TRP Channel
Transient receptor potential channels
TRP Channel Isoform Specific Products
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TRP Channel
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TRPA1
(34)
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TRPC3
(11)
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TRPC4
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TRPC5
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TRPC6
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TRPC7
(2)
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TRPM8
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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
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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 (583)
Related Products (583)
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Antibodies (3)
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TRP Channel Isoform Comparison
- 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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FGIN 1-27 (Standard)
0 ImagesCat. No.: HY-101059RCAS No.: 142720-24-9FGIN 1-27 (Standard) is the analytical standard of FGIN 1-27 (HY-101059). This product is intended for research and analytical applications. FGIN-1-27 is a blood-brain barrier-penetrant TSPO ligand with a Ki value of 5 nM. FGIN 1-27 inhibits PKC-β, PKA/CREB, p38/ERK MAPK, MITF, tyrosinase, TRP-1, and TRP-2, thereby inhibiting melanogenesis and pigmentation. FGIN-1-27 alleviates X-ray radiation-induced astrocyte mitochondrial hyperfunction, reduces ROS and superoxide production, inhibits excessive activation of A1-type astrocytes, downregulates GFAP and C3 protein expression, and restores astrocyte proliferative capacity. FGIN-1-27 produces anticonvulsant effects in normal mice; in diazepam-withdrawn mice, the brain MDR pathway becomes subsensitive, and the anticonvulsant activity disappears. FGIN-1-27 attenuates pigmentation in zebrafish embryos and ameliorates UVB-induced skin pigmentation in guinea pigs. FGIN-1-27 directly stimulates testicular Leydig cells while upregulating luteinizing hormone levels, causing an acute increase in serum testosterone in male rats. FGIN 1-27 can be used for research related to hyperpigmentation, epilepsy, brain injury, and other diseases. -
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DWP-05195
0 ImagesCat. No.: HY-167868CAS No.: 904309-12-2DWP-05195 is a TRPV1 antagonist that can inhibit the pain signal transduction. DWP-05195 induces ER stress-dependent apoptosis through the ROS-p38-CHOP pathway in human ovarian cancer cells. -
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2′-Deoxy-ADPR
0 ImagesCat. No.: HY-137704CAS No.: 111864-49-42′-Deoxy-ADPR is an agonist for transient receptor potential melastatin 2 channel (TRPM2 channel). 2′-Deoxy-ADPR may acts as the signaling molecule in Jurkat T-lymphocytes. -
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Crotamiton (Standard)
0 ImagesCrotamiton (Standard) is the analytical standard of Crotamiton. This product is intended for research and analytical applications. Crotamiton is a TRPV4 inhibitor. Crotamiton inhibits TRPV4 currents. Crotamiton inhibits TRPV4 selective agonist-induced pruritus-related behaviors in mice. Crotamiton inhibits Histamine- and Chloroquine-induced calcium influx via the H1R/TRPV1, MRGPRA3/TRPA1 pathways, and also suppresses calcium influx in primary mouse dorsal root ganglion neurons. Crotamiton is applicable to research related to pruritus, scabies, and non-scabietic pruritus. -
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N-Oleoyldopamine (Standard)
0 ImagesCat. No.: HY-108448RCAS No.: 105955-11-1Synonyms: OLDA (Standard)N-Oleoyldopamine (Standard) is the analytical standard of N-Oleoyldopamine (HY-108448). This product is intended for research and analytical applications. N-Oleoyldopamine (OLDA) is a product of condensation of oleic acid and dopamine (DA) and an endogenous TRPV1 selective agonist. N-Oleoyldopamine (OLDA) can crosses the blood-brain barrier. N-oleoyl-dopamine protects the heart against ischemia-reperfusion injury via activation of TRPV1. -
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N-Arachidonyldopamine (Standard)
0 ImagesCat. No.: HY-110018RCAS No.: 199875-69-9N-Arachidonyldopamine (Standard) is the analytical standard of N-Arachidonyldopamine (HY-110018). This product is intended for research and analytical applications. N-Arachidonyldopamine is a potent and selective endogenous CB1 receptor agonist with a Ki of 250 nM. N-Arachidonyldopamine is also a potent and selective TRPV1 agonist an with EC50 of ~ 50 nM. -
