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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4359 |
VAS2870
|
NADPH | Metabolism |
VAS2870 是一种NADPH 氧化酶抑制剂。 | |||
T8408 |
GKT136901
AK120765 |
NADPH-oxidase; NADPH | Immunology/Inflammation; Metabolism |
GKT136901 (AK120765) 是选择性的和具有口服活性的 NADPH 氧化酶 NOX-1/4抑制剂,Ki 分别为 160 和 165 nM。它具有抗炎症活性。它也是一种选择性和直接的过氧亚硝酸清除剂。它可用于糖尿病肾病,中风和神经退行性疾病的研究。 | |||
T8107 |
GLX351322
|
NADPH-oxidase; NADPH | Immunology/Inflammation; Metabolism |
GLX351322 抑制 NADPH 氧化酶 4 (Nox4) 。在 NOX4 过表达的细胞中,抑制过氧化氢的产生,IC50值为 5 μM。 | |||
T15433 |
GSK2795039
|
Apoptosis; Reactive Oxygen Species; ROS; NADPH | Apoptosis; Immunology/Inflammation; Metabolism; NF-κB |
GSK2795039 是一种 NADPH 氧化酶 2 抑制剂,可抑制活性氧产生和 NADPH 消耗,同时可减少细胞凋亡。 | |||
T6099 |
Setanaxib
GKT137831 |
NADPH-oxidase; Ferroptosis; NADPH | Apoptosis; Immunology/Inflammation; Metabolism |
Setanaxib (GKT137831) 是一种有效的特异性双重 NADPH 氧化酶 (NOX1/4) 抑制剂,Ki 分别为140和110nM。 | |||
T22990 |
ML-090
Fluoflavine |
NADPH-oxidase; Others | Immunology/Inflammation; Others |
ML-090 是 NOX1 特异性抑制剂 (IC50 = 90 nM),对 NOX1 的特异性高于 NOX2、NOX3、NOX4(所有 IC50 > 10 μM)100倍。 | |||
T7042 |
1,5-Isoquinolinediol
|
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
1,5-Isoquinolinediol 是一种多聚(ADP-核糖)合成酶抑制剂,对PARP1的IC50值为 0.39 µM。它用于研究 PARP1 在 DNA 修复和氧化应激诱导的细胞死亡中的作用。 | |||
T7191 |
Diphenyleneiodonium chloride
二苯基氯化碘盐,DPI |
NOS; Reactive Oxygen Species; NADPH; TRP/TRPV Channel | Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; NF-κB |
Diphenyleneiodonium chloride (DPI) 是 NADPH 氧化酶抑制剂,也是 TRPA1激活剂,EC50为 1 - 3 μM 。它选择性抑制胞内活性氧。 | |||
T10353 |
APX-115 free base
Ewha-18278 free base |
NADPH-oxidase; NADPH | Immunology/Inflammation; Metabolism |
APX-115 free base (Ewha-18278 free base) 是口服具有活性的、非选择性的 Nox 抑制剂,对 Nox1,Nox2和 Nox4的 Ki 分别为 1.08 μM,0.57 μM 和 0.63 μM。它能够有效预防糖尿病小鼠的肾损伤。 | |||
T38423 |
CL097
CL097 |
Reactive Oxygen Species; TLR | Immunology/Inflammation; Metabolism; NF-κB |
CL097 是 TLR7 和 TLR8 的有效激动剂。 CL097 诱导巨噬细胞中的促炎细胞因子和 NADPH 氧化酶引发,从而增加 fMLF 刺激的 ROS 产生。 | |||
T83625 |
iNOS-IN-14
3-bromo-1H-indazole-7-carbonitrile |
NOS | Immunology/Inflammation |
iNOS-IN-14 (3-bromo-1H-indazole-7-carbonitrile) 是一种有效的一氧化氮合酶(NOS)抑制剂,抑制nNOS的NADPH氧化酶活性。 | |||
T29097 |
VAS 3947
VA-S3947,VA S3947,VAS3947 |
Apoptosis; NADPH-oxidase | Apoptosis; Immunology/Inflammation |
VAS 3947 是一种特异的 NADPH 氧化酶 (NOX) 抑制剂。VAS 3947具有强大的抗血小板作用, 通过 UPR 激活,主要由于蛋白质聚集和错误折叠,独立于抗 NOX 活性诱导细胞凋亡。 | |||
T38404 |
MJ33 lithium salt
|
ROS | Immunology/Inflammation |
MJ33 lithium salt 是 NADPH 氧化酶 2 型介导的 ROS 生成抑制剂,是一种氟化磷脂类似物,可抑制过氧化物还蛋白 6 (Prdx6) 的磷脂酶 A2 (PLA2) 活性,可用于研究急性肺损伤。 | |||
TP1886L1 |
NoxA1ds acetate(1435893-78-9 free base)
|
