ID: ALA4794968

Max Phase: Preclinical

Molecular Formula: C23H25N5O3

Molecular Weight: 419.49

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC(Cn1nnc2cc(C#Cc3ccc(CN4CCOCC4)cc3)ccc21)N(O)C=O

Standard InChI:  InChI=1S/C23H25N5O3/c1-18(28(30)17-29)15-27-23-9-8-20(14-22(23)24-25-27)5-2-19-3-6-21(7-4-19)16-26-10-12-31-13-11-26/h3-4,6-9,14,17-18,30H,10-13,15-16H2,1H3

Standard InChI Key:  UOMUPOGAPKMXHS-UHFFFAOYSA-N

Associated Targets(non-human)

UDP-3-O-acyl-GlcNAc deacetylase 700 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 419.49Molecular Weight (Monoisotopic): 419.1957AlogP: 1.90#Rotatable Bonds: 6
Polar Surface Area: 83.72Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.25CX Basic pKa: 6.75CX LogP: 2.43CX LogD: 2.51
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.28Np Likeness Score: -1.51

References

1. Furuya T,Shapiro AB,Comita-Prevoir J,Kuenstner EJ,Zhang J,Ribe SD,Chen A,Hines D,Moussa SH,Carter NM,Sylvester MA,Romero JAC,Vega CV,Sacco MD,Chen Y,O'Donnell JP,Durand-Reville TF,Miller AA,Tommasi RA.  (2020)  N-Hydroxyformamide LpxC inhibitors, their in vivo efficacy in a mouse Escherichia coli infection model, and their safety in a rat hemodynamic assay.,  28  (24): [PMID:33160146] [10.1016/j.bmc.2020.115826]

Source