GPCR/G protein
GPCR/G protein(G 蛋白偶联受体/G 蛋白)
- Neuropeptide FF/AF Receptors(49)
- Formyl Peptide Receptors(11)
- 5-HT Receptor(504)
- Acetylcholine(29)
- Adenosine Deaminase(9)
- Adenosine Receptor(132)
- Adenosine Kinase(4)
- Adiponectin Receptor(3)
- Adrenergic Receptor(421)
- Adrenergic Transporters(5)
- Apelin Receptor(9)
- Angiotensin Receptor(114)
- Bombesin Receptors(23)
- Bradykinin Receptors(29)
- Calcitonin and Related Receptors(10)
- Cannabinoid Receptor(160)
- Calcimimetic Agent(2)
- CaSR(20)
- CCK1 Receptors(7)
- CCK2 Receptors(7)
- CCR(81)
- Chemokine Receptors(25)
- CRF1 Receptors(9)
- CRF2 Receptors(3)
- CXCR(80)
- CysLT1 receptor(1)
- Endothelin Receptor(52)
- EP1 Receptor(2)
- EP4 Receptor(3)
- ERRγ(1)
- ETA Receptors(5)
- ETB Receptors(5)
- Free Fatty Acid Receptors(18)
- Galanin Receptors(11)
- Ghrelin Receptors(12)
- GHSR(21)
- GIP Receptor(5)
- Glucagon Receptor(61)
- Glucocorticoid Receptor(97)
- GLUT1(1)
- Gonadotropin-Releasing Hormone Receptors(3)
- GPCR19(12)
- GPR109A(4)
- GPR119(10)
- GPR120(9)
- GPR35(10)
- GPR44(1)
- GPR55(11)
- Hydroxycarboxylic Acid Receptors(5)
- Leukotriene Receptor(58)
- LPA Receptor(12)
- LPL Receptor(60)
- LTD4 Receptor(1)
- mGluR (119)
- Melanin-concentrating Hormone Receptors(7)
- Melanocortin (MC) Receptors(58)
- Melatonin Receptors(24)
- Motilin Receptor(7)
- MT Receptor(1)
- Non-selective CRF(7)
- Neurotensin Receptors(24)
- NK2 Receptors(7)
- NK3 Receptor(6)
- NOP Receptor(20)
- NPY Receptors(28)
- Orexin(3)
- Orphan 7-TM Receptors(6)
- OX Receptor(48)
- Oxytocin Receptors(22)
- P2Y Receptor(62)
- PACAP Receptors(3)
- PAF Receptors(8)
- Peptide Receptors(14)
- PGD2 Receptor(1)
- Prostaglandin Receptor(172)
- Protease-Activated Receptors(10)
- Prostanoid Receptors
- RGS(2)
- S1P receptor(8)
- Secretin Receptors(1)
- Sensory Neuron-Specific Receptors(1)
- Somatostatin Receptor(39)
- Sigma Receptor(59)
- Vasopressin Receptor(35)
- 17,20-lyase(5)
- Ras(142)
- Urotensin-II Receptor(11)
- VIP Receptors(7)
- EBI2/GPR183(7)
- TSH Receptor(11)
- NK Receptor(1)
- GPR81(1)
- C3aR(1)
- CysLT2 receptor(1)
- S1P receptor inhibitor(22)
- CCKB(1)
- FFAR1 (GPR40)(20)
- GPR84(8)
- Neuromedin U Receptors(2)
- Kisspeptin Receptor(5)
- CRFR(25)
- RGS Protein(5)
- Urotensin Receptor(6)
- Cholecystokinin Receptor(25)
- GPR139(4)
- mAChR(185)
- MCHR1 (GPR24)(16)
- Neurokinin Receptor(75)
- Neuropeptide S Receptor(1)
- GPBA Receptor(1)
- Trace Amine 1 Receptor(2)
- GPCR protein(1)
- FFAR3(1)
- cGMP(27)
- GRK(1)
- GPR88
- Amylin Receptor
- Arrestin
- GCGR(2)
- GLP Receptor(2)
- Mas-related G-protein-coupled Receptor (MRGPR)
- Succinate Receptor 1
- PTHR(1)
- Protease Activated Receptor (PAR)(2)
- Free Fatty Acid Receptor(1)
- Formyl Peptide Receptor (FPR)(1)
GPCR/G protein 相关产品(3377)
- GC25728PF-4136309CAS: 857679-55-1
PF-4136309 (INCB8761, PF-04136309) is a potent, selective, and orally bioavailable CCR2 antagonist with an IC50 of 5.2 nM for human CCR2.
