ID: ALA4642371

Max Phase: Preclinical

Molecular Formula: C19H23N5

Molecular Weight: 321.43

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCCCc1nc2c(N)nc3cc(C#N)ccc3c2n1CC(C)C

Standard InChI:  InChI=1S/C19H23N5/c1-4-5-6-16-23-17-18(24(16)11-12(2)3)14-8-7-13(10-20)9-15(14)22-19(17)21/h7-9,12H,4-6,11H2,1-3H3,(H2,21,22)

Standard InChI Key:  FOLKUNKWCIRWGQ-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)

Toll-like receptor 7/8 156 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: 321.43Molecular Weight (Monoisotopic): 321.1953AlogP: 4.04#Rotatable Bonds: 5
Polar Surface Area: 80.52Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.59CX LogP: 4.22CX LogD: 4.22
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.77Np Likeness Score: -1.23

References

1. Hunt JR, Kleindl PA, Moulder KR, Prisinzano TE, Forrest ML..  (2020)  Further exploration of the structure-activity relationship of imidazoquinolines; identification of potent C7-substituted imidazoquinolines.,  30  (2): [PMID:31784317] [10.1016/j.bmcl.2019.126788]

Source