ID: ALA4457485

Max Phase: Preclinical

Molecular Formula: C38H23F4N9O

Molecular Weight: 697.66

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Fc1ccc(-c2nc(-c3cccc(-n4cc(-c5nc(Nc6ccccc6F)nc(Nc6ccccc6F)n5)nn4)c3)oc2-c2ccc(F)cc2)cc1

Standard InChI:  InChI=1S/C38H23F4N9O/c39-25-16-12-22(13-17-25)33-34(23-14-18-26(40)19-15-23)52-36(45-33)24-6-5-7-27(20-24)51-21-32(49-50-51)35-46-37(43-30-10-3-1-8-28(30)41)48-38(47-35)44-31-11-4-2-9-29(31)42/h1-21H,(H2,43,44,46,47,48)

Standard InChI Key:  CYMDGQVQSFQHOZ-UHFFFAOYSA-N

Associated Targets(non-human)

Streptococcus gordonii 131 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

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: 697.66Molecular Weight (Monoisotopic): 697.1962AlogP: 9.15#Rotatable Bonds: 9
Polar Surface Area: 119.47Molecular Species: NEUTRALHBA: 10HBD: 2
#RO5 Violations: 2HBA (Lipinski): 10HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 10.33CX Basic pKa: CX LogP: 10.10CX LogD: 10.10
Aromatic Rings: 8Heavy Atoms: 52QED Weighted: 0.14Np Likeness Score: -1.34

References

1. Patil PC, Tan J, Demuth DR, Luzzio FA..  (2019)  'Second-generation' 1,2,3-triazole-based inhibitors of Porphyromonas gingivalis adherence to oral streptococci and biofilm formation.,  10  (2): [PMID:30881614] [10.1039/C8MD00405F]

Source