Sodium salt (1S,8bR)-1-((R)-1-hydroxy-ethyl)-2-oxo-1,2,5,6,7,8,8a,8b-octahydro-azeto[2,1-a]isoindole-4-carboxylate

ID: ALA367717

Chembl Id: CHEMBL367717

PubChem CID: 44385877

Max Phase: Preclinical

Molecular Formula: C13H16NNaO4

Molecular Weight: 251.28

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C3CCCCC3[C@H]12.[Na+]

Standard InChI:  InChI=1S/C13H17NO4.Na/c1-6(15)9-10-7-4-2-3-5-8(7)11(13(17)18)14(10)12(9)16;/h6-7,9-10,15H,2-5H2,1H3,(H,17,18);/q;+1/p-1/t6-,7?,9-,10-;/m1./s1

Standard InChI Key:  FHHAVNAFQUMYML-IECICGCHSA-M

Associated Targets(non-human)

blaY Beta-lactamase 1 (50 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: 251.28Molecular Weight (Monoisotopic): 251.1158AlogP: 0.74#Rotatable Bonds: 2
Polar Surface Area: 77.84Molecular Species: ACIDHBA: 3HBD: 2
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 3.91CX Basic pKa: CX LogP: 0.04CX LogD: -3.17
Aromatic Rings: Heavy Atoms: 18QED Weighted: 0.71Np Likeness Score: 0.83

References

1. Copar A, Prevec T, Anzic B, Mesar T, Selic L, Vilar M, Solmajer T..  (2002)  Design, synthesis and bioactivity evaluation of tribactam beta lactamase inhibitors.,  12  (6): [PMID:11959006] [10.1016/s0960-894x(02)00061-6]

Source