ID: ALA4218708

Max Phase: Preclinical

Molecular Formula: C20H12FN5O2

Molecular Weight: 373.35

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(c1cncnc1)c1cc(C(=O)Nc2cccc(F)n2)c2ncccc2c1

Standard InChI:  InChI=1S/C20H12FN5O2/c21-16-4-1-5-17(25-16)26-20(28)15-8-13(7-12-3-2-6-24-18(12)15)19(27)14-9-22-11-23-10-14/h1-11H,(H,25,26,28)

Standard InChI Key:  KCEPSLKHOIYLKI-UHFFFAOYSA-N

Associated Targets(non-human)

Metabotropic glutamate receptor 5 4372 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 373.35Molecular Weight (Monoisotopic): 373.0975AlogP: 3.04#Rotatable Bonds: 4
Polar Surface Area: 97.73Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.48CX Basic pKa: 2.48CX LogP: 2.67CX LogD: 2.67
Aromatic Rings: 4Heavy Atoms: 28QED Weighted: 0.44Np Likeness Score: -1.35

References

1. Felts AS, Rodriguez AL, Morrison RD, Blobaum AL, Byers FW, Daniels JS, Niswender CM, Conn PJ, Lindsley CW, Emmitte KA..  (2018)  Discovery of 6-(pyrimidin-5-ylmethyl)quinoline-8-carboxamide negative allosteric modulators of metabotropic glutamate receptor subtype 5.,  28  (10): [PMID:29705142] [10.1016/j.bmcl.2018.04.053]

Source