Коефіціент розподілу (Ukrainian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Коефіціент розподілу" in Ukrainian language version.

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41doi.org

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27nih.gov

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actachemscand.org

Collander R, Lindholm M, Haug CM, Stene J, Sörensen NA (1951). The partition of organic compounds. between higher alcohols and water (PDF). Acta Chem. Scand. 5: 774—780. doi:10.3891/acta.chem.scand.05-0774. Архів оригіналу (PDF) за 19 липня 2021. Процитовано 26 травня 2022.

archive.org

4.2.4: Partition and Distribution Coefficients. Handbook of Essential Pharmacokinetics, Pharmacodynamics and Drug Metabolism for Industrial Scientists. New York: Kluwer Academic/Plenum Publishers. 2001. с. 44. ISBN 978-1-4757-8693-4.
Chapter 10: Physiological Drug Distribution and Protein Binding. Applied Biopharmaceutics & Pharmacokinetics (вид. 6th). New York: McGraw-Hill Medical. 2012. с. 211. ISBN 978-0-07-160393-5.
Chapter 3: Free Energy and Phase Diagrams. An Introduction to Aspects of Thermodynamics and Kinetics Relevant to Materials Science (вид. 3rd). Amsterdam: Elsevier. 2007. с. 98. ISBN 978-0-08-054968-2. Solid–solid equilibria equivalent to the solid–liquid case
Partition Coefficient. Compendium of Chemical Terminology: IUPAC Recommendations. Oxford: Blackwell Science. 1997. doi:10.1351/goldbook. ISBN 978-0-86542-684-9.
Lipophilicity Profiles: Theory and Measurement. Pharmacokinetic Optimization in Drug Research: Biological, Physicochemical, and Computational Strategies. Weinheim: Wiley-VCH. 2001. с. 275–304. doi:10.1002/9783906390437.ch17. ISBN 978-3-906390-22-2.
Chapter 4: The Hydrophobic Properties of Molecules. Quantitative Drug Design: A critical introduction (вид. 2nd). Boca Raton: CRC Press/Taylor & Francis. 2010. с. 66–73. ISBN 978-1-4200-7099-6.
Chapter 5: Calculation of Octanol-Water Partition Coefficients from Fragments, etc.. Substituent Constants for Correlation Analysis in Chemistry and Biology. New York: John Wiley & Sons Ltd. 1979. ISBN 978-0-471-05062-9.
Octanol log P. Exploring QSAR, Hydrophobic, Electronic, and Steric Constants. Washington, DC: American Chemical Society. 1995. ISBN 978-0-8412-3060-6.
Lipophilicity in Drug Action and Toxicology. New York: John Wiley & Sons Ltd. 1996. с. 439 pages. ISBN 978-3-527-29383-4.
Chapter 3: Methods of pK_a Prediction. pK_a Prediction for Organic Acids and Bases. London: Chapman & Hall. 1981. с. 21–26. doi:10.1007/978-94-009-5883-8. ISBN 978-0-412-22190-3.
Octanol-water partition coefficients : fundamentals and physical chemistry. Chichester: Wiley. 1997. ISBN 0-471-97397-1. OCLC 36430034.
Hendriks AJ, van der Linde A, Cornelissen G, Sijm DT (July 2001). The power of size. 1. Rate constants and equilibrium ratios for accumulation of organic substances related to octanol-water partition ratio and species weight. Environmental Toxicology and Chemistry. 20 (7): 1399—420. doi:10.1002/etc.5620200703. PMID 11434281.

ddbst.com

Octanol–Water Partition Coefficients. ddbst.com. Архів оригіналу за 20 березня 2016. Процитовано 19 березня 2016.
Dortmund Data Bank (DDB). Dortmund Data Bank Software & Separation Technology (DDBST) GmbH. Архів оригіналу за 25 січня 2021. Процитовано 20 травня 2020.

