ID: ALA5183971

Max Phase: Preclinical

Molecular Formula: C21H19Cl2N3

Molecular Weight: 384.31

Associated Items:

Representations

Canonical SMILES:  Clc1ccc(-c2ccc3nc(Cl)nc(N[C@@H]4C[C@H]5CC[C@@H]4C5)c3c2)cc1

Standard InChI:  InChI=1S/C21H19Cl2N3/c22-16-6-3-13(4-7-16)14-5-8-18-17(11-14)20(26-21(23)25-18)24-19-10-12-1-2-15(19)9-12/h3-8,11-12,15,19H,1-2,9-10H2,(H,24,25,26)/t12-,15+,19+/m0/s1

Standard InChI Key:  HWUWNFWEFPZCPR-IOHHAYIISA-N

Associated Targets(Human)

GABA-B receptor 281 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus 284745 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 384.31Molecular Weight (Monoisotopic): 383.0956AlogP: 6.20#Rotatable Bonds: 3
Polar Surface Area: 37.81Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 2.34CX LogP: 6.20CX LogD: 6.20
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.55Np Likeness Score: -0.70

References

1. Huszár J, Petró JL, Hadady Z, Bobok AÁ, Sághy K, Halász AS, Hornyánszky G, Román V, Greiner I, Éles J..  (2022)  6-Aryl-quinazolines as novel GABAB receptor positive allosteric modulators.,  67  [PMID:35367591] [10.1016/j.bmcl.2022.128714]

Source