메뉴 건너뛰기




Volumn 10, Issue 4, 2005, Pages 289-295

Predicting aqueous solubility from structure

Author keywords

[No Author keywords available]

Indexed keywords

DIMETHYL SULFOXIDE; SOLVENT; WATER;

EID: 13544270908     PISSN: 13596446     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1359-6446(04)03365-3     Document Type: Review
Times cited : (180)

References (63)
  • 1
    • 13544272536 scopus 로고
    • Body water in man. I. Total body water in normal subjects and edematous patients
    • Musha D. Body water in man. I. Total body water in normal subjects and edematous patients. Tohoku J. Exp. Med. 63:1956;309-317
    • (1956) Tohoku J. Exp. Med. , vol.63 , pp. 309-317
    • Musha, D.1
  • 2
    • 0031024171 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • Lipinski C.A., et al. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev. 23:1997;3-25
    • (1997) Adv. Drug Deliv. Rev. , vol.23 , pp. 3-25
    • Lipinski, C.A.1
  • 3
    • 0345732338 scopus 로고    scopus 로고
    • Physical and molecular properties of agrochemicals: An analysis of screen inputs, hits, leads and products
    • Clarke E.D., Delaney J.S. Physical and molecular properties of agrochemicals: An analysis of screen inputs, hits, leads and products. Chimia (Aarau). 57:2003;731-734
    • (2003) Chimia (Aarau) , vol.57 , pp. 731-734
    • Clarke, E.D.1    Delaney, J.S.2
  • 4
    • 0036761676 scopus 로고    scopus 로고
    • Improvement of "hit-to-lead" optimization by integration of in vitro HTS experimental models for early determination of pharmacokinetic properties
    • Kariv I., et al. Improvement of "hit-to-lead" optimization by integration of in vitro HTS experimental models for early determination of pharmacokinetic properties. Comb. Chem. High Throughput Screen. 5:2002;459-472
    • (2002) Comb. Chem. High Throughput Screen. , vol.5 , pp. 459-472
    • Kariv, I.1
  • 5
    • 0036174062 scopus 로고    scopus 로고
    • Prediction of the aqueous solubility: Comparison of the general solubility equation and the method using an amended solvation energy relationship
    • Yang G., et al. Prediction of the aqueous solubility: comparison of the general solubility equation and the method using an amended solvation energy relationship. J. Pharm. Sci. 91:2002;517-533
    • (2002) J. Pharm. Sci. , vol.91 , pp. 517-533
    • Yang, G.1
  • 6
    • 2342635206 scopus 로고    scopus 로고
    • Application of high-perfomance liquid chromatography based measurements of lipophilicity to model biological distribution
    • Valko K. Application of high-perfomance liquid chromatography based measurements of lipophilicity to model biological distribution. J. Chromatogr. A. 1037:2004;299-310
    • (2004) J. Chromatogr. A. , vol.1037 , pp. 299-310
    • Valko, K.1
  • 7
  • 8
    • 10644235575 scopus 로고    scopus 로고
    • Streamlined system for purifying and quantifying a diverse library of compounds and the effect of compound concentration measurements on the accurate interpretation of biological assay results
    • Popa-Burke I.G., et al. Streamlined system for purifying and quantifying a diverse library of compounds and the effect of compound concentration measurements on the accurate interpretation of biological assay results. Anal. Chem. 76:2004;7278-7287
    • (2004) Anal. Chem. , vol.76 , pp. 7278-7287
    • Popa-Burke, I.G.1
  • 9
    • 0036589825 scopus 로고    scopus 로고
    • Progress in computational methods for the prediction of ADMET properties
    • Clark D.E., Grootenhuis P.D.J. Progress in computational methods for the prediction of ADMET properties. Curr. Opin. Drug Discov. Devel. 5:2002;382-390
    • (2002) Curr. Opin. Drug Discov. Devel. , vol.5 , pp. 382-390
