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(E,4S,5S)-3-Hexylidene-dihydro-4-hydroxy-5-methylfuran-2(3H)-one ID: ALA4203689
Chembl Id: CHEMBL4203689
PubChem CID: 142746544
Max Phase: Preclinical
Molecular Formula: C11H18O3
Molecular Weight: 198.26
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: CCCCC/C=C1/C(=O)O[C@@H](C)[C@H]1O
Standard InChI: InChI=1S/C11H18O3/c1-3-4-5-6-7-9-10(12)8(2)14-11(9)13/h7-8,10,12H,3-6H2,1-2H3/b9-7+/t8-,10+/m0/s1
Standard InChI Key: SNDXBSGFPBRWRF-BJHGEIEHSA-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: 198.26Molecular Weight (Monoisotopic): 198.1256AlogP: 1.80#Rotatable Bonds: 4Polar Surface Area: 46.53Molecular Species: NEUTRALHBA: 3HBD: 1#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0CX Acidic pKa: 13.31CX Basic pKa: CX LogP: 2.50CX LogD: 2.50Aromatic Rings: 0Heavy Atoms: 14QED Weighted: 0.43Np Likeness Score: 2.41
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 ]