GPCR / G Protein

产品 51 到 100 共 860个

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  1. YC-1 (Lificiguat)

    Catalog No. A12402
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    sGC activator
    YC-1 (Lificiguat)是可溶性胍基环化酶(sGC)的直接活化剂,独立于一氧化氮。 了解更多
  2. Linaclotide

    Catalog No. A13834
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    Guanylate cyclase C 激动剂
    Linaclotide是鸟苷酸环化酶2C的肽激动剂。 了解更多
  3. BAY 41-2272

    Catalog No. A15891
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    sGC activator?
    BAY 41-2272是一种直接且不依赖NO的可溶性鸟苷酸环化酶(sGC)刺激物。 了解更多
  4. Vericiguat

    Catalog No. A21031
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    guanylate cyclase stimulator
    Vericiguat (BAY1021189) is a potent, orally available and soluble guanylate cyclase stimulator. 了解更多
  5. Olinciguat

    Catalog No. A13670
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    guanylate cyclase (sGC) stimulator
    Olinciguat (IW-1701) is an oral guanylate cyclase (sGC) stimulator with concentration-dependent stimulation of sGC in purified rat and human enzyme assays and a whole cell assay. 了解更多
  6. Cinaciguat

    Catalog No. A21283
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    sGC activator
    Cinaciguat is an activator of guanylate cyclase (sGC), and used for acute decompensated heart failure. 了解更多
  7. NS-2028

    Catalog No. A21643
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    sGC inhibitor
    NS-2028 is a highly selective soluble Guanylyl Cyclase (sGC) inhibitor with IC50 values of 30 nM and 200 nM for basal and NO-stimulated enzyme activity. 了解更多
  8. GSK221149A (Retosiban)

    Catalog No. A13106
    Oxytocin Receptor 拮抗剂
    GSK221149A (Retosiban)是一种口服药物,可作为选择性纳摩尔(Ki = 0.65 nM)催产素受体拮抗剂,其选择性是相关血管加压素受体的> 1400倍。 了解更多
  9. Atosiban

    Catalog No. A14334
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    peptide Oxytocin Receptor 抑制剂
    Atosiban是一种肽催产素受体抑制剂。 了解更多
  10. PF-3274167

    Catalog No. A13754
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    Oxytocin 拮抗剂
    PF-3274167是一种高亲和力非肽催产素受体(OTR)拮抗剂,Ki为9.5 nM。 了解更多
  11. SHR1653

    Catalog No. A18575
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    Oxytocin receptor antagonist
    SHR1653 is a highly potent, selective and brain penetrated oxytocin receptor (OTR) antagonist, with an IC50 of 15 nM for hOTR. 了解更多
  12. Oxytocin

    Catalog No. A17988
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    oxytocin receptor ligand
    Oxytocin (α-Hypophamine) is a mammalian neurohypophysial hormone; its actions are mediated by specific, high-affinity oxytocin receptors; ligand of oxytocin receptor. 了解更多
  13. Carbetocin

    Catalog No. A18080
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    peripheral oxytocin receptors agonist
    Carbetocin (Lonactene; Duratocin) is an obstetric drug used to control postpartum hemorrhage and bleeding after giving birth; an agonist at peripheral oxytocin receptors. 了解更多
  14. L-371,257

    Catalog No. A21219
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    oxytocin receptor antagonist
    L-371,257 is an orally bioavailable, non-blood-brain barrier penetrant, selective and competitive antagonist of oxytocin receptor (pA2=8.4) with high affinity at both the oxytocin receptor (Ki=19 nM) and vasopressin V1a receptor (Ki=3.7 nM). 了解更多
  15. Siramesine Hydrochloride

    Catalog No. A12479
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    Sigma-2 receptor 激动剂
    Siramesine Hydrochloride是一种选择性sigma-2受体激动剂,已被证明可触发癌细胞的细胞死亡并在体内表现出强大的抗癌活性。 了解更多
  16. S1RA (E-52862)

    Catalog No. A12504
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    sigma-1 receptor 拮抗剂
    S1RA是一种选择性sigma-1受体拮抗剂,据报道其结合亲和力为Ki = 17.0±7.0 nM,对sigma-2受体具有选择性,并且对其他170种受体,酶,转运蛋白和离子通道具有选择性。 了解更多
  17. Siramesine

    Catalog No. A13036
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    Sigma-2 receptor 激动剂
    Siramesine是一种溶酶体去污剂,诱导细胞保护性自噬体积累。 了解更多
  18. UMB24

    Catalog No. A13513
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    Sigma2 拮抗剂
    UMB24是推定的sigma2优选拮抗剂。 了解更多
  19. BD-1047 2HBr

