ID: ALA4442966

Max Phase: Preclinical

Molecular Formula: C18H19N3O4

Molecular Weight: 341.37

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC(C)CC(C)(O)c1cn(C2=CC(=O)c3cccc(O)c3C2=O)nn1

Standard InChI:  InChI=1S/C18H19N3O4/c1-10(2)8-18(3,25)15-9-21(20-19-15)12-7-14(23)11-5-4-6-13(22)16(11)17(12)24/h4-7,9-10,22,25H,8H2,1-3H3

Standard InChI Key:  ZAWKKFCMFOXGOT-UHFFFAOYSA-N

Associated Targets(non-human)

P2X purinoceptor 7 169 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Peritoneal macrophage 1554 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: 341.37Molecular Weight (Monoisotopic): 341.1376AlogP: 2.16#Rotatable Bonds: 4
Polar Surface Area: 105.31Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.14CX Basic pKa: CX LogP: 2.90CX LogD: 2.83
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.88Np Likeness Score: 0.35

References

1. Pacheco PAF, Galvão RMS, Faria AFM, Von Ranke NL, Rangel MS, Ribeiro TM, Bello ML, Rodrigues CR, Ferreira VF, da Rocha DR, Faria RX..  (2019)  8-Hydroxy-2-(1H-1,2,3-triazol-1-yl)-1,4-naphtoquinone derivatives inhibited P2X7 Receptor-Induced dye uptake into murine Macrophages.,  27  (8): [PMID:30528164] [10.1016/j.bmc.2018.11.036]

Source