Cholesterol
Synonyms: cholesterol, "Cholesterin", "Cholesteryl alcohol", "Cholest-5-en-3beta-ol", "Cholestrin", "Dusoran", "Dusoline", "Cordulan", "Cholesterine", "Hydrocerin", "Cholestrol", "Kathro", "Dythol", "Lanol", "Super hartolan", "Provitamin D", "Cholesterol base H", "Lidinite", "Nimco cholesterol base H", "Lidinit", "(-)-Cholesterol", "Tegolan (VAN)", "Cholest-5-en-3-beta-ol", "5:6-Cholesten-3beta-ol", "Tegolan", "3beta-Hydroxycholest-5-ene", "5-Cholesten-3beta-ol", "3-beta-Hydroxycholest-5-ene", "(3beta)-cholest-5-en-3-ol",
Source: Cholesterol is a natural component of most biological membranes.
Identifiers:
IUPAC Name: (3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
CAS Number: 57-88-5
PubChem ID: 5997
InChiKey: HVYWMOMLDIMFJA-DPAQBDIFSA-N
Canonical SMILES: CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C
Structural Properties:
Molecular Formula: C27H46O
Molecular Weight: 386,700
Pharmacophore Features:
Number of bond donors: 1
Number of bond acceptors: 1
Number of atoms different from hydrogen: 28
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2D structure (.sdf)
3D structure (.sdf)
3D structure (.mol2)
3D structure (.pdb)
3D structure (.pdbqt)
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Evidence Supporting This Chemical as an Emerging Contaminant
Baldwin, A. K., Corsi, S. R., De Cicco, L. A., Lenaker, P. L., Lutz, M. A., Sullivan, D. J., & Richards, K. D. (2016). Organic contaminants in Great Lakes tributaries: Prevalence and potential aquatic toxicity. Science of the Total Environment, 554, 42-52.