TRP Channel
Transient receptor potential channels
TRP Channel Isoform Specific Products
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TRP Channel
(342)
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TRPA1
(34)
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TRPC3
(11)
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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
(31)
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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 (584)
Related Products (584)
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Antibodies (3)
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TRP Channel Isoform Comparison
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N-Stearoyl valine
0 ImagesCat. No.: HY-N22000CAS No.: 14379-32-9N-Stearoyl valine is an N-acyl derivative of valine. N-Stearoyl valine antagonizes intracellular calcium mobilization by binding to the TRPV3 channel as a bioactive endogenous ligand of transient receptor potential (TRP) channels. N-Stearoyl valine participates in physiological processes such as lipid metabolism and cell signal transduction as an endogenous metabolite. N-Stearoyl valine is also a flavor compound. N-Stearoyl valine can be used in research on biomarker detection, animal nutrition and amino acid metabolism, and the development of the food and beverage industry. -
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Olvanil (Standard)
0 ImagesCat. No.: HY-101323RCAS No.: 58493-49-5Synonyms: NE-19550 (Standard); N-Vanillyloleamide (Standard)Olvanil (Standard) is the analytical standard of Olvanil. This product is intended for research and analytical applications. Olvanil (NE-19550) is an analgesic and an agonist of transient receptor potential vanilloid type 1 (TRPV1) channels with an EC50 of 0.7 nM. -
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- SB-705498 (Standard)
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(S)-ABT-102 (Standard)
0 ImagesCat. No.: HY-10635ARCAS No.: 808756-70-9(S)-ABT-102 (Standard) is the analytical standard of (S)-ABT-102 (HY-10635A). This product is intended for research and analytical applications. (S)-ABT-102 is a TRPV1 Antagonist, with an IC50 of 123 nM. (S)-ABT-102 has analgesic activity. -
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- AC4
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Amiloride-15N3
0 ImagesCat. No.: HY-B0285SCAS No.: 1217169-93-1Synonyms: MK-870-15N3Amiloride-15N3 (MK-870-15N3) is 15N labeled Amiloride. Amiloride (MK-870) is an inhibitor of both epithelial sodium channel (ENaC) and urokinase-type plasminogen activator receptor (uTPA). Amiloride is a blocker of polycystin-2 (PC2; TRPP2) channel. -
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EIPA hydrochloride (Standard)
0 ImagesSynonyms: L593754 hydrochloride (Standard); MH 12-43 hydrochloride (Standard); Ethylisopropylamiloride hydrochloride (Standard)EIPA (hydrochloride) (Standard) is the analytical standard of EIPA (hydrochloride). This product is intended for research and analytical applications. EIPA (L593754) hydrochloride is an orally active TRPP3 channel inhibitor with an IC50 of 10.5 μM. EIPA hydrochloride also enhances autophagy by inhibiting Na+/H+-exchanger 3 (NHE3). EIPA hydrochloride inhibits macropinocytosis as well. EIPA hydrochloride can be used in the research of inflammation and cancers, such as gastric cancer, colon carcinoma, pancreatic carcinoma. -
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AMG-628
0 ImagesCat. No.: HY-W931056CAS No.: 862269-93-0AMG-628 is an orally active inhibitor for TRPV1, that inhibits Capsaicin (HY-10448) or acid (pH 5)-induced Ca2+ influx into TRPV1- expressing CHO cell with IC50 of 4.9 and 3.1 nM. AMG-628 exhibits analgesic activity in Capsaicin (HY-10448)-induced rat model, and exhibits a half-life of 2.4 h in rats. -
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Zerencotrep (Standard)
0 ImagesCat. No.: HY-101507RCAS No.: 1628287-16-0Synonyms: Pico145 (Standard); HC-608 (Standard)Zerencotrep (Standard) is the analytical standard of Zerencotrep (HY-101507). This product is intended for research and analytical applications. Pico145 (HC-608) is a remarkable inhibitor of TRPC1/4/5 channels, inhibits (-)-englerin A-activated TRPC4/TRPC5 channels, with IC50s of 0.349 and 1.3 nM in cells, and shows no effect on TRPC3, TRPC6, TRPV1, TRPV4, TRPA1, TRPM2, TRPM8. -
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Icilin (Standard)
0 ImagesCat. No.: HY-11062RCAS No.: 36945-98-9Synonyms: AG-3-5 (Standard)Icilin (Standard) is the analytical standard of Icilin (HY-11062). This product is intended for research and analytical applications. Icilin (AG-3-5) is a super-agonist of the transient receptor potential M8 (TRPM8) ion channel. Icilin activates TRPM8 in EGTA in a dose-dependent manner (EC50=1.4 μM). Icilin is a "super-cooling agent" . Icilin attenuates autoimmune neuroinflammation through modulation of the T-cell response. -
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Mavatrep-d6
0 ImagesCat. No.: HY-16935SSynonyms: JNJ-39439335-d6Mavatrep-d6 (JNJ-39439335-d6) is a deuterated labeled Mavatrep (HY-16935). 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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Linopirdine (Standard)
