4-(1-(1-(4-Methoxybenzoyl)piperidin-4-yl)-1H-imidazol-5-yl)-phenyl 3-Cyanobenzenesulfonate

ID: ALA4531079

PubChem CID: 142737915

Max Phase: Preclinical

Molecular Formula: C29H26N4O5S

Molecular Weight: 542.62

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1ccc(C(=O)N2CCC(n3cncc3-c3ccc(OS(=O)(=O)c4cccc(C#N)c4)cc3)CC2)cc1

Standard InChI:  InChI=1S/C29H26N4O5S/c1-37-25-9-7-23(8-10-25)29(34)32-15-13-24(14-16-32)33-20-31-19-28(33)22-5-11-26(12-6-22)38-39(35,36)27-4-2-3-21(17-27)18-30/h2-12,17,19-20,24H,13-16H2,1H3

Standard InChI Key:  KFKLUYHZCSGRBR-UHFFFAOYSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA4531079

    ---

Associated Targets(Human)

P2RX7 Tchem P2X purinoceptor 7 (5534 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

Calculated Properties

Molecular Weight: 542.62Molecular Weight (Monoisotopic): 542.1624AlogP: 4.68#Rotatable Bonds: 7
Polar Surface Area: 114.52Molecular Species: NEUTRALHBA: 8HBD:
#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): #RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 6.44CX LogP: 3.67CX LogD: 3.64
Aromatic Rings: 4Heavy Atoms: 39QED Weighted: 0.31Np Likeness Score: -1.25

References

1. Park JH, Williams DR, Lee JH, Lee SD, Lee JH, Ko H, Lee GE, Kim S, Lee JM, Abdelrahman A, Müller CE, Jung DW, Kim YC..  (2016)  Potent Suppressive Effects of 1-Piperidinylimidazole Based Novel P2X7 Receptor Antagonists on Cancer Cell Migration and Invasion.,  59  (16): [PMID:27427902] [10.1021/acs.jmedchem.5b01690]

Source