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Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|July 4, 2006
Utility of the mouse dermal promotion assay in comparing the tumorigenic potential of cigarette mainstream smokeCarr J Smith, Thomas A Perfetti, Rajni Garg, et al.Bioorganic & Medicinal Chemistry|June 6, 2003
QSAR of apoptosis induction in various cancer cellsCorwin Hansch, Ali Jazirehi, Suresh Babu Mekapati, et al.Journal of Medicinal Chemistry|November 11, 2005
Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship studyCynthia D Selassie, Sanjay Kapur, Rajeshwar P Verma, et al.Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|November 25, 2003
Percutaneous penetration enhancers in cigarette mainstream smokeCarr J Smith, Thomas A Perfetti, Rajni Garg, et al.Bioorganic & Medicinal Chemistry|January 23, 2003
Quantitative structure-activity relationships of phenolic compounds causing apoptosisCorwin Hansch, Benjamin Bonavida, Ali R Jazirehi, et al.Journal of Chemical Information and Computer Sciences|January 28, 2003
On the role of polarizability in chemical-biological interactionsCorwin Hansch, Wayne E Steinmetz, Albert J Leo, et al.Chemical Research in Toxicology|March 19, 2003
Synthesis, cytotoxicity, and QSAR analysis of X-thiophenols in rapidly dividing cellsRajeshwar P Verma, Sanjay Kapur, Omar Barberena, et al.European Journal of Medicinal Chemistry|November 6, 2012
Novel peptidomimetic compounds containing redox active chalcogens and quinones as potential anticancer agentsSaad Shaaban, Randi Diestel, Bettina Hinkelmann, et al.Toxicological Sciences : an Official Journal of the Society of Toxicology|September 7, 2002
The relative toxicity of substituted phenols reported in cigarette mainstream smokeCarr J Smith, Thomas A Perfetti, Michael J Morton, et al.Journal of Inorganic Biochemistry|December 21, 2011
An in vitro comparative assessment with a series of new triphenyltin(IV) 2-/4-[(E)-2-(aryl)-1-diazenyl]benzoates endowed with anticancer activities: structural modifications, analysis of efficacy and cytotoxicity involving human tumor cell linesTushar S Basu Baul, Anup Paul, Lorenzo Pellerito, et al.Pageof 6