    • Clark, D.E.1    Grootenhuis, P.D.J.2
  • 10
    • 0038745774 scopus 로고    scopus 로고
    • Estimation of aqueous solubility by the general solubility equation (GSE) the easy way
    • Sanghvi T., et al. Estimation of aqueous solubility by the general solubility equation (GSE) the easy way. QSAR & Combinatorial Science. 22:2003;258-262
    • (2003) QSAR & Combinatorial Science , vol.22 , pp. 258-262
    • Sanghvi, T.1
  • 11
    • 0034608316 scopus 로고    scopus 로고
    • Prediction of drug solubility from Monte Carlo simulations
    • Jorgensen W.L., Duffy E.M. Prediction of drug solubility from Monte Carlo simulations. Bioorg. Med. Chem. Lett. 10:2000;1155-1158
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 1155-1158
    • Jorgensen, W.L.1    Duffy, E.M.2
  • 12
    • 0035765458 scopus 로고    scopus 로고
    • Cellular automata models of aqueous solution systems
    • K.B. Lipkowitz, Boyd D.B. Wiley-VCH
    • Kier L.B., et al. Cellular automata models of aqueous solution systems. Lipkowitz K.B., Boyd D.B. Reviews in Computational Chemistry. 17:2001;205-254 Wiley-VCH
    • (2001) Reviews in Computational Chemistry , vol.17 , pp. 205-254
    • Kier, L.B.1
  • 13
    • 0000870032 scopus 로고
    • The fantastic combinations of John Conway's new solitaire game "life"
    • Gardner M. The fantastic combinations of John Conway's new solitaire game "life" Sci. Am. 223:1970;120-123
    • (1970) Sci. Am. , vol.223 , pp. 120-123
    • Gardner, M.1
  • 14
    • 0002522655 scopus 로고
    • Continuum solvation models: Classical and quantum mechanical implementations
    • K.B. Lipkowitz, Boyd D.B. Wiley-VCH
    • Cramer C.J., Truhlar D.G. Continuum solvation models: Classical and quantum mechanical implementations. Lipkowitz K.B., Boyd D.B. Reviews in Computational Chemistry. 6:1995;1-72 Wiley-VCH
    • (1995) Reviews in Computational Chemistry , vol.6 , pp. 1-72
    • Cramer, C.J.1    Truhlar, D.G.2
  • 15
    • 0037196325 scopus 로고    scopus 로고
    • Prediction of aqueous solubility of drugs and pesticides with COSMO-RS
    • Klamt A. Prediction of aqueous solubility of drugs and pesticides with COSMO-RS. J. Comput. Chem. 23:2002;275-281
    • (2002) J. Comput. Chem. , vol.23 , pp. 275-281
    • Klamt, A.1
  • 16
    • 0001344176 scopus 로고
    • Estimating entropies and enthalpies of fusion of organic compounds
    • Chickos J.S., et al. Estimating entropies and enthalpies of fusion of organic compounds. J. Org. Chem. 56:1991;927-938
    • (1991) J. Org. Chem. , vol.56 , pp. 927-938
    • Chickos, J.S.1
  • 20
    • 0041698448 scopus 로고    scopus 로고
    • Molecular descriptors influencing melting point and their role in classification of solid drugs
    • Bergström C.A.S., et al. Molecular descriptors influencing melting point and their role in classification of solid drugs. J. Chem. Inf. Comput. Sci. 43:2003;1177-1185
    • (2003) J. Chem. Inf. Comput. Sci. , vol.43 , pp. 1177-1185
    • Bergström, C.A.S.1
  • 22
    • 0041731599 scopus 로고    scopus 로고
    • Prediction of aqueous solubility of a diverse set of compounds using quantitative structure-property relationships
    • Cheng A., Merz K.M. Prediction of aqueous solubility of a diverse set of compounds using quantitative structure-property relationships. J. Med. Chem. 46:2003;3572-3580
    • (2003) J. Med. Chem. , vol.46 , pp. 3572-3580
    • Cheng, A.1    Merz, K.M.2
  • 23
    • 2942704243 scopus 로고    scopus 로고
    • ESOL: Estimating aqueous solubility directly from molecular structure
    • Delaney J.S. ESOL: Estimating aqueous solubility directly from molecular structure. J. Chem. Inf. Comput. Sci. 44:2004;1000-1005
    • (2004) J. Chem. Inf. Comput. Sci. , vol.44 , pp. 1000-1005
    • Delaney, J.S.1
  • 25
