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Search Results for " conductance "

Targets Recommended: CFTR Autophagy

79

抑制剂 & 化合物

2

天然产物

4

重组蛋白

3

同位素标记化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T3135	KM11060	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	KM11060 是 F508del-CFTR 运输缺陷的新型校正剂，可纠正 F508del-CFTR 运输，增加质膜上功能性 CFTR 的数量。它可用于 F508del-CFTR 加工缺陷的研究和囊性纤维化治疗剂的开发。
T1634	Glibenclamide 格列本脲,Glyburide	Potassium Channel; Mitochondrial Metabolism; CFTR; P-gp; Autophagy	Autophagy; Membrane transporter/Ion channel; Metabolism; Neuroscience
	Glibenclamide (Glyburide) 是一种具有口服活性的 ATP 敏感的 K+通道抑制剂，可研究糖尿病和肥胖。它抑制 P-糖蛋白，可直接结合并阻断 KATP 的 SUR1亚基并抑制囊性纤维化跨膜传导调节蛋白。它通过诱导膜离子通透性干扰线粒体生物能，可诱导自噬。
T1805	Ataluren PTC124	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	Ataluren (PTC124) 是一种可口服的 CFTR-G542X 无义等位基因抑制剂。
T14935	Elexacaftor VX-445	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	Elexacaftor (VX-445) 是一种囊性纤维化跨膜电导调节因子 (CFTR) 校正剂。它促进CFTR 的加工和转运，增加细胞表面CFTR 的数量。
T16681	Nesolicaftor PTI-428	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	Nesolicaftor (PTI-428) 特异性增强囊性纤维化跨膜电导调节蛋白合成。
T5312	CFTR corrector 2 FDL169	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	CFTR corrector 2 (FDL169) 是一种新型有效的囊性纤维化跨膜电导调节因子(CFTR)调节剂，用于治疗携带 F508del 突变的囊性纤维化患者。
T9499	Icenticaftor QBW251	CFTR	Membrane transporter/Ion channel
	Icenticaftor (QBW251) 是一种具有口服活性CFTR 通道增强剂，可用于慢性阻塞性肺疾病 (COPD) 和囊性纤维化研究，对F508del 和G551D CFTR 的EC50分别为 79 和 497 nM。
T2451	GlyH-101 GlyH 101	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	GlyH-101 是一种可渗透入细胞的 CFTR 阻断剂，Ki 为1.4 uM。
T7083	GLPG1837 ABBV-974	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	GLPG1837 (ABBV-974) 是一种有效的 CFTR 增强剂，对其 F508del 和 G551D 的 EC50 分别为 3 nM 和 339 nM。
T2588	Ivacaftor Ivacaftor (VX-770),VX-770,依伐卡托	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	Ivacaftor (VX-770) 是一种 CFTR 增强剂，靶向G551D-CFTR 和F508del-CFTR 的EC50分别为100 和 25 nM。
T1874	PPQ-102 PPQ102,CFTR Inhibitor,PPQ 102	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	PPQ-102 (CFTR Inhibitor) 是一种CFTR 抑制剂，可以完全抑制CFTR 氯化物电流，IC50为90 nM。
T10591	BPO-27 racemate BPO-27 (racemate)	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	BPO-27 racemate (BPO-27(racemate)) 是一种CFTR 抑制剂，IC50为8 nM。
T9522	Rimtuzalcap CAD-1883	Potassium Channel	Membrane transporter/Ion channel
