"Flexible-Acceptor" General Solubility Equation for beyond Rule of 5 Drugs

被引:21
作者
Avdeef, Alex [1 ]
Kansy, Manfred [1 ]
机构
[1] In ADME Res, New York, NY 10128 USA
关键词
Kier Phi flexibility; Abraham H-bond basicity; aqueous intrinsic solubility; rule of 5 (Ro5); beyond Ro5 (bRo5); general solubility equation (GSE); flexible-acceptor general solubility equation; GSE(Phi; B); partial least-squares (PLS); intramolecular hydrogen bonding (IMHB); AQUEOUS SOLUBILITY; SOLUBLE DRUGS; PREDICTION; PERMEABILITY; DISSOLUTION; RIFAMPICIN; COMBINATION; FORMULATION; ABSORPTION; PACLITAXEL;
D O I
10.1021/acs.molpharmaceut.0c00689
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
This study describes a novel nonlinear variant of the well-known Yalkowsky general solubility equation (GSE). The modified equation can be trained with small molecules, mostly from the Lipinski Rule of 5 (Ro5) chemical space, to predict the intrinsic aqueous solubility, S0, of large molecules (MW > 800 Da) from beyond the rule of 5 (bRo5) space, to an accuracy almost equal to that of a recently described random forest regression (RFR) machine learning analysis. The new approach replaces the GSE constant factors in the intercept (0.5), the octanol-water log P (-1.0), and melting point, mp (-0.01) terms with simple exponential functions incorporating the sum descriptor, Phi+B (Kier F molecular flexibility and Abraham H-bond acceptor potential). The constants in the modified three-variable (log P, mp, Phi+B) equation were determined by partial least-squares (PLS) refinement using a smallmolecule log S-0 training set (n = 6541) of mostly druglike molecules. In this "flexible-acceptor" GSE(Phi,B) model, the coefficient of log P (normally fixed at -1.0) varies smoothly from -1.1 for rigid nonionizable molecules (Phi+B = 0) to -0.39 for typically flexible (Phi similar to 20, B similar to 6) large molecules. The intercept (traditionally fixed at +0.5) varies smoothly from +1.9 for completely inflexible small molecules to -2.2 for typically flexible large molecules. The mp coefficient (-0.007) remains practically constant, near the traditional value (-0.01) for most molecules, which suggests that the small-to-large molecule continuum is mainly solvation responsive, apparently with only minor changes in the crystal lattice contributions. For a test set of 32 large molecules (e.g., cyclosporine A, gramicidin A, leuprolide, nafarelin, oxytocin, vancomycin, and mostly natural-product-derived therapeutics used in infectious/viral diseases, in immunosuppression, and in oncology) the modified equation predicted the intrinsic solubility with a root-mean-square error of 1.10 log unit, compared to 3.0 by the traditional GSE, and 1.07 by RFR.
引用
收藏
页码:3930 / 3940
页数:11
相关论文
共 72 条
[1]   The correlation and prediction of the solubility of compounds in water using an amended solvation energy relationship [J].
Abraham, MH ;
Le, J .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1999, 88 (09) :868-880
[2]   Dissolution test as a surrogate for quality evaluation of rifampicin containing fixed dose combination formulations [J].
Agrawal, S ;
Panchagnula, R .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 287 (1-2) :97-112
[3]   Comments on prediction of the aqueous solubility using the general solubility equation (GSE) versus a genetic algorithm and a support vector machine model [J].
Alantary, Doaa ;
Yalkowsky, Samuel .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2018, 23 (07) :739-740
[4]   NOVEL CYTOTOXIC 3'-(TERT-BUTYL) 3'-DEPHENYL ANALOGS OF PACLITAXEL AND DOCETAXEL [J].
ALI, SM ;
HOEMANN, MZ ;
AUBE, J ;
MITSCHER, LA ;
GEORG, GI ;
MCCALL, R ;
JAYASINGHE, LR .
JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (19) :3821-3828
[5]  
ANDREW MARY LOU, 1959, ANTIBIOT AND CHEMOTHER, V9, P277
[6]  
Anik S. T., 1991, PEPTIDES DRUG DELIVE, P769
[7]   Comparative studies of the enhancing effects of cyclodextrins on the solubility and oral bioavailability of tacrolimus in rats [J].
Arima, H ;
Yunomae, K ;
Miyake, K ;
Irie, T ;
Hirayama, F ;
Uekama, K .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 90 (06) :690-701
[8]   Can small drugs predict the intrinsic aqueous solubility of 'beyond Rule of 5' big drugs? [J].
Avdeef, Alex ;
Kansy, Manfred .
ADMET AND DMPK, 2020, 8 (03) :180-+
[9]   Prediction of aqueous intrinsic solubility of druglike molecules using Random Forest regression trained with Wiki-pS0 database [J].
Avdeef, Alex .
ADMET AND DMPK, 2020, 8 (01) :29-77
[10]   Suggested Improvements for Measurement of Equilibrium Solubility-pH of Ionizable Drugs [J].
Avdeef, Alex .
ADMET AND DMPK, 2015, 3 (02) :84-109