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)
- GC37973ZT-12-037-01CAS: 2328073-61-4纯度: >98.00%
ZT-12-037-01 is a specific and ATP-competitive STK19 inhibitor with IC50s of 23.96 nM and 27.94 nM for STK19 (WT) and STK19 (D89N), respectively. It displays extremely high kinase selectivity using KINOMEscan against a panel of 468 diverse kinases using an in vitro ATP-site competition binding assay at 1 μM.
- GC37983β3-AR agonist 1CAS: 1283125-73-4
β3-AR agonist 1 (compound 15) 是一种高效选择性的,可口服的 β3-肾上腺素能受体 (β3-AR) 激动剂 (EC50=18 nM),对 β1-、β2-、α1A-AR 无活性 (β1/β3, β2/β3, α1A/β3>556倍)。
- GC38007β-Melanocyte Stimulating Hormone (MSH), human TFA纯度: >99.50%
β-Melanocyte Stimulating Hormone (MSH), human TFA, 是一个 22 肽,是一种内源性黑皮质素-4 受体 (melanocortin-4 receptor; MC4-R) 激动剂。
- GC38013[Sar9,Met(O2)11]-Substance P TFACAS: 2828433-10-7纯度: >99.50%
[Sar9,Met(O2)11]-Substance P TFA 是一种选择性的速激肽 NK1 受体激动剂。
- GC38038Sigma-1 receptor antagonist 1CAS: 1639220-19-1纯度: >99.50%
Sigma?1 receptor antagonist 1 (compound 137) 是一种高效选择性的 sigma-1 受体 (σ1R) 拮抗剂,对 σ1R 具有高亲和力 (Ki = 1.06 nM)。Sigma?1 receptor antagonist 1 具有抗神经痛活性,有作为治疗神经性疼痛药物的前景。
- GC38039Sigma-1 receptor antagonist 2CAS: 1639220-15-7纯度: >99.50%
Sigma-1 receptor antagonist 2 是一种有效的选择性 sigma 1 受体 (σ1R) 拮抗剂,对 σ1 和 σ2 受体的 Ki 分别为 3.88 和 1288 nM。
- GC38048Sigma-1 receptor antagonist 3CAS: 1639220-17-9纯度: >99.00%
Sigma-1 receptor antagonist 3 (化合物 135) 是有效的,选择性 Sigma-1 (σ1) 受体拮抗剂,Ki 为 1.14 nM。Sigma-1 receptor antagonist 3 抑制 hERG,IC50 为 1.54μM。Sigma-1 receptor antagonist 3 用于治疗神经性疼痛。
- GC38099HigenamineCAS: 5843-65-2
Demethyl-Coclaurine (Higenamine, Norcoclaurine), the key component of the Chinese herb aconite root, is a beta-2 adrenergic receptor (β2-AR) agonist. Demethyl-Coclaurine stimulates AKT phosphorylation and requires PI3K activation for the anti-apoptotic effect in cardiomyocytes.
- GC38104A2aR/A2bR antagonist-1CAS: 2239273-34-6纯度: >99.50%
An adenosine A 2A and A 2B receptor dual antagonist
- GC38107SNT-207858 free baseCAS: 1104662-66-9纯度: >98.00%
SNT-207858 free base 是一种选择性,能透过血脑屏障的,有口服活性的黑皮质素 (melanocortin; MC-4) 受体拮抗剂,SNT-207858 free base 抑制与 MC-4 受体结合,IC50 为 22 nM。SNT-207858 抑制 MC-4 活性,IC50 为 11 nM。
- GC381082-Methyl-5-HTCAS: 78263-90-8纯度: >98.00% / >95.00%
2-Methyl-5-HT (2-Methyl-5-hydroxytryptamine) 是一种有效的选择性 5-HT3 受体激动剂。2-Methyl-5-HT 显示出抗抑郁样作用。
- GC38111Rac-VU 6008667CAS: 2092917-63-8
Rac-VU 6008667 是毒蕈碱乙酰胆碱受体亚型 5 (M5 NAM) 的选择性负变构调节剂,对于人和大鼠的 IC50 值分别为 1.2 μM 和 1.6 μM。Rac-VU 6008667 具有高 CNS 渗透性。
- GC38133Tirzepatide (TFA)
Tirzepatide TFA (LY3298176 TFA) 是葡萄糖依赖性胰岛素营养多肽 (GIP) 和胰高血糖素样肽-1 (GLP-1) 受体双重激动剂,正在开发用于治疗 2 型糖尿病。
- GC38217VUF11207 fumarateCAS: 1785665-61-3纯度: >98.50%
VUF11207 fumarate是一种高效的趋化因子受体CXCR7激动剂(pK i =8.1),VUF11207 fumarate能够有效诱导CXCR7与其下游效应蛋白β-arrestin2的募集(pEC 50 =8.8),并促进受体的内化过程(pEC 50 =7.9)。
- GC38237Higenamine hydrochlorideCAS: 11041-94-4纯度: >99.00%
Higenamine (Norcoclaurine, (+-)-Demethylcoclaurine), also known as Norcoclaurine HCl, is a non-selective β2 adrenoceptor agonist which is a chemical compound naturally occurring in a number of plants.
