메뉴 건너뛰기




Volumn 16, Issue 6, 2004, Pages 369-378

Probability rule for chiral recognition

Author keywords

Binding statistics; Chiral discrimination; Chiral recognition; Chiral statistics; CHIRBASE; Receptor affinity distribution (RAD); SMED; String model

Indexed keywords

ARTICLE; BIOCHEMISTRY; CHIRALITY; COMBINATORIAL CHEMISTRY; ENANTIOMER; ENERGY; ISOMER; MATHEMATICAL ANALYSIS; MATHEMATICAL MODEL; MOLECULAR BIOLOGY; MOLECULAR INTERACTION; MOLECULAR MODEL; MOLECULAR RECOGNITION; OGSTON THREE POINT INTERACTION MODEL; PRIORITY JOURNAL; PROBABILITY; PROTEIN DOMAIN; STATISTICAL ANALYSIS;

EID: 3042638110     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/chir.20049     Document Type: Article
Times cited : (34)

References (96)
  • 1
    • 0029824691 scopus 로고    scopus 로고
    • Stereochemical aspects of drug action and disposition
    • Eichelbaum M, Gross AS. Stereochemical aspects of drug action and disposition. Adv Drug Res 1996;28:1-64.
    • (1996) Adv Drug Res , vol.28 , pp. 1-64
    • Eichelbaum, M.1    Gross, A.S.2
  • 2
    • 0000328349 scopus 로고    scopus 로고
    • Liquid chromatography as a measurement tool for chiral interactions
    • Ringo MC, Evans CE. Liquid chromatography as a measurement tool for chiral interactions. Anal Chem News Features 1998: 315A-321.
    • (1998) Anal Chem News Features
    • Ringo, M.C.1    Evans, C.E.2
  • 3
    • 0031028851 scopus 로고    scopus 로고
    • Explanation of where and how enantioselective binding takes place on permethylated beta-cyclodextrin, a chiral stationary phase used in gas chromatography
    • Lipkowitz KB, Pearl G, Coner B, Peterson MA. Explanation of where and how enantioselective binding takes place on permethylated beta-cyclodextrin, a chiral stationary phase used in gas chromatography. J Am Chem Soc 1997;119:600-610.
    • (1997) J Am Chem Soc , vol.119 , pp. 600-610
    • Lipkowitz, K.B.1    Pearl, G.2    Coner, B.3    Peterson, M.A.4
  • 4
    • 0033862856 scopus 로고    scopus 로고
    • Atomistic modeling of enantioselective binding
    • Lipkowitz KB. Atomistic modeling of enantioselective binding. Acc Chem Res 2000;33:555-562.
    • (2000) Acc Chem Res , vol.33 , pp. 555-562
    • Lipkowitz, K.B.1
  • 5
    • 0018774004 scopus 로고
    • Separation of D and L amino acids by liquid chromatography: Use of chiral eluants
    • Hare PE, Gil-Av E. Separation of D and L amino acids by liquid chromatography: use of chiral eluants. Science 1979;204:1226-1228.
    • (1979) Science , vol.204 , pp. 1226-1228
    • Hare, P.E.1    Gil-Av, E.2
  • 8
    • 0016859743 scopus 로고
    • Chromatographic resolution of enantiomers selective review
    • Lochmuller CH, Souter RW. Chromatographic resolution of enantiomers selective review. J Chromatogr 1975;113:283-302.
    • (1975) J Chromatogr , vol.113 , pp. 283-302
    • Lochmuller, C.H.1    Souter, R.W.2
  • 9
    • 0037008247 scopus 로고    scopus 로고
    • Preparative liquid chromatography
    • Guiochon G. Preparative liquid chromatography. J Chromatogr A 2002;965:129-161.
    • (2002) J Chromatogr A , vol.965 , pp. 129-161
    • Guiochon, G.1
  • 10
    • 0000087554 scopus 로고    scopus 로고
    • Enantioselective binding in gas chromatography: A computational study of chiral selection by permethyl-beta-cyclodextrin
    • Lipkowitz KB, Coner B, Peterson MA, Morreale A. Enantioselective binding in gas chromatography: a computational study of chiral selection by permethyl-beta-cyclodextrin. J Phys Organ Chem 1997;10: 311-322.
    • (1997) J Phys Organ Chem , vol.10 , pp. 311-322
    • Lipkowitz, K.B.1    Coner, B.2    Peterson, M.A.3    Morreale, A.4
  • 11
    • 0033962554 scopus 로고    scopus 로고
    • Enantiodiscrimination by a quinine-based chiral stationary phase: A computational study
    • Schefzick S, Lindner W, Lipkowitz KB, Jalaie M. Enantiodiscrimination by a quinine-based chiral stationary phase: a computational study. Chirality 2000;12:7-15.
