(2R)-4-(6-((3-Fluoro-1-methylazetidin-3-yl)buta-1,3-diyn-1-yl)-3-oxo-1H-pyrrolo[1,2-c]imidazol-2(3H)-yl)-N-hydroxy-2-methyl-2-(methylsulfonyl)butanamide

ID: ALA4534343

Chembl Id: CHEMBL4534343

PubChem CID: 135315359

Max Phase: Preclinical

Molecular Formula: C20H23FN4O5S

Molecular Weight: 450.49

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  CN1CC(F)(C#CC#Cc2cc3n(c2)C(=O)N(CC[C@](C)(C(=O)NO)S(C)(=O)=O)C3)C1

Standard InChI:  InChI=1S/C20H23FN4O5S/c1-19(17(26)22-28,31(3,29)30)8-9-24-12-16-10-15(11-25(16)18(24)27)6-4-5-7-20(21)13-23(2)14-20/h10-11,28H,8-9,12-14H2,1-3H3,(H,22,26)/t19-/m1/s1

Standard InChI Key:  SKEFWYGKZDVQQO-LJQANCHMSA-N

Alternative Forms

  1. Parent:

    ALA4534343

    ---

Associated Targets(non-human)

Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lpxC UDP-3-O-acyl-GlcNAc deacetylase (448 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lpxC UDP-3-O-acyl-GlcNAc deacetylase (700 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

Calculated Properties

Molecular Weight: 450.49Molecular Weight (Monoisotopic): 450.1373AlogP: -0.02#Rotatable Bonds: 5
Polar Surface Area: 111.95Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: HBA (Lipinski): 9HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 8.67CX Basic pKa: 4.00CX LogP: -0.58CX LogD: -0.61
Aromatic Rings: 1Heavy Atoms: 31QED Weighted: 0.37Np Likeness Score: -0.25

References

1. Panchaud P, Surivet JP, Diethelm S, Blumstein AC, Gauvin JC, Jacob L, Masse F, Mathieu G, Mirre A, Schmitt C, Enderlin-Paput M, Lange R, Gnerre C, Seeland S, Herrmann C, Locher HH, Seiler P, Ritz D, Rueedi G..  (2020)  Optimization of LpxC Inhibitor Lead Compounds Focusing on Efficacy and Formulation for High Dose Intravenous Administration.,  63  (1): [PMID:31804829] [10.1021/acs.jmedchem.9b01605]

Source