- GC38352Orexin A (human, rat, mouse) (TFA)纯度: >99.00%
Orexin A human, rat, mouse TFA 是一种 33 氨基酸兴奋性神经肽。Orexin A human, rat, mouse TFA 作用于 2 种特异性 G 蛋白偶联体 (GPCR):orexin-1 (OX1) 和 orexin-2 (OX2)。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC37969 | Ziprasidone D8 | 1126745-58-1 | - | |
An internal standard for the quantification of ziprasidone | ||||
| GC37973 | ZT-12-037-01 | 2328073-61-4 | >98.00% | |
ZT-12-037-01 is a specific and ATP-competitive STK19 inhibitor with IC50s of 23.96 nM and 27.94 nM for STK19 (WT) and STK19 (D89N), respectively. It displays extremely high kinase selectivity using KINOMEscan against a panel of 468 diverse kinases using an in vitro ATP-site competition binding assay at 1 μM. | ||||
| GC37983 | β3-AR agonist 1 | 1283125-73-4 | - | |
β3-AR agonist 1 (compound 15) 是一种高效选择性的,可口服的 β3-肾上腺素能受体 (β3-AR) 激动剂 (EC50=18 nM),对 β1-、β2-、α1A-AR 无活性 (β1/β3, β2/β3, α1A/β3>556倍)。 | ||||
| GC38007 | β-Melanocyte Stimulating Hormone (MSH), human TFA | - | >99.50% | |
β-Melanocyte Stimulating Hormone (MSH), human TFA, 是一个 22 肽,是一种内源性黑皮质素-4 受体 (melanocortin-4 receptor; MC4-R) 激动剂。 | ||||
| GC38013 | [Sar9,Met(O2)11]-Substance P TFA | 2828433-10-7 | >99.50% | |
[Sar9,Met(O2)11]-Substance P TFA 是一种选择性的速激肽 NK1 受体激动剂。 | ||||
| GC38029 | DHPG | 146255-66-5 | >99.00% / >99.50% | |
An agonist of group I mGluRs | ||||
| GC38038 | Sigma-1 receptor antagonist 1 | 1639220-19-1 | >99.50% | |
Sigma?1 receptor antagonist 1 (compound 137) 是一种高效选择性的 sigma-1 受体 (σ1R) 拮抗剂,对 σ1R 具有高亲和力 (Ki = 1.06 nM)。Sigma?1 receptor antagonist 1 具有抗神经痛活性,有作为治疗神经性疼痛药物的前景。 | ||||
| GC38039 | Sigma-1 receptor antagonist 2 | 1639220-15-7 | >99.50% | |
Sigma-1 receptor antagonist 2 是一种有效的选择性 sigma 1 受体 (σ1R) 拮抗剂,对 σ1 和 σ2 受体的 Ki 分别为 3.88 和 1288 nM。 | ||||
| GC38048 | Sigma-1 receptor antagonist 3 | 1639220-17-9 | >99.00% | |
Sigma-1 receptor antagonist 3 (化合物 135) 是有效的,选择性 Sigma-1 (σ1) 受体拮抗剂,Ki 为 1.14 nM。Sigma-1 receptor antagonist 3 抑制 hERG,IC50 为 1.54μM。Sigma-1 receptor antagonist 3 用于治疗神经性疼痛。 | ||||
| GC38099 | Higenamine | 5843-65-2 | - | |
Demethyl-Coclaurine (Higenamine, Norcoclaurine), the key component of the Chinese herb aconite root, is a beta-2 adrenergic receptor (β2-AR) agonist. Demethyl-Coclaurine stimulates AKT phosphorylation and requires PI3K activation for the anti-apoptotic effect in cardiomyocytes. | ||||
