ID: ALA5177753

Max Phase: Preclinical

Molecular Formula: C32H30F3N7O2

Molecular Weight: 601.63

Associated Items:

Representations

Canonical SMILES:  CNC(=O)c1ccc(-c2ccc(=O)n(CCc3ccc4ncc(-c5cnn(C6CCNCC6)c5)cc4c3)n2)cc1C(F)(F)F

Standard InChI:  InChI=1S/C32H30F3N7O2/c1-36-31(44)26-4-3-21(16-27(26)32(33,34)35)29-6-7-30(43)41(40-29)13-10-20-2-5-28-22(14-20)15-23(17-38-28)24-18-39-42(19-24)25-8-11-37-12-9-25/h2-7,14-19,25,37H,8-13H2,1H3,(H,36,44)

Standard InChI Key:  PGYVYYYFZQHUPY-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: 601.63Molecular Weight (Monoisotopic): 601.2413AlogP: 4.87#Rotatable Bonds: 7
Polar Surface Area: 106.73Molecular Species: BASEHBA: 8HBD: 2
#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.76CX Basic pKa: 10.12CX LogP: 3.43CX LogD: 0.82
Aromatic Rings: 5Heavy Atoms: 44QED Weighted: 0.28Np Likeness Score: -1.42

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