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Cat. No. | Product Name | ||
---|---|---|---|
L8700 | 铁死亡化合物库 | 779 compounds | |
779 种与铁死亡通路相关的化合物,可用于高通量和高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T83972 |
NOX-6-18
GPR132 antagonist 1,GPR132-B-160 |
GPR | Endocrinology/Hormones; GPCR/G Protein |
NOX-6-18 (GPR132-B-160) 是一种具有高效性和选择性的 GPR132 拮抗剂,具有促进胰岛素分泌活性,可以调节胰岛内的巨噬细胞重编程,减少体重增加。 | |||
T73718 |
MDCG sodium
NOX 100 sodium,N-methyl-N-dithiocarboxyglucamine sodium |
Endogenous Metabolite | Metabolism |
MDCG sodium (N-methyl-N-dithiocarboxyglucamine sodium) 是一种金属螯合剂,可促进Cd的胆道排泄。 | |||
T33716 |
Norathiol
NOX-100,NOX100,NOX 100 |
Endogenous Metabolite | Metabolism |
Norathiol (N-methyl-N-dithiocarboxyglucamine) 是一种镉中毒解毒剂,也是一种金属螯合剂,可促进 109Cd 的排泄,可以用于治疗镉中毒。 | |||
T4359 |
VAS2870
|
NADPH | Metabolism |
VAS2870 是一种NADPH 氧化酶抑制剂。 | |||
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。 | |||
T68796 |
Thr101
|
Others | Others |
Thr101, also known as NOX Inhibitor VII, is a dose-dependent inhibitor of HDAC1, HDAC3, HDAC4, HDAC5, HDAC6, HDAC7, HDAC8, and HDAC9. Thr101 is also a NOX inhibitor. | |||
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。 | |||
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。 | |||
T81647 |
NOX2-IN-2
|
Others | Others |
NOX2-IN-2(化合物33)作为一种高效的NOX2抑制剂,其作用机制是针对p47phox-p22phox的蛋白-蛋白相互作用,具有0.24 μM的Ki值。该化合物能够抑制NOX2在细胞内产生的ROS。 | |||
T81648 |
NOX2-IN-1
|
Others | Others |
NOX2-IN-1 是 NOX2 (烟酰胺腺嘌呤二核苷酸磷酸氧化酶异构体 2) 的抑制剂。该化合物旨在针对 p47phox-p22phox 蛋白间相互作用,展现出优秀的结合亲和力及细胞活性。 | |||
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。 | |||
T1586 |
Tenoxicam
Ro-12-0068,替诺昔康,Tenoxicamum,Mobiflex,Tilcotil |
COX | Immunology/Inflammation; Neuroscience |
Tenoxicam (Tilcotil) 是一种抗炎化合物,具有退热止痛作用。 | |||
T25944 |
Phenoxyacetone
苯氧乙酮,NSC-1876,NSC 1876,NSC1876 |
Others | Others |
Phenoxyacetone (NSC-1876) 可抑制乙酰胆碱酯酶。 | |||
T50115 |
3-phenoxy-8-azabicyclo[3.2.1]octane HCl
|
Others | Others |
3-phenoxy-8-azabicyclo[3.2.1]octane hydrochloride 是一种合成化合物,属于氮杂双环辛烷类。它是多巴胺D2受体的强效和选择性激动剂,被广泛用于研究多巴胺信号传导的机制及其在各种生理和病理过程中的作用。 | |||
T22678 |
3,5-Bis(4-nitrophenoxy)benzoic acid
3,5-二(4-硝基苯氧基)苯甲酸,Compound W |
Gamma-secretase | Neuroscience; Proteases/Proteasome; Stem Cells |
3,5-Bis(4-nitrophenoxy)benzoic acid (Compound W) 是 γ-secretase 抑制剂。它导致 Aβ42 和 notch-1 Aβ-like peptide 25 (Nβ25) 的释放水平降低。它是母体血清中 3,3’-diiodothyronine sulfate (T2S) 的交叉反应物质,可作为胎儿甲状腺功能减退的标志物。 | |||
T5200 |
Indirubin-3'-monoxime
靛玉红-3' -单肟,Indirubin-3'-oxime |