    Catalog No. A13196
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    Sigma-1 拮抗剂
    BD-1047 2HBr是sigma受体的选择性功能拮抗剂,在动物模型中显示出抗精神病活性,可预测精神分裂症的疗效。 了解更多
  20. SA-4503

    Catalog No. A12984
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    sigma 1 receptor(σ1R) 激动剂
    SA4503是选择性sigma 1受体(σ1R)激动剂;对(+)-[3H]喷他佐辛标记的sigma 1受体亚型具有高亲和力(IC50 = 17.4+/-1.9 nM);对sigma 2受体的亲和力低100倍。 了解更多
  21. Glycerol phenylbutyrate

    Catalog No. A18201
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    sigma-2 (σ2) receptor ligand
    Glycerol phenylbutyrate is a sigma-2 (σ2) receptor ligand, with a pKi of 8.02. 了解更多
  22. 4-IBP

    Catalog No. A12314
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    σ1 激动剂
    4-IBP is a selective ??1 agonist with a high level of affinity for the ??1 receptor (Ki = 1.7 nM) and a moderate affinity for the ??2 receptor (Ki = 25.2 nM) . 了解更多
  23. E1R

    Catalog No. A18825
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    sigma-1 receptors modulator
    E1R is a novel positive allosteric modulator of sigma-1 receptors. 了解更多
  24. Sigma-1 receptor antagonist 2

    Catalog No. A18504
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    sigma 1 receptor antagonist
    Sigma-1 receptor antagonist 2 is a potent and selective sigma 1 receptor (??1 R) antagonist with Kis of 3.88 and 1288 nM for ??1 and ??2 receptor, respectively. 了解更多
  25. Sigma-1 receptor antagonist 3

    Catalog No. A18501
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    Sigma-1 receptor antagonist
    Sigma-1 receptor antagonist 3 (compound135) is a potent and selective Sigma-1 (??1) receptor antagonist with a Ki of 1.14 nM. 了解更多
  26. Cutamesine

    Catalog No. A21152
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    sigma 1 receptor agonist
    Cutamesine (SA4503; AGY-94806) is a selective sigma 1 receptor(??1R) agonist; high affinity for the sigma 1 receptor subtype labeled by (+)-[3H]pentazocine (IC50= 17.4??1.9 nM); 100-fold less affinity for the sigma 2 receptor. 了解更多
  27. Ditolylguanidine

    Catalog No. A21268
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    Sigma receptor agonist
    Ditolylguanidine (1,3-Di-o-tolylguanidine) is an agonist of sigma receptor (??1/??2 receptor). 了解更多
  28. Desmopressin

    Catalog No. A12351
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    Desmopressin是一种合成的加压素类似物,在V1B和V2受体上起激动剂的作用(EC50值分别为11.4和23.9 nM,Ki值分别为5.84和65.9 nM)。 了解更多
  29. Tolvaptan

    Catalog No. A11594
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    vasopressin receptor 2 拮抗剂
    Tolvaptan是一种选择性的竞争性精氨酸加压素受体2拮抗剂,IC50为1.28μM。 了解更多
  30. OPC21268

    Catalog No. A15784
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    vasopressin V1 拮抗剂
    OPC21268是一种非肽AVP受体V(Vasopressin Receptor)拮抗剂,对V1受体的选择性是V2受体的1000倍。 了解更多
  31. Vasopressin antagonist 1867

    Catalog No. A16188
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    V1b receptor 拮抗剂
    Vasopressin antagonist 1867,可口服和选择性V1b受体拮抗剂(hV1b抑制作用的IC50值为3 nM,相对于hV1a,hV2和hOT表现出> 1000倍的选择性)。 了解更多
  32. Mozavaptan

    Catalog No. A16622
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    nonpeptide vasopressin V2 receptor antagonist
    Mozavaptan (OPC31260) is a orally effective, nonpeptide vasopressin V2 receptor antagonist with an IC50 of 14 nM. 了解更多
  33. Lixivaptan

    Catalog No. A21279
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    vasopressin receptor V2 antagonist
    Lixivaptan (VPA-985, WAY-VPA 985) is an orally active and selective vasopressin receptor V2 antagonist, with IC50 values of 1.2 and 2.3 nM for human and rat V2, respectively. 了解更多
  34. RG7713

    Catalog No. A21380
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    Brain-Penetrant Vasopressin 1a (V1a) receptor antagonist
    RG7713 (RO5028442) is a highly potent and selective Brain-Penetrant Vasopressin 1a (V1a) receptor antagonist with Kis of 1 nM (hV1a) and 39 nM (mV1a). 了解更多
  35. MK 3207 HCl

