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)
- GC60630Befiradol hydrochlorideCAS: 2436760-81-3纯度: >99.50%
Befiradolhydrochloride(NLX-112hydrochloride)是选择性的5-羟色胺1A(5-HT)1A受体激动剂。
- GC60662Brexpiprazole S-oxideCAS: 1191900-51-2
BrexpiprazoleS-oxide(DM-3411)是Brexpiprazole的主要代谢产物,并通过细胞色素P4503A4(CYP3A4)代谢。Brexpiprazole是一种非典型抗精神病药,是人5-HT1A和多巴胺受体的部分激动剂,Ki分别为0.12nM和0.3nM。Brexpiprazole也是5-HT2A受体的拮抗剂,Ki为0.47nM。
- GC60679CCR2 antagonist 4CAS: 226226-39-7纯度: >99.50%
CCR2antagonist4(Teijincompound1)是一种高效、特异的CCR2拮抗剂,对CCR2b的IC50值为180nM。CCR2antagonist4对MCP-1诱导的趋化作用有较强的抑制作用,其IC50为24nM。
- GC60724Corticotropin-releasing factor (human) (acetate)纯度: >98.50%
Corticotropin-releasingfactorhumanacetate(HumanCRFacetate)能够刺激垂体前叶的促肾上腺皮质激素的合成和分泌。
- GC60748Dehydro OlmesartanCAS: 172875-98-8
DehydroOlmesartan是Olmesartan的衍生物。Olmesartan是血管紧张素II受体(AT1R)拮抗剂,可用于高血压的研究。
- GC60758DeschloroclozapineCAS: 1977-07-7纯度: >98.00%
Deschloroclozapine是一种高亲和力、选择性且代谢稳定的毒蕈碱DREADD激动剂,Deschloroclozapine能快速穿透血脑屏障,有效激活兴奋性hM3Dq和抑制性hM4Di DREADD受体。
- GC60764Diacetolol D7CAS: 1346604-19-0
DiacetololD7是Diacetolol的氘代物。Diacetolol是Acebutolol的主要代谢产物。Diacetolol是一种β-肾上腺素受体(β-adrenoceptor)阻断剂和抗心律失常药。
- GC60767Dibenamine hydrochlorideCAS: 55-43-6纯度: >98.00%
Dibenamine (N-(2-Chloroethyl)dibenzylamine, Sympatholytin, Dibenzylchlorethamine) is an irreversible blocker of α1 adrenoceptors.
- GC60846FlesinoxanCAS: 98206-10-1纯度: >99.00%
Flesinoxan是一种降压剂,是一种有效的,高亲和力的选择性的5-羟色胺1A(5-HT1A)受体激动剂,EC50值为24nM。Flesinoxan还具有有效的抗焦虑/抗抑郁作用。
- GC60877GLP-2(3-33)CAS: 275801-62-2纯度: >99.00%
GLP-2(3-33)由二肽基肽酶IV(DPPIV)产生,是一种GLP-2受体部分激动剂(EC50=5.8nM)。
- GC60914Hydrocortisone hemisuccinateCAS: 2203-97-6纯度: >98.00%
Hydrocortisone hemisuccinate (A-hydrocort, Hydrocortisone 21-hemisuccinate), a physiological glucocorticoid with anti-inflammatory properties, is an inhibitor of proinflammatory cytokine with IC50 of 6.7 μM and 21.4 μM for Interleukin-6 (IL-6) and IL-3, respectively.
- GC60915Hydroxy ziprasidoneCAS: 884305-08-2
Hydroxyziprasidone是Ziprasidone的杂质。Ziprasidone,一种抗精神药物,是5-HT和多巴胺(dopaminereceptor)受体拮抗剂。
- GC60957Jatrorrhizine hydroxideCAS: 483-43-2纯度: >98.00%
Jatrorrhizine (Neprotin, Yatrorizine), one of the active constituents of Coptis chinensis Franch, has multiple bioactivities, such as hypoglycemic, antimicrobial, and antioxidant activities. It is an inhibitor of AChE with IC50 of 872 nM and demonstrates >115-fold selectivity for AChE over BuChE.
