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GPCR/G protein

G protein–coupled receptors (GPCRs) which are also known as seven-transmembrane domain receptors, 7TM receptors, heptahelical receptors, serpentine receptor, and G protein–linked receptors (GPLR), constitute a large protein family of receptors, that detect molecules outside the cell and activate internal signal transduction pathways and, ultimately, cellular responses. Coupling with G proteins, they are called seven-transmembrane receptors because they pass through the cell membrane seven times.

Products for GPCR/G protein

  1. Cat.No. Product Name Information
  2. BCC5662 IPAG IPAG
  3. BCC6987 SB 216641 hydrochloride SB 216641 hydrochloride
  4. BCC6010 Cortistatin 14 Cortistatin 14, human, rat (CST-14, human, rat), a neuropeptide with neuronal depressant and sleep modulating properties, can bind to all five cloned somatostatin receptors (SSTRs) and ghrelin receptor to exert its biological activities and co-exists with GABA within the cortex and hippocampus. Cortistatin 14
  5. BCC6968 SC 19220 SC 19220
  6. BCC5892 GLP-2 (rat) GLP-2 (rat)
  7. BCC1380 Atrasentan hydrochloride Atrasentan hydrochloride (ABT-627 hydrochloride) is a selective endothelin A receptor antagonist with an IC50 of 0.0551 nM for ETA. Atrasentan hydrochloride
  8. BCC8020 Prosaptide TX14(A) Prosaptide TX14(A)
  9. BCC1107 4-Acetyl Ramelteon 4-Acetyl Ramelteon
  10. BCC7040 SB 221284 SB 221284
  11. BCC6706 Methiothepin maleate Methiothepin maleate
  12. BCC7633 SN 003 SN 003
  13. BCC7395 T 98475 T 98475
  14. BCC7361 NNC 26-9100 NNC 26-9100
  15. BCC7559 LY 334370 hydrochloride LY 334370 hydrochloride
  16. BCC6035 SB 243213 dihydrochloride SB 243213 hydrochloride is an orally active, selective and high-affinity 5-hydroxytryptamine (5-HT)2C receptor antagonist with a pKi of 9.37 and a pKb of 9.8 for human 5-HT2C receptor. SB 243213 hydrochloride has improved anxiolytic profile and has the potential for schizophrenia and motor disorders. SB 243213 dihydrochloride
  17. BCC5755 Ac-RYYRWK-NH2 Ac-RYYRWK-NH2
  18. BCC5736 Ac-RYYRIK-NH2 Ac-RYYRIK-NH2
  19. BCC6723 4-PPBP maleate 4-PPBP maleate
  20. BCC6743 3-AQC 3-AQC
  21. BCC1724 LY341495 LY341495 is a metabotropic glutamate receptor (mGluR) antagonist with IC50s of 2.9 nM, 10 nM, 170 nM for mGluR-2, mGluR-3, mGluR-8, respectively. LY341495
  22. BCC6882 Spiperone hydrochloride Spiperone hydrochloride
  23. BCC6944 AM 281 Potent, selective CB1 antagonist/inverse agonist AM 281
  24. BCC7512 Ro 04-6790 Ro 04-6790
  25. BCC5766 Orexin B (mouse) Orexin B, rat, mouse is an endogenous agonist at Orexin receptor with Kis of 420 and 36 nM for OX1 and OX2, respectively. Orexin B (mouse)
  26. BCC1595 glucagon receptor antagonists 3 Glucagon receptor antagonists-3 is a highly potent glucagon receptor antagonist. glucagon receptor antagonists 3
  27. BCC1594 glucagon receptor antagonists 2 Glucagon receptor antagonists-2 is a highly potent glucagon receptor antagonist. glucagon receptor antagonists 2
  28. BCC7785 NF 340 NF 340
