TRP Channel
Transient receptor potential channels
TRP Channel Isoform Specific Products
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TRP Channel
(336)
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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
(4)
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TRPV1
(60)
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TRPV2
(5)
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TRPV3
(15)
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TRPV4
(29)
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TRPV6
(4)
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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 (569)
Related Products (569)
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Antibodies (3)
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TRP Channel Isoform Comparison
- Palvanil
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8-Gingerol (Standard)
0 ImagesCat. No.: HY-N0447RCAS No.: 23513-08-88-Gingerol (Standard) is the analytical standard of 8-Gingerol. This product is intended for research and analytical applications. 8-Gingerol, found in the rhizomes of ginger (Z. officinale) with oral bioavailability, activates TRPV1, with an EC50 of 5.0 μM. 8-Gingerol inhibits COX-2, and inhibits the growth of H. pylori in vitro. -
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Pulegone-d8
0 ImagesCat. No.: HY-N1500S1CAS No.: 62385-90-4Pulegone-d8 is deuterated labeled Pulegone (HY-N1500). 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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Dihydrocapsaicin-d3
0 ImagesCat. No.: HY-N0361SCAS No.: 1330261-21-6Dihydrocapsaicin-d3 is the deuterium labeled Dihydrocapsaicin (HY-N0361). Dihydrocapsaicin, a capsaicin, is a potent and selective TRPV1 (transient receptor potential vanilloid channel 1) agonist. Dihydrocapsaicin reduces AIF, Bax, and Caspase-3 expressions, and increased Bcl-2, Bcl-xL and p-Akt levels. Dihydrocapsaicin enhances the hypothermia-induced neuroprotection following ischemic stroke via PI3K/Akt regulation in rat. -
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Phanginin J
0 ImagesCat. No.: HY-N21629CAS No.: 1011528-67-8Phanginin J is a Cassane-type furanoditerpene found in the seeds of Caesalpinia sappan L. Phanginin J docks with the TRPV1 molecule and may inhibit nociceptive sensory signal transduction by antagonizing TRPV1. Phanginin J can be used in research related to chemotherapy-induced peripheral neuropathy (CIPN). -
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GRC-6211
0 ImagesCat. No.: HY-105324CAS No.: 1166398-35-1GRC-6211 is an orally active and selective TRPV1 antagonist. GRC-6211 exhibits anti-inflammation effect. -
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Cyclic ADP-ribose diammonium
0 ImagesCat. No.: HY-N7395BSynonyms: cADPR diammoniumCyclic ADP-ribose diammonium (cADPR diammonium) is a potent second messenger for calcium mobilization that is synthesized from NAD+ by an ADP-ribosyl cyclase. Cyclic ADP-ribose diammonium increases cytosolic calcium mainly by Ryanodine receptor-mediated release from endoplasmic reticulum and also by extracellular influx through the opening of TRPM2 channels. -
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TRPM4-IN-4
0 ImagesCat. No.: HY-183268TRPM4-IN-4 (Compound 118) is a selective TRPM4 inhibitor with an IC50 value of 0.339 μM against hTRPM4. TRPM4-IN-4 inhibits hTRPM4 and mTRPM4. TRPM4-IN-4 can be used for the research of colorectal cancer. -
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Hydroxy-α-sanshool (Standard)
0 ImagesCat. No.: HY-N6825RCAS No.: 83883-10-7Hydroxy-α-sanshool (Standard) is the analytical standard of Hydroxy-α-sanshool. This product is intended for research and analytical applications. Hydroxy-α-sanshool is a transient receptor potential ankyrin 1 (TRPA1) and TRP vanilloid 1 (TRPV1) agonist with EC50s of 69 and 1.1 μM, respectively. Hydroxy-α-sanshool can be used for pain research. -
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- AZ12099548
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N-Arachidonyldopamine-d8
0 ImagesCat. No.: HY-110018SCAS No.: 1159908-42-5N-Arachidonyldopamine-d8 is the deuterium labeled N-Arachidonyldopamine. -
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TRPC5-IN-4
0 ImagesCat. No.: HY-144429CAS No.: 2762315-39-7TRPC5-IN-4 is potent and safe TRPC inhibitor with IC50 value of 14.07 nM and 65 nM for TRPC5 and TRPC4, respectively. TRPC5-IN-4 shows no damage on the cellular component of liver and kidney. TRPC5-IN-4 can be used for the research of chronic kidney disease (CKD). -
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- GSK2332255B
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DD-161515
0 ImagesCat. No.: HY-183857CAS No.: 410080-55-6DD-161515 is a TRPV1/VR1 inhibitor with an IC50 of 0.7 μM in rats. DD-161515 binds to an allosteric site of TRPV1 distinct from that of capsaicin, blocks channel opening, inhibits receptor-mediated calcium ion influx, reduces the excitability of peripheral sensory nerve fibers, and thereby inhibits nociception induced by heat and transmission of chemically induced pain signals. DD-161515 can be used in studies related to inflammatory pain. -
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BCTC (Standard)
0 ImagesBCTC (Standard) is the analytical standard of BCTC. This product is intended for research and analytical applications. BCTC is an orally active current inhibitor of vanilloid receptor type 1 (VR1). BCTC is a transient receptor potential cation channel subfamily M member 8 (TRPM8) and transient receptor potential vanilloid 1 (TRPV1) antagonist. BCTC is an insulin sensitizer and secretor. BCTC has anticancer and analgesic effects. -
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RhTx
0 ImagesCat. No.: HY-P10654CAS No.: 2861260-80-0 -
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EIPA (Standard)
0 ImagesSynonyms: L593754 (Standard); MH 12-43 (Standard); Ethylisopropylamiloride (Standard)EIPA (Standard) is the analytical standard of EIPA. This product is intended for research and analytical applications. EIPA (L593754) is an orally active TRPP3 channel inhibitor with an IC50 of 10.5 μM. EIPA also enhances autophagy by inhibiting Na+/H+-exchanger 3 (NHE3). EIPA inhibits macropinocytosis as well. EIPA can be used in the research of inflammation and cancers, such as gastric cancer, colon carcinoma, pancreatic carcinoma. -
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(E)-3-Benzo[1,3]dioxol-5-yl-N,N-diphenyl-2-propenamide
0 ImagesCat. No.: HY-185173CAS No.: 1309389-73-8(E)-3-Benzodioxol-5-yl-N,N-diphenyl-2-propenamide is a chemically synthesized flavoring substance and can be found in toothpaste products. (E)-3-Benzodioxol-5-yl-N,N-diphenyl-2-propenamide is non-genotoxic, shows no genotoxic activity in bacterial reverse mutation and in vitro mammalian cell micronucleus assays. (E)-3-Benzodioxol-5-yl-N,N-diphenyl-2-propenamide does not induce prenatal developmental toxicity in rats. -
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Nonivamide (Standard)
0 ImagesSynonyms: Pelargonic acid vanillylamide (Standard); Nonanoic acid vanillylamide (Standard); Pseudocapsaicin (Standard)Nonivamide (Standard) is the analytical standard of Nonivamide. This product is intended for research and analytical applications. Nonivamide is aloading...Please select quantityGet QuoteAugust 31
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A-889425
0 ImagesCat. No.: HY-133166CAS No.: 1072921-02-8A-889425 is an oral active selective TRPV1 receptor antagonist with the with an IC50 of 335 nM (rat) and 34 nM (human). A-889425 has good penetration into the CNS and reduces mechanical allodynia and spinal neuron responses to mechanical stimulation of Complete Freund's adjuvant (HY-153808)-inflamed rat hind paws. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.