ID: ALA476623

Max Phase: Preclinical

Molecular Formula: C24H26O3

Molecular Weight: 362.47

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): 2,6-Bis(4-Ethoxybenzylidene)Cyclohexanone
Synonyms from Alternative Forms(1):

    Canonical SMILES:  CCOc1ccc(/C=C2\CCC/C(=C\c3ccc(OCC)cc3)C2=O)cc1

    Standard InChI:  InChI=1S/C24H26O3/c1-3-26-22-12-8-18(9-13-22)16-20-6-5-7-21(24(20)25)17-19-10-14-23(15-11-19)27-4-2/h8-17H,3-7H2,1-2H3/b20-16+,21-17+

    Standard InChI Key:  KBKAXUOCBIAHQQ-NWILIBCHSA-N

    Associated Targets(Human)

    KB 17409 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Estradiol 17-beta-dehydrogenase 3 821 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    11-beta-hydroxysteroid dehydrogenase 1 5910 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    11-beta-hydroxysteroid dehydrogenase 2 1168 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Associated Targets(non-human)

    Testosterone 17-beta-dehydrogenase 3 232 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    11-beta-hydroxysteroid dehydrogenase 1 202 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    11-beta-hydroxysteroid dehydrogenase 2 82 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

    Properties

    Molecular Weight: 362.47Molecular Weight (Monoisotopic): 362.1882AlogP: 5.70#Rotatable Bonds: 6
    Polar Surface Area: 35.53Molecular Species: NEUTRALHBA: 3HBD: 0
    #RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
    CX Acidic pKa: CX Basic pKa: CX LogP: 6.00CX LogD: 6.00
    Aromatic Rings: 2Heavy Atoms: 27QED Weighted: 0.62Np Likeness Score: -0.42

    References

    1. Liang G, Shao L, Wang Y, Zhao C, Chu Y, Xiao J, Zhao Y, Li X, Yang S..  (2009)  Exploration and synthesis of curcumin analogues with improved structural stability both in vitro and in vivo as cytotoxic agents.,  17  (6): [PMID:19243951] [10.1016/j.bmc.2008.10.044]
    2. 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]
    3. Lin H, Hu GX, Guo J, Ge Y, Liang G, Lian QQ, Chu Y, Yuan X, Huang P, Ge RS..  (2013)  Mono-carbonyl curcumin analogues as 11β-hydroxysteroid dehydrogenase 1 inhibitors.,  23  (15): [PMID:23800686] [10.1016/j.bmcl.2013.05.080]

    Source