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Cat. No. Product Name Information
PC-45355

Nonivamide

TRPV1 agonist

Nonivamide is a capsaicin analog that acts as an agonist of TRPV1 channel.
PC-26459

IMTU

TRPV1 antagonist

IMTU is a potent and selective TRPV1 antagonist with IC50 of 128.34 nM, significantly inhibits the capsaicin-induced calcium influx.
PC-26458

HKC54

TRPV2 antagonist

HKC54 is a potent, selective TRPV2 antagonist with IC50 of 0.4 uM, 50-fold selectivity over TRPV1 and ∼70-fold selectivity over TRPA1.
PC-26401

RN-1665

TRPV4 antagonist

RN-1665 is a potent, selective and orally active TRPV4 antagonist with IC50 of 0.26 μM and 0.39 μM for hTRPV4 and rTRPV4, exhibits excellent selectivity for related TRP receptors such as TRPV1, TRPV3 and TRPM8.
PC-26099

DWP05195

TRPV1 antagonist

DWP05195 (DWP-05195) is a transient receptor potential vanilloid 1 (TRPV1) antagonist.
PC-26098

Vocacapsaicin hydrochloride

TRPV1 agonist

Vocacapsaicin hydrochloride (CA-008) is a non-opioid, water-soluble and injectable prodrug of capsaicin, a potent agonist of TRPV1 channel.
PC-25977

TRPM8 inhibitor PBMC

TRPM8 antagonist

PBMC is a highly specific and potent TRPM8 antagonist with IC50 of 0.4-0.6 nM in whole-cell voltage clamp assays.
PC-25933

AV3-1

TRPV3 activator

AV3-1 (TRPV3 activator 1) is a specific small molecule TRPV3 activator with EC50 of 2.0 μM for mouse TRPV3 and 7.2 μM for human TRPV3.
PC-25855

Olvanil

TRPV1 agonist

Olvanil (NE-19550, N-Vanillyloleamide) is a potent, selective agonist of transient receptor potential vanilloid type 1 (TRPV1) channels with EC50 of 0.7 nM.
PC-25854

Capsiate

TRPV1 agonist

Capsiate is a non-pungent capsaicin analog and potent, selective TRPA1 agonist, evokes inward currents at -60 mV in the HEK293 cells expressing TRPV1with EC50 of 290 nM.
PC-25781

PPZ2

TRPC3/C6/C7 activator

PPZ2 is a selective activator of TRPC3/TRPC6/TRPC7, activates DAG-activated TRPC3/TRPC6/TRPC7 channels, promotes neurite outgrowth and neuronal survival via downstream Ca2+-dependent signals.
PC-25780

L687

TRPC3/C6/C7 activator

L687 is a potent, specific TRPC3/C6/C7 activator, induces cellular antisense oligonucleotide (ASO) uptake, also induces dextran uptake and increases endocytosis.

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