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Ion Channel/Membrane Transporter
TRP Channel

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TRP Channel

Chemical Structure Cat. No. Product Name CAS No.
Farnesyl diphosphate Chemical Structure
BCP48857 Farnesyl diphosphate 13058-04-3
Farnesyl pyrophosphate, a 15-carbon isoprenoid, is a metabolic intermediate of the mevalonate (MVA) pathway.
IA-alkyne Chemical Structure
BCP47204 IA-alkyne 930800-38-7
IA-alkyne is a novel thiol-reactive and clickable proble for protein-protein interaction studies
EIPA Chemical Structure
BCP44873 EIPA 1154-25-2
EIPA is a selective blocker of Na+/H+ antiport.
WS-12 Chemical Structure
BCP43788 WS-12 68489-09-8
WS12 is a potent TRPM8 agonist. It acts as a cooling agent with EC50 value of 193 nM. It robustly activated TRPM8 in low micromolar concentrations, thus displaying a higher potency and efficacy compared to menthol.
Pyr3 Chemical Structure
BCP42100 Pyr3 1160514-60-2
Pyr3 is a selective antagonist of the canonical transient receptor potential channel 3 (TRPC3).
ML-SA1 Chemical Structure
BCP41268 ML-SA1 332382-54-4
ML-SA1 is an agonist of transient receptor potential mucolipin 1 (TRPML1).
GSK2798745 Chemical Structure
BCP38659 GSK2798745 1419609-94-1
GSK2798745 is a potent and selective TRPV4 Ion Channel Inhibitor with IC50 = 1.8 nM.
AM12 Chemical Structure
BCP37833 AM12 2387510-84-9
AM12 inhibits Lanthanide-evoked TRPC5 activity with an IC50 of 0.28 μM.
AC1903 Chemical Structure
BCP37804 AC1903 831234-13-0
AC1903 is a specific blocker of TRPC5 channel activity. It has been shown to suppress severe proteinuria and prevent podocyte loss.
GSK2193874 Chemical Structure
BCP36070 GSK2193874 1336960-13-4
GSK2193874 is an orally active, potent, and selective TRPV4 antagonist with IC50s of 2 nM and 40 nM for rTRPV4 and hTRPV4.
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