	Rimtuzalcap (CAD-1883) 是首创的，选择性的小电导钙激活钾通道 (SK 通道) 正变构调节剂。Rimtuzalcap 可用于运动障碍的研究，包括脊髓小脑性共济失调 (SCA)和特发性震颤 (ET)。
T2486	IOWH-032 IOWH032,IOWH 032	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	IOWH-032 (IOWH032) 是一种合成 CFTR 抑制剂，可用于研究治疗霍乱、腹泻和分泌性腹泻，在T84和CHO-CFTR 细胞实验中IC50为1.01 uM。
T2595	Lumacaftor 鲁玛卡托,VX-809,VRT 826809	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	Lumacaftor (VRT 826809) 是一种 CFTR 调节剂，可纠正 CFTR 蛋白的折叠和运输。它增强了 FRT 细胞中 F508del-CFTR 蛋白的成熟，EC50为100 nM。
T2355	CFTR(inh)-172 CFTRinh 172,CFTR Inhibitor-172,CFTRinh-172,CFTRinh172	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	CFTR(inh)-172 (CFTR Inhibitor-172) 是一种不依赖电压的选择性 CFTR 抑制剂，在2分钟内可逆地抑制CFTR 短路电流的Ki 值为300 nM。
T2263	Tezacaftor VX661,1-(2,2-二氟-1,3-苯并二氧戊环-5-基)-N-[1-[(2R)-2,3-二羟基丙基]-6-氟-2-(2-羟基-1,1-二甲基乙基)-1H-吲哚-5-基]-环丙烷甲酰胺	CFTR; Autophagy	Autophagy; Membrane transporter/Ion channel
	Tezacaftor (VX661) 是一种小分子，可用作囊性纤维化跨膜电导调节器基因功能的校正剂。
T20341	DNDS	CFTR	Membrane transporter/Ion channel
	DNDS 是电压依赖性囊性纤维化跨膜电导调节剂 (CFTR) 的通道阻滞剂。
T23471	TRAM 39 2-Chloro-alpha,alpha-diphenylbenzeneacetonitrile,TRAM-39,ZINC27105797,2-(2-chlorophenyl)-2,2-diphenylacetonitrile	Potassium Channel	Membrane transporter/Ion channel
	TRAM 39 (2-Chloro-α,α-diphenylbenzeneacetonitrile)是一种选择性的中间传导性钙离子激活的K+通道的阻断剂。
T63806	CFTR corrector 8	CFTR	Membrane transporter/Ion channel
	CFTR corrector 8 is a highly effective modulator of the cystic fibrosis transmembrane conductance regulator (CFTR). This compound is specifically designed for utilization in research related to cystic fibrosis, a genetic disorder primarily affecting the lungs and digestive system [1].
TP1932L1	[D-Trp7,9,10]-Substance P acetate	Others	Others
	[D-Trp7,9,10]-Substance P acetate 是 substance P 的类似物，substance P 可通过烟碱乙酰胆碱受体抑制离子电导。
T7512	BMS-191011 BMS-A	Potassium Channel	Membrane transporter/Ion channel
	BMS-191011 (BMS-A) 是一种大电导 Ca2+激活的钾通道 (Ca2+-activated potassium (maxi-K) channel) 激活剂，在中风模型中有研究价值。
T16346	NS1652	Chloride channel	Membrane transporter/Ion channel
	NS1652 是可逆阴离子电导抑制剂，在人和小鼠的红细胞中，可以抑制氯离子通道，IC50值为 1.6 μM。
T26955	Cavosonstat N91115,N 91115,N-91115	GSNOR; CFTR	Membrane transporter/Ion channel; Metabolism
	Cavosonstat (N91115) 是一种口服活性 S-亚硝基谷胱甘肽还原酶(GSNOR)抑制剂，可促进囊性纤维化跨膜传导调节器(CFTR)成熟和质膜稳定。
T4294	NS 11021 NS11021	Potassium Channel	Membrane transporter/Ion channel
	NS 11021 (NS11021) 是特异性 Ca2+激活的大电导 K+(KCa1.1)通道激活剂。当浓度高于0.3 μM 时，它通过平行移动通道激活曲线产生更多负电位，以浓度依赖的方式激活 KCa1.1。
