TRP Channel
Transient receptor potential channels
TRP Channel Isoform Specific Products
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TRP Channel
(340)
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TRPA1
(33)
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TRPC3
(10)
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TRPC4
(8)
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TRPC5
(19)
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TRPC6
(4)
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TRPC7
(2)
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TRPM8
(24)
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TRPM2
(5)
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TRPM3
(9)
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TRPM4
(4)
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TRPM7
(1)
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TRPML1
(4)
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TRPML2
(4)
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TRPML3
(5)
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TRPV1
(60)
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TRPV2
(5)
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TRPV3
(15)
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TRPV4
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TRPV6
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All Product Categories
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TRP Channel Inhibitors
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TRP Channel Agonists
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TRP Channel Antagonists
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TRP Channel Activators
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TRP Channel Modulators
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TRP Channel Controls
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TRP Channel Ligands
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TRP Channel Related Products (577)
Related Products (577)
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Antibodies (3)
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TRP Channel Isoform Comparison
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HC-067047 hydrochloride
0 ImagesCat. No.: HY-W721480CAS No.: 1481646-76-7 -
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Glucoputranjivin
0 ImagesCat. No.: HY-N15422CAS No.: 18432-16-1Glucoputranjivin (compound 1) is a reference compound that can be used for qualitative and quantitative determinations of active compounds in SO. -
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GSK2193874 (Standard)
0 ImagesGSK2193874 (Standard) is the analytical standard of GSK2193874 (HY-100720). This product is intended for research and analytical applications. GSK2193874 is an orally active, potent, and selective TRPV4 antagonist with IC50s of 2 nM and 40 nM for rTRPV4 and hTRPV4. -
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N-Oleoyl valine
0 ImagesCat. No.: HY-118535CAS No.: 60374-41-6N-Oleoyl valine is a N-acyl valine compound that acts as a TRPV3 receptor antagonist. -
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(±)-Evodiamine (Standard)
0 Images(±)-Evodiamine Standard is the analytical standard of (±)-Evodiamine (HY-N0114A). This product is intended for research and analytical applications. (±)-Evodiamine is an orally active indoloquinazoline alkaloid composed of equal amounts of enantiomers, with (+)-Evodiamine exerting the primary biological functions. (±)-Evodiamine is a Top1 inhibitor and a TRPV1 receptor agonist. (±)-Evodiamine induces cell cycle arrest and apoptosis by inhibiting Top1 and disrupting Tubulin polymerization, suppresses oncogenic signaling pathways such as NF-κB and Akt, and specifically agonizes TRPV1 receptors to regulate neuropeptide release and energy metabolism. (±)-Evodiamine is used in research on traumatic brain injury, obesity, cancer, neuropathy, dry eye disease, and colitis. -
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HC-030031 (Standard)
0 ImagesHC-030031 (Standard) is the analytical standard of HC-030031. This product is intended for research and analytical applications. HC-030031 is a potent and selective TRPA1 inhibitor, which antagonizes AITC- and formalin-evoked calcium influx with IC50s of 6.2±0.2 and 5.3±0.2 μM, respectively. -
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(E/Z)-Capsaicin-d3
0 ImagesCat. No.: HY-10448SCAS No.: 1185237-43-7(E/Z)-Capsaicin-d3 is the deuterium labeled (E/Z)-Capsaicin[1]. -
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Bisandrographolide A
0 ImagesCat. No.: HY-N2940CAS No.: 160498-00-0Synonyms: BAABisandrographolide A (BAA) activates TRPV4 channel with an EC50 of 790-950 nM. Bisandrographolide A can bind to CD81 and suppress its function. Bisandrographolide A is an anti-inflammatory, immunostimulant, and antihypertensive compound. -
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Mavatrep (Standard)