- GC25756PirenperoneCAS: 75444-65-4
Pirenperone (R-47456, R-50656), a quinazoline derivative, is a selective antagonist of SR-2A (5-HT2 serotonin receptor) when employed in low doses. Pirenperone behaves like a typical neuroleptic when used in higher doses (greater than 0.1 mg/kg).
- GC25786PropafenoneCAS: 54063-53-5
Propafenone (SA-79) is an orally active sodium channel blocking agent and a beta-adrenoceptor (β-adrenergic receptor) antagonist. Propafenone offers a broad spectrum of activity in the treatment of cardiac arrhythmias.
- GC25898SB 200646CAS: 143797-63-1
SB 200646 (SB 200646A) is a potent, selective and oral-active antagonist of 5-HT2B/2C over 5-HT2A receptor with 50 fold selectivity. The pKi for rat 5-HT2C receptor, rat 5-HT2B receptor and rat 5-HT2A receptor are 6.9, 7.5 and 5.2, respectively. SB 200646 has electrophysiological and anxiolytic properties in vivo.
- GC26016TSHR antagonist S37CAS: 1217616-61-9
TSHR antagonist S37 is a selective and competitive antagonist of the thyrotropin receptor (TSHR).
- GC30008Ceruletide (Caerulein)CAS: 17650-98-5纯度: >99.50%
Ceruletide 作为一种十肽和一种有效的胆囊收缩剂,对人类和动物的胆囊肌肉和胆管具有直接的痉挛作用。
- GC30092Salmeterol (GR33343X)CAS: 89365-50-4纯度: >99.50%
Salmeterol (Astmerole, GR-33343X, SN408D) is a long-acting beta2-adrenergic receptor agonist with Ki value of 1.5 nM for WT β2AR and shows very high selectivity for the WT β2AR(β1Ki/β2Ki ratio of approximately 1500).
- GC30104Fezolinetant (ESN-364)CAS: 1629229-37-3纯度: >98.00%
Fezolinetant (ESN-364) 是一种神经激肽 3 受体 (NK3R) 的拮抗剂,用于治疗更年期潮热。
- GC30194JNJ-10229570CAS: 524923-88-4纯度: >98.00%
JNJ-10229570 (UNII-N9IX402L35) is a potent MC1R and MC5R antagonist.
- GC30206Roluperidone (CYR-101)CAS: 359625-79-9纯度: >99.50%
A dual antagonist of 5-HT 2A and σ 2 receptors
- GC30273Tedatioxetine hydrobromide (Lu AA 24530 hydrobromide)CAS: 960151-65-9纯度: >99.50%
Tedatioxetine (Lu AA24530) hydrobromide 可作为 5-HT2A、5-HT2C、5-HT3 和 α;1A-肾上腺素受体拮抗剂,可作为 5-羟色胺和去甲肾上腺素 (NE) 的首选三重再摄取抑制剂 (TRI)。
- GC30280Chlorpromazine D6 hydrochlorideCAS: 1228182-46-4纯度: >99.50%
Chlorpromazine D6 hydrochloride是 Chlorpromazine 的氘代物,可被用于 NMR、GC-MS 或 LC-MS 分析中的内标品,用于定量分析。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC25728 | PF-4136309 | 857679-55-1 | - | |
PF-4136309 (INCB8761, PF-04136309) is a potent, selective, and orally bioavailable CCR2 antagonist with an IC50 of 5.2 nM for human CCR2. | ||||
| GC25756 | Pirenperone | 75444-65-4 | - | |
Pirenperone (R-47456, R-50656), a quinazoline derivative, is a selective antagonist of SR-2A (5-HT2 serotonin receptor) when employed in low doses. Pirenperone behaves like a typical neuroleptic when used in higher doses (greater than 0.1 mg/kg). | ||||
| GC25786 | Propafenone | 54063-53-5 | - | |
Propafenone (SA-79) is an orally active sodium channel blocking agent and a beta-adrenoceptor (β-adrenergic receptor) antagonist. Propafenone offers a broad spectrum of activity in the treatment of cardiac arrhythmias. | ||||
| GC25898 | SB 200646 | 143797-63-1 | - | |
