(E)-2-(4-chlorostyryl)-N-(3-methoxypropyl)benzo[g]quinazolin-4-amine

ID: ALA3425698

PubChem CID: 118736572

Max Phase: Preclinical

Molecular Formula: C24H22ClN3O

Molecular Weight: 403.91

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  COCCCNc1nc(/C=C/c2ccc(Cl)cc2)nc2cc3ccccc3cc12

Standard InChI:  InChI=1S/C24H22ClN3O/c1-29-14-4-13-26-24-21-15-18-5-2-3-6-19(18)16-22(21)27-23(28-24)12-9-17-7-10-20(25)11-8-17/h2-3,5-12,15-16H,4,13-14H2,1H3,(H,26,27,28)/b12-9+

Standard InChI Key:  DURBPTOEENKJRD-FMIVXFBMSA-N

Molfile:  

     RDKit          2D

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   -2.5978    1.5002    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8968    0.7501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8968   -0.7501    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5978   -1.5002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2989   -0.7501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.5002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.5002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2989    0.7501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1981    1.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4967    0.7456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7980    1.4933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  -10.3962    1.4933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3962    2.9933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0972    3.7433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7981    2.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4355    3.5933    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.9017   -3.7496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9048   -5.2504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2806    0.7501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2806   -0.7501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5978   -1.5002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8968   -0.7501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8968    0.7501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5978    1.5002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2057   -5.9989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2087   -7.4998    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2488   -8.0983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
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  7 22  2  0
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  1 19  1  0
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 20 27  1  0
 27 28  1  0
 28 29  1  0
M  END

Alternative Forms

  1. Parent:

    ALA3425698

    ---

Associated Targets(non-human)

ftsZ Cell division protein ftsZ (97 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: 403.91Molecular Weight (Monoisotopic): 403.1451AlogP: 6.06#Rotatable Bonds: 7
Polar Surface Area: 47.04Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 4.08CX LogP: 6.25CX LogD: 6.25
Aromatic Rings: 4Heavy Atoms: 29QED Weighted: 0.30Np Likeness Score: -0.84

References

1. Nepomuceno GM, Chan KM, Huynh V, Martin KS, Moore JT, O'Brien TE, Pollo LA, Sarabia FJ, Tadeus C, Yao Z, Anderson DE, Ames JB, Shaw JT..  (2015)  Synthesis and Evaluation of Quinazolines as Inhibitors of the Bacterial Cell Division Protein FtsZ.,  (3): [PMID:25815151] [10.1021/ml500497s]

Source