GSK-3; Lipoxygenase; CDK | Cell Cycle/Checkpoint; Metabolism; PI3K/Akt/mTOR signaling; Stem Cells |
Indirubin-3'-monoxime (Indirubin-3'-oxime) 是一种有效的 GSK3β 抑制剂,IC50值为 22 nM。它对 CDK5/p25、CDK1/cyclin B 和CDk2/cyclin E 也有作用,IC50值分别为 100、180 和 250 nM。 | |||
T0274 |
Cinoxacin
西诺沙星,Compound 64716 |
Topoisomerase; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Cinoxacin (Compound 64716) 是一种喹诺酮类的合成抗生素, 与Oxolinic acid 和 Nalidixic acid 活性相似。 | |||
T16961 |
Supinoxin
RX-5902 |
Apoptosis; DNA/RNA Synthesis | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Supinoxin (RX-5902) 是磷酸化 p68 RNA 解旋酶的强效口服活性抑制剂,是一种抗肿瘤试剂。它与 Y593 磷酸化的 p68 相互作用并减弱 β-catenin 的核穿梭性。它诱导细胞凋亡并抑制 TNBC 癌细胞系的生长,IC50的范围为 10 nM 至 20 nM。 | |||
T2222 |
Carbinoxamine Maleate Salt
Lergefin,马来酸罗托沙敏,CarbinoxaMine Maleate |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Carbinoxamine Maleate Salt (Lergefin) 是一种乙醇胺类 H1 抗组胺药,具有温和的抗毒蕈碱和镇静作用。 | |||
T3431 |
Pardoprunox hydrochloride
SLV-308 hydrochloride,DU-126891 hydrochloride,帕多芦诺盐酸盐 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Pardoprunox hydrochloride (SLV-308 hydrochloride) 是多巴胺受体 D2、D3部分激动剂和5-HT1A 激动剂,pEC50分别为 8、9.2 和 6.3。 | |||
T68166 |
Traxanox
|
Others | Others |
Traxanox 是一种可口服的利尿剂。Traxanox 在体外增强小鼠腹膜巨噬细胞或大鼠腹膜多形核白细胞对酵母颗粒的吞噬作用。Traxanox 对抑制BALB/c小鼠抗体产生的恢复作用。 | |||
T7564 |
Chlorphenoxamine
Contristamine,氯苯沙明 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Chlorphenoxamine (Contristamine) 是一种抗组胺药和抗胆碱能药,用作止痒药和抗帕金森病药。 | |||
T14955 |
Chlorthenoxazine
氯西诺嗪,Chlorethylbenzmethoxazone |
Immunology/Inflammation related | Immunology/Inflammation |
Chlorthenoxazine (Chlorethylbenzmethoxazone) 是非甾体抗炎药。 | |||
T33479 |
Monoxerutin
Z 12007,MonoHER,7-Monohydroxyethylrutosid |
Antioxidant | oxidation-reduction |
Monoxerutin (MonoHER) 是一种血管扩张剂,具有抗氧化活性,可防止阿霉素诱导的小鼠心脏毒性,可用于研究急性呼吸系统综合征。 | |||
T20672 |
Quinoxyfen
DE-795,DE795,Legend,DE 795 |
Antifungal | Microbiology/Virology |
Quinoxyfen 具有抗菌活性,可用用于研究白粉病。 | |||
T1158 |
Phenoxybenzamine hydrochloride
苯氧苯札明,NCI-c01661,NSC 37448,盐酸酚苄明,Phenoxybenzamine HCl |
CaMK; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Phenoxybenzamine hydrochloride (NCI-c01661) 是一种选择性的 α-adrenoceptor 和 calmodulin 的抑制剂,是常用的抗高血压药。 | |||
T68161L |
Tienoxolol FA
Tienoxolol FA (90055-97-3 Free base) |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Tienoxolol FA 是一种小分子 β-肾上腺素能受体拮抗剂,可用于治疗心血管疾病和研究高血压、心机缺血。 | |||
T16522 |
Phenoxodiol
脱氢雌马酚,Dehydroequol,Idronoxil,Haginin E |
Apoptosis; IAP; Caspase; Topoisomerase; p53 | Apoptosis; DNA Damage/DNA Repair; Proteases/Proteasome |
