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Chemical Structure Cat. No. Product Name CAS No.
N-Methyldopamine hydrochloride Chemical Structure
BCP35497 N-Methyldopamine hydrochloride 62-32-8
N-Methyldopamine hydrochloride is an andregenic and dopamine receptor agonist; active metabolite of Ibopramine.
Nebivolol Chemical Structure
BCP35441 Nebivolol 99200-09-6
Nebivolol is a beta-blocker and antihypertensive medication that has additional vasodilatory activity mediated by nitric oxide release. Nebivolol has yet to be linked to instances of clinically apparent liver injury.
Neostigmine bromide Chemical Structure
BCP35352 Neostigmine bromide 114-80-7
Neostigmine Bromide is a cholinesterase inhibitor used in the treatment of myasthenia gravis.
ML417 Chemical Structure
BCP35340 ML417 1386162-69-1
ML417 is a selective and brain penetrant D3 dopamine receptor (D3R) agonist, with an EC50 of 38 nM. ML417 potently promotes D3R-mediated β-arrestin translocation, G protein mediated signaling, and pERK phosphorylation with minimal effects on other GPCR-mediated signaling. ML417 exhibits neuroprotection against toxin-induced neurodegeneration of dopaminergic neurons.
p-MPPI monohydrochloride Chemical Structure
BCP35226 p-MPPI monohydrochloride 220643-77-6
p-MPPI monohydrochloride is a selective 5-HT1A serotonin receptor antagonist, crossing the blood-brain barrier.
Metipranolol Chemical Structure
BCP35224 Metipranolol 22664-55-7
Metipranolol is a non-selective beta blocker used in eye drops to treat glaucoma. It is rapidly metabolized into desacetylmetipranolol.
URB 937 Chemical Structure
BCP35209 URB 937 1357160-72-5
URB 937 is a FAAH inhibitor and increases anandamide levels.
KN92 Chemical Structure
BCP35203 KN92 176708-42-2
KN-92 is an inactive derivative of KN-93.
PSEM 89S TFA Chemical Structure
BCP35173 PSEM 89S TFA 1336913-03-1
PSEM 89S TFA is a selective and brain penetrant agonists for the resulting ion channels. PSEM 89S TFA is orthogonally selective for Q79G and L141F, respectively.
Tranylcipromine Chemical Structure
BCP35142 Tranylcipromine 155-09-9
Tranylcypromine, an amphetamine derivative, has been found to be a MAO inhibitor that could be used an antidepressant agent and anxiolytic drug.
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