ID: ALA3903175

Max Phase: Preclinical

Molecular Formula: C25H19N3O4

Molecular Weight: 425.44

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1nn(Cc2ccc(Oc3ccccc3)cc2)c2nc(-c3ccco3)cc(C(=O)O)c12

Standard InChI:  InChI=1S/C25H19N3O4/c1-16-23-20(25(29)30)14-21(22-8-5-13-31-22)26-24(23)28(27-16)15-17-9-11-19(12-10-17)32-18-6-3-2-4-7-18/h2-14H,15H2,1H3,(H,29,30)

Standard InChI Key:  GYXFBYPMROKCLN-UHFFFAOYSA-N

Associated Targets(non-human)

Induced myeloid leukemia cell differentiation protein Mcl-1 homolog 108 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Apoptosis regulator Bcl-2 542 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bcl-2-like protein 1 598 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: 425.44Molecular Weight (Monoisotopic): 425.1376AlogP: 5.54#Rotatable Bonds: 6
Polar Surface Area: 90.38Molecular Species: ACIDHBA: 6HBD: 1
#RO5 Violations: 1HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 3.51CX Basic pKa: 1.78CX LogP: 4.53CX LogD: 1.30
Aromatic Rings: 5Heavy Atoms: 32QED Weighted: 0.38Np Likeness Score: -1.51

References

1.  (2016)  Small molecule inhibitors of MCL-1 and uses thereof, 

Source

Source(1):