GPCR / G Protein

产品 401 到 450 共 860个

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  1. 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
  2. Kainic acid monohydrate

    Catalog No. A13485
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    Kainate receptor 激动剂
    Kainic acid monohydrate是海藻酸酯类离子型谷氨酸受体激动剂。可在体内诱发癫痫发作和神经退行性变,也已用于在啮齿动物中诱发实验性癫痫和检查兴奋性诱发的神经元凋亡机制。 了解更多
  3. Noopept

    Catalog No. A15189
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    Noopept是在俄罗斯和周边国家/地区推广并指定为促智剂的药物。 了解更多
  4. VU0364289

    Catalog No. A15832
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    mGluR5 Modulator
    VU0364289是新型N-芳基哌嗪mGlu5阳性变构调节剂。 了解更多
  5. (S)-3,5-DHPG

    Catalog No. A16108
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    mGluR 激动剂
    (S)-3,5-DHPG是I类代谢型谷氨酸受体(mGluRs)的激动剂,与mGluR1a和mGluR5a(分别为Ki = 0.9和3.9 uM)结合,但不与离子型谷氨酸受体结合。 了解更多
  6. VU 0364770

    Catalog No. A12139
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    mGlu4 receptors modulator
    VU 0364770是mGlu4受体的正变构调节剂,在表达mGlu4的HEK 293细胞中EC50值为290 nM。 了解更多
  7. LY2979165

    Catalog No. A11487
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    mGlu2 激动剂
    LY2979165是mglu2激动剂。 了解更多
  8. VU6005649

    Catalog No. A17023
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    CNS penetrant mGlu7/8 receptor 激动剂
    VU6005649是一种CNS渗透性mGlu7/8受体激动剂,对mGlu7受体和mGlu8受体的EC50分别为0.65 μM和2.6 μM。 了解更多
  9. VU0652835

    Catalog No. A18885
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    mGlu5 modulator
    VU0652835 is a metabotropic glutamate receptor subtype 5 (mGlu5) negative allosteric modulator with an IC50 of 81 nM. 了解更多
  10. CPPHA

    Catalog No. A15053
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    mGluR1 modulator
    CPPHA是mGluR5受体的选择性正变构调节剂。 了解更多
  11. MTEP hydrochloride

    Catalog No. A15174
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    mGlu5 拮抗剂
    MTEP hydrochloride是一种有效的,选择性和非竞争性的mGlu5拮抗剂,IC50和Ki分别为5 nM和16 nM。 了解更多
  12. DL-AP3

    Catalog No. A15378
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    mGluR1 拮抗剂
    DL-AP3是D-AP3和L-AP3的外消旋制剂,是磷酸丝氨酸磷酸酶的抑制剂和代谢型谷氨酸受体(mGluR)的拮抗剂,阻断了由mGluR介导的磷酸肌醇转换。 了解更多
  13. CBiPES HCl

    Catalog No. A15811
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    mGlu2 receptor modulator
    CBiPES HCl是mGluR-2的选择性正变构调节剂,IC50值为98.2 nM。 了解更多
  14. LY2794193

    Catalog No. A19131
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    mGlu3 receptor agonist
    LY2794193 is a highly potent and selective mGlu3 receptor agonist (hmGlu3 Ki=0.927 nM??EC50=0.47 nM; hmGlu2 Ki=412 nM??EC50=47.5 nM). 了解更多
  15. BMT-145027

    Catalog No. A12457
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    mGluR5 positive allosteric modulator
    BMT-145027 is an mGluR5 positive allosteric modulator without inherent agonist activity, exhibits an EC50 of 47 nM. 了解更多
  16. Lu AF21934

    Catalog No. A12140
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    mGlu4 receptor modulator
    Lu AF21934 is a selective and brain-penetrant mGlu4 receptor positive allosteric modulator with an IC50 of 500 nM for human mGlu4. 了解更多
  17. Dipraglurant

    Catalog No. A11382
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    mGluR5 antagonists
    Dipraglurant (ADX 48621) is a mGluR5 antagonists with IC50 of 0.021 μM. 了解更多
  18. ADX88178

    Catalog No. A20922
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    mGluR4 PAM
    ADX88178 is a potent metabotropic glutamate receptor 4 positive allosteric modulator (mGluR4 PAM) with an EC50 of 4 nM for human mGluR4. 了解更多
  19. LY2812223