  29. BCC7426 PD 176252 PD176252 is a potent antagonist of neuromedin-B preferring (BB1) and gastrin-releasing peptide-preferring (BB2) receptor with Kis of 0.17 nM and 1 nM for human BB1 and BB2 receptors, and 0.66 nM, 16 nM for Rat BB1 and BB2 receptors, respectively; PD176252 is also an agonist of N-Formyl peptide receptor1/2 (FPR1/FPR2), with EC50s of 0.31 and 0.66 μM in HL-60 cells. PD 176252
  30. BCC1982 Talnetant hydrochloride Talnetant Hcl(SB 223412 Hcl) is a potent and selective NK3 receptor antagonist(ki=1.4 nM, hNK-3-CHO); 100-fold selective for the hNK-3 versus hNK-2 receptor, with no affinity for the hNK-1 at concentrations up to 100 uM. Talnetant hydrochloride
  31. BCC7311 2'-MeCCPA 2'-MeCCPA
  32. BCC5764 Orexin A (human, rat, mouse) Orexin A human, rat, mouse, a 33 amino acid excitatory neuropeptide, orchestrates diverse central and peripheral processes. Orexin A human, rat, mouse is a specific, high-affinity agonist for G-protein-coupled receptor OX1R. Orexin A human, rat, mouse has a role in the regulation of feeding behavior. Orexin A human, rat, mouse is an effective anti-nociceptive and anti-hyperalgesic agent in mice and rats. Orexin A (human, rat, mouse)
  33. BCC5765 Orexin B (human) Orexin B, human is an endogenous agonist at Orexin receptor with Kis of 420 and 36 nM for OX1 and OX2, respectively. Orexin B (human)
  34. BCC6832 BD 1063 dihydrochloride BD1063 dhydrochloride is a potent and selective sigma 1 receptor antagonist. BD 1063 dihydrochloride
  35. BCC6684 MR 16728 hydrochloride MR 16728 hydrochloride
  36. BCC5657 L-693,403 maleate L-693,403 maleate
  37. BCC5673 SB 203186 hydrochloride SB 203186 hydrochloride
  38. BCC5819 HS 014 HS 014
  39. BCC5703 Nocistatin (bovine) Nocistatin (bovine)
  40. BCC7364 (1R,1'S,3'R/1R,1'R,3'S)-L-054,264 (1R,1'S,3'R/1R,1'R,3'S)-L-054,264
  41. BCC1674 JWH 073 JWH 073
  42. BCC6006 CART (55-102) (rat) CART (55-102) (rat)
  43. BCC7718 Org 12962 hydrochloride Org 12962 hydrochloride
  44. BCC6008 CART (62-76) (rat, human) CART (62-76) (rat, human)
  45. BCC5936 SB 265610 SB-265610 is a selective, competitive, nonpeptide and allosteric CXCR2 antagonist. SB-265610 blocks rat cytokine-induced neutrophil chemoattractant-1 (CINC-1)-induced calcium mobilization and neutrophil chemotaxis with IC50s of 3.7 nM and 70 nM, respectively. SB 265610
  46. BCC6650 m-Chlorophenylbiguanide hydrochloride m-Chlorophenylbiguanide hydrochloride
  47. BCC5820 HS 024 HS 024
  48. BCC5732 Nocistatin (human) Nocistatin (human)
  49. BCC6291 Org 37684 Org 37684
  50. BCC5701 [Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 [Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2
  51. BCC6007 CART (55-102) (human) CART (55-102) (human)
  52. BCC6858 WB 4101 hydrochloride WB 4101 hydrochloride
  53. BCC5959 Apelin-17 (human, bovine) Apelin-17 (human, bovine)
  54. BCC7358 [Pyr1]-Apelin-13 [Pyr1]-Apelin-13 is a highly potent, selective endogenous apelin receptor (APJ) agonist. [Pyr1]-Apelin-13
  55. BCC7916 SB 268262 SB 268262
  56. BCC7423 (±)-J 113397 Potent and selective NOP antagonist (±)-J 113397