Phenoxodiol (Idronoxil) 是合成genestein 的类似物,激活线粒体caspase 系统,抑制XIAP,使癌细胞对fas 介导的凋亡敏感。它在细胞周期的G1/S 期诱导细胞周期阻滞,通过独立于p53的方式上调p21WAF1。它通过稳定可分裂复合物抑制DNA 拓扑异构酶II,从而阻止DNA 复制。 | |||
T20293 |
Phenoxyethanol
NSC 1864,乙二醇苯醚,NSC-1864,NSC1864 |
Others; Antibacterial | Microbiology/Virology; Others |
Phenoxyethanol (NSC-1864) 是广谱抗菌剂,被用作化妆品、疫苗和纺织品中的防腐剂。它是呼吸作用氧化磷酸化的解偶联剂,竞争性地抑制苹果酸脱氢酶。 | |||
T1190 |
Cefmenoxime hydrochloride
Cefmenoxime hemihydrochloride,SCE-1365 hemihydrochloride,盐酸头孢甲肟 |
Antibacterial; Antibiotic; Antifection | Microbiology/Virology |
Cefmenoxime hydrochloride (Cefmenoxime hemihydrochloride) 是一种头孢类抗生素,可通过静脉内或肌肉内给药。 它对大多数常见的革兰氏阳性和革兰氏阴性微生物有活性,是一种肠杆菌科抑制剂,并且对 β-内酰胺酶的水解具有高度抗性。 | |||
T0917 |
Sulfaquinoxaline sodium salt
SQ-Na,磺胺喹恶啉钠盐,Sulfaquinoxaline sodium,磺胺喹啉钠 |
Antibacterial; Antibiotic; Parasite | Microbiology/Virology |
Sulfaquinoxaline sodium salt (SQ-Na) 是一种兽用广谱抗菌剂,有抗革兰氏阴性菌和革兰氏阳性菌活性。Sulfaquinoxaline 能用于预防球虫病和细菌感染。 | |||
T22424 |
1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea
|
Apoptosis; STAT | Apoptosis; JAK/STAT signaling; Stem Cells |
SC-1 是一种 Sorafenib 的衍生物,可抑制 STAT3磷酸化,通过依赖 SHP-1 的 STAT3失活诱导细胞凋亡,具有抗癌作用。 | |||
T19633 |
Ionox 330
Antioxidant 40,BRN 2034522,Ahydol,Antioxidant 330,抗氧剂 330,AO-40 |
Others | Others |
Ionox 330 (Ahydol) 是一种用作抗氧化剂的烷基酚化合物。 | |||
T64388 |
3-Phenoxybenzaldehyde
|
Complement System | Immunology/Inflammation |
3-Phenoxybenzaldehyde 是补体经典途径抑制剂,IC50= 1388μM。 | |||
T27417L |
Glutathione arsenoxide hydrochloride
GSAO HCl,Glutathione arsenoxide hydrochloride(1271726-51-2 Free base) |
Apoptosis; AChR | Apoptosis; Neuroscience |
Glutathione arsenoxide hydrochloride (Glutathione arsenoxide hydrochloride(1271726-51-2 Free base)) 是一种潜在的抗癌活性分子和肿瘤代谢抑制剂。Glutathione arsenoxide hydrochloride 靶向线粒体内膜腺嘌呤核苷酸转移酶 (ANT),对细胞增殖有抑制作用,促进细胞凋亡。Glutathione arsenoxide hydrochloride 可用于识别如蛋白质二硫异构酶一样的细胞表面蛋白质。 | |||
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。 | |||
T9434 |
3-Phenoxybenzaldehyde cyanohydrin
三苯氧基苯甲醛,2-Hydroxy-2-(3-phenoxyphenyl)acetonitrile |
Others | Others |
3-Phenoxybenzaldehyde cyanohydrin (2-Hydroxy-2-(3-phenoxyphenyl)acetonitrile) 是拟除虫菊酯类杀虫剂如氯菊酯的中间体。 | |||
T50113 |
(4R)-3-[2-(4-chlorophenoxy)-2-methylpropanoyl]-1,3-thiazolidine-4-carboxylic acid
|
Others | Others |
(4R)-3-[2-(4-chlorophenoxy)-2-methylpropanoyl]-1,3-thiazolidine-4-carboxylic acid 可用于化学和生命科学领域的研究。 | |||
T20824 |
Cyanox CY 1790
Lowinox 1790,Irganox 3790,抗氧化剂 TH-1790,Antioxidant 1790,Irganox-3790,DN 90 |
Others | Others |
Cyanox CY 1790 (Irganox-3790) 是一种具有抗氧化活性的试剂。 | |||
