TRP/TRPV Channel
TRP (Transient Receptor Potential) channels, including the TRPV subfamily, are a group of ion channels involved in various sensory processes, such as temperature sensation, pain perception, and osmoregulation. TRP channels are widely expressed in different tissues and play a role in physiological responses to environmental stimuli. The TRPV channels, in particular, are involved in detecting temperature changes and are implicated in conditions such as chronic pain, inflammation, and cancer. At CymitQuimica, we offer a comprehensive range of TRP/TRPV channel modulators to support your research in sensory biology, pain management, and signal transduction.
Found 96 products of "TRP/TRPV Channel"
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Vocacapsaicin hydrochloride
CAS:Vocacapsaicin hydrochloride (CA-008 hydrochloride) is a non-opioid TRPV1 agonist, a raw material for capsaicin, and is used for pain relief.Formula:C26H42ClN3O4Purity:99.66% - 99.80%Color and Shape:SolidMolecular weight:496.08BI-749327
CAS:BI-749327 is a high selectivity and orally bioavailable antagonist of TRPC6 (IC50s: 13 nM, 19 nM and 15 nM for mouse, human and guinea pig TRPC6).Formula:C23H21F3N4O2Purity:99.68% - 99.84%Color and Shape:SolidMolecular weight:442.43Ref: TM-T10537
1mg126.00€2mg168.00€5mg260.00€10mg409.00€25mg597.00€50mg782.00€100mg1,044.00€500mg2,088.00€1mL*10mM (DMSO)285.00€(Z)-Capsaicin
CAS:(Z)-Capsaicin (Zucapsaicin) is a medication used to treat osteoarthritis of the knee and Others neuropathic pain.(Z)-Capsaicin is a synthetic cis isomer of
Formula:C18H27NO3Purity:97.33% - 98.91%Color and Shape:SolidMolecular weight:305.41GFB-8438
CAS:GFB-8438 is a potent and subtype selective inhibitor of TRPC5(IC50s of 0.18 and 0.29 μM of hTRPC5 and hTRPC4, respectively).Formula:C16H14ClF3N4O2Purity:99.58%Color and Shape:SolidMolecular weight:386.76Ref: TM-T11394
2mg35.00€5mg52.00€10mg81.00€25mg117.00€50mg170.00€100mg250.00€200mg369.00€1mL*10mM (DMSO)58.00€TRPV4 agonist-1 free base
CAS:TRPV4 agonist-1 free base (OUN67600) is an agonist of transient receptor potential vanilloid 4 (TRPV4;EC50 of 60 nM, in the hTRPV4 Ca2+ assay).Formula:C25H22F2N4O2Purity:99.79%Color and Shape:SolidMolecular weight:448.46IA-Alkyne
CAS:IA-Alkyne: TRPC agonist, cysteine-reactivity probe, potential in respiratory infection study.Formula:C8H12INOPurity:99.76%Color and Shape:SolidMolecular weight:265.09Ref: TM-T15543
1mg56.00€5mg119.00€10mg177.00€25mg250.00€50mg313.00€100mg432.00€1mL*10mM (DMSO)114.00€RN-1665
CAS:RN-1665 is a potent and selective TRPV4 receptor antagonist.Formula:C20H24F5N3O3S2Purity:99.96%Color and Shape:SoildMolecular weight:513.54GSK2798745
CAS:GSK2798745 is an orally active transient receptor potential vanilloid 4 (TRPV4) ion channel blocker (IC50s: 1.8 and 1.6 nM for hTRPV4 and rTRPV4).Formula:C25H28N6O3Color and Shape:SolidMolecular weight:460.53TRPM8 antagonist 3
CAS:TRPM8 antagonist 3 is a blocker of TRPM8 (IC50 = 11 nM).Formula:C13H12N2O4SPurity:99.74%Color and Shape:SolidMolecular weight:292.31AP 18
CAS:AP-18 is a potent and selective TRPA1 inhibitor.
