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Isoforms Recommended:	TRPM8

Results for "

TRPM8

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Bacterial (2) Calcium Channel (1) Cannabinoid Receptor (2) CGRP Receptor (2) Drug Intermediate (2) Drug Metabolite (1) Endogenous Metabolite (5) Environmental Pollutants (4) ERK (1) Insulin Receptor (2) Interleukin Related (3) Isotope-Labeled Compounds (4) MMP (1) NF-κB (2) NOD-like Receptor (NLR) (1) p38 MAPK (1) Parasite (1) PKA (1) PKC (1) Reactive Oxygen Species (ROS) (1) Reference Standards (8) Small Interfering RNA (siRNA) (3) TNF Receptor (2) TRP Channel (53)
By Research Areas:	Cancer (16) Cardiovascular Disease (4) Endocrinology (1) Infection (3) Inflammation/Immunology (13) Metabolic Disease (9) Neurological Disease (34)
Oligonucleotides:	Flavoring Agents (1) Rat Pre-designed siRNA Sets (1) Mouse Pre-designed siRNA Sets (1) Human Pre-designed siRNA Sets (1) siRNAs (3)

Inhibitors & Agonists

Biochemical Assay Reagents

Natural
Products

Isotope-Labeled Compounds

Antibodies

Oligonucleotides

Cat. No.	상품명	Target	연구분야	Chemical Structure

HY-75161

(-)-Menthol 4 Publications Verification	Environmental Pollutants Endogenous Metabolite TRP Channel	Cancer
(-)-Menthol is a key component of peppermint oil that binds and activates transient receptor potential melastatin 8 (TRPM8), a Ca ²⁺-permeable nonselective cation channel, to increase [Ca ²⁺]_i . Antitumor activity .

HY-11062

Icilin 1 Publications Verification AG-3-5	TRP Channel	Neurological Disease Inflammation/Immunology
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 .

HY-108449

Acoltremon 2 Publications Verification WS-12; AR-15512; AVX-012	TRP Channel	Neurological Disease
Acoltremon (WS-12; AR-15512) is a potent and selective *TRPM8* agonist, the menthol derivative, as a cooling agent. Acoltremon shows analgesic effect, and can be used in chronic neuropathic pain research .

HY-B0985

Phenazopyridine hydrochloride 2 Publications Verification	TRP Channel	Neurological Disease
Phenazopyridine hydrochlorideis a competitive SARM1 inhibitor, with IC₅₀ 145 μM. Phenazopyridine hydrochlorideis a *TRPM8* antagonist. Phenazopyridine hydrochloride has a local anesthetic/analgesic effect. Phenazopyridine hydrochlorideis used to relieve painful symptoms of conditions such as cystitis and urethritis. Phenazopyridine hydrochloridecan promote neuronal differentiation and can also be used in the study of traumatic brain injury, peripheral neuropathy and neurodegenerative diseases .

HY-W014325

TRPM8 agonist WS-3 Framidice 3	TRP Channel Endogenous Metabolite	Neurological Disease Metabolic Disease Cancer
TRPM8 agonist WS-3 is an specific agonist of *TRPM8* with an EC₅₀ of 3.7 μM. TRPM8 agonist WS-3 inhibits epileptic seizures through a TRPM8 dependent mechanism. TRPM8 agonist WS-3 can be used for research on epilepsy and other conditions .

HY-19960

BCTC 5 Publications Verification	TRP Channel Insulin Receptor CGRP Receptor	Neurological Disease Metabolic Disease Cancer
BCTC is an orally active current inhibitor of vanilloid receptor type 1 (VR1). BCTC is a transient receptor potential cation channel subfamily M member 8 (TRPM8) and transient receptor potential vanilloid 1 (TRPV1) antagonist. BCTC is an insulin sensitizer and secretor. BCTC has anticancer and analgesic effects .

HY-101507

Zerencotrep Maximum Cited Publications 13 Publications Verification Pico145; HC-608	TRP Channel	Cancer
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 .

HY-18662

RQ-00203078 5+ Cited Publications	TRP Channel	Neurological Disease Cancer
RQ-00203078 is a highly selective, potent and orally active *TRPM8* antagonist with IC₅₀s of 5.3 nM and 8.3 nM for rat and human *TRPM8* channels, respectively. RQ-00203078 shows little inhibitory action against TRPV1, TRPA1, TRPV4, or TRPM2 channels .

