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JT010

Chemical Structure : JT010

CAS No.: 917562-33-5

JT010 (JT-010)

Catalog No.: PC-49684Not For Human Use, Lab Use Only.

JT010 (JT-010) is a potent, site-selective and covalent TRPA1 agonist, opens the TRPA1 channel by covalently and site-selectively binding to Cys621 with EC50 of 0.65 nM.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

JT010 (JT-010) is a potent, site-selective and covalent TRPA1 agonist, opens the TRPA1 channel by covalently and site-selectively binding to Cys621 with EC50 of 0.65 nM.
JT010 is highly selective for TRPA1 over TRPV1, TRPV3, TRPV4, TRPM2, TRPM8, and TRPC5 (EC50 values >1 uM).
JT010 (10 nM) failed to stimulate calcium influx in the C621S mutant cells but induced calcium influx in the wild type cells.
JT010 could induce TRPA1-specific pain model. increased the intracellular calcium concentration and extracellular signal-regulated kinase 1/2 phosphorylation, and up-regulated alkaline phosphatase mRNA in human dental pulp cells.
Topical treatment of TRPA1 specific agonist JT010 increased UVB-induced skin pigmentation in guinea pigs.

Physicochemical Properties

M.Wt 354.85
Formula C16H19ClN2O3S
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

2-chloro-N-(4-(4-methoxyphenyl)thiazol-2-yl)-N-(3-methoxypropyl)acetamide

References

1. Takaya J, et al. J Am Chem Soc. 2015 Dec 23;137(50):15859-64.

2. Heber S, et al. J Neurosci. 2019 May 15;39(20):3845-3855.

3. Tazawa K, et al. Am J Pathol. 2020 Dec;190(12):2417-2426.

4. Wu W, et al. Exp Dermatol. 2022 Oct 27. doi: 10.1111/exd.14693.

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