ID: ALA3116317

Max Phase: Preclinical

Molecular Formula: C17H20N4O3

Molecular Weight: 328.37

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COC(=O)c1ccc2c(c1)nc(N)c1nc(C)n(CC(C)(C)O)c12

Standard InChI:  InChI=1S/C17H20N4O3/c1-9-19-13-14(21(9)8-17(2,3)23)11-6-5-10(16(22)24-4)7-12(11)20-15(13)18/h5-7,23H,8H2,1-4H3,(H2,18,20)

Standard InChI Key:  WMYKXORUYKRBKG-UHFFFAOYSA-N

Associated Targets(Human)

Toll-like receptor 8 1853 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Toll-like receptor 7 2626 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

TLR7 and TLR8 70 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 328.37Molecular Weight (Monoisotopic): 328.1535AlogP: 2.03#Rotatable Bonds: 3
Polar Surface Area: 103.26Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 4.08CX LogP: 1.54CX LogD: 1.54
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.71Np Likeness Score: -0.59

References

1. Schiaffo CE, Shi C, Xiong Z, Olin M, Ohlfest JR, Aldrich CC, Ferguson DM..  (2014)  Structure-activity relationship analysis of imidazoquinolines with Toll-like receptors 7 and 8 selectivity and enhanced cytokine induction.,  57  (2): [PMID:24383475] [10.1021/jm4004957]

Source