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)
- GC61076MLS000532223CAS: 16616-39-0纯度: >99.00%
MLS000532223 is a high affinity, selective inhibitor of Rho family GTPases with EC50 ranging from 16 μM to 120 μM.
- GC61108Naftidrofuryl oxalateCAS: 3200-06-4纯度: >95.00%
Naftidrofuryloxalate(Nafronyloxalatesalt)是在外周血和脑血管病症如血管扩张药的管理中使用的药物,增加细胞氧化能力,且是一种5-HT2受体拮抗剂。
- GC61118Nebentan potassiumCAS: 342005-82-7纯度: >99.00%
Nebentanpotassium(YM598)是一种有效的具有口服活性的非肽类内皮素受体(ETAreceptor)拮抗剂,通过Bosentan修饰得到。Nebentanpotassium抑制[125I]内皮素-1与人内皮素ETA和ETB受体结合,Ki分别为0.697nM和569nM。Nebentanpotassium可用于改善肺心病和心肌梗死的相关研究。
- GC61153Olmesartan medoxomil impurity CCAS: 879562-26-2
OlmesartanmedoxomilimpurityC是Olmesartanmedoxomil的杂质。Olmesartanmedoxomil是一种有效的选择性的血管紧张素(angiotensinAT1)受体抑制剂,IC50为66.2μM。
- GC61154Olmesartan methyl esterCAS: 1347262-29-6
Olmesartanmethylester是Olmesartanmedoxomil合成的中间体。Olmesartanmedoxomil是一种有效的选择性的血管紧张素(angiotensinAT1)受体拮抗剂,IC50为66.2μM。
- GC61167Paliperidone palmitateCAS: 199739-10-1纯度: >98.00%
Paliperidone Palmitate (9-hydroxyrisperidone palmitate) is a palmitate ester of paliperidone, which is a dopamine antagonist and 5-HT2A antagonist of the atypical antipsychotic class.
- GC61208Propranolol D7 hydrochlorideCAS: 1613439-56-7纯度: >99.00%
PropranololD7hydrochloride是Propranololhydrochloride的氘代物。Propranololhydrochloride是一种非选择性的β-adrenergicreceptor(βAR)拮抗剂,对β1AR和β2AR具有高亲和力,Ki值分别为1.8nM和0.8nM。Propranololhydrochloride抑制[3H]-DHA与大鼠脑膜制剂的结合,IC50为12nM。Propranololhydrochloride用于高血压,嗜铬细胞瘤,心肌梗塞,心律不齐,心绞痛和肥大心肌病的相关研究。
- GC61219PS372424 hydrochlorideCAS: 1596362-29-6纯度: >96.00%
PS372424hydrochloride,CXCL10的三个氨基酸片段,是一种特异的人CXCR3激动剂,具有抗炎活性。在关节炎炎症模型中,PS372424hydrochloride可抑制T细胞迁移。
- GC61320Terazosin dimer impurity dihydrochlorideCAS: 1486464-41-8
Terazosindimerimpuritydihydrochloride是Terazosin的二聚体,也是Terazosin的杂质。Terazosin是喹唑啉衍生物,是竞争性的,具有口服活性的α1-肾上腺素(α1-adrenoceptor)受体拮抗剂。
- GC61389Ziprasidone amino acidCAS: 1159977-64-6
Ziprasidoneaminoacid(ZiprasidoneImpurityC)是Ziprasidone的杂质。Ziprasidone是5-HT和多巴胺(dopaminereceptor)受体拮抗剂,具有抗精神病活性。
- GC61413J-2156 TFACAS: 2387505-73-7纯度: >99.50%
J-2156TFA是一种高效,选择性的生长抑素受体4型(SST4)激动剂,对于人和大鼠SST4受体的IC50分别为0.05nM和0.07nM。J-2156TFA具有抗炎作用,可以缓解大鼠同侧后爪的机械性异常性疼痛和机械性痛觉过敏。
- GC61486Neurokinin A TFACAS: 2828433-19-6纯度: >99.00%
Neurokinin A TFA是一种内源性的速激肽家族神经肽,是神经激肽2受体(NK2R)的强效选择性激动剂。
- GC61496Angiotensin (1-7) (acetate)CAS: 2855063-75-9纯度: >98.50%
Angiotensin (1-7) (Ang-(1-7), Angiotensin fragment 1-7) is a bioactive component of the renin-angiotensin system that is formed endogenously from either Ang I or Ang II. Angiotensin (1-7) is a canine ACE inhibitor with an IC50 of 0.65 μM and inhibits the activity mediated by myostatin through Mas receptor.