    • 0018709674 scopus 로고
    • Chance factors in studies of quantitative structure-activity relationships
    • Topliss J.G., Edwards R.P. Chance factors in studies of quantitative structure-activity relationships. J. Med. Chem. 22:1979;1238-1244
    • (1979) J. Med. Chem. , vol.22 , pp. 1238-1244
    • Topliss, J.G.1    Edwards, R.P.2
  • 26
    • 0020748239 scopus 로고
    • Computer-intensive methods in statistics
    • Diaconis P., Efron B. Computer-intensive methods in statistics. Sci. Am. 248:1983;116-130
    • (1983) Sci. Am. , vol.248 , pp. 116-130
    • Diaconis, P.1    Efron, B.2
  • 27
    • 0002851282 scopus 로고
    • The evolution of the concept of molecular similarity
    • M.A. Johnson, & G.M. Maggiora. Wiley
    • Rouvray D.H. The evolution of the concept of molecular similarity. Johnson M.A., Maggiora G.M. Concepts and Applications of Molecular Similarity. 1990;15-42 Wiley
    • (1990) Concepts and Applications of Molecular Similarity , pp. 15-42
    • Rouvray, D.H.1
  • 28
    • 0032841864 scopus 로고    scopus 로고
    • The correlation and prediction of the solubility of compounds in water using an amended solvation energy relationship
    • Abraham M.H., Le J. The correlation and prediction of the solubility of compounds in water using an amended solvation energy relationship. J. Pharm. Sci. 88:1999;868-880
    • (1999) J. Pharm. Sci. , vol.88 , pp. 868-880
    • Abraham, M.H.1    Le, J.2
  • 29
    • 0000381930 scopus 로고    scopus 로고
    • Prediction of hydrophobic (lipophilic) properties of small organic molecules using fragmental methods: An analysis of ALOG P and CLOG P methods
    • Ghose A.K., et al. Prediction of hydrophobic (lipophilic) properties of small organic molecules using fragmental methods: An analysis of ALOG P and CLOG P methods. J. Phys. Chem. A. 102:1998;3762-3772
    • (1998) J. Phys. Chem. a , vol.102 , pp. 3762-3772
    • Ghose, A.K.1
  • 30
    • 0028974572 scopus 로고
    • AQUAFAC: Aqueous functional group activity coefficients: Application to the estimation of aqueous solubility
    • Myrdal P.B., et al. AQUAFAC: Aqueous functional group activity coefficients: Application to the estimation of aqueous solubility. Chemosphere. 24:1995;1619-1637
    • (1995) Chemosphere , vol.24 , pp. 1619-1637
    • Myrdal, P.B.1
  • 31
    • 0028990049 scopus 로고
    • Group contribution methods to estimate water solubility of organic chemicals
    • Kuhne R., et al. Group contribution methods to estimate water solubility of organic chemicals. Chemosphere. 30:1995;2061-2077
    • (1995) Chemosphere , vol.30 , pp. 2061-2077
    • Kuhne, R.1
  • 32
    • 0026914713 scopus 로고
    • Estimation of aqueous solubility of organic compounds by the group contribution approach. Application to the study of biodegradation
    • Klopman G. Estimation of aqueous solubility of organic compounds by the group contribution approach. application to the study of biodegradation. J. Chem. Inf. Comput. Sci. 32:1992;474-482
    • (1992) J. Chem. Inf. Comput. Sci. , vol.32 , pp. 474-482
    • Klopman, G.1
  • 33
    • 0037065199 scopus 로고    scopus 로고
    • Group-contribution-based estimation of octanol/water partition coefficient and aqueous solubility
    • Marrero J., Gani R. Group-contribution-based estimation of octanol/water partition coefficient and aqueous solubility. Ind. Eng. Chem. Res. 41:2002;6623-6633
    • (2002) Ind. Eng. Chem. Res. , vol.41 , pp. 6623-6633
    • Marrero, J.1    Gani, R.2
  • 34
    • 1842639123 scopus 로고    scopus 로고
    • A universal molecular descriptor system for prediction of Log P, LogS, LogBB, and absorption
    • Sun H. A universal molecular descriptor system for prediction of Log P, LogS, LogBB, and absorption. J. Chem. Inf. Comput. Sci. 44:2004;748-757