doi.org

Leo A, Hansch C, Elkins D (1971). Partition coefficients and their uses. Chem. Rev. 71 (6): 525—616. doi:10.1021/cr60274a001.
Partition Coefficient. Compendium of Chemical Terminology: IUPAC Recommendations. Oxford: Blackwell Science. 1997. doi:10.1351/goldbook. ISBN 978-0-86542-684-9.
Lipophilicity Profiles: Theory and Measurement. Pharmacokinetic Optimization in Drug Research: Biological, Physicochemical, and Computational Strategies. Weinheim: Wiley-VCH. 2001. с. 275–304. doi:10.1002/9783906390437.ch17. ISBN 978-3-906390-22-2.
Pagliara A, Carrupt PA, Caron G, Gaillard P, Testa B (1997). Lipophilicity Profiles of Ampholytes. Chemical Reviews. 97 (8): 3385—3400. doi:10.1021/cr9601019. PMID 11851494.
Scherrer RA, Howard SM (January 1977). Use of distribution coefficients in quantitative structure-activity relationships. Journal of Medicinal Chemistry. 20 (1): 53—8. doi:10.1021/jm00211a010. PMID 13215.
Manners CN, Payling DW, Smith DA (March 1988). Distribution coefficient, a convenient term for the relation of predictable physico-chemical properties to metabolic processes. Xenobiotica; the Fate of Foreign Compounds in Biological Systems. 18 (3): 331—50. doi:10.3109/00498258809041669. PMID 3289270.
Wolfenden R (January 1978). Interaction of the peptide bond with solvent water: a vapor phase analysis. (primary). Biochemistry. 17 (1): 201—4. doi:10.1021/bi00594a030. PMID 618544.
Collander R, Lindholm M, Haug CM, Stene J, Sörensen NA (1951). The partition of organic compounds. between higher alcohols and water (PDF). Acta Chem. Scand. 5: 774—780. doi:10.3891/acta.chem.scand.05-0774. Архів оригіналу (PDF) за 19 липня 2021. Процитовано 26 травня 2022.
Whitehead KE, Geankoplis CJ (1955). Separation of Formic and Sulfuric Acids by Extraction. Ind. Eng. Chem. 47 (10): 2114—2122. doi:10.1021/ie50550a029.
Brodsky J, Ballschmiter K (1988). Reversed phase liquid chromatography of PCBs as a basis for calculation of water solubility and K_ow for polychlorobiphenyls. Fresenius' Z. Anal. Chem. 331 (3–4): 295—301. doi:10.1007/BF00481899.
Sangster J (1989). Octanol–Water Partition Coefficients of Simple Organic Compounds (PDF). Journal of Physical and Chemical Reference Data. 18 (3): 1111—1227. Bibcode:1989JPCRD..18.1111S. doi:10.1063/1.555833. Архів оригіналу (PDF) за 4 березня 2016. Процитовано 26 травня 2022.
Mannhold R, Poda GI, Ostermann C, Tetko IV (March 2009). Calculation of molecular lipophilicity: State-of-the-art and comparison of log P methods on more than 96,000 compounds. Journal of Pharmaceutical Sciences. 98 (3): 861—93. doi:10.1002/jps.21494. PMID 18683876.
Leeson PD, Springthorpe B (November 2007). The influence of drug-like concepts on decision-making in medicinal chemistry. Nature Reviews. Drug Discovery. 6 (11): 881—90. doi:10.1038/nrd2445. PMID 17971784.
Role of Physicochemical Properties and Ligand Lipophilicity Efficiency in Addressing Drug Safety Risks. Annual Reports in Medicinal Chemistry. Т. 45. 2010. с. 381—391. doi:10.1016/S0065-7743(10)45023-X. ISBN 978-0-12-380902-5.
Bodor N, Buchwald P (April 1999). Recent advances in the brain targeting of neuropharmaceuticals by chemical delivery systems. Advanced Drug Delivery Reviews. 36 (2–3): 229—254. doi:10.1016/S0169-409X(98)00090-8. PMID 10837718.
Eisenberg D, McLachlan AD (1986). Solvation energy in protein folding and binding. Nature. 319 (6050): 199—203. Bibcode:1986Natur.319..199E. doi:10.1038/319199a0. PMID 3945310.
