2,4-pentanedione

2,4-pentanedione is a lipid of Fatty Acyls (FA) class. The related lipids are Butyrates.

Cross Reference

Introduction

To understand associated biological information of 2,4-pentanedione, 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 2,4-pentanedione?

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 2,4-pentanedione

PubChem Associated disorders and diseases

What pathways are associated with 2,4-pentanedione

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 2,4-pentanedione?

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

What functions are associated with 2,4-pentanedione?

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

What lipids are associated with 2,4-pentanedione?

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 2,4-pentanedione?

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

What common seen animal models are associated with 2,4-pentanedione?

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

NCBI Entrez Crosslinks

All references with 2,4-pentanedione

Download all related citations
Per page 10 20 50 100 | Total 1027
Authors Title Published Journal PubMed Link
pmid:25894207
pmid:25832649
pmid:25772881
pmid:25765264
Mahnir VM et al. Modification of arginine in sea anemone toxin RTX-III from Radianthus macrodactylus. 1989 Toxicon pmid:2573177
pmid:25411917
pmid:25173924
Dai X et al. Acetylation-dependent regulation of essential iPS-inducing factors: a regulatory crossroad for pluripotency and tumorigenesis. 2014 Cancer Med pmid:25116380
pmid:25084441
AuBuchon JP and Brightman A Use of indium-111 as a red cell label. 1989 Transfusion pmid:2493173
pmid:24858353
pmid:24769359
Korsager S et al. Direct route to 1,3-diketones by palladium-catalyzed carbonylative coupling of aryl halides with acetylacetone. 2013 Chemistry pmid:24353081
Sharpe RJ et al. Asymmetric synthesis of the aminocyclitol pactamycin, a universal translocation inhibitor. 2013 J. Am. Chem. Soc. pmid:24245656
Triantis C et al. Synthesis and characterization of fac-[M(CO)3(P)(OO)] and cis-trans-[M(CO)2(P)2(OO)] complexes (M = Re, (99m)Tc) with acetylacetone and curcumin as OO donor bidentate ligands. 2013 Inorg Chem pmid:24199833
Allen JG et al. Metabolism of debrisoquine sulfate. Identification of some urinary metabolites in rat and man. 1975 Sep-Oct Drug Metab. Dispos. pmid:241613
Wang M et al. Photodegradation of Acid Orange 7 in a UV/acetylacetone process. 2013 Chemosphere pmid:24079997
Shah J et al. Validated spectrofluorimetric method for determination of sulpiride in commercial formulations using Hantzsch condensation reaction. 2013 Pak J Pharm Sci pmid:24035947
Minaga T et al. Enzymatic degradation of succinyl-coenzyme A by rat liver homogenates. 1978 Biochim. Biophys. Acta pmid:23860
Rostami-Charati F et al. A facile one-pot synthesis of functionalized 1,3-oxathiolan-2-yliden derivatives: multicomponent reaction of oxiranes in water. 2014 Comb. Chem. High Throughput Screen. pmid:23755720
Siegel D et al. Controlling detrimental effects of metal cations in the quantification of energy metabolites via ultrahigh pressure-liquid chromatography-electrospray-tandem mass spectrometry by employing acetylacetone as a volatile eluent modifier. 2013 J Chromatogr A pmid:23643099
Narayanaperumal S et al. Basic-functionalized recyclable ionic liquid catalyst: A solvent-free approach for Michael addition of 1,3-dicarbonyl compounds to nitroalkenes under ultrasound irradiation. 2013 Ultrason Sonochem pmid:23218731
Al-Etaibi AM et al. A facile synthesis of new monoazo disperse dyes derived from 4-hydroxyphenylazopyrazole-5-amines: evaluation of microwave assisted dyeing behavior. 2012 Molecules pmid:23178305
El-Sonbati AZ et al. Supramolecular structure and spectral studies on mixed-ligand complexes derived from β-diketone with azodye rhodanine derivatives. 2012 Spectrochim Acta A Mol Biomol Spectrosc pmid:23036937
Sun Z et al. A general chelate-assisted co-assembly to metallic nanoparticles-incorporated ordered mesoporous carbon catalysts for Fischer-Tropsch synthesis. 2012 J. Am. Chem. Soc. pmid:23020275
pmid:23007529
Park H et al. Fe(II) complexes that mimic the active site structure of acetylacetone dioxygenase: O2 and NO reactivity. 2012 Inorg Chem pmid:22974346
Zhuang Y and Cao L Sensitive fluorescence detection of etimicin based on derivatives of formaldehyde and acetylacetone. 2013 J Fluoresc pmid:22918626
pmid:22915372
pmid:22906488
pmid:22891995
Mohammadi K and Rastegari M New tetradentate Schiff bases of 2,2-dimethyl-1,3-diaminopropane and acetylacetone derivatives and their vanadyl complexes. 2012 Spectrochim Acta A Mol Biomol Spectrosc pmid:22885931
pmid:22876815
pmid:22861660
pmid:22850856
pmid:22850842
pmid:22849122
pmid:22835057
pmid:22819396
pmid:22813988
pmid:22785355
pmid:22782337
pmid:22772805
Chalifoux WA et al. Direct and highly regioselective and enantioselective allylation of β-diketones. 2012 Nature pmid:22763452
pmid:22762956
pmid:22730344
Åšwiderek K et al. A theoretical study of carbon-carbon bond formation by a Michael-type addition. 2012 Org. Biomol. Chem. pmid:22722380
pmid:22714784
pmid:22714120
pmid:22709348