Neuronal Signaling

产品 201 到 250 共 365个

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  1. Radiprodil

    Catalog No. A21193
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    NMDA NR2B antagonist
    Radiprodil (RGH-896) is an orally active and selective NMDA NR2B antagonist. A potential therapeutic agent in treatment of neuropathic pain and possibly other chronic pain conditions. 了解更多
  2. NMDA-IN-1

    Catalog No. A21419
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    NMDA antagonist
    NMDA-IN-1 is a potent and NR2B-selective NMDA antagonist with Ki of 0.85 nM. 了解更多
  3. 7-Chlorokynurenic acid sodium salt

    Catalog No. A21879
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    NMDA receptor antagonist
    7-Chlorokynurenic acid sodium salt is a potent and selective antagonist of the glycine B coagonist site of the N-methyl-D-aspartate (NMDA) receptor (IC50=0.56 μM). 了解更多
  4. SDZ 220-581 hydrochloride, SDZ220-581, SDZ-220-581

    Catalog No. A21897
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    NMDA receptor antagonist
    SDZ 220-581 hydrochloride is an orally active, potent, competitive NMDA receptor antagonist with pKi value of 7.7. 了解更多
  5. Rislenemdaz

    Catalog No. A21907
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    NMDA receptor GluN2B antagonist
    Rislenemdaz (CERC-301) is an orally bioavailable and selective N-methyl-D-aspartate (NMDA) receptor subunit 2B (GluN2B) antagonist with Ki and IC50 of 8.1 nM and 3.6 nM, respectively. 了解更多
  6. Memantine hydrochloride

    Catalog No. A11708
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    NMDA receptor 拮抗剂
    Memantine hydrochloride是nmda受体的拮抗剂,与离子通道位点结合。它还是CYP2B6和CYP2D6抑制剂,作用于重组CYP2B6和CYP2D6,Ki分别为0.51 nM和94.9 μM。它被用于治疗帕金森综合征。 了解更多
  7. Orphenadrine citrate

    Catalog No. A11712
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    NMDA receptor 拮抗剂
    Orphenadrine柠檬酸盐是NMDA受体拮抗剂,Ki为6.0μM,还是HERG钾离子通道阻断剂。 了解更多
  8. Felbamate

    Catalog No. A11862
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    Felbamate是NMDA相关甘氨酸结合位点的拮抗剂。 了解更多
  9. MDL 29951

    Catalog No. A13729
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    NMDA receptor 拮抗剂
    MDL-29951是在体外和体内均能激活NMDA受体的新型甘氨酸拮抗剂(Ki = 0.14 mM,[3H]甘氨酸结合)。 了解更多
  10. NVP-AAM077 Tetrasodium Hydrate (PEAQX)

    Catalog No. A14071
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    NMDA receptors 拮抗剂
    NVP-AAM077抑制成年小鼠在脑室下区域和齿状回中的祖细胞增殖,并降低了齿状回中的新生细胞的存活。 了解更多
  11. ARL-15896

    Catalog No. A13858
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    NMDA receptor ion channel 拮抗剂
    ARL-15896是新型的N-甲基-D-天冬氨酸受体离子通道拮抗剂。 了解更多
  12. GLYX-13 (Rapastinel)

    Catalog No. A13576
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    NMDAR modulator
    GLYX-13 (Rapastinel)是NMDA受体甘氨酸位点的选择性弱部分激动剂。 了解更多
  13. Ibotenic Acid

    Catalog No. A14006
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    NMDA& mGlu receptor 激动剂
    Ibotenic Acid是最初从鹅膏菌属物种中分离出来的一种神经兴奋性氨基酸,它起着NMDA和代谢型谷氨酸受体激动剂的作用。 了解更多
  14. CIQ

    Catalog No. A15523
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    NMDA receptors Potentiator
    CIQ是包含NR2C或NR2D亚基的NMDA受体的亚基选择性增强剂。 了解更多
  15. RO 25-6981 maleate

    Catalog No. A16083
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    NMDA receptors blocker
    RO 25-6981 maleate是含有NR2B亚基的NMDA受体的强效和选择性活性依赖性阻断剂。克隆的受体亚基组合NR1C/NR2B和NR1C/NR2A的IC50值分别为0.009和52 uM。 了解更多
  16. CNQX

    Catalog No. A16109
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    AMPA/kainate 拮抗剂
    CNQX是一种竞争性的非NMDA谷氨酸受体拮抗剂(AMPA和海藻酸酯受体的IC50分别为0.3和1.5 uM,而NMDA受体的IC50 = 25 uM)。 了解更多
  17. Ro 25-6981 maleate