Miyamoto S, Kollman PA (September 1993). What determines the strength of noncovalent association of ligands to proteins in aqueous solution?. Proceedings of the National Academy of Sciences of the United States of America. 90 (18): 8402—6. Bibcode:1993PNAS...90.8402M. doi:10.1073/pnas.90.18.8402. PMC 47364. PMID 8378312.
Cronin D, Mark T (2006). The Role of Hydrophobicity in Toxicity Prediction. Current Computer-Aided Drug Design. 2 (4): 405—413. doi:10.2174/157340906778992346.
Heuel-Fabianek B (2006). Partition Coefficients (K_d) for the Modelling of Transport Processes of Radionuclides in Groundwater (PDF). Current Computer-Aided Drug Design. 2 (4): 405—413. doi:10.2174/157340906778992346. Архів оригіналу (PDF) за 7 жовтня 2021. Процитовано 26 травня 2022.
Noble A (July 1993). Partition coefficients (n-octanol—water) for pesticides. Journal of Chromatography A. 642 (1–2): 3—14. doi:10.1016/0021-9673(93)80072-G.
Dearden JC, Bresnan GM (1988). The Measurement of Partition Coefficients. Quantitative Structure-Activity Relationships. 7 (3): 133—144. doi:10.1002/qsar.19880070304.
Andrés A, Rosés M, Ràfols C, Bosch E, Espinosa S, Segarra V, Huerta JM (August 2015). Setup and validation of shake-flask procedures for the determination of partition coefficients (log D) from low drug amounts. European Journal of Pharmaceutical Sciences. 76: 181—91. doi:10.1016/j.ejps.2015.05.008. PMID 25968358. {{cite journal}}: |hdl-access= вимагає |hdl= (довідка)
Valkó K (May 2004). Application of high-performance liquid chromatography based measurements of lipophilicity to model biological distribution. Journal of Chromatography A. 1037 (1–2): 299—310. doi:10.1016/j.chroma.2003.10.084. PMID 15214672.
Ulmeanu SM, Jensen H, Bouchard G, Carrupt PA, Girault HH (August 2003). 11095_2004_Article_468694.pdf&response-content-type=application%2Fpdf&AWSAccessKeyId=ded3589a13b4450889b2f728d54861a6&Expires=1626819250&Signature=3AJg%2F4E0vRhKdraPr47uSGPhhx0%3D Water-oil partition profiling of ionized drug molecules using cyclic voltammetry and a 96-well microfilter plate system. Pharmaceutical Research. 20 (8): 1317—22. doi:10.1023/A:1025025804196. PMID 12948031. Архів оригіналу (PDF) за 19 липня 2021. Процитовано 26 травня 2022.
Scholz F, Komorsky-Lovrić Š, Lovrić M (February 2000). A new access to Gibbs energies of transfer of ions across liquid|liquid interfaces and a new method to study electrochemical processes at well-defined three-phase junctions. Electrochemistry Communications (англ.). 2 (2): 112—118. doi:10.1016/S1388-2481(99)00156-3. Архів оригіналу за 4 травня 2018. Процитовано 26 травня 2022.
Bond AM, Marken F (1994). Mechanistic aspects of the electron and ion transport processes across the electrode. Journal of Electroanalytical Chemistry. 372 (1–2): 125—135. doi:10.1016/0022-0728(93)03257-P.
Nieto-Draghi C, Fayet G, Creton B, Rozanska X, Rotureau P, de Hemptinne JC, Ungerer P, Rousseau B, Adamo C (December 2015). A General Guidebook for the Theoretical Prediction of Physicochemical Properties of Chemicals for Regulatory Purposes. Chemical Reviews. 115 (24): 13093—164. doi:10.1021/acs.chemrev.5b00215. PMID 26624238.
Judson R, Richard A, Dix DJ, Houck K, Martin M, Kavlock R, Dellarco V, Henry T, Holderman T, Sayre P, Tan S, Carpenter T, Smith E (May 2009). The toxicity data landscape for environmental chemicals. Environmental Health Perspectives. 117 (5): 685—95. doi:10.1289/ehp.0800168. PMC 2685828. PMID 19479008.
