Kuramochi, H <br/><br/>
Conformational studies and electronic structures of tamoxifen and toremifene and their allylic carbocations proposed as reactive intermediates leading to DNA adduct formation.  [electronic resource] 

 -  Journal of medicinal chemistry  Jul 1996 
 - 2877-86 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0022-2623 
<br/><br/><label>Standard No.: </label>10.1021/jm960255g  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Antineoplastic Agents, Hormonal--chemistry<br/>Chemical Phenomena<br/>Chemistry, Physical<br/>Computer Simulation<br/>Crystallography, X-Ray<br/>DNA Adducts--chemistry<br/>Drug Stability<br/>Electrochemistry<br/>Estrogen Antagonists--chemistry<br/>Hydroxylation<br/>Models, Molecular<br/>Molecular Conformation<br/>Molecular Structure<br/>Tamoxifen--analogs & derivatives<br/>Thermodynamics<br/>Toremifene--chemistry