Neuronal Signaling

产品 1 到 50 共 365个

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  1. Bitopertin

    Catalog No. A15021
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    Glycine reuptake 抑制剂
    Bitopertin是一种有效的非竞争性甘氨酸再摄取抑制剂(GlyT1)。 了解更多
  2. Bitopertin (R enantiomer)

    Catalog No. A15022
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    Glycine reuptake 抑制剂
    Bitopertin (R enantiomer)是一种有效的非竞争性甘氨酸再摄取抑制剂(GlyT1)。 了解更多
  3. Amoxapine

    Catalog No. A16406
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    Amoxapine是一种三环二苯并x氮杂(N-芳基哌嗪),其作用与其他几种三环抗抑郁药相似,阿莫沙平抑制GLYT2a转运活性,IC50为92 μM。 了解更多
  4. LY2365109 hydrochloride

    Catalog No. A21779
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    GlyT1 inhibitor
    LY2365109 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
  5. Prasugrel (Effient)

    Catalog No. A10748
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    platelet inhibitor
    Prasugrel (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
  6. (+)-Clopidogrel hydrogen sulfate (Plavix)

    Catalog No. A10233
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    (+)-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
  7. Ticagrelor (AZD6140)

    Catalog No. A11238
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    P2Y12 拮抗剂
    Ticagrelor (AZD6140)是第一个可逆结合的口服P2Y(12)受体拮抗剂,可阻断ADP诱导的血小板聚集。 了解更多
  8. MRS 2578

    Catalog No. A11486
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    P2Y6 Receptor 拮抗剂
    MRS 2578是P2Y6核苷酸受体的选择性拮抗剂。 了解更多
  9. AZD1283

    Catalog No. A15443
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    P2Y12 receptor 拮抗剂
    AZD1283是P2Y12受体的有效拮抗剂,EC50为3.0 ug/kg/min,TI> 10;结合IC50为11 nM。 了解更多
  10. Methylthioadenosine

    Catalog No. A16106
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    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
  11. Prasugrel Hydrochloride

    Catalog No. A16144
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    P2Y12 拮抗剂
    Prasugrel Hydrochloride是噻吩并吡啶ADP受体(P2Y12)拮抗剂,用于减少血栓性心血管事件。 了解更多
  12. Clopidogrel

    Catalog No. A21206
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    platelet inhibitor
    Clopidogrel 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
  13. BPTU

    Catalog No. A16952
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    P2Y1 拮抗剂
    BPTU是P2Y1拮抗剂。已经显示出它具有抗血栓形成的功效并减少了出血的可能性。 了解更多
  14. Cangrelor Tetrasodium

    Catalog No. A17919
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    P2Y12 receptors inhibitor
    Cangrelor 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
  15. Vicagrel

    Catalog No. A18586
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    P2Y12 platelet inhibitor
    Vicagrel, an acetate derivative of Clopidogrel, is a P2Y12 platelet inhibitor potentially for the treatment of thrombosis. 了解更多
  16. Clopidogrel thiolactone

    Catalog No. A20862
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    P2Y12 receptor inhibitor
    Clopidogrel thiolactone is a P2Y12 receptor inhibitor, is a potent antiplatelet agent. 了解更多
  17. Elinogrel

    Catalog No. A21468
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    platelet P2Y12 antagonist
    Elinogrel (PRT060128) is a potent, direct acting, competitive, and reversible platelet P2Y12 antagonist (IC50=20 nM). It is orally and intravenously available and has potent antiplatelet effects. 了解更多
  18. GW791343 HCl

    Catalog No. A11107
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    P2X7 modulator
    GW791343 HCl充当人P2X7的负变构调节剂(pIC50 = 6.9-7.2)和大鼠P2X7的正变构调节剂。 了解更多
  19. Ticlopidine HCl

    Catalog No. A11690
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    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
  20. A 740003

    Catalog No. A11316
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    P2X7 receptor 拮抗剂
    A740003是P2X7受体的新型竞争性拮抗剂(人的IC50值= 40 nM,大鼠的IC50值= 18 nM)。 了解更多
  21. NF 279

    Catalog No. A11972
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    P2X1 拮抗剂
    NF279是一种苏拉明类似物,可作为P2X受体的高选择性,竞争性和可逆性ATP拮抗剂(平滑肌中IC50/KB1μM)。 了解更多
  22. A-317491 sodium salt hydrate

    Catalog No. A12412
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    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
  23. A-804598

    Catalog No. A16066
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    P2X7 receptor 拮抗剂
    A-804598是一种P2X7选择性竞争性拮抗剂,对人,大鼠和小鼠通道的IC50值分别为11、10和9 nM。 了解更多
  24. A-438079 HCl

    Catalog No. A12597
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    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
  25. A 438079 hydrochloride