Matter H, Baringhaus KH, Naumann T, Klabunde T, Pirard B (September 2001). Computational approaches towards the rational design of drug-like compound libraries. Combinatorial Chemistry & High Throughput Screening. 4 (6): 453—75. doi:10.2174/1386207013330896. PMID 11562252.
Schuffenhauer A, Ruedisser S, Marzinzik AL, Jahnke W, Blommers M, Selzer P, Jacoby E (2005). Library design for fragment based screening. Current Topics in Medicinal Chemistry. 5 (8): 751—62. doi:10.2174/1568026054637700. PMID 16101415.
Ghose AK, Crippen GM (1986). Atomic Physicochemical Parameters for Three-Dimensional Structure-Directed Quantitative Structure–Activity Relationships I. Partition Coefficients as a Measure of Hydrophobicity. Journal of Computational Chemistry. 7 (4): 565—577. doi:10.1002/jcc.540070419. Архів оригіналу (PDF) за 19 липня 2021. Процитовано 26 травня 2022. {{cite journal}}: |hdl-access= вимагає |hdl= (довідка)
Cheng T, Zhao Y, Li X, Lin F, Xu Y, Zhang X, Li Y, Wang R, Lai L (2007). Computation of octanol-water partition coefficients by guiding an additive model with knowledge. Journal of Chemical Information and Modeling. 47 (6): 2140—8. doi:10.1021/ci700257y. PMID 17985865. Архів оригіналу за 28 березня 2012. Процитовано 26 травня 2022.
Moriguchi I, Hirono S, Liu Q, Nakagome I, Matsushita Y (1992). Simple method of calculating octanol/water partition coefficient. Chem. Pharm. Bull. 40 (1): 127—130. doi:10.1248/cpb.40.127.
Ghose AK, Viswanadhan VN, Wendoloski JJ (1998). Prediction of Hydrophobic (Lipophilic) Properties of Small Organic Molecules Using Fragmental Methods: An Analysis of AlogP and ClogP Methods. Journal of Physical Chemistry A. 102 (21): 3762—3772. Bibcode:1998JPCA..102.3762G. doi:10.1021/jp980230o.
Chapter 3: Methods of pK_a Prediction. pK_a Prediction for Organic Acids and Bases. London: Chapman & Hall. 1981. с. 21–26. doi:10.1007/978-94-009-5883-8. ISBN 978-0-412-22190-3.
Pinsuwan S, Li A, Yalkowsky SH (May 1995). Correlation of Octanol/Water Solubility Ratios and Partition Coefficients. Journal of Chemical & Engineering Data. 40 (3): 623—626. doi:10.1021/je00019a019.
Wang J, Hou T (June 2011). Recent advances on aqueous solubility prediction. Combinatorial Chemistry & High Throughput Screening. 14 (5): 328—38. doi:10.2174/138620711795508331. PMID 21470182.
Skyner RE, McDonagh JL, Groom CR, van Mourik T, Mitchell JB (March 2015). A review of methods for the calculation of solution free energies and the modelling of systems in solution (PDF). Physical Chemistry Chemical Physics. 17 (9): 6174—91. Bibcode:2015PCCP...17.6174S. doi:10.1039/c5cp00288e. PMID 25660403.
Hodges G, Eadsforth C, Bossuyt B, Bouvy A, Enrici MH, Geurts M та ін. (2019). A comparison of log Kow (n-octanol–water partition coefficient) values for non-ionic, anionic, cationic and amphoteric surfactants determined using predictions and experimental methods. Environmental Sciences Europe. 31 (1). doi:10.1186/s12302-018-0176-7.
Hendriks AJ, van der Linde A, Cornelissen G, Sijm DT (July 2001). The power of size. 1. Rate constants and equilibrium ratios for accumulation of organic substances related to octanol-water partition ratio and species weight. Environmental Toxicology and Chemistry. 20 (7): 1399—420. doi:10.1002/etc.5620200703. PMID 11434281.
Cumming H, Rücker C (September 2017). Octanol-Water Partition Coefficient Measurement by a Simple ¹H NMR Method. ACS Omega. 2 (9): 6244—6249. doi:10.1021/acsomega.7b01102. PMC 6644330. PMID 31457869.