    • (2000) Chirality , vol.12 , pp. 7-15
    • Schefzick, S.1    Lindner, W.2    Lipkowitz, K.B.3    Jalaie, M.4
  • 12
    • 0037167008 scopus 로고    scopus 로고
    • Elucidation of the chiral recognition mechanism of cinchona alkaloid carbamate-type receptors for 3,5-dinitrobenzoyl amino acids
    • Maier NM, Schefzick S, Lombardo GM, Feliz M, Rissanen K, Lindner W, Lipkowitz KB. Elucidation of the chiral recognition mechanism of cinchona alkaloid carbamate-type receptors for 3,5-dinitrobenzoyl amino acids. J Am Chem Soc 2002;124:8611-8629.
    • (2002) J Am Chem Soc , vol.124 , pp. 8611-8629
    • Maier, N.M.1    Schefzick, S.2    Lombardo, G.M.3    Feliz, M.4    Rissanen, K.5    Lindner, W.6    Lipkowitz, K.B.7
  • 13
    • 0035854402 scopus 로고    scopus 로고
    • Quantitative structure-enantioselective retention relationships for chromatographic separation of arylalkylcarbinols on Pirkle type chiral stationary phases
    • Suzuki T, Timofei S, luoras BE, Uray G, Verdino P, Fabian WM. Quantitative structure-enantioselective retention relationships for chromatographic separation of arylalkylcarbinols on Pirkle type chiral stationary phases. J Chromatogr A 2001;922:13-23.
    • (2001) J Chromatogr A , vol.922 , pp. 13-23
    • Suzuki, T.1    Timofei, S.2    Luoras, B.E.3    Uray, G.4    Verdino, P.5    Fabian, W.M.6
  • 14
    • 0030702922 scopus 로고    scopus 로고
    • Locating regions of maximum chiral discrimination: A computational study of enantioselection on a popular chiral stationary phase used in chromatography
    • Lipkowitz KB, Coner R, Peterson MA. Locating regions of maximum chiral discrimination: A computational study of enantioselection on a popular chiral stationary phase used in chromatography. J Am Chem Soc 1997;119:11269-11276.
    • (1997) J Am Chem Soc , vol.119 , pp. 11269-11276
    • Lipkowitz, K.B.1    Coner, R.2    Peterson, M.A.3
  • 15
    • 0037506742 scopus 로고    scopus 로고
    • Comparison of two methods for the gas chromatographic determination of thermodynamic parameters of enantioselectivity
    • Spanik I, Krupcik J, Schurig V. Comparison of two methods for the gas chromatographic determination of thermodynamic parameters of enantioselectivity. J Chromatogr A 1999;843:123-128.
    • (1999) J Chromatogr A , vol.843 , pp. 123-128
    • Spanik, I.1    Krupcik, J.2    Schurig, V.3
  • 16
    • 0025826099 scopus 로고
    • Theoretical approach to the gaschromatographic separation of enantiomers on dissolved cyclodextrin derivatives
    • Jung M, Schmalzing D, Schurig V. Theoretical approach to the gaschromatographic separation of enantiomers on dissolved cyclodextrin derivatives. J Chromatogr 1991;552:43-57.
    • (1991) J Chromatogr , vol.552 , pp. 43-57
    • Jung, M.1    Schmalzing, D.2    Schurig, V.3
  • 17
    • 0037844272 scopus 로고    scopus 로고
    • Apparent and true enantioselectivity in enantioseparations
    • Gotmar G, Fornstedt T, Guiochon G. Apparent and true enantioselectivity in enantioseparations. Chirality 2000;12:558-564.
    • (2000) Chirality , vol.12 , pp. 558-564
    • Gotmar, G.1    Fornstedt, T.2    Guiochon, G.3
  • 18
    • 0025685319 scopus 로고
    • A vivid model illustrating chiral recognition induced by achiral structures
    • Davankov VA, Meyer VR, Rais M. A vivid model illustrating chiral recognition induced by achiral structures. Chirality 1990;2:208-210.
    • (1990) Chirality , vol.2 , pp. 208-210
    • Davankov, V.A.1    Meyer, V.R.2    Rais, M.3
  • 19
    • 0346734382 scopus 로고    scopus 로고
    • Modeling of the separation of two enantiomers using a microbore column
    • Zhou D, Kaczmarski K, Cavazzini A, Liu X, Guiochon G. Modeling of the separation of two enantiomers using a microbore column. J Chromatogr A 2003;1020:199-217.
    • (2003) J Chromatogr A , vol.1020 , pp. 199-217
    • Zhou, D.1    Kaczmarski, K.2    Cavazzini, A.3    Liu, X.4    Guiochon, G.5
  • 20
    • 0141670647 scopus 로고    scopus 로고
    • Adsorption isotherms and retention behavior of 1,1′-bis(2-naphthol) on CHIRIS AD1 and CHIRIS AD2 columns
    • Skavrada M, Jandera P, Cherrak DE, Aced A, Guiochon G. Adsorption isotherms and retention behavior of 1,1′-bis(2-naphthol) on CHIRIS AD1 and CHIRIS AD2 columns. J Chromatogr A 2003;1016: 143-154.