HY-112430

TRPM8 antagonist 2 1 Publications Verification	TRP Channel	Neurological Disease
TRPM8 antagonist 2 is a potent and selective *TRPM8* antagonist, with an IC₅₀ of 0.2 nM, used in the research of neuropathic pain syndromes.

HY-165559

Trpvicin	TRP Channel	Inflammation/Immunology
Trpvicin is a potent and subtype-selective TRPV3 inhibitor with IC₅₀s of 0.41 and 0.22 μM for hTRPV3-WT and hTRPV3-G573S mutant, respectively. Trpvicin exhibits minimal effects on other TRP family members (such as TRPV1/2/4/5/6, TRPA1 and TRPM8). Trpvicin inhibits the TRPV3 channel by stabilizing it in a closed state via VSLD-PD binding. Trpvicin accesses additional binding sites inside the central cavity of the G573S mutant to remodel symmetry and block the channel. Trpvicin inhibits itch and hair loss in mouse models. Trpvicin can be used for study of inflammation and immunology .

HY-100345

AMTB hydrochloride 2 Publications Verification	TRP Channel	Neurological Disease Cancer
AMTB hydrochloride is a selective TRPM8 channel blocker. AMTB hydrochloride inhibits icilin-induced TRPM8 channel activation with a pIC₅₀ of 6.23. AMTB hydrochloride can be used for the research of the overactive bladder and painful bladder syndrome. AMTB hydrochloride is a non-selective inhibitor of voltage-gated sodium channels (Na_V) .

HY-115506

PF-05105679	TRP Channel	Neurological Disease
PF-05105679, a chemical probe, is an orally active and selective *TRPM8* antagonist with an IC₅₀ of 103 nM. PF-05105679 has the potential for cold-related pain .

HY-112703

AMG 333	TRP Channel	Cardiovascular Disease Neurological Disease
AMG 333 is an orally active and highly selective *TRPM8* antagonist with an IC₅₀ of 13 nM.

HY-N8264

Moringin 1 Publications Verification	TRP Channel	Neurological Disease Inflammation/Immunology Cancer
Moringin is a potent and selective TRPA1 ion channel natural agonist with an EC₅₀ of 3.14 μM. Moringin does not activate or activates very weakly the vanilloids somatosensory channels TRPV1, TRPV2, TRPV3 and TRPV4, and the melastatin cooling receptor TRPM8. Moringin has hypoglycemic, antimicrobial, anti-inflammatory, anticancer and neuroprotection activities .

HY-110181

M8-B 1 Publications Verification	TRP Channel	Metabolic Disease
M8-B is a potent transient receptor potential melastatin-8 (TRPM8) antagonist. M8-B blocks cold-induced and TRPM8-agonist-induced activation TRPM8 channels. M8-B decreases deep body temperature (Tb) .

HY-N7144A

Citronellyl acetate	Environmental Pollutants PKC TRP Channel PKA	Neurological Disease
Citronellyl acetate, a monoterpene product of the secondary metabolism of plants, is an orally active antinociceptive agent. Citronellyl acetate modulates TRPV1, *TRPM8, ASIC, glutamate receptors, PKC, and PKA*-mediated nociception. Citronellyl acetate can be used for the research of acute pain .

HY-145124

TRPM8 antagonist 3	TRP Channel	Others
TRPM8 antagonist 3 is a novel *TRPM8* blocker with an IC₅₀ value of 11 nM.

HY-109087

Elismetrep MT-8554	TRP Channel	Cardiovascular Disease Neurological Disease
Elismetrep (MT-8554) is a *TRPM8* antagonist. Elismetrep reduces the frequency of vasomotor symptoms. Elismetrep can be used for study of pain .

HY-16162A

D-3263 hydrochloride 1 Publications Verification	TRP Channel	Cancer
D-3263 hydrochloride is an enteric-coated, orally bioavailable (transient receptor potential melastatin member 8) *TRPM8* agonist.

HY-110199

TC-I 2014	TRP Channel	Neurological Disease
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 .

HY-19976

RN-1747 5 Publications Verification	TRP Channel	Cardiovascular Disease Metabolic Disease
RN-1747 is a selective TRPV4 channel agonist, with EC₅₀ values of 0.77 μM, 4.0 μM and 4.1 μM for hTRPV4, mTRPV4 and rTRPV4, respectively. RN-1747 acts as an antagonist of *TRPM8, with an IC₅₀* of 4 μM. Topical cutaneous administration of RN-1747 induces hypothermia, increases tail heat loss via cutaneous vasodilation, and promotes cold-seeking behavior in rats. Intracerebroventricular administration of RN-1747 does not induce hypothermia in rats .

