N-(3-chloro-5-(4-(dimethylamino)piperidin-1-yl)phenyl)-4-fluoro-7-methyl-1H-indole-2-carboxamide

ID: ALA5093241

PubChem CID: 166632475

Max Phase: Preclinical

Molecular Formula: C23H26ClFN4O

Molecular Weight: 428.94

Molecule Type: Unknown

Names and Identifiers

Canonical SMILES:  Cc1ccc(F)c2cc(C(=O)Nc3cc(Cl)cc(N4CCC(N(C)C)CC4)c3)[nH]c12

Standard InChI:  InChI=1S/C23H26ClFN4O/c1-14-4-5-20(25)19-13-21(27-22(14)19)23(30)26-16-10-15(24)11-18(12-16)29-8-6-17(7-9-29)28(2)3/h4-5,10-13,17,27H,6-9H2,1-3H3,(H,26,30)

Standard InChI Key:  CYMUKCDJRAOOBQ-UHFFFAOYSA-N

Molfile:  

 
     RDKit          2D

 30 33  0  0  0  0  0  0  0  0999 V2000
   26.4500  -27.2644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4488  -28.0840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1569  -28.4929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1551  -26.8556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8637  -27.2608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8685  -28.0794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.6485  -28.3279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.1259  -27.6628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.6408  -27.0034    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   27.1527  -26.0384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.9431  -27.6580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.3558  -28.3632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   30.3475  -26.9479    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   31.1647  -26.9430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.5754  -27.6502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.3918  -27.6457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.7970  -26.9351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.3799  -26.2275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.5648  -26.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.7818  -25.5160    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   27.1579  -29.3101    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
   33.5984  -25.5139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.0002  -24.8064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.5884  -24.1001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.7703  -24.1059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.3640  -24.8179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.9930  -23.3901    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   34.8102  -23.3855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.5804  -22.6848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8042  -28.3512    0.0000 Cl  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
  8  9  1  0
  9  5  1  0
  4 10  1  0
  8 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 14  1  0
 18 20  1  0
  3 21  1  0
 20 22  1  0
 20 26  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 24 27  1  0
 27 28  1  0
 27 29  1  0
 16 30  1  0
M  END

Alternative Forms

1. Parent:

   

   ALA5093241

   ---

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Unknown

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 428.94

Molecular Weight (Monoisotopic): 428.1779

AlogP: 5.05

#Rotatable Bonds: 4

Polar Surface Area: 51.37

Molecular Species: BASE

HBA: 3

HBD: 2

#RO5 Violations: 1

HBA (Lipinski): 5

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 1

CX Acidic pKa: 11.95

CX Basic pKa: 9.78

CX LogP: 4.48

CX LogD: 2.13

Aromatic Rings: 3

Heavy Atoms: 30

QED Weighted: 0.61

Np Likeness Score: -1.92

References

1. Lampe JW, Alford JS, Boriak-Sjodin PA, Brach D, Cosmopoulos K, Duncan KW, Eckley ST, Foley MA, Harvey DM, Motwani V, Munchhof MJ, Raimondi A, Riera TV, Tang C, Thomenius MJ, Totman J, Farrow NA..  (2021)  Discovery of a First-in-Class Inhibitor of the Histone Methyltransferase SETD2 Suitable for Preclinical Studies.,  12  (10.0): [PMID:34671445] [10.1021/acsmedchemlett.1c00272]

Source

Source(1):

• Scientific Literature