    • (2003) J Chromatogr A , vol.1016 , pp. 143-154
    • Skavrada, M.1    Jandera, P.2    Cherrak, D.E.3    Aced, A.4    Guiochon, G.5
  • 21
    • 0035515269 scopus 로고    scopus 로고
    • Nonlinear effects in LC and chiral LC
    • Fornstedt T, Guiochon G. Nonlinear effects in LC and chiral LC. Anal Chem 2001;73:608A-617A.
    • (2001) Anal Chem , vol.73
    • Fornstedt, T.1    Guiochon, G.2
  • 22
    • 0035847272 scopus 로고    scopus 로고
    • Separation of enantiomers: Needs, challenges, perspectives
    • Maier NM, Franco P, Lindner W. Separation of enantiomers: needs, challenges, perspectives. J Chromatogr A 2001;906:3-33.
    • (2001) J Chromatogr A , vol.906 , pp. 3-33
    • Maier, N.M.1    Franco, P.2    Lindner, W.3
  • 23
    • 0035975877 scopus 로고    scopus 로고
    • Quantitative affinity chromatography
    • Winzor DJ. Quantitative affinity chromatography. J Biochem Biophys Methods 2001;49:99-121.
    • (2001) J Biochem Biophys Methods , vol.49 , pp. 99-121
    • Winzor, D.J.1
  • 24
    • 0000469640 scopus 로고
    • Quantitative affinity chromatography. Determination of binding constants by elution with competitive inhibitors
    • Dunn BM, Chaiken IM. Quantitative affinity chromatography. Determination of binding constants by elution with competitive inhibitors. Proc Natl Acad Sci USA 1974;71:2382-2385.
    • (1974) Proc Natl Acad Sci USA , vol.71 , pp. 2382-2385
    • Dunn, B.M.1    Chaiken, I.M.2
  • 25
    • 0023046684 scopus 로고
    • Analytical affinity chromatography in studies of molecular recognition in biology: A review
    • Chaiken IM. Analytical affinity chromatography in studies of molecular recognition in biology: a review. J Chromatogr 1986;376: 11-32.
    • (1986) J Chromatogr , vol.376 , pp. 11-32
    • Chaiken, I.M.1
  • 26
    • 0036107851 scopus 로고    scopus 로고
    • Towards a general model for protein-substrate stereoselectivity
    • Sundaresan V, Abrol R. Towards a general model for protein-substrate stereoselectivity. Protein Sci 2002;11:1330-1339.
    • (2002) Protein Sci , vol.11 , pp. 1330-1339
    • Sundaresan, V.1    Abrol, R.2
  • 27
    • 0024834111 scopus 로고
    • A general criterion for molecular recognition: Implications for chiral interactions
    • Topiol S. A general criterion for molecular recognition: implications for chiral interactions. Chirality 1989;1:69-79.
    • (1989) Chirality , vol.1 , pp. 69-79
    • Topiol, S.1
  • 28
    • 0024824483 scopus 로고
    • A vivid model of chiral recognition
    • Meyer VR, Rais M. A vivid model of chiral recognition. Chirality 1989; 1:167-169.
    • (1989) Chirality , vol.1 , pp. 167-169
    • Meyer, V.R.1    Rais, M.2
  • 29
    • 0033945847 scopus 로고    scopus 로고
    • Sites of binding and orientation in a four-location model for protein stereospecificity
    • Mesecar AD, Koshland DE. Sites of binding and orientation in a four-location model for protein stereospecificity. Iubmb Life 2000;49:457-466.
    • (2000) Iubmb Life , vol.49 , pp. 457-466
    • Mesecar, A.D.1    Koshland, D.E.2
  • 30
    • 0030936156 scopus 로고    scopus 로고
    • Is chiral recognition a three-point process?
    • Booth TD, Wahnon D, Wainer IW. Is chiral recognition a three-point process? Chirality 1997;9:96-98.
    • (1997) Chirality , vol.9 , pp. 96-98
    • Booth, T.D.1    Wahnon, D.2    Wainer, I.W.3
  • 31
    • 0034076152 scopus 로고    scopus 로고
    • An exactly solvable Ogston model of gel electrophoresis. V. Attractive gel-analyte interactions and their effects on the Ferguson plot
    • Labrie J, Mercier JF, Slater GW. An exactly solvable Ogston model of gel electrophoresis. V. Attractive gel-analyte interactions and their effects on the Ferguson plot. Electrophoresis 2000;21:823-833.
    • (2000) Electrophoresis , vol.21 , pp. 823-833
    • Labrie, J.1    Mercier, J.F.2    Slater, G.W.3
  • 32
    • 0030254780 scopus 로고    scopus 로고
    • The agonistic binding site at the histamine H2 receptor. I. Theoretical investigations of histamine binding to an oligopeptide mimicking a part of the fifth transmembrane alpha-helix
    • Nederkoorn PH, van Lenthe JH, van der Goot H, Donne-Op den Kelder GM, Timmerman H. The agonistic binding site at the histamine H2 receptor. I. Theoretical investigations of histamine binding to an oligopeptide mimicking a part of the fifth transmembrane alpha-helix. J Comput Aid Mol Des 1996;10:461-478.
