Octane

Octane is a lipid of Fatty Acyls (FA) class. The involved functions are known as enzyme activity and Synthesis. Octane often locates in Mitochondrial matrix.

Cross Reference

Introduction

To understand associated biological information of Octane, 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 Octane?

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

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with Octane

MeSH term MeSH ID Detail
Tuberculosis D014376 20 associated lipids
Dermatitis, Contact D003877 59 associated lipids
Dermatitis, Occupational D009783 12 associated lipids
Colonic Neoplasms D003110 161 associated lipids
Sarcoma 180 D012510 21 associated lipids
Body Weight D001835 333 associated lipids
Acute Kidney Injury D058186 34 associated lipids
Hypersensitivity, Delayed D006968 43 associated lipids
Chemical and Drug Induced Liver Injury D056486 39 associated lipids
Mast-Cell Sarcoma D012515 9 associated lipids
Per page 10 20 | Total 15

PubChem Associated disorders and diseases

What pathways are associated with Octane

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 Octane?

Related references are published most in these journals:

Location Cross reference Weighted score Related literatures
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What functions are associated with Octane?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with Octane?

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

What genes are associated with Octane?

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

What common seen animal models are associated with Octane?

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

NCBI Entrez Crosslinks

All references with Octane

Download all related citations
Per page 10 20 50 100 | Total 1789
Authors Title Published Journal PubMed Link
Gianoulis TA et al. Genomic analysis of the hydrocarbon-producing, cellulolytic, endophytic fungus Ascocoryne sarcoides. 2012 PLoS Genet. pmid:22396667
Pareja M et al. Herbivory by a Phloem-feeding insect inhibits floral volatile production. 2012 PLoS ONE pmid:22384116
van der Peet P et al. Discovery of inhibitors of Leishmania β-1,2-mannosyltransferases using a click-chemistry-derived guanosine monophosphate library. 2012 PLoS ONE pmid:22393429
Banerjee C et al. Tuning the probe location on zwitterionic micellar system with variation of pH and addition of surfactants with different alkyl chains: solvent and rotational relaxation studies. 2012 J Phys Chem B pmid:22900581
Li W et al. New approach to the preparation of bicyclo octane derivatives via the enantioselective cascade reaction catalyzed by chiral diamine-Ni(OAc)2 complex. 2012 Org. Biomol. Chem. pmid:22588686
Cheung DL Molecular simulation of hydrophobin adsorption at an oil-water interface. 2012 Langmuir pmid:22591377
Ramus K et al. Sorption-induced effects of humic substances on mass transfer of organic pollutants through aqueous diffusion boundary layers: the example of water/air exchange. 2012 Environ. Sci. Technol. pmid:22268690
Orzechowski K et al. Electric permittivity anomaly close to the critical consolute point of a nitrobenzene + octane liquid mixture. 2012 J Phys Chem B pmid:22276572
Zeeb B et al. Influence of interfacial properties on Ostwald ripening in crosslinked multilayered oil-in-water emulsions. 2012 J Colloid Interface Sci pmid:22958854
Liu XY et al. Oxidative dearomatization/intramolecular Diels-Alder cycloaddition cascade for the syntheses of (±)-atisine and (±)-isoazitine. 2012 Org. Biomol. Chem. pmid:22193953
Vincent M and Gallay J Water gradient in the membrane-water interface: a time-resolved study of the series of n-(9-anthroyloxy) stearic acids incorporated in AOT/water/iso-octane reverse micelles. 2012 J Phys Chem B pmid:22233168
Watanabe Y et al. Design and synthesis of novel opioid ligands with an azabicyclo[2.2.2]octane skeleton and their pharmacologies. 2012 Bioorg. Med. Chem. Lett. pmid:22445285
Grant C et al. Tools for characterizing the whole-cell bio-oxidation of alkanes at microscale. 2012 Biotechnol. Bioeng. pmid:22473845
Pasquale S et al. Giant regular polyhedra from calixarene carboxylates and uranyl. 2012 Nat Commun pmid:22510690
Skinner-Adams TS et al. The frequency of malaria is similar among women receiving either lopinavir/ritonavir or nevirapine-based antiretroviral treatment. 2012 PLoS ONE pmid:22509297
Mann RS et al. Induced release of a plant-defense volatile 'deceptively' attracts insect vectors to plants infected with a bacterial pathogen. 2012 PLoS Pathog. pmid:22457628
Neckameyer WS and Bhatt P Neurotrophic actions of dopamine on the development of a serotonergic feeding circuit in Drosophila melanogaster. 2012 BMC Neurosci pmid:22413901
Campbell BC et al. Chemosensitization as a means to augment commercial antifungal agents. 2012 Front Microbiol pmid:22393330
Karukstis KK et al. Biologically relevant lyotropic liquid crystalline phases in mixtures of n-octyl β-D-glucoside and water. Determination of the phase diagram by fluorescence spectroscopy. 2012 J Phys Chem B pmid:22385304
Tang MW et al. A review of the virological efficacy of the 4 World Health Organization-recommended tenofovir-containing regimens for initial HIV therapy. 2012 Clin. Infect. Dis. pmid:22357809