ID: ALA3091633

Max Phase: Preclinical

Molecular Formula: C23H21NO6

Molecular Weight: 407.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1nc(Cc2cccc(Oc3ccccc3)c2)c(CCC(=O)O)c(C(=O)O)c1O

Standard InChI:  InChI=1S/C23H21NO6/c1-14-22(27)21(23(28)29)18(10-11-20(25)26)19(24-14)13-15-6-5-9-17(12-15)30-16-7-3-2-4-8-16/h2-9,12,27H,10-11,13H2,1H3,(H,25,26)(H,28,29)

Standard InChI Key:  XICUGIVKIBHPFC-UHFFFAOYSA-N

Associated Targets(Human)

P2X purinoceptor 7 5534 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

P2X purinoceptor 3 1991 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

P2X purinoceptor 1 68 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: 407.42Molecular Weight (Monoisotopic): 407.1369AlogP: 4.19#Rotatable Bonds: 8
Polar Surface Area: 116.95Molecular Species: ACIDHBA: 5HBD: 3
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 2.72CX Basic pKa: 3.40CX LogP: 3.69CX LogD: -2.25
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.51Np Likeness Score: -0.09

References

1. Cho JH, Jung KY, Jung Y, Kim MH, Ko H, Park CS, Kim YC..  (2013)  Design and synthesis of potent and selective P2X₃ receptor antagonists derived from PPADS as potential pain modulators.,  70  [PMID:24246730] [10.1016/j.ejmech.2013.10.026]

Source