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Cat. No. | Product Name | Target | Signaling Pathways |
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T38003 |
Levofloxacin N-oxide
|
Others | Others |
Levofloxacin N-oxide 是从左氧氟沙星中分离出来的杂质。 | |||
T31532 |
Disperse Red 1
Celliton Scarlet B,Neosetile Scarlet B,Diacelliton Scarlet B,Fenacet Scarlet B,分散红 1,Celliton Red B |
Others | Others |
Disperse Red 1 (Celliton Scarlet B) 是偶氮苯衍生物,是偶氮纺织品染料,普遍用于纺织工业中的聚酯织物染色。 | |||
T22309 |
2,5-Dimethyl-3(2H)-furanone
2,5-二甲基-3(2H)-呋喃酮,2,5-Dimethyl-2,3-dihydrofuran-3-one |
Others | Others |
2,5-Dimethyl-3(2H)-furanone (2,5-Dimethyl-2,3-dihydrofuran-3-one) 是一种调味物质,无遗传毒性。 | |||
TN2258 |
Tartrazine
酒石黄,FD&C Yellow No. 5,Acid Yellow 23,酸性黄 23 |
Others | Others |
Tartrazine (Acid Yellow 23) 是偶氮型酸性染料,是橙黄色粉末,溶于水中呈黄色,常用作食品着色的合成柠檬黄色偶氮染料。 | |||
T1887 |
Inauhzin
INZ |
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Inauhzin (INZ) 是一种新型小分子,通过抑制 SIRT1 活性有效地重新激活 p53,促进人 Y 细胞的 p53 依赖性凋亡,在 A549 细胞中的IC50为3 uM。 | |||
T2204 |
Diaveridine
二氨藜芦啶,EGIS-5645,敌菌净,CCRIS-3784,AI3-23935 |
DHFR; Antifolate; Antibacterial | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Diaveridine (AI3-23935) 是二氢叶酸还原酶的抑制剂,对于野生型 DHFR 的Ki 值为 11.5 nM。它也是一种抗菌剂。 | |||
T19051 |
Reactive Blue 4
活性艳蓝X-ARL,活性蓝4 |
Others | Others |
Reactive Blue 4 是蒽醌类染料,具有植物毒性、细胞毒性和基因毒性。它可作为单一的比色化学传感器,用于在水介质中连续测定具有不同光学响应的多种分析物。 | |||
T69840 |
MX106
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MX106 is a survivin inhibitor which induces degradation of XIAP and/or cIAP1, and suppresses genotoxic NF-kappaB activation. | |||
T36952 |
N-Nitroso Fluoxetine
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N-Nitroso fluoxetine is a derivative of fluoxetine.1It is genotoxic toS. typhimuriumwhen used at concentrations ranging from 0.06 to 0.12 mg/ml. | |||
T40740 |
Dibromochloroacetaldehyde
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Dibromochloroacetaldehyde, a trihalogenated acetaldehyde compound, is present as a byproduct in drinking water. It exhibits genotoxic properties. | |||
T69845 |
MX107
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MX107 is a survivin inhibitor which induces degradation of XIAP and/or cIAP1, and suppresses genotoxic NF-kappaB activation. | |||
T39657 |
Cyanazine
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Cyanazine, a triazine herbicide, is utilized for effective control of a diverse range of grass and broadleaf weeds. It has been scientifically validated as non-genotoxic. | |||
T28117 |
MSN-50
MSN50,MSN 50 |
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MSN-50, an inhibitor of Bax and Bak oligomerization, inhibits liposome permeabilization, prevents genotoxic cell death and promotes neuroprotection. | |||
T32272 |
Jatropham
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Jatropham 是一种天然化合物,从百合花中分离得到。它被证明具有调节和降低 zeocin 的细胞毒性和遗传毒性/致裂作用的潜力。 | |||
T41127 | Bromochloroacetaldehyde | ||
Bromochloroacetaldehyde is a dihalogenated acetaldehyde compound that is commonly found as a byproduct in drinking water. It exhibits genotoxic properties. | |||
T69434 | Methapyrilene fumarate | ||