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Lazertinib (Standard)
0 ImagesCat. No.: HY-109061RCAS No.: 1903008-80-9Synonyms: YH25448 (Standard); GNS-1480 (Standard)Lazertinib (Standard) is the analytical standard of Lazertinib (HY-109061). This product is intended for research and analytical applications. Lazertinib (YH25448) is a potent, selective, CNS-penetrant, orally available and irreversible EGFR tyrosine Kinase inhibitor, exhibiting high selectivity for activating (EGFRm) and T790M resistance mutations. Lazertinib inhibits phosphorylation of EGFR, AKT and ERK, leading to apoptosis and suppression of tumor growth in mouse H1975-luc brain metastasis xenograft models. Lazertinib can be used in the study of non-small cell lung cancer. -
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ML-SA1 (Standard)
0 ImagesCat. No.: HY-108462RCAS No.: 332382-54-4ML-SA1 (Standard) is the analytical standard of ML-SA1 (HY-108462). This product is intended for research and analytical applications. ML-SA1, as a selective TRPML agonist, inhibits Dengue virus 2 (DENV2) and Zika virus (ZIKV) by promoting lysosomal acidification and protease activity. The IC50 value of ML-SA1 against DENV2 RNA and ZIKV RNA is 8.3 μM and 52.99 μM, respectively. ML-SA1 induces autophagy. ML-SA1 can be used for the research of broad-spectrum antiviral. -
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Pregnenolone monosulfate sodium (Standard)
0 ImagesCat. No.: HY-110189RCAS No.: 1852-38-6Synonyms: 3β-Hydroxy-5-pregnen-20-one monosulfate sodium (Standard)Pregnenolone monosulfate (sodium) (Standard) is the analytical standard of Pregnenolone monosulfate (sodium). This product is intended for research and analytical applications. Pregnenolone monosulfate sodium (3β-Hydroxy-5-pregnen-20-one monosulfate sodium) is a powerful neurosteroid, the main precursor of various steroid hormones including steroid ketones. Pregnenolone monosulfate sodium acts as a signaling-specific inhibitor of cannabinoid CB1 receptor, inhibits the effects of tetrahydrocannabinol (THC) that are mediated by the CB1 receptors. Pregnenolone monosulfate sodium can protect the brain from cannabis intoxication. Pregnenolone monosulfate sodium is also a TRPM3 channel activator, and also can weakly activate TRPM1 channels. -
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TC-I 2014 (Standard)
0 ImagesCat. No.: HY-110199RCAS No.: 1221349-53-6TC-I 2014 (Standard) is the analytical standard of TC-I 2014 (HY-110199). This product is intended for research and analytical applications. TC-I 2014 (compound 5) is a potent and orally active Benzimidazole-containing transient receptor potential melastatin 8 (TRPM8) antagonist, with IC50 values of 0.8 nM, 3.0 nM and 4.4 nM for canine, human and rat channels respectively. TC-I 2014 exhibits antiallodynic properties in pain models. -
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8-Br-7-CH-ADPR
0 ImagesCat. No.: HY-134268CAS No.: 1011457-95-6Synonyms: 8-Bromo-7-deazaadenosine-5'-O-diphosphoribose8-Br-7-CH-ADPR (8-Bromo-7-deazaadenosine-5'-O-diphosphoribose) is a specific TRPM2 antagonist that inhibits TRPM2 activation by binding to the NUDT9 homology domain of the TRPM2 channel, thereby controlling the influx of cations through the cell membrane channel. 8-Br-7-CH-ADPR can be used to study the role of TRPM2 in pathological processes such as cell death, neurodegenerative diseases, myocardial infarction, and diabetes. -
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AM-0902 (Standard)
0 ImagesCat. No.: HY-108329RCAS No.: 1883711-97-4 -
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MSK-195
0 ImagesCat. No.: HY-123428CAS No.: 289902-82-5MSK-195 is a potent agonist of TRPV1, with a potency of 120 nM and an efficacy of 71% in arteriolar response. -
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Mesendogen (Standard)
0 ImagesCat. No.: HY-103073RCAS No.: 864716-85-8Mesendogen (Standard) is the analytical standard of Mesendogen (HY-103073). This product is intended for research and analytical applications. Mesendogen is a TRPM6 inhibitor. Mesendogen enhances the mesoderm and definitive endoderm (DE) differentiations of human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs). Mesendogen can be used for the research of magnesium homeostasis during early embryonic cell development. -
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A778317
0 ImagesCat. No.: HY-121122CAS No.: 808756-64-1 -
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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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