- GC60965Keto ZiprasidoneCAS: 884305-07-1
KetoZiprasidone是Ziprasidone的杂质。Ziprasidone,一种抗精神药物,是5-HT和多巴胺(dopaminereceptor)受体拮抗剂。
- GC60969KRAS inhibitor-9CAS: 300809-71-6纯度: >99.50%
KRASinhibitor-9是有效的KRAS抑制剂(Kd=92μM),阻止GTP-KRAS的形成和KRAS下游激活。KRASinhibitor-9以中等的结合亲和力与KRASG12D,KRASG12C和KRASQ61H蛋白结合。KRASinhibitor-9导致G2/M细胞周期停滞并诱导凋亡(apoptosis)。KRASinhibitor-9选择性抑制具有KRAS突变的NSCLC细胞的增殖,但不抑制正常肺细胞的增殖。KRASinhibitor-9
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC60615 | AZD2423 | 1229603-37-5 | >98.50% | |
AZD2423是一种有效的、选择性的、口服生物利用的、非竞争性的CCR2趋化因子受体负向变构调节剂。AZD2423对CCR2Ca2+通量的IC50为1.2nM。 | ||||
| GC60619 | BA 1 TFA | - | >99.50% | |
BA 1 TFA 是铃蟾肽 (BB) 受体家族的有效激动剂。 | ||||
| GC60630 | Befiradol hydrochloride | 2436760-81-3 | >99.50% | |
Befiradolhydrochloride(NLX-112hydrochloride)是选择性的5-羟色胺1A(5-HT)1A受体激动剂。 | ||||
| GC60662 | Brexpiprazole S-oxide | 1191900-51-2 | - | |
BrexpiprazoleS-oxide(DM-3411)是Brexpiprazole的主要代谢产物,并通过细胞色素P4503A4(CYP3A4)代谢。Brexpiprazole是一种非典型抗精神病药,是人5-HT1A和多巴胺受体的部分激动剂,Ki分别为0.12nM和0.3nM。Brexpiprazole也是5-HT2A受体的拮抗剂,Ki为0.47nM。 | ||||
| GC60679 | CCR2 antagonist 4 | 226226-39-7 | >99.50% | |
CCR2antagonist4(Teijincompound1)是一种高效、特异的CCR2拮抗剂,对CCR2b的IC50值为180nM。CCR2antagonist4对MCP-1诱导的趋化作用有较强的抑制作用,其IC50为24nM。 | ||||
| GC60717 | Clonidine | 4205-90-7 | >98.50% / >99.50% | |
Clonidine HCl(Kapvay) is a direct-acting α2 adrenergic agonist with an ED50 of 0.02±0.01 mg/kg. | ||||
| GC60724 | Corticotropin-releasing factor (human) (acetate) | - | >98.50% | |
Corticotropin-releasingfactorhumanacetate(HumanCRFacetate)能够刺激垂体前叶的促肾上腺皮质激素的合成和分泌。 | ||||
| GC60748 | Dehydro Olmesartan | 172875-98-8 | - | |
DehydroOlmesartan是Olmesartan的衍生物。Olmesartan是血管紧张素II受体(AT1R)拮抗剂,可用于高血压的研究。 | ||||
| GC60758 | Deschloroclozapine | 1977-07-7 | >98.00% | |
Deschloroclozapine是一种高亲和力、选择性且代谢稳定的毒蕈碱DREADD激动剂,Deschloroclozapine能快速穿透血脑屏障,有效激活兴奋性hM3Dq和抑制性hM4Di DREADD受体。 | ||||
| GC60764 | Diacetolol D7 | 1346604-19-0 | - | |
DiacetololD7是Diacetolol的氘代物。Diacetolol是Acebutolol的主要代谢产物。Diacetolol是一种β-肾上腺素受体(β-adrenoceptor)阻断剂和抗心律失常药。 | ||||
| GC60767 | Dibenamine hydrochloride | 55-43-6 | >98.00% | |
Dibenamine (N-(2-Chloroethyl)dibenzylamine, Sympatholytin, Dibenzylchlorethamine) is an irreversible blocker of α1 adrenoceptors. | ||||
| GC60790 | Doxazosin D8 | 1126848-44-9 | - | |
An internal standard for the quantification of doxazosin | ||||
