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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. BCC6197 BAY 60-6583 BAY 60-6583 is a potent and high-affinity agonist of adenosine A2B receptor (EC50 = 3 nM) over A1, A2A, and A3 receptors. BAY 60-6583 binds to mouse, rabbit, and dog A2BAR with Ki values of 750 nM, 340 nM and 330 nM, respectively. BAY 60-6583 has a cardioprotective effect in a myocardial ischemia model. BAY 60-6583
  3. BCC7421 TCB-2 TCB-2
  4. BCC6452 ELN441958 ELN-441958 is a potent, neutral antagonist of B1 receptor, inhibits the binding of the B1 agonist ligand [3H]DAKD to IMR-90 cells with Ki of 0.26 nM. ELN441958
  5. BCC5123 Almorexant hydrochloride Almorexant hydrochloride (ACT 078573 hydrochloride) is a potent and competitive dual orexin 1 receptor (OX1)/orexin 2 receptor (OX2) antagonist with Ki values of 1.3 and 0.17 nM, respectively. Almorexant hydrochloride
  6. BCC6221 CS 2100 CS 2100
  7. BCC7977 Lu AA 47070 Lu AA 47070
  8. BCC4063 TCS 1102 TCS 1102 is a potent, dual orexin receptor antagonist (Ki values are 0.2 and 3 nM for OX2 and OX1 receptors respectively). TCS 1102
  9. BCC7459 PSB 0474 PSB 0474
  10. BCC1767 MK-6892 MK-6892 is a potent, selective, and full agonist for the high affinity nicotinic acid (NA) receptor GPR109A. Ki and GTPγS EC50 of MK-6892 on the Human GPR109A is 4 nM and 16 nM, respectively. MK-6892
  11. BCC5370 AZD1283 AZD1283 is a potent antagonist of the P2Y12 receptor with EC50 of 3.0 ug/kg/min, TI >10; with binding IC50 of 11 nM. AZD1283
  12. BCC5840 Neuromedin N (rat, mouse, porcine, canine) Neuromedin N is a potent modulator of dopamine D2 receptor agonist binding in rat neostriatal membranes. Neuromedin N (rat, mouse, porcine, canine)
  13. BCC4152 GSK962040 hydrochloride Camicinal hydrochloride (GSK962040 hydrochloride) is a small molecule, selective motilin receptor agonist with pEC50 of 7.9. GSK962040 hydrochloride
  14. BCC4756 AdipoRon AdipoRon is an orally active adiponectin receptor (AdipoR) agonist, binding to AdipoR1 and AdipoR2 with Kds of 1.8 and 3.1 μM, respectively. AdipoRon
  15. BCC6318 LUF 6283 LUF 6283
  16. BCC7796 (±)-PPCC oxalate (±)-PPCC oxalate
  17. BCC6633 (S)-(-)-Atenolol (S)-(-)-Atenolol
  18. BCC6772 2-Iodomelatonin 2-Iodomelatonin is a potent agonist of melatonin receptor 1 (MT1) with a Ki value of 28 pM, it is more 5-fold selective for MT1 over MT2. 2-iodomelatonin can be used to identify, characterize and localize melatonin binding sites in the brain and peripheral tissues. 2-Iodomelatonin
  19. BCC5505 LCZ696 LCZ696 (Sacubitril/Valsartan), comprised Valsartan (an ARB) and Sacubitril (AHU377) in 1:1 molar ratio, is a first-in-class, orally bioavailable, and dual-acting angiotensin receptor-neprilysin (ARN) inhibitor for hypertension and heart failure. LCZ696 ameliorates diabetic cardiomyopathy by inhibiting inflammation, oxidative stress and apoptosis. LCZ696
  20. BCC5810 GRP (human) Gastrin-Releasing Peptide, human (GRP) belongs to the bombesin-like peptide family, and is not a classical hypothalamic-hypophyseal regulatory hormone since it plays only a perfunctory role in the mediation of pituitary hormone release. GRP (human)
  21. BCC5719 [Ac-Tyr1,D-Phe2]GRF 1-29, amide (human) [Ac-Tyr1,D-Phe2]GRF 1-29, amide (human)