T60653	CFTR corrector 9	CFTR	Membrane transporter/Ion channel
	CFTR corrector 9是一种囊性纤维化跨膜传导调节蛋白 (CFTR)调节剂。CFTR corrector 9 可用于研究囊性纤维化 (CF) 和其他 CFTR 相关疾病。
T30293	Bamocaftor VX-659	CFTR	Membrane transporter/Ion channel
	Bamocaftor是一种CFTR通道（DeltaF508-CFTR突变）矫正器，适用于 CF 跨膜传导调节器，被设计用于恢复 F508del-CFTR 蛋白功能。联合使用 tezacaftor 和 VX-561 治疗 F508del/MF 的囊性纤维化患者。
T12256	NS8593 hydrochloride NS8593 HCl	Potassium Channel	Membrane transporter/Ion channel
	NS8593 hydrochloride (NS8593 HCl) 是选择性的 SK 通道抑制剂。它可逆抑制 SK3介导的电流，Kd 值为 77 nM。它抑制所有 SK1-3亚型的 Ca2+依赖性 (在 0.5 μM Ca2+时，Kd 分别为 0.42、0.60 和 0.73 μM)，并且不影响中间电导和大电导的钙激活钾通道。
T4612	NS309	EGFR; Potassium Channel; HER	Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors
	NS309 是选择性钙依赖性钾离子通道 SK/IK 的激活剂，在 BK 通道上没有激活作用。
T6186	TRAM-34 Triarylmethane-34,TRAM 34	Potassium Channel; IκB/IKK	Membrane transporter/Ion channel; NF-κB
	TRAM-34 (Triarylmethane-34) 是一种高选择性的钙激活 K+通道 (IKCa1)阻断剂，Kd 值为 20 nM。
T10977	DCEBIO	Potassium Channel	Membrane transporter/Ion channel
	DCEBIO 是1-EBIO 的衍生物，是 T84 结肠细胞中Cl-分泌的极有效的激活剂。DCEBIO 通过激活 hIK1 K+通道和顶端膜的 Cl-传导促进 Cl-的分泌。
T10776	CFTR corrector 4	CFTR	Membrane transporter/Ion channel
	CFTR corrector 4是一种高效且可口服的囊性纤维化跨膜电导调节剂 (CFTR)，是一种有效的 (R，R) 型活性对映体。CFTR corrector 4 可以增加细胞表面的 CFTR 水平，是用来研究囊性纤维化的潜在化合物。
T19658	Enflurane NSC115944,Ethrane,NSC-115944,恩氟烷,Efrane,NSC 115944	Others	Others
	Enflurane (Efrane) 是一种挥发性麻醉剂，是 Chara australis 高电导 Ca2+ 激活的 K+ 通道的有效抑制剂。安氟醚是通过顶空气相色谱-质谱法监测卤化挥发性麻醉剂的内标。它可以快速调整麻醉深度，而脉搏或呼吸频率几乎没有变化。
T16345	NS13001 N-(4-chlorophenyl)-2-(3,5-dimethylpyrazol-1-yl)-9-methylpurin-6-amine,N-(4-Chlorophenyl)-2-(3,5-dimethyl-1H-pyrazol-1-yl)-9-methyl-9H-purin-6-amine	Potassium Channel	Membrane transporter/Ion channel
	NS13001 (N-(4-Chlorophenyl)-2-(3,5-dimethyl-1H-pyrazol-1-yl)-9-methyl-9H-purin-6-amine) 是口服有效的 SK 通道选择性正向变构调节剂。NS13001 对 SK2 和 SK3 通道的 EC50分别为 1.8 μM 和 0.14 μM。NS13001 在脊髓小脑共济失调 2 型和其他小脑共济失调方面具有研究价值。
T15286	Flindokalner BMS-204352	Potassium Channel	Membrane transporter/Ion channel
	Flindokalner (BMS-204352) 是一种钾离子通道调节剂。它是大电导钙激活 K 通道正向调节剂。它是在 HEK293 细胞中表达的所有神经元 Kv7通道亚型的正调节剂。它在 Kv7.1 通道 (Ki=3.7 μM) 处显示负调节活性，并充当 GABAA 受体的负调节剂。它在体内显示出抗焦虑功效。
T0782	Benzthiazide Aquatag,苄噻嗪,Lemazide,Dihydrex	Carbonic Anhydrase	Metabolism
	Benzthiazide (Lemazide) 是长效利尿剂及抗高血压剂。它也是碳酸酐酶 9 的抑制剂，他对 CA9，CA2 和 CA1 的 Ki 分别为 8.0，8.8 和 10 nM。它对肿瘤细胞增殖具有抑制作用。