| GC60829 | Exendin-3/4 (59-86) | 1263874-37-8 | >97.00% | |
Exendin-3/4(59-86)是Exendin-4多肽衍生物。 | ||||
| GC60846 | Flesinoxan | 98206-10-1 | >99.00% | |
Flesinoxan是一种降压剂,是一种有效的,高亲和力的选择性的5-羟色胺1A(5-HT1A)受体激动剂,EC50值为24nM。Flesinoxan还具有有效的抗焦虑/抗抑郁作用。 | ||||
| GC60876 | GLP-1(7-36), amide TFA | - | >99.00% | |
GLP-1(7-36),amideTFA是一种主要的肠道激素,在葡萄糖的刺激下,它能促使胰岛β细胞分泌胰岛素。 | ||||
| GC60877 | GLP-2(3-33) | 275801-62-2 | >99.00% | |
GLP-2(3-33)由二肽基肽酶IV(DPPIV)产生,是一种GLP-2受体部分激动剂(EC50=5.8nM)。 | ||||
| GC60899 | Hibifolin | 55366-56-8 | >98.00% | |
Hibifolin (Gossypetin-8-O-β-D-glucuronide) is a flavonol glycoside and acts as a potential inhibitor of adenosine deaminase (ADA) with a Ki of 49.92 μM. Hibifolin prevents β-amyloid-induced neurotoxicity in cultured cortical neurons. | ||||
| GC60914 | Hydrocortisone hemisuccinate | 2203-97-6 | >98.00% | |
Hydrocortisone hemisuccinate (A-hydrocort, Hydrocortisone 21-hemisuccinate), a physiological glucocorticoid with anti-inflammatory properties, is an inhibitor of proinflammatory cytokine with IC50 of 6.7 μM and 21.4 μM for Interleukin-6 (IL-6) and IL-3, respectively. | ||||
| GC60915 | Hydroxy ziprasidone | 884305-08-2 | - | |
Hydroxyziprasidone是Ziprasidone的杂质。Ziprasidone,一种抗精神药物,是5-HT和多巴胺(dopaminereceptor)受体拮抗剂。 | ||||
| GC60938 | Iprindole | 5560-72-5 | >98.00% | |
Iprindole具有抗抑郁的生物活性,是一种弱的去甲肾上腺素和5-HT摄取的抑制剂。 | ||||
| GC60957 | Jatrorrhizine hydroxide | 483-43-2 | >98.00% | |
Jatrorrhizine (Neprotin, Yatrorizine), one of the active constituents of Coptis chinensis Franch, has multiple bioactivities, such as hypoglycemic, antimicrobial, and antioxidant activities. It is an inhibitor of AChE with IC50 of 872 nM and demonstrates >115-fold selectivity for AChE over BuChE. | ||||
| GC60965 | Keto Ziprasidone | 884305-07-1 | - | |
KetoZiprasidone是Ziprasidone的杂质。Ziprasidone,一种抗精神药物,是5-HT和多巴胺(dopaminereceptor)受体拮抗剂。 | ||||
| GC60969 | KRAS inhibitor-9 | 300809-71-6 | >99.50% | |
KRASinhibitor-9是有效的KRAS抑制剂(Kd=92μM),阻止GTP-KRAS的形成和KRAS下游激活。KRASinhibitor-9以中等的结合亲和力与KRASG12D,KRASG12C和KRASQ61H蛋白结合。KRASinhibitor-9导致G2/M细胞周期停滞并诱导凋亡(apoptosis)。KRASinhibitor-9选择性抑制具有KRAS突变的NSCLC细胞的增殖,但不抑制正常肺细胞的增殖。KRASinhibitor-9 | ||||
| GC60971 | L-692429 | 145455-23-8 | >99.50% | |
L-692429(MK-0751)是一种苯并内酰胺的衍生物,也是一种非肽基生长激素促分泌素(GHS)激动剂。L-692429以Ki值为63nM来结合G蛋白偶联受体(Gprotein-coupledreceptor)。 | ||||
