5-(4-chlorophenyl)-9-(4-chlorophenylmethylene)-2-thioxo-6,7,8,9-tetrahydropyrimido[4,5-b]quinolin-4-one

ID: ALA520498

PubChem CID: 44582924

Max Phase: Preclinical

Molecular Formula: C24H17Cl2N3OS

Molecular Weight: 466.39

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  O=c1[nH]c(=S)[nH]c2nc3c(c(-c4ccc(Cl)cc4)c12)CCC/C3=C\c1ccc(Cl)cc1

Standard InChI:  InChI=1S/C24H17Cl2N3OS/c25-16-8-4-13(5-9-16)12-15-2-1-3-18-19(14-6-10-17(26)11-7-14)20-22(27-21(15)18)28-24(31)29-23(20)30/h4-12H,1-3H2,(H2,27,28,29,30,31)/b15-12+

Standard InChI Key:  WHHZQYBYWJCUON-NTCAYCPXSA-N

Molfile:  

     RDKit          2D

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   -1.4384   -5.0007    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -5.7184  -12.4168    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
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M  END

Associated Targets(non-human)

Kidney (678 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Brain (4256 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

Calculated Properties

Molecular Weight: 466.39Molecular Weight (Monoisotopic): 465.0469AlogP: 6.83#Rotatable Bonds: 2
Polar Surface Area: 61.54Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 8.52CX Basic pKa: 1.98CX LogP: 8.04CX LogD: 8.01
Aromatic Rings: 4Heavy Atoms: 31QED Weighted: 0.32Np Likeness Score: -0.77

References

1. El-Gazzar AB, Youssef MM, Youssef AM, Abu-Hashem AA, Badria FA..  (2009)  Design and synthesis of azolopyrimidoquinolines, pyrimidoquinazolines as anti-oxidant, anti-inflammatory and analgesic activities.,  44  (2): [PMID:18462840] [10.1016/j.ejmech.2008.03.022]

Source