T25446	Gea 857 Gea857,Gea-857	Others	Others
	Gea 857 is a potassium conductance putative blocker.
T23648	AF-2785	Others	Others
	In epididymal epithelial cells, AF-2785 inhibits cystic fibrosis transmembrane conductance regulator Cl(-) channels.
T29040	UCCF-029 UC(CF)-029,UC(CF) 029,UCCF029,UC(CF)029	Others	Others
	UCCF-029 is an activator of cystic fibrosis transmembrane conductance regulator (CFTR).
T71598	AqB011	Others	Others
	AqB011 is a selective blocker of the Aquaporin-1 ion channel conductance, slowing cancer cell migration.
T71599	AqB007	Others	Others
	AqB007 is a selective blocker of the Aquaporin-1 ion channel conductance, thereby slowing cancer cell migration.
T24137	HENA	Others	Others
	HENA is a novel activator of large conductance, voltage- and Ca2+-gated K+ (BK) channels.
T13705	GLPG2451	Cysteine Protease	Proteases/Proteasome
	GLPG2451 is a cystic fibrosis transmembrane conductance regulator (CFTR) potentiator. It effectively potentiates low temperature rescued F508del CFTR (EC50: 11.1 nM).
T24004	Ditran	Others	Others
	Ditran is an agent of anticholinergic. It also blocking end-plate ion conductance.
TP2059	Charybdotoxin
	Specific inhibitor of the big conductance Ca2+-activated K+ channel.
T28195	NS004 NS 004,NS-004	Others	Others
	NS004 is a large-conductance K+ channel opener, it inhibits mitochondrial function in glioma cells.
T13704	GLPG-3221	Others	Others
	GLPG-3221 can be uesd for the treatment of cystic fibrosis.GLPG-3221 is a potent, orally active corrector of CFTR (cystic fibrosis transmembrane conductance regulator), with an EC50 of 105 nM.
T25074	Ambasilide Ambasilidum	Others	Others
	Ambasilide 是一种 III 类抗心律失常化合物，钾离子通道阻滞剂，它通过改变电导而不是通过影响门控机制发挥作用。
T37821	AP 14145 hydrochloride	Others	Others
	KCa2 (small conductance Ca2+-activated potassium) channel negative allosteric modulator (IC50 = 1.1 μM). Increases the EC50 of Ca2+ on KCa2.3 channels by ~3-fold. Prolongs atrial effective refractory period (AERP) in rats. Reduces atrial fibrillation (AF) duration and prolongs atrial refractoriness without affecting ventricular refractory period in an animal AF model. Diness et al (2017) Termination of vernakalant-resistant atrial fibrillation by inhibition of small-conductance Ca2+-activated K+...
T74417	Vanzacaftor	Others	Others
	Vanzacaftor 是一种囊性纤维化跨膜电导调节体（CFTR）的调节剂，用于研究囊性纤维化。