    • (1996) J Comput Aid Mol Des , vol.10 , pp. 461-478
    • Nederkoorn, P.H.1    Van Lenthe, J.H.2    Van Der Goot, H.3    Donne-Op Den Kelder, G.M.4    Timmerman, H.5
  • 33
    • 0030256228 scopus 로고    scopus 로고
    • The agonistic binding site at the histamine H2 receptor. II. Theoretical investigations of histamine binding to receptor models of the seven alpha-helical transmembrane domain
    • Nederkoorn PH, van Gelder EM, Donne-Op den Kelder GM, Timmerman H. The agonistic binding site at the histamine H2 receptor. II. Theoretical investigations of histamine binding to receptor models of the seven alpha-helical transmembrane domain. J Comput Aid Mol Des 1996;10:479-489.
    • (1996) J Comput Aid Mol Des , vol.10 , pp. 479-489
    • Nederkoorn, P.H.1    Van Gelder, E.M.2    Donne-Op Den Kelder, G.M.3    Timmerman, H.4
  • 34
    • 0035567118 scopus 로고    scopus 로고
    • Chiral recognition in gas-phase cyclodextrin: Amino acid complexes-is the three point interaction still valid in the gas phase?
    • Ahn S, Ramirez J, Grigorean G, Lebrilla CB. Chiral recognition in gas-phase cyclodextrin: amino acid complexes-is the three point interaction still valid in the gas phase? J Am Soc Mass Spectrom 2001;12:278-287.
    • (2001) J Am Soc Mass Spectrom , vol.12 , pp. 278-287
    • Ahn, S.1    Ramirez, J.2    Grigorean, G.3    Lebrilla, C.B.4
  • 35
    • 0020868572 scopus 로고
    • Three-point attachment: Past, present, but no future
    • Bentley R. Three-point attachment: past, present, but no future. Trans NY Acad Sci 1983;41:5-24.
    • (1983) Trans NY Acad Sci , vol.41 , pp. 5-24
    • Bentley, R.1
  • 36
    • 0030933019 scopus 로고    scopus 로고
    • The nature of chiral recognition: Is it a three point interaction?
    • Davankov VA. The nature of chiral recognition: is it a three point interaction? Chirality 1997;9:99-102.
    • (1997) Chirality , vol.9 , pp. 99-102
    • Davankov, V.A.1
  • 39
    • 0034809582 scopus 로고    scopus 로고
    • Enhancement of enanfiomeric excess by ligand distortion
    • Lipkowitz KB, Schefzick S, Avnir D. Enhancement of enanfiomeric excess by ligand distortion. J Am Chem Soc 2001;123:6710-6711.
    • (2001) J Am Chem Soc , vol.123 , pp. 6710-6711
    • Lipkowitz, K.B.1    Schefzick, S.2    Avnir, D.3
  • 40
    • 0014757146 scopus 로고
    • Interaction between asymmetric solutes and solvents. Peptide derivatives as stationary phases in gas liquid partition chromatography
    • Feibush B, Gil-Av E. Interaction between asymmetric solutes and solvents. Peptide derivatives as stationary phases in gas liquid partition chromatography. Tetrahedron 1970;26:1361-1368.
    • (1970) Tetrahedron , vol.26 , pp. 1361-1368
    • Feibush, B.1    Gil-Av, E.2
  • 41
    • 0037112479 scopus 로고    scopus 로고
    • Extrathermodynamic relationships in reversed-phase liquid chromatography
    • Miyabet K, Guiochon G. Extrathermodynamic relationships in reversed-phase liquid chromatography. Anal Chem 2002;74: 5754-5465.
    • (2002) Anal Chem , vol.74 , pp. 5754-5465
    • Miyabet, K.1    Guiochon, G.2
  • 42
    • 0036882648 scopus 로고    scopus 로고
    • Thermodynamic interpretation of retention equilibrium in reversed-phase liquid chromatography based on enthalpy-entropy compensation
    • Miyabet K, Guiochon G. Thermodynamic interpretation of retention equilibrium in reversed-phase liquid chromatography based on enthalpy-entropy compensation. Anal Chem 2002;74:5982-5992.
    • (2002) Anal Chem , vol.74 , pp. 5982-5992
    • Miyabet, K.1    Guiochon, G.2
  • 43
    • 0037035817 scopus 로고    scopus 로고
    • Effects of temperature on retention of chiral compounds on a ristocetin A chiral stationary phase
    • Peter A, Vekes E, Armstrong DW. Effects of temperature on retention of chiral compounds on a ristocetin A chiral stationary phase. J Chromatogr A 2002;958:89-107.
    • (2002) J Chromatogr A , vol.958 , pp. 89-107
    • Peter, A.1    Vekes, E.2    Armstrong, D.W.3
  • 44
    • 0036032998 scopus 로고    scopus 로고
    • Liquid chromatographic retention behavior and enantiomeric separation of three chiral center beta-blocker drug (nadolol) using heptakis (6-azido-6-deoxy-2, 3-di-O-phenylcarbamolyted) beta-cyclodextrin bonded chiral stationary phase
    • Wang X, Ching CB. Liquid chromatographic retention behavior and enantiomeric separation of three chiral center beta-blocker drug (nadolol) using heptakis (6-azido-6-deoxy-2, 3-di-O-phenylcarbamolyted) beta-cyclodextrin bonded chiral stationary phase. Chirality 2002;14:798-805.