    Catalog No. A10598
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    CGRP Receptor 拮抗剂
    MK 3207 hydrochloride是一种有效的CGRP受体拮抗剂,IC50为0.12 nM。 了解更多
  36. MK-0974 (Telcagepant)

    Catalog No. A11255
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    CGRP receptor 拮抗剂
    MK-0974 (Telcagepant)是人和恒河猴CGRP受体的有效和选择性拮抗剂。 了解更多
  37. BMS-927711

    Catalog No. A13102
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    CGRP receptor 拮抗剂
    BMS-927711是一种有效的,选择性的,竞争性的人降钙素基因相关肽(CGRP)受体拮抗剂,已显示出体内功效,而没有血管收缩作用。 了解更多
  38. MK-3207

    Catalog No. A15165
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    CGRP Receptor 拮抗剂
    MK-3207是一种有效且口服可生物利用的CGRP受体拮抗剂(IC50 = 0.12 nM;Ki = 0.024 nM);对人类AM1,AM2,CTR和AMY3具有高度选择性。 了解更多
  39. CGRP 8-37 (human)

    Catalog No. A16949
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    CGRP receptor 拮抗剂
    CGRP 8-37 (human)是人降钙素基因相关肽(hCGRP)片段,也是CGRP受体的拮抗剂。序列:Val-Thr-His-Arg-Leu-Ala-Gly-Leu-Leu-Ser-Arg-Ser-Gly-Gly-Val-Val-Lys-Asn-Asn-Phe-Val-Pro-Thr-Asn- Val-Gly-Ser-Lys-Ala-Phe;VTHRLAGLLSRSGGVVKNNFVPTNVGSKAF。 了解更多
  40. Olcegepant

    Catalog No. A11512
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    CGRP1 receptor
    Olcegepant is a potent and selective non-peptide antagonist of the calcitonin gene-related peptide 1 (CGRP1) receptor with IC50 of 0.03 nM and Ki of 14.4 pM for human CGRP. 了解更多
  41. Ubrogepant

    Catalog No. A21670
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    CGRP antagonist
    Ubrogepant (MK-1602) is a novel oral calcitonin gene-related peptide receptor (CGRP) antagonist in development for acute treatment of migraine. 了解更多
  42. Olcegepant hydrochloride

    Catalog No. A21900
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    CGRP1 receptor antagonist
    Olcegepant hydrochloride is the first potent and selective non-peptide antagonist of the calcitonin gene-related peptide 1 (CGRP1) receptor with IC50 of 0.03 nM and with a Ki of 14.4 pM for human CGRP. 了解更多
  43. FTY720 (Fingolimod)

    Catalog No. A10408
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    S1P Receptor 拮抗剂
    FTY720 (Fingolimod)是ISP-1(肉豆蔻酸)的衍生物,ISP-1是中国草药Iscaria sinclarii的真菌代谢物,也是鞘氨醇的结构类似物。 了解更多
  44. BAF312 (Siponimod)

    Catalog No. A12906
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    S1PR1/S1PR5 抑制剂
    BAF312 (Siponimod)是下一代有效的1-磷酸鞘氨醇(S1P)受体激动剂,对S1P1和S1P5具有选择性。 了解更多
  45. PF-543

    Catalog No. A13039
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    SphK1 抑制剂
    PF-543是一种新型选择性SK-1抑制剂,可与鞘氨醇竞争性抑制SK-1活性。 了解更多
  46. ABC294640

    Catalog No. A12614
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    SphK2 抑制剂
    ABC294640是一种口服的芳基金刚烷化合物,是鞘氨醇激酶2(SK2)的选择性抑制剂,Ki 为 9.8 μM,具有潜在的抗肿瘤活性。 了解更多
  47. CYM 5442 HCl

    Catalog No. A13637
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    EDG-1 (S1P1) 激动剂
    CYM 5442 HCl是一种有效的体外选择性EDG-1(S1P1)激动剂(EC50 = 1.35 nM)。 了解更多
  48. PF-543 Citrate

    Catalog No. A15210
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    SphK1 抑制剂
    PF-543 Citrate是一种新型的SphK1细胞渗透抑制剂,K(i)为3.6 nM,PF-543具有鞘氨醇竞争性,对SphK1的选择性是SphK2同种型的100倍以上。 了解更多
  49. RPC1063 (Ozanimod)

    Catalog No. A15819
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    S1PR1 modulators
    RPC1063 (Ozanimod)是选择性的鞘氨醇1磷酸酯受体调节剂和方法,可用于治疗与S1P1-β相关的疾病。 了解更多
  50. NS13001

    Catalog No. A15833
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    SK2 modulator
    NS13001是选择性的SK2/3调节剂,可作为治疗SCA2和其他可能的小脑共济失调的潜在治疗剂。 了解更多

产品 51 到 100 共 860个

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