1,5-bis(3-methoxy-4-(tetrahydro-2H-pyran-3-yloxy)phenyl)penta-1,4-dien-3-one

ID: ALA1091227

PubChem CID: 46886165

Max Phase: Preclinical

Molecular Formula: C29H34O7

Molecular Weight: 494.58

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  COc1cc(/C=C/C(=O)/C=C/c2ccc(OC3CCCOC3)c(OC)c2)ccc1OC1CCCOC1

Standard InChI:  InChI=1S/C29H34O7/c1-31-28-17-21(9-13-26(28)35-24-5-3-15-33-19-24)7-11-23(30)12-8-22-10-14-27(29(18-22)32-2)36-25-6-4-16-34-20-25/h7-14,17-18,24-25H,3-6,15-16,19-20H2,1-2H3/b11-7+,12-8+

Standard InChI Key:  RFKDCBFGFBWCFB-MKICQXMISA-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: 494.58Molecular Weight (Monoisotopic): 494.2305AlogP: 5.12#Rotatable Bonds: 10
Polar Surface Area: 72.45Molecular Species: NEUTRALHBA: 7HBD:
#RO5 Violations: 1HBA (Lipinski): 7HBD (Lipinski): #RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.03CX LogD: 5.03
Aromatic Rings: 2Heavy Atoms: 36QED Weighted: 0.42Np Likeness Score: 0.24

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