glycodeoxycholic acid (steraloids inc)
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Glycodeoxycholic Acid, supplied by steraloids inc, used in various techniques. Bioz Stars score: 94/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sodium+glycodeoxycholate/5%CE%B2-CHOLANIC+ACID-3%CE%B1%2C+12%CE%B1-DIOL+N-(CARBOXYMETHYL)-AMIDE+SODIUM+SALT/pmc12386833-213-77-79
Average 94 stars, based on 4 article reviews
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Concentration Assay:Article Title: Improved analysis of bile acids in tissues and intestinal contents of rats using LC/ESI-MS Article Snippet: Cholic acid (5b-cholanic acid-3a,7a,12a-triol, CA), a-muricholic acid (5b-cholanic acid-3a,6b,7a-triol, aMCA), b-muricholic acid (5b-cholanic acid-3a,6b,7b-triol, bMCA), v-muricholic acid (5b-cholanic acid-3a,6a,7b-triol, vMCA), chenodeoxycholic acid (5b-cholanic acid-3a,7a-diol, CDCA), deoxycholic acid (5b-cholanic acid-3a,12a-diol, DCA), hyodeoxycholic acid (5b-cholanic acid3a,6a-diol, HDCA), Article Title: Investigation of Glycochenodeoxycholate Sulfate and Chenodeoxycholate Glucuronide as Surrogate Endogenous Probes for Drug Interaction Studies of OATP1B1 and OATP1B3 in Healthy Japanese Volunteers. Article Snippet: Purpose To assess the use of glycochenodeoxycholate-3sulfate (GCDCA-S) and chenodeoxycholate 3or 24glucuronide (CDCA-3G or -24G) as surrogate endogenous substrates in the investigation of drug interactions involving OATP1B1 and OATP1B3.. Methods Uptake of GCDCA-S and CDCA-24G was examined in HEK293 cells transfected with cDNA for OATP1B1, OATP1B3, and NTCP and in cryopreserved human hepatocytes.. Plasma concentrations of bile acids and their metabolites (GCDCA-S, CDCA-3G, and CDCA-24G) were determined by LC–MS/MS in eight healthy volunteers with or without administration of rifampicin (600 mg, po). Transformation Assay:Article Title: Improved analysis of bile acids in tissues and intestinal contents of rats using LC/ESI-MS Article Snippet: Cholic acid (5b-cholanic acid-3a,7a,12a-triol, CA), a-muricholic acid (5b-cholanic acid-3a,6b,7a-triol, aMCA), b-muricholic acid (5b-cholanic acid-3a,6b,7b-triol, bMCA), v-muricholic acid (5b-cholanic acid-3a,6a,7b-triol, vMCA), chenodeoxycholic acid (5b-cholanic acid-3a,7a-diol, CDCA), deoxycholic acid (5b-cholanic acid-3a,12a-diol, DCA), hyodeoxycholic acid (5b-cholanic acid3a,6a-diol, HDCA), Article Title: Investigation of Glycochenodeoxycholate Sulfate and Chenodeoxycholate Glucuronide as Surrogate Endogenous Probes for Drug Interaction Studies of OATP1B1 and OATP1B3 in Healthy Japanese Volunteers. Article Snippet: Purpose To assess the use of glycochenodeoxycholate-3sulfate (GCDCA-S) and chenodeoxycholate 3or 24glucuronide (CDCA-3G or -24G) as surrogate endogenous substrates in the investigation of drug interactions involving OATP1B1 and OATP1B3.. Methods Uptake of GCDCA-S and CDCA-24G was examined in HEK293 cells transfected with cDNA for OATP1B1, OATP1B3, and NTCP and in cryopreserved human hepatocytes.. Plasma concentrations of bile acids and their metabolites (GCDCA-S, CDCA-3G, and CDCA-24G) were determined by LC–MS/MS in eight healthy volunteers with or without administration of rifampicin (600 mg, po). Clinical Proteomics:Article Title: Improved analysis of bile acids in tissues and intestinal contents of rats using LC/ESI-MS Article Snippet: Cholic acid (5b-cholanic acid-3a,7a,12a-triol, CA), a-muricholic acid (5b-cholanic acid-3a,6b,7a-triol, aMCA), b-muricholic acid (5b-cholanic acid-3a,6b,7b-triol, bMCA), v-muricholic acid (5b-cholanic acid-3a,6a,7b-triol, vMCA), chenodeoxycholic acid (5b-cholanic acid-3a,7a-diol, CDCA), deoxycholic acid (5b-cholanic acid-3a,12a-diol, DCA), hyodeoxycholic acid (5b-cholanic acid3a,6a-diol, HDCA), Article Title: Investigation of Glycochenodeoxycholate Sulfate and Chenodeoxycholate Glucuronide as Surrogate Endogenous Probes for Drug Interaction Studies of OATP1B1 and OATP1B3 in Healthy Japanese Volunteers. Article Snippet: Purpose To assess the use of glycochenodeoxycholate-3sulfate (GCDCA-S) and chenodeoxycholate 3or 24glucuronide (CDCA-3G or -24G) as surrogate endogenous substrates in the investigation of drug interactions involving OATP1B1 and OATP1B3.. Methods Uptake of GCDCA-S and CDCA-24G was examined in HEK293 cells transfected with cDNA for OATP1B1, OATP1B3, and NTCP and in cryopreserved human hepatocytes.. Plasma concentrations of bile acids and their metabolites (GCDCA-S, CDCA-3G, and CDCA-24G) were determined by LC–MS/MS in eight healthy volunteers with or without administration of rifampicin (600 mg, po). |
