ID: ALA3706693

Max Phase: Preclinical

Molecular Formula: C14H8N6O7S

Molecular Weight: 404.32

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cccc2sc(Nc3c([N+](=O)[O-])cc([N+](=O)[O-])c4no[n+]([O-])c34)nc12

Standard InChI:  InChI=1S/C14H8N6O7S/c1-26-8-3-2-4-9-12(8)16-14(28-9)15-10-6(18(21)22)5-7(19(23)24)11-13(10)20(25)27-17-11/h2-5H,1H3,(H,15,16)

Standard InChI Key:  KOLWYXRJFLDNQN-UHFFFAOYSA-N

Associated Targets(non-human)

Vibrio sp. (72 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 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: 404.32Molecular Weight (Monoisotopic): 404.0175AlogP: 2.64#Rotatable Bonds: 5
Polar Surface Area: 173.40Molecular Species: ACIDHBA: 11HBD: 1
#RO5 Violations: 1HBA (Lipinski): 13HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 2.77CX Basic pKa: CX LogP: 3.19CX LogD: 1.58
Aromatic Rings: 4Heavy Atoms: 28QED Weighted: 0.30Np Likeness Score: -1.51

References

1. Chugunova E, Boga C, Sazykin I, Cino S, Micheletti G, Mazzanti A, Sazykina M, Burilov A, Khmelevtsova L, Kostina N..  (2015)  Synthesis and antimicrobial activity of novel structural hybrids of benzofuroxan and benzothiazole derivatives.,  93  [PMID:25707015] [10.1016/j.ejmech.2015.02.023]

Source