6-{[(1R,2S)-2-Acetamidocyclohexyl]amino}-5-cyano-2-(3-methylanilino)pyridine-3-carboxamide

ID: ALA4552333

PubChem CID: 155554641

Max Phase: Preclinical

Molecular Formula: C22H26N6O2

Molecular Weight: 406.49

Molecule Type: Unknown

Names and Identifiers

Canonical SMILES:  CC(=O)N[C@H]1CCCC[C@H]1Nc1nc(Nc2cccc(C)c2)c(C(N)=O)cc1C#N

Standard InChI:  InChI=1S/C22H26N6O2/c1-13-6-5-7-16(10-13)26-22-17(20(24)30)11-15(12-23)21(28-22)27-19-9-4-3-8-18(19)25-14(2)29/h5-7,10-11,18-19H,3-4,8-9H2,1-2H3,(H2,24,30)(H,25,29)(H2,26,27,28)/t18-,19+/m0/s1

Standard InChI Key:  ONCURUYZPHWULO-RBUKOAKNSA-N

Molfile:  

 
     RDKit          2D

 30 32  0  0  0  0  0  0  0  0999 V2000
   31.7535  -10.0333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.7523  -10.8528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.4604  -11.2618    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   33.1700  -10.8523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.1672  -10.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.4586   -9.6244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.8711   -9.6172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.5773   -9.2059    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   33.8784  -11.2598    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   33.8797  -12.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.1696  -12.4819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.1690  -13.2955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.8755  -13.7068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.5844  -13.2983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.5867  -12.4785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.2935  -12.0684    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   31.0430   -9.6263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.0428   -8.8091    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   30.3354  -10.0350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.0443  -11.2608    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   31.0437  -12.0780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.3355  -12.4845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.3345  -13.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.0424  -13.7109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.7528  -13.2985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.7503  -12.4834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.6263  -13.7086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.0021  -12.4755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.7090  -12.0654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.0039  -13.2927    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  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  7  8  3  0
  5  7  1  0
  4  9  1  0
 10  9  1  1
 10 11  1  0
 10 15  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  1
 17 18  1  0
 17 19  2  0
  1 17  1  0
  2 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
 26 21  1  0
 23 27  1  0
 16 28  1  0
 28 29  1  0
 28 30  2  0
M  END

Alternative Forms

1. Parent:

   

   ALA4552333

   ---

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: 406.49

Molecular Weight (Monoisotopic): 406.2117

AlogP: 2.96

#Rotatable Bonds: 6

Polar Surface Area: 132.93

Molecular Species: NEUTRAL

HBA: 6

HBD: 4

#RO5 Violations: ┄

HBA (Lipinski): 8

HBD (Lipinski): 5

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: 13.29

CX Basic pKa: 1.84

CX LogP: 3.81

CX LogD: 3.81

Aromatic Rings: 2

Heavy Atoms: 30

QED Weighted: 0.58

Np Likeness Score: -1.13

References

1. Taniguchi T, Inagaki H, Baba D, Yasumatsu I, Toyota A, Kaneta Y, Kiga M, Iimura S, Odagiri T, Shibata Y, Ueda K, Seo M, Shimizu H, Imaoka T, Nakayama K..  (2019)  Discovery of Novel Pyrido-pyridazinone Derivatives as FER Tyrosine Kinase Inhibitors with Antitumor Activity.,  10  (5): [PMID:31097992] [10.1021/acsmedchemlett.8b00631]

Source

Source(1):

• Scientific Literature