Crystal and molecular structure of an enantiomeric gossypol-acetic acid clathrate

被引:9
作者
Dowd, MK
Thomas, LM
Calhoun, MC
机构
[1] USDA ARS, So Reg Res Ctr, New Orleans, LA 70124 USA
[2] Iowa State Univ, Dept Chem, Ames, IA 50011 USA
[3] Texas Agr Expt Stn, San Angelo, TX 76901 USA
关键词
gossypol; gossypol acetic acid; gossypol enantiomers; inclusion compounds; isomers; isomer separation;
D O I
10.1007/s11746-999-0148-6
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Single crystals of gossypol with three molecules of acetic acid (gossypol triacetic acid) were grown from solutions of gossypol acetic acid and acetone. The crystals were unstable in air but could be stabilized for X-ray diffraction analysis by coating the crystal surfaces with a thin layer of mineral oil. The gossypol triacetic acid complex (C30H30O8. 3C(2)H(4)O(2)) forms an orthorhombic crystal system with P2(1)2(1)2(1) (Z = 4) symmetry.. Unit cell dimensions were a = 9.0208(7) Angstrom, b = 17.4884(10) Angstrom, and c = 24.358(2), Angstrom yielding a volume of 3842.7(5) Angstrom(3) and a density of 1.2077(2) g/cm(3). As with all previously reported crystals of gossypol, the gossypol molecules were of the aldehyde tautomer, and the two planar naphthalene rings were approximately perpendicular. Acetic acid molecules were found to lie in channels within the gossypol matrix. Individual crystals contained only one gossypol enantiomer, but both enantiomers crystallized from solution. Although the crystal habit could not be used to distinguish between the gossypol enantiomers, a fragment of the crystal could be derivatized and analyzed by high-performance liquid chromatography for this purpose. The ability to grow large, nonracemic crystals leads to a simple procedure for separating small quantities of the individual gossypol enantiomers.
引用
收藏
页码:1343 / 1350
页数:8
相关论文
共 36 条
[1]  
Allen F.H., 1993, CHEM AUTOMAT NEWS, V8, P31
[2]   TABLES OF BOND LENGTHS DETERMINED BY X-RAY AND NEUTRON-DIFFRACTION .1. BOND LENGTHS IN ORGANIC-COMPOUNDS [J].
ALLEN, FH ;
KENNARD, O ;
WATSON, DG ;
BRAMMER, L ;
ORPEN, AG ;
TAYLOR, R .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1987, (12) :S1-S19
[3]   ANTIPROLIFERATIVE EFFECT OF GOSSYPOL AND ITS OPTICAL ISOMERS ON HUMAN REPRODUCTIVE CANCER CELL-LINES [J].
BAND, V ;
HOFFER, AP ;
BAND, H ;
RHINEHARDT, AE ;
KNAPP, RC ;
MATLIN, SA ;
ANDERSON, DJ .
GYNECOLOGIC ONCOLOGY, 1989, 32 (03) :273-277
[4]  
BENZ CC, 1990, MOL PHARMACOL, V37, P840
[5]  
Berardi L. C., 1980, Toxic constituents of plant foodstuffs., P183
[6]  
CHANGFU X, 1982, SCI SINICA B, V25, P1194
[7]   ON ENANTIOMORPH-POLARITY ESTIMATION [J].
FLACK, HD .
ACTA CRYSTALLOGRAPHICA SECTION A, 1983, 39 (NOV) :876-881
[8]   LATTICE INCLUSION-COMPOUNDS OF GOSSYPOL - STRUCTURE OF THE 2-3 GOSSYPOL-BENZALDEHYDE COORDINATOCLATHRATE [J].
GDANIEC, M ;
IBRAGIMOV, BT ;
TALIPOV, SA .
ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 1991, 47 :573-577
[9]  
GDANIEC M, 1995, POL J CHEM, V69, P1133
[10]  
GDANIEC M, 1994, POL J CHEM, V68, P733