Home   >  
Ion Channel/Membrane Transporter
  >  
TRP Channel

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

TRP Channel

Chemical Structure Cat. No. Product Name CAS No.
ABT-102 Chemical Structure
BCP27708 ABT-102 808756-71-0
ABT 102 is a selective transient receptor potential vanilloid 1 (TRPV1) receptor antagonist with IC50 values to be 5-7 nM.
N-(p-amylcinnamoyl) Anthranilic Acid Chemical Structure
BCP30845 N-(p-amylcinnamoyl) Anthranilic Acid 110683-10-8
N-(p-amylcinnamoyl) Anthranilic Acid (ACA) is a broad spectrum Phospholipase A2 (PLA2) inhibitor and TRP channel blocker. N-(p-amylcinnamoyl) Anthranilic Acid (ACA) is also an effective reversible inhibitor of calcium-activated chloride channels, has potential to treat arrhythmia.
AMG-333 Chemical Structure
BCP30858 AMG-333 1416799-28-4
AMG 333 is a potent and highly selective TRPM8 antagonist with an IC50 of 13 nM.
Elismetrep Chemical Structure
BCP30294 Elismetrep 1400699-64-0
Elismetrep is a non-opioid analgesic drug candidate.
SAR7334 Chemical Structure
BCP11028 SAR7334 1333210-07-3
SAR7334 is a potent TRPC6 (Transient receptor potential cation channel, subfamily C, member 6) inhibitor.
Icilin Chemical Structure
BCP27818 Icilin 36945-98-9
Icilin(AG 3-5) is a synthetic super-agonist of TRPM8 ion channel.
HC-070 Chemical Structure
BCP29966 HC-070 1628291-95-1
HC-070 is a potent inhibitor of TRPC4 and TRPC5, leading to anxiolytic and antidepressant effects in mice.
ML 204 Chemical Structure
BCP28617 ML 204 5465-86-1
ML204 is a novel potent antagonist that selectively modulates native TRPC4/C5 ion channels.
TRPM8 antagonist 14 Chemical Structure
BCP29863 TRPM8 antagonist 14 259674-19-6
TRPM8 antagonist 14 is a potent, selective TRPM8 antagonist with IC50 of 0.2 nM in calcium influx assays, shows no activity on TRPV1; shows significant target coverage in both an icilin-induced WDS (at 1-30 mg/kg s.c.) and oxaliplatin-induced cold allodynia (at 0.1-1 μg s.c.) mice models.
Probenecid Chemical Structure
BCP21785 Probenecid 57-66-9
Probenecid is a potent and selective agonist of transient receptor potential vanilloid 2 (TRPV2) channels.
123下一页末页共 41 条记录 1 / 5 页 
0086-13720134139