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
(29)
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TRPV6
(4)
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All Product Categories
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TRP Channel Inhibitors
(164)
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TRP Channel Agonists
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TRP Channel Antagonists
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TRP Channel Activators
(85)
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TRP Channel Modulators
(22)
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TRP Channel Controls
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TRP Channel Ligands
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TRP Channel Related Products (574)
Related Products (574)
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Antibodies (3)
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TRP Channel Isoform Comparison
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TRPM5 agonist-1
0 ImagesCat. No.: HY-178236CAS No.: 2768029-03-2TRPM5 agonist-1 is an orally active TRPM5 agonist with a pEC50 of 8.1. TRPM5 agonist-1 shows excellent selectivity (> 100-fold) versus related cation channels (TRPM8, TRPV1, TRPV4, TRPA1, TRPM4). TRPM5 agonist-1 exhibits locally acting stimulatory effect on gastrointestinal transit in mice. TRPM5 agonist-1 can be used for research on promoting gastric motility. -
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Citronellyl acetate (Standard)
0 ImagesCat. No.: HY-N7144ARCAS No.: 150-84-5Citronellyl acetate (Standard) is the analytical standard of Citronellyl acetate (HY-N7144A). This product is intended for research and analytical applications. Citronellyl acetate is a monoterpene product of the secondary metabolism of plants, with antinociceptive activity. Citronellyl acetate exhibits pro-apoptotic activity in human hepatoma cells. Citronellyl acetate shows fungicidal, larvicidal, bactericidal and repelling/insecticidal effects. -
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Englerin A (Standard)
0 ImagesCat. No.: HY-133168RCAS No.: 1094250-15-3Englerin A (Standard) is the analytical standard of Englerin A. This product is intended for research and analytical applications. Englerin A is a potent and selective activator of TRPC4 and TRPC5 channels, with EC50s of 11.2 and 7.6 nM, respectively. Englerin A can induce renal carcinoma cells death by elevated Ca2+ influx and Ca2+ cell overload. -
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FAAH-IN-10
0 ImagesCat. No.: HY-184331FAAH-IN-10 is a FAAH inhibitor and TRPV1 antagonist, with an IC50 of 0.57 μM against human FAAH. FAAH-IN-10 regulates FAAH activity, antagonizes TRPV1 activity, and exhibits analgesic and anti-inflammatory activities. FAAH-IN-10 does not induce TRPV1-mediated hyperthermia. FAAH-IN-10 can be used for pain-related research. -
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8,9-Epoxyeicosatrienoic acid
0 ImagesCat. No.: HY-113488CAS No.: 81246-85-78,9-Epoxyeicosatrienoic acid has an unique protective effect on glomeruli. 8,9-Epoxyeicosatrienoic acid blocks the increase in glomerular albumin permeability caused by circulating permeability factor (FSPF). 8,9-Epoxyeicosatrienoic acid can be used for the research of glomerular dysfunction. -
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AMG9678
0 ImagesCat. No.: HY-104062CAS No.: 1159997-27-9AMG9678 is a potent, selective, orally active antagonist of TRPM8 with an IC50 of 31.2 nM. -
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TRPML modulator 1
0 ImagesCat. No.: HY-169824CAS No.: 2171065-77-1TRPML modulator 1 (compound A12) is a TRPML modulator that promotes autophagy. TRPML modulator 1 AC50 in the TFEB test is less than 2 mM. -
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TRPV1 antagonist 11
0 ImagesCat. No.: HY-176063CAS No.: 3084843-71-7TRPV1 antagonist 11 (compound 2ac) is a potent TRPV1 antagonist with an IC50 of 29.3 nM. TRPV1 antagonist 11 is a potent μ-opioid receptor (MOR) agonist with a Ki of 60.3 nM. TRPV1 antagonist 11, a pyrimidine piperazine, exhibits pain relieving effects by antagonizing TRPV1 and stimulating MOR. TRPV1 antagonist 11 shows a potent, dose-dependent anti-nociceptive effect in a Formalin-induced pain model in mice. -
