ID: ALA2030362

Max Phase: Preclinical

Molecular Formula: C18H27N5O3

Molecular Weight: 361.45

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Nc1nc(OCC2CCCC2)ncc1C(=O)NCCCN1CCCC1=O

Standard InChI:  InChI=1S/C18H27N5O3/c19-16-14(11-21-18(22-16)26-12-13-5-1-2-6-13)17(25)20-8-4-10-23-9-3-7-15(23)24/h11,13H,1-10,12H2,(H,20,25)(H2,19,21,22)

Standard InChI Key:  QWPFMNIDBBBCSH-UHFFFAOYSA-N

Associated Targets(Human)

DNA ligase 1 262 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 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: 361.45Molecular Weight (Monoisotopic): 361.2114AlogP: 1.37#Rotatable Bonds: 8
Polar Surface Area: 110.44Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.59CX Basic pKa: 4.49CX LogP: 1.26CX LogD: 1.26
Aromatic Rings: 1Heavy Atoms: 26QED Weighted: 0.68Np Likeness Score: -1.36

References

1. Gu W, Wang T, Maltais F, Ledford B, Kennedy J, Wei Y, Gross CH, Parsons J, Duncan L, Arends SJ, Moody C, Perola E, Green J, Charifson PS..  (2012)  Design, synthesis and biological evaluation of potent NAD+-dependent DNA ligase inhibitors as potential antibacterial agents. Part I: aminoalkoxypyrimidine carboxamides.,  22  (11): [PMID:22560473] [10.1016/j.bmcl.2012.04.037]

Source