化合物

Cat.No: T3135

Target: CFTR, Autophagy

Cat.No: T1634

Synonym: 格列本脲,Glyburide

Target: Potassium Channel, Mitochondrial Metabolism, CFTR, P-gp, Autophagy

Cat.No: T1805

Synonym: PTC124

Target: CFTR, Autophagy

Cat.No: T14935

Synonym: VX-445

Target: CFTR, Autophagy

Cat.No: T16681

Synonym: PTI-428

Target: CFTR, Autophagy

CFTR corrector 2

Cat.No: T5312

Synonym: FDL169

Target: CFTR, Autophagy

Cat.No: T9499

Synonym: QBW251

Target: CFTR

Cat.No: T2451

Synonym: GlyH 101

Target: CFTR, Autophagy

Cat.No: T7083

Synonym: ABBV-974

Target: CFTR, Autophagy

Cat.No: T2588

Synonym: Ivacaftor (VX-770),VX-770,依伐卡托

Target: CFTR, Autophagy

Cat.No: T1874

Synonym: PPQ102,CFTR Inhibitor,PPQ 102

Target: CFTR, Autophagy

BPO-27 racemate

Cat.No: T10591

Synonym: BPO-27 (racemate)

Target: CFTR, Autophagy

Cat.No: T9522

Synonym: CAD-1883

Target: Potassium Channel

Cat.No: T2486

Synonym: IOWH032,IOWH 032

Target: CFTR, Autophagy

Cat.No: T2595

Synonym: 鲁玛卡托,VX-809,VRT 826809

Target: CFTR, Autophagy

Cat.No: T2355

Synonym: CFTRinh 172,CFTR Inhibitor-172,CFTRinh-172,CFTRinh172

Target: CFTR, Autophagy

Cat.No: T2263

Synonym: VX661,1-(2,2-二氟-1,3-苯并二氧戊环-5-基)-N-[1-[(2R)-2,3-二羟基丙基]-6-氟-2-(2-羟基-1,1-二甲基乙基)-1H-吲哚-5-基]-环丙烷甲酰胺

Target: CFTR, Autophagy

Cat.No: T20341

Target: CFTR

Cat.No: T23471

Synonym: 2-Chloro-alpha,alpha-diphenylbenzeneacetonitrile,TRAM-39,ZINC27105797,2-(2-chlorophenyl)-2,2-diphenylacetonitrile

Target: Potassium Channel

CFTR corrector 8

Cat.No: T63806

Target: CFTR

[D-Trp7,9,10]-Substance P acetate

Cat.No: TP1932L1

Target: Others

Cat.No: T7512

Synonym: BMS-A

Target: Potassium Channel

Cat.No: T16346

Target: Chloride channel

Cat.No: T26955

Synonym: N91115,N 91115,N-91115

Target: GSNOR, CFTR

Cat.No: T4294

Synonym: NS11021

Target: Potassium Channel

CFTR corrector 9

Cat.No: T60653

Target: CFTR

Cat.No: T30293

Synonym: VX-659

Target: CFTR

NS8593 hydrochloride

Cat.No: T12256

Synonym: NS8593 HCl

Target: Potassium Channel

Cat.No: T4612

Target: EGFR, Potassium Channel, HER

Cat.No: T6186

Synonym: Triarylmethane-34,TRAM 34

Target: Potassium Channel, IκB/IKK

Cat.No: T10977

Target: Potassium Channel

CFTR corrector 4

Cat.No: T10776

Target: CFTR

Cat.No: T19658

Synonym: NSC115944,Ethrane,NSC-115944,恩氟烷,Efrane,NSC 115944

Target: Others

Cat.No: T16345

Synonym: N-(4-chlorophenyl)-2-(3,5-dimethylpyrazol-1-yl)-9-methylpurin-6-amine,N-(4-Chlorophenyl)-2-(3,5-dimethyl-1H-pyrazol-1-yl)-9-methyl-9H-purin-6-amine

Target: Potassium Channel

Cat.No: T15286

Synonym: BMS-204352

Target: Potassium Channel

Cat.No: T0782

Synonym: Aquatag,苄噻嗪,Lemazide,Dihydrex

Target: Carbonic Anhydrase

Cat.No: T25446

Synonym: Gea857,Gea-857

Target: Others

Cat.No: T23648

Target: Others

Cat.No: T29040

Synonym: UC(CF)-029,UC(CF) 029,UCCF029,UC(CF)029

Target: Others

Cat.No: T71598

Target: Others

Cat.No: T71599

Target: Others

Cat.No: T24137

Target: Others

Cat.No: T13705

Target: Cysteine Protease

Cat.No: T24004

Target: Others

Cat.No: TP2059

Cat.No: T28195

Synonym: NS 004,NS-004

Target: Others

Cat.No: T13704

Target: Others

Cat.No: T25074

Synonym: Ambasilidum

Target: Others

AP 14145 hydrochloride

Cat.No: T37821

Target: Others

Cat.No: T74417

Target: Others

Cat. No.	Product Name	Target	Signaling Pathways
T5065	GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD Monosodium-GMP,cGMP sodium salt,鸟苷-3',5'-环磷酸一钠盐,Cyclic GMP	PKA	Tyrosine Kinase/Adaptors
	GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD (cGMP sodium salt) 也称为 cGMP，是一种细胞调节剂，被描述为第二信使。它的水平随着各种激素的增加而增加，包括乙酰胆碱、胰岛素和催产素。 cGMP 激活蛋白激酶 G(PKG) 并调节离子通道电导，信号传导影响多种过程，包括平滑肌松弛和增殖、光转导和能量稳态。
T73764	L-Palmitoylcarnitine TFA	Others	Others
	L-Palmitoylcarnitine TFA 是一种长链酰基肉碱和脂肪酸代谢产物，在缺血期间积聚于肌膜并扰乱膜脂环境。L-Palmitoylcarnitine TFA 通过与Kir6.2的相互作用抑制KATP 通道活性，而不影响单通道电导。

