ID: ALA5186157

Max Phase: Preclinical

Molecular Formula: C14H13N3O

Molecular Weight: 239.28

Associated Items:

Representations

Canonical SMILES:  COc1ccc(-c2nc3ccccn3c2N)cc1

Standard InChI:  InChI=1S/C14H13N3O/c1-18-11-7-5-10(6-8-11)13-14(15)17-9-3-2-4-12(17)16-13/h2-9H,15H2,1H3

Standard InChI Key:  ITUOXVCQWLKCGP-UHFFFAOYSA-N

Associated Targets(Human)

Toll-like receptor 9 943 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Toll-like receptor 7 2626 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: 239.28Molecular Weight (Monoisotopic): 239.1059AlogP: 2.59#Rotatable Bonds: 2
Polar Surface Area: 52.55Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 6.74CX LogP: 1.90CX LogD: 1.81
Aromatic Rings: 3Heavy Atoms: 18QED Weighted: 0.75Np Likeness Score: -1.63

References

1. Das N, Bandopadhyay P, Roy S, Sinha BP, Dastidar UG, Rahaman O, Pal S, Ganguly D, Talukdar A..  (2022)  Development, Optimization, and In Vivo Validation of New Imidazopyridine Chemotypes as Dual TLR7/TLR9 Antagonists through Activity-Directed Sequential Incorporation of Relevant Structural Subunits.,  65  (17.0): [PMID:35959635] [10.1021/acs.jmedchem.2c00386]

Source