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

ID: ALA1090244

PubChem CID: 46886113

Max Phase: Preclinical

Molecular Formula: C29H32O5

Molecular Weight: 460.57

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  O=C1/C(=C/c2ccc(OC3CCCOC3)cc2)CC/C1=C\c1ccc(OC2CCCOC2)cc1

Standard InChI:  InChI=1S/C29H32O5/c30-29-23(17-21-5-11-25(12-6-21)33-27-3-1-15-31-19-27)9-10-24(29)18-22-7-13-26(14-8-22)34-28-4-2-16-32-20-28/h5-8,11-14,17-18,27-28H,1-4,9-10,15-16,19-20H2/b23-17+,24-18+

Standard InChI Key:  RFWQDJMWKUXTKI-GJHDBBOXSA-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: 460.57Molecular Weight (Monoisotopic): 460.2250AlogP: 5.63#Rotatable Bonds: 6
Polar Surface Area: 53.99Molecular Species: NEUTRALHBA: 5HBD:
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): #RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.67CX LogD: 5.67
Aromatic Rings: 2Heavy Atoms: 34QED Weighted: 0.52Np Likeness Score: -0.07

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