    Catalog No. A13144
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    NMDA receptors Blocker
    Ro 25-6981是N-甲基-D-天冬氨酸(NMDA)受体的高亲和力,强效选择性阻断剂。 了解更多
  18. 7CKA

    Catalog No. A17070
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    NMDA receptor 拮抗剂
    7CKA是在甘氨酸位点起作用的NMDA受体拮抗剂。 了解更多
  19. D-AP5

    Catalog No. A17044
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    NMDA 拮抗剂
    D-AP5是一种选择性的N-甲基-D-天冬氨酸(NMDA)受体拮抗剂,可竞争性抑制NMDA受体的谷氨酸结合位点。 了解更多
  20. Neu-2000

    Catalog No. A17033
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    NMDA receptor 拮抗剂
    Neu-2000是可能用于治疗中风的NMDA受体拮抗剂。 了解更多
  21. Mephenesin

    Catalog No. A17493
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    NMDA receptor antagonist
    Mephenesin is an NMDA receptor antagonist, is a centrally acting muscle relaxant. 了解更多
  22. Glycine

    Catalog No. A17936
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    NMDA antagonist
    AZD-4282, also known as aminoacetic acid and glycine, is a N-methyl-D-aspartate (NMDA) receptor antagonist potentially for the treatment of neuropathic pain. 了解更多
  23. GNE 0723

    Catalog No. A12757
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    NMDAR modulator
    GNE 0723 is a brain permeable positive allosteric modulator of NMDAR, with an EC50 of 21 nM for GluN2A, 7.4 and 6.2 μM for GluN2C and GluN2D, respectively. 了解更多
  24. CaMKII-IN-1

    Catalog No. A21034
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    CaMKII inhibitor
    CaMKII-IN-1 is a potent and highly selective CaMKII inhibitor with IC50 of 63 nM. 了解更多
  25. KN-62

    Catalog No. A11473
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    CaM kinase II 抑制剂
    KN-62是一种有效,选择性的钙调蛋白依赖性蛋白激酶 II (CaMK-II)抑制剂。 了解更多
  26. CID 2011756

    Catalog No. A12416
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    PKD 抑制剂
    CID 2011756是一种蛋白激酶D(PKD)抑制剂(PKD2,PKD3和PKD1的IC50值分别为0.6、0.7和3.2μM)。 了解更多
  27. kb NB 142-70

    Catalog No. A12423
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    PKD 抑制剂
    kb NB 142-70是一种选择性蛋白激酶D(PKD)抑制剂(PKD1、2和3的IC50值分别为28.3、58.7和53.2 nM)。 了解更多
  28. Phenoxybenzamine hydrochloride

    Catalog No. A10719
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    α-adrenergic (AR) 拮抗剂/CaM 抑制剂
    Phenoxybenzamine hydrochloride是一种细胞可渗透的,非特异性的,不可逆的α-肾上腺素(AR)拮抗剂,也可作为CaM抑制剂。 了解更多
  29. KN-93

    Catalog No. A13276
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    CaM kinase II 抑制剂
    KN-93是多功能Ca++/钙调蛋白依赖性蛋白激酶的抑制剂。 了解更多
  30. CID 755673

    Catalog No. A13804
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    PKD 抑制剂
    CID755673是一种具有细胞活性的泛PKD1/2/3抑制剂,IC50值分别为180 nM,280nM,以及227 nM。 了解更多
  31. KN-93 Phosphate

    Catalog No. A14288
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    CaMKII 抑制剂
    KN-93 Phosphate是一种有效且特异性的Ca2+/钙调蛋白依赖性蛋白激酶II(CaMKII)抑制剂,Ki为0.37μM,对APK,PKC,MLCK或Ca2+-PDE活性无明显抑制作用。 了解更多
  32. NH125

    Catalog No. A14307
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    eEF-2 抑制剂
    NH125是选择性eEF-2激酶抑制剂。 了解更多
  33. K252a

    Catalog No. A13897
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    CaMK/Phosphorylase 抑制剂
    K252a是CaM激酶和磷酸化酶激酶的高效细胞渗透抑制剂(IC50分别为1.8和1.7 nmol/L)。 了解更多
  34. A-484954

    Catalog No. A13447
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    eEF2K (CAMKIII) 抑制剂
    A-484954是一种有效的、选择性的真核细胞延长因子-2激酶(eEF2K)抑制剂。 了解更多
  35. KN-92

