24,25-dihydrolanosterol

24,25-dihydrolanosterol is a lipid of Sterol Lipids (ST) class. The involved functions are known as Binding (Molecular Function), Force, Molecular Dynamics and Synthesis. The related lipids are Sterols and Steroids.

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Introduction

To understand associated biological information of 24,25-dihydrolanosterol, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with 24,25-dihydrolanosterol?

There are no associated biomedical information in the current reference collection.

No disease MeSH terms mapped to the current reference collection.

PubChem Associated disorders and diseases

What pathways are associated with 24,25-dihydrolanosterol

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with 24,25-dihydrolanosterol?

There are no associated biomedical information in the current reference collection.

What functions are associated with 24,25-dihydrolanosterol?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with 24,25-dihydrolanosterol?

Related references are published most in these journals:

Lipid concept Cross reference Weighted score Related literatures
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What genes are associated with 24,25-dihydrolanosterol?

There are no associated biomedical information in the current reference collection.

What common seen animal models are associated with 24,25-dihydrolanosterol?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with 24,25-dihydrolanosterol

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pmid:
Buurman ET et al. Utilization of target-specific, hypersensitive strains of Saccharomyces cerevisiae to determine the mode of action of antifungal compounds. 2005 Antimicrob. Agents Chemother. pmid:15917573
Warrilow AG et al. Expression, purification, and characterization of Aspergillus fumigatus sterol 14-alpha demethylase (CYP51) isoenzymes A and B. 2010 Antimicrob. Agents Chemother. pmid:20660663
Aoyama Y and Yoshida Y Different substrate specificities of lanosterol 14a-demethylase (P-45014DM) of Saccharomyces cerevisiae and rat liver for 24-methylene-24,25-dihydrolanosterol and 24,25-dihydrolanosterol. 1991 Biochem. Biophys. Res. Commun. pmid:1872829
Ačimovič J et al. Circadian rhythm of cholesterol synthesis in mouse liver: a statistical analysis of the post-squalene metabolites in wild-type and Crem-knock-out mice. 2011 Biochem. Biophys. Res. Commun. pmid:21531203
Aoyama Y et al. Structural analysis of the interaction between the side-chain of substrates and the active site of lanosterol 14 alpha-demethylase (P-450(14)DM) of yeast. 1992 Biochim. Biophys. Acta pmid:1504086
Sood R and Kinnunen PK Cholesterol, lanosterol, and ergosterol attenuate the membrane association of LL-37(W27F) and temporin L. 2008 Biochim. Biophys. Acta pmid:18358828
Sonoda Y et al. Purification of a human cytochrome P-450 isozyme catalyzing lanosterol 14 alpha-demethylation. 1993 Biochim. Biophys. Acta pmid:8399332
Moroyama T et al. Changes in sterol metabolism in the skin of developing chick embryo and alterations in the presence of an anticholesterolemic agent and a chemical carcinogen. 1982 Biochim. Biophys. Acta pmid:6812647
Sukhanova A et al. Targeting C4-demethylating genes in the cholesterol pathway sensitizes cancer cells to EGF receptor inhibitors via increased EGF receptor degradation. 2013 Cancer Discov pmid:23125191