375365

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Triarylmethanes, a new class of cx50 inhibitors.

Silke B Bodendiek et al.

Frontiers in pharmacology, 3, 106-106 (2012-06-12)

The paucity of specific pharmacological agents has been a major impediment for delineating the roles of gap junction (GJ) channels formed by connexin proteins in physiology and pathophysiology. Here, we used the selective optimization of side activities (SOSA) approach, which

Theoretical investigations on the molecular structure and vibrational spectral analysis of 4-methyl 2-phenylimidazole.

Erdogdu Y, et al.

Optics and Spectroscopy, 113(6), 596-606 (2012)

Physical properties of a bisphenol-F epoxy containing a silica filler treated with silane coupling agents.

Case SL and Ward TC.

Journal of Adhesion, 79(2), 105-121 (2003)

Cure profiles, crosslink density, residual stresses, and adhesion in a model epoxy.

Case SL, et al.

Polymer, 46(24), 1083-1040 (2005)

Rhodium (III)-catalyzed CH activation of phenylazoles toward CN bond cleavage of diazabicyclic olefins: A facile access to mono-and biscyclopentenyl-functionalized aza-heteroaromatics

Praveen P, et al.

Synlett, 25, 0275-0279 (2014)

Tumor-specific cytotoxic activity and type of cell death induced by 4-trifluoromethylimidazoles in human oral squamous cell carcinoma cell lines.

Fumihiro Takekawa et al.

Anticancer research, 27(6B), 4065-4069 (2008-01-30)

Fourteen 4-trifluoromethylimidazole derivatives were investigated for their cytotoxicity against three human normal cells (gingival fibroblast HGF, pulp cell HPC and periodontal ligament fibroblast HPLF) and four human tumor cell lines (oral squamous cell carcinoma HSC-2, HSC-3, HSC-4 and promyelocytic leukemia

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