(3Z,3'E,4S,4'S,5S,5'S)-3,3'-(decane-1,10-diylidene)bis(4-hydroxy-5-methyldihydrofuran-2(3H)-one)

ID: ALA5267528

Chembl Id: CHEMBL5267528

Max Phase: Preclinical

Molecular Formula: C20H30O6

Molecular Weight: 366.45

Associated Items:

Names and Identifiers

Canonical SMILES:  C[C@@H]1OC(=O)/C(=C\CCCCCCCC/C=C2/C(=O)O[C@@H](C)[C@H]2O)[C@@H]1O

Standard InChI:  InChI=1S/C20H30O6/c1-13-17(21)15(19(23)25-13)11-9-7-5-3-4-6-8-10-12-16-18(22)14(2)26-20(16)24/h11-14,17-18,21-22H,3-10H2,1-2H3/b15-11-,16-12+/t13-,14-,17+,18+/m0/s1

Standard InChI Key:  KCJDQTLZAGPZQB-FBPJLDJHSA-N

Alternative Forms

  1. Parent:

    ALA5267528

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Associated Targets(Human)

PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 366.45Molecular Weight (Monoisotopic): 366.2042AlogP: 2.57#Rotatable Bonds: 9
Polar Surface Area: 93.06Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 13.01CX Basic pKa: CX LogP: 3.64CX LogD: 3.64
Aromatic Rings: Heavy Atoms: 26QED Weighted: 0.37Np Likeness Score: 1.29

References

1. 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