Catalog |
name |
Description |
price |
R-C-2475 |
Revefenacin CAS:864750-70-9 |
Revefenacin(TD-4208;GSK1160724)is a potent mAChR antagonist;has a high affinity on M3 receptor with a Ki of 0.18nM. |
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R-C-2476 |
Diphemanil Methylsulfate CAS:62-97-5 |
Diphemanil Methylsulfate is a quaternary ammonium anticholinergic,it binds muscarinic acetycholine receptors(mAchR). |
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R-C-2477 |
Glycopyrrolate CAS:596-51-0 |
Glycopyrrolate(Glycopyrronium,Robinul,Gastrodyn)is a muscarinic antagonist used as an antispasmodic,in some disorders of the gastrointestinal tract,and to reduce salivation with some anesthetics. |
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R-C-2478 |
Tropisetron CAS: 89565-68-4 |
Tropisetron(SDZ-ICS-930 free base)is a selective 5-HT3 receptor antagonist and α7-nicotinic receptor agonist with an IC50 of 70.1±0.9nM for 5-HT3 receptor. |
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R-C-2479 |
Thonzylamine CAS:91-85-0 |
Thonzylamine is an orally active H1 histamine receptor antagonist,exhibits good antihistaminic and antianaphylactic properties.Thonzylamine can be used for the research of hypersensitivity diseases,nasal congestion,allergic conjunctivitis and other allergic diseases. |
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R-C-2480 |
Caulophylline (N-Methylcytisine) CAS:486-86-2 |
Caulophylline(N-Methylcytisine,Caulophyllin,NMC)is a tricyclic quinolizidine alkaloid with anti-inflammatory activities.Caulophylline binds to nicotinic acetylcholine receptors(nAChR)from squid optical ganglia with Kd of 50nM. Caulophylline significantly reduces myeloperoxidase(MPO)activity,blocks the activation of NF-κB by inhibiting IκB and IKK phosphorylation. |
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R-C-2489 |
BRL 54443 CAS:57477-39-1 |
BRL 54443 is a potent 5-HT1E/1F receptor agonist(Ki values are 1.1nM and 0.7 nM respectively);displays>30-fold selectivity over other 5-HT and dopamine receptors. |
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R-C-2541 |
Oxiracetam CAS:62613-82-5 |
Oxiracetam is a cyclic derivative of γ-aminobutyric acid(GABA)which has been commonly used as nootropic drug to treat cognitive impairments. |
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R-C-2542 |
Prasugrel CAS:150322-43-3 |
Prasugrel(PCR 4099),a thienopyridine and prodrug,inhibits platelet function.Prasugrel is an orally active and potent P2Y12 receptor antagonist,and inhibits ADP-induced platelet aggregation. |
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R-C-2543 |
Agomelatine (S-20098) CAS:138112-76-2 |
Agomelatine(S-20098)is a specific agonist of MT1 and MT2 receptors with Kis of 0.1,0.06,0.12, and 0.27nM for CHO-hMT1,HEK-hMT1,CHO-hMT2,and HEK-hMT2,respectively.Agomelatine is a selective 5-HT2C receptor antagonist with pKis of 6.4 and 6.2 at native(porcine)and cloned, human 5-HT2C receptors, respectively. |
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