HY-N7117

1,4-Cineole	Environmental Pollutants TRP Channel	Neurological Disease
1,4-Cineole is an oxygenated monoterpene found in eucalyptus oil. 1,4-Cineole is a *hTRPM8* and hTRPA1 agonist. 1,4-Cineole can increase intracellular Ca ²⁺ concentration. 1,4-Cineole exhibits anti-anxiety and anti-depression effects. 1,4-Cineole can be used for the research of neurological disease, such as depression .

HY-B1173

(+)-Camphor 1 Publications Verification D-(+)-Camphor; (1R)-(+)-Camphor	Environmental Pollutants Bacterial	Neurological Disease Inflammation/Immunology Cancer
(+)-Camphor (D-(+)-Camphor; (1R)-(+)-Camphor) is an isomer of Camphor. Camphor is an agonist of monoterpenoid transient receptor potential (TRP) channels (such as TRPV1, TRPV3, *TRPM8) and an inhibitor of TRPA1* channels. Camphor's derivatives have multiple biological activities, including antibacterial, antiviral, antioxidant, analgesic and anticancer. Camphor can selectively activate cold-sensitive TRP channels and inhibit TRPA1-mediated nociceptive signals. Camphor stimulates the cold-sensing nerve endings in the skin and regulates the activity of ion channels to exert analgesic, anti-inflammatory and anti-itching effects. It also has anti-proliferative and anti-mutagenic activities on tumor cells, which may be related to inhibiting ribosome function or inducing cell apoptosis. Camphor can be absorbed through the skin and (+)-Camphor can be used in the study of muscle and joint pain and inflammation .

HY-108461

TRPM8-IN-1	TRP Channel	Neurological Disease
TRPM8-IN-1 (example 14) is an inhibitor of transient receptor potential melastatin-8 (TRPM8) channels, IC₅₀<5 μM .

HY-104059

AMG2850 1 Publications Verification	TRP Channel	Inflammation/Immunology
AMG2850 is a potent, orally bioavailable and selective transient receptor potential melastatin 8 (TRPM8) antagonist .

HY-126593

Cryosim-3	TRP Channel	Others
Cryosim-3 is a selective TRPM8 receptor agonist. Cryosim-3 increases tear secretion and relieves ocular discomfort in animal models .

HY-177763

TRPM8 receptor agonist-1	TRP Channel	Neurological Disease
TRPM8 receptor agonist-1 (Example 81) is a *TRPM8* receptor agonist. TRPM8 receptor agonist-1 can trigger the inward flow of calcium, sodium and other ions within the cell, causing the cell membrane to depolarize and triggering an action potential. TRPM8 receptor agonist-1 can activate signals related to the swallowing reflex and can be used for the research of oropharyngeal dysphagia .

HY-75161R

(-)-Menthol (Standard)	Reference Standards TRP Channel Endogenous Metabolite	Cancer
(-)-Menthol (Standard) is the analytical standard of (-)-Menthol. This product is intended for research and analytical applications. (-)-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-B0985A

Phenazopyridine 2 Publications Verification	TRP Channel	Neurological Disease
Phenazopyridine is a competitive SARM1 inhibitor, with IC₅₀ 145 μM. Phenazopyridine is a *TRPM8* antagonist. Phenazopyridine has a local anesthetic/analgesic effect. Phenazopyridine is used to relieve painful symptoms of conditions such as cystitis and urethritis. Phenazopyridine can promote neuronal differentiation and can also be used in the study of traumatic brain injury, peripheral neuropathy and neurodegenerative diseases .

HY-160900

RN-1665 1 Publications Verification	TRP Channel	Others
RN-1665 is an orally active TRPV4 antagonist that exhibits excellent selectivity for related TRP receptors such as TRPV1, TRPV3 and TRPM8. RN-1665 is a TRPV4 probe for focus screens, with IC50s of 0.26 μM and 0.39 μM for hTRPV4 and rTRPV4 from human and rat, respectively .

HY-144372

TRPV1 antagonist 3	TRP Channel	Neurological Disease
TRPV1 antagonist 3 (Compound 7q) is a potent TRPV1 antagonist with an IC₅₀ of 2.66 nM against capsaicin. TRPV1 antagonist 3 is mode-selective, oral bioavailable (F = 60%) and CNS-penetrant .