NADPH-oxidase | Immunology/Inflammation |
NoxA1ds acetate(1435893-78-9 free base) 是一种有效的选择性 NADPH 氧化酶 1 (NOX1) 抑制剂 (IC50 : 20 nM)。对 NOX1 的选择性优于对 NOX2、NOX4、NOX5 和黄嘌呤氧化酶的选择性。它抑制 HT-29 人结肠癌细胞中 NOX1 衍生的 O2 产生。在体外缺氧条件下减弱 VEGF 诱导的人肺动脉内皮细胞迁移。 | |||
T22096 |
L 012 sodium salt
|
Others | Others |
L 012 sodium salt 是一种 luminol 类似物,是一种广泛使用的活性氧和活性氮的化学发光(CL)探针 的化学发光 (CL) 探针。L 012 sodium salt 广泛用于检测 NADPH 氧化酶 (Nox) 衍生的超氧化物 (O2•−) ,用于发现 Nox 抑制剂。 | |||
T15300 |
Fluorofenidone
AKF-PD |
Others | Others |
Fluorofenidone (AKF-PD) 是 AMR69 的类似物,抗纤维化活性与 AMR69相同,但 Fluorofenidone 的毒性更低,半衰期长。它部分通过 PI3K/Akt 信号通路抑制 NADPH 氧化酶和细胞外基质 (ECM) 的沉积,能够减少肾间质纤维化的发生。 | |||
T10354 |
APX-115
Ewha-18278 |
NADPH-oxidase | Immunology/Inflammation |
APX-115 (Ewha-18278) (Ewha-18278) 是一种有效的,口服活性的,非选择性 Nox 抑制剂,对 Nox1,Nox2 和 Nox4 的 Ki 值分别为 1.08 μM,0.57 μM 和 0.63 μM。APX-115 可有效预防糖尿病小鼠的肾损伤。 | |||
T13112 |
Tat-NR2B9c
Tat-NR2Bct,NA-1 |
NO Synthase; iGluR | Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience |
Tat-NR2B9c (NA-1) 是一种突触后密度-95(PSD-95)抑制剂,具有神经保护和抗癫痫作用。Tat-NR2B9c 可抑制PSD-95d2、 PSD-95d1 和 PSD-95,可阻止NMDA诱导的神经元NADPH氧化酶的激活,从而阻断超氧化物的产生,可减少中风后急性期的缺血性损伤。 | |||
T0825 |
Ebselen
SPI-1005,PZ-51,依布硒,CCG-39161 |
Phosphatase; Virus Protease; Calcium Channel; COX; HIV Protease | Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Ebselen (CCG-39161) 是一种谷胱甘肽过氧化物酶模拟物,是电压依赖性钙通道阻断剂。它抑制Mpro 和COVID-19病毒,是HIV-1衣壳 CTD 二聚化的抑制剂,具有抗炎、抗癌和抗氧化活性。 | |||
T12781 |
RV01
|
Others | Others |
RV01 是一种新型的白藜芦醇喹啉取代类似物,可抑制 DNA 损伤,降低乙醇诱导的乙醛脱氢酶 (ALDH2) 的 mRNA 表达,具有清除羟自由基的活性。RV01 降低 iNOS 的表达,具有抗神经炎症作用。RV01降低肿瘤坏死因子-a (TNF-a)和白细胞介素-6 (IL-6) mRNA 水平和分泌,抑制lps 诱导的ROS 生成和烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶活化,降低toll 样受体4 (TLR4)的蛋白表达,抑制lps 诱导的丝裂原活化蛋白激酶(MAPK)和核转录因子-кB (NF-кB)信号通路的激活。 | |||
T69630 |
Diphenyleneiodonium (free base)
|
Others | Others |
Diphenyleneiodonium (free base) is an NADPH oxidase inhibitor. | |||
T71513 |
GK-136901
|
Others | Others |
GK-136901 is a first-in-class, potent, and orally bioavailable NADPH oxidase isoform 4 (Nox4) inhibitor. | |||
T80243 |
gp91 ds-tat
|
||
gp91 ds-tat 是一种生物活性肽,作为(NADPH氧化酶组装肽抑制剂)。 | |||
T78592 |
Diapocynin
Dehydrodiacetovanillone |
Others | Others |
Diapocynin (DeHydrodiacetovanillone),Apocynin的二聚体,是具有口服活性的NADPH氧化酶抑制剂。具备抗炎、神经保护及抗氧化效果。 | |||
T11333 |
Fulvene-5
|
Others | Others |
Fulvene-5 is a chemical compound that exhibits antitumor activity. It functions as a potent inhibitor of NADPH oxidase 4 (NOX4) and possesses antioxidant properties. Additionally, Fulvene-5 acts as a reactive oxygen species (ROS) modifying agent and a powerful radioprotector. | |||
TP2083 |
Ac9-25
|
||
