BCC1324
A-867744
A-867744 is a highly potent and selective type II positive allosteric modulator (PAM) of the alpha7 nicotinic acetylcholine receptors (nAChR) with an EC50 of 1.0 μM.
BCN1946
Hyoscyamine
L-Hyoscyamine is a chemical compound, a tropane alkaloid it is the levo-isomer to atropine.
BCC4582
Trospium chloride
Trospium Chloride is a competitive muscarinic cholinergic receptor antagonist.
BCC4563
Neostigmine Bromide
Neostigmine Bromide is a cholinesterase inhibitor used in the treatment of myasthenia gravis.
BCC4148
Tarafenacin D-tartrate
Tarafenacin D-tartrate (SVT-40776 D-tartrate) is a highly selective M3 muscarinic receptor antagonist (Ki= 0.19 nM), ~200 fold selectivity over M2 receptor.
BCC1068
Rocuronium Bromide
Rocuronium Bromide (ORG 9426 Bromide) is an aminosteroid non-depolarizing neuromuscular blocker or muscle relaxant used in modern anaesthesia, to facilitate endotracheal intubation and to provide skeletal musclerelaxation during surgery or mechanical ventilation.
BCC5512
mAChR-IN-1
mAChR-IN-1 is a potent muscarinic cholinergic receptor(mAChR) antagonist with IC50 of 17 nM.
BCC1900
Rivastigmine
Rivastigmine, an cholinesterase inhibitor(IC50= 5.5 uM), inhibits both butyrylcholinesterase and acetylcholinesterase IC50 value: 5.5 uM Target: AChE Rivastigmine is a parasympathomimetic or cholinergic agent for the treatment of mild to moderate dementia of the Alzheimer's type and dementia due to Parkinson's disease.
BCC4054
(R)-(+)-Tolterodine
Tolterodine(PNU-200583) is a potent muscarinic receptor antagonists that show selectivity for the urinary bladder over salivary glands in vivo.
BCC3851
Rivastigmine Tartrate
Rivastigmine tartrate, an cholinesterase inhibitor(IC50= 5.5 uM), inhibits both butyrylcholinesterase and acetylcholinesterase IC50 value: 5.5 uM Target: AChE Rivastigmine is a parasympathomimetic or cholinergic agent for the treatment of mild to moderate dementia of the Alzheimer's type and dementia due to Parkinson's disease.
BCC2000
Tiotropium Bromide
Tiotropium Bromide (BA679 BR) is a muscarinic acetylcholine receptor (mAChR) antagonist that blocks the binding of the acetylcholine ligand and subsequent opening of the ligand-gated ion channel.
BCC4585
Tiotropium Bromide hydrate
Tiotropium Bromide hydrate is a monohydrate of tiotropium bromide (Spiriva; Tiova; BA 679BR; tiopropium) that is an anticholinergic and bronchodilator and a muscarinic receptor antagonist.
BCC4146
Xanomeline oxalate
Xanomeline oxalate (LY246708 oxalate) is a selective M1 muscarinic receptor agonist.
BCC1906
Rocuronium
Rocuronium (Org-9426) is an aminosteroid non-depolarizing neuromuscular blocker or muscle relaxant used in modern anaesthesia.
BCN6255
Pregnenolone
Pregnenolone (3β-Hydroxy-5-pregnen-20-one) is a powerful neurosteroid, the main precursor of various steroid hormones including steroid ketones. Pregnenolone acts as a signaling-specific inhibitor of cannabinoid CB1 receptor, inhibits the effects of tetrahydrocannabinol (THC) that are mediated by the CB1 receptors. Pregnenolone can protect the brain from cannabis intoxication.
BCC4149
Oxybutynin chloride
Oxybutynin chloride is an anticholinergic agent, which inhibits vascular Kv channels in a concentration-dependent manner, with an IC50 of 11.51 μM.
BCC4574
Tropicamide
Tropicamide is an anticholinergic and a muscarinic receptor subtype M4-preferring antagonist .
BCC5559
Nitenpyram
Nitenpyram is a calss of neonicotinoid and an insect nicotinic acetylcholine receptor (nAChR) agonist with an IC50 of 14 nM. Nitenpyram is an oral fast-acting insecticide used to suppress sucking insects on companion animals.
BCC4577
Methscopolamine
Methscopolamine (Pamine) is a muscarinic acetylcholine receptor blocker.
BCC4578
Pancuronium dibromide
Pancuronium Dibromide is a bis-quaternary steroid that is a competitive nicotinic antagonist.
BCC5193
Solifenacin hydrochloride
Solifenacin hydrochloride (YM905 hydrochloride) is a muscarinic receptor antagonist, with pKis of 7.6, 6.9 and 8.0 for M1, M2 and M3 receptors, respectively.
BCN2869
Galantamine hydrobromide
Galanthamine hydrobromide is a long-acting, centrally active acetylcholinesterase(AChE) inhibitor (IC50 = 410 nM) and allosteric potentiator at neuronal nicotinic ACh receptors.