HY-W014394

Vanillyl butyl ether	TRP Channel Parasite	Infection Cardiovascular Disease
Vanillyl butyl ether is a major contributor to the characteristic flavor and fragrance of vanilla. Vanillyl butyl ether is one of the eco-friendly and nontoxic substances. Vanillyl butyl ether exhibits mutually inhibitory effects on mammalian TRPV1 and *TRPM8* channels. Vanillyl butyl ether shows repellency activity against Tribolium castaneum, T. confusum and L. bostrychophila. Vanillyl butyl ether acts as a mild warming agent, providing a warming sensation and enhancing blood circulation .

HY-126941

Hecogenin acetate	ERK MMP Reactive Oxygen Species (ROS) NF-κB p38 MAPK NOD-like Receptor (NLR) TRP Channel TNF Receptor Interleukin Related	Infection Neurological Disease Inflammation/Immunology Endocrinology
Hecogenin acetate is an orally active steroid saponin aglycone with extensive biological activities. Hecogenin acetate inhibits the phosphorylation of NF-κB and p38 MAPK signaling pathways, antagonizes *TRPA1/TRPM8* channels, inhibits the production of pro-inflammatory cytokines, and has anti-inflammatory and analgesic effects. Hecogenin acetate inhibits the production of ROS and the activation of NLRP3 inflammasome; downregulates the expression of MMP-2, and has neuroprotective and anti-tumor activities. Hecogenin acetate enhances gastric mucosal defense and promotes ulcer healing. Hecogenin acetate can be used in combination with certain antibiotics to regulate bacterial efflux pumps and restore antibiotic sensitivity .

HY-174846

TRPM8 antagonist 4 prodrug	Cannabinoid Receptor TRP Channel Drug Intermediate	Neurological Disease Inflammation/Immunology
TRPM8 antagonist 4 prodrug (Compound 8b) is an orally active CB₂R agonist (EC₅₀: 51.2 nM) and a weak *TRPM8* antagonist. TRPM8 antagonist 4 prodrug is a prodrug of TRPM8 antagonist 4 (HY-174825). TRPM8 antagonist 4 prodrug exhibits anti-inflammatory and analgesic activities and can be used in the research of inflammation-related pain disorders .

HY-174825

TRPM8 antagonist 4	TRP Channel Cannabinoid Receptor Interleukin Related TNF Receptor	Inflammation/Immunology
TRPM8 antagonist 4 is a CB2R partial agonist (EC₅₀=54.2 nM, K_i=3.2 μM) and *TRPM8* antagonists (IC₅₀=42.3 nM) with high functional selectivity and good physicochemical properties. TRPM8 antagonist 4 has significant anti-inflammatory and analgesic effects and good safety, reduces the mRNA expression of TNF-α, IL-6, and IL-1β .

HY-N7536

Voacangine	TRP Channel	Others
Voacangine is an antagonist for TRPV1 and *TRPM8* but as an agonist for TRPA1 (EC₅₀=8 μM). Voacangine competitively blockes capsaicin binding to TRPV1 (IC₅₀=50 μM). Voacangine competitively inhibits the binding of menthol to *TRPM8* (IC₅₀=9 μM) and it shows noncompetitive inhibition against icilin (IC₅₀=7 μM). Voacangine selectively abrogates chemical agonist-induced *TRPM8* activation and did not affect cold-induced activation. Voacangine is an alkaloid isolated from the root bark of Voacanga africana .

HY-W014325R

TRPM8 agonist WS-3 (Standard) Framidice 3 (Standard)	Reference Standards TRP Channel Endogenous Metabolite	Neurological Disease Metabolic Disease Cancer
TRPM8 agonist WS-3 (Standard) is the analytical standard of TRPM8 agonist WS-3. This product is intended for research and analytical applications. TRPM8 agonist WS-3 is an specific agonist of *TRPM8* with an EC₅₀ of 3.7 μM. TRPM8 agonist WS-3 inhibits epileptic seizures through a TRPM8 dependent mechanism. TRPM8 agonist WS-3 can be used for research on epilepsy and other conditions .

HY-130074

FEMA 4809	TRP Channel	Neurological Disease
FEMA 4809 is a TRPM8 receptor agonist (EC₅₀=0.2 nM) for use as a cooling agent. TRPM8 is the ion channel responsible for the cool perception .