0 ImagesCat. No.: HY-16935RCAS No.: 956274-94-5Synonyms: JNJ-39439335 (Standard)Mavatrep (Standard) is the analytical standard of Mavatrep. This product is intended for research and analytical applications. Mavatrep (JNJ-39439335) is an orally active, selective and potent TRPV1 antagonist with high affinity for hTRPV1 channels (Ki=6.5 nM). Mavatrep antagonizes capsaicin-induced Ca2+ influx with an IC50 value of 4.6 nM. Mavatrep can be used in some studies of neuropathic pain. -
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(Rac)-AMG 628
0 ImagesCat. No.: HY-123374CAS No.: 862269-73-6(Rac)-AMG 628 is the racemate of AMG 628, a potent TRPV1 antagonist with an IC50 of 3.7nM. AMG 628 can be used in chronic pain research. -
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Pyr3 (Standard)
0 ImagesCat. No.: HY-108465RCAS No.: 1160514-60-2 -
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Pulegone (Standard)
0 ImagesPulegone (Standard) is the analytical standard of Pulegone (HY-N1500). This product is intended for research and analytical applications. Pulegone is a monoterpene ketone compound widely present in the essential oils of many plants. Pulegone can also be used as a bird repellent. Pulegone has multiple activities such as anti-inflammatory, antibacterial, antifungal, and anti-hyperalgesic effects. Pulegone is particularly effective against bacteria of the Salmonella species. -
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CIM0216 (Standard)
0 ImagesCat. No.: HY-110220RCAS No.: 1031496-06-6CIM0216 (Standard) is the analytical standard of CIM0216 (HY-110220). This product is intended for research and analytical applications. CIM0216, a synthetic TRPM3 ligand, acts as a potent and selective agonist of TRPM3. CIM0216 exhibits selectivity for TRPM3 over TRPM1, TRPM2 and TRPM4-8. CIM0216 acts in a TRPM3-dependent manner to induce pain and evoke neuropeptide release from sensory nerve terminals in vitro. CIM0216 is a powerful tool for studies of the physiological functions of TRPM3, and can be used for neurogenic inflammation research. -
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ASP7663 (Standard)
0 ImagesCat. No.: HY-101907RCAS No.: 1190217-35-6 -
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Acoltremon (Standard)
0 ImagesCat. No.: HY-108449RCAS No.: 68489-09-8Synonyms: WS-12 (Standard); AR-15512 (Standard); AVX-012 (Standard)Acoltremon (Standard) is the analytical standard of Acoltremon (HY-108449). This product is intended for research and analytical applications. Acoltremon (WS-12; AR-15512) is a potent and selective TRPM8 agonist, the menthol derivative, as a cooling agent. Acoltremon shows analgesic effect, and can be used in chronic neuropathic pain research. -
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- AMG9810 (Standard)
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Diphenyleneiodonium chloride (Standard)
0 ImagesCat. No.: HY-100965RCAS No.: 4673-26-1Synonyms: DPI (Standard)Diphenyleneiodonium chloride (Standard) is the analytical standard of Diphenyleneiodonium chloride (HY-100965). This product is intended for research and analytical applications. Diphenyleneiodonium chloride is a NADPH oxidase (NOX) inhibitor and also functions as a TRPA1 activator with an EC50 of 1 to 3 μM. Diphenyleneiodonium chloride selectively inhibits intracellular reactive oxygen species. -
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Taurultam
0 ImagesTaurultam is the major active hydrolytic metabolite of Taurolidine (HY-W011522), which selectively activates hTRPA1 to trigger effects in sensory neurons. Taurultam exhibits activity against SARS-CoV-2 variants, influenza A viruses (H1N1, H3N2) and influenza B viruses. Taurultam induces mild tracheal sensory nerve stimulation and CGRP release in mice. Taurultam can be used in studies related to SARS-CoV-2 infection, influenza virus infection, and co-infection with SARS-CoV-2 and influenza A virus. -
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Methyl syringate (Standard)
0 ImagesMethyl syringate is a selective TRPA1 agonist. Methyl syringate regulates food intake and gastric emptying through a TRPA1-mediated pathway. Methyl syringate is an efficient phenolic mediator for bacterial and fungal laccases. Methyl syringate is a chemical marker of Asphodel monofloral honey. Methyl syringate contributes to the antibacterial activity of honey. Methyl syringate inhibits aflatoxin production. Methyl syringate can contribute to weight suppression. Methyl syringate can be studies for cancer prevention (e.g. lung cancer), suppression of hypoxia-induced inflammatory response and tumorigenesis. -
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(Z)-Capsaicin (Standard)
0 ImagesCat. No.: HY-B1583RCAS No.: 25775-90-0Synonyms: Zucapsaicin (Standard); Civamide (Standard); cis-Capsaicin (Standard) -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
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