(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

Alternative Forms

  1. Parent:

    ALA4215365

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Associated Targets(Human)

KEAP1 Tclin Kelch-like ECH-associated protein 1 (1736 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARA Tclin Peroxisome proliferator-activated receptor alpha (9197 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARD Tchem Peroxisome proliferator-activated receptor delta (6293 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 170.21Molecular Weight (Monoisotopic): 170.0943AlogP: 1.02#Rotatable Bonds: 2
Polar 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: 1.61
Aromatic 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]

Source