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Chemical Structure Cat. No. Product Name CAS No.
Talinolol Chemical Structure
BCP30483 Talinolol 57460-41-0
Talinolol is a beta(1)-adrenergic receptor antagonist and a probe drug for P-glycoprotein (P-gp) activity in humans.
Ganaxolone Chemical Structure
BCP30445 Ganaxolone 38398-32-2
Ganaxolone, also known as CCD 1042 and C1042, is a CNS-selective GABAA modulator that acts on well-characterized targets in the brain known to have anxiolytic and anticonvulsant effects. Ganaxolone protects against seizures in diverse animal models, including the pentylenetetrazol, 6 Hz and amygdala kindling models. Ganaxolone is a positive allosteric modulator of the action of the GABAA receptor and, unlike benzodiazepines, there does not appear to be tolerance to the anticonvulsant effects of ganaxolone.
ent Naxagolide Hydrochloride Chemical Structure
BCP21508 ent Naxagolide Hydrochloride 100935-99-7
ent Naxagolide is a S-isomer of Naxagolide.
Atracurium besylate Chemical Structure
BCP22909 Atracurium besylate 64228-81-5
Atracurium Besylate is a neuromuscular blocking agent with ED95 of 0.2 mg/kg.
Metopimazine Acid Chemical Structure
BCP15668 Metopimazine Acid 18182-00-8
Metopimazine Acid is the acid metabolite of Metopimazine.
Metopimazine Sulfoxide Chemical Structure
BCP15667 Metopimazine Sulfoxide 18181-99-2
Metopimazine Sulfoxide is a metabolite of Metopimazine in dogs and rabbits.
CHF 5074 Chemical Structure
BCP30410 CHF 5074 749269-83-8
CHF5074 is a novel γ-secretase modulator, reduces Aβ42 and Aβ40 secretion, with an IC50 of 3.6 and 18.4 μM, respectively.
A-381393 Chemical Structure
BCP30376 A-381393 726174-00-1
A-381393 is a potent and selective agonist of the dopamine D4 receptor.
Homovanillyl alcohol Chemical Structure
BCP30361 Homovanillyl alcohol 2380-78-1
Homovanillyl alcohol is a metabolite of hydroxytyrosol, which in turn is a metabolite of the neurotransmitter dopamine.
(S)-B-973B Chemical Structure
BCP30366 (S)-B-973B 2244989-34-0
(S)-B-973B is a potent allosteric agonism and positive allosteric modulation (ago-PAM) for α7 nAChR, with antinociceptive activity.
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