(S)-5-fluoro-2-(pyrrolidin-3-yl)benzo[d]oxazole

ID: ALA4098081

Chembl Id: CHEMBL4098081

PubChem CID: 45784336

Max Phase: Preclinical

Molecular Formula: C11H11FN2O

Molecular Weight: 206.22

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Fc1ccc2oc([C@H]3CCNC3)nc2c1

Standard InChI:  InChI=1S/C11H11FN2O/c12-8-1-2-10-9(5-8)14-11(15-10)7-3-4-13-6-7/h1-2,5,7,13H,3-4,6H2/t7-/m0/s1

Standard InChI Key:  FEVDTPYNDIOAPF-ZETCQYMHSA-N

Alternative Forms

Associated Targets(Human)

MPO Tchem Myeloperoxidase (1002 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NHDF (1164 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

LPO Lactoperoxidase (91 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: 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: 206.22Molecular Weight (Monoisotopic): 206.0855AlogP: 2.04#Rotatable Bonds: 1
Polar Surface Area: 38.06Molecular Species: BASEHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 10.27CX LogP: 1.40CX LogD: -1.32
Aromatic Rings: 2Heavy Atoms: 15QED Weighted: 0.78Np Likeness Score: -1.38

References

1. Soubhye J, Chikh Alard I, Aldib I, Prévost M, Gelbcke M, De Carvalho A, Furtmüller PG, Obinger C, Flemmig J, Tadrent S, Meyer F, Rousseau A, Nève J, Mathieu V, Zouaoui Boudjeltia K, Dufrasne F, Van Antwerpen P..  (2017)  Discovery of Novel Potent Reversible and Irreversible Myeloperoxidase Inhibitors Using Virtual Screening Procedure.,  60  (15): [PMID:28671460] [10.1021/acs.jmedchem.7b00285]

Source