- GC61499Neuropeptide Y (human) (TFA)纯度: >98.50%
NeuropeptideY(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。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC60998 | LMD-009 | 950195-51-4 | >99.50% | |
LMD-009是选择性CCR8非肽激动剂。LMD-009以高效力介导趋化性,肌醇磷酸盐积累和钙释放,EC50为11至87nM。 | ||||
| GC61067 | Mirtazapine D3 | 1216678-68-0 | - | |
An Analytical Reference Material | ||||
| GC61076 | MLS000532223 | 16616-39-0 | >99.00% | |
MLS000532223 is a high affinity, selective inhibitor of Rho family GTPases with EC50 ranging from 16 μM to 120 μM. | ||||
| GC61108 | Naftidrofuryl oxalate | 3200-06-4 | >95.00% | |
Naftidrofuryloxalate(Nafronyloxalatesalt)是在外周血和脑血管病症如血管扩张药的管理中使用的药物,增加细胞氧化能力,且是一种5-HT2受体拮抗剂。 | ||||
| GC61118 | Nebentan potassium | 342005-82-7 | >99.00% | |
Nebentanpotassium(YM598)是一种有效的具有口服活性的非肽类内皮素受体(ETAreceptor)拮抗剂,通过Bosentan修饰得到。Nebentanpotassium抑制[125I]内皮素-1与人内皮素ETA和ETB受体结合,Ki分别为0.697nM和569nM。Nebentanpotassium可用于改善肺心病和心肌梗死的相关研究。 | ||||
| GC61153 | Olmesartan medoxomil impurity C | 879562-26-2 | - | |
OlmesartanmedoxomilimpurityC是Olmesartanmedoxomil的杂质。Olmesartanmedoxomil是一种有效的选择性的血管紧张素(angiotensinAT1)受体抑制剂,IC50为66.2μM。 | ||||
| GC61154 | Olmesartan methyl ester | 1347262-29-6 | - | |
Olmesartanmethylester是Olmesartanmedoxomil合成的中间体。Olmesartanmedoxomil是一种有效的选择性的血管紧张素(angiotensinAT1)受体拮抗剂,IC50为66.2μM。 | ||||
| GC61167 | Paliperidone palmitate | 199739-10-1 | >98.00% | |
Paliperidone Palmitate (9-hydroxyrisperidone palmitate) is a palmitate ester of paliperidone, which is a dopamine antagonist and 5-HT2A antagonist of the atypical antipsychotic class. | ||||
| GC61208 | Propranolol D7 hydrochloride | 1613439-56-7 | >99.00% | |
PropranololD7hydrochloride是Propranololhydrochloride的氘代物。Propranololhydrochloride是一种非选择性的β-adrenergicreceptor(βAR)拮抗剂,对β1AR和β2AR具有高亲和力,Ki值分别为1.8nM和0.8nM。Propranololhydrochloride抑制[3H]-DHA与大鼠脑膜制剂的结合,IC50为12nM。Propranololhydrochloride用于高血压,嗜铬细胞瘤,心肌梗塞,心律不齐,心绞痛和肥大心肌病的相关研究。 | ||||
| GC61219 | PS372424 hydrochloride | 1596362-29-6 | >96.00% | |
PS372424hydrochloride,CXCL10的三个氨基酸片段,是一种特异的人CXCR3激动剂,具有抗炎活性。在关节炎炎症模型中,PS372424hydrochloride可抑制T细胞迁移。 | ||||
| GC61234 | Rebamipide D4 | 1219409-06-9 | - | |
An internal standard for the quantification of rebamipide | ||||
| GC61268 | SB 243213 | 200940-22-3 | >98.50% | |
A 5-HT 2C receptor inverse agonist | ||||
| GC61281 | SKF-83566 | 99295-33-7 | >99.00% | |
A dopamine D 1 receptor antagonist | ||||
| GC61320 | Terazosin dimer impurity dihydrochloride | 1486464-41-8 | - | |
Terazosindimerimpuritydihydrochloride是Terazosin的二聚体,也是Terazosin的杂质。Terazosin是喹唑啉衍生物,是竞争性的,具有口服活性的α1-肾上腺素(α1-adrenoceptor)受体拮抗剂。 | ||||
| GC61377 | VU0119498 | 79183-37-2 | >99.50% | |
An M 1 , M 3 , and M 5 muscarinic receptor positive allosteric modulator | ||||
| GC61378 | VU0238441 | 85511-68-8 | - | |
VU0238441 is a pan muscarinic acetylcholine receptor (mAChR) positive allosteric modulator (PAM) with EC50 of 2.1 μM, 2.2 μM, 2.8 μM, 3.2 μM and >10 μM for M5, M3, M2, M1 and M4, respectively. | ||||
| GC61387 | Zamifenacin | 127308-82-1 | >99.50% | |
A muscarinic M 3 receptor antagonist | ||||
| GC61389 | Ziprasidone amino acid | 1159977-64-6 | - | |
Ziprasidoneaminoacid(ZiprasidoneImpurityC)是Ziprasidone的杂质。Ziprasidone是5-HT和多巴胺(dopaminereceptor)受体拮抗剂,具有抗精神病活性。 | ||||
| GC61401 | Oxatomide | 60607-34-3 | >99.00% | |
Oxatomide是一种口服活性的H1受体拮抗剂(抗组胺药)。 | ||||
| GC61413 | J-2156 TFA | 2387505-73-7 | >99.50% | |
J-2156TFA是一种高效,选择性的生长抑素受体4型(SST4)激动剂,对于人和大鼠SST4受体的IC50分别为0.05nM和0.07nM。J-2156TFA具有抗炎作用,可以缓解大鼠同侧后爪的机械性异常性疼痛和机械性痛觉过敏。 | ||||
| GC61464 | GR 125743 | 148547-33-5 | >99.50% | |
GR125743是一种选择性的5-HT1B/1D受体拮抗剂,与野生型的人h5-HT1B和5-HT1D结合的pKi分别为8.85和8.31。GR125743可用于帕金森病和心血管疾病的研究。 | ||||
| GC61486 | Neurokinin A TFA | 2828433-19-6 | >99.00% | |
Neurokinin A TFA是一种内源性的速激肽家族神经肽,是神经激肽2受体(NK2R)的强效选择性激动剂。 | ||||
| GC61496 | Angiotensin (1-7) (acetate) | 2855063-75-9 | >98.50% | |
Angiotensin (1-7) (Ang-(1-7), Angiotensin fragment 1-7) is a bioactive component of the renin-angiotensin system that is formed endogenously from either Ang I or Ang II. Angiotensin (1-7) is a canine ACE inhibitor with an IC50 of 0.65 μM and inhibits the activity mediated by myostatin through Mas receptor. | ||||
| GC61499 | Neuropeptide Y (human) (TFA) | - | >98.50% | |
NeuropeptideY(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。 | ||||
