ID: ALA571255

Max Phase: Preclinical

Molecular Formula: C12H13BrO3

Molecular Weight: 285.14

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(CBr)CC(Cc1ccccc1)C(=O)O

Standard InChI:  InChI=1S/C12H13BrO3/c13-8-11(14)7-10(12(15)16)6-9-4-2-1-3-5-9/h1-5,10H,6-8H2,(H,15,16)

Standard InChI Key:  RHPUFCREMWHRIP-UHFFFAOYSA-N

Associated Targets(Human)

Carboxypeptidase A1 146 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: 285.14Molecular Weight (Monoisotopic): 284.0048AlogP: 2.28#Rotatable Bonds: 6
Polar Surface Area: 54.37Molecular Species: ACIDHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 3.73CX Basic pKa: CX LogP: 2.78CX LogD: -0.52
Aromatic Rings: 1Heavy Atoms: 16QED Weighted: 0.82Np Likeness Score: 0.28

References

1. Wang SF, Tian GR, Zhang WZ, Jin JY..  (2009)  Characterization of alpha-nitromethyl ketone as a new zinc-binding group based on structural analysis of its complex with carboxypeptidase A.,  19  (17): [PMID:19646864] [10.1016/j.bmcl.2009.07.060]

Source