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)
- GC151401-oleoyl-2-hydroxy-sn-glycero-3-phosphate (sodium salt)CAS: 325465-93-8纯度: >95.00% / >99.00% / >98.00%
1-油酰基溶血磷脂酸(1-油酰基-sn-甘油-3-磷酸)钠作为一种有效的生物活性磷脂,是LPA受体激活剂[2]。
- GC15428H2L 5765834CAS: 420841-84-5纯度: >99.00%
H2L 5765834 是溶血磷脂酸受体 LPA1、LPA3 和 LPA5 的拮抗剂,IC50 分别为 94、752 和 463 nM。
- GC15505MethylprednisoloneCAS: 83-43-2纯度: >99.50% / >98.00%
甲泼尼龙是皮质类固醇,可作用于糖皮质激素受体并抑制皮质醇分泌,其IC50为1.7ng/ml。
- GC15653PF-05212384 (PKI-587)CAS: 1197160-78-3纯度: >98.00%
PF-05212384 (PKI-587) 是一种高效的PI3K/mTOR双重抑制剂,对PI3Kα(IC 50 =0.4nM)、PI3Kβ(IC 50 =6nM)、PI3Kγ(IC 50 =8nM)、PI3Kδ(IC 50 =6nM)和mTOR(IC 50 =1.4nM)都具有抑制效果。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC15107 | Clomipramine HCl | 17321-77-6 | >99.00% | |
A tricyclic antidepressant | ||||
| GC15121 | Lasmiditan | 439239-90-4 | - | |
An Analytical Reference Standard | ||||
| GC15140 | 1-oleoyl-2-hydroxy-sn-glycero-3-phosphate (sodium salt) | 325465-93-8 | >95.00% / >99.00% / >98.00% | |
1-油酰基溶血磷脂酸(1-油酰基-sn-甘油-3-磷酸)钠作为一种有效的生物活性磷脂,是LPA受体激活剂[2]。 | ||||
| GC15144 | (±)-PPCC oxalate | 932736-90-8 | - | |
sigma (σ) receptor ligand | ||||
| GC15153 | Almotriptan Malate | 181183-52-8 | >98.00% | |
An agonist of 5-HT 1B and 5-HT 1D receptors | ||||
| GC15220 | AM095 | 1345614-59-6 | >99.50% | |
AM095是一种选择性、具有口服活性的LPA1受体拮抗剂,对小鼠LPA1的IC 50 值为0.73μM。 | ||||
| GC15223 | Tropisetron Hydrochloride | 105826-92-4 | >99.50% | |
A 5-HT 3 receptor antagonist | ||||
| GC15317 | SB408124 | 288150-92-5 | >98.50% | |
A potent orexin 1 receptor antagonist | ||||
| GC15331 | Prednisolone | 50-24-8 | >98.00% | |
The active metabolite of prednisone | ||||
| GC15332 | Ticagrelor | 274693-27-5 | >99.50% | |
A reversible purinergic P2Y 12 receptor antagonist | ||||
| GC15374 | BD 1047 dihydrobromide | 138356-21-5 | >98.00% | |
A selective antagonist of σ 1 receptors | ||||
| GC15414 | AM1241 | 444912-48-5 | - | |
AM1241是一种氨基烷基吲哚类似物,是II型大麻素受体(CB2)的选择性配体,对CB2受体的亲和力(K i =3.4nM)高于对CB1受体(K i =280nM)。 | ||||
| GC15428 | H2L 5765834 | 420841-84-5 | >99.00% | |
H2L 5765834 是溶血磷脂酸受体 LPA1、LPA3 和 LPA5 的拮抗剂,IC50 分别为 94、752 和 463 nM。 | ||||
| GC15463 | Iloperidone | 133454-47-4 | >99.50% | |
An atypical antipsychotic | ||||
| GC15465 | N-[2-(Piperidinylamino)ethyl]-4-iodobenzamide | 155054-42-5 | - | |
σ-1 selective ligand | ||||
| GC15489 | RS 504393 | 300816-15-3 | >98.00% | |
RS 504393是一种选择性的CCR2趋化因子受体拮抗剂,对人类重组CCR2受体和CCR1受体的IC 50 值分别为89nM和100μM。 | ||||
| GC15505 | Methylprednisolone | 83-43-2 | >99.50% / >98.00% | |
甲泼尼龙是皮质类固醇,可作用于糖皮质激素受体并抑制皮质醇分泌,其IC50为1.7ng/ml。 | ||||
| GC15534 | SB-674042 | 483313-22-0 | >99.50% | |
A potent and selective orexin 1 receptor antagonist | ||||
| GC15574 | Taranabant | 701977-09-5 | >99.00% | |
A CB 1 receptor inverse agonist | ||||
| GC15575 | Tolvaptan | 150683-30-0 | >98.00% | |
A vasopressin V 2 receptor antagonist | ||||
| GC15629 | Tizanidine | 51322-75-9 | - | |
An α 2 -adrenergic receptor agonist | ||||
| GC15653 | PF-05212384 (PKI-587) | 1197160-78-3 | >98.00% | |
PF-05212384 (PKI-587) 是一种高效的PI3K/mTOR双重抑制剂,对PI3Kα(IC 50 =0.4nM)、PI3Kβ(IC 50 =6nM)、PI3Kγ(IC 50 =8nM)、PI3Kδ(IC 50 =6nM)和mTOR(IC 50 =1.4nM)都具有抑制效果。 | ||||
| GC15668 | Meprednisone | 1247-42-3 | >99.50% | |
A corticosteroid | ||||
| GC15687 | Azasetron HCl | 123040-16-4 | >98.00% | |
A 5-HT 3 receptor antagonist | ||||