HY-RS15118

TRPM8 Human Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
TRPM8 Human Pre-designed siRNA Set A contains three designed siRNAs for TRPM8 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

TRPM8 Human Pre-designed siRNA Set A TRPM8 Human Pre-designed siRNA Set A

HY-108449S

Acoltremon-d3 WS-12-d₃; AR-15512-d₃; AVX-012-d₃	Isotope-Labeled Compounds TRP Channel	Neurological Disease
Acoltremon-d₃ (WS-12-d₃) is the deuterium labeled Acoltremon (HY-108449). Acoltremon is a potent and selective TRPM8 agonist, the menthol derivative, as a cooling agent. Acoltremon shows analgesic effect, and can be used in chronic neuropathic pain research .

HY-RS16771

Trpm8 Mouse Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
Trpm8 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Trpm8 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

Trpm8 Mouse Pre-designed siRNA Set A Trpm8 Mouse Pre-designed siRNA Set A

HY-RS23211

Trpm8 Rat Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
Trpm8 Rat Pre-designed siRNA Set A contains three designed siRNAs for Trpm8 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

Trpm8 Rat Pre-designed siRNA Set A Trpm8 Rat Pre-designed siRNA Set A

HY-N1369S1

Menthol-d2	Calcium Channel Isotope-Labeled Compounds	Neurological Disease
Menthol-d₂ is deuterated labeled Menthol (HY-N1369). Menthol is an analgesic and TRPM8 modulator. TRPM8 is a cold temperature sensing ion channel, and Menthol can regulate TRPM8 to exert analgesic and anti-irritation mechanisms. Menthol stimulates cold receptors and produces a cooling sensation by inhibiting Ca++ currents in neuronal cell membranes .

HY-104061

AMG8788	TRP Channel	Others
AMG8788 is a potent, selective, orally active antagonist of *TRPM8* with an IC₅₀ of 63.2 nM .

HY-117372

DFL23448	TRP Channel	Metabolic Disease
DFL23448 is a selective transient receptor potential melastatin-8 (TRPM8) antagonist. DFL23448 shows IC₅₀ values of 10 and 21 nM in hTRPM8 human embryonic kidney 293 cells activated by Cooling Agent 10 or cold. DFL23448 has limited activity (IC₅₀ >10 μM) at transient receptor potential vanilloids TRPV1, TRPA1, or TRPV4 or at various G protein-coupled receptors. DFL23448 can modify bladder function and reduce bladder overactivity in awake rats .

HY-178393

TRPM2-IN-2	TRP Channel	Neurological Disease Metabolic Disease
TRPM2-IN-2 is a potent and selective *TRPM2* inhibitor (IC₅₀ = 0.66 μM) with minimal activity against TRPM8 and TRPV1 (IC₅₀ >10 μM). TRPM2-IN-2 exhibits robust neuroprotective effects in both in vitro oxygen-glucose deprivation/reperfusion (OGD/R) model and in vivo transient middle cerebral artery occlusion (tMCAO) mouse model. TRPM2-IN-2 can be used for ischemic stroke research .

HY-178236

TRPM5 agonist-1	TRP Channel	Metabolic Disease
TRPM5 agonist-1 is an orally active *TRPM5* agonist with a pEC₅₀ of 8.1. TRPM5 agonist-1 shows excellent selectivity (> 100-fold) versus related cation channels (TRPM8, TRPV1, TRPV4, TRPA1, TRPM4). TRPM5 agonist-1 exhibits locally acting stimulatory effect on gastrointestinal transit in mice. TRPM5 agonist-1 can be used for research on promoting gastric motility .

HY-N9484S

Menthofuran-13C2	Drug Metabolite Isotope-Labeled Compounds	Others
Menthofuran- ¹³C₂ is ¹³C labeled Menthol (HY-N1369). Menthol is an analgesic and *TRPM8* modulator. TRPM8 is a cold temperature sensing ion channel, and Menthol can regulate TRPM8 to exert analgesic and anti-irritation mechanisms. Menthol stimulates cold receptors and produces a cooling sensation by inhibiting Ca ⁺⁺ currents in neuronal cell membranes. Menthol also improves oral nicotine rejection in mice .