N-terminal peptide of Annexin I (AI/Lipocortin I) that inhibits leukocyte extravasation. Acts as a formyl peptide receptor 1 (FPR1) ligand and stimulates neutrophil NADPH oxidase activation. | |||
T75813 |
Ac9-25 TFA
|
||
Ac9-25 TFA, 膜联蛋白 I N 端肽,作为甲酰肽受体(FPR)的激动剂,能激活中性粒细胞NADPH氧化酶通过FPR。 | |||
TP1886 |
NoxA1ds
|
||
Potent and selective NADPH oxidase 1 (NOX1) inhibitor (IC50 = 20 nM). Exhibits selectivity for NOX1 over NOX2, NOX4, NOX5 and xanthine oxidase. Inhibits NOX1-derived O2- production in HT-29 human colon cancer cells. Attenuates VEGF-induced human pulmonary | |||
T35393 |
gp91ds-tat
gp91ds-tat |
NADPH-oxidase | Immunology/Inflammation |
gp91ds-tat 是一种 NADPH 氧化酶(NADPH oxidase)的肽抑制剂,由与人类免疫缺陷病毒-tat 肽相连的 gp91phox 序列组成。tat 序列促进了这种肽进入细胞。 | |||
T75949 |
NoxA1ds TFA
|
||
NoxA1ds TFA is a potent and selective inhibitor of NADPH oxidase 1 (NOX1), with an inhibition concentration (IC50) of 20 nM, demonstrating selectivity over NOX2, NOX4, NOX5, and xanthine oxidase. It effectively inhibits NOX1-derived O2- production in HT-29 human colon cancer cells and attenuates VEGF-induced migration of human pulmonary artery endothelial cells under hypoxic conditions in vitro. | |||
T73896 |
Glucose-6-phosphate dehydrogenase
|
Others | Others |
Glucose-6-phosphate dehydrogenase 是戊糖磷酸途径的限速酶。Glucose-6-phosphate dehydrogenase 是抗氧化途径、一氧化氮合酶、NADPH 氧化酶、细胞色素 p450 等系统中 NADPH 的主要来源。Glucose-6-phosphate dehydrogenase 可用于糖尿病、醛固酮诱导的内皮功能障碍和癌症的研究。 | |||
T60517 |
CL097 hydrochloride
|
Others | Others |
CL097 hydrochloride 是一种有效的 TLR7和 TLR8激动剂。CL097 hydrochloride 可在巨噬细胞中诱导促炎细胞因子和 NADPH 氧化酶启动活性,从而增加 fMLF 刺激的ROS 产生。 | |||
TP1585 |
sgp91 ds-tat Peptide 2, scrambled
|
||
This peptide is a scrambled sequence of NADPH oxidase assembly peptide inhibitor gp91 ds-tat. It is used as a control peptide. It is two amino acid residues shorter at the N-terminus compared to the scrambled gp91 ds-tat. | |||
T38646 |
GKT136901 hydrochloride
GKT136901 hydrochloride |
Others | Others |
GKT136901 hydrochloride is a powerful, selective, and orally active inhibitor of NADPH oxidase (NOX1/4). It exhibits K i values of 160 nM and 165 nM against NOX1 and NOX4, respectively. Additionally, GKT136901 hydrochloride demonstrates selectivity and direct scavenging ability towards peroxynitrite. This compound finds utility in studying diabetic nephropathy, stroke, neurodegeneration, and possesses anti-inflammatory properties. | |||
T75815 |
WKYMVM-NH2 TFA
|
||
WKYMVM-NH2 TFA 是一种高效的 N-甲酰肽受体 FPR1 与 FPRL1/2 激动剂,具备激活白细胞功效特性,包括趋化性、补体受体-3 的激活以及 NADPH 氧化酶的激活。 | |||
TP1948 |
PBP10
PBP 10 |
||
Selective formyl peptide receptor 2 (FPR2) antagonist; cell permeable. Selectively inhibits FPR2-mediated NADPH oxidase activity but has no effect on FPR1 signaling in neutrophils. Displays PIP2 binding activity in vitro and blocks cell motility. Also exh | |||
