GPCR / G Protein

产品 601 到 650 共 860个

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  1. GSK726701A

    Catalog No. A20101
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    EP4 partial agonist
    GSK726701A is a novel prostaglandin E2 receptor 4 (EP4) partial agonist with a pEC50 of 7.4. 了解更多
  2. Aligeron

    Catalog No. A13241
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    prostaglandin (PG) antagonist
    Aligeron is a non-selective prostaglandin (PG) antagonist, and has vasodilatory properties. 了解更多
  3. CAY10471 Racemate

    Catalog No. A11760
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    Prostaglandin D2 receptor CRTH2 antagonist
    CAY10471 Racemate (TM30089 Racemate) is a potent and highly selective prostaglandin D2 receptor CRTH2 antagonist. 了解更多
  4. ONO-AE3-208

    Catalog No. A11516
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    EP4 antagonist
    ONO-AE3-208 is an EP4 antagonist, and suppresses cell invasion, migration, and metastasis of prostate cancer. 了解更多
  5. (+)-Cloprostenol

    Catalog No. A12979
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    prostaglandin F2α (PGF2α) analogue
    (+)-Cloprostenol is a prostaglandin F2α (PGF2α) analogue, and shows selective agonistic activity at the prostaglandin receptor. 了解更多
  6. MK-2894 sodium salt

    Catalog No. A11498
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    EP4 antagonist
    MK-2894 sodium salt is a highly potent and selective second generation EP4 antagonist. 了解更多
  7. Terutroban

    Catalog No. A20884
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    thromboxane-prostaglandin receptor antagonist
    Terutroban is a thromboxane-prostaglandin receptor antagonist. 了解更多
  8. AGN 210676

    Catalog No. A21281
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    prostaglandin EP2 agonist
    AGN 210676 is a selective prostaglandin EP2 agonist extracted from patent US20070203222A1, Compound example 23, has an EC50 of 5 nM. 了解更多
  9. CJ-42794

    Catalog No. A21948
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    EP4 antagonist
    CJ-42794 is a selective prostaglandin E receptor subtype 4 (EP4) antagonist, inhibits [3H]-PGE2 binding to the human EP4 receptor with a mean pKi of 8.5, a binding affinity that was at least 200-fold more selective for the human EP4 receptor than other human EP receptor subtypes (EP1, EP2, and EP3). 了解更多
  10. Treprostinil sodium

    Catalog No. A21046
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    DP1/EP2 agonist
    Treprostinil sodium is a potent DP1 and EP2 agonist with EC50 values of 0.6??0.1 and 6.2??1.2 nM, respectively. 了解更多
  11. Laropiprant (MK0524)

    Catalog No. A11483
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    DP1 抑制剂
    Laropiprant (MK0524)与烟酸合用可降低血液胆固醇。是一种有效的,选择性的 DP receptor 拮抗剂,Ki 值为 0.57 nM,对 TP 受体的 Ki 值为 2.95 nM。 了解更多
  12. Ozagrel hydrochloride

    Catalog No. A11742
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    Thromboxane A2 synthesis 抑制剂
    Ozagrel hydrochloride是一种抗血小板剂,用作血栓烷a2合成抑制剂。 了解更多
  13. MK-2894

    Catalog No. A11497
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    EP4 receptor 拮抗剂
    MK-2894是一种高度有效和选择性的第二代EP4拮抗剂。 了解更多
  14. Cloprostenol (sodium salt)

    Catalog No. A13498
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    cloprostenol是前列腺素F2α(PGF2α)的合成类似物。它在仓鼠和大鼠中终止妊娠的效力分别是PGF2α的200倍和100倍,而没有与PGF2α相关的副作用。 了解更多
  15. BAY-u 3405

    Catalog No. A13751
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    dual 拮抗剂 of TP/DP2
    BAY-u 3405是用于治疗变应性鼻炎的经过批准的人用药物,已证明其具有作为血栓烷受体(TP受体)的拮抗剂的活性。 了解更多
  16. NS-304 (Selexipag)

    Catalog No. A13880
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    prostacyclin receptor 激动剂
    NS-304 (Selexipag)是一种选择性的前列环素IP1受体激动剂(人和大鼠IP受体的Ki值为260和2100 nM,EP1-4,DP,FP和TP受体的Ki值为> 10μM)。 了解更多
  17. Saikosaponin B2

    Catalog No. A14600
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    Prostanoid activator
    Saikosaponin B2是皂苷激活剂。 了解更多
  18. GW627368

