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

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Chemical Compound Review:

Tevenel 2,2-dichloro-N-[(1S,2R)-1,3- dihydroxy-1-(4...

Synonyms: amp-3, CHEMBL454640, SureCN1448436, AC1Q3GZB, AR-1H7256, ...

Yatscoff, R.W. et al., Wallace, R.B. et al.

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High impact information on Tevenel

Each resistant cell line had an identical growth rate in the presence and absence of 100 mug Tevenel/ml [1].
A clone of Chinese hamster ovary (CHO) cells, BT3, resistant to Tevenel, the sulfamoyl analog of chloramphenicol has been isolated [2].

References

Selection of mammalian cells resistant to a chloramphenicol analog. Wallace, R.B., Freeman, K.B. J. Cell Biol. (1975) [Pubmed]
Cybrid formation with recipient cell lines containing dominant phenotypes. Yatscoff, R.W., Mason, J.R., Patel, H.V., Freeman, K.B. Somatic Cell Genet. (1981) [Pubmed]

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