ID: ALA5170241

Max Phase: Preclinical

Molecular Formula: C33H32F3N7O3

Molecular Weight: 631.66

Associated Items:

Representations

Canonical SMILES:  CNC(=O)c1ccc(-c2ccc(=O)n(CCc3ccc4ncc(-c5cnn(CCN6CCOCC6)c5)cc4c3)n2)cc1C(F)(F)F

Standard InChI:  InChI=1S/C33H32F3N7O3/c1-37-32(45)27-4-3-23(18-28(27)33(34,35)36)30-6-7-31(44)43(40-30)9-8-22-2-5-29-24(16-22)17-25(19-38-29)26-20-39-42(21-26)11-10-41-12-14-46-15-13-41/h2-7,16-21H,8-15H2,1H3,(H,37,45)

Standard InChI Key:  HMTIVTZESXYYSZ-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: 631.66Molecular Weight (Monoisotopic): 631.2519AlogP: 4.28#Rotatable Bonds: 9
Polar Surface Area: 107.17Molecular Species: NEUTRALHBA: 9HBD: 1
#RO5 Violations: 1HBA (Lipinski): 10HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.75CX Basic pKa: 6.96CX LogP: 3.58CX LogD: 3.45
Aromatic Rings: 5Heavy Atoms: 46QED Weighted: 0.26Np Likeness Score: -1.80

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