T0717 |
Enoxacin hydrate
CI-919 hydrate,Enoxacin Sesquihydrate,依诺沙星半水合物,AT-2266 hydrate,依诺沙星倍半水合物 |
DNA gyrase; DNA/RNA Synthesis; Topoisomerase; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Enoxacin hydrate (AT-2266 hydrate) 是氟喹诺酮,可干扰DNA 复制,抑制细菌 DNA 促旋酶 (IC50=126 µg/ml) 和拓扑异构酶 IV (IC50=26.5 µg/ml)。它是特异性癌症生长抑制剂,抑制革兰氏阳性和阴性细菌。 | |||
T10459 |
Banoxantrone dihydrochloride
AQ4N dihydrochloride,AZD1689 2HCl |
NOS | Immunology/Inflammation |
Banoxantrone dihydrochloride (AQ4N dihydrochloride) 是一种新型缺氧细胞毒素,通过 iNOS 依赖机制选择性地杀死缺氧细胞。 | |||
T9058 |
Bisphenoxyethanolfluorene
|
Others | Others |
Bisphenoxyethanolfluorene 是一种高稳定性的新型有机化工原料,主要用于合成耐热、透明性和高折射率的高分子单体。 | |||
T1639 |
Amlexanox
氨来呫诺,CHX3673,Amoxanox,氨来诺,AA673 |
IL Receptor; FGFR; Others; IκB/IKK | Angiogenesis; Immunology/Inflammation; NF-κB; Others; Tyrosine Kinase/Adaptors |
Amlexanox (AA673) 是一种特异性的 IKKε和 TBK1抑制剂,其 IC50=1-2 μM。 | |||
T19679 |
Benoxaprofen
氧苯恶唑丙酸,NSC 299582,LY-90459,Benoxaphen. Compound 90459 |
COX | Immunology/Inflammation; Neuroscience |
Benoxaprofen (NSC-299582) 是长效的、强效的抗炎和解热化合物,在体外具有较弱的对环氧合酶的抑制作用,也可以抑制脂氧合酶,在一些炎症动物模型中抑制单核细胞迁移。 | |||
T5938 |
4-Phenoxybenzylamine
|
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
4-Phenoxybenzylamine 通过稳定无活性构象来抑制NS3蛋白的功能,对 HCV NS3/4a 的 IC50 约为 500 μM。 | |||
T1401 |
Meclofenoxate hydrochloride
Meclofenoxate (Centrophenoxine) HCl,Lucidril,盐酸甲氯芬酯,Cerutil,盐酸甲氯酚酯,Meclofenoxate HCl |
Lipoxygenase; COX; AChR; iGluR | Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Meclofenoxate hydrochloride (Lucidril) 是二甲基氨基乙醇和对氯苯氧乙酸的酯,有刺激记忆和提高认知的活性。 | |||
T3263 |
(6R,7S)-Cefminox sodium heptahydrate
Meicelin,头孢米诺钠,Cefminox Sodium,Alteporina,Tencef |
Antibiotic | Microbiology/Virology |
(6R,7S)-Cefminox sodium heptahydrate (Meicelin) 是一种 Cefminox sodium heptahydrate 的异构体。它也是一种具有广谱抗菌活性的 β-内酰胺头孢菌素抗生素。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7732 |
Carbenoxolone
Biogastrone,甘珀酸,Carbenoxolona,Carbenoxolone,Bioral |
Dehydrogenase; Gap Junction Protein | Cytoskeletal Signaling; Metabolism |
Carbenoxolone (Carbenoxolona) 是 11β-HSD 和 gap junction connexin 通道的抑制剂。 Carbenoxolone 抑制巨噬细胞迁移到心房并防止脂肪肝的发展。 | |||
T5S0658 |
Corynoxine
柯诺辛,柯诺辛碱 |
Autophagy | Autophagy |
Corynoxine 是从大叶钩藤中分离出的一种四环羟吲哚生物碱。它是一种自噬增强剂,可通过Akt/mTOR 途径促进 α-突触核蛋白的清除。 | |||
T6S0654 |
Isocorynoxeine
7-Isocorynoxeine,异去氢钩藤碱 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Isocorynoxeine (7-Isocorynoxeine) 是钩藤中的一种生物碱,剂量依赖性抑制5-HT2A 受体介导的电流反应,IC50为 72.4 μM。 | |||
TN1527 |
(-)-Corynoxidine