    • (2004) J. Chem. Inf. Comput. Sci. , vol.44 , pp. 748-757
    • Sun, H.1
  • 35
    • 1542741028 scopus 로고    scopus 로고
    • ADME evaluation in drug discovery: 4. Prediction of aqueous solubility based on atom contribution approach
    • Hou T.J., et al. ADME evaluation in drug discovery: 4. Prediction of aqueous solubility based on atom contribution approach. J. Chem. Inf. Comput. Sci. 44:2004;266-275
    • (2004) J. Chem. Inf. Comput. Sci. , vol.44 , pp. 266-275
    • Hou, T.J.1
  • 36
    • 0001645890 scopus 로고    scopus 로고
    • Estimation of aqueous solubility for a diverse set of organic compounds based on molecular topology
    • Huuskonen J. Estimation of aqueous solubility for a diverse set of organic compounds based on molecular topology. J. Chem. Inf. Comput. Sci. 40:2000;773-777
    • (2000) J. Chem. Inf. Comput. Sci. , vol.40 , pp. 773-777
    • Huuskonen, J.1
  • 37
    • 0035498340 scopus 로고    scopus 로고
    • Development of quantitative structure-property relationship models for early ADME evaluation in drug discovery: 1. Aqueous solubility
    • Liu R., So S. Development of quantitative structure-property relationship models for early ADME evaluation in drug discovery: 1. Aqueous solubility. J. Chem. Inf. Comput. Sci. 41:2001;1633-1639
    • (2001) J. Chem. Inf. Comput. Sci. , vol.41 , pp. 1633-1639
    • Liu, R.1    So, S.2
  • 38
    • 0035526162 scopus 로고    scopus 로고
    • Estimation of aqueous solubility of chemical compounds using E-state indices
    • Tetko I.V., et al. Estimation of aqueous solubility of chemical compounds using E-state indices. J. Chem. Inf. Comput. Sci. 41:2001;1488-1493
    • (2001) J. Chem. Inf. Comput. Sci. , vol.41 , pp. 1488-1493
    • Tetko, I.V.1
  • 39
    • 0000805679 scopus 로고
    • The molecular connectivity Chi indexes and Kappa shape indexes in structure-property modeling
    • K.B. Lipkowitz, Boyd D.B. Wiley-VCH
    • Hall L.H., Kier L.B. The molecular connectivity Chi indexes and Kappa shape indexes in structure-property modeling. Lipkowitz K.B., Boyd D.B. Reviews in Computational Chemistry. 2:1991;367-422 Wiley-VCH
    • (1991) Reviews in Computational Chemistry , vol.2 , pp. 367-422
    • Hall, L.H.1    Kier, L.B.2
  • 40
    • 0034751673 scopus 로고    scopus 로고
    • Simultaneous prediction of aqueous solubility and octanol/water partition coefficient based on descriptors derived from molecular structure
    • Livingstone D.J., et al. Simultaneous prediction of aqueous solubility and octanol/water partition coefficient based on descriptors derived from molecular structure. J. Comput. Aided Mol. Des. 15:2001;741-752
    • (2001) J. Comput. Aided Mol. Des. , vol.15 , pp. 741-752
    • Livingstone, D.J.1
  • 41
    • 0034833042 scopus 로고    scopus 로고
    • Estimation of water solubility from atom-type electrotopological state indices
    • Huuskonen J. Estimation of water solubility from atom-type electrotopological state indices. Environ. Toxicol. Chem. 20:2001;491-497
    • (2001) Environ. Toxicol. Chem. , vol.20 , pp. 491-497
    • Huuskonen, J.1
  • 42
    • 0034527396 scopus 로고    scopus 로고
    • Prediction of aqueous solubility for a diverse set of organic compounds based on atom-type electrotopological state indices
    • Huuskonen J. Prediction of aqueous solubility for a diverse set of organic compounds based on atom-type electrotopological state indices. Eur. J. Med. Chem. 35:2000;1081-1088
    • (2000) Eur. J. Med. Chem. , vol.35 , pp. 1081-1088
    • Huuskonen, J.1
  • 44
    • 0347419177 scopus 로고    scopus 로고
    • Prediction of aqueous solubility of organic compounds by topological descriptors
