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Tenapanor hydrochloride

更新时间:2025-08-27 12:22:16

Tenapanor hydrochloride结构式
Tenapanor hydrochloride结构式
品牌特惠专场
常用名 Tenapanor hydrochloride 英文名 Tenapanor hydrochloride
CAS号 1234365-97-9 分子量 1217.970
密度 N/A 沸点 N/A
分子式 C50H68Cl6N8O10S2 熔点 N/A
MSDS N/A 闪点 N/A

 Tenapanor hydrochloride用途


盐酸替那泊(AZD1722)是一种有效的口服活性钠/氢交换异构体3(NHE3)抑制剂。盐酸替纳帕诺主要通过减少被动细胞旁磷酸盐通量来减少肠道磷酸盐吸收。盐酸替那泊具有研究高磷血症的潜力[1][2]。

 Tenapanor hydrochloride名称

英文名 tenapanor hydrochloride
英文别名 更多

 Tenapanor hydrochloride生物活性

描述 盐酸替那泊(AZD1722)是一种有效的口服活性钠/氢交换异构体3(NHE3)抑制剂。盐酸替纳帕诺主要通过减少被动细胞旁磷酸盐通量来减少肠道磷酸盐吸收。盐酸替那泊具有研究高磷血症的潜力[1][2]。
相关类别
体内研究 盐酸替纳帕诺(0.15,0.5 mg/kg;p.o.)减少大鼠被动细胞旁磷酸盐吸收[1]。盐酸替那泊钠(0.15 mg/kg;p.o.;连续11天每天两次)可增加大鼠尿磷排泄的减少[2]。动物模型:大鼠(肠环模型)[1]剂量:0.15,0.5 mg/kg给药:P.o.结果:通过减少高磷酸盐餐后的尿磷酸盐和钠排泄以及增加到盲肠的钠和磷酸盐输送,减少被动细胞旁磷酸盐吸收。动物模型:8周,250g雄性Sprague–Dawley大鼠[2]剂量:0.15mg/kg与司维拉姆(0%、0.75%、1.5%和3%(wt/wt))联合给药:口服灌胃;连续11天每天两次结果:显著增加尿磷排泄的减少。
参考文献

[1]. King AJ, et al. Inhibition of sodium/hydrogen exchanger 3 in the gastrointestinal tract by tenapanor reduces paracellular phosphate permeability. Sci Transl Med. 2018 Aug 29;10(456):eaam6474.

[2]. King AJ, et al. Combination treatment with tenapanor and sevelamer synergistically reduces urinary phosphorus excretion in rats. Am J Physiol Renal Physiol. 2021 Jan 1;320(1):F133-F144.

 Tenapanor hydrochloride物理化学性质

分子式 C50H68Cl6N8O10S2
分子量 1217.970
精确质量 1214.263062
InChIKey VFRAXTZDILCRKY-OWRGXFNZSA-N
SMILES CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCNS(=O)(=O)c3cccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)c3)c2)C1.Cl.Cl

 Tenapanor hydrochloride靶点实验

查看更多实验

实验名称:Reduction in serum phosphorus level in Sprague-Dawley rat model of uremia-associated ...
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL3881411
实验名称:Inhibition of human NHE3-mediated sodium-dependant hydrogen ion antiport in Opossum k...
来源:ChEMBL
靶标:Sodium/hydrogen exchanger 3
External Id:CHEMBL3881404
实验名称:Inhibition of human Nap2B expressed in HEK293 cells assessed as inhibition of Pi upta...
来源:ChEMBL
靶标:Nucleosome assembly protein 1-like 4
External Id:CHEMBL3881405
实验名称:Reduction in plasma creatinine level in Sprague-Dawley rat model of uremia-associated...
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL3881416
实验名称:Reduction in plasma phosphorus level in Sprague-Dawley rat model of uremia-associated...
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL3881417
实验名称:Reduction in plasma FGF23 level in Sprague-Dawley rat model of uremia-associated vasc...
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL3881418
实验名称:Reduction in creatinine clearance in Sprague-Dawley rat model of uremia-associated va...
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL3881419
实验名称:Reduction in serum calcium level in Sprague-Dawley rat model of uremia-associated vas...
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL3881412
实验名称:Reduction in serum creatinine level in Sprague-Dawley rat model of uremia-associated ...
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL3881413
实验名称:Reduction in blood urea nitrogen level in Sprague-Dawley rat model of uremia-associat...
来源:ChEMBL
靶标:Rattus norvegicus
External Id:CHEMBL3881414
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 Tenapanor hydrochloride英文别名

tenapanor HCl
N,N'-(10,17-Dioxo-3,6,21,24-tetraoxa-9,11,16,18-tetraazahexacosane-1,26-diyl)bis{3-[(4S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydro-4-isoquinolinyl]benzenesulfonamide} dihydrochloride
tenapanor hydrochloride
50605O2ZNS
RDX5791
AZD1722 hydrochloride
1,1'-(butane-1,4-diyl)bis{3-[2-(2-{2-[({3-[(4S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl]phenyl}sulfonyl)amino]ethoxy}ethoxy)ethyl]urea} dihydrochloride
Benzenesulfonamide, N,N'-(10,17-dioxo-3,6,21,24-tetraoxa-9,11,16,18-tetraazahexacosane-1,26-diyl)bis[3-[(4S)-6,8-dichloro-1,2,3,4-tetrahydro-2-methyl-4-isoquinolinyl]-, hydrochloride (1:2)
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