Neuronal Signaling
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Bitopertin
Catalog No. A15021 -
Bitopertin (R enantiomer)
Catalog No. A15022 -
LY2365109 hydrochloride
Catalog No. A21779 GlyT1 inhibitorLY2365109 hydrochloride is a potent and selective GlyT1 inhibitor, with an IC50 of 15.8 nM for glycine uptake in cells over-expressing hGlyT1a. 了解更多 -
Prasugrel (Effient)
Catalog No. A10748 platelet inhibitorPrasugrel (Effient)是一种新型的血小板抑制剂,用于减少急性冠脉综合征(PCI)患者的血栓性心血管事件(包括支架血栓形成)。 了解更多 -
(+)-Clopidogrel hydrogen sulfate (Plavix)
Catalog No. A10233 (+)-Clopidogrel hydrogen sulfate (Plavix)是一种口服的,噻吩吡啶类抗血小板药物。 了解更多 -
Ticagrelor (AZD6140)
Catalog No. A11238 -
AZD1283
Catalog No. A15443 -
Methylthioadenosine
Catalog No. A16106 Methylthioadenosine是存在于所有哺乳动物组织中的天然存在的含硫核苷。 了解更多 -
Prasugrel Hydrochloride
Catalog No. A16144 -
Clopidogrel
Catalog No. A21206 platelet inhibitorClopidogrel is a well-known and orally active platelet inhibitor that targets P2Y12 receptor. Clopidogrel is used to inhibit blood clots in coronary artery disease, peripheral vascular disease, and cerebrovascular disease. 了解更多 -
Cangrelor Tetrasodium
Catalog No. A17919 P2Y12 receptors inhibitorCangrelor Tetrasodium is a high-affinity, reversible inhibitor of P2Y12 receptors that causes almost complete inhibition of ADP-induced platelet aggregate. It is a modified ATP derivative stable to enzymatic degradation. Unlike clopidogrel (Plavix), which is a prodrug, cangrelor is an active drug not requiring metabolic conversion. 了解更多 -
Clopidogrel thiolactone
Catalog No. A20862 P2Y12 receptor inhibitorClopidogrel thiolactone is a P2Y12 receptor inhibitor, is a potent antiplatelet agent. 了解更多 -
GW791343 HCl
Catalog No. A11107 -
Ticlopidine HCl
Catalog No. A11690 Ticlopidine是一种二磷酸腺苷(ADP)受体抑制剂。它通过阻断ADP受体来改变血小板膜的功能,从而抑制血小板聚集。这防止了糖蛋白IIb/IIIa的构象变化,从而使血小板与血纤蛋白原结合。 了解更多 -
NF 279
Catalog No. A11972 -
A-317491 sodium salt hydrate
Catalog No. A12412 P2X3 and P2X2/3 receptor 拮抗剂A-317491 sodium salt hydrate是一种非核苷酸的P2X3和P2X2/3受体拮抗剂,可抑制受体介导的钙通量。 了解更多 -
A-438079 HCl
Catalog No. A12597 P2X7 receptor 拮抗剂A-438079 HCl是一种竞争性P2X7受体拮抗剂(抑制人重组P2X7细胞系中Ca2+流入的pIC50 = 6.9)。在其他P2受体上没有活性(IC50 > 10 uM)。 了解更多 -
A 438079 hydrochloride
Catalog No. A14983 P2X7 receptor 拮抗剂A 438079 hydrochloride是一种竞争性P2X7受体拮抗剂(抑制人重组P2X7细胞系中Ca2+流入的pIC50 = 6.9)。 了解更多 -
JNJ-54175446
Catalog No. A18675 P2X7 receptor antagonistJNJ-54175446 is a potent and selective brain penetrant P2X7 receptor antagonist, with pIC50s of 8.46 and 8.81 for hP2X7 receptor and rP2X7 receptor, respectively. 了解更多 -
A 839977
Catalog No. A21178 -
CE-224535
Catalog No. A21183 -
GW791343 trihydrochloride
Catalog No. A21204 P2X7 allosteric modulatorGW791343 3Hcl is a P2X7 allosteric modulator; exhibits species-specific activity and acts as a negative allosteric modulator of human P2X7 (pIC50 = 6.9 - 7.2). 了解更多 -
Minodronic acid
Catalog No. A21975 purinergic P2X2/3 receptors antagonistMinodronic acid (YM-529) is an antagonist of purinergic P2X2/3 receptors involved in pain. 了解更多 -
PNU-120596
Catalog No. A11203 -
Adiphenine HCl
Catalog No. A11716 -
Methyllycaconitine citrate
Catalog No. A12681 Methyllycaconitine citrate是含有α7的神经元烟碱受体(Ki = 1.4 nM)的有效拮抗剂。与浓度大于40 nM的α4β2和α6β2受体相互作用。 了解更多 -
Tropisetron HCL
Catalog No. A14375 5-HT3 receptor 拮抗剂Tropisetron HCL是选择性的5-HT3受体拮抗剂和α7烟碱样受体激动剂,对5-HT3受体的IC50为70.1±0.9 nM。 了解更多 -
Bephenium hydroxynaphthoate
Catalog No. A17391 B-type AChR activatorBephenium hydroxynaphthoate is an anthelmintic agent formerly used in the treatment of hookworm infections and ascariasis; B-type AChR activator. 了解更多 -
Varenicline Hydrochloride
Catalog No. A21539 α4β2 nAChR partial agonistVarenicline Hydrochloride (CP 526555 hydrochloride) is a high affinity, selective α4β2 nicotine acetylcholine receptor (nAChR) partial agonist and full α7 nAChR agonist. 了解更多 -
Tebanicline hydrochloride
Catalog No. A21918 nAChR modulatorTebanicline hydrochloride (ABT594 hydrochloride) is a nAChR modulator with potent, orally effective analgesic activity. 了解更多 -
PNU 282987
Catalog No. A11233 -
Ispronicline (TC-1734, AZD-3480)
Catalog No. A14183 nAChR 激动剂Ispronicline (TC-1734,AZD-3480)是神经元烟碱乙酰胆碱受体部分激动剂。Ispronicline是亚型选择性的,主要与a4b2亚型结合。它具有抗抑郁、益智和神经保护作用。 了解更多 -
Sofinicline (ABT-894, A-422894)
Catalog No. A13842 -
5-Iodo-A-85380 2HCl
Catalog No. A13639 -
A-582941
Catalog No. A13539 -
EVP-6124 (Encenicline)
Catalog No. A15086 nAChR 抑制剂EVP-6124 (Encenicline)是α7神经元烟碱乙酰胆碱受体(nAChRs)的新型部分激动剂;显示对α7nAChRs的选择性,并且不激活或抑制异聚体α4β2nAChRs。 了解更多