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GPCR/G Protein
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Neuro Signaling Pathway
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Protease/Metabolic Enzyme
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Research Areas
- Metabolic Disease
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Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Ammonia Series
- Azaindazole
- Pyridazine Series
- Nucleoside Series
- Quinazoline
- Pyrazole Series
- Boric acid
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- Pyrrole Series
- Thiophene Series
- Saccharide
- Azaindole
- Indole Series
- Piperidine Series
- Indazole Series
- Heterocyclic Series
- Benzene Series
- Pyridine Series
Raw Materials
TRP Channel
Chemical Structure | Cat. No. | Product Name | CAS No. |
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BCP49641 | Fospropofol | 258516-89-1 | |
Fospropofol is a water soluble prodrug and is converted to propofol in the liver.
|
BCP49138 | TRPV4 agonist-1 New | 2314467-59-7 | |
TRPV4 agonist-1 free base is a transient receptor potential vanilloid 4 (TRPV4) agonist with an EC50 of 60 nM in the hTRPV4 Ca2+ assay.
|
BCP49136 | TRPV4 agonist-1 New | 2314467-60-0 | |
TRPV4 agonist-1 is a transient receptor potential vanilloid 4 (TRPV4) agonist with an EC50 of 60 nM in the hTRPV4 Ca2+ assay.
|
BCP24615 | AMTB hydrochloride New | 926023-82-7 | |
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 (NaV).
|
BCP48932 | TRPM4-IN-5 New | 351424-20-9 | |
TRPM4-IN-5 is a potent and selective inhibitor of the cation channel TRPM4.
|
BCP48857 | Farnesyl diphosphate New | 13058-04-3 | |
Farnesyl pyrophosphate, a 15-carbon isoprenoid, is a metabolic intermediate of the mevalonate (MVA) pathway.
|
BCP47204 | IA-alkyne New | 930800-38-7 | |
IA-alkyne is a novel thiol-reactive and clickable proble for protein-protein interaction studies
|
BCP44873 | EIPA New | 1154-25-2 | |
EIPA is a selective blocker of Na+/H+ antiport.
|
BCP43788 | WS-12 New | 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.
|
BCP42100 | Pyr3 New | 1160514-60-2 | |
Pyr3 is a selective antagonist of the canonical transient receptor potential channel 3 (TRPC3).
|