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.

Cross Reference

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
Loading... please refresh the page if content is not showing up.

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

Download all related citations
Per page 10 20 50 | Total 30
Authors Title Published Journal PubMed Link
Jennings GK et al. Spin equilibrium and Oâ‚‚-binding kinetics of Mycobacterium tuberculosis CYP51 with mutations in the histidine-threonine dyad. 2014 J. Inorg. Biochem. pmid:24793591
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
Keber R et al. Male germ cell-specific knockout of cholesterogenic cytochrome P450 lanosterol 14α-demethylase (Cyp51). 2013 J. Lipid Res. pmid:23509403
Keber R et al. Mouse knockout of the cholesterogenic cytochrome P450 lanosterol 14alpha-demethylase (Cyp51) resembles Antley-Bixler syndrome. 2011 J. Biol. Chem. pmid:21705796
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
Liu XT et al. Antibacterial compounds from mushrooms I: a lanostane-type triterpene and prenylphenol derivatives from Jahnoporus hirtus and Albatrellus flettii and their activities against Bacillus cereus and Enterococcus faecalis. 2010 Planta Med. pmid:19644795
Zhu J et al. Effects of FoxO4 overexpression on cholesterol biosynthesis, triacylglycerol accumulation, and glucose uptake. 2010 J. Lipid Res. pmid:20037138
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
Chen CK et al. Trypanosoma cruzi CYP51 inhibitor derived from a Mycobacterium tuberculosis screen hit. 2009 PLoS Negl Trop Dis pmid:19190730
Lange Y et al. Effectors of rapid homeostatic responses of endoplasmic reticulum cholesterol and 3-hydroxy-3-methylglutaryl-CoA reductase. 2008 J. Biol. Chem. pmid:18024962
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
Nguyen AD et al. Hypoxia stimulates degradation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase through accumulation of lanosterol and hypoxia-inducible factor-mediated induction of insigs. 2007 J. Biol. Chem. pmid:17635920
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
Kavtaradze LK et al. A low-toxicity method for the separation of lanosterol and dihydrolanosterol from commercial mixtures. 2004 Steroids pmid:15465116
Berger A et al. Cholesterol-lowering properties of Ganoderma lucidum in vitro, ex vivo, and in hamsters and minipigs. 2004 Lipids Health Dis pmid:14969592
Liu XY et al. Creating new supramolecular materials by architecture of three-dimensional nanocrystal fiber networks. 2002 J. Am. Chem. Soc. pmid:12475350
Sonoda Y et al. Purification of a human cytochrome P-450 isozyme catalyzing lanosterol 14 alpha-demethylation. 1993 Biochim. Biophys. Acta pmid:8399332
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
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
Nes WD et al. Concerning the role of 24,25-dihydrolanosterol and lanostanol in sterol biosynthesis by cultured cells. 1989 Mar-May Steroids pmid:2799854