elsevier.com

linkinghub.elsevier.com

Scholz F, Komorsky-Lovrić Š, Lovrić M (February 2000). A new access to Gibbs energies of transfer of ions across liquid|liquid interfaces and a new method to study electrochemical processes at well-defined three-phase junctions. Electrochemistry Communications (англ.). 2 (2): 112—118. doi:10.1016/S1388-2481(99)00156-3. Архів оригіналу за 4 травня 2018. Процитовано 26 травня 2022.

epa.gov

nepis.epa.gov

Wasik SP, Tewari YB, Miller MM, Martire DE (1981). Octanol–Water Partition Coefficients and Aqueous Solubilities of Organic Compounds. NBS Techn. Rep. 81 (2406): S1—56. Архів оригіналу за 13 листопада 2021. Процитовано 21 червня 2022.

epfl.ch

infoscience.epfl.ch

Ulmeanu SM, Jensen H, Bouchard G, Carrupt PA, Girault HH (August 2003). 11095_2004_Article_468694.pdf&response-content-type=application%2Fpdf&AWSAccessKeyId=ded3589a13b4450889b2f728d54861a6&Expires=1626819250&Signature=3AJg%2F4E0vRhKdraPr47uSGPhhx0%3D Water-oil partition profiling of ionized drug molecules using cyclic voltammetry and a 96-well microfilter plate system. Pharmaceutical Research. 20 (8): 1317—22. doi:10.1023/A:1025025804196. PMID 12948031. Архів оригіналу (PDF) за 19 липня 2021. Процитовано 26 травня 2022.

fz-juelich.de

juser.fz-juelich.de

Heuel-Fabianek B (2006). Partition Coefficients (K_d) for the Modelling of Transport Processes of Radionuclides in Groundwater (PDF). Current Computer-Aided Drug Design. 2 (4): 405—413. doi:10.2174/157340906778992346. Архів оригіналу (PDF) за 7 жовтня 2021. Процитовано 26 травня 2022.

harvard.edu

ui.adsabs.harvard.edu

Sangster J (1989). Octanol–Water Partition Coefficients of Simple Organic Compounds (PDF). Journal of Physical and Chemical Reference Data. 18 (3): 1111—1227. Bibcode:1989JPCRD..18.1111S. doi:10.1063/1.555833. Архів оригіналу (PDF) за 4 березня 2016. Процитовано 26 травня 2022.
Eisenberg D, McLachlan AD (1986). Solvation energy in protein folding and binding. Nature. 319 (6050): 199—203. Bibcode:1986Natur.319..199E. doi:10.1038/319199a0. PMID 3945310.
Miyamoto S, Kollman PA (September 1993). What determines the strength of noncovalent association of ligands to proteins in aqueous solution?. Proceedings of the National Academy of Sciences of the United States of America. 90 (18): 8402—6. Bibcode:1993PNAS...90.8402M. doi:10.1073/pnas.90.18.8402. PMC 47364. PMID 8378312.
Ghose AK, Viswanadhan VN, Wendoloski JJ (1998). Prediction of Hydrophobic (Lipophilic) Properties of Small Organic Molecules Using Fragmental Methods: An Analysis of AlogP and ClogP Methods. Journal of Physical Chemistry A. 102 (21): 3762—3772. Bibcode:1998JPCA..102.3762G. doi:10.1021/jp980230o.
Skyner RE, McDonagh JL, Groom CR, van Mourik T, Mitchell JB (March 2015). A review of methods for the calculation of solution free energies and the modelling of systems in solution (PDF). Physical Chemistry Chemical Physics. 17 (9): 6174—91. Bibcode:2015PCCP...17.6174S. doi:10.1039/c5cp00288e. PMID 25660403.

