rac-7-[(2-Aminocyclohexyl)amino]-8-chloro-5-(3-methylanilino)pyrido[3,4-d]pyridazin-4(3H)-one

ID: ALA4524587

PubChem CID: 155520028

Max Phase: Preclinical

Molecular Formula: C20H23ClN6O

Molecular Weight: 398.90

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1cccc(Nc2nc(NC3CCCCC3N)c(Cl)c3cn[nH]c(=O)c23)c1

Standard InChI:  InChI=1S/C20H23ClN6O/c1-11-5-4-6-12(9-11)24-18-16-13(10-23-27-20(16)28)17(21)19(26-18)25-15-8-3-2-7-14(15)22/h4-6,9-10,14-15H,2-3,7-8,22H2,1H3,(H,27,28)(H2,24,25,26)

Standard InChI Key:  YIFKWRHDBDXBPE-UHFFFAOYSA-N

Molfile:  

 
     RDKit          2D

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   24.7631   -4.1093    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   25.4728   -3.6998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.4699   -2.8772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.0562   -2.8808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.7588   -2.4759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.7595   -1.6695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.0593   -1.2618    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   23.3566   -1.6666    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   23.3543   -2.4792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.6468   -2.8881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.3470   -4.1083    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   23.3464   -4.9255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.6382   -5.3320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.6372   -6.1484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.3452   -6.5584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.0555   -6.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.0530   -5.3309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9290   -6.5561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.1811   -4.1073    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   26.1824   -4.9245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.4724   -5.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.4717   -6.1430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.1782   -6.5543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.8871   -6.1458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.8894   -5.3260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.5963   -4.9159    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   26.1749   -2.4639    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
  5  1  2  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
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  5  6  1  0
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  1 12  1  0
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 15 19  1  0
  3 20  1  0
 20 21  1  0
 21 22  1  0
 21 26  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
  4 28  1  0
M  END

Alternative Forms

  1. Parent:

    ALA4524587

    ---

Associated Targets(Human)

FER Tclin Tyrosine-protein kinase FER (2362 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

BaF3 (4657 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 398.90Molecular Weight (Monoisotopic): 398.1622AlogP: 3.71#Rotatable Bonds: 4
Polar Surface Area: 108.72Molecular Species: BASEHBA: 6HBD: 4
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 5#RO5 Violations (Lipinski):
CX Acidic pKa: 9.48CX Basic pKa: 10.11CX LogP: 4.32CX LogD: 2.58
Aromatic Rings: 3Heavy Atoms: 28QED Weighted: 0.53Np Likeness Score: -1.15

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