T62004 |
(Rac)-Nebivolol
|
Others | Others |
(Rac)-Nebivolol ((Rac)-R 065824) 是 Nebivolol 的外消旋异构体。Nebivolol 是一种选择性的β1 肾上腺素能受体拮抗剂(IC50= 0.8 nM)。Nebivolol 显示血管舒张活性。在乙醇引起心脏毒性的早期阶段,Nebivolol 能预防 Nox2/NADPH 氧化酶上调和脂质过氧化。 | |||
T63847 |
1-Oleoyl-2-hydroxy-sn-glycero-3-phospho-L-serine sodium
|
Others | Others |
Oleoyl-2-hydroxy-sn-glycero-3-phospho-L-serine sodium (18:1 Lyso-PS) 是一种改性 PS 产品,经由 NADPH 氧化酶激活及 Lyso-PS 信号转导后得到。Oleoyl-2-hydroxy-sn-glycero-3-phospho-L-serine sodium 能够利用巨噬细胞 G2A 功能,增强现有的受体/配体系统,进而解决中性粒细胞炎症。 | |||
TP1891 |
MMK 1
|
||
Potent and selective human formyl peptide receptor FPR2 agonist (EC50 values are 1, 2 and > 10 000 nM at mFRP2, hFPR2 and hFPR1 respectively). Induces migration of human monocytes and neutrophils via a chemotactic mechanism and enhances production of proi | |||
TP1948L |
PBP 10 acetate(794466-43-6 Free base)
|
||
PBP 10 acetate(794466-43-6 Free base) 是一种选择性甲酰肽受体 2 (FPR2) 拮抗剂。 PBP 10 acetate 选择性抑制 FPR2 介导的 NADPH 氧化酶活性,但对中性粒细胞中的 FPR1 信号传导没有影响。 PBP 10 acetate 在体外表现出 PIP2 结合活性并阻断细胞运动。 PBP 10 acetate 通过抑制病毒诱导的 ERK 激活而表现出针对流感病毒的抗病毒活性。 | |||
T37583 |
XTT (sodium salt hydrate)
|
||
XTT is a cell-impermeable, negatively charged tetrazolium dye that produces a water-soluble formazan when reduced at the cell surface by cellular-derived NADH and an electron mediator.1,2It is frequently used in colorimetric assays to measure cell proliferation, cytotoxicity, and apoptosis.3 1.Berridge, M.V., Tan, A.S., and Herst, P.M.Tetrazolium dyes as tools in cell biology: New insights into their cellular reductionBiotechnol. Ann. Rev.11127-152(2005) 2.Berridge, M.V., and Tan, A.S.Trans-plas... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6391 |
Apocynin
香草乙酮,Acetovanillone,Acetoguaiacone,NSC 2146,罗布麻宁 |
Apoptosis; NADPH; Autophagy | Apoptosis; Autophagy; Metabolism |
Apocynin (NSC 2146) 是一种选择性NADPH-氧化酶抑制剂,IC50为10 μM。 | |||
TN2126 |
Quercetin-3-O-glucose-6''-acetate
6"-O-Acetylisoquercitrin,槲皮素-3-O-葡萄糖苷-6′′-乙酯 |
NADPH-oxidase; ROS; NADPH | Immunology/Inflammation; Metabolism |
Quercetin-3-O-glucose-6''-acetate (6"-O-Acetylisoquercitrin) 是 NADPH 氧化酶的抑制剂。 Quercetin-3-O-glucose-6''-acetate 具有抗氧化活性。 | |||
T5S2343 |
Acetylshikonin
乙酰紫草素,Acetyl shikonin |
Others; P450; AChE | Metabolism; Neuroscience; Others |
Acetylshikonin 来源于紫草根,具有抗癌、抗炎作用。它是一种 AChE 抑制剂,具有很强的抗凋亡活性。它是一种非选择性的细胞色素 P450抑制剂,对所有 P450 亚型抑制的 IC50值范围为 1.4-4.0 μM。 | |||
TN2039 |
Panaxydol
|
cAMP; p38 MAPK; JNK | GPCR/G Protein; MAPK |
