(3E)-N-(4-(methylsulfonyl)phenyl)-N'-(2-oxo-3-((1-methyl-1H-imidazol-2-yl)methylene)indolin-5-yl)urea

ID: ALA3735019

PubChem CID: 127037285

Max Phase: Preclinical

Molecular Formula: C21H19N5O4S

Molecular Weight: 437.48

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  Cn1ccnc1/C=C1/C(=O)Nc2ccc(NC(=O)Nc3ccc(S(C)(=O)=O)cc3)cc21

Standard InChI:  InChI=1S/C21H19N5O4S/c1-26-10-9-22-19(26)12-17-16-11-14(5-8-18(16)25-20(17)27)24-21(28)23-13-3-6-15(7-4-13)31(2,29)30/h3-12H,1-2H3,(H,25,27)(H2,23,24,28)/b17-12+

Standard InChI Key:  ATIJRGHGXSCRHK-SFQUDFHCSA-N

Molfile:  

     RDKit          2D

 31 34  0  0  0  0  0  0  0  0999 V2000
    3.7889    0.0269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5889    0.0182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7138    1.2033    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2917    0.7475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0028    1.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3155    0.7475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3155   -0.7475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0028   -1.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2917   -0.7475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7138   -1.2033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1855   -2.6254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1889   -3.7475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2891   -3.5814    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8927   -4.9546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2267   -5.9530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5222   -5.1969    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6236   -5.6733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6187   -1.4919    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6267   -2.9927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9300   -3.7369    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9380   -5.2378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2396   -5.9835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2445   -7.4835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9480   -8.2378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9530   -9.7386    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9938  -10.3358    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9156  -10.3418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9564  -10.9386    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6465   -7.4922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6415   -5.9922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5905   -3.5979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  4  9  1  0
  9 10  1  0
  2 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 12 16  1  0
 16 17  1  0
  7 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 25 28  2  0
 24 29  1  0
 29 30  2  0
 21 30  1  0
 19 31  2  0
M  END

Alternative Forms

1. Parent:

   

   ALA3735019

   ---

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: 437.48

Molecular Weight (Monoisotopic): 437.1158

AlogP: 2.96

#Rotatable Bonds: 4

Polar Surface Area: 122.19

Molecular Species: NEUTRAL

HBA: 6

HBD: 3

#RO5 Violations: ┄

HBA (Lipinski): 9

HBD (Lipinski): 3

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: 10.92

CX Basic pKa: 5.96

CX LogP: 1.58

CX LogD: 1.57

Aromatic Rings: 3

Heavy Atoms: 31

QED Weighted: 0.54

Np Likeness Score: -1.48

References

1. Sestito S, Nesi G, Daniele S, Martelli A, Digiacomo M, Borghini A, Pietra D, Calderone V, Lapucci A, Falasca M, Parrella P, Notarangelo A, Breschi MC, Macchia M, Martini C, Rapposelli S..  (2015)  Design and synthesis of 2-oxindole based multi-targeted inhibitors of PDK1/Akt signaling pathway for the treatment of glioblastoma multiforme.,  105  [PMID:26498573] [10.1016/j.ejmech.2015.10.020]

Source

Source(1):

• Scientific Literature