ID: ALA5275869

Max Phase: Preclinical

Molecular Formula: C37H47F7N4O7

Molecular Weight: 564.75

Associated Items:

Representations

Canonical SMILES:  O=C(O)C(F)(F)F.O=C(O)C(F)(F)F.O=C(c1ccc(OC2CCNCC2)c(C2CCCCC2)c1)N1CCC(Oc2cc(F)cc(N3CCNCC3)c2)CC1

Standard InChI:  InChI=1S/C33H45FN4O3.2C2HF3O2/c34-26-21-27(37-18-14-36-15-19-37)23-30(22-26)40-29-10-16-38(17-11-29)33(39)25-6-7-32(41-28-8-12-35-13-9-28)31(20-25)24-4-2-1-3-5-24;2*3-2(4,5)1(6)7/h6-7,20-24,28-29,35-36H,1-5,8-19H2;2*(H,6,7)

Standard InChI Key:  JGCMQALWSTZHLW-UHFFFAOYSA-N

Associated Targets(Human)

beta-catenin-B-cell lymphoma 9 protein complex 525 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 564.75Molecular Weight (Monoisotopic): 564.3476AlogP: 5.10#Rotatable Bonds: 7
Polar Surface Area: 66.07Molecular Species: BASEHBA: 6HBD: 2
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 9.87CX LogP: 4.24CX LogD: 0.42
Aromatic Rings: 2Heavy Atoms: 41QED Weighted: 0.49Np Likeness Score: -0.72

References

1. Li Z, Zhang M, Teuscher KB, Ji H..  (2021)  Discovery of 1-Benzoyl 4-Phenoxypiperidines as Small-Molecule Inhibitors of the β-Catenin/B-Cell Lymphoma 9 Protein-Protein Interaction.,  64  (15.0): [PMID:34270257] [10.1021/acs.jmedchem.1c00596]

Source