ID: ALA5272334

Max Phase: Preclinical

Molecular Formula: C24H23N3O3

Molecular Weight: 401.47

Associated Items:

Representations

Canonical SMILES:  COc1ccc(Cc2nc3cc(NC(=O)[C@H](N)Cc4ccccc4)ccc3o2)cc1

Standard InChI:  InChI=1S/C24H23N3O3/c1-29-19-10-7-17(8-11-19)14-23-27-21-15-18(9-12-22(21)30-23)26-24(28)20(25)13-16-5-3-2-4-6-16/h2-12,15,20H,13-14,25H2,1H3,(H,26,28)/t20-/m1/s1

Standard InChI Key:  FWRWQIYOIQDTFK-HXUWFJFHSA-N

Associated Targets(non-human)

Mycobacterium tuberculosis 203094 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: 401.47Molecular Weight (Monoisotopic): 401.1739AlogP: 3.94#Rotatable Bonds: 7
Polar Surface Area: 90.38Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.87CX Basic pKa: 8.00CX LogP: 3.66CX LogD: 2.96
Aromatic Rings: 4Heavy Atoms: 30QED Weighted: 0.49Np Likeness Score: -0.85

References

1. Pepi MJ, Chacko S, Kopetz N, Boshoff HIM, Cuny GD, Hedstrom L..  (2023)  Nonhydrolyzable d‑phenylalanine-benzoxazole derivatives retain antitubercular activity.,  80  [PMID:36572353] [10.1016/j.bmcl.2022.129116]

Source