2-[4-(2-Oxo-4H-benzo[d][1,3]oxazin-1-yl)-piperidin-1-yl]-N-(9-oxo-9H-fluoren-4-yl)-acetamide

ID: ALA536275

Chembl Id: CHEMBL536275

PubChem CID: 10481215

Max Phase: Preclinical

Molecular Formula: C28H26ClN3O4

Molecular Weight: 467.53

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Cl.O=C(CN1CCC(N2C(=O)OCc3ccccc32)CC1)Nc1cccc2c1-c1ccccc1C2=O

Standard InChI:  InChI=1S/C28H25N3O4.ClH/c32-25(29-23-10-5-9-22-26(23)20-7-2-3-8-21(20)27(22)33)16-30-14-12-19(13-15-30)31-24-11-4-1-6-18(24)17-35-28(31)34;/h1-11,19H,12-17H2,(H,29,32);1H

Standard InChI Key:  DVIGMRVHCMNLPR-UHFFFAOYSA-N

Associated Targets(non-human)

Npy5r Neuropeptide Y receptor type 5 (108 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

Calculated Properties

Molecular Weight: 467.53Molecular Weight (Monoisotopic): 467.1845AlogP: 4.46#Rotatable Bonds: 4
Polar Surface Area: 78.95Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 12.67CX Basic pKa: 6.02CX LogP: 3.52CX LogD: 3.50
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.48Np Likeness Score: -0.69

References

1. Torrens A, Mas J, Port A, Castrillo JA, Sanfeliu O, Guitart X, Dordal A, Romero G, Fisas MA, Sánchez E, Hernández E, Pérez P, Pérez R, Buschmann H..  (2005)  Synthesis of new benzoxazinone derivatives as neuropeptide Y5 antagonists for the treatment of obesity.,  48  (6): [PMID:15771450] [10.1021/jm049599u]

Source