    • (2002) Chirality , vol.14 , pp. 798-805
    • Wang, X.1    Ching, C.B.2
  • 45
    • 0025949252 scopus 로고
    • Reconstruction of the antibody affinity distribution from experimental binding data by a minimum cross-entropy procedure
    • Yee E. Reconstruction of the antibody affinity distribution from experimental binding data by a minimum cross-entropy procedure. J Theor Biol 1991;153:205-227.
    • (1991) J Theor Biol , vol.153 , pp. 205-227
    • Yee, E.1
  • 46
    • 84988099160 scopus 로고
    • Diluted modified cyclodextrins as chiral stationary phases influence of the polysiloxane solvent - Heptakis (2,3-di-o-acetyl-6-o-tert- butyldimethylsilyl)-beta-cyclodextrin
    • Dietrich A, Maas B, Mosandl A. Diluted modified cyclodextrins as chiral stationary phases influence of the polysiloxane solvent - heptakis (2,3-di-o-acetyl-6-o-tert-butyldimethylsilyl)-beta-cyclodextrin. J High Resol Chromatogr 1995;18:152-156.
    • (1995) J High Resol Chromatogr , vol.18 , pp. 152-156
    • Dietrich, A.1    Maas, B.2    Mosandl, A.3
  • 47
    • 0037207248 scopus 로고    scopus 로고
    • Effect of temperature on the reversal in the retention order of the enantiomers of mosapride on Chiral-AGP
    • Karlsson A, Skoog A, Ohlen K. Effect of temperature on the reversal in the retention order of the enantiomers of mosapride on Chiral-AGP. J Biochem Biophys Methods 2002;54:347-356.
    • (2002) J Biochem Biophys Methods , vol.54 , pp. 347-356
    • Karlsson, A.1    Skoog, A.2    Ohlen, K.3
  • 48
    • 0029794940 scopus 로고    scopus 로고
    • Quantifying biological specificity: The statistical mechanics of molecular recognition
    • Janin J. Quantifying biological specificity: the statistical mechanics of molecular recognition. Proteins 1996;25:438-445.
    • (1996) Proteins , vol.25 , pp. 438-445
    • Janin, J.1
  • 49
    • 0036386869 scopus 로고    scopus 로고
    • Test of a statistical model for molecular recognition in biological repertoires
    • Rosenwald S, Kafri R, Lancet D. Test of a statistical model for molecular recognition in biological repertoires. J Theor Biol 2002;216:327-336.
    • (2002) J Theor Biol , vol.216 , pp. 327-336
    • Rosenwald, S.1    Kafri, R.2    Lancet, D.3
  • 50
    • 0024834111 scopus 로고
    • A general criterion for molecular recognition - Implications for chiral interactions
    • Topiol S. A general criterion for molecular recognition - implications for chiral interactions. Chirality 1989;1:69-79.
    • (1989) Chirality , vol.1 , pp. 69-79
    • Topiol, S.1
  • 51
    • 0024472594 scopus 로고
    • Immune network theory
    • Perelson AS. Immune network theory. Immunol Rev 1989;110:5-36.
    • (1989) Immunol Rev , vol.110 , pp. 5-36
    • Perelson, A.S.1
  • 52
    • 84955373821 scopus 로고
    • Molecular recognition in biology: Models for analysis of protein-ligand interactions
    • Behr JP, editor. New York: John Wiley & Sons
    • Lancet D, Horovitz A, Katchalski-Katzir E. Molecular recognition in biology: models for analysis of protein-ligand interactions. In: Behr JP, editor. The lock-and-key principle, vol. 2. New York: John Wiley & Sons; 1994. p 25-71.
    • (1994) The Lock-and-key Principle , vol.2 , pp. 25-71
    • Lancet, D.1    Horovitz, A.2    Katchalski-Katzir, E.3
  • 53
    • 0033609160 scopus 로고    scopus 로고
    • Explaining high alloreactivity as a quantitative consequence of affinity-driven thymocyte selection
    • Detours V, Perelson AS. Explaining high alloreactivity as a quantitative consequence of affinity-driven thymocyte selection. Proc Natl Acad Sci USA 1999;96:5153-5158.
    • (1999) Proc Natl Acad Sci USA , vol.96 , pp. 5153-5158
    • Detours, V.1    Perelson, A.S.2
  • 54
    • 0034682496 scopus 로고    scopus 로고
    • The paradox of alloreactivity and self MHC restriction: Quantitative analysis and statistics
    • Detours V, Perelson AS. The paradox of alloreactivity and self MHC restriction: quantitative analysis and statistics. Proc Natl Acad Sci USA 2000;97:8479-8483.
