(E)-5,6-Dimethoxy-2-{3-[(piperidin-1-yl)methyl]-benzylidene}-2,3-dihydroinden-1-one

ID: ALA475161

PubChem CID: 25197632

Max Phase: Preclinical

Molecular Formula: C24H27NO3

Molecular Weight: 377.48

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  COc1cc2c(cc1OC)C(=O)/C(=C/c1cccc(CN3CCCCC3)c1)C2

Standard InChI:  InChI=1S/C24H27NO3/c1-27-22-14-19-13-20(24(26)21(19)15-23(22)28-2)12-17-7-6-8-18(11-17)16-25-9-4-3-5-10-25/h6-8,11-12,14-15H,3-5,9-10,13,16H2,1-2H3/b20-12+

Standard InChI Key:  YUVGMQGHHQRBBC-UDWIEESQSA-N

Molfile:  

     RDKit          2D

 28 31  0  0  0  0  0  0  0  0999 V2000
    8.7897  -20.2762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5441  -20.6096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4593  -21.4319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6491  -21.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2366  -22.3160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4116  -22.3160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9991  -21.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4116  -20.8885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2366  -20.8885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6173  -19.4660    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2600  -20.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9717  -20.6096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6875  -20.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4034  -20.6096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4034  -21.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6875  -21.8471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9717  -21.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1151  -20.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8310  -20.6096    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.5468  -20.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2585  -20.6096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2585  -21.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5468  -21.8471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8310  -21.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1741  -21.6002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7616  -22.3160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9991  -23.0319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1741  -23.0319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  1  9  1  0
  4  9  2  0
  1 10  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 12 17  2  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 19 24  1  0
 18 19  1  0
 14 18  1  0
  2 11  2  0
 25 26  1  0
  7 25  1  0
 27 28  1  0
  6 27  1  0
M  END

Alternative Forms

1. Parent:

   

   ALA475161

   (E)-5,6-Dimethoxy-2-{3-[(piperidin-1-yl)methyl]-benzylidene}-2,3-dihydroinden-1-one

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: 377.48

Molecular Weight (Monoisotopic): 377.1991

AlogP: 4.51

#Rotatable Bonds: 5

Polar Surface Area: 38.77

Molecular Species: NEUTRAL

HBA: 4

HBD: ┄

#RO5 Violations: ┄

HBA (Lipinski): 4

HBD (Lipinski): ┄

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: ┄

CX Basic pKa: 8.45

CX LogP: 4.37

CX LogD: 3.29

Aromatic Rings: 2

Heavy Atoms: 28

QED Weighted: 0.72

Np Likeness Score: -0.42

References

1. Sheng R, Xu Y, Hu C, Zhang J, Lin X, Li J, Yang B, He Q, Hu Y..  (2009)  Design, synthesis and AChE inhibitory activity of indanone and aurone derivatives.,  44  (1): [PMID:18436348] [10.1016/j.ejmech.2008.03.003]

2. Chitranshi N, Gupta S, Tripathi PK, Seth PK.  (2013)  New molecular scaffolds for the design of Alzheimers acetylcholinesterase inhibitors identified using ligand- and receptor-based virtual screening,  22  (5): [10.1007/s00044-012-0227-3]

Source

Source(1):

• Scientific Literature