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)
- GC13814Adrenalone HClCAS: 62-13-5纯度: >98.00%
Decoyinine (Angustmycin A), a specific inhibitor of bacterial GMPS, has been isolated from Streptomyces .
- GC13906Nebivolol hydrochlorideCAS: 152520-56-4纯度: >99.50% / >98.00%
Nebivolol hydrochloride是第三代β1肾上腺素受体选择性拮抗剂,Nebivolol hydrochloride通过高选择性阻断β1受体并激活一氧化氮(NO)介导的血管扩张双重机制发挥降压作用,同时对外周血管阻力、代谢及性功能影响。
- GC14033ICI 118,551 hydrochlorideCAS: 72795-01-8纯度: >98.00% / >99.50%
ICI 118,551 hydrochloride是一种选择性β2-肾上腺素受体拮抗剂。
- GC14350CYM 50358 hydrochloride纯度: >97.00%
CYM 50358 hydrochloride是一种有效的、选择性的鞘氨醇-1-磷酸4(S1P4)受体拮抗剂,通过拮抗S1P4受体发挥作用。
- GC14518Asenapine hydrochlorideCAS: 1412458-61-7纯度: >99.50%
Asenapine hydrochloride 是一种抗精神病药,是一种 5-HT (1A, 1B, 2A, 2B, 2C, 5A, 6, 7) 和多巴胺 (D2, D3, D4) 受体拮抗剂,Ki 值为 0.03-4.0 nM,作用 5- HT 和多巴胺受体分别为 1.3、0.42、1.1 nM。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC13747 | Vilanterol | 503068-34-6 | - | |
A β 2 -AR agonist | ||||
| GC13814 | Adrenalone HCl | 62-13-5 | >98.00% | |
Decoyinine (Angustmycin A), a specific inhibitor of bacterial GMPS, has been isolated from Streptomyces . | ||||
| GC13871 | Duloxetine HCl | 136434-34-9 | >99.50% | |
A serotonin and norepinephrine reuptake inhibitor | ||||
| GC13906 | Nebivolol hydrochloride | 152520-56-4 | >99.50% / >98.00% | |
Nebivolol hydrochloride是第三代β1肾上腺素受体选择性拮抗剂,Nebivolol hydrochloride通过高选择性阻断β1受体并激活一氧化氮(NO)介导的血管扩张双重机制发挥降压作用,同时对外周血管阻力、代谢及性功能影响。 | ||||
| GC13911 | S1RA hydrochloride | 1265917-14-3 | >99.00% | |
A σ 1 receptor antagonist | ||||
| GC13966 | CS 2100 | 913827-99-3 | - | |
CS 2100 (Compound 10b) 是一种有效的、选择性的、口服活性的和 S1P3 保留的 S1P1 激动剂,对人 S1P1 的 EC50 为 4.0 nM。 | ||||
| GC13974 | Salbutamol Sulfate | 51022-70-9 | >98.00% | |
A β 2 -AR agonist | ||||
| GC13993 | Terazosin HCl | 70024-40-7 | >99.50% | |
A potent and selective α 1 -AR antagonist | ||||
| GC14021 | Betaxolol | 63659-18-7 | >99.00% | |
An Analytical Reference Standard | ||||
| GC14032 | Clonidine HCl | 4205-91-8 | >99.50% | |
An α 2 -adrenergic receptor agonist | ||||
| GC14033 | ICI 118,551 hydrochloride | 72795-01-8 | >98.00% / >99.50% | |
ICI 118,551 hydrochloride是一种选择性β2-肾上腺素受体拮抗剂。 | ||||
| GC14067 | Prasugrel hydrochloride | 389574-19-0 | >99.50% | |
A prodrug form of R-99224 | ||||
| GC14145 | (R,R)-Formoterol | 67346-49-0 | >98.00% | |
β2-selective adrenergic agonist | ||||
| GC14160 | Blonanserin | 132810-10-7 | >98.50% | |
A dopamine and serotonin receptor antagonist | ||||
| GC14220 | Scopine | 498-45-3 | >98.00% | |
A metabolite of scopolamine | ||||
| GC14262 | Desvenlafaxine Succinate | 386750-22-7 | >99.50% | |
An active metabolite of venlafaxine | ||||
| GC14350 | CYM 50358 hydrochloride | - | >97.00% | |
CYM 50358 hydrochloride是一种有效的、选择性的鞘氨醇-1-磷酸4(S1P4)受体拮抗剂,通过拮抗S1P4受体发挥作用。 | ||||
| GC14412 | CCG-63808 | 620113-73-7 | - | |
CCG-63808 是 G 蛋白信号 (RGS) 蛋白调节剂的可逆抑制剂。 | ||||
| GC14436 | H2L5186303 | 139262-76-3 | >98.00% | |
H2L5186303是一种选择性的溶血磷脂酸2受体(LPA2;IC₅₀=9nM)的拮抗剂。 | ||||
| GC14437 | Vortioxetine (Lu AA21004) HBr | 960203-27-4 | >99.50% | |
A multimodal serotonergic agent | ||||
| GC14512 | Fenspiride HCl | 5053-08-7 | >99.50% | |
A histamine H 1 receptor antagonist | ||||
| GC14518 | Asenapine hydrochloride | 1412458-61-7 | >99.50% | |
Asenapine hydrochloride 是一种抗精神病药,是一种 5-HT (1A, 1B, 2A, 2B, 2C, 5A, 6, 7) 和多巴胺 (D2, D3, D4) 受体拮抗剂,Ki 值为 0.03-4.0 nM,作用 5- HT 和多巴胺受体分别为 1.3、0.42、1.1 nM。 | ||||
| GC14532 | TC-G 1006 | 1324003-64-6 | >99.50% | |
S1P1 Agonist III 是一种有效且具有口服活性的 S1P1 激动剂,EC50 为 18 nM; S1P3 上没有活动。 | ||||
| GC14536 | Metoprolol Tartrate | 56392-17-7 | - | |
An Analytical Reference Standard | ||||
