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Cannabinoid Receptor(大麻素受体)

The cannabinoid receptor (CB1 and CB2) is a member of G-protein coupled receptor which plays a significant role in physiologic processes such as cognitive and immune functions.

Products for  Cannabinoid Receptor

  1. Cat.No. 产品名称 Information
  2. GC10907 (±)-SLV 319 A selective antagonist of CB1
  3. GC10028 (R)-SLV 319 The inactive enantiomer of SLV 319
  4. GC63410 (Rac)-MRI-1867 (Rac)-MRI-1867 ((Rac)-MRI-1867, Compound 6b) 是一种大麻素受体 1 型 (CB1R)/iNOS 拮抗剂,对 CB1R 的 Ki 为 5.7 nM。
  5. GC10753 (S)-SLV 319 A selective antagonist of CB1
  6. GC16403 2-Arachidonoyl Glycerol

    Endogenous CB1 and CB2 receptor agonist

  7. GC16196 2-Palmitoylglycerol An endogenous fatty acid ester
  8. GC17100 4-Quinolone-3-Carboxamide CB2 Ligand An Analytical Reference Standard
  9. GC15850 4-Quinolone-3-Carboxamide Furan CB2 Agonist Selective CB2 agonist
  10. GC16480 AM 281 A CB1 receptor antagonist/inverse agonist
  11. GC62835 AM-6538 AM6538 是一种长效、高亲和力、伪不可逆的 cannabinoid (CB) 拮抗剂。AM6538 是利莫那班的结构类似物。AM6538可有效评价大麻素完全和部分激动剂的表观疗效。AM6538 可能在未来需要暂时减少大麻素受体可用性的研究中有用。
  12. GC15414 AM1241 A CB2 receptor agonist and inverse agonist
  13. GC15717 AM251 A CB1 receptor antagonist
  14. GC15093 AM4113 A CB1 receptor neutral antagonist
  15. GC10147 AM630 An inverse agonist at CB2 and partial agonist at CB1 receptors
  16. GC14661 AM6545 A peripherally restricted CB1 receptor antagonist
  17. GC35339 Anandamide An endogenous cannabinoid
  18. GC18435 Arachidonoyl 2'-Chloroethylamide A potent and selective CB1 receptor agonist
  19. GC16826 Arachidonoyl amide An AEA analog with similar biological activity
  20. GC18097 Arachidonoyl Serinol A CB1 receptor agonist
  21. GC11849 Arachidonyl serotonin An inhibitor of FAAH
  22. GC10205 Arvanil A structural analog of capsaicin with analgesic activity
  23. GC14115 AVE-1625 A potent CB1 receptor antagonist
  24. GC62855 AZD1940 AZD1940 是一种具有口服活性,高亲和力的大麻素 CB1/CB2 受体激动剂,对 CB1R 和 CB2R 的 pKi 值分别为 7.93 和 9.06,并具有强大的镇痛作用。
  25. GC61778 BAY 38-7271 BAY38-7271是一个选择性、高效的大麻素受体CB1/CB2激动剂,对人重组CB1和CB2作用的Ki值分别为1.85nM和5.96nM。BAY38-7271具有很强的神经保护特性。
  26. GC19060 Bay 59-3074 A partial agonist of CB1 and CB2 receptors
  27. GC11376 BML-190 A CB2 receptor inverse agonist
  28. GC66030 CB1 agonist 1 CB1 agonist 1 (compound 22) 是 CB1 的激动剂。CB1 agonist 1 与 CB1 受体的亲和力的 pIC50 值为 5.7。CB1 agonist 1可以用于大脑失调的研究。
  29. GC31306 CB1 antagonist 1

    CB1antagonist1是CB1receptor的拮抗剂,可用于代谢综合征、肥胖、神经炎性疾病、认知障碍和精神病、胃肠功能紊乱和心血管疾病的研究。

  30. GC30935 CB1-IN-1 CB1-IN-1是一种新型外周大麻素-1受体(CB1R)拮抗剂,作用于CB1R(EC50=3nM)和CB2R,Ki值分别为0.3nM和21nM。
  31. GC33756 CB2R-IN-1 CB2R-IN-1是一种有效的cannabinoidCB2受体反向激动剂,Ki为0.9nM。
  32. GC18110 COR 170 COR 170 (11u) 是一种选择性 CB2 反向激动剂,它是一种 4-喹诺酮-3-羧酸衍生物,对 CB2 受体的 Ki 值为 3.8 nM。
  33. GC17205 CP-945598 HCl A selective CB1 receptor antagonist
  34. GC50579 Ec2la Ec2la 是一种口服活性大麻素 2 型受体 (CB2Rs) 正变构调节剂。
  35. GC11760 GW842166X A CB2 receptor agonist
  36. GC17133 Hemopressin (human, mouse) Hemopressin 是一种衍生自血红蛋白 α1 链的九肽,最初是从大鼠脑匀浆中分离出来的。
  37. GC17116 Hemopressin (rat) Hemopressin (rat) 是一种衍生自血红蛋白 α1 链的九肽,最初是从大鼠脑匀浆中分离出来的。
  38. GC13660 JD5037 JD5037 是一种有效的 CB1R 拮抗剂,IC50 为 1.5 nM。
  39. GC16644 JTE 907 A selective CB2 receptor inverse agonist
  40. GC18496 Leelamine (hydrochloride) An inhibitor of pyruvate dehydrogenase kinase
  41. GC50273 LEI 101 hydrochloride Potent and selective CB2 partial agonist; orally biovailable
  42. GC12538 LH 21 Weak CB1 antagonist
  43. GC13318 LY 320135 A selective CB1 receptor antagonist
  44. GC19231 LY2828360 A selective CB2 receptor agonist
  45. GC12420 MAFP An inhibitor of MAGL, FAAH, cPLA2, and iPLA2
  46. GC15788 MJ 15 A potent CB1 receptor antagonist
  47. GC11453 ML-191 An antagonist of GPR55
  48. GC14626 MM-22

    biotinylated anandamide analog acts as a probe for visualizing the accumulation and intracellular trafficking of anandamide

  49. GC14750 N-Arachidonylglycine A metabolite of anandamide with analgesic activity
  50. GC31536 N-Oleoyl glycine

    A putative substrate for peptidyl glycine α-amidating enzyme

  51. GC18041 NESS 0327 A potent CB1 receptor antagonist

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