    • Yan A., Gasteiger J. Prediction of aqueous solubility of organic compounds by topological descriptors. QSAR & Combinatorial Science. 22:2003;821-829
    • (2003) QSAR & Combinatorial Science , vol.22 , pp. 821-829
    • Yan, A.1    Gasteiger, J.2
  • 45
    • 0036757543 scopus 로고    scopus 로고
    • High-throughput, in silico prediction of aqueous solubility based on one- and two-dimensional descriptors
    • Engkvist O., Wrede P. High-throughput, in silico prediction of aqueous solubility based on one- and two-dimensional descriptors. J. Chem. Inf. Comput. Sci. 42:2002;1247-1249
    • (2002) J. Chem. Inf. Comput. Sci. , vol.42 , pp. 1247-1249
    • Engkvist, O.1    Wrede, P.2
  • 46
    • 0035470294 scopus 로고    scopus 로고
    • A fuzzy ARTMAP based on quantitative structure-property relationships (QSPRs) for predicting aqueous solubility of organic compounds
    • Yaffe D. A fuzzy ARTMAP based on quantitative structure-property relationships (QSPRs) for predicting aqueous solubility of organic compounds. J. Chem. Inf. Comput. Sci. 41:2001;1177-1207
    • (2001) J. Chem. Inf. Comput. Sci. , vol.41 , pp. 1177-1207
    • Yaffe, D.1
  • 47
    • 0037361981 scopus 로고    scopus 로고
    • Prediction of aqueous solubility of organic compounds based on a 3D structure representation
    • Yan A., Gasteiger J. Prediction of aqueous solubility of organic compounds based on a 3D structure representation. J. Chem. Inf. Comput. Sci. 43:2003;429-434
    • (2003) J. Chem. Inf. Comput. Sci. , vol.43 , pp. 429-434
    • Yan, A.1    Gasteiger, J.2
  • 48
    • 4344667602 scopus 로고    scopus 로고
    • Linear and nonlinear functions on modeling of aqueous solubility of organic compounds by two structure representation methods
    • Yan A., et al. Linear and nonlinear functions on modeling of aqueous solubility of organic compounds by two structure representation methods. J. Comput. Aided Mol. Des. 18:2004;75-87
    • (2004) J. Comput. Aided Mol. Des. , vol.18 , pp. 75-87
    • Yan, A.1
  • 49
    • 0000055756 scopus 로고    scopus 로고
    • QM/NN QSPR models with error estimation: Vapor pressure and log P
    • Beck B., et al. QM/NN QSPR models with error estimation: Vapor pressure and log P. J. Chem. Inf. Comput. Sci. 40:2000;1046-1051
    • (2000) J. Chem. Inf. Comput. Sci. , vol.40 , pp. 1046-1051
    • Beck, B.1
  • 51
    • 0242384972 scopus 로고    scopus 로고
    • Estimation of the aqueous solubility of organic compounds using molecular connectivity indices
    • Zhong C., Hu Q. Estimation of the aqueous solubility of organic compounds using molecular connectivity indices. J. Pharm. Sci. 92:2003;2284-2294
    • (2003) J. Pharm. Sci. , vol.92 , pp. 2284-2294
    • Zhong, C.1    Hu, Q.2
  • 52
    • 4043112686 scopus 로고    scopus 로고
    • Global and local computational models for aqueous solubility prediction of drug-like molecules
    • Bergström C.A.S., et al. Global and local computational models for aqueous solubility prediction of drug-like molecules. J. Chem. Inf. Comput. Sci. 44:2004;1477-1488
    • (2004) J. Chem. Inf. Comput. Sci. , vol.44 , pp. 1477-1488
    • Bergström, C.A.S.1
  • 53
    • 0036179179 scopus 로고    scopus 로고
    • Quantitative structure/property relationship analysis on aqueous solubility using genetic algorithm-combined partial least squares method
    • Wanchana S., et al. Quantitative structure/property relationship analysis on aqueous solubility using genetic algorithm-combined partial least squares method. Pharmazie. 57:2002;127-129
    • (2002) Pharmazie , vol.57 , pp. 127-129
    • Wanchana, S.1
  • 54
    • 0037498037 scopus 로고    scopus 로고
    • Prediction of aqueous solubility and partition coefficient optimized by a genetic algorithm based descriptor selection method