Panaxydol has anti-cancer activity, can inhibit the growth and apoptosis of cancer cells, the signaling mechanisms involve a [Ca(2+)](i) increase, JNK and p38 MAPK activation, cAMP, MAP kinase and ROS generation through NADPH oxidase and mitochondria. | |||
TN6515 |
Selaginellin
|
||
Selaginellin has a neuroprotective effect against L-glutamate-induced neurotoxicity through mechanisms related to anti-oxidation and anti-apoptosis via scavenging reactive oxygen species and up-regulating the expression of klotho gene. Selaginellin shows |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-01746 |
NOX4 Protein, Human, Recombinant (E. coli, His)
Kidney superoxide-producing NADPH oxidase,... |
Human | E. coli |
NOX4 Protein, Human, Recombinant (E. coli, His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 28.8 kDa and the accession number is Q9NPH5. | |||
TMPH-01744 |
NOX1 Protein, Human, Recombinant (His)
NADH/NADPH mitogenic oxidase subunit P65-M... |
Human | E. coli |
NOH-1S is a voltage-gated proton channel that mediates the H(+) currents of resting phagocytes and other tissues. It participates in the regulation of cellular pH and is blocked by zinc. NOH-1L is a pyridine nucleotide-dependent oxidoreductase that generates superoxide and might conduct H(+) ions as part of its electron transport mechanism, whereas NOH-1S does not contain an electron transport chain. NOX1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-10xHis t... | |||
TMPH-01745 |
NOX4 Protein, Human, Recombinant (Cell-Free, His)
NOX4,Kidney oxidase-1,Renal NAD(P)H-oxidase |
Human | E. coli |
NOX4 Protein, Human, Recombinant (Cell-Free, His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 69.8?kDa and the accession number is Q9NPH5. | |||
TMPJ-00848 |
NCF1 Protein, Human, Recombinant (His)
Nox-organizing protein 2/SH3 and PX domain-containing protei... |
Human | E. coli |
Neutrophil cytosol factor 1( NCF1) is a 47 kDa cytosolic subunit of neutrophil NADPH oxidase. This oxidase is characterized as a multicomponent enzyme which is activated to produce superoxide anion. NCF2, NCF1, and a membrane bound cytochrome b558 are required for the activation of the latent NADPH oxidase. The human NCF1 gene encodes a 390 amino acids protein without a signal peptide. The NCF1 gene interacts with other subunits of nicotinamide adenine dinucleotide phosphate-oxidase (NADPH) and ... | |||
TMPH-03751 |
CYBB Protein, Human, Recombinant (His)
NADPH oxidase 2,Heme-binding membrane glyc... |
Human | E. coli |
Critical component of the membrane-bound oxidase of phagocytes that generates superoxide. It is the terminal component of a respiratory chain that transfers single electrons from cytoplasmic NADPH across the plasma membrane to molecular oxygen on the exterior. Also functions as a voltage-gated proton channel that mediates the H(+) currents of resting phagocytes. It participates in the regulation of cellular pH and is blocked by zinc. | |||