  57. BCC7220 L-803,087 trifluoroacetate L-803087 is a potent and selective somatostatin sst4 receptor agonist with a Ki of 0.7 nM, which is > 280-fold higher than other somatostatin receptors. L-803087 facilitates AMPA-mediated hippocampal synaptic responses in vitro and increases kainate-induced seizures in mice. L-803,087 trifluoroacetate
  58. BCC7221 L-817,818 L-817,818
  59. BCC6029 BX 471 BX471 (ZK-811752) is an orally active, potent and selective non-peptide CCR1 antagonist with a Ki of 1 nM, and exhibits 250-fold selectivity for CCR1 over CCR2, CCR5 and CXCR4. BX 471
  60. BCC1777 MPEP Hydrochloride MPEP hydrochloride is a potent and highly selective non-competitive antagonist at the mGlu5 receptor subtype with IC50 of 36 nM. MPEP Hydrochloride
  61. BCC6973 DH 97 DH 97
  62. BCC5868 Antisauvagine-30 Antisauvagine-30
  63. BCC7480 Antalarmin hydrochloride Antalarmin hydrochloride
  64. BCC5891 GLP-2 (human) GLP-2(1-33) (human) is an enteroendocrine hormone which can bind to the GLP-2 receptor and stimulate the growth of intestinal epithelium. GLP-2 (human)
  65. BCC3814 Mirabegron (YM178) Mirabegron is a selective β3-adrenoceptor agonist with EC50 of 22.4 nM. Mirabegron (YM178)
  66. BCC1483 Cinacalcet Cinacalcet (AMG 073) is an orally active, allosteric agonist of Ca receptor (CaR), used for cardiovascular disease treatment. Cinacalcet
  67. BCC5992 R 892 R 892
  68. BCC7011 Abn-CBD Abn-CBD
  69. BCC5911 Apelin-36 (rat, mouse) Apelin-36 (rat, mouse)
  70. BCC4320 Terbutaline Sulfate Terbutaline sulfate is a β2-adrenergic receptor agonist; a fast-acting bronchodilator and a tocolytic to delay premature labor. Terbutaline Sulfate
  71. BCC4341 Xylazine HCl Xylazine hydrochloride (BAY 1470 hydrochloride) is a strong α2-adrenergic agonist whose effects are mediated via stimulation of central α2-receptors. Xylazine hydrochloride is used as a sedative, analgesic and muscle relaxant in veterinary medicine. Xylazine HCl
  72. BCC4333 Oxymetazoline HCl Oxymetazoline HCl
  73. BCC4337 Ritodrine HCl Ritodrine hydrochloride (DU21220 hydrochloride) is a β-2 adrenergic receptor agonist. Ritodrine HCl
  74. BCC4327 Guanabenz Acetate Guanabenz (Acetate) (BR-750) is an alpha-2 selective adrenergic agonist used as an antihypertensive agent. Guanabenz Acetate
  75. BCC7289 2-Palmitoylglycerol 2-Palmitoylglycerol
  76. BCC6094 MEN 11270 MEN 11270
  77. BCC5781 [Arg14,Lys15]Nociceptin [Arg14,Lys15]Nociceptin
  78. BCC5629 Methylprednisolone Sodium Succinate 6α-Methylprednisolone 21-hemisuccinate sodium salt is a glucocorticoid of slightly longer half-life than that of Prednisolone. Methylprednisolone Sodium Succinate
  79. BCC5897 Tabimorelin hemifumarate Tabimorelin hemifumarate
  80. BCC1312 5-Iodotubercidin 5-Iodotubercidin (NSC 113939), an ATP mimetic, is a potent adenosine kinase inhibitor with an IC50 of 26 nM. 5-Iodotubercidin (NSC 113939) initiates glycogen synthesis in isolated hepatocytes by causing inactivation of phosphorylase and activation of glycogen synthase. 5-Iodotubercidin (NSC 113939) also inhibits CK1, insulin receptor tyrosine kinase, phosphorylase kinase, PKA, CK2, PKC and Haspin. 5-Iodotubercidin
