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. 2018 Nov 8;9:1283. doi: 10.3389/fphar.2018.01283

Table 1.

Critical micellar concentrations (CMC) of natural bile acids and semisynthetic keto-derivatives.

Bile acid Abbreviation Position and orientation of OH groups CMC [mM]
Natural bile acids [18, 20]
Cholic acid CA 3α 7α 12α 11–13
Chenodeoxycholic acid CDCA 3α 7α 4–9
Deoxycholic acid DCA 3α 12α 3–10
Ursodeoxycholic acid UDCA 3α 7β 7–19
Taurocholic acid TCA 3α 7α 12α 6–10
Glycocholic acid GCA 3α 7α 12α 10–12
Tauro-chenodeoxycholic acid TCDCA 3α 7α 3
Glyco-chenodeoxycholic acid GCDCA 3α 7α 2–6
Tauro-deoxycholic acid TDCA 3α 12α 2
Glyco-deoxycholic acid GDCA 3α 12α 2–6
Tauro-ursodeoxycholic acid TUDCA 3α 7β 2
Glyco-ursodeoxycholic acid GUDCA 3α 7β 4
Semisynthetic keto derivatives [29]
12-monoketocholic acid 12-MKC 3α 7α 67
7-monoketocholic acid 7-MKC 3α 12α 68
7,12-diketocholic acid 7,12-DKC 3α 95
3,7,12-triketocholic acid 3,7,12-TKC / 135
12-monoketodeoxycholic acid 12-MKDC 3α 20