4-Chloro-3-methoxy-N-pyridin-2-yl-benzenesulfonamide

Modify Date: 2026-04-12 22:00:58

4-Chloro-3-methoxy-N-pyridin-2-yl-benzenesulfonamide Structure
4-Chloro-3-methoxy-N-pyridin-2-yl-benzenesulfonamide structure
Common Name 4-Chloro-3-methoxy-N-pyridin-2-yl-benzenesulfonamide
CAS Number 409357-24-0 Molecular Weight 298.75
Density N/A Boiling Point N/A
Molecular Formula C12H11ClN2O3S Melting Point N/A
MSDS N/A Flash Point N/A

 Names

Name 4-Chloro-3-methoxy-N-pyridin-2-yl-benzenesulfonamide

 Chemical & Physical Properties

Molecular Formula C12H11ClN2O3S
Molecular Weight 298.75
InChIKey YDFWVQDTODNHNL-UHFFFAOYSA-N
SMILES COC1=C(C=CC(=C1)S(=O)(=O)NC2=CC=CC=N2)Cl

 Bioassay

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Name: A screen for compounds that inhibit cell wall-associated teichoic acid synthesis in S...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: N/A
External Id: HMS704
Name: Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: HCMV UL50
External Id: HMS1262
Name: Chemical Probes of Kaposi's Sarcoma Herpes Virus Latent Infection
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: ORF 73 [Human herpesvirus 8 type M]
External Id: HMS791
Name: Small-molecule inhibitors of ST2 (IL1RL1)
Source: 20881
Target: interleukin-1 receptor-like 1 isoform [homo sapiens]
External Id: ST2_IL33_Inhibitors_Primary_Screening_77700
Name: Inhibitors of CDC25B-CDK2/CyclinA interaction
Source: Center for Chemical Genomics, University of Michigan
External Id: MScreen:TargetID_600
Name: High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS1303
Name: A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS979
Name: Alphascreen assay for small molecules abrogating mHTT-CaM Interaction
Source: 24983
Target: Huntingtin
External Id: KUHTS-Muma KU-CaM-Htt INH-01
Name: A screen for compounds that inhibit viral RNA polymerase binding and polymerization a...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: Chain A, Poliovirus Polymerase With Gtp
External Id: HMS750
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