GX 201
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    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 462578

CAS#: 1788071-27-1

Description: GX 201 is a potent and selective Nav1.7 blocker and an analgesic.


Chemical Structure

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GX 201
CAS# 1788071-27-1

Theoretical Analysis

MedKoo Cat#: 462578
Name: GX 201
CAS#: 1788071-27-1
Chemical Formula: C25H27ClF4N2O4S
Exact Mass: 562.13
Molecular Weight: 563.005
Elemental Analysis: C, 53.33; H, 4.83; Cl, 6.30; F, 13.50; N, 4.98; O, 11.37; S, 5.69

Price and Availability

Size Price Availability Quantity
10mg USD 585 2 Weeks
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Synonym: GX 201; GX-201; GX201

IUPAC/Chemical Name: 4-[[1-[[2-Chloro-5-(trifluoromethyl)phenyl]methyl]-4-piperidinyl]methoxy]-5-cyclopropyl-2-fluoro-N-(methylsulfonyl)benzamide

InChi Key: KYBPOTYVFWNSGS-UHFFFAOYSA-N

InChi Code: InChI=1S/C25H27ClF4N2O4S/c1-37(34,35)31-24(33)20-11-19(16-2-3-16)23(12-22(20)27)36-14-15-6-8-32(9-7-15)13-17-10-18(25(28,29)30)4-5-21(17)26/h4-5,10-12,15-16H,2-3,6-9,13-14H2,1H3,(H,31,33)

SMILES Code: O=C(NS(=O)(C)=O)C1=CC(C2CC2)=C(OCC3CCN(CC4=CC(C(F)(F)F)=CC=C4Cl)CC3)C=C1F

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >3 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 563.00 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Shields SD, Deng L, Reese RM, et al. Insensitivity to Pain upon Adult-Onset Deletion of Nav1.7 or Its Blockade with Selective Inhibitors. J Neurosci. 2018;38(47):10180-10201. doi:10.1523/JNEUROSCI.1049-18.2018

2: Bankar G, Goodchild SJ, Howard S, et al. Selective NaV1.7 Antagonists with Long Residence Time Show Improved Efficacy against Inflammatory and Neuropathic Pain. Cell Rep. 2018;24(12):3133-3145. doi:10.1016/j.celrep.2018.08.063