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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Authors Title Published Journal PubMed Link
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
Kavtaradze LK et al. A low-toxicity method for the separation of lanosterol and dihydrolanosterol from commercial mixtures. 2004 Steroids pmid:15465116
Chen CK et al. Trypanosoma cruzi CYP51 inhibitor derived from a Mycobacterium tuberculosis screen hit. 2009 PLoS Negl Trop Dis pmid:19190730
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
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
Keber R et al. Male germ cell-specific knockout of cholesterogenic cytochrome P450 lanosterol 14α-demethylase (Cyp51). 2013 J. Lipid Res. pmid:23509403
Zhu J et al. Effects of FoxO4 overexpression on cholesterol biosynthesis, triacylglycerol accumulation, and glucose uptake. 2010 J. Lipid Res. pmid:20037138
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
Evans JL and Gealt MA The sterols of growth and stationary phases of Aspergillus nidulans cultures. 1985 J. Gen. Microbiol. pmid:3884732
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