5-(2-chlorobenzyl)thieno[3,2-c]pyridin-5-ium

ID: ALA3526248

Chembl Id: CHEMBL3526248

Cas Number: 721387-90-2

PubChem CID: 12570096

Max Phase: Preclinical

Molecular Formula: C14H11ClNS+

Molecular Weight: 260.77

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Clc1ccccc1C[n+]1ccc2sccc2c1

Standard InChI:  InChI=1S/C14H11ClNS/c15-13-4-2-1-3-11(13)9-16-7-5-14-12(10-16)6-8-17-14/h1-8,10H,9H2/q+1

Standard InChI Key:  OQXLLGWEACZMFD-UHFFFAOYSA-N

Alternative Forms

Associated Targets(Human)

CYP2B6 Tchem Cytochrome P450 2B6 (1338 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver microsome (8277 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

CYP2B4 Cytochrome P450 2B4 (31 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

Calculated Properties

Molecular Weight: 260.77Molecular Weight (Monoisotopic): 260.0295AlogP: 3.89#Rotatable Bonds: 2
Polar Surface Area: 3.88Molecular Species: NEUTRALHBA: 1HBD:
#RO5 Violations: HBA (Lipinski): 1HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 0.02CX LogD: 0.02
Aromatic Rings: 3Heavy Atoms: 17QED Weighted: 0.62Np Likeness Score: -1.51

References

1. Talakad JC, Shah MB, Walker GS, Xiang C, Halpert JR, Dalvie D..  (2011)  Comparison of in vitro metabolism of ticlopidine by human cytochrome P450 2B6 and rabbit cytochrome P450 2B4.,  39  (3): [PMID:21156812] [10.1124/dmd.110.037101]

Source