Corynoxidine |
Antibacterial; AChE; Antifection | Microbiology/Virology; Neuroscience |
(-)-Corynoxidine 是一种源自 Stephania succifera 块茎的 AChE 抑制剂。 Corynoxidine 对金黄色葡萄球菌和耐甲氧西林金黄色葡萄球菌具有不同程度的抗菌活性。 | |||
T0073 |
Octinoxate
2-Ethylhexyl 4-methoxycinnamate,ethylhexyl methoxycinnamate,Octyl 4-methoxycinnamate,甲氧基肉桂酸辛酯,Octyl methoxycinnamate,对甲氧基肉桂酸辛酯 |
Others | Others |
Octyl 4-methoxycinnamate 是一种有机化合物,能够吸收来自太阳的UV-B射线,保护皮肤免受损伤,也可用于减少疤痕的外观,常用于是防晒霜和唇膏等化妆品中。Octinoxate 具有雄激素和雌激素作用。 | |||
T9932 |
2(1H)-Quinoxalinone
|
Others | Others |
2(1H)-Quinoxalinone 是从 Clitoria ternatea 和 Hibiscus rosa sinensis 等食用花卉中提取的天然产物。 | |||
TN3110 |
5-Geranoxy-7-methoxycoumarin
|
Anti-infection; Antibacterial; Antifungal | Microbiology/Virology |
5-Geranoxy-7-methoxycoumarin 是一种香豆素。它诱导细胞凋亡,具有抗癌、抗真菌和抗菌活性。 | |||
T1468 |
Lornoxicam
Ro 13-9297,Chlortenoxicam,TS110,氯诺昔康 |
COX; Endogenous Metabolite | Immunology/Inflammation; Metabolism; Neuroscience |
Lornoxicam (Chlortenoxicam) 是一种新型非甾体抗炎药,是高活性 COX-1 和 COX-2 抑制剂,IC50 分别为 5 和 8 nM。 | |||
T7932 |
[(2-Methoxyphenoxy)Methyl]Oxirane
|
Others | Others |
[(2-Methoxyphenoxy)Methyl]Oxirane 是一种天然产物。 | |||
T6S0655 |
Corynoxeine
|
ERK | MAPK |
Corynoxeine 是从钩藤中分离的一种天然产物,是 PDGF-BB 诱导血管平滑肌细胞 (VSMCs) 增殖过程中的 ERK1/ERK2抑制剂。 | |||
T9894 |
2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethyl methanesulfonate
|
Others | Others |
2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethyl methanesulfonate 是一种天然产物,可作为参考标准。 | |||
T5143 |
Corynoxine hydrochloride(6877-32-3(free base))
|
Autophagy | Autophagy |
Corynoxine hydrochloride(6877-32-3(free base)) 是一种天然羟吲哚生物碱,可在不同的神经元细胞系(包括 N2a 和 SHSY-5Y 细胞)中诱导自噬。 | |||
TQ0258 |
Corynoxine B
柯诺辛碱 B,柯诺辛碱B |
Autophagy | Autophagy |
Corynoxine B is a Beclin-1-dependent autophagy inducer. It is an natural alkaloid isolated from Uncaria rhynchophylla (Miq.) Jacks (Gouteng in Chinese). | |||
T75438 |
Corynoxine hydrochloride
|
Others | Others |
Corynoxine hydrochloride 是一种从Uncaria macrophylla 中分离出的四环羟吲哚生物碱。Corynoxine hydrochloride 是一种天然的自噬增强剂,可通过Akt/mTOR 途径促进 α-突触核蛋白的清除。 | |||
TN1607 |
Epicorynoxidine
|
Others | Others |
Epicorynoxidine 是一种从 Corydalis tashiroi 植物中提取的生物碱。 | |||
TN3801 |
methoxyphenoxy]oxane-3,4,5-triol
Dehydrodiconiferyl alcohol 4-O-beta-D-glucopyranoside |
Others | Others |
Dehydrodiconiferyl alcohol 4-O-beta-D-glucopyranoside is a natural product from Ligusticopsis wallichiana (DC) Pimenov & Kljuykov. | |||
T10010 | 1-(2-Quinoxalinyl)-1,2,3,4-butanetetrol | Others | Others |
