ID: ALA3274655

Max Phase: Preclinical

Molecular Formula: C9H13N3O6S

Molecular Weight: 291.29

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cn1c([N+](=O)[O-])cnc1S(=O)(=O)CCCCC(=O)O

Standard InChI:  InChI=1S/C9H13N3O6S/c1-11-7(12(15)16)6-10-9(11)19(17,18)5-3-2-4-8(13)14/h6H,2-5H2,1H3,(H,13,14)

Standard InChI Key:  GSQCHYKNEGOEMI-UHFFFAOYSA-N

Associated Targets(non-human)

Bacteroides fragilis 1445 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Clostridium perfringens 1165 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Neisseria gonorrhoeae 1461 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Trichomonas vaginalis 2376 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Candida albicans 78123 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: 291.29Molecular Weight (Monoisotopic): 291.0525AlogP: 0.36#Rotatable Bonds: 7
Polar Surface Area: 132.40Molecular Species: ACIDHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 3.07CX Basic pKa: CX LogP: 0.23CX LogD: -3.23
Aromatic Rings: 1Heavy Atoms: 19QED Weighted: 0.44Np Likeness Score: -1.10

References

1. Tweit RC, Muir RD, Ziecina S..  (1977)  Nitroimidazoles with antibacterial activity against Neisseria gonorrhoeae.,  20  (12): [PMID:412966] [10.1021/jm00222a036]

Source