Formula:C11H12ClNOPurity:99.85% - 99.96%Color and Shape:SolidMolecular weight:209.67CBP-1008
CBP-1008 is a dual-ligand peptide-drug conjugate (PDC) with MMAE, targeting folate receptor (FRα) and TRPV6. It exhibits high binding affinity to FRα and low affinity to TRPV6. CBP-1008 shows antitumor activity and can be utilized for research in advanced solid tumors such as colorectal cancer, breast cancer, non-small cell lung cancer, ovarian cancer, adrenocortical carcinoma, and follicular dendritic cell sarcoma.Color and Shape:Odour SolidOleoyl Serotonin
CAS:Oleoyl Serotonin is an antagonist of hTRPV1 with an IC50 of 2.57 μM.Formula:C28H44N2O2Purity:99.88%Color and Shape:SolidMolecular weight:440.66Ref: TM-T22124
5mg62.00€10mg87.00€25mg173.00€50mg299.00€100mg520.00€500mg1,134.00€1mL*10mM (DMSO)90.00€NGD-8243
CAS:NGD-8243 (N-[4-(trifluoromethyl)phenyl]-7-[3-(trifluoromethyl)pyridin-2-yl]quinazolin-4-amine) is a TRPV1 inhibitor and can be used in studies for preventionFormula:C21H12F6N4Purity:95.26%Color and Shape:SolidMolecular weight:434.34L-R4W2
CAS:Vanilloid TRPV1 (VR1) receptor antagonist peptide (IC50 ~ 0.1 μM); blocks Ca2+ currents in dorsal root ganglion neurons. Analgesic in vivo.Formula:C46H71N21O6Purity:98%Color and Shape:SolidMolecular weight:1014.2TRPA1-IN-2
CAS:TRPA1-IN-2 is a potent and orally active TRPA1 inhibitor with an IC50 value of 0.04 µM.TRPA1-IN-2 has anti-inflammatory activity.Formula:C24H25F3N4OPurity:98.93%Color and Shape:SoildMolecular weight:442.48Ref: TM-T77511
1mg56.00€5mg129.00€10mg188.00€25mg319.00€50mg447.00€100mg600.00€200mg807.00€1mL*10mM (DMSO)142.00€(S)-ABT 102
CAS:N-[(1S)-1H-inden-1-yl]-N'-indazol-4-ylurea is a strong TRPV1 blocker with a 123 nM IC50 against capsaicin.Formula:C21H24N4OPurity:99.65% - 99.77%Color and Shape:SoildMolecular weight:348.44Ref: TM-T29522L
1mg73.00€5mg149.00€10mg212.00€25mg319.00€50mg447.00€100mg610.00€200mg822.00€1mL*10mM (DMSO)154.00€PF-04745637
CAS:PF-04745637 is a potent and selective TRPA1 antagonist with an IC50 of 17 nM[1].Formula:C27H32ClF3N2O2Purity:98.88% - 99.3%Color and Shape:SolidMolecular weight:509Ref: TM-T64337
1mg73.00€5mg145.00€10mg197.00€25mg333.00€50mg475.00€100mg655.00€200mg882.00€1mL*10mM (DMSO)163.00€Resolvin D2
CAS:Resolvin D2 (RvD2) is a TRPV1 inhibitor and pro-ablative mediator with anti-inflammatory, anti-infective and pro-ablative effects.Formula:C22H32O5Purity:98%Color and Shape:SolidMolecular weight:376.49N-Oleoyl Valine Ammonium salt
N-Oleoyl Valine Ammonium salt is an N-acyl amide compound that is a TRPV3 antagonist and can be used to study inflammation.Formula:C23H46N2O3Purity:99.72%Color and Shape:SolidMolecular weight:398.62Cyclic ADP-Ribose (ammonium salt)
Cyclic ADP-Ribose (ammonium salt) (cADPR) is an NAD⁺ metabolite that triggers Ca²⁺ release from ER stores via ryanodine receptors, relevant to inflammation research.Formula:C15H21N5O13P2·xNH3Color and Shape:SolidBTD
CAS:BTD is a TRPC5 activator that activates heteromeric channel complexes composed of TRPC5 and its closest relatives TRPC1 or TRPC4.Formula:C24H33N3O4SColor and Shape:SolidMolecular weight:459.6Phenazopyridine
CAS:Phenazopyridine is an orally administered azo dye with local analgesic effects on urinary tract infections,. against SARM1 and TRPM8.Formula:C11H11N5Purity:99.98%Color and Shape:SolidMolecular weight:213.24Pico145
