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

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Chemical Compound Review:

CCRIS 6327 trichloro-methyl-stannane

Synonyms: AG-I-01431, ACMC-20ake3, LS-2324, AC1Q3FSK, CTK3J7136, ...

Foti, C. et al., Dopp, E. et al.

Dopp, Hartmann, von Recklinghausen, Florea, Rabieh, Shokouhi, Hirner, Obe, Rettenmeier,

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High impact information on trichloro-methyl-stannane

After forced uptake by electroporation MMT, DMT and TMT induced significant DNA damage at non-cytotoxic concentrations [1].
The formation and stability of some carboxylate and hydroxycarboxylate (acetate, 1,2,3-propanetricarboxylate, 1,2,3,4-butanetetracarboxylate, malate and citrate) complexes of monomethyltin trichloride was studied potentiometrically at 25 degrees C and at different ionic strengths in NaNO3 aqueous solution [2].

References

The cyto- and genotoxicity of organotin compounds is dependent on the cellular uptake capability. Dopp, E., Hartmann, L.M., von Recklinghausen, U., Florea, A.M., Rabieh, S., Shokouhi, B., Hirner, A.V., Obe, G., Rettenmeier, A.W. Toxicology (2007) [Pubmed]
Interaction of alkyltin(IV) compounds with ligands of interest in the speciation of natural fluids: carboxylate and hydroxycarboxylate complexes of monomethyltin(IV) trichloride. Foti, C., Gianguzza, A., Sammartano, S. Annali di chimica. (2002) [Pubmed]

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