天然产物

GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD

Cat.No: T5065

Synonym: Monosodium-GMP,cGMP sodium salt,鸟苷-3',5'-环磷酸一钠盐,Cyclic GMP

Target: PKA

L-Palmitoylcarnitine TFA

Cat.No: T73764

Target: Others

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPH-00670	MscL Protein, E. coli O157:H7, Recombinant (B2M & His) mscL,Large-conductance mechanosensitive channel	E. coli	E. coli
	Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell. MscL Protein, E. coli O157:H7, Recombinant (B2M & His) is expressed in E. coli expression system with N-6xHis-B2M tag. The predicted molecular weight is 29.0 kDa and the accession number is P0A743.
TMPH-03209	CLNS1A Protein, Rabbit, Recombinant (His & Myc) I(Cln),Chloride conductance regulatory protein ICln...	Rabbit	E. coli
	CLNS1A Protein, Rabbit, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 33.4 kDa and the accession number is Q28678.
TMPH-01358	FXYD3 Protein, Human, Recombinant (His & SUMO) Phospholemman-like,Chloride conductance inducer pro...	Human	E. coli
	FXYD3 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 20.5 kDa and the accession number is Q14802.
TMPY-03629	Syntaxin 8 Protein, Human, Recombinant (His) CARB,syntaxin 8	Human	HEK293 Cells
	STX8, also known as syntaxin 8, directly interacts with HECTd3. STX8 forms the SNARE complex with syntaxin 7, vti1b and endobrevin. STX8 belongs to the syntaxin family. Members of this family are key molecules implicated in diverse vesicle docking and membrane fusion events. STX8 physically interacts with cystic fibrosis transmembrane conductance regulator (CFTR): recombinant syntaxin 8 binds CFTR in vitro and both proteins co-immunoprecipitate in HT29 cells. Syntaxin 8 regulates CFTR-mediated c...

重组蛋白

MscL Protein, E. coli O157:H7, Recombinant (B2M & His)

Cat.No: TMPH-00670

Species: E. coli

Expression System: E. coli

CLNS1A Protein, Rabbit, Recombinant (His & Myc)

Cat.No: TMPH-03209

Species: Rabbit

Expression System: E. coli

FXYD3 Protein, Human, Recombinant (His & SUMO)

Cat.No: TMPH-01358

Species: Human

Expression System: E. coli

Syntaxin 8 Protein, Human, Recombinant (His)

Cat.No: TMPY-03629

Species: Human

Expression System: HEK293 Cells

Cat. No.	Product Name	Target	Signaling Pathways
T27098	Ivacaftor-D9 deutivacaftor,CTP-656
	CTP-656, a cystic fibrosis transmembrane conductance regulator (CFTR) channel activator, is used potentially for the treatment of cystic fibrosis.
T71303	Flufenamic Acid-d4
	Flufenamic acid-d4 is intended for use as an internal standard for the quantification of flufenamic acid by GC- or LC-MS. Flufenamic acid is a non-steroidal anti-inflammatory drug (NSAID) and COX inhibitor (IC50s = 3 and 9.3 µM for human COX-1 and COX-2, respectively). Flufenamic acid inhibits TNF-α-induced increases in COX-2 levels and NF-κB activation in HT-29 colon cancer cells in a concentration-dependent manner. It inhibits calcium influx induced by fMLP or A23187 in human polymorphonuclear...
TMIH-0568	Tezacaftor-d4 VX-661-d4
	Tezacaftor-d4 是 Tezacaftor 的氘代化合物。Tezacaftor 的 CAS 号为 1152311-62-0。VX-661 是一种小分子，可用作囊性纤维化跨膜电导调节器基因功能的校正剂。

同位素标记化合物

Cat.No: T27098

Synonym: deutivacaftor,CTP-656

Flufenamic Acid-d4

Cat.No: T71303

Cat.No: TMIH-0568

Synonym: VX-661-d4

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