Chemical Component Summary | |
|---|---|
| Name | GAMMA-BUTYROLACTONE |
| Synonyms | DIHYDROFURAN-2(3H)-ONE |
| Identifiers | oxolan-2-one |
| Formula | C4 H6 O2 |
| Molecular Weight | 86.089 |
| Type | NON-POLYMER |
| Isomeric SMILES | C1CC(=O)OC1 |
| InChI | InChI=1S/C4H6O2/c5-4-2-1-3-6-4/h1-3H2 |
| InChIKey | YEJRWHAVMIAJKC-UHFFFAOYSA-N |
Chemical Details | |
|---|---|
| Formal Charge | 0 |
| Atom Count | 12 |
| Chiral Atom Count | 0 |
| Bond Count | 12 |
| Aromatic Bond Count | 0 |
Drug Info: DrugBank
| DrugBank ID | DB04699? |
|---|---|
| Name | gamma-Butyrolactone |
| Groups |
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| 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. |
| Synonyms |
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| Categories |
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| CAS number | 96-48-0 |
Drug Targets
| Name | Target Sequence | Pharmacological Action | Actions |
|---|---|---|---|
| O-GlcNAcase NagJ | MKRKMLKRLLTSAFACMFIANGLITTTVRAVGPKTGEENQVLVPNLNPTP... | unknown |
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison
T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS.
Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682
Related Resource References
| Resource Name | Reference |
|---|---|
| PubChem | 7302 |
| ChEMBL | CHEMBL95681 |
| ChEBI | CHEBI:42639 |
| CCDC/CSD | BICGUP, LUBMUS, AHULIB, FOMNAX, TITDAE, EYUHOV, GUZTOK, ZULJUO, QAHJOC, PECYIJ, QAVKIL, QAVJUW, KAWSAG |
| COD | 2100197 |