    Catalog No. A21100
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    mGlu2 receptor agonist
    LY2812223 is a highly potent, functionally selective mGlu2 receptor agonist with mGlu2 binding affinity for mGlu2 and mGlu3 (Ki=144 nM and 156 nM, respectively). 了解更多
  20. O-Phospho-L-serine

    Catalog No. A21159
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    group III mGluR receptors agonist
    O-Phospho-L-serine is the immediate precursor to L-serine in the serine synthesis pathway, and an agonist at the group III mGluR receptors (mGluR4, mGluR6, mGluR7, and mGluR8); O-Phospho-L-serine also acts as a weak antagonist for mGluR1 and a potent antagonist for mGluR2. 了解更多
  21. TCN238

    Catalog No. A21191
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    mGlu4 receptor modulator
    TCN238 is a positive allosteric mGlu4 receptor modulator with an EC50 of 1 μM. 了解更多
  22. Mavoglurant

    Catalog No. A21223
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    mGlu5 receptor antagonist
    Mavoglurant is a structurally novel, non-competitive mGlu5 receptor antagonist, has an IC50 of 30 nM in a functional assay with human mGluR5. 了解更多
  23. Basimglurant

    Catalog No. A21225
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    mGlu5 negative allosteric modulator
    Basimglurant (RG7090) is a potent, selective and orally available mGlu5 negative allosteric modulator with a Kd of 1.1 nM. 了解更多
  24. LY 541850

    Catalog No. A21651
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    mGlu2 agonist/mGlu3 antagonist
    LY541850 is a selective orthosteric mGlu2 agonist and mGlu3 antagonist with IC50 values of 0.161 μM and 0.038 μM, respectively. 了解更多
  25. Mavoglurant racemate

    Catalog No. A21799
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    mGlu5 receptor antagonist
    Mavoglurant (racemate) is the racemate of mavoglurant. Mavoglurant is a novel, non-competitive mGlu5 receptor antagonist. 了解更多
  26. L-APB

    Catalog No. A21872
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    mGluRs M3 agonist
    L-APB is a potent and specific agonist for the group III mGluRs, with EC50s of 0.13, 0.29, 1.0, 249 μM for mGlu4, mGlu8, mGlu6 and mGlu7 receptors, respectively. 了解更多
  27. (R)-ADX-47273

    Catalog No. A21887
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    mGluR5 positive allosteric modulator
    (R)-ADX-47273 is a potent mGluR5 positive allosteric modulator, with an EC50 of 168 nM for potentiation . 了解更多
  28. Methoxy-PEPy

    Catalog No. A21899
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    mGlu5 receptor antagonist
    Methoxy-PEPy is a potent and highly selective mGlu5 receptor antagonist with IC50 of 1 nM. 了解更多
  29. (1R,2S)-VU0155041

    Catalog No. A21933
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    partial mGluR4 agonist
    (1R,2S)-VU0155041, Cis regioisomer of VU0155041, is a partial mGluR4 agonist with an EC50 of 2.35 μM. 了解更多
  30. CHPG sodium salt

    Catalog No. A21968
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    mGluR5 agonist
    CHPG sodium salt is a selective mGluR5 agonist, and attenuates SO2-induced oxidative stress and inflammation through TSG-6/NF-κB pathway in BV2 microglial cells. 了解更多
  31. Auglurant

    Catalog No. A20958
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    mGlu5 antagonist
    Auglurant (VU0424238) is a novel and selective mGlu5 antagonist with an IC50 value of 11 nM (rat) and an IC50 value of 14 nM (human). Auglurant (VU0424238) has an acceptable CNS penetration. 了解更多
  32. Eglumegad

    Catalog No. A21005
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    group II (mGlu2/3) receptor agonist
    Eglumegad (LY354740) is a highly potent and selective group II (mGlu2/3) receptor agonist with IC50s of 5 and 24 nM on transfected human mGlu2 and mGlu3 receptors, respectively. 了解更多
  33. ADL5859 HCl

    Catalog No. A11072
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    Opioid Receptor 激动剂
    ADL5859 HCl是高效的选择性δ阿片受体激动剂,Ki值为0.84 nM,ED50值为20 nM。 了解更多
  34. JTC-801

    Catalog No. A11076
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    Opioid Receptor 拮抗剂
    JTC-801是nociceptin receptor(也称为ORL-1受体)的选择性拮抗剂。 了解更多
  35. MCOPPB 3HCl

