ID: ALA568021

Max Phase: Preclinical

Molecular Formula: C21H21N7O

Molecular Weight: 387.45

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCNC(=O)Nc1cn2c(-c3ncc(C)cn3)cc(-c3ccc(C)nc3)cc2n1

Standard InChI:  InChI=1S/C21H21N7O/c1-4-22-21(29)27-18-12-28-17(20-24-9-13(2)10-25-20)7-16(8-19(28)26-18)15-6-5-14(3)23-11-15/h5-12H,4H2,1-3H3,(H2,22,27,29)

Standard InChI Key:  PVKBVEDKZQIBPE-UHFFFAOYSA-N

Associated Targets(non-human)

DNA gyrase subunit B 35 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

ParE 35 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Streptococcus pyogenes 16140 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Streptococcus pneumoniae 31063 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: 387.45Molecular Weight (Monoisotopic): 387.1808AlogP: 3.61#Rotatable Bonds: 4
Polar Surface Area: 97.10Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.20CX Basic pKa: 5.31CX LogP: 2.64CX LogD: 2.63
Aromatic Rings: 4Heavy Atoms: 29QED Weighted: 0.56Np Likeness Score: -1.46

References

1. Starr JT, Sciotti RJ, Hanna DL, Huband MD, Mullins LM, Cai H, Gage JW, Lockard M, Rauckhorst MR, Owen RM, Lall MS, Tomilo M, Chen H, McCurdy SP, Barbachyn MR..  (2009)  5-(2-Pyrimidinyl)-imidazo[1,2-a]pyridines are antibacterial agents targeting the ATPase domains of DNA gyrase and topoisomerase IV.,  19  (18): [PMID:19683922] [10.1016/j.bmcl.2009.07.141]

Source