    Catalog No. A14983
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    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
  26. AF-353

    Catalog No. A13131
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    P2X3/P2X2/3 receptor 拮抗剂
    AF-353是一种新型、有效的P2X3/P2X2/3受体拮抗剂,可抑制人和大鼠的P2X3(pIC50 = 8.0)。 了解更多
  27. JNJ-54175446

    Catalog No. A18675
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    P2X7 receptor antagonist
    JNJ-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
  28. A 839977

    Catalog No. A21178
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    P2X7 selective antagonist
    A 839977 is a P2X7 selective antagonist. 了解更多
  29. CE-224535

    Catalog No. A21183
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    P2X7 receptor antagonist
    CE-224535 is a selective P2X7 receptor antagonist. 了解更多
  30. GW791343 trihydrochloride

    Catalog No. A21204
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    P2X7 allosteric modulator
    GW791343 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
  31. Minodronic acid

    Catalog No. A21975
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    purinergic P2X2/3 receptors antagonist
    Minodronic acid (YM-529) is an antagonist of purinergic P2X2/3 receptors involved in pain. 了解更多
  32. PNU-120596

    Catalog No. A11203
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    Nicotinic (α7) Receptor Modulator
    PNU-120596是α7神经元烟碱型乙酰胆碱受体的正变构调节剂。 了解更多
  33. Varenicline

    Catalog No. A10966
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    nAChR partial agonist
    Varenicline是烟碱样受体部分激动剂。 了解更多
  34. Adiphenine HCl

    Catalog No. A11716
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    AChR抑制剂
    Adiphenine Hydrochloride是烟碱受体抑制剂,IC50为15μM,用作解痉药物。 了解更多
  35. 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
  36. Tropisetron HCL

    Catalog No. A14375
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    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
  37. BNC375

    Catalog No. A18503
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    α7 nAChR Modulator
    BNC375 is a Potent, Selective, and Orally Available Type I Positive Allosteric Modulator of α7 nAChRs. 了解更多
  38. Bephenium hydroxynaphthoate

    Catalog No. A17391
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    B-type AChR activator
    Bephenium hydroxynaphthoate is an anthelmintic agent formerly used in the treatment of hookworm infections and ascariasis; B-type AChR activator. 了解更多
  39. CCMI

    Catalog No. A21534
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    α7 nAChR-positive allosteric modulator
    CCMI is a potent and selective α7 nAChR-positive allosteric modulator, does not bind to or activate α7 nAChRs via the orthosteric site, and causes significant positive modulation of agonist-induced currents at α7 nAChRs. 了解更多
  40. Varenicline Hydrochloride

    Catalog No. A21539
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    α4β2 nAChR partial agonist
    Varenicline 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
  41. Tebanicline hydrochloride

    Catalog No. A21918
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    nAChR modulator
    Tebanicline hydrochloride (ABT594 hydrochloride) is a nAChR modulator with potent, orally effective analgesic activity. 了解更多
  42. Bephenium

    Catalog No. A21680
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    AChR activator
    Bephenium is an anthelmintic agent formerly used in the treatment of hookworm infections and ascariasis; B-type AChR activator. 了解更多
  43. PNU 282987

    Catalog No. A11233
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    α7 nAChR 激动剂
    PNU 282987 (PNU-282,987)可作为神经烟碱乙酰胆碱受体α7亚型的有效选择性激动剂。 了解更多
  44. A-867744

    Catalog No. A11290
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    modulator of α7 nAChRs
    A-867744是α7烟碱乙酰胆碱受体的新型正变构调节剂。 了解更多
  45. Ispronicline (TC-1734, AZD-3480)

    Catalog No. A14183
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    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
  46. Sofinicline (ABT-894, A-422894)

    Catalog No. A13842
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    nAChR 激动剂
    Sofinicline (ABT-894,A-422894)是一种新型的烟碱型乙酰胆碱受体激动剂,可治疗注意力不足/多动症。 了解更多
  47. ABT-418 HCl

    Catalog No. A13688
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    nAChR 激动剂
    ABT-418 HCl是神经元烟碱型乙酰胆碱受体激动剂。 了解更多
  48. 5-Iodo-A-85380 2HCl

    Catalog No. A13639
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    nAChR 激动剂
    5-Iodo-A-85380 2HCl是针对a4b2和a6b2烟碱乙酰胆碱受体的强效亚型选择性激动剂。 了解更多
  49. A-582941

    Catalog No. A13539
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    α7 nAChR 激动剂
    A-582941是选择性的AChR a7部分激动剂。它对大鼠和人类a7受体均表现出高亲和力(Ki值分别为10.8和16.7 nM)。 了解更多
  50. EVP-6124 (Encenicline)

    Catalog No. A15086
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    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

产品 1 到 50 共 365个

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