ID: ALA462412

Max Phase: Preclinical

Molecular Formula: C14H26N2O6

Molecular Weight: 318.37

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCC(=O)OCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)CO

Standard InChI:  InChI=1S/C14H26N2O6/c1-4-11(19)22-8-7-15-10(18)5-6-16-13(21)12(20)14(2,3)9-17/h12,17,20H,4-9H2,1-3H3,(H,15,18)(H,16,21)/t12-/m0/s1

Standard InChI Key:  RDDMMYIBMXQVKV-LBPRGKRZSA-N

Associated Targets(non-human)

Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
coaA Pantothenate kinase (64 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: 318.37Molecular Weight (Monoisotopic): 318.1791AlogP: -1.06#Rotatable Bonds: 10
Polar Surface Area: 124.96Molecular Species: NEUTRALHBA: 6HBD: 4
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.68CX Basic pKa: CX LogP: -1.49CX LogD: -1.49
Aromatic Rings: 0Heavy Atoms: 22QED Weighted: 0.30Np Likeness Score: -0.12

References

1. Mercer AC, Meier JL, Hur GH, Smith AR, Burkart MD..  (2008)  Antibiotic evaluation and in vivo analysis of alkynyl Coenzyme A antimetabolites in Escherichia coli.,  18  (22): [PMID:18701278] [10.1016/j.bmcl.2008.07.078]

Source