ID: ALA4648327

Max Phase: Preclinical

Molecular Formula: C26H33N3O5

Molecular Weight: 467.57

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1cc(C(=O)N[C@@H]2C[C@H]3CCC[C@@H](C2)N3CC(=O)Nc2ccccc2)cc(OC)c1OC

Standard InChI:  InChI=1S/C26H33N3O5/c1-32-22-12-17(13-23(33-2)25(22)34-3)26(31)28-19-14-20-10-7-11-21(15-19)29(20)16-24(30)27-18-8-5-4-6-9-18/h4-6,8-9,12-13,19-21H,7,10-11,14-16H2,1-3H3,(H,27,30)(H,28,31)/t19-,20-,21+

Standard InChI Key:  GBPZEGDRVCGMTG-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: 467.57Molecular Weight (Monoisotopic): 467.2420AlogP: 3.47#Rotatable Bonds: 8
Polar Surface Area: 89.13Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.46CX Basic pKa: 7.21CX LogP: 2.48CX LogD: 2.27
Aromatic Rings: 2Heavy Atoms: 34QED Weighted: 0.62Np Likeness Score: -0.91

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