ID: ALA2230023

Max Phase: Preclinical

Molecular Formula: C10H6ClNO2S

Molecular Weight: 239.68

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=[N+]([O-])c1cc(Cl)ccc1-c1ccsc1

Standard InChI:  InChI=1S/C10H6ClNO2S/c11-8-1-2-9(7-3-4-15-6-7)10(5-8)12(13)14/h1-6H

Standard InChI Key:  NCCBXPUAWAEOAW-UHFFFAOYSA-N

Associated Targets(non-human)

Mycosphaerella arachidis 441 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium oxysporum 3998 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Botryosphaeria berengeriana 484 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium graminearum 1554 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Alternaria solani 773 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: 239.68Molecular Weight (Monoisotopic): 238.9808AlogP: 3.98#Rotatable Bonds: 2
Polar Surface Area: 43.14Molecular Species: HBA: 3HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.94CX LogD: 3.94
Aromatic Rings: 2Heavy Atoms: 15QED Weighted: 0.59Np Likeness Score: -2.41

References

1. Wang MZ, Xu H, Feng Q, Wang LZ, Wang SH, Li ZM..  (2009)  Design, synthesis, and fungicidal activity of novel analogues of pyrrolnitrin.,  57  (17): [PMID:19681615] [10.1021/jf902320e]

Source