ID: ALA3706692

Max Phase: Preclinical

Molecular Formula: C14H8N6O6S

Molecular Weight: 388.32

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ccc2nc(Nc3c([N+](=O)[O-])cc([N+](=O)[O-])c4no[n+]([O-])c34)sc2c1

Standard InChI:  InChI=1S/C14H8N6O6S/c1-6-2-3-7-10(4-6)27-14(15-7)16-11-8(18(21)22)5-9(19(23)24)12-13(11)20(25)26-17-12/h2-5H,1H3,(H,15,16)

Standard InChI Key:  UZIKBHQBFNIEQI-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: 388.32Molecular Weight (Monoisotopic): 388.0226AlogP: 2.94#Rotatable Bonds: 4
Polar Surface Area: 164.17Molecular Species: ACIDHBA: 10HBD: 1
#RO5 Violations: 0HBA (Lipinski): 12HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 2.27CX Basic pKa: CX LogP: 3.91CX LogD: 2.30
Aromatic Rings: 4Heavy Atoms: 27QED Weighted: 0.31Np Likeness Score: -1.75

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