The store will not work correctly when cookies are disabled.
JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.
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
28 31 0 0 0 0 0 0 0 0999 V2000
24.0551 -3.7003 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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
4 6 2 0
5 6 1 0
5 10 1 0
6 7 1 0
7 8 2 0
8 9 1 0
9 10 1 0
10 11 2 0
1 12 1 0
12 13 1 0
13 14 2 0
14 15 1 0
15 16 2 0
16 17 1 0
17 18 2 0
18 13 1 0
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 Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 398.90Molecular Weight (Monoisotopic): 398.1622AlogP: 3.71#Rotatable Bonds: 4Polar 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: 2.58Aromatic 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 ]