HY-B1173R

(+)-Camphor (Standard) D-(+)-Camphor (Standard); (1R)-(+)-Camphor (Standard)	Reference Standards Bacterial	Neurological Disease Inflammation/Immunology Cancer
(+)-Camphor (Standard) is the analytical standard of (+)-Camphor. This product is intended for research and analytical applications. (+)-Camphor (D-(+)-Camphor; (1R)-(+)-Camphor) is an isomer of Camphor. Camphor is an agonist of monoterpenoid transient receptor potential (TRP) channels (such as TRPV1, TRPV3, *TRPM8) and an inhibitor of TRPA1* channels. Camphor's derivatives have multiple biological activities, including antibacterial, antiviral, antioxidant, analgesic and anticancer. Camphor can selectively activate cold-sensitive TRP channels and inhibit TRPA1-mediated nociceptive signals. Camphor stimulates the cold-sensing nerve endings in the skin and regulates the activity of ion channels to exert analgesic, anti-inflammatory and anti-itching effects. It also has anti-proliferative and anti-mutagenic activities on tumor cells, which may be related to inhibiting ribosome function or inducing cell apoptosis. Camphor can be absorbed through the skin and (+)-Camphor can be used in the study of muscle and joint pain and inflammation .

HY-104062

AMG9678	TRP Channel	Others
AMG9678 is a potent, selective, orally active antagonist of *TRPM8* with an IC₅₀ of 31.2 nM .

Cat. No.	상품명	Category	Target	Chemical Structure

HY-75161

(-)-Menthol 4 Publications Verification	Structural Classification Other Monoterpenes Classification of Application Fields Terpenoids Labiatae Erythrina poeppigiana Plants Endogenous metabolite Disease Research Fields Source Classification Cancer	Environmental Pollutants Endogenous Metabolite TRP Channel
(-)-Menthol is a key component of peppermint oil that binds and activates transient receptor potential melastatin 8 (TRPM8), a Ca ²⁺-permeable nonselective cation channel, to increase [Ca ²⁺]_i . Antitumor activity .

HY-N8264

Moringin 1 Publications Verification	Structural Classification Natural Products Neurological Disease Classification of Application Fields Moringa oleifera Lam. Moringaceae Plants Inflammation/Immunology Disease Research Fields Source Classification	TRP Channel
Moringin is a potent and selective TRPA1 ion channel natural agonist with an EC₅₀ of 3.14 μM. Moringin does not activate or activates very weakly the vanilloids somatosensory channels TRPV1, TRPV2, TRPV3 and TRPV4, and the melastatin cooling receptor TRPM8. Moringin has hypoglycemic, antimicrobial, anti-inflammatory, anticancer and neuroprotection activities .

HY-N7144A

Citronellyl acetate	Infection Structural Classification Natural Products Classification of Application Fields Pelargonium hortorum Plants Geraniaceae Disease Research Fields Source Classification	Environmental Pollutants PKC TRP Channel PKA
Citronellyl acetate, a monoterpene product of the secondary metabolism of plants, is an orally active antinociceptive agent. Citronellyl acetate modulates TRPV1, *TRPM8, ASIC, glutamate receptors, PKC, and PKA*-mediated nociception. Citronellyl acetate can be used for the research of acute pain .

HY-N7117

1,4-Cineole	Structural Classification Other Monoterpenes Classification of Application Fields Terpenoids Ericaceae Plants Rhododendron anthopogonoides Maxim. Inflammation/Immunology Disease Research Fields Cancer	Environmental Pollutants TRP Channel
1,4-Cineole is an oxygenated monoterpene found in eucalyptus oil. 1,4-Cineole is a *hTRPM8* and hTRPA1 agonist. 1,4-Cineole can increase intracellular Ca ²⁺ concentration. 1,4-Cineole exhibits anti-anxiety and anti-depression effects. 1,4-Cineole can be used for the research of neurological disease, such as depression .

HY-B1173

(+)-Camphor 1 Publications Verification D-(+)-Camphor; (1R)-(+)-Camphor	Structural Classification Other Monoterpenes Classification of Application Fields Terpenoids Other Diseases Plants Lauraceae Cinnamomum camphora Disease Research Fields Source Classification	Environmental Pollutants Bacterial
(+)-Camphor (D-(+)-Camphor; (1R)-(+)-Camphor) is an isomer of Camphor. Camphor is an agonist of monoterpenoid transient receptor potential (TRP) channels (such as TRPV1, TRPV3, *TRPM8) and an inhibitor of TRPA1* channels. Camphor's derivatives have multiple biological activities, including antibacterial, antiviral, antioxidant, analgesic and anticancer. Camphor can selectively activate cold-sensitive TRP channels and inhibit TRPA1-mediated nociceptive signals. Camphor stimulates the cold-sensing nerve endings in the skin and regulates the activity of ion channels to exert analgesic, anti-inflammatory and anti-itching effects. It also has anti-proliferative and anti-mutagenic activities on tumor cells, which may be related to inhibiting ribosome function or inducing cell apoptosis. Camphor can be absorbed through the skin and (+)-Camphor can be used in the study of muscle and joint pain and inflammation .