  81. BCC7654 L-798,106 L-798106 is potent and highly selective prostanoid EP3 receptor antagonist (Ki=0.3 nM), it also has micromolar activities at the EP4, EP1 and EP2 receptors with Ki values of 916 nM, >5000 nM and >5000 nM at EP4, EP1 and EP2, respectively. L-798,106
  82. BCC7475 L-748,337 L-748,337
  83. BCC6279 FSLLRY-NH2 FSLLRY-NH2
  84. BCC6086 RWJ 52353 RWJ 52353
  85. BCC7991 TC-G 1000 TC-G 1000
  86. BCC7158 BIIE 0246 BIIE-0246 is a potent and highly selective non-peptide neuropeptide Y (NPY) Y2 receptor antagonist, with an IC50 of 15 nM. BIIE 0246
  87. BCC5366 AL 8810 AL 8810
  88. BCC5552 Fimasartan Fimasartan(BR-A-657) is a non-peptide angiotensin II receptor antagonist used for the treatment of hypertension and heart failure. Fimasartan
  89. BCC6657 Dihydroergocristine mesylate Dihydroergocristine mesylate (DHEC mesylate) is a inhibitor of γ-secretase (GSI), reduces the production of the Alzheimer's disease amyloid-β peptides, binds directly to γ-secretase and Nicastrin with equilibrium dissociation constants (Kd) of 25.7 nM and 9.8 μM, respectively. Dihydroergocristine mesylate
  90. BCC6056 SB 328437 SB 328437
  91. BCC6813 Agmatine sulfate Agmatine sulfate exerts modulatory action at multiple molecular targets, such as neurotransmitter systems, ion channels and nitric oxide synthesis. It is an endogenous agonist at imidazoline receptor and a NO synthase inhibitor. Agmatine sulfate
  92. BCC4289 SB-334867 hydrochloride SB-334867 (SB 334867A) is an excellent,selective and blood–brain barrier permeable orexin-1 (OX1) receptor antagonist, shows selectivity over OX2 (pKb=7.4), 100-fold over 5-HT2B, 5-HT2C with pKi values of 5.4 and 5.3, respectively. SB-334867 reduces ethanol consumption and inhibits the acquisition of morphine-induced sensitization to locomotor activity in vivo. 
SB-334867 hydrochloride
  93. BCC1362 Anamorelin Anamorelin is a novel ghrelin receptor agonist with EC50 value of 0.74 nM in the FLIPR assay. Anamorelin
  94. BCC7177 NNC 63-0532 NNC 63-0532
  95. BCC5796 Urotensin II (human) Urotensin II (114-124), human, an 11-amino acid residue peptide, is a potent vasoconstrictor and agonist for the orphan receptor GPR14. Urotensin II (human)
  96. BCC7656 SLV 320 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. Derenofylline suppresses cardiac fibrosis and attenuates albuminuria without affecting blood pressure in rats. SLV 320
  97. BCC5910 Apelin-36 (human) Apelin-36 (human)
  98. BCC7433 RWJ 56110 RWJ 56110
  99. BCC6106 MRE 3008F20 MRE3008F20 is a highly potent and selective antagonist of adenosine A3 receptor (AA3R), inhibits agonist-induced cAMP elevation in resting T lymphocytes with an IC50 of 5 nM. MRE 3008F20
  100. BCC7924 Talsupram hydrochloride Talsupram hydrochloride
  101. BCC7312 SEW 2871 SEW2871 is a highly selective, orally active S1P1 agonist with an EC50 of 13.8 nM. SEW2871 activates ERK, Akt, and Rac signaling pathways and induces S1P1 internalization and recycling. SEW2871 reduces lymphocyte numbers in blood and has therapeutic implications in contexts of diabetes, Alzheimer’s disease, liver fibrosis, and inflammatory responses. SEW 2871

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