  22. BCC6330 PG 106 PG 106
  23. BCC7852 MJ 15 MJ 15
  24. BCC6321 CYM 5541 CYM-5541 (ML249) is an selective and allosteric S1P3 receptor agonist with an EC50 between 72 and 132 nM. CYM 5541
  25. BCC7525 (R)-(+)-m-Nitrobiphenyline oxalate (R)-(+)-m-Nitrobiphenyline oxalate
  26. BCC1920 Salmeterol xinafoate Salmeterol xinafoate is a long-acting beta-2 adrenergic receptor (β2AR) agonist, with Ki of 1.5 nM for WT β2AR, and used for asthma treatment. Salmeterol xinafoate
  27. BCC1539 DY131 DY131(GSK 9089) is a novel selective agonist of ERRβ and ERRγ; displays minimal activity at ERRα, ERα and ERβ at concentrations up to 30 μM. DY131
  28. BCC4008 UNBS 5162 UNBS5162 is a pan-antagonist of CXCL chemokine expression, with anti-tumor activity. UNBS 5162
  29. BCC6114 MM-22 MM-22
  30. BCC4256 Betamethasone hydrochloride Betamethasone (hydrochloride) is a glucocorticoid steroid with anti-inflammatory and immunosuppressive properties. Betamethasone hydrochloride
  31. BCC4807 Nedaplatin Nedaplatin (NSC 375101D) is a derivative of cisplatin and DNA damage agent. Nedaplatin
  32. BCC4594 MPEP MPEP is a potent and highly selective non-competitive antagonist at the mGlu5 receptor subtype (IC50 = 36 nM) and a positive allosteric modulator at mGlu4 receptors. MPEP
  33. BCC5664 Metaphit Metaphit
  34. BCC7211 [D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P [D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P
  35. BCC7890 XCC XCC
  36. BCC7600 XAC XAC
  37. BCC5725 VIP (guinea pig) VIP (guinea pig)
  38. BCC4345 Cisatracurium Besylate Cisatracurium besylate (51W89) is a nondepolarizing neuromuscular blocking agent, antagonizing the action of acetylcholine by inhibiting neuromuscular transmission. Cisatracurium Besylate
  39. BCC6812 DTG Ditolylguanidine (1,3-Di-o-tolylguanidine) is an agonist of sigma receptor (σ1/σ2 receptor). DTG
  40. BCC6696 α-Methyl-5-hydroxytryptamine maleate α-Methyl-5-hydroxytryptamine maleate
  41. BCC5422 Eltoprazine hydrochloride Eltoprazine(DU28853) is a serenic or antiaggressive agent which as an agonist at the 5-HT1A and 5-HT1B receptors and as an antagonist at the 5-HT2C receptor. Eltoprazine hydrochloride
  42. BCC5421 Eltoprazine Eltoprazine hydrochloride (DU 28853 hydrochloride) is a serenic or antiaggressive agent which as an agonist at the 5-HT1A and 5-HT1B receptors and as an antagonist at the 5-HT2C receptor. Eltoprazine
  43. BCC6519 Metoprolol Succinate Metoprolol Succinate (Toprol XL) is a selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension. Metoprolol Succinate
  44. BCC7951 3,5-DHBA 3,5-Dihydroxybenzoic acid a potential biomarker for the consumption of many food products, including beer, nuts, peanut, and pulses. 3,5-DHBA
  45. BCC5768 Proglumide sodium salt Proglumide sodium is a nonpeptide and orally active cholecystokinin (CCK)-A/B receptors antagonist. Proglumide sodium selective blocks CCK’s effects in the central nervous system (CNS). Proglumide sodium has ability to inhibit gastric secretion and to protect the gastroduodenal mucosa. Proglumide sodium also has antiepileptic and antioxidant activities. Proglumide sodium salt

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