BCC3795
Ipratropium Bromide
Ipratropium Bromide is a muscarinic antagonist, bronchodilator, N-Isopropyl salt of atropine.
BCC4573
Otilonium Bromide
Octylonium bromide (SP63) is an antimuscarinic used as a spasmolytic agent.
BCN2913
Arecoline hydrobromide
Arecoline hydrobromide (Arecoline bromide) is a muscarinic acetylcholine receptor agonist.
BCN2868
Galantamine
Galanthamine is a potent acetylcholinesterase (AChE) inhibitor with an IC50 of 500 nM.
BCC5208
Flavoxate hydrochloride
Flavoxate Hydrochloride(DW-61 Hydrochloride) is a muscarinic AChR antagonist used in various urinary syndromes and as an antispasmodic.
BCN2170
Varenicline tartrate
Varenicline Tartrate(CP 526555;Champix) is a nicotinic receptor partial agonist; it stimulates nicotine receptors more weakly than nicotine itself does.
BCC4147
Tarafenacin
Tarafenacin(SVT-40776) is a highly selective M3 muscarinic receptor antagonist (Ki= 0.19 nM), ~200 fold selectivity over M2 receptor.
BCC4053
VU0152100
VU0152100 is a potent and selective allosteric potentiator of M4 mAChR with an EC50 of 380 ± 93 nM.
BCC4572
Orphenadrine Citrate
Orphenadrine citrate is a NMDA receptor antagonist with Ki of 6.0 +/- 0.7 μM, HERG potassium channel blocker.
BCC4581
PNU-120596
PNU-120596 (NSC 216666 ) is a potent and selective positive allosteric α7 nAChR modulator with an EC50 of 0.2 μM.
BCC2498
Vecuronium Bromide
Vecuronium bromide (ORG NC 45) is a nondepolarizing neuromuscular blocking agent of intermediate duration.
BCC4570
Homatropine Bromide
Homatropine Bromide is muscarinic AChR antagonist that is an anticholinergic medication.
BCC4274
Biperiden
Biperiden(KL 373) is an antiparkinsonian agent, which is the selective central M1 cholinoreceptors blocker.
BCC4568
Decamethonium Bromide
Decamethonium Bromide is a nicotinic AChR partial agonist and neuromuscular blocking agent.
BCC4561
Hexamethonium Bromide
Hexamethonium Dibromide is a selective antagonist of neuronal-type nicotinic AChR in ganglia.
BCC3833
Oxybutynin
Oxybutynin is an anticholinergic agent, which inhibits vascular Kv channels in a concentration-dependent manner, with an IC50 of 11.51 μM.
BCC4566
Bethanechol chloride
Bethanechol Chloride (Carbamyl-β-methylcholine chloride) is a selective muscarinic receptor agonist without any effect on nicotinic receptors.
BCC3728
Atropine sulfate monohydrate
Atropine sulfate monohydrate (Atropine sulfate hydrate) is a broad-spectrum and competitive muscarinic acetylcholine receptor (mAChR) antagonist with anti-myopia effect.
BCC4275
Glycopyrrolate
Glycopyrrolate (Glycopyrronium bromide) is a muscarinic competitive antagonist used as an antispasmodic.
BCN2197
Acetylcholine chloride
Acetylcholine chloride (ACh chloride) is a common neurotransmitter found in the central and peripheral nerve system.
BCC4564
Succinylcholine Chloride Dihydrate
Succinylcholine Chloride Dihydrate is a nicotinic AChR agonist and also acts as a depolarizing neuromuscular blocker.
BCC3716
Acetylcysteine
Acetylcysteine (N-Acetylcysteine) is a mucolytic agent which reduces the thickness of the mucus. Acetylcysteine is a ROS inhibitor. Acetylcysteine is a cysteine precursor, prevents hemin-induced ferroptosis by neutralizing toxic lipids generated by arachidonate-dependent activity of 5-lipoxygenases. Acetylcysteine induces cell apoptosis. Acetylcysteine also has anti-influenza virus activities.
BCC5517
TBPB
TBPB is an allosteric M1 mAChR agonist(EC50=289 nM) that regulates amyloid processing and produces antipsychotic-like activity in rats.
BCC4576
Gallamine Triethiodide
Gallamine Triethiodide is a synthetic nondepolarizing blocking drug.
BCC5054
Paroxetine HCl
Paroxetine hydrochloride is a potent selective serotonin-reuptake inhibitor, commonly prescribed as an antidepressant and has GRK2 inhibitory ability with IC50 of 14 μM.
BCC4571
Homatropine Methylbromide
Homatropine methylbromide (Homatropine methobromide) is muscarinic AChR antagonist, inhibits endothelial and smooth muscle muscarinic receptors of WKY-E and SHR-E with IC50 of 162.5 nM and 170.3 nM, respectively.
BCC5564
LY2119620
LY2119620 is a high-affinity muscarinic M2/M4 receptor agonist.