ID: ALA4761141

Max Phase: Preclinical

Molecular Formula: C24H20FN3O6S

Molecular Weight: 497.50

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1ccc(Cc2cn(C)c3ccc([N+](=O)[O-])cc23)cc1C(=O)NS(=O)(=O)c1ccc(F)cc1

Standard InChI:  InChI=1S/C24H20FN3O6S/c1-27-14-16(20-13-18(28(30)31)6-9-22(20)27)11-15-3-10-23(34-2)21(12-15)24(29)26-35(32,33)19-7-4-17(25)5-8-19/h3-10,12-14H,11H2,1-2H3,(H,26,29)

Standard InChI Key:  PSZLCCNFAPPZTO-UHFFFAOYSA-N

Associated Targets(non-human)

Porphyromonas gingivalis 651 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 497.50Molecular Weight (Monoisotopic): 497.1057AlogP: 3.94#Rotatable Bonds: 7
Polar Surface Area: 120.54Molecular Species: ACIDHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.20CX Basic pKa: CX LogP: 4.76CX LogD: 3.82
Aromatic Rings: 4Heavy Atoms: 35QED Weighted: 0.30Np Likeness Score: -1.31

References

1. Howard KC,Gonzalez OA,Garneau-Tsodikova S.  (2020)  Second Generation of Zafirlukast Derivatives with Improved Activity against the Oral Pathogen Porphyromonas gingivalis.,  11  (10): [PMID:33062172] [10.1021/acsmedchemlett.9b00614]

Source