    • (2000) Proc Natl Acad Sci USA , vol.97 , pp. 8479-8483
    • Detours, V.1    Perelson, A.S.2
  • 55
  • 56
    • 0027414469 scopus 로고
    • Probability model for molecular recognition in biological receptor repertoires: Significance to the olfactory system
    • Lancet D, Sadovsky E, Seidemann E. Probability model for molecular recognition in biological receptor repertoires: significance to the olfactory system. Proc Natl Acad Sci USA 1993;90:3715-3719.
    • (1993) Proc Natl Acad Sci USA , vol.90 , pp. 3715-3719
    • Lancet, D.1    Sadovsky, E.2    Seidemann, E.3
  • 59
    • 0035847236 scopus 로고    scopus 로고
    • Reviewing mobile phases used on Chiralcel OD through an application of data mining tools to CHIRBASE database
    • Piras P, Roussel C, Pierrot-Sanders J. Reviewing mobile phases used on Chiralcel OD through an application of data mining tools to CHIRBASE database. J Chromatogr A 2001;906:443-458.
    • (2001) J Chromatogr A , vol.906 , pp. 443-458
    • Piras, P.1    Roussel, C.2    Pierrot-Sanders, J.3
  • 60
    • 0030928811 scopus 로고    scopus 로고
    • An approach to discriminating 25 commercial chiral stationary phases from structural data sets extracted from a molecular database
    • Roussel C, Piras P, Heitmann I. An approach to discriminating 25 commercial chiral stationary phases from structural data sets extracted from a molecular database. Biomed Chromatogr 1997;11: 311-316.
    • (1997) Biomed Chromatogr , vol.11 , pp. 311-316
    • Roussel, C.1    Piras, P.2    Heitmann, I.3
  • 63
    • 0026749348 scopus 로고
    • Chromatographic resolution of the chiral isomers of several beta-blockers over cellulose tris(3,5-dimethylphenylcarbamate) chiral stationary phase
    • Ching CB, Lim BG, Lee EJ, Ng SC. Chromatographic resolution of the chiral isomers of several beta-blockers over cellulose tris(3,5- dimethylphenylcarbamate) chiral stationary phase. Chirality 1992;4: 174-177.
    • (1992) Chirality , vol.4 , pp. 174-177
    • Ching, C.B.1    Lim, B.G.2    Lee, E.J.3    Ng, S.C.4
  • 64
    • 0037172687 scopus 로고    scopus 로고
    • Enantioseparation of various amino acid derivatives on a quinine based chiral anion-exchange selector at variable temperature conditions. Influence of structural parameters of the analytes on the apparent retention and enantioseparation characteristics
    • Oberleitner WR, Maier NM, Lindner W. Enantioseparation of various amino acid derivatives on a quinine based chiral anion-exchange selector at variable temperature conditions. Influence of structural parameters of the analytes on the apparent retention and enantioseparation characteristics. J Chromatogr A 2002;960:97-108.
    • (2002) J Chromatogr A , vol.960 , pp. 97-108
    • Oberleitner, W.R.1    Maier, N.M.2    Lindner, W.3
  • 65
    • 0034646783 scopus 로고    scopus 로고
    • Quantitative chirality/enantioselectivity relations in large random supramolecular structures
    • Katzenelson O, Avnir D. Quantitative chirality/enantioselectivity relations in large random supramolecular structures. Chemistry 2000; 6:1346-1354.
    • (2000) Chemistry , vol.6 , pp. 1346-1354
    • Katzenelson, O.1    Avnir, D.2
  • 66
    • 0035844007 scopus 로고    scopus 로고
    • Effect of the mobile phase on the retention behaviour of optical isomers of carboxylic acids and amino acids in liquid chromatography on bonded Teicoplanin columns
    • Jandera P, Skavrada M, Klemmova K, Backovska V, Guiochon G. Effect of the mobile phase on the retention behaviour of optical isomers of carboxylic acids and amino acids in liquid chromatography on bonded Teicoplanin columns. J Chromatogr A 2001;917: 123-133.
    • (2001) J Chromatogr A , vol.917 , pp. 123-133
    • Jandera, P.1    Skavrada, M.2    Klemmova, K.3    Backovska, V.4    Guiochon, G.5
  • 67
    • 0033033223 scopus 로고    scopus 로고
    • Cyclodextrin derivatives as chiral selectors for direct gas chromatographic separation of enantiomers in the essential oil, aroma and flavour fields
    • Bicchi C, D'Amato A, Rubiolo P. Cyclodextrin derivatives as chiral selectors for direct gas chromatographic separation of enantiomers in the essential oil, aroma and flavour fields. J Chromatogr A 1999;843:99-121.
    • (1999) J Chromatogr A , vol.843 , pp. 99-121
    • Bicchi, C.1    D'Amato, A.2    Rubiolo, P.3
  • 68
    • 0016757920 scopus 로고
    • Theory of hapten binding to IgM: The question of repulsive interactions between binding sites
    • Goldstein B. Theory of hapten binding to IgM: the question of repulsive interactions between binding sites. Biophys Chem 1975;3: 363-367.
