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)
- GC34270Neuropeptide Y (29-64), amide, human TFA
NeuropeptideY(29-64),amide,human(TFA)和阿尔兹海默症相关,能够保护老鼠皮质神经元对抗淀粉样蛋白毒性。
- GC34304Befiradol hydrochloride (NLX-112 (hydrochloride))
Befiradolhydrochloride(NLX-112hydrochloride)是选择性的5-羟色胺1A(5-HT)1A受体激动剂。
- GC34326H-Val-Pro-Pro-OH TFACAS: 2828433-08-3纯度: >98.00%
H-Val-Pro-Pro-OH(TFA),是牛奶来源的脯氨酸肽衍生物,是血管紧张素I转化酶(ACE)的抑制剂,其IC50为9μM.
- GC34328Semaglutide TFA纯度: >99.50%
Semaglutide (Rybelsus, Ozempic, NN9535, OG217SC, NNC 0113-0217), a long-acting glucagon-like peptide 1 (GLP-1) analogue, is a GLP-1 receptor agonist with the potential for the treatment of type 2 diabetes mellitus (T2DM).
- GC34364OT antagonist 1 demethyl derivativeCAS: 2763705-17-3
OTantagonist1demethylderivative是OTantagonist1的去甲基化产物.OTantagonist1(Compound4)是一种有效的选择性催产素(Oxytocin)拮抗剂,Ki为50nM。
- GC34367(RS)-ButyryltimololCAS: 2320274-78-8
(RS)-Butyryltimolol是Butyryltimolol的外消旋体。Butyryltimolol是Timolol的丁酸酯。Timolol是非选择性β受体阻滞剂。
- GC34386ALX 40-4C Trifluoroacetate
ALX40-4CTrifluoroacetate是一种趋化因子受体(CXCR4)抑制剂,能够抑制SDF-1与CXCR4结合,Ki值为1μM,具有抗HIV-1作用;ALX40-4CTrifluoroacetate同时为APJ受体拮抗剂,IC50值为2.9μM。
- GC344276H05 trifluoroacetate (K-Ras inhibitor)
6H05 is a selective, and allosteric inhibitor of oncogenic K-Ras(G12C).
- GC34521CCR6 inhibitor 1CAS: 2437547-04-9纯度: >99.50%
CCR6inhibitor1是一种有效、选择性的CCR6抑制剂,对猴子和人CCR6的IC50值分别为0.45和6nM,对其选择性远高于人CCR1(IC50,>30000nM)和CCR7(IC50,9400nM)。CCR6inhibitor1显著抑制ERK磷酸化。可用于自身免疫病和癌症的研究。
- GC34575Eplivanserin mixtureCAS: 130581-13-4纯度: >99.50%
Eplivanserinmixture是一种选择性的血清素再摄取抑制剂,是5-HT2A受体的拮抗剂。化合物信息来自专利WO2005/002578A1。
- GC34684Neurokinin B TFACAS: 101536-55-4纯度: >98.00%
NeurokininBTFA属于速激肽家族。Neurokinin结合到一系列G蛋白偶联受体(GPCR)-包括神经激肽受体1(NK1R),NK2R和NK3R,且介导其生物学作用。
- GC34752Radioprotectin-1CAS: 1622006-09-0纯度: >99.50%
Radioprotectin-1是一种高效特异性的LPA2激动剂,EC50值为25nM(鼠源LPA2亚型)。
- GC34808SolabegronCAS: 252920-94-8纯度: >99.50%
Solabegron(GW427353)是β3肾上腺素能受体(β3-AR)的选择性激动剂,在中国仓鼠卵巢细胞中测得的EC50值为22nM。目前正在被用于开发治疗膀胱过度活跃和肠易激综合征。
- GC34840TirzepatideCAS: 2023788-19-2纯度: >98.00% / >98.50%
Tirzepatide是一种双重胰高血糖素样肽-1 (GLP-1)和葡萄糖依赖性胰岛素性多肽(GIP)受体激动剂,是2型糖尿病(T2DM)的前瞻性治疗药物。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC34249 | KQMEEEAVRLFIEWLKNGGPSSGAPPPS | - | - | |
KQMEEEAVRLFIEWLKNGGPSSGAPPPS是Exendin-4多肽衍生物。 | ||||
| GC34270 | Neuropeptide Y (29-64), amide, human TFA | - | - | |
NeuropeptideY(29-64),amide,human(TFA)和阿尔兹海默症相关,能够保护老鼠皮质神经元对抗淀粉样蛋白毒性。 | ||||
| GC34289 | Ivabradine D6 hydrochloride | - | - | |
IvabradineD6盐酸盐是Ivabradine的氘代化合物标准品。 | ||||
| GC34304 | Befiradol hydrochloride (NLX-112 (hydrochloride)) | - | - | |
Befiradolhydrochloride(NLX-112hydrochloride)是选择性的5-羟色胺1A(5-HT)1A受体激动剂。 | ||||
| GC34326 | H-Val-Pro-Pro-OH TFA | 2828433-08-3 | >98.00% | |
H-Val-Pro-Pro-OH(TFA),是牛奶来源的脯氨酸肽衍生物,是血管紧张素I转化酶(ACE)的抑制剂,其IC50为9μM. | ||||
