GLPG-1837
CAS No. 1654725-02-6
GLPG-1837 ( GLPG1837 | GLPG 1837 | ABBV-974 )
产品货号. M12524 CAS No. 1654725-02-6
GLPG-1837 (ABBV-974) 是一种有效的口服 CFTR 增强剂,对 F508del 和 G551D CFTR 的 EC50 分别为 3 nM 和 339 nM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥708 | 有现货 |
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| 10MG | ¥1169 | 有现货 |
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| 25MG | ¥1841 | 有现货 |
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| 50MG | ¥3143 | 有现货 |
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| 100MG | ¥4347 | 有现货 |
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| 200MG | ¥6057 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥748 | 有现货 |
|
生物学信息
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产品名称GLPG-1837
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述GLPG-1837 (ABBV-974) 是一种有效的口服 CFTR 增强剂,对 F508del 和 G551D CFTR 的 EC50 分别为 3 nM 和 339 nM。
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产品描述GLPG-1837 (ABBV-974)?is a potent, orally available CFTR potentiator with EC50 of 3 nM and 339 nM on F508del and G551D CFTR, respectively; shows enhanced efficacy on CFTR mutants harboring Class III mutations compared to Ivacaftor.Cystic Fibrosis,Phase 2 Clinical(In Vitro):GLPG1837 is a potent CFTR potentiator, with EC50s of 3 nM and 339 nM for F508del and G551D CFTR, respectively. GLPG1837 increases the conductivity of the G551D CFTR channel with obtained potency of 181 nM. GLPG1837 is reversible CFTR potentiator, with a the apparent affinity within a range of 0.2~2 μM.
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体外实验GLPG1837 is a potent CFTR potentiator, with EC50s of 3 nM and 339 nM for F508del and G551D CFTR, respectively. GLPG1837 increases the conductivity of the G551D CFTR channel with obtained potency of 181 nM. GLPG1837 is reversible CFTR potentiator, with a the apparent affinity within a range of 0.2~2 μM.
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体内实验——
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同义词GLPG1837 | GLPG 1837 | ABBV-974
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通路Apoptosis
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靶点CFTR
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受体F508delCFTR|G551DCFTR
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研究领域Other Indications
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适应症Fibrosis
化学信息
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CAS Number1654725-02-6
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分子量348.421
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分子式C16H20N4O3S
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纯度>98% (HPLC)
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溶解度Ethanol: 5 mg/mL; Water: Insoluble; DMSO: 60 mg/mL ( < 1 mg/ml refers to the product slightly soluble or insoluble )
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SMILESO=C(C1=NNC=C1)NC(S2)=C(C(N)=O)C3=C2C(C)(C)OC(C)(C)C3
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化学全称N-(3-carbamoyl-5,5,7,7-tetramethyl-4,7-dihydro-5H-thieno[2,3-c]pyran-2-yl)-1H-pyrazole-5-carboxamide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Van der Plas SE, et al. J Med Chem. 2017 Nov 17. doi: 10.1021/acs.jmedchem.7b01288.
产品手册
关联产品
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Ivacaftor hydrate
Ivacaftor (VX-770、VX770) 是一种有效的、口服生物可利用的 CFTR 增强剂,可增加 G551D- 和 F508del CFTR 介导的 Cl- 分泌,EC50 为 100 nM。
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Astressin 2B
Potent and selective corticotropin-releasing factor receptor 2 (CRF2) antagonist (IC50 values are 1.3 and > 500 nM for CRF2 and CRF1 respectively). Antagonizes CRF2-mediated inhibition of gastric emptying.
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Ivacaftor
Ivacaftor (VX-770、VX770) 是一种有效的、口服生物可利用的 CFTR 增强剂,可增加 G551D- 和 F508del CFTR 介导的 Cl- 分泌,EC50 为 100 nM。
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