Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Chemical Compound Review:

PubChem3118 4-methanoylbenzonitrile

Synonyms: PubChem8078, ARONIS24248, NSC-5091, AC-283, ACMC-1BQT2, ...

Itoh, T., Chen, Q. et al., Giraldi, T. et al.

Itoh,

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Disease relevance of p-Cyanobenzaldehyde

Two adducts derived from 2,6-dinitro- and 4-cyanobenzaldehyde were active against TLX5 lymphoma in mice [1].

High impact information on p-Cyanobenzaldehyde

The IC50 values of 4-cyanobenzaldehyde and 4-cyanobenzoic acid were estimated as 0.62 and 2.45 mM for monophenolase and as 0.72 and 1.40 mM for diphenolase, respectively [2].
The lowest excited triplet (T1) energies of p-methoxybenzaldehyde and p-cyanobenzaldehyde vapors estimated from the temperature dependence of the T2(n, pi*) phosphorescence and the S1(n, pi*) fluorescence spectra [3].

References

Antitumor activity of hydrazones and adducts between aromatic aldehydes and p-(3,3-dimethyl-1-triazeno)benzoic acid hydrazide. Giraldi, T., Goddard, P.M., Nisi, C., Sigon, F. Journal of pharmaceutical sciences. (1980) [Pubmed]
Inhibitory effect of 4-cyanobenzaldehyde and 4-cyanobenzoic acid on mushroom (Agaricus bisporus) tyrosinase. Chen, Q., Chen, Q.X., Qiu, L., Song, K.K., Huang, H. J. Protein Chem. (2003) [Pubmed]
The lowest excited triplet (T1) energies of p-methoxybenzaldehyde and p-cyanobenzaldehyde vapors estimated from the temperature dependence of the T2(n, pi*) phosphorescence and the S1(n, pi*) fluorescence spectra. Itoh, T. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. (2003) [Pubmed]

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