| GC38104 | A2aR/A2bR antagonist-1 | 2239273-34-6 | >99.50% | |
An adenosine A 2A and A 2B receptor dual antagonist | ||||
| GC38107 | SNT-207858 free base | 1104662-66-9 | >98.00% | |
SNT-207858 free base 是一种选择性,能透过血脑屏障的,有口服活性的黑皮质素 (melanocortin; MC-4) 受体拮抗剂,SNT-207858 free base 抑制与 MC-4 受体结合,IC50 为 22 nM。SNT-207858 抑制 MC-4 活性,IC50 为 11 nM。 | ||||
| GC38108 | 2-Methyl-5-HT | 78263-90-8 | >98.00% / >95.00% | |
2-Methyl-5-HT (2-Methyl-5-hydroxytryptamine) 是一种有效的选择性 5-HT3 受体激动剂。2-Methyl-5-HT 显示出抗抑郁样作用。 | ||||
| GC38111 | Rac-VU 6008667 | 2092917-63-8 | - | |
Rac-VU 6008667 是毒蕈碱乙酰胆碱受体亚型 5 (M5 NAM) 的选择性负变构调节剂,对于人和大鼠的 IC50 值分别为 1.2 μM 和 1.6 μM。Rac-VU 6008667 具有高 CNS 渗透性。 | ||||
| GC38112 | MRS-1191 | 185222-90-6 | >98.50% | |
MRS-1191 是一种有效的选择性的 A3 腺苷受体 (A3 adenosine receptor ) 拮抗剂,其 KB 值为 92 nM,对人 A3 受体的 Ki 值为 31.4 nM,对 CHO 细胞的 IC50 值为 120 nM。 | ||||
| GC38132 | Tirzepatide hydrochloride | - | >99.50% | |
Tirzepatide是一种双GIP和GLP-1受体激动剂,可以改善血糖控制和减轻体重。 | ||||
| GC38133 | Tirzepatide (TFA) | - | - | |
Tirzepatide TFA (LY3298176 TFA) 是葡萄糖依赖性胰岛素营养多肽 (GIP) 和胰高血糖素样肽-1 (GLP-1) 受体双重激动剂,正在开发用于治疗 2 型糖尿病。 | ||||
| GC38147 | Etelcalcetide hydrochloride | 1334237-71-6 | >98.00% | |
A peptide agonist of CaSR | ||||
| GC38148 | Etelcalcetide | 1262780-97-1 | - | |
A peptide agonist of CaSR | ||||
| GC38204 | SX-682 | 1648843-04-2 | >98.50% / >98.00% | |
SX-682是一种口服生物可利用的小分子CXCR1和CXCR2抑制剂,IC 50 值分别为31nM和21nM。 | ||||
| GC38217 | VUF11207 fumarate | 1785665-61-3 | >98.50% | |
VUF11207 fumarate是一种高效的趋化因子受体CXCR7激动剂(pK i =8.1),VUF11207 fumarate能够有效诱导CXCR7与其下游效应蛋白β-arrestin2的募集(pEC 50 =8.8),并促进受体的内化过程(pEC 50 =7.9)。 | ||||
| GC38227 | Gamma-Mangostin | 31271-07-5 | >99.50% | |
A xanthone with diverse biological activities | ||||
| GC38237 | Higenamine hydrochloride | 11041-94-4 | >99.00% | |
Higenamine (Norcoclaurine, (+-)-Demethylcoclaurine), also known as Norcoclaurine HCl, is a non-selective β2 adrenoceptor agonist which is a chemical compound naturally occurring in a number of plants. | ||||
| GC38352 | Orexin A (human, rat, mouse) (TFA) | - | >99.00% | |
Orexin A human, rat, mouse TFA 是一种 33 氨基酸兴奋性神经肽。Orexin A human, rat, mouse TFA 作用于 2 种特异性 G 蛋白偶联体 (GPCR):orexin-1 (OX1) 和 orexin-2 (OX2)。 | ||||
