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carboxytolbutamide

Known as: 1-butyl-3-(4-carboxyphenyl)sulfonylurea, 4-(((butylamino)carbonyl)amino)sulfonylbenzoic acid, tolbutamide carboxylic acid 
National Institutes of Health

Related topics

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2 relations

Broader (1)

Tolbutamide
analogs & derivatives

Papers overview

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Highly Cited
2003
Highly Cited
2003
Artemisinin autoinduction is caused by involvement of cytochrome P450 2B6 but not 2C9
Highly Cited
2002
Highly Cited
2002
Evaluation of cytochrome P4502C9 metabolic activity with tolbutamide in CYP2C9*1 heterozygotes
Multiple single‐nucleotide polymorphisms in the gene encoding cytochrome P450 (CYP) 2C9 have been identified, but the functional… 
Highly Cited
2001
Highly Cited
2001
Fluvoxamine inhibits the CYP2C9 catalyzed biotransformation of tolbutamide
Our objective was to examine the interaction between fluvoxamine and tolbutamide to confirm that fluvoxamine inhibits CYP2C9. 
Highly Cited
1996
Highly Cited
1996
Use of tolbutamide as a substrate probe for human hepatic cytochrome P450 2C9.
Highly Cited
1988
Highly Cited
1988
Characterization of the sulfonylurea receptor on beta cell membranes.
Highly Cited
1987
Highly Cited
1987
Increased cytosolic calcium. A signal for sulfonylurea-stimulated insulin release from beta cells.
Highly Cited
1987
Highly Cited
1987
The hypoglycemic sulfonylureas glyburide and tolbutamide inhibit fatty acid oxidation by inhibiting carnitine palmitoyltransferase.
  • G. Cook
  • The Journal of biological chemistry
  • 1987
  • Corpus ID: 19575672
1977
1977
In vitro insulin release from chicken pancreas.
1970
1970
Hepatic effect of sulfonylureas.
1961
1961
Kinetics of carboxytolbutamide excretion following tolbutamide and carboxytolbutamide administration.
The excretion kinetics of carboxytolbutamide after the oral ingestion of sodium tolbutamide of tolbutamide or tolbutamide free… 
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