nih.gov

pubmed.ncbi.nlm.nih.gov

Pagliara A, Carrupt PA, Caron G, Gaillard P, Testa B (1997). Lipophilicity Profiles of Ampholytes. Chemical Reviews. 97 (8): 3385—3400. doi:10.1021/cr9601019. PMID 11851494.
Scherrer RA, Howard SM (January 1977). Use of distribution coefficients in quantitative structure-activity relationships. Journal of Medicinal Chemistry. 20 (1): 53—8. doi:10.1021/jm00211a010. PMID 13215.
Manners CN, Payling DW, Smith DA (March 1988). Distribution coefficient, a convenient term for the relation of predictable physico-chemical properties to metabolic processes. Xenobiotica; the Fate of Foreign Compounds in Biological Systems. 18 (3): 331—50. doi:10.3109/00498258809041669. PMID 3289270.
Wolfenden R (January 1978). Interaction of the peptide bond with solvent water: a vapor phase analysis. (primary). Biochemistry. 17 (1): 201—4. doi:10.1021/bi00594a030. PMID 618544.
Mannhold R, Poda GI, Ostermann C, Tetko IV (March 2009). Calculation of molecular lipophilicity: State-of-the-art and comparison of log P methods on more than 96,000 compounds. Journal of Pharmaceutical Sciences. 98 (3): 861—93. doi:10.1002/jps.21494. PMID 18683876.
Leeson PD, Springthorpe B (November 2007). The influence of drug-like concepts on decision-making in medicinal chemistry. Nature Reviews. Drug Discovery. 6 (11): 881—90. doi:10.1038/nrd2445. PMID 17971784.
Bodor N, Buchwald P (April 1999). Recent advances in the brain targeting of neuropharmaceuticals by chemical delivery systems. Advanced Drug Delivery Reviews. 36 (2–3): 229—254. doi:10.1016/S0169-409X(98)00090-8. PMID 10837718.
Kubinyi H (March 1979). Nonlinear dependence of biological activity on hydrophobic character: the bilinear model. Il Farmaco; Edizione Scientifica. 34 (3): 248—76. PMID 43264.
Kubinyi H (1979). Lipophilicity and biological activity. Drug transport and drug distribution in model systems and in biological systems. Arzneimittel-Forschung. 29 (8): 1067—80. PMID 40579.
Eisenberg D, McLachlan AD (1986). Solvation energy in protein folding and binding. Nature. 319 (6050): 199—203. Bibcode:1986Natur.319..199E. doi:10.1038/319199a0. PMID 3945310.
Miyamoto S, Kollman PA (September 1993). What determines the strength of noncovalent association of ligands to proteins in aqueous solution?. Proceedings of the National Academy of Sciences of the United States of America. 90 (18): 8402—6. Bibcode:1993PNAS...90.8402M. doi:10.1073/pnas.90.18.8402. PMC 47364. PMID 8378312.
Andrés A, Rosés M, Ràfols C, Bosch E, Espinosa S, Segarra V, Huerta JM (August 2015). Setup and validation of shake-flask procedures for the determination of partition coefficients (log D) from low drug amounts. European Journal of Pharmaceutical Sciences. 76: 181—91. doi:10.1016/j.ejps.2015.05.008. PMID 25968358. {{cite journal}}: |hdl-access= вимагає |hdl= (довідка)
Valkó K (May 2004). Application of high-performance liquid chromatography based measurements of lipophilicity to model biological distribution. Journal of Chromatography A. 1037 (1–2): 299—310. doi:10.1016/j.chroma.2003.10.084. PMID 15214672.
Ulmeanu SM, Jensen H, Bouchard G, Carrupt PA, Girault HH (August 2003). 11095_2004_Article_468694.pdf&response-content-type=application%2Fpdf&AWSAccessKeyId=ded3589a13b4450889b2f728d54861a6&Expires=1626819250&Signature=3AJg%2F4E0vRhKdraPr47uSGPhhx0%3D Water-oil partition profiling of ionized drug molecules using cyclic voltammetry and a 96-well microfilter plate system. Pharmaceutical Research. 20 (8): 1317—22. doi:10.1023/A:1025025804196. PMID 12948031. Архів оригіналу (PDF) за 19 липня 2021. Процитовано 26 травня 2022.
