| Weight | 426.729 g/mol |
|---|---|
| Formula | C30H50O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
lanosterol (79-63-0)
Kryptosterol · 4,4,14 alpha-trimethyl-5 alpha-cholesta-8,24-dien-3 beta-ol
Score:
#1712 in Biochemistry
,
#3806 in Biology
,
#4789 in Chemistry
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- The presence of an R467K amino acid substitution and loss of allelic variation correlate with an azole-resistant lanosterol 14alpha demethylase in Candida albicans. (Antimicrobial Agents and Chemotherapy, 1997)
- Insig-mediated degradation of HMG CoA reductase stimulated by lanosterol, an intermediate in the synthesis of cholesterol (Cell Metabolism, 2005)
- From Lanosterol to Cholesterol: Structural Evolution and Differential Effects on Lipid Bilayers (Biophysical Journal, 2002)
- Molecular order and dynamics of phosphatidylcholine bilayer membranes in the presence of cholesterol, ergosterol and lanosterol: a comparative study using 2H-, 13C- and 31p-NMR spectroscopy (Biochimica et Biophysica Acta, 1995)
- Isolation of an Arabidopsis thaliana gene encoding cycloartenol synthase by functional expression in a yeast mutant lacking lanosterol synthase by the use of a chromatographic screen (Proceedings of the National Academy of Sciences of the United States of America, 1993)
- A Three-Dimensional Model of Lanosterol 14-Demethylase of Candida albicans and Its Interaction with Azole Antifungals (Journal of Medicinal Chemistry, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Kryptosterol
- 4,4,14 alpha-trimethyl-5 alpha-cholesta-8,24-dien-3 beta-ol
-
SMILESCC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C
-
InChIKeyCAHGCLMLTWQZNJ-UHFFFAOYSA-N
- Pubchem - lanosterol
- Wikipedia - lanosterol
Lanosterol is a tetracyclic triterpenoid and is the compound from which all animal and fungal steroids are derived. By contrast plant steroids are produced via cycloartenol.
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lanosterol
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