CAS:Pico145 (HC-608) is a remarkable inhibitor of TRPC1/4/5 channels.Formula:C23H20ClF3N4O5Purity:99.06%Color and Shape:SolidMolecular weight:524.88Ref: TM-T16532
1mg70.00€5mg150.00€10mg215.00€25mg358.00€50mg517.00€100mg707.00€200mg1,009.00€1mL*10mM (DMSO)167.00€TRPM4-IN-1
CAS:TRPM4-IN-1 (4-chloro-2-(2-(2-chlorophenoxy)acetamido)benzoic acid) is a potent and selective inhibitor of TRPM4 with an IC50 of 1.5 μM.Formula:C15H11Cl2NO4Purity:97.22%Color and Shape:SolidMolecular weight:340.16MK6-83
CAS:MK6-83 is the transient receptor potential channel ML3 agonist.Formula:C16H20N2O2S2Purity:99.5%Color and Shape:SolidMolecular weight:336.479-Phenanthrol
CAS:9-Phenanthrol is inhibitor of the transient receptor potential melastatin 4 (TRPM) channel, a Ca2+ -activated non-selective cation channel.Formula:C14H10OPurity:98.48%Color and Shape:SolidMolecular weight:194.23TC-I2000
CAS:TC-I2000 is an TRPM8 channel blocker. Inhibits icilin-induced TRPM8 channel activation in rTRPM8-expressing CHO cells with IC50 of 53 nM.Formula:C23H18F4N2OPurity:99.778%Color and Shape:SolidMolecular weight:414.4Ref: TM-T8449
5mg35.00€10mg50.00€25mg88.00€50mg119.00€100mg173.00€200mg259.00€1mL*10mM (DMSO)To inquireML204 hydrochloride
CAS:ML204 hydrochloride (ML204 HCl) is a TRPC4/TRPC5 channel antagonist.Formula:C15H19ClN2Color and Shape:SolidMolecular weight:262.78WS-12
CAS:WS-12 is a potent TRPM8 agonist that acts as a cooling agent (EC50 : 193 nM)Formula:C18H27NO2Purity:99.99%Color and Shape:Whitish To White Solid CrystallineMolecular weight:289.41HC-067047
CAS:HC-067047 is a potent and selective TRPV4 antagonist.Also inhibits the endogenous TRPV4-mediated response to 4α-PDH .Formula:C26H28F3N3O2Purity:99.45% - 99.97%Color and Shape:SolidMolecular weight:471.51cim0216
CAS:CIM0216 is a synthetic TRPM3 activator whose potency and apparent affinity greatly exceeds that of the canonical TRPM3 agonist.Formula:C21H21N3O2Purity:99.87%Color and Shape:SolidMolecular weight:347.41Ref: TM-T9263
1mg44.00€2mg56.00€5mg87.00€10mg138.00€25mg281.00€50mg442.00€100mg665.00€500mg1,378.00€1mL*10mM (DMSO)96.00€AMG 517
CAS:AMG 517 is an effective and specific TRPV1 antagonist, antagonizes proton (IC50: 0.76 nM), capsaicin (IC50: 0.62 nM) and heat activation (IC50: 1.3 nM) of TRPV1Formula:C20H13F3N4O2SPurity:99.77% - 99.85%Color and Shape:SolidMolecular weight:430.4GSK2193874
CAS:GSK2193874 was identified as a selective, orally active TRPV4 blocker.Formula:C37H38BrF3N4OPurity:99.99% - ≥95%Color and Shape:SolidMolecular weight:691.62Ref: TM-T5640
1mg43.00€2mg57.00€5mg81.00€10mg127.00€25mg246.00€50mg404.00€100mg602.00€1mL*10mM (DMSO)111.00€JNJ-17203212
CAS:JNJ-17203212 is a potent and selective antagonist of TRPV1 (human TRPV1 and rat TRPV1, IC50 of 65 nM and 102 nM).Formula:C17H15F6N5OPurity:99.18%Color and Shape:SolidMolecular weight:419.32M8-B Hydrochloride
CAS:M8-B Hydrochloride is a selective transient receptor potential melastatin-8 (TRPM8) channel antagonist.Formula:C22H25ClN2O3SPurity:99.33%Color and Shape:SolidMolecular weight:432.96Ref: TM-T8442
2mg35.00€5mg52.00€10mg74.00€25mg145.00€50mg226.00€100mg335.00€200mg469.00€1mL*10mM (DMSO)64.00€SB-366791
CAS:SB-366791 is a new and selective cinnamide TRPV1 antagonist.Formula:C16H14ClNO2Purity:99.51%Color and Shape:SolidMolecular weight:287.74Ononetin