    • (1975) Biophys Chem , vol.3 , pp. 363-367
    • Goldstein, B.1
  • 69
    • 0030597505 scopus 로고    scopus 로고
    • Size and connectivity of the idiotypic network are independent of the discreteness of the affinity distribution
    • Detours V, Sulzer B, Perelson AS. Size and connectivity of the idiotypic network are independent of the discreteness of the affinity distribution. J Theor Biol 1996;183:409-416.
    • (1996) J Theor Biol , vol.183 , pp. 409-416
    • Detours, V.1    Sulzer, B.2    Perelson, A.S.3
  • 71
    • 0013863816 scopus 로고
    • Comparison of experimental binding data and theoretical models in proteins containing subunits
    • Koshland DE Jr, Nemethy G, Filmer D. Comparison of experimental binding data and theoretical models in proteins containing subunits. Biochemistry 1966;5:365-385.
    • (1966) Biochemistry , vol.5 , pp. 365-385
    • Koshland Jr., D.E.1    Nemethy, G.2    Filmer, D.3
  • 72
    • 0030844327 scopus 로고    scopus 로고
    • Molecularly imprinted ligand-exchange adsorbents for the chiral separation of underivatized amino acids
    • Vidyasankar S, Ru M, Arnold FH. Molecularly imprinted ligand-exchange adsorbents for the chiral separation of underivatized amino acids. J Chromatogr A 1997;775:51-63.
    • (1997) J Chromatogr A , vol.775 , pp. 51-63
    • Vidyasankar, S.1    Ru, M.2    Arnold, F.H.3
  • 77
    • 0346199347 scopus 로고    scopus 로고
    • Power and measures of effect size in analysis of variance with fixed versus random nested factors
    • Siemer M, Joormann J. Power and measures of effect size in analysis of variance with fixed versus random nested factors. Psychol Methods 2003;8:497-517.
    • (2003) Psychol Methods , vol.8 , pp. 497-517
    • Siemer, M.1    Joormann, J.2
  • 78
    • 0035131982 scopus 로고    scopus 로고
    • The impact of genotyping error on family-based analysis of quantitative traits
    • Abecasis GR, Cherny SS, Cardon LR. The impact of genotyping error on family-based analysis of quantitative traits. Eur J Hum Genet 2001;9:130-134.
    • (2001) Eur J Hum Genet , vol.9 , pp. 130-134
    • Abecasis, G.R.1    Cherny, S.S.2    Cardon, L.R.3
  • 80
    • 0036782116 scopus 로고    scopus 로고
    • Putting chirality to work: The strategy of chiral switches
    • Agranat I, Caner H, Caldwell J. Putting chirality to work: the strategy of chiral switches. Nat Rev Drug Discov 2002;1:753-768.
    • (2002) Nat Rev Drug Discov , vol.1 , pp. 753-768
    • Agranat, I.1    Caner, H.2    Caldwell, J.3
  • 81
    • 0035808649 scopus 로고    scopus 로고
    • Influence of the solute hydrophobicity on the enantioselective adsorption of beta-blockers on a cellulase protein used as the chiral selector
    • Gotmar G, Fornstedt T, Andersson M, Guiochon G. Influence of the solute hydrophobicity on the enantioselective adsorption of beta-blockers on a cellulase protein used as the chiral selector. J Chromatogr A 2001;905:3-17.
    • (2001) J Chromatogr A , vol.905 , pp. 3-17
    • Gotmar, G.1    Fornstedt, T.2    Andersson, M.3    Guiochon, G.4
  • 82
    • 8944238475 scopus 로고    scopus 로고
    • Experimental and theoretical study of the adsorption behavior and mass transfer kinetics of propranolol enantiomers on cellulase protein as the selector
    • Fornstedt T, Zhong G, Bensetiti Z, Guiochon G. Experimental and theoretical study of the adsorption behavior and mass transfer kinetics of propranolol enantiomers on cellulase protein as the selector. Anal Chem 1996;68:2370-2378.
    • (1996) Anal Chem , vol.68 , pp. 2370-2378
    • Fornstedt, T.1    Zhong, G.2    Bensetiti, Z.3    Guiochon, G.4
  • 83
    • 3042653330 scopus 로고    scopus 로고
    • Enthalpy-entropy compensation for enantio-seperation on cellulose and amylose tris (3, 5-dimethyl-phenylcarbamate) derivatives as stationary phases
    • Kazusaki M, Shoda T, Kawabata H. Enthalpy-entropy compensation for enantio-seperation on cellulose and amylose tris (3, 5-dimethyl-phenylcarbamate) derivatives as stationary phases. Chromatography 2003;24:121-126.
    • (2003) Chromatography , vol.24 , pp. 121-126
    • Kazusaki, M.1    Shoda, T.2    Kawabata, H.3
  • 84
    • 0028274617 scopus 로고
    • Enantiomeric separation of chiral sulfoxides - Screening of cellulose-based sorbents with particular reference to cellulose tribenzoate
    • Kusters E, Loux V, Schmid E, Floersheim P. Enantiomeric separation of chiral sulfoxides - screening of cellulose-based sorbents with particular reference to cellulose tribenzoate. J Chromatogr A 1994; 666:421-432.