    Catalog No. A15525
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    EP4 receptor 拮抗剂
    GW627368是一种新型,有效且选择性的前列腺素EP4受体竞争拮抗剂(Ki = 100 nM),具有额外的人TP受体亲和力(Ki = 150 nM)。 了解更多
  19. MF498

    Catalog No. A15532
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    EP4 receptor 拮抗剂
    MF498是一种新型的选择性E前列腺素类受体4(EP4受体)拮抗剂,对EP4受体具有很强的结合亲和力,Ki为0.7 nM。 了解更多
  20. PF-04418948

    Catalog No. A12894
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    EP2 Receptor 拮抗剂
    PF-04418948是一种有效的选择性前列腺素EP2受体拮抗剂,IC50为16 nM。 了解更多
  21. CP544326 (Taprenepag)

    Catalog No. A15853
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    EP2 激动剂?
    CP544326 (Taprenepag)是一种有效的选择性前列腺素E2受体激动剂,EC50值为2.8 nM。 了解更多
  22. TG6-10-1

    Catalog No. A15968
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    Prostaglandin E2 receptor 拮抗剂
    TG6-10-1是前列腺素E2受体亚型EP2的有效和选择性拮抗剂。 了解更多
  23. Grapiprant (CJ-023423)

    Catalog No. A15964
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    prostaglandin EP4 receptor 拮抗剂
    Grapiprant (CJ-023423)是一种具有抗痛觉过敏特性的新型,有效且选择性的前列腺素EP4受体拮抗剂。 了解更多
  24. KAG-308

    Catalog No. A18389
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    EP4 激动剂
    KAG-308, a newly-identified EP4-selective agonist shows efficacy for treating ulcerative colitis and can bring about lower risk of colorectal carcinogenesis by oral administration. 了解更多
  25. Reversine

    Catalog No. A13250
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    human A3 adenosine receptor 拮抗剂 /Aurora 抑制剂
    Reversine是一种有效的人A3腺苷受体拮抗剂,Ki为0.66μM,是一种泛光A/B/C激酶抑制剂,IC50分别为12 nM/13 nM/20 nM。也用于干细胞去分化。 了解更多
  26. Pentostatin

    Catalog No. A11534
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    Adenosine deaminase 抑制剂
    Pentostatin是腺苷脱氨酶的不可逆抑制剂(Ki = 2.5 pM)。 了解更多
  27. MT-DADMe-ImmA

    Catalog No. A13651
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    human 5'-methylthioadenosine phosphorylase inhibitor
    MT-DADMe-ImmA is an inhibitor of human 5'-methylthioadenosine phosphorylase (MTAP) with a Ki of 90 pM. 了解更多
  28. A2A receptor antagonist 1

    Catalog No. A12567
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    adenosine A2A/A1 receptor antagonist
    A2A receptor antagonist 1 (CPI-444 analog) is an antagonist of both adenosine A2A receptor and A1 receptor with Kis of 4 and 264 nM, respectively. 了解更多
  29. AB-MECA

    Catalog No. A12189
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    A3 adenosine receptor agonist
    AB-MECA is a high affinity A3 adenosine receptor agonist, has high affinity for recombinant A1 and A3 receptors. 了解更多
  30. CGS 21680

    Catalog No. A11354
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    adenosine A2A receptor agonist
    CGS 21680 is a selective adenosine A2A receptor agonist, with a Ki of 27 nM. 了解更多
  31. APNEA

    Catalog No. A20845
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    A3 adenosine receptor agonist
    APNEA (N6-[2-(4-Aminophenyl)ethyl]adenosine) is a potent, non-selective A3 adenosine receptor agonist. 了解更多
  32. LAS101057

    Catalog No. A21203
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    A2B receptor antagonist
    LAS101057 is a potent, selective, and orally efficacious A2B receptor antagonist. 了解更多
  33. Tonapofylline

    Catalog No. A21328
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    adenosine A1 receptor antagonist
    Tonapofylline (BG 9928) is an orally active and selective adenosine A1 receptor antagonist with a Ki of 7.4 nM for human adenosine A1 receptor (hA1), which displays 915-fold selectivity versus human adenosine A2A receptor and 12-fold selectivity versus human adenosine A2B receptor and is used in development for the treatment of heart failure. 了解更多
  34. LUF6000