CAS:Ononetin (2',4'-Dihydroxy-2-(4-methoxyphenyl)acetophenone) is a TRPM3 channel blocker(IC50: 0.3 μM).Formula:C15H14O4Purity:98.06%Color and Shape:SolidMolecular weight:258.27Evifacotrep
CAS:Evifacotrep: TRPC5 antagonist for neurological disease research (WO2020061162, compound 100).Formula:C18H12ClF4N5O2Purity:98.6%Color and Shape:SolidMolecular weight:441.77Ref: TM-T40042
1mg92.00€5mg178.00€10mg286.00€25mg440.00€50mg655.00€100mg973.00€200mg1,468.00€1mL*10mM (DMSO)152.00€HC067047 Hydrochloride(883031-03-6 free base)
CAS:HC-067047 hydrochloride, a TRPV4 antagonist, selectively inhibits human, rat, and mouse currents with IC50s: 486 nM, 133 nM, and 17 nM.Formula:C26H29ClF3N3O2Purity:99.95%Color and Shape:SolidMolecular weight:507.98Ref: TM-T4680L
1mg88.00€5mg172.00€10mg259.00€25mg425.00€50mg598.00€100mg810.00€200mg1,074.00€1mL*10mM (DMSO)217.00€HC-030031
CAS:HC-030031 (TOSLAB 829227) is a potent TRPA1 inhibitor, which antagonizes AITC- and formalin-evoked calcium influx with IC50s of 6.2 and 5.3 μM, respectively.Formula:C18H21N5O3Purity:99.69% - ≥95%Color and Shape:SolidMolecular weight:355.39ML204
CAS:ML204 is a novel potent antagonist that selectively modulates native TRPC4/C5 ion channels.Formula:C15H18N2Purity:98.1% - 99.72%Color and Shape:SolidMolecular weight:226.32RN-1734
CAS:RN-1734 is selective TRPV4 channel antagonist(IC50 of 2.3 μM,5.9 μM,3.2 μM for hTRPV4, mTRPV4 and rTRPV4,respectively)Formula:C14H22Cl2N2O2SPurity:99.1% - 99.3%Color and Shape:SolidMolecular weight:353.31AMG 333
CAS:AMG 333 is TRPM8 antagonist with an IC50 of 13 nM,a Clinical Candidate for the Treatment of Migraine.Formula:C20H12F5N3O4Purity:99.95%Color and Shape:SolidMolecular weight:453.32Chembridge-5861528
CAS:Chembridge-5861528 (TCS 5861528) is a TRPA1 channel blocker that antagonizes AITC- and 4-HNE-evoked calcium influx with IC50 values of 14.3 and 18.7 μM.Formula:C19H23N5O3Purity:99.97%Color and Shape:SolidMolecular weight:369.42RQ-00203078
CAS:RQ-00203078 is a highly selective, potent and orally available TRPM8 antagonist.Formula:C21H13ClF6N2O5SPurity:98% - 99.6%Color and Shape:SolidMolecular weight:554.85A-967079
CAS:A 967079 is a potent, selective, and bioavailable inhibitor of the TRPA1 channel, with IC50 values of 67 and 289 nM for the human and rat isoforms, respectively
Formula:C12H14FNOPurity:98.34% - 99.75%Color and Shape:SolidMolecular weight:207.24ICILIN
CAS:ICILIN (AG-3-5) is a synthetic TRPM8 ion channel super-agonist.Formula:C16H13N3O4Purity:98.45% - ≥95%Color and Shape:Light Yellow SolidMolecular weight:311.29ASP7663
CAS:ASP7663 is a TRPA1 Receptor Agonist and exhibiting an abdominal analgesic effect in vivo.Formula:C14H14FNO3Purity:98.61%Color and Shape:SolidMolecular weight:263.26AM-0902
CAS:AM-0902 is a potent and specific TRPA1 antagonist (IC50s: 71/131 nM for rTRPA1 and hTRPA1).Formula:C17H15ClN6O2Purity:>99.99%Color and Shape:SolidMolecular weight:370.79SB 452533
CAS:SB 452533 is an antagonist of the vanilloid receptor 1(pKb: 7.8).Formula:C18H22BrN3OPurity:99.87%Color and Shape:SolidMolecular weight:376.29Ref: TM-T23322
2mg39.00€5mg60.00€10mg92.00€25mg173.00€50mg269.00€100mg389.00€200mg555.00€1mL*10mM (DMSO)73.00€PF-4840154
CAS:PF-4840154: potent TrpA1 agonist; EC50 of 97 nM (rat) & 23 nM (human); triggers nociception in mice.
