(E)-N1-(2-(4-chlorostyryl)-6-(thiophen-2-yl)quinazolin-4-yl)-N2,N2-dimethylethane-1,2-diamine

ID: ALA3425614

PubChem CID: 118736493

Max Phase: Preclinical

Molecular Formula: C24H23ClN4S

Molecular Weight: 435.00

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  CN(C)CCNc1nc(/C=C/c2ccc(Cl)cc2)nc2ccc(-c3cccs3)cc12

Standard InChI:  InChI=1S/C24H23ClN4S/c1-29(2)14-13-26-24-20-16-18(22-4-3-15-30-22)8-11-21(20)27-23(28-24)12-7-17-5-9-19(25)10-6-17/h3-12,15-16H,13-14H2,1-2H3,(H,26,27,28)/b12-7+

Standard InChI Key:  HZTZMSKFVZOBTO-KPKJPENVSA-N

Molfile:  

     RDKit          2D

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   -2.6111   -0.7486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2964   -1.4973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2964    1.4973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.7486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.7486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2964   -1.4973    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5929   -0.7486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5929    0.7486    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2964    1.4973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2995    2.9981    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6003    3.7467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6034    5.2475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9042    5.9961    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9067    7.1961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9424    5.3943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8942   -1.4964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1929   -0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4942   -1.4919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7933   -0.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0923   -1.4919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0923   -2.9919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7933   -3.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4943   -2.9919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1316   -3.5918    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.9086    1.5029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0476    2.9835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5150    3.2942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2640    1.9946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2594    0.8807    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  6  2  0
  5  4  2  0
  4  1  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
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  9 10  2  0
 10  5  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
  8 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 19  1  0
 22 25  1  0
  1 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 26  1  0
M  END

Alternative Forms

1. Parent:

   

   ALA3425614

   ---

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 435.00

Molecular Weight (Monoisotopic): 434.1332

AlogP: 6.16

#Rotatable Bonds: 7

Polar Surface Area: 41.05

Molecular Species: BASE

HBA: 5

HBD: 1

#RO5 Violations: 1

HBA (Lipinski): 4

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 1

CX Acidic pKa: ┄

CX Basic pKa: 8.75

CX LogP: 6.59

CX LogD: 5.22

Aromatic Rings: 4

Heavy Atoms: 30

QED Weighted: 0.38

Np Likeness Score: -1.43

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.,  6  (3): [PMID:25815151] [10.1021/ml500497s]

Source

Source(1):

• Scientific Literature