Publication Details

Category Text Publication
Reference Category Journals
DOI 10.1002/(SICI)1521-3838(199810)17:05<437::AID-QSAR437>3.0.CO;2-K
Title (Primary) A kinetic analysis of the conformational flexibility of steroid hormones
Author Ivanov, J.; Mekenyan, O.; Bradbury, S.P.; Schüürmann, G.
Journal Quantitative Structure-Activity Relationships
Year 1998
Department OEC; COE
Volume 17
Issue 5
Page From 437
Page To 449
Language englisch

For a set of 10 androgen steroids and estradiol (E2), the kinetic feasibility of conformation flexibility of the cyclic moieties was studied under the constraint of maintaining the B/C trans and C/D trans ring fusion of the natural and biologically active enantiomer. To this end, the conformational energy surface was quantified using the semiempirical quantum chemical AM1 model. The computational analysis included the location of Conformational transition states with associated barriers, and intrinsic reaction coordinate (IRC) calculations to characterize the trajectories of the rotations and the relationships of the transition states to neighbouring chair and twist conformations. Conformational transformations were observed only for the A and B rings except for E2, which yielded corresponding transformations for the B and C ring, respectively. Interestingly, the rotation barriers starting from the lowest-energy conformations differed substantially, ranging from below 10 kJ/mol for four compounds to 18–20 kJ/mol for another five compounds. Moreover, chair and twist conformations were found only for steroids with higher saturated rings, while semichairs and semitwists occurred for steroids with aromatic or partly unsaturated rings, and B-ring transformations lead to kinetically unstable conformations with very flat energy minima. Although the rotation barriers for most of the transitions are clearly above the thermal energy (kT) at room temperature when evaluated relative to the lowest-energy conformations, the associated energy demands are well below the gain in energy from ligand-receptor binding. The results suggest that conformer interconversion are feasible from both a thermodynamic and kinetic perspective, and support previous investigations in which conformer distributions rather than lowest energy confor-mations were considered when assessing hormone receptor topography and the biological activity of ligands.

Persistent UFZ Identifier
Ivanov, J., Mekenyan, O., Bradbury, S.P., Schüürmann, G. (1998):
A kinetic analysis of the conformational flexibility of steroid hormones
Quant. Struct.-Act. Relat. 17 (5), 437 - 449