HY-75161R

(-)-Menthol (Standard)	Structural Classification Other Monoterpenes Human Gut Microbiota Metabolites Microorganisms Terpenoids Labiatae Erythrina poeppigiana Plants Endogenous metabolite Source Classification	Reference Standards TRP Channel Endogenous Metabolite
(-)-Menthol (Standard) is the analytical standard of (-)-Menthol. This product is intended for research and analytical applications. (-)-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-W014394

Vanillyl butyl ether	Cardiovascular Disease Structural Classification Monophenols other families Classification of Application Fields Phenols Plants Disease Research Fields Source Classification	TRP Channel Parasite
Vanillyl butyl ether is a major contributor to the characteristic flavor and fragrance of vanilla. Vanillyl butyl ether is one of the eco-friendly and nontoxic substances. Vanillyl butyl ether exhibits mutually inhibitory effects on mammalian TRPV1 and *TRPM8* channels. Vanillyl butyl ether shows repellency activity against Tribolium castaneum, T. confusum and L. bostrychophila. Vanillyl butyl ether acts as a mild warming agent, providing a warming sensation and enhancing blood circulation .

HY-126941

Hecogenin acetate	Structural Classification Agave americana Linn. Agavaceae Plants Steroids Source Classification	ERK MMP Reactive Oxygen Species (ROS) NF-κB p38 MAPK NOD-like Receptor (NLR) TRP Channel TNF Receptor Interleukin Related
Hecogenin acetate is an orally active steroid saponin aglycone with extensive biological activities. Hecogenin acetate inhibits the phosphorylation of NF-κB and p38 MAPK signaling pathways, antagonizes *TRPA1/TRPM8* channels, inhibits the production of pro-inflammatory cytokines, and has anti-inflammatory and analgesic effects. Hecogenin acetate inhibits the production of ROS and the activation of NLRP3 inflammasome; downregulates the expression of MMP-2, and has neuroprotective and anti-tumor activities. Hecogenin acetate enhances gastric mucosal defense and promotes ulcer healing. Hecogenin acetate can be used in combination with certain antibiotics to regulate bacterial efflux pumps and restore antibiotic sensitivity .

HY-N7536

Voacangine	Alkaloids other families Classification of Application Fields Other Diseases Plants Disease Research Fields Indole Alkaloids Source Classification	TRP Channel
Voacangine is an antagonist for TRPV1 and *TRPM8* but as an agonist for TRPA1 (EC₅₀=8 μM). Voacangine competitively blockes capsaicin binding to TRPV1 (IC₅₀=50 μM). Voacangine competitively inhibits the binding of menthol to *TRPM8* (IC₅₀=9 μM) and it shows noncompetitive inhibition against icilin (IC₅₀=7 μM). Voacangine selectively abrogates chemical agonist-induced *TRPM8* activation and did not affect cold-induced activation. Voacangine is an alkaloid isolated from the root bark of Voacanga africana .

HY-B1173R

(+)-Camphor (Standard) D-(+)-Camphor (Standard); (1R)-(+)-Camphor (Standard)	Structural Classification Other Monoterpenes Terpenoids Plants Lauraceae Cinnamomum camphora Source Classification	Reference Standards Bacterial
(+)-Camphor (Standard) is the analytical standard of (+)-Camphor. This product is intended for research and analytical applications. (+)-Camphor (D-(+)-Camphor; (1R)-(+)-Camphor) is an isomer of Camphor. Camphor is an agonist of monoterpenoid transient receptor potential (TRP) channels (such as TRPV1, TRPV3, *TRPM8) and an inhibitor of TRPA1* channels. Camphor's derivatives have multiple biological activities, including antibacterial, antiviral, antioxidant, analgesic and anticancer. Camphor can selectively activate cold-sensitive TRP channels and inhibit TRPA1-mediated nociceptive signals. Camphor stimulates the cold-sensing nerve endings in the skin and regulates the activity of ion channels to exert analgesic, anti-inflammatory and anti-itching effects. It also has anti-proliferative and anti-mutagenic activities on tumor cells, which may be related to inhibiting ribosome function or inducing cell apoptosis. Camphor can be absorbed through the skin and (+)-Camphor can be used in the study of muscle and joint pain and inflammation .

