ID: ALA4114978

Max Phase: Preclinical

Molecular Formula: C22H22FN5O2

Molecular Weight: 407.45

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(-n2nccn2)c(C(=O)N2[C@H]3CC[C@@H]2[C@@H](COc2ccc(F)cn2)C3)c1

Standard InChI:  InChI=1S/C22H22FN5O2/c1-14-2-5-20(28-25-8-9-26-28)18(10-14)22(29)27-17-4-6-19(27)15(11-17)13-30-21-7-3-16(23)12-24-21/h2-3,5,7-10,12,15,17,19H,4,6,11,13H2,1H3/t15-,17+,19-/m1/s1

Standard InChI Key:  FNSBFXNNFNCHOW-HHXXYDBFSA-N

Associated Targets(Human)

Orexin receptor 1 5435 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Orexin receptor 2 5902 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: 407.45Molecular Weight (Monoisotopic): 407.1758AlogP: 3.18#Rotatable Bonds: 5
Polar Surface Area: 73.14Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 1.19CX LogP: 2.49CX LogD: 2.49
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.65Np Likeness Score: -1.29

References

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

Source

Source(1):