JT-010

Source: Wikipedia, the free encyclopedia.
JT-010
Names
Preferred IUPAC name
2-Chloro-N-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]-N-(3-methoxypropyl)acetamide
Identifiers
3D model (
JSmol
)
ChemSpider
  • InChI=1S/C16H19ClN2O3S/c1-21-9-3-8-19(15(20)10-17)16-18-14(11-23-16)12-4-6-13(22-2)7-5-12/h4-7,11H,3,8-10H2,1-2H3
    Key: KZMAWJRXKGLWGS-UHFFFAOYSA-N
  • O=C(N(C1=NC(C2=CC=C(OC)C=C2)=CS1)CCCOC)CCl
Properties
C16H19ClN2O3S
Molar mass 354.85 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

JT-010 is a chemical compound which acts as a potent, selective activator of the TRPA1 channel, and has been used to study the role of this receptor in the perception of pain, as well as other actions such as promoting repair of dental tissue after damage.[1][2][3][4]

See also

References

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