ID: ALA4799902

Max Phase: Preclinical

Molecular Formula: C20H11F3N2O4

Molecular Weight: 400.31

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ccoc1C(=O)Nc1c(F)cc(N2C(=O)c3ccccc3C2=O)c(F)c1F

Standard InChI:  InChI=1S/C20H11F3N2O4/c1-9-6-7-29-17(9)18(26)24-16-12(21)8-13(14(22)15(16)23)25-19(27)10-4-2-3-5-11(10)20(25)28/h2-8H,1H3,(H,24,26)

Standard InChI Key:  ZQOAYJJXKVBVJA-UHFFFAOYSA-N

Associated Targets(Human)

Metabotropic glutamate receptor 1 2309 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Metabotropic glutamate receptor 4 2320 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Metabotropic glutamate receptor 7 376 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: 400.31Molecular Weight (Monoisotopic): 400.0671AlogP: 4.06#Rotatable Bonds: 3
Polar Surface Area: 79.62Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.10CX Basic pKa: CX LogP: 3.67CX LogD: 3.67
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.53Np Likeness Score: -1.16

References

1. Davis DC,Bungard JD,Chang S,Rodriguez AL,Blobaum AL,Boutaud O,Melancon BJ,Niswender CM,Jeffrey Conn P,Lindsley CW.  (2021)  Lead optimization of the VU0486321 series of mGlu PAMs. Part 4: SAR reveals positive cooperativity across multiple mGlu receptor subtypes leading to subtype unselective PAMs.,  32  [PMID:33253881] [10.1016/j.bmcl.2020.127724]

Source