SB 200646 (SB 200646A) is a potent, selective and oral-active antagonist of 5-HT2B/2C over 5-HT2A receptor with 50 fold selectivity. The pKi for rat 5-HT2C receptor, rat 5-HT2B receptor and rat 5-HT2A receptor are 6.9, 7.5 and 5.2, respectively. SB 200646 has electrophysiological and anxiolytic properties in vivo. | ||||
| GC26002 | Trazodone | 19794-93-5 | >98.00% | |
Trazodone (AF-1161) is a 5-HT 2A/2C receptor antagonist that is used as an antidepressant for treating major depressive disorder and anxiety disorders. | ||||
| GC26016 | TSHR antagonist S37 | 1217616-61-9 | - | |
TSHR antagonist S37 is a selective and competitive antagonist of the thyrotropin receptor (TSHR). | ||||
| GC26027 | V-0219 | 878453-71-5 | - | |
V-0219 is an orally active, positive allosteric modulator (PAM) of the glucagon-like peptide-1 receptor (GLP-1R), can be used for obesity-associated diabetes research. | ||||
| GC26069 | WAY-639889 | 432506-24-6 | - | |
WAY-639889 is a bioactive compound relative to neuropeptide Y-5. | ||||
| GC26144 | Menthol | 1490-04-6 | - | |
Menthol 是个天然的止痛剂。Menthol 通过抑制神经元细胞膜的 Ca ++ 电流,刺激冷感受器,从而产生凉的感觉。 | ||||
| GC30008 | Ceruletide (Caerulein) | 17650-98-5 | >99.50% | |
Ceruletide 作为一种十肽和一种有效的胆囊收缩剂,对人类和动物的胆囊肌肉和胆管具有直接的痉挛作用。 | ||||
| GC30058 | GLP-1(7-37) | 106612-94-6 | >99.50% | |
GLP-1(7-37)是一种截短的胰高血糖素样肽,对GLP-1受体的EC 50 值为0.9 ± 0.1nM。 | ||||
| GC30068 | Taprenepag (CP-544326) | 752187-80-7 | >99.50% | |
A potent EP 2 receptor agonist | ||||
| GC30092 | Salmeterol (GR33343X) | 89365-50-4 | >99.50% | |
Salmeterol (Astmerole, GR-33343X, SN408D) is a long-acting beta2-adrenergic receptor agonist with Ki value of 1.5 nM for WT β2AR and shows very high selectivity for the WT β2AR(β1Ki/β2Ki ratio of approximately 1500). | ||||
| GC30095 | SB-423562 | 351490-27-2 | >99.50% | |
SB-423562是一种短效的(CaR)拮抗剂。 | ||||
| GC30104 | Fezolinetant (ESN-364) | 1629229-37-3 | >98.00% | |
Fezolinetant (ESN-364) 是一种神经激肽 3 受体 (NK3R) 的拮抗剂,用于治疗更年期潮热。 | ||||
| GC30188 | Dapiprazole hydrochloride | 72822-13-0 | >99.50% | |
An α-adrenergic receptor antagonist | ||||
| GC30194 | JNJ-10229570 | 524923-88-4 | >98.00% | |
JNJ-10229570 (UNII-N9IX402L35) is a potent MC1R and MC5R antagonist. | ||||
| GC30198 | Dolasetron Mesylate hydrate | 878143-33-0 | >99.00% | |
A 5-HT 3 receptor antagonist | ||||
| GC30206 | Roluperidone (CYR-101) | 359625-79-9 | >99.50% | |
A dual antagonist of 5-HT 2A and σ 2 receptors | ||||
| GC30224 | FPTQ | 864863-72-9 | >99.50% | |
FPTQ是mGluR1拮抗剂,在人和老鼠上IC50是6nM和4nM | ||||
| GC30254 | HAEGTFT | 926018-95-3 | >99.00% | |
HAEGTFT是GLP-1多肽N-端的1-7残基。 | ||||
| GC30273 | Tedatioxetine hydrobromide (Lu AA 24530 hydrobromide) | 960151-65-9 | >99.50% | |
Tedatioxetine (Lu AA24530) hydrobromide 可作为 5-HT2A、5-HT2C、5-HT3 和 α;1A-肾上腺素受体拮抗剂,可作为 5-羟色胺和去甲肾上腺素 (NE) 的首选三重再摄取抑制剂 (TRI)。 | ||||
| GC30280 | Chlorpromazine D6 hydrochloride | 1228182-46-4 | >99.50% | |
Chlorpromazine D6 hydrochloride是 Chlorpromazine 的氘代物,可被用于 NMR、GC-MS 或 LC-MS 分析中的内标品,用于定量分析。 | ||||
| GC30299 | GSK726701A | 945721-87-9 | >98.50% | |
GSK726701A是前列腺素E2受体4(EP4)的部分激动剂,pEC50为7.4。 | ||||
