ID: ALA4205831

Max Phase: Preclinical

Molecular Formula: C21H15F2N5O2

Molecular Weight: 407.38

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccnc(NC(=O)c2cc(C(F)(F)c3cncnc3)cc3cccnc23)c1

Standard InChI:  InChI=1S/C21H15F2N5O2/c1-30-16-4-6-26-18(9-16)28-20(29)17-8-14(7-13-3-2-5-27-19(13)17)21(22,23)15-10-24-12-25-11-15/h2-12H,1H3,(H,26,28,29)

Standard InChI Key:  ZUKQQYGHLFIREM-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: 407.38Molecular Weight (Monoisotopic): 407.1194AlogP: 3.82#Rotatable Bonds: 5
Polar Surface Area: 89.89Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.49CX Basic pKa: 4.15CX LogP: 2.87CX LogD: 2.87
Aromatic Rings: 4Heavy Atoms: 30QED Weighted: 0.54Np Likeness Score: -1.12

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