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Cat. No. Product Name Information
PC-70039

RN-9893

TRPV4 inhibitor

RN-9893 (RN9893) is a potent, selective orally-bioavailable TRPV4 antagonist with IC50 of 320, 420 and 660 nM for mouse, human and rat TRPV4 channels, respectively.
PC-60025

AC1903

AC1903 is a potent, specific TRPC5 channel inhibitor with IC50 of 14.7 uM.
PC-60019

2-APB

TRP channel inhibitor

2-APB (2-Aminoethoxydiphenylborane) is a membrane permeable IP3 receptor antagonist and broad TRP channels (TRPC5, TRPM2) blocker.
PC-45654

GSK-1016790A

TRPV4 agonist

GSK-1016790A is a potent TRPV4 channel agonist, induces Ca2+ influx in HEK cells expressing human TRPV4 with EC50 of 2.1 nM.
PC-45790

Clemizole hydrochloride

TRPC5 inhibitor

Clemizole hydrochloride is an H1 histamine receptor antagonist that substantially inhibits HCV replication by suppression of NS4B's RNA binding (IC50=24 nM) with little toxicity for the host cells.
PC-45789

Clemizole

TRPC5 inhibitor

An H1 histamine receptor antagonist that substantially inhibits HCV replication by suppression of NS4B's RNA binding (IC50=24 nM) with little toxicity for the host cells.
PC-42591

Capsaicin

TRPV1 agonist

Capsaicin is an active component of chili pepper, potent agonist of TRPV1 channel with EC50 of 0.29 uM.
PC-42799

Icilin

TRPM8 agonist

Icilin (AG-3-5) is asuper-cooling agent that fuctions as a potent TRPM8 agonist with EC50 of 0.2 uM.
PC-45042

SN-2

TRPML3 activator

SN-2 (TRPML3 activator SN-2) is a small molecule activator of the TRPML3 ion channel with EC50 of 1.13 uM strongly potentiates TRPML3 activation with low extracytosolic [Na(+)].
PC-45093

Mavatrep

TRPV1 inhibitor

Mavatrep (JNJ-39439335) is a selective, high-affinity TRPV1 antagonist with IC50 of 4.6 nM (inhibition of capsaicin-induced Ca(2+) influx).
PC-45772

RN-1734

TRPV4 inhibitor

RN-1734 (RN1734) is a potent, selective TRPV4 antagonist with IC50 of 2.3, 3.2 and 5.9 uM for hTRPV4, rTRPV4 and mTRPV4 channels, respectively.
PC-42062

JNJ-17203212

TRPV1 antagonist

JNJ-17203212 is a potent, selective and orally bioavailable TRPV1 receptor antagonist with IC50 of 65 nM and 102 nM for hTRPV1 and rTRPV1, respectively.

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