    Catalog No. A21532
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    A3 adenosine receptor allosteric modulator
    LUF6000 is an allosteric modulator of the human A3 adenosine receptor (AR). 了解更多
  35. EHNA hydrochloride

    Catalog No. A21585
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    Adenosine deaminase inhibitor
    EHNA hydrochloride is a specific inhibitor of adenosine deaminase, prevents dAdo degradation and increases mitochondrial dATP levels in fibroblasts. 了解更多
  36. Rolofylline

    Catalog No. A21649
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    adenosine A1 receptor antagonist
    Rolofylline (KW-3902) is a potent, selective adenosine A1 receptor antagonist that is under development for the treatment of patients with acute congestive heart failure and renal impairment. 了解更多
  37. Derenofylline

    Catalog No. A21990
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    adenosine A1 receptor antagonist
    Derenofylline (SLV 320) is a potent, selective and orally active adenosine A1 receptor antagonist, with Ki values of 1 nM, 200 nM and 398 nM for human A1, A3 and A2A receptors respectively. 了解更多
  38. MRS 1754

    Catalog No. A21998
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    A2B adenosine receptor antagonist
    MRS 1754 is a selective antagonist radioligand for A2B adenosine receptor with very low affinity for A1 and A3 receptors of both humans and rats. 了解更多
  39. N6-Cyclohexyladenosine

    Catalog No. A21008
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    A1 receptor agonist
    N6-Cyclohexyladenosine is a selective A1 receptor agonist (EC50 = 8.2 nM). 了解更多
  40. Istradefylline (KW-6002)

    Catalog No. A11451
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    A2A 拮抗剂
    Istradefylline (KW-6002)是A2A受体的选择性拮抗剂。 了解更多
  41. SYN-115 (Tozadenant)

    Catalog No. A11560
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    A2a receptor 拮抗剂
    SYN115是口服,有效和选择性的腺苷2a(A2a)受体抑制剂,作用于人类和恒河猴的 adenosine A2A 受体,Ki 值分别为 11.5 nM 和 6 nM。 了解更多
  42. CGS 21680 HCl Hydrate

    Catalog No. A11619
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    Adenosine A2A Receptor 激动剂
    CGS 21680 HCl是一种特定的腺苷A2A亚型受体激动剂。 了解更多
  43. Adenosine

    Catalog No. A10040
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    Adenosine在生化过程中起着重要作用,例如能量转移(如三磷酸腺苷(ATP)和二磷酸腺苷(ADP))以及信号传导中的环状单磷酸腺苷cAMP。 它也是一种抑制性神经递质。 了解更多
  44. Aminophylline

    Catalog No. A10066
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    Adenosine receptor 拮抗剂
    Aminophylline是一种非选择性的腺苷受体拮抗剂和磷酸二酯酶抑制剂,能够逆转局部缺血引起的bradyasystole。 了解更多
  45. Dyphylline

    Catalog No. A10339
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    Adenosine receptor 拮抗剂
    Dyphylline是黄嘌呤衍生物,具有支气管扩张药和血管扩张药的作用。 它充当腺苷受体拮抗剂和磷酸二酯酶抑制剂。 了解更多
  46. SCH 442416

    Catalog No. A12695
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    A2A Receptor 拮抗剂
    SCH 442416是一种选择性的腺苷A2A受体拮抗剂。以高亲和力结合人和大鼠A2A受体(Ki值分别为0.048和0.5 nM)。在体外对hA2A的选择性比hA1高> 23000倍,并且对hA2B和hA3受体的亲和力最小(IC50> 10μM)。 了解更多
  47. Tamsulosin hydrochloride

    Catalog No. A12846
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    Tamsulosin hydrochloride是前列腺素α1A肾上腺素受体的拮抗剂。 了解更多
  48. CVT 6883

    Catalog No. A13745
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    adenosine A2B receptors 拮抗剂
    CVT-6883是一种选择性的A2B腺苷拮抗剂,代表了一种治疗心肺疾病的新型潜在方法。 了解更多
  49. Capadenoson

    Catalog No. A14159
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    Adenosine Receptor 激动剂
    Capadenoson是腺苷A1受体的选择性激动剂。 了解更多
  50. 5-Iodotubercidin

    Catalog No. A13948
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    Adenosine kinase 抑制剂
    5-Iodotubercidin是一种有效的腺苷激酶抑制剂,IC50为26 nM。 了解更多

产品 601 到 650 共 860个

每页
页面:
  1. 11
  2. 12
  3. 13
  4. 14
  5. 15

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