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(E,4S,5S)-3-Butylidene-dihydro-4-hydroxy-5-methylfuran-2(3H)-one ID: ALA4215365
Chembl Id: CHEMBL4215365
PubChem CID: 142746547
Max Phase: Preclinical
Molecular Formula: C9H14O3
Molecular Weight: 170.21
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: CCC/C=C1/C(=O)O[C@@H](C)[C@H]1O
Standard InChI: InChI=1S/C9H14O3/c1-3-4-5-7-8(10)6(2)12-9(7)11/h5-6,8,10H,3-4H2,1-2H3/b7-5+/t6-,8+/m0/s1
Standard InChI Key: WQLMRKLWOQAVAU-MGRRSFKLSA-N
Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 170.21Molecular Weight (Monoisotopic): 170.0943AlogP: 1.02#Rotatable Bonds: 2Polar Surface Area: 46.53Molecular Species: NEUTRALHBA: 3HBD: 1#RO5 Violations: ┄HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): ┄CX Acidic pKa: 13.31CX Basic pKa: ┄CX LogP: 1.61CX LogD: 1.61Aromatic Rings: ┄Heavy Atoms: 12QED Weighted: 0.50Np Likeness Score: 2.73
References 1. Lee J, Mailar K, Yoo OK, Choi WJ, Keum YS.. (2018) Marliolide inhibits skin carcinogenesis by activating NRF2/ARE to induce heme oxygenase-1., 150 [PMID:29525432 ] [10.1016/j.ejmech.2018.02.068 ] 2. Ahn S, Basavana Gowda MK, Lee M, Masagalli JN, Mailar K, Choi WJ, Noh M.. (2020) Novel linked butanolide dimer compounds increase adiponectin production during adipogenesis in human mesenchymal stem cells through peroxisome proliferator-activated receptor γ modulation., 187 [PMID:31865018 ] [10.1016/j.ejmech.2019.111969 ]