ID: ALA4647997

Max Phase: Preclinical

Molecular Formula: C25H30ClN3O4

Molecular Weight: 471.99

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1cc(OC)cc(C(=O)N[C@@H]2C[C@H]3CCC[C@@H](C2)N3CC(=O)Nc2ccc(Cl)cc2)c1

Standard InChI:  InChI=1S/C25H30ClN3O4/c1-32-22-10-16(11-23(14-22)33-2)25(31)28-19-12-20-4-3-5-21(13-19)29(20)15-24(30)27-18-8-6-17(26)7-9-18/h6-11,14,19-21H,3-5,12-13,15H2,1-2H3,(H,27,30)(H,28,31)/t19-,20-,21+

Standard InChI Key:  WEKBLDZYQSQSGL-MZADTFQBSA-N

Associated Targets(Human)

C-X-C chemokine receptor type 6 264 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 471.99Molecular Weight (Monoisotopic): 471.1925AlogP: 4.11#Rotatable Bonds: 7
Polar Surface Area: 79.90Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.40CX Basic pKa: 7.10CX LogP: 3.25CX LogD: 3.07
Aromatic Rings: 2Heavy Atoms: 33QED Weighted: 0.63Np Likeness Score: -1.25

References

1. Peddibhotla S, Hershberger PM, Jason Kirby R, Sugarman E, Maloney PR, Hampton Sessions E, Divlianska D, Morfa CJ, Terry D, Pinkerton AB, Smith LH, Malany S..  (2020)  Discovery of small molecule antagonists of chemokine receptor CXCR6 that arrest tumor growth in SK-HEP-1 mouse xenografts as a model of hepatocellular carcinoma.,  30  (4): [PMID:31882297] [10.1016/j.bmcl.2019.126899]

Source