Methapyrilene fumarate is a histamine H1 antagonist with sedative action used as a hypnotic and in allergies. It is a hepatocarcinogen in sufficiently high doses, inducing mutations through an indirect genotoxic mechanism; e.g., via an oxidative mechanism or interaction with chromosomal proteins. | |||
T74465 |
Colibactin
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Colibactin 是一种复杂的次级代谢产物,由一些具有遗传毒性的肠道大肠杆菌菌株产生。Colibactin 具有研究结直肠癌的潜力。 | |||
T81748 |
MRV03-069
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MRV03-069(化合物3)为一种选择性ClbP抑制剂,具备阻止Colibactin对真核细胞基因毒性的能力,适用于结直肠癌的研究。 | |||
T74985 | MRV03-037 | ||
MRV03-037 是一种选择性的大肠杆菌素活化肽酶 (ClbP) 抑制剂,能阻断Colibactin 对真核细胞的基因毒性作用。MRV03-037 可以防止肠道细菌基因毒素的产生。 | |||
T78549 |
Ethylene glycol dimethacrylate
|
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
Ethylene glycol dimethacrylate 是一种具有细胞毒性和基因毒性作用的甲基丙烯酸酯单体。它可增加人牙龈成纤维细胞 (HGF) 内的活性氧 (ROS) 产生,引发 DNA 损伤和细胞凋亡 (apoptosis),并使细胞周期在 G1/G0 期停滞。 | |||
T81749 |
MRV03-068
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MRV03-068(化合物2)作为一种选择性的ClbP抑制剂,有效抑制Colibactin对真核细胞的基因毒性。该化合物在结直肠癌研究中具有潜在应用价值。 | |||
T73517 |
RK-701
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RK-701 是一种G9a 高选择性且非遗传毒性的抑制剂,IC50值为 23-27 nM。RK-701 选择性的上调 HbF、γ- Globin、BGLT3 的表达,下调 H3K9me2 的表达。RK-701 也对 BCL11A 和 ZBTB7A 有抑制作用。 | |||
T60888 | NiCur | ||
NiCur 可阻断CBP HAT 活性并在基因毒性应激时下调 p53 的激活。NiCur 是CBP 组蛋白乙酰转移酶 (HAT)的有效选择性抑制剂,IC50值为 0.35 μΜ。 NiCur 可用于机制研究,不影响目标蛋白的表达。 | |||
T63337 | CYP2C19-IN-1 | ||
CYP2C19-IN-1 是强效的,无遗传毒性的、无肝脏毒性的 CYP2C19 抑制剂。 CYP2C19-IN-1 能够抑制 RNA 依赖的 RNA 聚合酶 (RdRP) (Ki: 6.16 μM),能够用于研究寨卡病毒 (ZIKV) 感染。 | |||
T36235 |
5-Chlorouracil
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5-Chlorouracil is a chlorinated derivative of the pyrimidine nucleoside base uracil . In vivo, it is converted into chlorodeoxyuridine, which is mutagenic and genotoxic.1 Uracil is chlorinated at the 5 position in a cell-free myeloperoxidase, peroxide, and chloride system in which hypochlorous acid is formed.2 5-Chlorouracil has been found in human neutrophils stimulated with phorbol 12-myristate 13-acetate in vitro and in inflammatory human exudate isolated from sites of superficial infection. ... | |||
T69908 |
Pidnarulex HCl
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Pidnarulex HCl is the salt form of CX-5461, a first-in-class non-genotoxic small molecule targeted inhibitor of RNA polymerase I (Pol I) that activates the p53 pathway without causing DNA damage. CX-5461 selectively inhibits rRNA synthesis by Pol I in the nucleolus, but does not inhibit mRNA synthesis by RNA Polymerase II (Pol II) and does not inhibit DNA replication or protein synthesis. Inhibition of Pol I results in nucleolar stress and release of ribosomal proteins (RP) from the nucleolus. T... | |||
T36241 |
Arecaidine propargyl ester (hydrobromide)
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Arecaidine propargyl ester is an agonist of M2muscarinic acetylcholine receptors (mAChRs).1It selectively binds to M2over M1, M3, M4, and M5mAChRs in CHO cells expressing the human receptors (Kis = 0.0871, 1.23, 0.851, 0.977, and 0.933 μM, respectively). Arecaidine propargyl ester induces contractions in isolated guinea pig atrium (pD2= 8.67). It induces apoptosis and the production of reactive oxygen species (ROS) in U87 and U251 glioblastoma cells when used at a concentration of 100 μM.2Arecai... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T19137 |
