ID: ALA3343819

Max Phase: Preclinical

Molecular Formula: C27H24ClF2NO3Se

Molecular Weight: 526.44

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cl.O=C(c1ccc(OCCN2CCOCC2)cc1)c1c(-c2ccc(F)cc2)[se]c2cc(F)ccc12

Standard InChI:  InChI=1S/C27H23F2NO3Se.ClH/c28-20-5-1-19(2-6-20)27-25(23-10-7-21(29)17-24(23)34-27)26(31)18-3-8-22(9-4-18)33-16-13-30-11-14-32-15-12-30;/h1-10,17H,11-16H2;1H

Standard InChI Key:  RYKSDCYQFHVQBD-UHFFFAOYSA-N

Associated Targets(Human)

MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

MG-22A (171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 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: 526.44Molecular Weight (Monoisotopic): 527.0811AlogP: #Rotatable Bonds:
Polar Surface Area: Molecular Species: HBA: HBD:
#RO5 Violations: HBA (Lipinski): HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: CX LogD:
Aromatic Rings: Heavy Atoms: QED Weighted: Np Likeness Score:

References

1. Arsenyan P, Paegle E, Domracheva I, Gulbe A, Kanepe-Lapsa I, Shestakova I..  (2014)  Selenium analogues of raloxifene as promising antiproliferative agents in treatment of breast cancer.,  87  [PMID:25282270] [10.1016/j.ejmech.2014.09.088]

Source