ID: ALA2397603

Max Phase: Preclinical

Molecular Formula: C25H25NO3

Molecular Weight: 387.48

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCC(=O)Nc1ccc(/C(=C(\CC)c2ccc(O)cc2)c2ccc(O)cc2)cc1

Standard InChI:  InChI=1S/C25H25NO3/c1-3-23(17-7-13-21(27)14-8-17)25(19-9-15-22(28)16-10-19)18-5-11-20(12-6-18)26-24(29)4-2/h5-16,27-28H,3-4H2,1-2H3,(H,26,29)/b25-23-

Standard InChI Key:  BKSHYWRYPXOKGP-BZZOAKBMSA-N

Associated Targets(Human)

DNA topoisomerase I 7553 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

DNA topoisomerase II alpha 6317 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MSTO-211H 316 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HeLa 62764 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MCF7 126967 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: 387.48Molecular Weight (Monoisotopic): 387.1834AlogP: 5.82#Rotatable Bonds: 6
Polar Surface Area: 69.56Molecular Species: NEUTRALHBA: 3HBD: 3
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski): 1
CX Acidic pKa: 8.57CX Basic pKa: CX LogP: 5.82CX LogD: 5.79
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.47Np Likeness Score: -0.34

References

1. Christodoulou MS, Fokialakis N, Passarella D, García-Argáez AN, Gia OM, Pongratz I, Dalla Via L, Haroutounian SA..  (2013)  Synthesis and biological evaluation of novel tamoxifen analogues.,  21  (14): [PMID:23735829] [10.1016/j.bmc.2013.05.012]

Source