    • Wegner J.K., Zell A. Prediction of aqueous solubility and partition coefficient optimized by a genetic algorithm based descriptor selection method. J. Chem. Inf. Comput. Sci. 43:2003;1077-1084
    • (2003) J. Chem. Inf. Comput. Sci. , vol.43 , pp. 1077-1084
    • Wegner, J.K.1    Zell, A.2
  • 55
    • 0345548663 scopus 로고    scopus 로고
    • Support vector machines for the estimation of aqueous Solubility
    • Lind P., Maltseva T. Support vector machines for the estimation of aqueous Solubility. J. Chem. Inf. Comput. Sci. 43:2003;1855-1859
    • (2003) J. Chem. Inf. Comput. Sci. , vol.43 , pp. 1855-1859
    • Lind, P.1    Maltseva, T.2
  • 56
    • 0035526164 scopus 로고    scopus 로고
    • Search for predictive generic model of aqueous solubility using Bayesian neural nets
    • Bruneau P. Search for predictive generic model of aqueous solubility using Bayesian neural nets. J. Chem. Inf. Comput. Sci. 41:2001;1605-1616
    • (2001) J. Chem. Inf. Comput. Sci. , vol.41 , pp. 1605-1616
    • Bruneau, P.1
  • 57
    • 0036115689 scopus 로고    scopus 로고
    • Estimation of aqueous solubility of organic compounds with QSPR approach
    • Gao H., et al. Estimation of aqueous solubility of organic compounds with QSPR approach. Pharm. Res. 19:2002;497-503
    • (2002) Pharm. Res. , vol.19 , pp. 497-503
    • Gao, H.1
  • 58
    • 0347717608 scopus 로고    scopus 로고
    • In silico prediction of aqueous solubility, human plasma protein binding and volume of distribution of compounds from calculated pKa and Alog P98 values
    • Lobell M., Sivarajah V. In silico prediction of aqueous solubility, human plasma protein binding and volume of distribution of compounds from calculated pKa and Alog P98 values. Mol. Divers. 7:2003;69-87
    • (2003) Mol. Divers. , vol.7 , pp. 69-87
    • Lobell, M.1    Sivarajah, V.2
  • 59
    • 0037204544 scopus 로고    scopus 로고
    • Prediction of drug solubility from structure
    • Jorgensen W.L., Duffy E.M. Prediction of drug solubility from structure. Adv. Drug Deliv. Rev. 54:2002;355-366
    • (2002) Adv. Drug Deliv. Rev. , vol.54 , pp. 355-366
    • Jorgensen, W.L.1    Duffy, E.M.2
  • 60
    • 11144253884 scopus 로고    scopus 로고
    • Aqueous solubility in discovery, chemistry, and assay changes
    • Lipinski C.A. Aqueous solubility in discovery, chemistry, and assay changes. Methods and Principles in Medicinal Chemistry. 18:2003;215-231
    • (2003) Methods and Principles in Medicinal Chemistry , vol.18 , pp. 215-231
    • Lipinski, C.A.1
  • 61
    • 33745301826 scopus 로고    scopus 로고
    • Building classification models for DMSO solubility: Comparison of five methods
    • Philadelphia, PA, USA, August 22-26
    • Lu, J. and Bakken, G.A. (2004) Building classification models for DMSO solubility: Comparison of five methods. Abstracts of Papers, 228th ACS National Meeting, Philadelphia, PA, USA, August 22-26
    • (2004) Abstracts of Papers, 228th ACS National Meeting
    • Lu, J.1    Bakken, G.A.2
  • 62
    • 4544285614 scopus 로고    scopus 로고
    • In silico estimation of DMSO solubility of organic compounds for bioscreening
    • Balakin K.V., et al. In silico estimation of DMSO solubility of organic compounds for bioscreening. J. Biomol. Screen. 9:2004;22-31
    • (2004) J. Biomol. Screen. , vol.9 , pp. 22-31
    • Balakin, K.V.1
  • 63
    • 0036179239 scopus 로고    scopus 로고
    • Experimental and computational screening models for prediction of aqueous drug solubility
    • Bergström C.A.S., et al. Experimental and computational screening models for prediction of aqueous drug solubility. Pharm. Res. 19:2002;182-188
    • (2002) Pharm. Res. , vol.19 , pp. 182-188
    • Bergström, C.A.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.