13391-36-1Relevant academic research and scientific papers
CoMFA study of novel phenyl ring-substituted 3α- (diphenylmethoxy)tropane analogues at the dopamine transporter
Newman, Amy Hauck,Izenwasser, Sari,Robarge, Michael J.,Kline, Richard H.
, p. 3502 - 3509 (2007/10/03)
A series of phenyl ring-substituted analogues of 3α- (diphenylmethoxy)tropane (benztropine) has been prepared as novel probes for the dopamine transporter. Cross-validated comparative molecular field analysis (CoMFA) models of the binding domain on the do
Stabilities of Carbonium Ions. IV. Steric Effects in the Solvolysis of Substituted Diphenylmethyl Chlorides
Bolton, Roger,Burley, Rita E.,Williams, Nigel J.
, p. 625 - 634 (2007/10/02)
The replacement of ortho-hydrogen atoms by methyl groups in diphenylmethyl chloride has three distinguishable results upon the rate of solvolysis.Firstly, the alkyl group activates by its electronic effect; secondly, steric interactions diminish all obsse
Synthesis and quantitative structure-activity relationships of antibacterial 1-(substituted benzhydryl)-4-(5-nitro-2- furfurylideneamino)piperazines
Yung,Gilroy,Mahony
, p. 900 - 905 (2007/10/04)
1-Benzhydryl-4-(5-nitro-2-furfurylideneamino)piperazine and 11 substituted analogs were prepared and examined for in vitro antimicrobial activity. The compounds were active against Bacillus cereus 7, Bacillus megaterium 122, Bacillus subtilis 104, Clostridium perfringens 13, and the tetracycline-resistant Clostridium perfringens 37. Regression analyses on the antibacterial activity data based on the Hansch approach, using π, π2, and σ parameters, yielded several statistically significant correlation equations. 1-Benzhydryl-4-(5-nitro-2-furfurylideneamino)piperazine stopped the protein and DNA syntheses in C. perfringens 13, as indicated by precipitable radioactivity. The compound, however, showed no effect on the cell wall synthesis in the bacteria.
