ID: ALA3116323

Max Phase: Preclinical

Molecular Formula: C19H24N4O3

Molecular Weight: 356.43

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCc1nc2c(N)nc3cc(C(=O)OC)ccc3c2n1C[C@H](C)O

Standard InChI:  InChI=1S/C19H24N4O3/c1-4-5-6-15-22-16-17(23(15)10-11(2)24)13-8-7-12(19(25)26-3)9-14(13)21-18(16)20/h7-9,11,24H,4-6,10H2,1-3H3,(H2,20,21)/t11-/m0/s1

Standard InChI Key:  MUXBNOKWIARUJW-NSHDSACASA-N

Associated Targets(Human)

TLR7 and TLR8 121 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

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: 356.43Molecular Weight (Monoisotopic): 356.1848AlogP: 2.68#Rotatable Bonds: 6
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: 4.06CX LogP: 2.85CX LogD: 2.85
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.66Np Likeness Score: -0.74

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