| GC34328 | Semaglutide TFA | - | >99.50% | |
Semaglutide (Rybelsus, Ozempic, NN9535, OG217SC, NNC 0113-0217), a long-acting glucagon-like peptide 1 (GLP-1) analogue, is a GLP-1 receptor agonist with the potential for the treatment of type 2 diabetes mellitus (T2DM). | ||||
| GC34339 | CXCR7 modulator 2 | 2227426-37-9 | >98.00% | |
CXCR7modulator2是CXCR7的调节剂,其Ki值为13nM。 | ||||
| GC34364 | OT antagonist 1 demethyl derivative | 2763705-17-3 | - | |
OTantagonist1demethylderivative是OTantagonist1的去甲基化产物.OTantagonist1(Compound4)是一种有效的选择性催产素(Oxytocin)拮抗剂,Ki为50nM。 | ||||
| GC34367 | (RS)-Butyryltimolol | 2320274-78-8 | - | |
(RS)-Butyryltimolol是Butyryltimolol的外消旋体。Butyryltimolol是Timolol的丁酸酯。Timolol是非选择性β受体阻滞剂。 | ||||
| GC34386 | ALX 40-4C Trifluoroacetate | - | - | |
ALX40-4CTrifluoroacetate是一种趋化因子受体(CXCR4)抑制剂,能够抑制SDF-1与CXCR4结合,Ki值为1μM,具有抗HIV-1作用;ALX40-4CTrifluoroacetate同时为APJ受体拮抗剂,IC50值为2.9μM。 | ||||
| GC34408 | Monohydroxy Netupitant D6 | - | - | |
MonohydroxyNetupitantD6是MonohydroxyNetupitant的氘代化合物标准品。 | ||||
| GC34418 | Netupitant D6 (CID-6451149 D6) | - | - | |
An internal standard for the quantification of netupitant | ||||
| GC34427 | 6H05 trifluoroacetate (K-Ras inhibitor) | - | - | |
6H05 is a selective, and allosteric inhibitor of oncogenic K-Ras(G12C). | ||||
| GC34464 | AM-4668 | 1011531-27-3 | >99.00% | |
AM-4668是一种GPR40激动剂,用于2型糖尿病研究。在A9细胞中和CHO细胞,激活GPR40的EC50分别为3.6nM和36nM。 | ||||
| GC34521 | CCR6 inhibitor 1 | 2437547-04-9 | >99.50% | |
CCR6inhibitor1是一种有效、选择性的CCR6抑制剂,对猴子和人CCR6的IC50值分别为0.45和6nM,对其选择性远高于人CCR1(IC50,>30000nM)和CCR7(IC50,9400nM)。CCR6inhibitor1显著抑制ERK磷酸化。可用于自身免疫病和癌症的研究。 | ||||
| GC34542 | CRF, bovine TFA | - | - | |
CRF,bovine(TFA)是一种有效的CRF受体激动剂,能够取代[125I-Tyr]ovineCRF,Ki值为3.52nM。 | ||||
| GC34575 | Eplivanserin mixture | 130581-13-4 | >99.50% | |
Eplivanserinmixture是一种选择性的血清素再摄取抑制剂,是5-HT2A受体的拮抗剂。化合物信息来自专利WO2005/002578A1。 | ||||
| GC34683 | Neurokinin A(4-10) TFA | - | >98.00% | |
NeurokininA(4-10)TFA是速激肽NK2受体激动剂。 | ||||
| GC34684 | Neurokinin B TFA | 101536-55-4 | >98.00% | |
NeurokininBTFA属于速激肽家族。Neurokinin结合到一系列G蛋白偶联受体(GPCR)-包括神经激肽受体1(NK1R),NK2R和NK3R,且介导其生物学作用。 | ||||
| GC34752 | Radioprotectin-1 | 1622006-09-0 | >99.50% | |
Radioprotectin-1是一种高效特异性的LPA2激动剂,EC50值为25nM(鼠源LPA2亚型)。 | ||||
| GC34775 | SBI-115 | 882366-16-7 | >99.50% / >98.00% | |
SBI-115是一种G蛋白胆汁酸偶联受体1(TGR5;GPCR19)拮抗剂。 | ||||
| GC34808 | Solabegron | 252920-94-8 | >99.50% | |
Solabegron(GW427353)是β3肾上腺素能受体(β3-AR)的选择性激动剂,在中国仓鼠卵巢细胞中测得的EC50值为22nM。目前正在被用于开发治疗膀胱过度活跃和肠易激综合征。 | ||||
| GC34840 | Tirzepatide | 2023788-19-2 | >98.00% / >98.50% | |
Tirzepatide是一种双重胰高血糖素样肽-1 (GLP-1)和葡萄糖依赖性胰岛素性多肽(GIP)受体激动剂,是2型糖尿病(T2DM)的前瞻性治疗药物。 | ||||
| GC34859 | VU0650786 | 1809085-30-0 | >99.50% | |
VU0650786是有效的、选择性的、能透过中枢神经系统的,谷氨酸受体亚型3(mGlu3)的负变构调节剂,IC50值为392nM。VU0650786在啮齿动物中具有抗抑郁和抗焦虑活性。 | ||||