Formula:C26H38N6O2Purity:>99.99%Color and Shape:SolidMolecular weight:466.62Pyr10
CAS:Pyr10, a pyrazole derivative, selectively inhibits TRPC3, not STIM1/Orai1, with IC50 of 0.72 μM in TRPC3-HEK293, and 13.08 μM in BRL-2H3 cells.Formula:C18H13F6N3O2SPurity:99.69% - 99.7%Color and Shape:SolidMolecular weight:449.37SB-705498
CAS:SB705498 is a TRPV1 antagonist for hTRPV1. SB-705498 has been investigated for the treatment of Rhinitis, Chronic Cough, and Non-allergic Rhinitis.Formula:C17H16BrF3N4OPurity:99.57% - ≥95%Color and Shape:SolidMolecular weight:429.23Vanilloid receptor antagonist 1
CAS:Vanilloid receptor antagonist 1 (4-(7-Hydroxy-2-isopropyl-4-oxoquinazolin-3(4H)-yl)benzonitrile) is a potent vanilloid receptor TRPV1 antagonist.Formula:C18H15N3O2Purity:98.14%Color and Shape:SolidMolecular weight:305.33AMG9810
CAS:AMG 9810 blocks capsaicin's action on TRPV1; human IC50=24.5 nM, rat IC50=85.6 nM.Formula:C21H23NO3Purity:99.79% - 99.95%Color and Shape:SolidMolecular weight:337.41Ref: TM-T7189
2mg34.00€5mg48.00€10mg58.00€25mg110.00€50mg177.00€100mg286.00€200mg425.00€1mL*10mM (DMSO)50.00€Optovin
CAS:Optovin is a TRPA1 activator, which is reversibly photoactivated.Formula:C15H13N3OS2Purity:99.47% - 99.67%Color and Shape:SolidMolecular weight:315.41Ref: TM-T6617
2mg39.00€5mg57.00€10mg93.00€25mg160.00€50mg250.00€100mg406.00€200mg592.00€1mL*10mM (DMSO)64.00€MDR-652
CAS:MDR-652 is a highly specific and efficacious agonist of nonpungent transient receptor potential vanilloid 1 (TRPV1) with Ki value of 11.4 nM and 23.8 nM forFormula:C22H23ClFN3O2SPurity:99.96%Color and Shape:SolidMolecular weight:447.95Ref: TM-T22360
1mg60.00€2mg87.00€5mg130.00€10mg178.00€25mg331.00€50mg512.00€100mg707.00€200mg973.00€1mL*10mM (DMSO)142.00€RN-1747
CAS:RN-1747: TRPV4 agonist (EC50: human 0.77 μM, mouse 4.0 μM, rat 4.1 μM), TRPM8 antagonist (IC50: 4 μM).Formula:C17H18ClN3O4SPurity:99.29%Color and Shape:SolidMolecular weight:395.86AMTB hydrochloride
CAS:AMTB HCl: Novel TRPM8 blocker, relieves pain, treats urinary issues, moderates bladder reflexes in rats.Formula:C23H27ClN2O2SPurity:99.08%Color and Shape:SolidMolecular weight:430.99Ref: TM-T19723
1mg34.00€5mg74.00€10mg119.00€25mg250.00€50mg424.00€100mg627.00€200mg890.00€1mL*10mM (DMSO)87.00€TRPM8 antagonist 2
CAS:TRPM8 antagonist 2 is a potent and selective TRPM8 antagonist with an IC50 of 0.2 nM. TRPM8 antagonist 2 is used in the research of neuropathic pain syndromes.Formula:C26H26N2O2Purity:98.1%Color and Shape:SolidMolecular weight:398.5Ref: TM-T5698
1mg34.00€5mg66.00€10mg99.00€25mg167.00€50mg260.00€100mg416.00€200mg600.00€1mL*10mM (DMSO)73.00€AC1903
CAS:AC1903 is a specific inhibitor of TRPC5 channel, and has been shown to suppress severe proteinuria and prevent podocyte loss.Formula:C19H17N3OPurity:98.45%Color and Shape:SolidMolecular weight:303.36JNJ-28583113
CAS:JNJ-28583113 is a TRPM2 antagonist, inducing phosphorylation of GSK3α and β subunits, protecting cells from oxidative stress-induced cell death.Formula:C19H21F3N2O2Purity:98.57%Color and Shape:SolidMolecular weight:366.38Ref: TM-T74779