    Catalog No. A10561
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    NOP receptor 激动剂
    MCOPPB 3HCl是一种用作伤害感受器受体的有效和选择性激动剂的化合物,pKi为10.07。 了解更多
  36. BRL 52537 HCl

    Catalog No. A11210
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    Opioid Receptors 激动剂
    BRL 52537 hydrochloride是一种高度选择性和有效的κ阿片类激动剂(Ki = 0.24 nM)。比吗啡强25倍。 了解更多
  37. Alvimopan (ADL 8-2698)

    Catalog No. A11292
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    Opioid 拮抗剂
    Alvimopan (ADL 8-2698)表现为外周作用的opioid拮抗剂,Alvimopan竞争性结合胃肠道中的mu-opioid receptor。 了解更多
  38. BAN ORL 24

    Catalog No. A11322
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    NOP 拮抗剂
    BAN ORL 24是一种强效选择性NOP受体拮抗剂。 了解更多
  39. Trimebutine

    Catalog No. A11718
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    Trimebutine是一种具有抗毒蕈碱和弱μ阿片激动剂作用的药物。 了解更多
  40. Nalfurafine hydrochloride

    Catalog No. A12579
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    opioid κ-selective 激动剂
    Nalfurafine hydrochloride是一种κ-opioid激动剂。 了解更多
  41. U-69593

    Catalog No. A14187
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    κ1-opioid receptor 激动剂
    U-69593是有效的选择性κ1阿片受体激动剂(EC50 = 80-109 nM)。在体内有活性。抗伤害感受。 了解更多
  42. ADL5747

    Catalog No. A13479
    δ opioid receptor 激动剂
    ADL5747是一种选择性的非肽类δ opioid激动剂。 了解更多
  43. Alvimopan dihydrate

    Catalog No. A14991
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    ?-opioid receptor 激动剂
    Alvimopan dihydrate (LY 246736,ADL 8-2698)是一种外周作用的类阿片受体(PAM-OR,IC50 = 1.7 nM)拮抗剂,可促进术后胃肠道恢复。 了解更多
  44. Alvimopan monohydrate

    Catalog No. A14992
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    ?-opioid receptor 激动剂
    Alvimopan monohydrate是一种外围作用的类阿片受体(PAM-OR,IC50 = 1.7 nM)拮抗剂,可促进术后肠胃的恢复。 了解更多
  45. Naloxegol Oxalate

    Catalog No. A15972
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    Opioid 拮抗剂
    Naloxegol Oxalate是用于治疗阿片类药物引起的便秘的外周选择性阿片类药物拮抗剂。 了解更多
  46. Docusate Sodium

    Catalog No. A16155
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    Docusate Sodium是一种用于治疗便秘的泻药,对于便秘,由于使用了鸦片制剂,可能与刺激性泻药一起使用,可以通过口腔或直肠服用。 了解更多
  47. Cebranopadol (GRT-6005)

    Catalog No. A12670
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    Opioid Receptor 激动剂
    Cebranopadol是一种有效的伤害感受器/孤儿蛋白FQ肽(NOP)和阿片受体激动剂。作用于人NOP,MOP,KOP 和δ-阿片肽(DOP)受体,Ki/EC50 分别为 0.9 nM/13 nM,0.7 nM/1.2 nM,2.6 nM/17 nM,18 nM/110 nM。 了解更多
  48. Bevenopran

    Catalog No. A17110
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    opioid receptor antagonis
    Bevenopran,也称为CB-5945,ADL-5945,MK-2402,OpRA III,是一种外周选择性μ-和δ-阿片样物质受体拮抗剂。 了解更多
  49. Trimebutine maleate

    Catalog No. A18115
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    ?- opioid receptor agonist
    Trimebutine Maleate is a drug with antimuscarinic and weak mu opioid agonist effects. Trimebutine Maleate modulates the calcium and potassium channels, relieves abdominal pain in patients with irritable bowel syndrome. 了解更多
  50. BTRX-335140

    Catalog No. A18583
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    κ opioid receptor antagonist
    BTRX-335140 (CYM-53093) is a potent and selective, orally active κ opioid receptor (KOR) antagonist, has antagonist activity for κOR, μOR and δOR with IC50 values of 0.8 nM, 110 nM, and 6500 nM, respectively. 了解更多

产品 401 到 450 共 860个

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  2. 8
  3. 9
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