    • (1994) J Chromatogr A , vol.666 , pp. 421-432
    • Kusters, E.1    Loux, V.2    Schmid, E.3    Floersheim, P.4
  • 85
    • 0035847280 scopus 로고    scopus 로고
    • Separation of enantiomers by gas chromatography
    • Schurig V. Separation of enantiomers by gas chromatography. J Chromatogr A 2001;906:275-299.
    • (2001) J Chromatogr A , vol.906 , pp. 275-299
    • Schurig, V.1
  • 86
    • 0028351604 scopus 로고
    • Changes in chiral selectivity with temperature for an ovomucoid protein-based column
    • Kirkland KM, Mccombs DA. Changes in chiral selectivity with temperature for an ovomucoid protein-based column. J Chromatogr A 1994;666:211-219.
    • (1994) J Chromatogr A , vol.666 , pp. 211-219
    • Kirkland, K.M.1    Mccombs, D.A.2
  • 88
    • 0037080470 scopus 로고    scopus 로고
    • Reversal of elution order during the chiral separation in high performance liquid chromatography
    • Okamoto M. Reversal of elution order during the chiral separation in high performance liquid chromatography. J Pharm Biomed Anal 2002;27:401-407.
    • (2002) J Pharm Biomed Anal , vol.27 , pp. 401-407
    • Okamoto, M.1
  • 89
    • 0010642665 scopus 로고
    • A study of multispecific interactions by quantative affinity chromatography
    • Chaiken IM, Wilcheck M, Parkih I, editors. Orlando: Academic Press
    • Inman JK. A study of multispecific interactions by quantative affinity chromatography. In: Chaiken IM, Wilcheck M, Parkih I, editors. Affinity chromatography and biological recognition. Orlando: Academic Press; 1983.
    • (1983) Affinity Chromatography and Biological Recognition
    • Inman, J.K.1
  • 90
    • 0001329819 scopus 로고    scopus 로고
    • Chirality of large random supra-molecular structures
    • Katzenelson O, HelOr HZ, Avnir D. Chirality of large random supra-molecular structures. Chem Eur J 1996;2:174-181.
    • (1996) Chem Eur J , vol.2 , pp. 174-181
    • Katzenelson, O.1    HelOr, H.Z.2    Avnir, D.3
  • 91
    • 0035408563 scopus 로고    scopus 로고
    • Thin-layer chromatography-a useful technique for the separation of enantiomers
    • Bereznitski Y, Thompson R, O'Neill E, Grinberg N. Thin-layer chromatography-a useful technique for the separation of enantiomers. J AOAC Int 2001;84:1242-1251.
    • (2001) J AOAC Int , vol.84 , pp. 1242-1251
    • Bereznitski, Y.1    Thompson, R.2    O'Neill, E.3    Grinberg, N.4
  • 92
    • 0029803925 scopus 로고    scopus 로고
    • Chiral separations by nonaqueous capillary electrophoresis
    • Wang F, Khaledi MG. Chiral separations by nonaqueous capillary electrophoresis. Anal Chem 1996;68:3460-3467.
    • (1996) Anal Chem , vol.68 , pp. 3460-3467
    • Wang, F.1    Khaledi, M.G.2
  • 93
    • 0038777333 scopus 로고    scopus 로고
    • Enantioselective ligand exchange in modern separation techniques
    • Davankov VA. Enantioselective ligand exchange in modern separation techniques. J Chromatogr A 2003;1000:891-915.
    • (2003) J Chromatogr A , vol.1000 , pp. 891-915
    • Davankov, V.A.1
  • 94
    • 0034332612 scopus 로고    scopus 로고
    • Identification of chiral selectors from a 200-member parallel combinatorial library
    • Wang Y, Bluhm LH, Li T. Identification of chiral selectors from a 200-member parallel combinatorial library. Anal Chem 2000;72:5459-5465.
    • (2000) Anal Chem , vol.72 , pp. 5459-5465
    • Wang, Y.1    Bluhm, L.H.2    Li, T.3
  • 95
    • 0036745525 scopus 로고    scopus 로고
    • Combinatorial enantiomeric separation of diverse compounds using capillary array electrophoresis
    • Zhong W, Yeung ES. Combinatorial enantiomeric separation of diverse compounds using capillary array electrophoresis. Electrophoresis 2002;23:2996-3005.
    • (2002) Electrophoresis , vol.23 , pp. 2996-3005
    • Zhong, W.1    Yeung, E.S.2
  • 96
    • 0141675068 scopus 로고    scopus 로고
    • Chiral recognition: Design and preparation of chiral stationary phases using selectors derived from ugi multicomponent condensation reactions and a combinatorial approach
    • Brahmachary E, Ling FH, Svec F, Frechet JM. Chiral recognition: design and preparation of chiral stationary phases using selectors derived from ugi multicomponent condensation reactions and a combinatorial approach. J Comb Chem 2003;5:441-450.
    • (2003) J Comb Chem , vol.5 , pp. 441-450
    • Brahmachary, E.1    Ling, F.H.2    Svec, F.3    Frechet, J.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.