HY-N7117R

1,4-Cineole (Standard)	Structural Classification Other Monoterpenes Terpenoids Ericaceae Plants Rhododendron anthopogonoides Maxim.	Reference Standards TRP Channel
1,4-Cineole (Standard) is the analytical standard of 1,4-Cineole (HY-N7117). 1,4-Cineole is an oxygenated monoterpene found in eucalyptus oil. 1,4-Cineole is a *hTRPM8* and hTRPA1 agonist. 1,4-Cineole can increase intracellular Ca ²⁺ concentration. 1,4-Cineole exhibits anti-anxiety and anti-depression effects. 1,4-Cineole can be used for the research of neurological disease, such as depression .

Cat. No.	상품명	Chemical Structure

HY-108449S

Acoltremon-d3
Acoltremon-d₃ (WS-12-d₃) is the deuterium labeled Acoltremon (HY-108449). Acoltremon is a potent and selective TRPM8 agonist, the menthol derivative, as a cooling agent. Acoltremon shows analgesic effect, and can be used in chronic neuropathic pain research .

HY-N1369S1

Menthol-d2
Menthol-d₂ is deuterated labeled Menthol (HY-N1369). Menthol is an analgesic and TRPM8 modulator. TRPM8 is a cold temperature sensing ion channel, and Menthol can regulate TRPM8 to exert analgesic and anti-irritation mechanisms. Menthol stimulates cold receptors and produces a cooling sensation by inhibiting Ca++ currents in neuronal cell membranes .

HY-N9484S

Menthofuran-13C2

Menthofuran- ¹³C₂ is ¹³C labeled Menthol (HY-N1369). Menthol is an analgesic and TRPM8 modulator. TRPM8 is a cold temperature sensing ion channel, and Menthol can regulate TRPM8 to exert analgesic and anti-irritation mechanisms. Menthol stimulates cold receptors and produces a cooling sensation by inhibiting Ca ⁺⁺ currents in neuronal cell membranes. Menthol also improves oral nicotine rejection in mice .

HY-W711474

(-)-Menthol-d4
(-)-Menthol-d₄ is the deuterium labeled (-)-Menthol (HY-75161). (-)-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 .

Host:	Rabbit (2)
Reactivity:	Human (2) Rat (1) Mouse (2)
Application:	IHC-P (1) ICC/IF (2) WB (2)
Isotype:	IgG (2)
Conjugation:	Non-conjugated (2)
Clonality:	Monoclonal (1) Recombinant (1)
Modification:	Unmodified (1)

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HY-P81864

	TRPM8 Antibody (YA1609) LTrpC6; MGC2849; Transient receptor potential p8; Trp p8; TRPM8; TRPP8	WB, ICC/IF	Human, Mouse
	TRPM8 Antibody (YA1609) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to TRPM8.

HY-P810995

	TRPM8 Antibody LTRPC6, TRPP8, TRPM8, Transient receptor potential cation channel subfamily M member 8, Long transient receptor potential channel 6, Transient receptor potential p8, LTrpC-6, LTrpC6, Trp-p8	WB, IHC-P, ICC/IF	Human, Mouse, Rat
	TRPM8 Antibody is a Rabbit-derived and non-conjugated IgG Polyclonal antibody, targeting to TRPM8.

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Cat. No.	상품명		Classification

HY-75161

(-)-Menthol 4 Publications Verification		Flavoring Agents
(-)-Menthol is a key component of peppermint oil that binds and activates transient receptor potential melastatin 8 (TRPM8), a Ca ²⁺-permeable nonselective cation channel, to increase [Ca ²⁺]_i . Antitumor activity .

HY-RS15118

TRPM8 Human Pre-designed siRNA Set A		siRNAs Human Pre-designed siRNA Sets
TRPM8 Human Pre-designed siRNA Set A contains three designed siRNAs for TRPM8 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

HY-RS16771

Trpm8 Mouse Pre-designed siRNA Set A		siRNAs Mouse Pre-designed siRNA Sets
Trpm8 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Trpm8 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

HY-RS23211

Trpm8 Rat Pre-designed siRNA Set A		siRNAs Rat Pre-designed siRNA Sets
Trpm8 Rat Pre-designed siRNA Set A contains three designed siRNAs for Trpm8 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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