I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
Biospecific adsorption of carbonic anhydrase to self-assembled monolayers of alkanethiolates that present benzenesulfonamide groups on gold. Biospecific binding of carbonic anhydrase to mixed sams presenting benzenesulfonamide ligands led to a model system for studying lateral steric effects. Benzenesulfonamide modifications at c-7 of ciprofloxacin change its primary target instreptococcus pneumoniae from topoisomerase iv to gyrase. Polar substitutions in the benzenesulfonamide ring of celecoxib afford a potent 1,5-diarylpyrazole class of COX-2 inhibitors.
Milan Mrksich,; Jocelyn R. Grunwell,; George M. Whitesides .Biospecific Adsorption of Carbonic Anhydrase to Self-Assembled Monolayers of Alkanethiolates That Present Benzenesulfonamide Groups on Gold. J. Am. Chem. Soc., . 1995, 117 (48),12009-12010.
Joydeep Lahiri,; Lyle Isaacs,; Bartosz Grzybowski,; Jeffrey D. Carbeck,; George M. Whitesides. title . Langmuir. 1999, 15(21),7186-7198.
해저드 설명서 (EU): H302
Harmful if swallowed.
주의 설명서: P280f
Wear protective clothing.