TRP Channels are a group of ion channels that are primarily found on the plasma membrane of various types of human and animal cells. There are about 28 TRP channels, and many of them are structurally related to one another. These are divided into two major categories: TRPC ("C" for canonical), TRPV ("V" for vanilloid), TRPM ("M" for melastatin), TRPN, and TRPA are all members of Group 1. There are two members of group 2: TRPP (for polycystic) and TRPML (for mucolipin). A large number of these channels mediate a wide range of sensations, including pain, hotness, warmth, or coldness, various tastes, pressure, and vision. Cations like sodium, calcium, and magnesium are relatively non-selectively permeable to TRP channels. The fruit fly Drosophila trp-mutant strain is where TRP channels were first identified. TRP channels are later discovered in vertebrates, where they are widely expressed in a variety of cell types and tissues. TRP channels are crucial for human health because at least four diseases are caused by mutations in these channels.
| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
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V70122 | (1S,2S)-ML-SI3 ((+)-trans-ML-SI3) | 2563870-87-9 | (1S,2S)-ML-SI3 is the trans-isomer of ML-SI3 and is a TRPML inhibitor. |
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V70167 | (R)-Methanandamide (AM-356) | 157182-49-5 | (R)-Methanandamide (AM-356), an analog of the endocannabinoid ligand Anandamide, is a potent CB1 agonist/activator with a Ki of 20 nM. |
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V70142 | (Rac)-Dalzanemdor ((Rac)-SAGE-718) | 2216703-16-9 | (Rac)-Dalzanemdor ((Rac)-SAGE-718) is an isomer of Dalzanemdor. |
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V81847 | 2-(2-Methylbenzamido)acetic acid-d7 (2-methylhippuric acid d7) | 1216430-90-8 | 2-(2-Methylbenzamido)acetic acid-d7 is the deuterium labelled form of 2-(2-Methylbenzamido)acetic acid. |
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V70119 | 4-(Phenyldiazenyl)benzoic acid | 1562-93-2 | 4-(Phenyldiazenyl)benzoic acid is a photosensitive and controllable TRPA1 agonist that could be utilized as a pharmacological tool to study pain signaling. |
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V70162 | 5-Iodoresiniferatoxin (I-RTX) | 535974-91-5 | 5-Iodoresiniferatoxin (I-RTX) is a selective TRPV1 antagonist (inhibitor) with IC50 of 0.7 and 5.4 nM for rat and human receptors, respectively. |
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V70152 | 6'-Iodoresiniferatoxin (6'-IRTX) | 335151-55-8 | 6'-Iodoresiniferatoxin (6'-IRTX) is a TRPV1 agonist that may be utilized in the research/study of neuropathic pain. |
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V6545 | A-967079 | 1170613-55-4 | A-967079 is a novel, potent, CNS-penetrant and selective blocker/antagonist TRPA1 channel (IC50s of 67 nM and 289 nM at human and rat TRPA1 receptors), with analgesic and antiinflammatory effects and is used in scientific research, but has not been developed for medical use. |
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V10018 | AC1903 | 831234-13-0 | AC1903 is a selective and specific inhibitor of TRPC5 with podocyte protective properties. |
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V6708 | Adarotene (ST1926) | 496868-77-0 | Adarotene (ST-1926),a synthetic, phenolic hydroxyl retinoid with proapoptotic activity,is an atypical retinoid and a promising anti-tumour agent with selective apoptotic activity on the leukaemic blast. |
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V39083 | Adenosine 5′-diphosphoribose sodium | 68414-18-6 | Adenosine 5′-diphosphoribose sodium (ADP ribose sodium) is a novel nicotinamide adenine nucleotide (NAD+) metabolite, and is the most potent and primary intracellular Ca2+-permeable cation TRPM2 channel activator. |
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V6706 | AM-0902 | 1883711-97-4 | AM-0902 is a novel, potent and selective Transient Receptor Potential A1 (TRPA1) antagonist withIC50s of 71 and 131 nM forrTRPA1andhTRPA1, respectively. |
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V3458 | AMG 333 | 1416799-28-4 | AMG 333 is a novel, potent and highly selectiveTRPM8antagonist with anIC50of 13 nMand 20 nM for hTRPM8 and rTRPM8, respectively. |
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V3400 | AMG 9810 | 545395-94-6 | AMG9810 (AMG-9810) is a nove, potent, selective and competitive antagonist of vanilloid receptor 1 (TRPV1) with cancer-promoting effects. |
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V6811 | ASP7663 | 1190217-35-6 | ASP7663 is an selective and orally bioavailable TRPA1 activator, acting by stimulating 5-HT release from QGP-1 cells and exhibiting an abdominal analgesic effect in vivo. |
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V70123 | BAY-390 | 2741956-55-6 | BAY-390 is a selective, cross-species active, brain-penetrating TRPA1 inhibitor. |
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V5910 | BCTC | 393514-24-4 | BCTC is a selective and orally bioactive vanilloid receptor 1 (TRPV1 receptor) antagonist. |
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V30488 | Beta-Eudesmol | 473-15-4 | Beta-Eudesmol has anticancer and anti~inflammatory activities. |
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V4712 | BI-749327 | 2361241-23-6 | BI-749327 (BI749327) is a novel, potent and orally bioavailableantagonist of Transient receptor potential canonical type 6 (TRPC6) with the potential to be used for treating PAH (pulmonary arterial hypertension) and PH (pulmonary hypertension) due to respiratory diseases or hypoxemia. |
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V70154 | Bisandrographolide A (BAA) | 160498-00-0 | Bisandrographolide A (BAA) activates TRPV4 channels with EC50 of 790-950 nM. |
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