MiMeDB: Showing metabocard for gamma-Decalactone (MMDBc0033643)

Plant

Xenobiotic

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-11-19 04:57:10 UTC

Update Date

2025-01-16 04:44:12 UTC

Metabolite ID

MMDBc0033643

Metabolite Identification

Common Name

gamma-Decalactone

Description

xi-5-Hexyldihydro-2(3H)-furanone, also known as 4-hexyl-4-butanolide or gamma-lactone decanoic acid, belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a carboxy group on the carbon adjacent to the oxygen atom. xi-5-Hexyldihydro-2(3H)-furanone has been detected, but not quantified, in fruits. This could make XI-5-hexyldihydro-2(3H)-furanone a potential biomarker for the consumption of these foods.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
4-Decanolide	ChEBI
4-Hexyl-gamma-butyrolactone	ChEBI
4-Hydroxydecanoic acid gamma-lactone	ChEBI
5-Hexyldihydro-2(3H)-furanone	ChEBI
5-Hexyloxolan-2-one	ChEBI
5-Hexyltetrahydro-2-furanone	ChEBI
Decan-4-olide	ChEBI
gamma-Decanolactone	ChEBI
gamma-Hexyl-gamma-butyrolactone	ChEBI
gamma-N-Decalactone	ChEBI
gamma-N-Hexyl-gamma-butyrolactone	ChEBI
4-Hexyl-g-butyrolactone	Generator
4-Hexyl-γ-butyrolactone	Generator
4-Hydroxydecanoate g-lactone	Generator
4-Hydroxydecanoate gamma-lactone	Generator
4-Hydroxydecanoate γ-lactone	Generator
4-Hydroxydecanoic acid g-lactone	Generator
4-Hydroxydecanoic acid γ-lactone	Generator
g-Decanolactone	Generator
Γ-decanolactone	Generator
g-Hexyl-g-butyrolactone	Generator
Γ-hexyl-γ-butyrolactone	Generator
g-N-Decalactone	Generator
Γ-N-decalactone	Generator
g-N-Hexyl-g-butyrolactone	Generator
Γ-N-hexyl-γ-butyrolactone	Generator
g-Decalactone	Generator
Γ-decalactone	Generator

Molecular Formula

C₁₀H₁₈O₂

Average Mass

170.2487

Monoisotopic Mass

170.1306798

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

706-14-9

SMILES

Not Available

InChI Identifier

InChI=1S/C10H18O2/c1-2-3-4-5-6-9-7-8-10(11)12-9/h9H,2-8H2,1H3

InChI Key

IFYYFLINQYPWGJ-UHFFFAOYSA-N

Chemical Taxonomy

Functional Ontology

Not Available

Physical Properties

State

Not Available

Predicted Properties

Not Available

Spectra

Not Available

Chromatographic Retention Times and Retention Indices

Retention Times

Chromatography Type	Technique	Column	Deposition Date	Retention Time (s)
Liquid Chromatography	HILIC	Waters Acquity UPLC-BEH Amide column (eluted)	2025-10-24	196.6
Liquid Chromatography	HILIC	Accucore 150 Amide HILIC (void)	2025-10-24	25.5
Liquid Chromatography	Reversed-phase	Hypersil Gold 1.9 µm C18 (eluted)	2025-10-24	405.9
Liquid Chromatography	Reversed-phase	Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) (eluted)	2025-10-24	643.5
Liquid Chromatography	Reversed-phase	XBridge C18 3.5u 2.1x50 mm (eluted)	2025-10-24	579.2
Liquid Chromatography	Reversed-phase	Ascentis Express C18 (void)	2025-10-24	404.3
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	2059.0
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (void)	2025-10-24	89.5
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC (eluted)	2025-10-24	393.5
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	480.0
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-24	385.3
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	230.6
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	162.6
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (void)	2025-10-24	91.4
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-24	474.5
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	365.9
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	347.6
Liquid Chromatography	Reversed-phase	Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex (eluted)	2025-10-24	1268.1
Liquid Chromatography	Reversed-phase	Waters Atlantis T3 (2.1 x 150 mm, 5 um) (eluted)	2025-10-24	1209.5

Retention Indices

Not Available

Biological Properties

Cellular Locations

Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	1	Human feces; Human saliva	Unknown

Exposure Sources

Food Exposures

Other Exposures

Source Type	Data Source	Reference
Cosmetics	U.S. Environmental Protection Agency	CompTox
Domestics	U.S. Environmental Protection Agency	CompTox
Food Additive	U.S. Food and Drug Administration	FDA

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Gamma-Decalactone

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

145740

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Loscos N, Hernandez-Orte P, Cacho J, Ferreira V: Release and formation of varietal aroma compounds during alcoholic fermentation from nonfloral grape odorless flavor precursors fractions. J Agric Food Chem. 2007 Aug 8;55(16):6674-84. doi: 10.1021/jf0702343. Epub 2007 Jul 7. [PubMed:17616208 ]
Yannai, Shmuel (2004). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. Boca Raton: Chapman & Hall/CRC..

Showing metabocard for gamma-Decalactone (MMDBc0033643)

MOL for #<Metabolite:0x00007f9ad8579ae8>

3D MOL for #<Metabolite:0x00007f9ad8579ae8>

3D SDF for #<Metabolite:0x00007f9ad8579ae8>

3D-SDF for #<Metabolite:0x00007f9ad8579ae8>

PDB for #<Metabolite:0x00007f9ad8579ae8>

3D PDB for #<Metabolite:0x00007f9ad8579ae8>

SMILES for #<Metabolite:0x00007f9ad8579ae8>

INCHI for #<Metabolite:0x00007f9ad8579ae8>

Structure for #<Metabolite:0x00007f9ad8579ae8>

3D Structure for #<Metabolite:0x00007f9ad8579ae8>