ID: ALA2262039

Max Phase: Preclinical

Molecular Formula: C14H11ClN4O2SSe

Molecular Weight: 413.75

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(S(=O)(=O)n2nnnc2[Se]c2ccc(Cl)cc2)cc1

Standard InChI:  InChI=1S/C14H11ClN4O2SSe/c1-10-2-6-12(7-3-10)22(20,21)19-14(16-17-18-19)23-13-8-4-11(15)5-9-13/h2-9H,1H3

Standard InChI Key:  YLDMPIDTYKROSV-UHFFFAOYSA-N

Associated Targets(non-human)

Pseudomonas aeruginosa 123386 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Listeria monocytogenes 2626 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bacillus cereus 7522 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Salmonella enteritidis 727 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Yersinia enterocolitica 166 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: UnknownTopical: 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: 413.75Molecular Weight (Monoisotopic): 413.9456AlogP: #Rotatable Bonds:
Polar Surface Area: Molecular Species: HBA: HBD:
#RO5 Violations: HBA (Lipinski): HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: CX LogD:
Aromatic Rings: Heavy Atoms: QED Weighted: Np Likeness Score:

References

1. Yldrr Y, Us MF, Colak N, Ozkan H, Yavuz S, Disli A, Ozturk S, Turker L.  (2009)  The synthesis and investigation of the antimicrobial activity of some new phenylselanyl-1-(toluene-4-sulfonyl)-1H-tetrazole derivatives,  18  (2): [10.1007/s00044-008-9110-7]

Source