Basic Info

Common NameGamma-Butyrolactone(F04716)
2D Structure
Description

One of the furans with a carbonyl thereby forming a cyclic lactone. It is an endogenous compound made from gamma-aminobutyrate and is the precursor of gamma-hydroxybutyrate. It is also used as a pharmacological agent and solvent.

FRCD IDF04716
CAS Number96-48-0
PubChem CID7302
FormulaC4H6O2
IUPAC Name

oxolan-2-one

InChI Key

YEJRWHAVMIAJKC-UHFFFAOYSA-N

InChI

InChI=1S/C4H6O2/c5-4-2-1-3-6-4/h1-3H2

Canonical SMILES

C1CC(=O)OC1

Isomeric SMILES

C1CC(=O)OC1

WikipediaGamma-Butyrolactone
Synonyms
        
            gamma-Butyrolactone
        
            96-48-0
        
            4-Butyrolactone
        
            dihydrofuran-2(3H)-one
        
            BUTYROLACTONE
        
            4-Butanolide
        
            1,4-Butanolide
        
            2-Oxolanone
        
            4-Hydroxybutyric acid lactone
        
            4-Deoxytetronic acid
        
Classifies
                

                  
                    Predicted: Animal Toxin
                  

                
        
Update DateNov 13, 2018 17:07

Chemical Taxonomy

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassLactones
SubclassGamma butyrolactones
Intermediate Tree NodesNot available
Direct ParentGamma butyrolactones
Alternative Parents
Molecular FrameworkAliphatic heteromonocyclic compounds
SubstituentsGamma butyrolactone - Tetrahydrofuran - Carboxylic acid ester - Oxacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as gamma butyrolactones. These 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 ketone group on the carbon adjacent to the oxygen atom.

Properties

Property NameProperty Value
Molecular Weight86.09
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Complexity67.9
Monoisotopic Mass86.037
Exact Mass86.037
XLogP-0.6
Formal Charge0
Heavy Atom Count6
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

ADMET

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.9837
Human Intestinal AbsorptionHIA+0.9894
Caco-2 PermeabilityCaco2+0.6346
P-glycoprotein SubstrateNon-substrate0.8319
P-glycoprotein InhibitorNon-inhibitor0.9572
Non-inhibitor0.9896
Renal Organic Cation TransporterNon-inhibitor0.8004
Distribution
Subcellular localizationMitochondria0.6416
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8264
CYP450 2D6 SubstrateNon-substrate0.8742
CYP450 3A4 SubstrateNon-substrate0.7067
CYP450 1A2 InhibitorNon-inhibitor0.8028
CYP450 2C9 InhibitorNon-inhibitor0.8599
CYP450 2D6 InhibitorNon-inhibitor0.9398
CYP450 2C19 InhibitorNon-inhibitor0.8187
CYP450 3A4 InhibitorNon-inhibitor0.9841
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9591
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9180
Non-inhibitor0.9700
AMES ToxicityNon AMES toxic0.9480
CarcinogensNon-carcinogens0.9049
Fish ToxicityLow FHMT0.8394
Tetrahymena Pyriformis ToxicityLow TPT0.8364
Honey Bee ToxicityHigh HBT0.7581
BiodegradationReady biodegradable0.9342
Acute Oral ToxicityIII0.8098
Carcinogenicity (Three-class)Non-required0.6946

Model Value Unit
Absorption
Aqueous solubility1.0072LogS
Caco-2 Permeability1.6053LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.7154LD50, mol/kg
Fish Toxicity2.5087pLC50, mg/L
Tetrahymena Pyriformis Toxicity-1.5950pIGC50, ug/L

References

TitleJournalDatePubmed ID
Streptogramins - two are better than one!Int J Med Microbiol2014 Jan24119565
In vivo functions of the gamma-butyrolactone autoregulator receptor inStreptomyces ambofaciens producing spiramycin.Biotechnol Lett2008 May18058070
Inverse gas chromatographic evaluation of the influence of soy protein on thebinding of selected butter flavor compounds in a wheat soda cracker system.J Agric Food Chem2006 Jul 2616848540
Cloning and in vivo functional analysis by disruption of a gene encoding thegamma-butyrolactone autoregulator receptor from Streptomyces natalensis.Arch Microbiol2005 Dec16228193
The role of GABAB receptors in the discriminative stimulus effects of gamma-hydroxybutyrate in rats: time course and antagonism studies.J Pharmacol Exp Ther2003 May12606639
Adverse events, including death, associated with the use of 1,4-butanediol.N Engl J Med2001 Jan 1111150358
Volatile compounds produced from monosodium glutamate in common food cooking.J Agric Food Chem2000 Jun10888564

Targets

General Function:
Zinc ion binding
Specific Function:
Nuclear receptor that binds DNA as a monomer to ROR response elements (RORE) containing a single core motif half-site 5'-AGGTCA-3' preceded by a short A-T-rich sequence. Key regulator of cellular differentiation, immunity, peripheral circadian rhythm as well as lipid, steroid, xenobiotics and glucose metabolism. Considered to have intrinsic transcriptional activity, have some natural ligands like oxysterols that act as agonists (25-hydroxycholesterol) or inverse agonists (7-oxygenated sterols), enhancing or repressing the transcriptional activity, respectively. Recruits distinct combinations of cofactors to target gene regulatory regions to modulate their transcriptional expression, depending on the tissue, time and promoter contexts. Regulates the circadian expression of clock genes such as CRY1, ARNTL/BMAL1 and NR1D1 in peripheral tissues and in a tissue-selective manner. Competes with NR1D1 for binding to their shared DNA response element on some clock genes such as ARNTL/BMAL1, CRY1 and NR1D1 itself, resulting in NR1D1-mediated repression or RORC-mediated activation of the expression, leading to the circadian pattern of clock genes expression. Therefore influences the period length and stability of the clock. Involved in the regulation of the rhythmic expression of genes involved in glucose and lipid metabolism, including PLIN2 and AVPR1A. Negative regulator of adipocyte differentiation through the regulation of early phase genes expression, such as MMP3. Controls adipogenesis as well as adipocyte size and modulates insulin sensitivity in obesity. In liver, has specific and redundant functions with RORA as positive or negative modulator of expression of genes encoding phase I and Phase II proteins involved in the metabolism of lipids, steroids and xenobiotics, such as SULT1E1. Also plays also a role in the regulation of hepatocyte glucose metabolism through the regulation of G6PC and PCK1. Regulates the rhythmic expression of PROX1 and promotes its nuclear localization (By similarity). Plays an indispensable role in the induction of IFN-gamma dependent anti-mycobacterial systemic immunity (PubMed:26160376).Isoform 2: Essential for thymopoiesis and the development of several secondary lymphoid tissues, including lymph nodes and Peyer's patches. Required for the generation of LTi (lymphoid tissue inducer) cells. Regulates thymocyte survival through DNA-binding on ROREs of target gene promoter regions and recruitment of coactivaros via the AF-2. Also plays a key role, downstream of IL6 and TGFB and synergistically with RORA, for lineage specification of uncommitted CD4(+) T-helper (T(H)) cells into T(H)17 cells, antagonizing the T(H)1 program. Probably regulates IL17 and IL17F expression on T(H) by binding to the essential enhancer conserved non-coding sequence 2 (CNS2) in the IL17-IL17F locus. May also play a role in the pre-TCR activation cascade leading to the maturation of alpha/beta T-cells and may participate in the regulation of DNA accessibility in the TCR-J(alpha) locus.
Gene Name:
RORC
Uniprot ID:
P51449
Molecular Weight:
58194.845 Da
References
  1. Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]