    Catalog No. A15137
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    CaMK-II 抑制剂
    KN-92是KN-93的非活性衍生物。KN-93是Ca2+/钙调蛋白依赖性激酶II(CaMKII)的选择性抑制剂,竞争性阻断CaM与激酶的结合(Ki = 370 nM)。 了解更多
  36. KN-92 hydrochloride

    Catalog No. A15138
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    CaMK-II 抑制剂
    KN-92 hydrochloride是KN-93的阴性对照。 了解更多
  37. KN-92 phosphate

    Catalog No. A15139
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    CaMKII 抑制剂
    KN-92 phosphate是KN-93的非活性衍生物。KN-93是Ca2+/钙调蛋白依赖性激酶II(CaMKII)的选择性抑制剂,竞争性阻断CaM与激酶的结合(Ki = 370 nM)。 了解更多
  38. CID 797718

    Catalog No. A13809
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    PKD1 抑制剂
    CID797718是CID755673(Adooq目录号A13804)的结构类似物。它是效力降低10倍的PKD1抑制剂,IC50值为7.0+/-0.8 uM。 了解更多
  39. CRT-0066101

    Catalog No. A16318
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    PKD 抑制剂
    CRT-0066101是有效,选择性的蛋白激酶D(PKD)抑制剂;抑制所有PKD同工型(PKD1,PKD3和PKD2的IC50值分别为1、2和2.5 nM)。 了解更多
  40. STO-609 acetate

    Catalog No. A16345
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    CaMKK 抑制剂
    STO-609是钙/钙调蛋白依赖性激酶激酶(CaMKK)亚型CaMKKα和CaMKKβ(Ki分别为80和15 ng/ml)的细胞渗透性抑制剂。 了解更多
  41. Pitofenone Hydrochloride

    Catalog No. A17053
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    Antispasmodic Agent
    Pitofenone Hydrochloride是抗痉化合物。它是乙酰胆碱酯酶活性的有效抑制剂。 了解更多
  42. Tacrine HCl

    Catalog No. A17374
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    AChE & butyrylcholinesterase inhibitor
    Tacrine is a derivative of aminoacridine that functions as an inhibitor of both acetylcholinesterase (AChE) and butyrylcholinesterase (IC50s = 31 and 26.5 nM, respectively). 了解更多
  43. Pralidoxime Iodide

    Catalog No. A17526
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    Cholinesterase Reactivator
    Pralidoxime iodide is a Cholinesterase Reactivator. 了解更多
  44. Nerolidol

    Catalog No. A17599
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    AChE inhibitor
    Nerolidol is a synthetic AChE inhibitor and F0F1-ATP synthase modulator. It acts as a sedative, inhibits growth of bacteria and fungi, and decreases the mitochondrial transmembrane electric potential to induce cell death in hepatocarcinoma cells. 了解更多
  45. Edrophonium chloride

    Catalog No. A17794
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    acetylcholinesterase inhibitor
    Edrophonium Chloride, also known as Tensilon, is an acetylcholinesterase inhibitor used in cardiac arrhythmias and in the diagnosis of myasthenia gravis. Edrophonium Chloride has also been used as an antidote to curare principles. 了解更多
  46. Galanthamine

    Catalog No. A12483
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    AChE inhibitor
    Galanthamine is a potent acetylcholinesterase (AChE) inhibitor with an IC50 of 500 nM. 了解更多
  47. MHP 133

    Catalog No. A20058
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    AChE /M1/M2/5HT4/I2 inhibitor
    MHP 133 is a drug with multiple CNS targets, and inhibits acetylcholinesterase (AChE) with Ki of 69 μM; also active against muscarinic M1 and M2 receptors, serotonin 5HT4 receptors, and imidazole I2 receptors. 了解更多
  48. Acetyllovastatin

    Catalog No. A19111
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    AChE inhibitor
    Acetyllovastatin, a acetate of Lovastatin, presentes a moderate inhibitory effect against the enzyme acetylcholinesterase with an IC50 of 79 μg/mL. Lovastatin has been found to display antifungal activity, and suppresses proliferation of a number of transformed cell lines. 了解更多
  49. (R)-Rivastigmine D6 tartrate

    Catalog No. A21454
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    cholinesterase inhibitor
    (R)-Rivastigmine D6 (tartrate) is the deuterium labeled (R)-Rivastigmine, which is an cholinesterase inhibitor. 了解更多
  50. (+)-Phenserine

    Catalog No. A20993
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    cholinesterase noncompetitive inhibitor
    (+)-Phenserine is a novel selective cholinesterase noncompetitive inhibitor with an IC50 of 45.3 μM. 了解更多

产品 201 到 250 共 365个

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