TMPY-04475 |
RFK Protein, Human, Recombinant (His)
riboflavin kinase,RIFK |
Human | E. coli |
Flavokinase is a member of the transferases family, specifically those transferring phosphorus-containing groups (phosphotransferases) with an alcohol group as acceptor. Flavokinase is an essential enzyme that catalyzes the phosphorylation of riboflavin (vitamin B2) to form flavin mononucleotide (FMN), an obligatory step in vitamin B2 utilization and flavin cofactor synthesis. It has been proposed that TNF, through the activation of the flavokinase gene, enhances the incorporation of FAD in NADP... | |||
TMPY-02439 |
Rac2 Protein, Human, Recombinant (His)
p21-Rac2,HSPC022,Gx,EN-7,ras-related C3 botulinum toxin subs... |
Human | E. coli |
Ras-related C3 botulinum toxin substrate 2 (Rac2) is a small G-protein belonging to the Ras subfamily of the GTPase family. Rac2 acts as an "on / off" switch for signal transduction cascades and motilities. When GDP is attached to the small G-protein, the enzyme is inactivated. Release of the GDP and replace of the GTP cativate the GTPasee. Rac2 remains active until the GTP is hydrolyzed to GDP. Rac2 is a hematopoietic-specific Rho family GTPase implicated as an important constituent of the NADP... | |||
TMPY-01187 |
Rac1 Protein, Human, Recombinant (GST)
Rac-1,p21-Rac1,MIG5,ras-related C3 botulinum toxin substrate... |
Human | Baculovirus Insect Cells |
RAC1 is a GTPase that belongs to the RAS superfamily of small GTP-binding proteins. Members of this superfamily appear to regulate a diverse array of cellular events, including the control of cell growth, cytoskeletal reorganization, and the activation of protein kinases. Two transcript variants encoding different isoforms have been found for RAC1 gene. RAC1 is a plasma membrane-associated small GTPase which cycles between active GTP-bound and inactive GDP-bound states. In its active state, bind... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T71328 |
Theobromine-d6
|
||
Theobromine-d6 is intended for use as an internal standard for the quantification of theobromine by GC- or LC-MS. Theobromine is a methylxanthine alkaloid and derivative of caffeine that has been found in cocoa beans and has diverse biological activities. It is an adenosine A1 receptor antagonist. Theobromine increases AMPK phosphorylation and inhibits adipocyte differentiation, ERK and JNK phosphorylation, and IL-6 and TNF-α production in 3T3-L1 preadipocytes cultured in differentiation medium.... |