Cholic Acid | C24H40O5 | CID 221493 - PubChem
Cholic acid is a bile acid that is 5beta-cholan-24-oic acid bearing three alpha-hydroxy substituents at position 3, 7 and 12. It has a role as a human metabolite and a mouse metabolite. It is a bile acid, a C24-steroid, a 3alpha-hydroxy steroid, a 7alpha-hydroxy steroid, a 12alpha-hydroxy steroid and a trihydroxy-5beta-cholanic acid.
Cholic acid - Wikipedia
Cholic acid, also known as 3α,7α,12α-trihydroxy-5β-cholan-24-oic acid is a primary bile acid [3] that is insoluble in water (soluble in alcohol and acetic acid), it is a white crystalline substance. Salts of cholic acid are called cholates.
Structure and Dynamics of Cholic Acid and Dodecylphosphocholine-Cholic ...
The chemical (A) and 3-dimensional (B) structures of cholic acid (3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholan-24-oic acid) with standard numbering. In (B), oxygen and carbon atoms are in red and ice blue, respectively.
Bile acids: Chemistry, physiology, and pathophysiology - PMC
Stereostructure of cholic acid. A: Space-filling model; B: Calculated molecular lipophilic potential. Blue colour shows polar surface and red colour shows apolar surface; C: Cartoon representation (as introduced by Small).
Hydrophobic Tetramer Structures of Cholic Acid
Cholic acid (CA) is a primary bile acid which possesses facial amphiphilicity and self-assembly ability. CA is slightly soluble in water, which makes it impossible to form the self-assembled structures spontaneously in aqueous solutions.
Cholic acid - NIST Chemistry WebBook
Chemical structure: This structure is also available as a 2d Mol file; Stereoisomers: 3Beta,7beta,12beta-trihydroxy-5beta-cholan-24-oic acid
Structure Database (LMSD) - LIPID MAPS
The structure of sodium 3α,7α,12α-trihydroxy-5β-cholan-24-oate monohydrate (sodium cholate monohydrate), Acta Cryst B, 1980 DOI: 10.1107/S056774088000310X
We observed that the assembly of cholic acid can recognize organic guests in size, shape, polarity and chirality much more efficiently than that of deoxycholic acid.
Cholic acid monohydrate, also space group P21, (Lessinger, 1982), contains bilayers of yet another sort, in which tetrahedrally hydrogen-bonded water
Cholic Acid - 药物在线
Structure and synthesis: Fieser, Fieser, Steroids (Reinhold, New York, 1959). Properties: Plates from dil acetic acid. Bitter taste with sweetish aftertaste. When anhydr, mp 198°. [a]D20 +37° (c = 0.6 in alcohol). pK = 6.4. Not precipitated by digitonin.