1-(2-Quinoxalinyl)-1,2,3,4-butanetetrol is an endogenous metabolite. | |||
T19091 |
2-(2',3',4'-Trihydroxybutyl)quinoxaline
|
Others | Others |
2-(2',3',4'-Trihydroxybutyl)quinoxaline is a food metabolite. | |||
T81458 |
Pinofuranoxin A
|
||
Pinofuranoxin A 对Athelia rolfsii和Phytophthora cambivora的生长展现出了完全抑制效果。 | |||
T35359 |
3-Phenoxybenzoic acid
3-Phenoxybenzoic acid,m-phenoxybenzoic acid,3-PBA |
Others | Others |
3-phenoxybenzoic acid (3-PBA) 是拟除虫菊酯的中间代谢产物,比其母体化合物毒性更高,并已在牛奶、土壤和人类尿液中检测到。 | |||
T3834 |
8-Epideoxyloganic acid
8-表去氧马钱酸 |
ROS; Immunology/Inflammation related | Immunology/Inflammation |
8-Epideoxyloganic acid 是从 Incarvillea delavayi 中分离得到的一种环烯醚萜苷。它具有微弱的缓解疼痛活性。 | |||
T3S1416 |
Decursin
Decursinol angelate,前胡素,(+)-Decursin,紫花前胡素 |
Apoptosis; PKC | Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling |
Decursin (Decursinol angelate) 是一种细胞毒性剂,是一种来自朝鲜当归根的有效蛋白激酶 C 激活剂。它通过 Hippo/YAP 信号通路抑制 HepG2 细胞的生长。它通过下调 CXCR7 表达来抑制胃癌中的肿瘤生长,迁移和侵袭。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-01276 |
ENOX1 Protein, Human, Recombinant (His)
Ecto-NOX disulfide-thiol exchanger 1,ENOX1... |
Human | E. coli |
Probably acts as a terminal oxidase of plasma electron transport from cytosolic NAD(P)H via hydroquinones to acceptors at the cell surface. Hydroquinone oxidase activity alternates with a protein disulfide-thiol interchange/oxidoreductase activity which may control physical membrane displacements associated with vesicle budding or cell enlargement. The activities oscillate with a period length of 24 minutes and play a role in control of the ultradian cellular biological clock. | |||
TMPJ-00848 |
NCF1 Protein, Human, Recombinant (His)
Nox-organizing protein 2/SH3 and PX domain-containi... |
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-01277 |
ENOX2 Protein, Human, Recombinant
ENOX2,APK1 antigen,Cytosolic ovarian carcinoma anti... |
Human | E. coli |
May be involved in cell growth. Probably acts as a terminal oxidase of plasma electron transport from cytosolic NAD(P)H via hydroquinones to acceptors at the cell surface. Hydroquinone oxidase activity alternates with a protein disulfide-thiol interchange/oxidoreductase activity which may control physical membrane displacements associated with vesicle budding or cell enlargement. The activities oscillate with a period length of 22 minutes and play a role in control of the ultradian cellular biol... | |||
TMPH-01278 |
ENOX2 Protein, Human, Recombinant (His & Myc)
Cytosolic ovarian carcinoma antigen 1,Ecto-NOX disu... |
Human | E. coli |