Nieto-Draghi C, Fayet G, Creton B, Rozanska X, Rotureau P, de Hemptinne JC, Ungerer P, Rousseau B, Adamo C (December 2015). A General Guidebook for the Theoretical Prediction of Physicochemical Properties of Chemicals for Regulatory Purposes. Chemical Reviews. 115 (24): 13093—164. doi:10.1021/acs.chemrev.5b00215. PMID 26624238.
Judson R, Richard A, Dix DJ, Houck K, Martin M, Kavlock R, Dellarco V, Henry T, Holderman T, Sayre P, Tan S, Carpenter T, Smith E (May 2009). The toxicity data landscape for environmental chemicals. Environmental Health Perspectives. 117 (5): 685—95. doi:10.1289/ehp.0800168. PMC 2685828. PMID 19479008.
Matter H, Baringhaus KH, Naumann T, Klabunde T, Pirard B (September 2001). Computational approaches towards the rational design of drug-like compound libraries. Combinatorial Chemistry & High Throughput Screening. 4 (6): 453—75. doi:10.2174/1386207013330896. PMID 11562252.
Schuffenhauer A, Ruedisser S, Marzinzik AL, Jahnke W, Blommers M, Selzer P, Jacoby E (2005). Library design for fragment based screening. Current Topics in Medicinal Chemistry. 5 (8): 751—62. doi:10.2174/1568026054637700. PMID 16101415.
Rutkowska E, Pajak K, Jóźwiak K (2013). Lipophilicity--methods of determination and its role in medicinal chemistry (PDF). Acta Poloniae Pharmaceutica. 70 (1): 3—18. PMID 23610954. Архів оригіналу (PDF) за 19 липня 2021. Процитовано 26 травня 2022.
Cheng T, Zhao Y, Li X, Lin F, Xu Y, Zhang X, Li Y, Wang R, Lai L (2007). Computation of octanol-water partition coefficients by guiding an additive model with knowledge. Journal of Chemical Information and Modeling. 47 (6): 2140—8. doi:10.1021/ci700257y. PMID 17985865. Архів оригіналу за 28 березня 2012. Процитовано 26 травня 2022.
Wang J, Hou T (June 2011). Recent advances on aqueous solubility prediction. Combinatorial Chemistry & High Throughput Screening. 14 (5): 328—38. doi:10.2174/138620711795508331. PMID 21470182.
Skyner RE, McDonagh JL, Groom CR, van Mourik T, Mitchell JB (March 2015). A review of methods for the calculation of solution free energies and the modelling of systems in solution (PDF). Physical Chemistry Chemical Physics. 17 (9): 6174—91. Bibcode:2015PCCP...17.6174S. doi:10.1039/c5cp00288e. PMID 25660403.
Hendriks AJ, van der Linde A, Cornelissen G, Sijm DT (July 2001). The power of size. 1. Rate constants and equilibrium ratios for accumulation of organic substances related to octanol-water partition ratio and species weight. Environmental Toxicology and Chemistry. 20 (7): 1399—420. doi:10.1002/etc.5620200703. PMID 11434281.
Cumming H, Rücker C (September 2017). Octanol-Water Partition Coefficient Measurement by a Simple ¹H NMR Method. ACS Omega. 2 (9): 6244—6249. doi:10.1021/acsomega.7b01102. PMC 6644330. PMID 31457869.

ncbi.nlm.nih.gov

Miyamoto S, Kollman PA (September 1993). What determines the strength of noncovalent association of ligands to proteins in aqueous solution?. Proceedings of the National Academy of Sciences of the United States of America. 90 (18): 8402—6. Bibcode:1993PNAS...90.8402M. doi:10.1073/pnas.90.18.8402. PMC 47364. PMID 8378312.
Judson R, Richard A, Dix DJ, Houck K, Martin M, Kavlock R, Dellarco V, Henry T, Holderman T, Sayre P, Tan S, Carpenter T, Smith E (May 2009). The toxicity data landscape for environmental chemicals. Environmental Health Perspectives. 117 (5): 685—95. doi:10.1289/ehp.0800168. PMC 2685828. PMID 19479008.
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