0 ImagesCat. No.: HY-W020468RCAS No.: 105431-72-9Synonyms: DuP 996 (Standard)Linopirdine (DuP 996) is an orally active, selective M-type K+ current (IM; Kv7; KCNQ Channels) inhibitor with an IC50 of 2.4 μM. Linopirdine is a TRPV1 agonist. Linopirdine, a putative cognition enhancing agent, increases acetylcholine release in rat brain tissue. -
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2-Aminoethyl diphenylborinate (Standard)
0 ImagesCat. No.: HY-W009724RCAS No.: 524-95-8Synonyms: 2-APB (Standard)2-Aminoethyl diphenylborinate (Standard) is the analytical standard of 2-Aminoethyl diphenylborinate (HY-W009724). This product is intended for research and analytical applications. 2-Aminoethyl diphenylborinate (2-APB) is a cell-permeable inhibitor of Inositol triphosphate receptor (IP3R). 2-Aminoethyl diphenylborinate also inhibits the store-operated Ca2+ (SOC) channel and activates some TRP channels (V1, V2 and V3). Additionally, 2-Aminoethyl diphenylborinate has inhibitory effects on vasospasm. At high concentrations, it exhibits specific anti-inflammatory and antioxidant effects in neural tissue. -
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Resiniferatoxin (Standard)
0 ImagesCat. No.: HY-N2333RCAS No.: 57444-62-9Synonyms: (+)-Resiniferatoxin (Standard)Resiniferatoxin (Standard) is the analytical standard of Resiniferatoxin (HY-N2333). This product is intended for research and analytical applications. Resiniferatoxin ((+)-Resiniferatoxin), is a selective agonist of transient receptor potential vanilloid 1 (TRPV1) receptor agonist. Resiniferatoxin can be isolated from the Euphorbia resinifera plant. Resiniferatoxin eliminates TRPV1+ primary sensory afferents and blunt cardiac sympathetic afferent reflex for a relatively long period. -
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4,5-Di-O-caffeoylquinic acid
0 ImagesSynonyms: 4,5-di-O-CQA4,5-Di-O-caffeoylquinic acid (4,5-di-O-CQA) is a natural product with multiple activities including anti-inflammatory, antioxidant, and antibacterial properties. 4,5-Di-O-caffeoylquinic acid induces intracellular Ca2+ influx, and inhibits hypoxia-induced COX-2 expression and cell migration via the TRPV1-mediated pathway. 4,5-Di-O-caffeoylquinic acid scavenges DPPH free radicals, inhibits Cu2+-mediated LDL oxidation, and reduces the production of TBARS. 4,5-Di-O-caffeoylquinic acid promotes intracellular ATP production, inhibits Aβ42 aggregation and β-sheet conversion, and protects neuroblastoma cells. 4,5-Di-O-caffeoylquinic acid inhibits the growth of Bacillus shigae. 4,5-Di-O-caffeoylquinic acid can be used in studies related to atherosclerosis, Alzheimer's disease, and bacterial infections. -
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Carvacryl acetate
0 ImagesCarvacryl acetate is an orally active and brain-penetrant TRPA1 receptor activator and Na+/K+-ATPase activator. Carvacryl acetate modulates GABAergic signaling, alters hippocampal GABA and glutamine levels, reduces lipid peroxidation and nitrite formation, scavenges hydroxyl radicals, and boosts glutathione and antioxidant enzyme activity. Carvacryl acetate inhibits Haemonchus contortus larval hatching, development, adult motility, and fecal egg counts, and induces adult worm structural damage. Carvacryl acetate can be used for the research of intestinal mucositis, gastrointestinal nematode infection, epilepsy, and neurodegenerative diseases. -
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A-784168 (Standard)
0 ImagesCat. No.: HY-108460RCAS No.: 824982-41-4A-784168 (Standard) is the analytical standard of A-784168 (HY-108460). This product is intended for research and analytical applications. A-784168 is a potent and orally active inhibitor of vanilloid receptor type 1 (TRPV1). Vanilloid receptor type 1 (TRPV1) is a ligand-gated nonselective cation channel that is considered to be an important integrator of various pain stimuli such as endogenous lipids, capsaicin, heat, and low pH. A-784168 has good CNS penetration. -
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9-Phenanthrol (Standard)
0 ImagesSynonyms: 9-Hydroxyphenanthrene (Standard); NSC 50554 (Standard)9-Phenanthrol (Standard) is the analytical standard of 9-Phenanthrol. This product is intended for research and analytical applications. 9-Phenanthrol (9-Hydroxyphenanthrene) is a selective TRPM4 inhibitor with an IC50 of 17 μM. 9-Phenanthrol has no inhibitory activity on TRPM5, TRPC6, and CFTR. 9-Phenanthrol can be used for the research of ischemia-reperfusion injury. -
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TRPMPZQ-IN-1
0 ImagesCat. No.: HY-175507TRPMPZQ-IN-1 (Compound 52) is a TRPMPZQ inhibitor, with an EC50 of 0.38 μM against TRPMPZQ from Spirometra erinaceieuropaei. TRPMPZQ-IN-1 exhibits antiparasitic activity, showing an EC50 of 4.3 μM against Echinococcus multilocularis. TRPMPZQ-IN-1 can be used in antiparasitic research. -
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Dihydrocapsiate (Standard)
0 ImagesCat. No.: HY-124073RCAS No.: 205687-03-2Dihydrocapsiate (Standard) is the analytical standard of Dihydrocapsiate. This product is intended for research and analytical applications. Dihydrocapsiate, as a compound of capsinoid family, is an orally active TRPV1 agonist. Dihydrocapsiate can be used for the research of metabolism disease. -
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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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