TCS 2210

95%

Reagent Code: #238950
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CAS Number 1201916-31-5

science Other reagents with same CAS 1201916-31-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.35 g/mol
Formula C₁₈H₁₇N₃O₃
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used as a selective antagonist for the TRPM8 ion channel, TCS 2210 is primarily employed in scientific research to study cold-sensing pathways and pain mechanisms related to temperature perception. It helps investigate the role of TRPM8 in conditions such as neuropathic pain, migraine, and overactive bladder. Due to its ability to block menthol- and cold-induced responses, it is a valuable tool in pharmacological studies aiming to develop new analgesic or urological treatments. Its selectivity makes it suitable for in vitro and in vivo experiments where precise modulation of TRPM8 activity is required.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿11,320.00
inventory 25mg
10-20 days ฿33,980.00
TCS 2210
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Used as a selective antagonist for the TRPM8 ion channel, TCS 2210 is primarily employed in scientific research to study cold-sensing pathways and pain mechanisms related to temperature perception. It helps investigate the role of TRPM8 in conditions such as neuropathic pain, migraine, and overactive bladder. Due to its ability to block menthol- and cold-induced responses, it is a valuable tool in pharmacological studies aiming to develop new analgesic or urological treatments. Its selectivity makes it s

Used as a selective antagonist for the TRPM8 ion channel, TCS 2210 is primarily employed in scientific research to study cold-sensing pathways and pain mechanisms related to temperature perception. It helps investigate the role of TRPM8 in conditions such as neuropathic pain, migraine, and overactive bladder. Due to its ability to block menthol- and cold-induced responses, it is a valuable tool in pharmacological studies aiming to develop new analgesic or urological treatments. Its selectivity makes it suitable for in vitro and in vivo experiments where precise modulation of TRPM8 activity is required.

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