1mg89.00€5mg204.00€10mg254.00€25mg409.00€50mg624.00€100mg795.00€200mg1,103.00€1mL*10mM (DMSO)225.00€SAR7334
CAS:SAR7334 (TRCP6-IN-1) is a potent and specific inhibitor of TRPC6(IC50 of 7.9 nM).Formula:C21H22ClN3OPurity:99.62% - 99.71%Color and Shape:SolidMolecular weight:367.87Ref: TM-T12849
1mg67.00€2mg88.00€5mg152.00€10mg236.00€25mg295.00€50mg349.00€100mg439.00€200mg628.00€1mL*10mM (DMSO)166.00€JYL 1421
CAS:JYL 1421 (SC 0030) is an antagonist of TRPV1 receptor (IC50 = 8 nM).Formula:C20H26FN3O2S2Purity:98.83%Color and Shape:SolidMolecular weight:423.57Ref: TM-T15634
1mg66.00€5mg177.00€10mg289.00€25mg580.00€50mg888.00€100mg1,414.00€200mg1,882.00€1mL*10mM (DMSO)170.00€Asivatrep
CAS:Asivatrep (PAC14028) is a selective and potent antagonist of transient receptor potential vanilloid subtype 1 (TRPV1) for the study of atopic dermatitis.Formula:C21H22F5N3O3SPurity:95.13%Color and Shape:SolidMolecular weight:491.48TRPV4 agonist-1
CAS:TRPV4 agonist-1 is an agonist of TRPV4 (EC50: 60 nM in the hTRPV4 Ca2+ assay).Formula:C25H23ClF2N4O2Purity:98%Color and Shape:SolidMolecular weight:484.93TRPC6-PAM-C20
CAS:TRPC6-PAM-C20, a selective enhancer for TRPC6, boosts calcium in HEK cells and OAG-related platelet clumping, EC50: 2.37μM.Formula:C22H21NO4Purity:98.16%Color and Shape:SolidMolecular weight:363.41D-3263 hydrochloride
CAS:D-3263 hydrochloride (D3263 HCl salt) is enteric-coated, orally bioavailable transient receptor potential melatonin member 8 (TRPM8) agonist.
Formula:C21H32ClN3O3Purity:99.93%Color and Shape:SolidMolecular weight:409.95TRPV3 antagonist 74a
CAS:TRPV3 antagonist 74a (TRPV3 74a) is a specific TRPV3 antagonist for the study of neurological disorders.Formula:C17H17F3N2O2Purity:≥98.0%Color and Shape:SolidMolecular weight:338.32GSK1702934A
CAS:GSK1702934A is a TRPC3 agonist with pro-arrhythmic and positive inotropic effects and is used in the study of diabetes mellitus.Formula:C22H25N3O2SPurity:98.15%Color and Shape:SolidMolecular weight:395.52N-Oleoyl Valine
CAS:N-Oleoyl valine, an N-acyl amine, antagonizes TRPV3 for thermoregulation; rises post-cold exposure; elevates in mouse lung injury.Formula:C23H43NO3Molecular weight:381.59TRPM4-IN-2
CAS:NBA, or TRPM4-IN-2, is a potent TRPM4 inhibitor with IC50 of 0.16 μM, used in prostate and colorectal cancer research.Formula:C19H14ClNO4Purity:99.21%Color and Shape:SolidMolecular weight:355.77AM12
CAS:AM12 inhibits Lanthanide-evoked TRPC5 activity (IC50: 0.28 μM).Formula:C15H9BrO5Purity:98%Color and Shape:SolidMolecular weight:349.13RN9893
CAS:RN9893 is a selective and potent TRPV4 receptor antagonist with IC50 values of 320, 420 and 660 nM for TRPV4 receptors in mouse, human and rat, respectively.Formula:C21H23F3N4O5SPurity:99.99%Color and Shape:SolidMolecular weight:500.49HC-070
CAS:HC-070 is a TRPC5 and TRPC4 antagonist (IC50 = 9.3 nM and 46 nM).Formula:C22H20Cl2N4O4Purity:98.48%Color and Shape:SolidMolecular weight:475.32Ref: TM-T15465