4'-Methylacetophenone
|
Others | Others |
4′-methylacetophenone 是一种香料,普遍存在于食品中的挥发性化合物和某些天然复合物中。 | |||
T10148 |
4-Hydroxynonenal
4-羟基壬烯醛,4-HNE |
Dehydrogenase; Endogenous Metabolite | Metabolism |
4-Hydroxynonenal (4-HNE) 是一种 α,β 不饱和羟基烯醛,可作为氧化/亚硝化应激生物标志物。它是ALDH2的底物和抑制剂。它可以调节许多信号传导过程,主要是通过与蛋白质,核酸和膜脂质中具有亲核官能团的共价加合物形成的。它通过线粒体在癌症中起重要作用。 | |||
T19081 |
1,3-Dithiane
1,3-Dithian,M-DITHIANE,1,3-Dithiacyclohexane,1,3-二噻烷 |
Anti-infection; Endogenous Metabolite; Antibacterial | Metabolism; Microbiology/Virology |
1,3-Dithiane (1,3-Dithian) 是一种受保护的甲醛阴离子等价物,可用作有用的标记合成子。它是在煮熟的牛肉提取物中发现的含硫美拉德反应产物 。 | |||
TN1886 |
Lucidin primeveroside
Lucidin 3-O-primeveroside,亮黄素3-桑色素酊 |
Topoisomerase | DNA Damage/DNA Repair |
Lucidin primeveroside (Lucidin 3-O-primeveroside) 是从茜草的根粉中分离得到的天然产物,可用作着色剂和食用色素。 Lucidin Primeveroside 可以在小鼠体内代谢转化为基因毒性化合物 Lucidin。 | |||
T22857 |
Illudin S
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Apoptosis; DNA Alkylator/Crosslinker; Antifungal | Apoptosis; DNA Damage/DNA Repair; Microbiology/Virology |
Illudin S (ILS)是一种真菌倍半萜次生代谢物,具有很强的遗传毒性和细胞毒性 | |||
TJS0405 |
Lucidin
NSC 30546,芦西定;卢西定,卢西定,亮黄素,Henine |
Others | Others |
Lucidin (NSC-30546) 是茜草中的一种天然成分,可以诱导细菌和哺乳动物细胞的突变。 | |||
T37101 |
1-Hydroxyanthraquinone
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DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
1-Hydroxyanthraquinone 是口服有效的天然产物,来源于植物 Tabebuia avellanedae,显示出致癌活性。 | |||
TN2245 |
Sunset Yellow FCF
Food Yellow 3,Orange Yellow S,Sunset yellow,CI 15985 |
Androgen Receptor | Endocrinology/Hormones |
Sunset Yellow FCF (Sunset yellow) 是一种橙色偶氮染料,吸光度具有pH 依赖性。Sunset Yellow FCF 可在食品,化妆品和药品中使用,在许多食品中用作着色剂食品添加剂,它们可能具有细胞毒性和遗传毒性,因此在使用这些材料作为食品添加剂时必须小心。 | |||
TN4219 |
Homobaldrinal
|
Others | Others |
Homobaldrinal has low toxic activity. It has genotoxic activity in the Salmonella/microsome test and the SOS-chromotest. | |||
TN4913 |
Riddelline
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VEGFR; DNA/RNA Synthesis | Angiogenesis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Tyrosine Kinase/Adaptors |
Riddelline is a potent genotoxic agent in vitro and induces significant elevations in unscheduled DNA synthesis and S-phase synthesis in rat liver. | |||
TN3403 |
Djalonensone
交链孢霉甲基醚,Alternariol monomethyl ether |
Immunology/Inflammation related | Immunology/Inflammation |
Djalonensone (Alternariol monomethyl ether) 具有强大的 DPPH 自由基清除作用。 | |||
T35770 |
Cylindrospermopsin
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Cylindrospermopsin, a tricyclic uracil derivative, is a cyanobacterial toxin that was first discovered in an algal bloom contaminating a local drinking supply on Palm Island in Queensland, Australia after an outbreak of a mysterious disease. Cylindrospermopsin targets protein and glutathione synthesis in hepatocytes (IC50s = 1.3 and 2.4 µM, respectively), leading to cell death. [1] It has been shown to inhibit the activity of the uridine monophosphate synthase complex with a Ki value of 10 &... |