1. Membrane Transporter/Ion Channel
  2. TRP Channel

TRP Channel

TRP Channel (Transient receptor potential channel) is a group of ion channels located mostly on the plasma membrane of numerous human and animal cell types. There are about 28 TRP channels that share some structural similarity to each other. These are grouped into two broad groups: Group 1 includes TRPC ("C" for canonical), TRPV ("V" for vanilloid), TRPM ("M" for melastatin), TRPN, and TRPA. In group 2, there are TRPP ("P" for polycystic) and TRPML ("ML" for mucolipin). Many of these channels mediate a variety of sensations like the sensations of pain, hotness, warmth or coldness, different kinds of tastes, pressure, and vision. TRP channels are relatively non-selectively permeable to cations, including sodium, calcium and magnesium. TRP channels are initially discovered in trp-mutant strain of the fruit fly Drosophila. Later, TRP channels are found in vertebrates where they are ubiquitously expressed in many cell types and tissues. TRP channels are important for human health as mutations in at least four TRP channels underlie disease.

TRP Channel Related Products (60):

Cat. No. Product Name Effect Purity
  • HY-17386
    Rosiglitazone Modulator 99.21%
    Rosiglitazone (BRL49653) is a selective PPARγ agonist with EC50s of 30 nM, 100 nM and 60 nM for PPARγ1, PPARγ2, and PPARγ, respectively.
  • HY-10448
    Capsaicin Agonist 98.39%
    Capsaicin is a TRPV1 agonist with an EC50 of 0.29 μM in HEK293 cells.
  • HY-15640
    Capsazepine Antagonist >99.0%
    Capsazepine is a synthetic analogue of the sensory neurone excitotoxin, and an antagonist of TRPV1 receptor with an IC50 of 562 nM.
  • HY-101840
    EIPA Inhibitor 99.73%
    EIPA is a TRPP3 channel inhibitor with an IC50 of 10.5 μM. EIPA also inhibits Na+/H+-exchanger (NHE) and macropinocytosis.
  • HY-100965
    Diphenyleneiodonium chloride Activator 99.87%
    Diphenyleneiodonium chloride is a NADPH oxidase (NOX) inhibitor and also functions as a TRPA1 activator with an EC50 of 1 to 3 μM.
  • HY-112430
    TRPM8 Antagonist Antagonist 98.20%
    TRPM8 Antagonist is a potent and selective TRPM8 antagonist, with an IC50 of 0.2 nM, used in the research of neuropathic pain syndromes.
  • HY-108465
    Pyr3 Inhibitor 99.89%
    Pyr3 is a selective inhibitor of transient receptor potential canonical channel 3 (TRPC3), with an IC50 of 700 nM for TRPC3-mediated Ca2+ influx.
  • HY-75161
    (-)-Menthol Activator >98.0%
    (-)-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.
  • HY-15064
    HC-030031 Inhibitor 98.01%
    HC-030031 is a potent and selective TRPA1 inhibitor, which antagonizes AITC- and formalin-evoked calcium influx with IC50s of 6.2±0.2 and 5.3±0.2 μM, respectively.
  • HY-100001
    SKF-96365 hydrochloride Inhibitor 99.44%
    SKF-96365 hydrochloride is a non-selective TRP Channel blocker.
  • HY-B0545
    Probenecid Agonist 99.91%
    Probenecid is a potent and selective agonist of transient receptor potential vanilloid 2 (TRPV2) channels.
  • HY-100208
    HC-067047 Antagonist >98.0%
    HC-067047 is a potent and selective TRPV4 antagonist with IC50s of 48 nM, 133 nM, and 17 nM for human, rat, and mouse TRPV4.
  • HY-101736
    AMG9810 Antagonist 99.42%
    AMG9810 is a selective and competitive vanilloid receptor 1 (TRPV1) antagonist with IC50 values of 24.5 and 85.6 nM for human and rat TRPV1, repectively.
  • HY-19608
    GSK1016790A Agonist
    GSK1016790A is a potent transient receptor potential vanilloid 4 (TRPV4) activator.
  • HY-15699
    SAR7334 Inhibitor 99.91%
    SAR7334 is a potent TRPC6 (Transient receptor potential cation channel, subfamily C, member 6) inhibitor.
  • HY-18779
    PF-4840154 Agonist 99.59%
    PF-4840154 is a potent, selective agonist of the rat and human TrpA1 channel with EC50s of 97 and 23 nM, respectively.
  • HY-19975
    RN-1734 Antagonist 99.01%
    RN-1734 is selective antagonist of the TRPV4 channel, completely antagonizes 4αPDD-mediated activation of TRPV4 with comparable, low micromolar IC50values for all three species (hTRPV4: IC50 = 2.3 μM, mTRPV4: IC50 = 5.9 μM, rTRPV4: IC50 = 3.2 μM).
  • HY-15699A
    SAR7334 hydrochloride Inhibitor
    SAR7334 hydrochloride is a potent and specific TRPC6 inhibitor, inhibiting TRPC6 currents with IC50 of 7.9 nM.
  • HY-12245
    SB-366791 Antagonist 98.64%
    SB-366791 is a potent , competitive and selective vanilloid receptor (VR1/TRPV1) antagonist with IC50 of 5.7±1.2 nM target: VR1/TRPV1 IC 50: 5.7±1.2 nM [1] SB-366791 produced a concentration-dependent inhibition of the response to capsaicin with an apparent pKb of 7.74±0.08.
  • HY-10634
    AMG 517 Antagonist 99.87%
    AMG 517 is a potent and selective vanilloid receptor-1 (TRPV1) antagonist with an IC50 of 0.5 nM.
Isoform Specific Products

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