May be involved in cell growth. Probably acts as a terminal oxidase of plasma electron transport from cytosolic NAD(P)H via hydroquinones to acceptors at the cell surface. Hydroquinone oxidase activity alternates with a protein disulfide-thiol interchange/oxidoreductase activity which may control physical membrane displacements associated with vesicle budding or cell enlargement. The activities oscillate with a period length of 22 minutes and play a role in control of the ultradian cellular biol... | |||
TMPH-01744 |
NOX1 Protein, Human, Recombinant (His)
NADH/NADPH mitogenic oxidase subunit P65-MOX,NADPH oxidase 1... |
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,Kidney ... |
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. | |||
TMPH-01746 |
NOX4 Protein, Human, Recombinant (E. coli, His)
Kidney superoxide-producing NADPH oxidase,NOX4,NADP... |
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-00361 |
Beta-mammal toxin Cn2 Protein, Centruroides noxius, Recombinant (His)
Toxin 2,Beta-mammal toxin Cn2,Toxin II.9.2.2 |
Centruroides noxius | P. pastoris (Yeast) |
Mammal beta-toxins bind voltage-independently at site-4 of sodium channels (Nav) and shift the activation voltage to more negative potentials. This toxin is active against mammals. Beta-mammal toxin Cn2 Protein, Centruroides noxius, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 9.6 kDa and the accession number is P01495. | |||
TMPY-02391 |
SUMO1 Protein, Human, Recombinant (His)
small ubiquitin-like modifier 1,SMT3C,SMT3,SMT3H3,UBL1,SENP2... |
Human | E. coli |
Small ubiquitin-like modifier protein (SUMO) modification is a highly dynamic process, catalyzed by SUMO-specific activating (E1), conjugating (E2) and ligating (E3) enzymes, and reversed by a family of SUMO-specific proteases (SENPs). Small ubiquitin-like modifier 1 (SUMO1) is a member of the superfamily of ubiquitin-like proteins. Despite its structural similarity with ubiquitin, SUMO1 does not seem to play any role in protein degradation. SUMO1 plays an important role in modulation of NOX act... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19201 |
Banoxantrone-d12 dihydrochloride
AQ4N D12 dihydrochloride |
Others | Others |
Banoxantrone D12 (AQ4N D12) dihydrochloride is the deuterium-labeled Banoxantrone. Banoxantrone is a bioreductive agent that can be reduced to a stable, DNA-affinity compound AQ4, which is a topoisomerase II inhibitor. | |||
TMIH-0418 |
Ozenoxacin-d3
|
||
