ID: ALA5205446

Max Phase: Preclinical

Molecular Formula: C28H23F3N6O3

Molecular Weight: 548.53

Representations

Canonical SMILES:  CNC(=O)c1ccc(-c2ccc(=O)n(CCOc3ccc4ncc(-c5cnn(C)c5)cc4c3)n2)cc1C(F)(F)F

Standard InChI:  InChI=1S/C28H23F3N6O3/c1-32-27(39)22-5-3-17(13-23(22)28(29,30)31)25-7-8-26(38)37(35-25)9-10-40-21-4-6-24-18(12-21)11-19(14-33-24)20-15-34-36(2)16-20/h3-8,11-16H,9-10H2,1-2H3,(H,32,39)

Standard InChI Key:  DHFFKLIQPPSHSV-UHFFFAOYSA-N

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type:

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Properties

Molecular Weight: 548.53

Molecular Weight (Monoisotopic): 548.1784

AlogP: 4.32

#Rotatable Bonds: 7

Polar Surface Area: 103.93

Molecular Species: NEUTRAL

HBA: 8

HBD: 1

#RO5 Violations: 1

HBA (Lipinski): 9

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 1

CX Acidic pKa: 13.75

CX Basic pKa: 4.02

CX LogP: 3.41

CX LogD: 3.41

Aromatic Rings: 5

Heavy Atoms: 40

QED Weighted: 0.33

Np Likeness Score: -1.89

References

1. Wang C, Li J, Qu L, Tang X, Song X, Yang F, Chen X, Lin Q, Lin W, Zhou Y, Tu Z, Chen Y, Zhang Z, Lu X..  (2022)  Discovery of D6808, a Highly Selective and Potent Macrocyclic c-Met Inhibitor for Gastric Cancer Harboring MET Gene Alteration Treatment.,  65  (22.0): [PMID:36355693] [10.1021/acs.jmedchem.2c00981]

Source

Source(1):

• Scientific Literature