Müller R., Ekberg B., and Mosbach K. Direct enantioseparation of ß-adrenergic blockers using a chiral stationary phase prepared by molecular imprinting. J. Am. Chem. Soc. 113 (1991) 9358-9360
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 9358-9360
    • Fischer, L.1    Müller, R.2    Ekberg, B.3    Mosbach, K.4
  • 6
    • 33745502124 scopus 로고
    • Peptidomimetics for receptor ligands-Discovery, development, and medical properties
    • Giannis A., and Kolter T. Peptidomimetics for receptor ligands-Discovery, development, and medical properties. Angew. Chemie Int. Ed. Engl. 32 (1993) 1244-1267
    • (1993) Angew. Chemie Int. Ed. Engl. , vol.32 , pp. 1244-1267
    • Giannis, A.1    Kolter, T.2
  • 7
  • 8
    • 0019407381 scopus 로고
    • On the attribution and additivity of binding energies
    • Jencks W.P. On the attribution and additivity of binding energies. Proc. Natl. Acad. Sci. USA 78 (1978) 4046-4050
    • (1978) Proc. Natl. Acad. Sci. USA , vol.78 , pp. 4046-4050
    • Jencks, W.P.1
  • 9
    • 0000665502 scopus 로고
    • Binding studies on substrate- and enantio-selective molecularly imprinted polymers
    • Kempe M., and Mosbach K. Binding studies on substrate- and enantio-selective molecularly imprinted polymers. Anal. Lett. 24 (1991) 1137-1145
    • (1991) Anal. Lett. , vol.24 , pp. 1137-1145
    • Kempe, M.1    Mosbach, K.2
  • 10
    • 0000546426 scopus 로고
    • Enzyme mimicking polymers exhibiting specific substrate binding and catalytic functions
    • Leonhardt A., and Mosbach K. Enzyme mimicking polymers exhibiting specific substrate binding and catalytic functions. Reactive Polymers 6 (1987) 285-290
    • (1987) Reactive Polymers , vol.6 , pp. 285-290
    • Leonhardt, A.1    Mosbach, K.2
  • 11
    • 0029742633 scopus 로고    scopus 로고
    • Carbon-carbon bond formation using substrate selective catalytic polymers prepared by molecular imprinting.: An artificial aldolase
    • in press
    • Matsui, J., Nicholls, I.A., Karube, I., & Mosbach, K. (1996). Carbon-carbon bond formation using substrate selective catalytic polymers prepared by molecular imprinting.: An artificial aldolase. J., Org. Chem. 61, in press.
    • (1996) J., Org. Chem , vol.61
    • Matsui, J.1    Nicholls, I.A.2    Karube, I.3    Mosbach, K.4
  • 12
  • 13
    • 77956764030 scopus 로고
    • Framsfällning av polymerer genom molekylavtryck för använding vid stereooch enantioselektiva synteser styrda primärt av icke-kovalenta interaktioner. Swedish
    • Patent Application 9203913-0, Worldwide patent pending
    • Mosbach, K., Nicholls, I.A., & Ramström, O. (1992). Framsfällning av polymerer genom molekylavtryck för använding vid stereooch enantioselektiva synteser styrda primärt av icke-kovalenta interaktioner. Swedish Patent Application 9203913-0, Worldwide patent pending.
    • (1992)
    • Mosbach, K.1    Nicholls, I.A.2    Ramström, O.3
  • 15
    • 77956812049 scopus 로고
    • Design, synthesis and opioid receptor binding of some novel benzazepine constrained leucine enkephalin mimetics
    • in press
    • Nicholls, I.A. & Alewood, P.F. (1994). Design, synthesis and opioid receptor binding of some novel benzazepine constrained leucine enkephalin mimetics. J. Chem. Research, in press.
