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Items: 1 to 20 of 79

1.
2.

Prediction of aqueous solubility from SCRATCH.

Jain P, Yalkowsky SH.

Int J Pharm. 2010 Jan 29;385(1-2):1-5. doi: 10.1016/j.ijpharm.2009.10.003. Epub 2009 Oct 9.

PMID:
19819319
3.

Estimating the melting point, entropy of fusion, and enthalpy of fusion of organic compounds via SPARC.

Whiteside TS, Hilal SH, Brenner A, Carreira LA.

SAR QSAR Environ Res. 2016 Aug;27(8):677-701. doi: 10.1080/1062936X.2016.1217270.

PMID:
27586365
4.

Effect of molecular symmetry on melting temperature and solubility.

Pinal R.

Org Biomol Chem. 2004 Sep 21;2(18):2692-9. Epub 2004 Aug 20.

PMID:
15351835
5.

Prediction of solubility curves and melting properties of organic and pharmaceutical compounds.

Nordström FL, Rasmuson AC.

Eur J Pharm Sci. 2009 Feb 15;36(2-3):330-44. doi: 10.1016/j.ejps.2008.10.009. Epub 2008 Oct 30.

PMID:
19022383
6.

Estimation of the ideal solubility (crystal-liquid fugacity ratio) of organic compounds.

Yalkowsky SH, Wu M.

J Pharm Sci. 2010 Mar;99(3):1100-6. doi: 10.1002/jps.21897. Review.

PMID:
19739108
7.

Capturing the crystal: prediction of enthalpy of sublimation, crystal lattice energy, and melting points of organic compounds.

Salahinejad M, Le TC, Winkler DA.

J Chem Inf Model. 2013 Jan 28;53(1):223-9. doi: 10.1021/ci3005012. Epub 2013 Jan 2. Erratum in: J Chem Inf Model. 2013 Mar 25;53(3):737.

PMID:
23215043
8.

Thermodynamic and structural aspects of sulfonamide crystals and solutions.

Perlovich GL, Tkachev VV, Strakhova NN, Kazachenko VP, Volkova TV, Surov OV, Schaper KJ, Raevsky OA.

J Pharm Sci. 2009 Dec;98(12):4738-55. doi: 10.1002/jps.21784.

PMID:
19408296
9.

Melting point, boiling point, and symmetry.

Abramowitz R, Yalkowsky SH.

Pharm Res. 1990 Sep;7(9):942-7.

PMID:
2235894
10.

Prediction of aqueous solubility of organic compounds by the general solubility equation (GSE).

Ran Y, Jain N, Yalkowsky SH.

J Chem Inf Comput Sci. 2001 Sep-Oct;41(5):1208-17.

PMID:
11604020
11.

[Calculation of mobility and entropy of the binding of molecules by crystals].

Garbuzynskiy SO, Finkelstein AV.

Mol Biol (Mosk). 2016 May-Jun;50(3):520-9. doi: 10.7868/S0026898416020063. Russian.

12.

Estimating the Aqueous Solubility of Pharmaceutical Hydrates.

Franklin SJ, Younis US, Myrdal PB.

J Pharm Sci. 2016 Jun;105(6):1914-1919. doi: 10.1016/j.xphs.2016.03.040.

13.

Is universal, simple melting point prediction possible?

Preiss UP, Beichel W, Erle AM, Paulechka YU, Krossing I.

Chemphyschem. 2011 Nov 18;12(16):2959-72. doi: 10.1002/cphc.201100522. Epub 2011 Sep 29.

PMID:
21956860
14.

The QSAR prediction of melting point, a property of environmental relevance.

Dearden JC.

Sci Total Environ. 1991 Dec;109-110:59-68.

PMID:
1815377
15.

Estimation of the aqueous solubility I: application to organic nonelectrolytes.

Jain N, Yalkowsky SH.

J Pharm Sci. 2001 Feb;90(2):234-52.

PMID:
11169540
17.

Estimation of aqueous solubility of organic compounds by using the general solubility equation.

Ran Y, He Y, Yang G, Johnson JL, Yalkowsky SH.

Chemosphere. 2002 Aug;48(5):487-509.

PMID:
12146628
18.

Melting studies of short DNA hairpins: influence of loop sequence and adjoining base pair identity on hairpin thermodynamic stability.

Vallone PM, Paner TM, Hilario J, Lane MJ, Faldasz BD, Benight AS.

Biopolymers. 1999 Oct 5;50(4):425-42.

PMID:
10423551
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