ID: ALA5204053

Max Phase: Preclinical

Molecular Formula: C31H33F3N6O2

Molecular Weight: 578.64

Associated Items:

Representations

Canonical SMILES:  CNC(=O)c1ccc(-c2ccc(=O)n(CCc3ccc4ncc(NCCN5CCCCC5)cc4c3)n2)cc1C(F)(F)F

Standard InChI:  InChI=1S/C31H33F3N6O2/c1-35-30(42)25-7-6-22(19-26(25)31(32,33)34)28-9-10-29(41)40(38-28)15-11-21-5-8-27-23(17-21)18-24(20-37-27)36-12-16-39-13-3-2-4-14-39/h5-10,17-20,36H,2-4,11-16H2,1H3,(H,35,42)

Standard InChI Key:  NULBWEXDJCDLOD-UHFFFAOYSA-N

Associated Targets(Human)

Hepatocyte growth factor receptor 10718 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Hs746T 53 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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

Properties

Molecular Weight: 578.64Molecular Weight (Monoisotopic): 578.2617AlogP: 4.98#Rotatable Bonds: 9
Polar Surface Area: 92.15Molecular Species: BASEHBA: 7HBD: 2
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.75CX Basic pKa: 8.91CX LogP: 4.05CX LogD: 2.53
Aromatic Rings: 4Heavy Atoms: 42QED Weighted: 0.29Np Likeness Score: -1.70

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