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GX 201

Catalog No. T9647   CAS 1788071-27-1
Synonyms: GX-201

GX 201 is a selective NaV1.7 inhibitor, IC50 of < 3.2 nM for hNaV1.7.

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GX 201 Chemical Structure
GX 201, CAS 1788071-27-1
Pack Size Availability Price/USD Quantity
1 mg In stock $ 131.00
5 mg In stock $ 328.00
10 mg In stock $ 493.00
25 mg In stock $ 788.00
50 mg In stock $ 1,120.00
100 mg In stock $ 1,490.00
500 mg In stock $ 2,960.00
1 mL * 10 mM (in DMSO) In stock $ 363.00
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Purity: 99.46%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description GX 201 is a selective NaV1.7 inhibitor, IC50 of < 3.2 nM for hNaV1.7.
In vivo GX 201 has a relatively long half-life in mice. GX 201 produces analgesia at a free plasma concentration about 3 times the IC50 for high-affinity channel block. GX 201 inhibits nociceptive responses induced by formalin and inflammatory pain caused by complete Freund’s adjuvant (CFA)[1].
Synonyms GX-201
Molecular Weight 563
Formula C25H27ClF4N2O4S
CAS No. 1788071-27-1

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 60 mg/mL (106.6 mM), Sonification is recommended.

TargetMolReferences and Literature

1. Girish Bankar, et al. Selective Na V 1.7 Antagonists with Long Residence Time Show Improved Efficacy against Inflammatory and Neuropathic Pain. Cell Rep. 2018 Sep 18;24(12):3133-3145.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Bioactive Compounds Library Max Bioactive Compound Library Anti-Cancer Compound Library

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Keywords

GX 201 1788071-27-1 Membrane transporter/Ion channel Sodium Channel GX-201 GX201 inhibitor inhibit

 

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