1mg84.00€5mg160.00€10mg236.00€25mg406.00€50mg572.00€100mg772.00€200mg1,035.00€1mL*10mM (DMSO)165.00€ABT 102
CAS:ABT 102 (CHEMBL398338) is a selective antagonist of transient receptor potential vanilloid 1 (TRPV1) receptor.Formula:C21H24N4OPurity:98.38% - 99.86%Color and Shape:SolidMolecular weight:348.44Ref: TM-T29522
1mg109.00€5mg235.00€10mg349.00€25mg532.00€50mg745.00€100mg999.00€200mg1,333.00€1mL*10mM (DMSO)245.00€Olvanil
CAS:Olvanil (N-Vannilyloleoylamide) is a vanilloid receptor agonist with EC50 of 0.7nM.Formula:C26H43NO3Purity:99.58%Color and Shape:SolidMolecular weight:417.62Ref: TM-T23106
2mg34.00€5mg49.00€10mg75.00€25mg145.00€50mg236.00€100mg385.00€200mg560.00€1mL*10mM (DMSO)50.00€Elismetrep
CAS:Elismetrep (MT-8554) is an orally available TRPM8 inhibitor with potential analgesic activity for the study of vasomotor symptoms in postmenopausal women.Formula:C27H21F3N2O5SPurity:99.37% - 99.93%Color and Shape:SolidMolecular weight:542.53TC-I 2014
CAS:TC-I 2014 shows antiallodynic properties in pain models.Formula:C23H19F6N3OPurity:99.07%Color and Shape:SolidMolecular weight:467.41Ref: TM-T17006
1mg57.00€5mg120.00€10mg192.00€25mg385.00€50mg620.00€100mg1,018.00€200mg1,378.00€1mL*10mM (DMSO)126.00€MSP3
CAS:MSP3 is an agonist of TRPV1 (EC50 = 0.87 μM) and shows antinociceptive and neuroprotective effects.Formula:C16H19NO3SPurity:99.89%Color and Shape:SolidMolecular weight:305.39Ref: TM-T28118
2mg33.00€5mg50.00€10mg80.00€25mg161.00€50mg243.00€100mg358.00€200mg505.00€1mL*10mM (DMSO)71.00€Pyr3
CAS:Pyr3 selectively blocks TRPC3 channels, reducing Ca2+ influx; it's effective at 700 nM.Formula:C16H11Cl3F3N3O3Purity:98.04%Color and Shape:SolidMolecular weight:456.63Ref: TM-T16687
1mg35.00€2mg52.00€5mg77.00€10mg97.00€25mg215.00€50mg363.00€100mg512.00€200mg738.00€500mg1,121.00€1mL*10mM (DMSO)86.00€Mavatrep
CAS:Mavatrep (JNJ-39439335) is a selective antagonist of TRPV1 with Ki of 6.5 nM and can be used for studies about inflammatory pain.Formula:C25H21F3N2OPurity:98.51% - 99.31%Color and Shape:SolidMolecular weight:422.44Ref: TM-T16014
1mg63.00€2mg90.00€5mg137.00€10mg215.00€25mg385.00€50mg618.00€100mg888.00€200mg1,243.00€1mL*10mM (DMSO)150.00€FEMA-4809
CAS:FEMA-4809 activates TRPM8, the ion channel for cold sensation, and is used as a cooling agent.Formula:C17H17N3O2SPurity:99.9%Color and Shape:SolidMolecular weight:327.4Ref: TM-T27308
1mg34.00€5mg73.00€10mg110.00€25mg180.00€50mg255.00€100mg363.00€200mg497.00€1mL*10mM (DMSO)84.00€SET 2
CAS:SET 2 is an antagonist of transient receptor potential vanilloid type 2(TRPV2) with an IC50 of 0.46 μM. SET 2 shows selectivity over TRPV1, TRPV3 and TRPV4.Formula:C17H21F3N4O2SPurity:99.77%Color and Shape:SolidMolecular weight:402.43Ref: TM-T37097
5mg55.00€10mg92.00€25mg168.00€50mg284.00€100mg414.00€500mgTo inquire1mL*10mM (DMSO)67.00€MK-2295
CAS:MK-2295 is a potent TRPV1 antagonist. MK-2295 can be used in studies about the treatment of chronic pain.Formula:C27H31FN6O2Purity:98.83% - 99.44%Color and Shape:SolidMolecular weight:490.57Mesendogen
