ID: ALA4454630

Max Phase: Preclinical

Molecular Formula: C23H25N3O

Molecular Weight: 359.47

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1cccc(C#CC=C2CCN(C(=O)NC(C)c3ccccc3)CC2)n1

Standard InChI:  InChI=1S/C23H25N3O/c1-18-8-6-12-22(24-18)13-7-9-20-14-16-26(17-15-20)23(27)25-19(2)21-10-4-3-5-11-21/h3-6,8-12,19H,14-17H2,1-2H3,(H,25,27)

Standard InChI Key:  FNHKUHMKWHDZML-UHFFFAOYSA-N

Associated Targets(Human)

Metabotropic glutamate receptor 5 5733 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Metabotropic glutamate receptor 1 1186 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: 359.47Molecular Weight (Monoisotopic): 359.1998AlogP: 4.23#Rotatable Bonds: 2
Polar Surface Area: 45.23Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 4.19CX LogP: 3.53CX LogD: 3.53
Aromatic Rings: 2Heavy Atoms: 27QED Weighted: 0.82Np Likeness Score: -1.08

References

1. Graziani D, Caligari S, Callegari E, De Toma C, Longhi M, Frigerio F, Dilernia R, Menegon S, Pinzi L, Pirona L, Tazzari V, Valsecchi AE, Vistoli G, Rastelli G, Riva C..  (2019)  Evaluation of Amides, Carbamates, Sulfonamides, and Ureas of 4-Prop-2-ynylidenecycloalkylamine as Potent, Selective, and Bioavailable Negative Allosteric Modulators of Metabotropic Glutamate Receptor 5.,  62  (3): [PMID:30624919] [10.1021/acs.jmedchem.8b01226]

Source