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(-)-Menthol-d4
0 ImagesCat. No.: HY-W711474CAS No.: 1450828-98-4(-)-Menthol-d4 is the deuterium labeled (-)-Menthol (HY-75161). (-)-Menthol is a key component of peppermint oil that binds and activates transient receptor potential melastatin 8 (TRPM8), a Ca2+-permeable nonselective cation channel, to increase [Ca2+]i. Antitumor activity. -
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Diisopropyl adipate (Standard)
0 ImagesCat. No.: HY-134098RCAS No.: 6938-94-9Synonyms: Adipic acid diisopropyl ester (Standard)Oxaloacetic acid (Standard) is the analytical standard of Oxaloacetic acid. This product is intended for research and analytical applications. Oxaloacetic acid (2-Oxosuccinic acid) is a metabolic intermediate involved in several ways, such as citric acid cycle, gluconeogenesis, the urea cycle, the glyoxylate cycle, amino acid synthesis, and fatty acid synthesis, whereby Oxaloacetic acid facilitates the clearance of reactive oxygen species (ROS) and improves mitochondrial function. -
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Rosiglitazone-d4-1
0 ImagesCat. No.: HY-17386S2CAS No.: 1132641-20-3Synonyms: BRL 49653-d4-1 -
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Sphingosylphosphorylcholine-d9
0 ImagesSphingosylphosphorylcholine-d9 is deuterium labeled Sphingosylphosphorylcholine. -
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TRPV4/TRPA1-IN-1
0 ImagesCat. No.: HY-122692CAS No.: 1532515-60-8TRPV4/TRPA1-IN-1 is a TRPV4/TRPA1 inhibitor that suppresses TRPV4/TRPA1-mediated calcium influx. TRPV4/TRPA1-IN-1 alleviates pain behaviors in a mouse trigeminal stimulation pain model and inhibits inflammation and pain-related behaviors in a mouse acute pancreatitis model. TRPV4/TRPA1-IN-1 can be used in research on acute pancreatitis. -
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Pregnenolone-d6
0 ImagesCat. No.: HY-B0151S3Synonyms: 3β-Hydroxy-5-pregnen-20-one-d6Pregnenolone-d6 (3β-Hydroxy-5-pregnen-20-one-d6) is the deuterium labeled Pregnenolone (HY-B0151) . Pregnenolone (3β-Hydroxy-5-pregnen-20-one) is a powerful neurosteroid, the main precursor of various steroid hormones including steroid ketones. Pregnenolone acts as a signaling-specific inhibitor of cannabinoid CB1 receptor, inhibits the effects of tetrahydrocannabinol (THC) that are mediated by the CB1 receptors. Pregnenolone can protect the brain from cannabis intoxication. Pregnenolone is also a TRPM3 channel activator, and also can weakly activate TRPM1 channels. -
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JNJ-38893777
0 ImagesCat. No.: HY-119121CAS No.: 951135-00-5JNJ-38893777 is an orally active and highly selective transient receptor potential vanilloid type 1 (TRPV1) channel antagonist. JNJ-38893777 inhibits neuronal hyperactivation and reduces inflammatory hyperalgesia. JNJ-38893777 is promising for research of migraine headaches, neuropathic and inflammatory pain. -
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TRPM2-IN-2
0 ImagesCat. No.: HY-178393TRPM2-IN-2 is a potent and selective TRPM2 inhibitor (IC50 = 0.66 μM) with minimal activity against TRPM8 and TRPV1 (IC50 >10 μM). TRPM2-IN-2 exhibits robust neuroprotective effects in both in vitro oxygen-glucose deprivation/reperfusion (OGD/R) model and in vivo transient middle cerebral artery occlusion (tMCAO) mouse model. TRPM2-IN-2 can be used for ischemic stroke research. -
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TRPV1 activator-1
0 ImagesCat. No.: HY-148751CAS No.: 1803181-80-7 -
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TRPV1 activator-2
0 ImagesCat. No.: HY-148752CAS No.: 17514-11-3TRPV1 activator-2 (compound 9), a capsaicin head analog, makes specific interactions with channel residues at the lipid-water. -
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TRPM8 antagonist 5
0 ImagesCat. No.: HY-189375TRPM8 antagonist 5 is a TRPM8 antagonist. TRPM8 antagonist 5 exhibits anticancer activity against melanoma and prostate cancer. TRPM8 antagonist 5 can be used for research on melanoma and prostate cancer. -
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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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