Ozenoxacin-d3 是 Ozenoxacin 的氘代化合物。Ozenoxacin 的 CAS 号为 245765-41-7。Ozenoxacin是一种新型喹诺酮类抗生素,能够抵抗大多数从在皮肤和软组织感染中分离的微生物。 | |||
TMIJ-0027 |
3-Methyl-2-quinoxalinecarboxylic Acid-d4
MQCA-d4 |
||
3-Methyl-2-quinoxalinecarboxylic Acid-d4 是 3-Methyl-2-quinoxalinecarboxylic Acid 的氘代化合物。3-Methyl-2-quinoxalinecarboxylic Acid 的 CAS 号为 74003-63-7。3-Methyl-2-quinoxalinecarboxylic acid 在生命科学相关研究中具有广泛的应用。 | |||
TMID-0030 |
4-Bromophenoxybenzene-d5
|
||
4-Bromophenoxybenzene-d5 是 4-Bromophenoxybenzene 的氘代化合物。4-Bromophenoxybenzene 的 CAS 号为 101-55-3。 | |||
TMID-0268 |
Enoxacin-d8 HCl
|
||
Enoxacin-d8 HCl 是 Enoxacin HCl 的氘代化合物。Enoxacin HCl 的 CAS 号为 74011-31-7。 | |||
T10458 |
Banoxantrone (D12)
Banoxantrone D12,AQ4N D12 |
Others | Others |
Banoxantrone D12 (AQ4N D12) is the deuterium-labeled Banoxantrone. Banoxantrone is a bioreductive agent that can be reduced to a stable, DNA-affinity compound AQ4, which is a topoisomerase II inhibitor. | |||
TMID-0127 |
MINOXIDIL-d10
|
||
MINOXIDIL-d10 是 MINOXIDIL 的氘代化合物。MINOXIDIL 的 CAS 号为 38304-91-5。Minoxidil 是一种是 ATP 敏感的钾通道 (KATP) 开放剂,可作为有效的口服降压药和外周血管舒张药,促进血管扩张并促进头发的生长。Minoxidil 还是一种大豆脂氧合酶的有效抑制剂,IC50为 20 μM。 | |||
T71212 |
Lornoxicam-d4
|
||
Lornoxicam-d4 is intended for use as an internal standard for the quantification of lornoxicam by GC- or LC-MS. Lornoxicam is a COX inhibitor and non-steroidal anti-inflammatory drug (NSAID) with anti-inflammatory and analgesic properties. It inhibits production of thromboxane B2 from arachidonic acid in HEL human erythroleukemic cells, which endogenously express COX-1, as well as inhibits LPS-induced formation of prostaglandin F1α from arachidonic acid in Mono-Mac-6 cells, which endogenously e... | |||
TMID-0054 |
2-Quinoxalinecarboxylic acid-d4
|
||
2-Quinoxalinecarboxylic acid-d4 是 2-Quinoxalinecarboxylic acid 的氘代化合物。2-Quinoxalinecarboxylic acid 的 CAS 号为 879-65-2。 | |||
TMIH-0542 |
Sulfaquinoxaline-d4
|
||
Sulfaquinoxaline-d4 是 Sulfaquinoxaline 的氘代化合物。 | |||
TMIJ-0433 |
2,4,5-Trichlorophenoxyacetic Acid-d4
|
||
2,4,5-Trichlorophenoxyacetic Acid-d4 是 2,4,5-Trichlorophenoxyacetic Acid 的氘代化合物。2,4,5-Trichlorophenoxyacetic Acid 的 CAS 号为 93-76-5。 | |||
TMIH-0230 |
Ezetimibe-d4 Phenoxy ß-D-Glucuronide
Ezetimibe Phenoxy Glucuronide-d4 |
||
Ezetimibe-d4 Phenoxy ß-D-Glucuronide 是 Ezetimibe Phenoxy ß-D-Glucuronide 的氘代化合物。Ezetimibe Phenoxy ß-D-Glucuronide 的 CAS 号为 190448-57-8。 | |||
TMID-0272 |
Cinoxacino-d8
|
||
Cinoxacino-d8 是 Cinoxacino 的氘代化合物。Cinoxacino 的 CAS 号为 28657-80-9。Cinoxacin是一种喹诺酮类的合成抗生素, 与Oxolinic acid和 Nalidixic acid活性相似。 |