ID: ALA2030372

Max Phase: Preclinical

Molecular Formula: C13H20N4O4

Molecular Weight: 296.33

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)Oc1nc(N)c(C(N)=O)c(O[C@H]2CCC[C@@H]2O)n1

Standard InChI:  InChI=1S/C13H20N4O4/c1-6(2)20-13-16-10(14)9(11(15)19)12(17-13)21-8-5-3-4-7(8)18/h6-8,18H,3-5H2,1-2H3,(H2,15,19)(H2,14,16,17)/t7-,8-/m0/s1

Standard InChI Key:  YDTZIAORSQUSGW-YUMQZZPRSA-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: 296.33Molecular Weight (Monoisotopic): 296.1485AlogP: 0.24#Rotatable Bonds: 5
Polar Surface Area: 133.58Molecular Species: NEUTRALHBA: 7HBD: 3
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.41CX Basic pKa: 3.88CX LogP: 1.33CX LogD: 1.33
Aromatic Rings: 1Heavy Atoms: 21QED Weighted: 0.71Np Likeness Score: 0.08

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