ID: ALA3343820

Max Phase: Preclinical

Molecular Formula: C25H24ClNO4Se

Molecular Weight: 480.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CN(C)CCOc1ccc(C(=O)c2[se]c3cc(O)ccc3c2-c2ccc(O)cc2)cc1.Cl

Standard InChI:  InChI=1S/C25H23NO4Se.ClH/c1-26(2)13-14-30-20-10-5-17(6-11-20)24(29)25-23(16-3-7-18(27)8-4-16)21-12-9-19(28)15-22(21)31-25;/h3-12,15,27-28H,13-14H2,1-2H3;1H

Standard InChI Key:  ALZCMKWBMQKXKY-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: 480.42Molecular Weight (Monoisotopic): 481.0792AlogP: #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