ID: ALA3663522

Max Phase: Preclinical

Molecular Formula: C22H18F4N6O

Molecular Weight: 458.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(c1cccc(F)c1-c1ncccn1)N1C2CCC1C(Nc1cnc(C(F)(F)F)cn1)C2

Standard InChI:  InChI=1S/C22H18F4N6O/c23-14-4-1-3-13(19(14)20-27-7-2-8-28-20)21(33)32-12-5-6-16(32)15(9-12)31-18-11-29-17(10-30-18)22(24,25)26/h1-4,7-8,10-12,15-16H,5-6,9H2,(H,30,31)

Standard InChI Key:  NWUAUSABGZEYEW-UHFFFAOYSA-N

Associated Targets(Human)

Orexin receptor 2 5902 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Orexin receptor 1 5435 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Orexin receptor 1 669 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: 458.42Molecular Weight (Monoisotopic): 458.1478AlogP: 3.95#Rotatable Bonds: 4
Polar Surface Area: 83.90Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 1.04CX LogP: 3.03CX LogD: 3.03
Aromatic Rings: 3Heavy Atoms: 33QED Weighted: 0.60Np Likeness Score: -1.10

References

1.  (2015)  Substituted 7-azabicyles and their use as orexin receptor modulators, 
2.  (2016)  Substituted 7-azabicycles and their use as orexin receptor modulators, 

Source

Source(1):