2,5-bis(3-methoxy-4-(tetrahydro-2H-pyran-3-yloxy)benzylidene)cyclopentanone

ID: ALA1089909

PubChem CID: 46886130

Max Phase: Preclinical

Molecular Formula: C31H36O7

Molecular Weight: 520.62

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  COc1cc(/C=C2\CC/C(=C\c3ccc(OC4CCCOC4)c(OC)c3)C2=O)ccc1OC1CCCOC1

Standard InChI:  InChI=1S/C31H36O7/c1-33-29-17-21(7-11-27(29)37-25-5-3-13-35-19-25)15-23-9-10-24(31(23)32)16-22-8-12-28(30(18-22)34-2)38-26-6-4-14-36-20-26/h7-8,11-12,15-18,25-26H,3-6,9-10,13-14,19-20H2,1-2H3/b23-15+,24-16+

Standard InChI Key:  OZBZOZIPHASEQY-DFEHQXHXSA-N

Molfile:  

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M  END

Associated Targets(Human)

HSD17B3 Tchem Estradiol 17-beta-dehydrogenase 3 (821 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hsd17b3 Testosterone 17-beta-dehydrogenase 3 (232 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: 520.62Molecular Weight (Monoisotopic): 520.2461AlogP: 5.65#Rotatable Bonds: 8
Polar Surface Area: 72.45Molecular Species: NEUTRALHBA: 7HBD:
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): #RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 5.36CX LogD: 5.36
Aromatic Rings: 2Heavy Atoms: 38QED Weighted: 0.42Np Likeness Score: 0.00

References

1. Hu GX, Liang G, Chu Y, Li X, Lian QQ, Lin H, He Y, Huang Y, Hardy DO, Ge RS..  (2010)  Curcumin derivatives inhibit testicular 17beta-hydroxysteroid dehydrogenase 3.,  20  (8): [PMID:20346654] [10.1016/j.bmcl.2010.02.089]

Source