CAS:Mesendogen is an inhibitor of transient receptor potential cation channel, subfamily M, member 6 (TRPM6) and 7 (TRPM7) and acts by inhibiting TRPM6/TRPM7Formula:C18H16ClF3N2OSPurity:99.66%Color and Shape:SolidMolecular weight:400.85GSK3395879
CAS:GSK3395879 is a selective and orally bioavailable antagonist of transient receptor potential vanilloid-4 (TRPV4) (IC50: 1 nM for hTRPV4).Formula:C20H15F4N3O5SPurity:98%Color and Shape:SolidMolecular weight:485.41PF-05105679
CAS:PF-05105679 is a selective TRPM8 antagonist (IC50 = 103 nM). PF-05105679 can be used in research on cold-related pain.Formula:C26H21FN2O3Purity:99.84%Color and Shape:SolidMolecular weight:428.45Ref: TM-T16483
1mg47.00€2mg60.00€5mg87.00€10mg145.00€25mg279.00€50mg425.00€100mg645.00€200mg895.00€1mL*10mM (DMSO)96.00€JT010
CAS:JT010 is an effective agonist of TRPA1 (EC50 = 0.65 nM).Formula:C16H19ClN2O3SPurity:99.75%Color and Shape:SolidMolecular weight:354.85A-1165442
CAS:A-1165442 is a competitive TRPV1 antagonist. For human TRPV, the IC50 values is 9 nM.Formula:C22H20ClF2N3O2Color and Shape:SolidMolecular weight:431.86AMG-0347
CAS:AMG-0347 inhibits TRPA1 ion channels in sensory neurons, blocking pain perception.Formula:C24H26F3N3O2Purity:99.93%Color and Shape:SolidMolecular weight:445.48Ref: TM-T29968
1mg215.00€5mg523.00€10mg695.00€25mg1,054.00€50mg1,414.00€100mg1,900.00€200mg2,565.00€1mL*10mM (DMSO)537.00€AMG2850
CAS:AMG2850 is a potent, orally bioavailable, and selective antagonist of transient receptor potential melastatin 8 (TRPM8).Formula:C19H17F6N3OPurity:99.84%Color and Shape:SolidMolecular weight:417.35Ref: TM-T10300
1mg71.00€5mg161.00€10mg235.00€25mg423.00€50mg627.00€100mg803.00€1mL*10mM (DMSO)172.00€ELP-004
CAS:ELP-004 is a TRPC channel inhibitor that blocks Ca2+ entry mediated by TRPC channels. It serves as an osteoclast inhibitor by preventing osteoclast differentiation. ELP-004 also hinders basal Ca2+ levels and the associated translocation of NFATc1 in inflammatory osteoclastogenesis. Additionally, it reduces bone erosion in mouse models of rheumatoid arthritis.Formula:C10H11Cl2NOColor and Shape:SolidMolecular weight:232.106TRPA1 Antagonist 1
CAS:TRPA1 Antagonist 1 is an antagonist of TRPA1(IC50: 8 nM) and is a methylene phosphate prodrug which converts to its active parent drug.Formula:C24H20F6N5Na2O7PSPurity:98%Color and Shape:SolidMolecular weight:713.45Apcin A HCL
CAS:Apcin A HCL is an Apcin derivative. Apcin A HCL is an anaphase-promoting complex (APC) inhibitor. Apcin-A HCL interacts strongly with Cdc20, and inhibits the ubiquitination of Cdc20 substrates. Apcin-A HCL can be used to synthesize the PROTAC CP5V [1].
Formula:C10H15Cl4N5O2Purity:99.30%Color and Shape:SolidMolecular weight:379.07Motugivatrep
CAS:Motugivatrep is a potent and selective TRPV1 antagonist that can be used to study TRPV1-related respiratory diseases.
Formula:C22H20F3NO3Purity:99.22%Color and Shape:SolidMolecular weight:403.39Ref: TM-T64312
Discontinued product
