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
(84)
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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
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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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(S)-AMG-628
0 ImagesCat. No.: HY-169780CAS No.: 862269-92-9(S)-AMG-628 (Compound 16q) is the S-isomer of AMG-628 (HY-123374). (S)-AMG-628 is the orally active antagonist for TRPV1, that inhibits the Capsaicin (HY-10448)- and acid-induced Ca2+-influx with IC50 of 7 nM and 5 nM in CHO cell. (S)-AMG-628 ameliorates Capsaicin-induced rats flinching, and reverses the thermal hypersensitivity in CFA-(HY-153808) induced inflammatory pain models. -
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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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HC-067047 (Standard)
0 ImagesHC-067047 (Standard) is the analytical standard of HC-067047 (HY-100208). This product is intended for research and analytical applications. HC-067047 is a potent and selective TRPV4 antagonist and reversibly inhibits currents through the human, rat, and mouse TRPV4 orthologs with IC50 values of 48 nM, 133 nM, and 17 nM, respectively. -
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- 20-Hydroxy-N-arachidonoyl taurine
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Cyclo(-asp-gly)
0 ImagesCat. No.: HY-W554764CAS No.: 52661-97-9Cyclo(-asp-gly) is a cyclic dipeptide composed of amino acids and is a potential TRPV1 stimulator. -
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MK6-83 (Standard)
0 ImagesCat. No.: HY-110238RCAS No.: 1062271-24-2 -
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BI-749327 (Standard)
0 ImagesCat. No.: HY-111925RCAS No.: 2361241-23-6BI-749327 (Standard) is the analytical standard of BI-749327 (HY-111925). This product is intended for research and analytical applications. BI-749327 is a potent, high selectivity and orally bioavailable TRPC6 antagonist, with IC50s of 13 nM, 19 nM and 15 nM for mouse, human and guinea pig TRPC6, respectively. BI-749327 is 85-fold more selective for mouse TRPC6 than TRPC3 and 42-fold versus TRPC7. -
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2'-Deoxyadenosine-5'-O-diphosphoribose sodium
0 ImagesCat. No.: HY-1814812'-Deoxyadenosine-5'-O-diphosphoribose sodium is a TRPM2 agonist. 2'-Deoxyadenosine-5'-O-diphosphoribose sodium enhances calcium-induced currents in inside-out patch-clamp experiments using HEK293 cells expressing human TRPM2. 2'-Deoxyadenosine-5'-O-diphosphoribose sodium is a substrate for Nucleoside Triphosphate Diphosphatase 9 (NUDT9). -
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Clemizole penicillin
0 ImagesCat. No.: HY-W754356CAS No.: 6011-39-8Clemizole penicillin is a composite preparation containing two active components, Clemizole (HY-30234) and penicillin, with antihistamine, anti-inflammatory, and bactericidal activities. The Clemizole component of Clemizole penicillin targets the H1 receptor, CrtN, and TRPC5 calcium channel, while penicillin exerts antibacterial effects. The clemizole contained in Clemizole penicillin acts as a reversible competitive inhibitor of the TRPC5 calcium channel; it also competitively targets the CrtN enzyme of Staphylococcus aureus to block staphyloxanthin biosynthesis. Clemizole penicillin can be used in research on lobar pneumonia and syphilis. -
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JT010 (Standard)
0 ImagesCat. No.: HY-111132RCAS No.: 917562-33-5JT010 (Standard) is the analytical standard of JT010 (HY-111132). This product is intended for research and analytical applications. JT010 is a covalent and site-selective TRPA1 agonist. JT010 can be used in myocardial infarction research. -
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SB 452533 (Standard)
0 ImagesCat. No.: HY-108458RCAS No.: 459429-39-1SB 452533 (Standard) is the analytical standard of SB 452533 (HY-108458). This product is intended for research and analytical applications. SB 452533 is a potent and selective TRPV1 antagonist with the pKb of 7.8. -
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AMG2850 (Standard)
0 ImagesCat. No.: HY-104059RCAS No.: 1470018-52-0AMG2850 (Standard) is the analytical standard of AMG2850 (HY-104059). This product is intended for research and analytical applications. AMG2850 is an orally active, blood-brain barrier-permeable selective TRPM8 competitive antagonist. AMG2850 abolishes the counterirritant effect of TRPM8 agonists, blocks TRPM8 activation induced by cold, (-)-Menthol (HY-75161) and Icilin (HY-11062), and exhibits selectivity over TRPA1, TRPV1, TRPV3 and TRPV4. AMG2850 is applicable for pain-related research. -
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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.