    • (1994) J. Chem. Research
    • Nicholls, I.A.1    Alewood, P.F.2
  • 16
    • 77956826168 scopus 로고
    • Rational CNS drug design - potential antihypertensive agents
    • Nicholls I.A., Alewood P.F., and Andrews P.R. Rational CNS drug design - potential antihypertensive agents. Aust. J. Hosp. Pharm. 20 (1990) 334-338
    • (1990) Aust. J. Hosp. Pharm. , vol.20 , pp. 334-338
    • Nicholls, I.A.1    Alewood, P.F.2    Andrews, P.R.3
  • 17
    • 0012048776 scopus 로고
    • 2-substituted 1, 3-benzodiazocines: Design, synthesis and evaluation as potential central nervous system active agents
    • s
    • Nicholls I.A., Alewood P.F., Brinkworth R.I., Morrison S.F., and Andrews P.R. 2-substituted 1, 3-benzodiazocines: Design, synthesis and evaluation as potential central nervous system active agents. J. Chem. Research (M 2811-2826 (1993) 408-409 s
    • (1993) J. Chem. Research (M , vol.2811-2826 , pp. 408-409
    • Nicholls, I.A.1    Alewood, P.F.2    Brinkworth, R.I.3    Morrison, S.F.4    Andrews, P.R.5
  • 18
    • 0028054257 scopus 로고
    • H-NMR and molecular modeling based conformational analysis of some N-alkyl-l- and 2-benzazepinones: Useful central nervous system agent design motifs
    • Nicholls I.A., Craik D.J., and Alewood P.F. H-NMR and molecular modeling based conformational analysis of some N-alkyl-l- and 2-benzazepinones: Useful central nervous system agent design motifs. Biochem. Biophys. Res. Commun. 205 (1994) 98-104
    • (1994) Biochem. Biophys. Res. Commun. , vol.205 , pp. 98-104
    • Nicholls, I.A.1    Craik, D.J.2    Alewood, P.F.3
  • 20
    • 0015101706 scopus 로고
    • Entropic contributions to rate accelerations in enzymic and intramolecular reactions and the chelate effect
    • Page M.I., and Jencks W.P. Entropic contributions to rate accelerations in enzymic and intramolecular reactions and the chelate effect. Proc. Natl. Acad. Sci. USA 68 (1971) 1678-1683
    • (1971) Proc. Natl. Acad. Sci. USA , vol.68 , pp. 1678-1683
    • Page, M.I.1    Jencks, W.P.2
  • 21
    • 0028209780 scopus 로고
    • Synthetic peptide receptor mimics: Highly stereoselective recognition in non-covalent molecularly imprinted polymers
    • in press
    • Ramström, O., Nicholls, LA., & Mosbach, K. (1994). Synthetic peptide receptor mimics: Highly stereoselective recognition in non-covalent molecularly imprinted polymers. Tetrahedron: Asymmetry 5, in press.
    • (1994) Tetrahedron: Asymmetry , vol.5
    • Ramström, O.1    Nicholls, L.A.2    Mosbach, K.3
  • 22
    • 9644258919 scopus 로고
    • The cost of conformational order: Entropy changes in molecular associations
    • Searle M.S., and Williams D.H. The cost of conformational order: Entropy changes in molecular associations. J. Am. Chem. Soc. 114 (1992) 10690-10697
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 10690-10697
    • Searle, M.S.1    Williams, D.H.2
  • 24
    • 0027447855 scopus 로고
    • Drug assay using antibody mimics made by molecular imprinting
    • Vlatakis G., Andersson L.I., Müller R., and Mosbach K. Drug assay using antibody mimics made by molecular imprinting. Nature (London 361 (1993) 645-647
    • (1993) Nature (London , vol.361 , pp. 645-647
    • Vlatakis, G.1    Andersson, L.I.2    Müller, R.3    Mosbach, K.4
  • 27
    • 77956838213 scopus 로고
    • Molecular basis of the activity of antibiotics of the vancomycin group: Guides for peptide-peptide binding
    • Brown C. (Ed), Academic Press, London
    • Williams D.H., Doig A.J., Cox J.P., Nicholls L.I.A., and Gardner M. Molecular basis of the activity of antibiotics of the vancomycin group: Guides for peptide-peptide binding. In: Brown C. (Ed). Chirality in Drug Design and Synthesis (1990), Academic Press, London 101-113
    • (1990) Chirality in Drug Design and Synthesis , pp. 101-113
    • Williams, D.H.1    Doig, A.J.2    Cox, J.P.3    Nicholls, L.I.A.4    Gardner, M.5
  • 28
    • 0022918163 scopus 로고
    • Molecular recognition in polymers prepared with templates
    • Polymeric Reagents and Catalysts Ford, W.T, Ed, pp, American Chemical Society, Washington DC
    • Wulff, G.I. (1986). Molecular recognition in polymers prepared with templates. In: Polymeric Reagents and Catalysts Ford, W.T., Ed.), pp. 186-230. ACS symposium series 308, American Chemical Society, Washington DC.
    • (1986) ACS symposium series , vol.308 , pp. 186-230
    • Wulff, G.I.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.