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3
Cat. No. | Product Name | Target | Signaling Pathways |
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T21859 |
ARM1
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Aminopeptidase; Epoxide Hydrolase | Metabolism |
ARM1 是氨基肽酶和环氧化物水解酶抑制剂,IC50分别为为7.61 µM 和12.4 µM。 | |||
T41319 |
D-Saccharic acid 1,4-lactone hydrate
|
Others | Others |
D-Saccharic acid 1,4-lactone hydrate 是β-葡萄糖醛酸酶的有效抑制剂(IC50=48.4 μM),可用作标准药物。D-Saccharic acid 1,4-lactone hydrate 显示出抗癌、解毒和抗氧化的活性性。 | |||
T14571 |
Bifenazate
|
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Bifenazate 是 GABA 受体的正向变构调节剂。 Bifenazate 是一种杀螨剂,可在 25 ppm 的浓度下控制 100% 的螨虫。 | |||
T40296 |
MCA17-1
MCA17-1 |
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MCA17-1 exhibits superior bioactivity compared to the positive control, obeticholic acid (OCA), in the treatment of liver fibrosis. | |||
T82398 |
Firefly Luciferase circRNA
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Firefly Luciferase circRNA 是一种从Photinus pyralis(萤火虫)分离的荧光素酶蛋白,适用于作为环状RNA转染的阳性对照,用于监测和优化转染效率。 | |||
T71097 |
DC-120
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DC-120 is an ATP competitive AKT kinase inhibitor that suppressed proliferation and induced apoptosis in liver cancer cells both in vitro and in vivo. DC120 blocked the phosphorylation of downstream molecules in the AKT signal pathway in dose- and time-dependent manners both in vitro and in vivo. DC120 inhibits AKT activity in vitro with an EC(50) of 153 nM. DC120 at 20 mg/kg/day inhibited the CNE2 xenograft tumor growth with a treated group/control group ratio of 38.1%, accompanied by increas... | |||
T82497 |
eGFP circRNA
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eGFP circRNA,能够编码由Aequorea victoria水母分离得到的绿色荧光蛋白。作为哺乳动物细胞培养中的常规直接检测报告蛋白,其在509 nm波长下发出鲜明的绿光。eGFP circRNA作为环状RNA转染的首选阳性对照,对于监测及提升转染效率具有重要意义。 | |||
T35422 |
5'-pApA (sodium salt)
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5'-pApA is a linearized form of cyclic di-AMP, a bacterial second messenger that activates the host innate immune system through stimulator of interferon genes (STING).1,2,3,4It is a metabolite of cyclic di-AMP formedviahydrolysis by various phosphodiesterases (PDEs).55'-pApA is intended for use as a negative control for cyclic di-AMP signaling. 1.Burdette, D.L., Monroe, K.M., Sotelo-Troha, K., et al.STING is a direct innate immune sensor of cyclic-di-GMPNature478(7370)515-518(2011) 2.Parvatiyar... | |||
T67442 |
CGP-53716
|
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The growth factors, platelet-derived growth factor (PDGF) and basic fibroblast growth factor (bFGF) play major roles in enhanced smooth muscle cells growth in rodent blood vessels after vascular injury. Tyrosine kinase inhibition has been shown to be effective in blocking tyrosine phosphorylation at the PDGF and bFGF receptors in cultured fibroblast and vascular smooth muscle cells which in turn inhibits their proliferation[1]. CGP 53716 is a specific PDGFR tyrosine kinase inhibitor on SMC (smoo... | |||
T36629 | Givinostat | ||
Givinostat (ITF-2357) is a HDAC inhibitor with an IC50 of 198 and 157 nM for HDAC1 and HDAC3, respectively. Givinostat (ITF2357) suppresses total LPS-induced IL-1β production robustly compared with the reduction by ITF3056. At 25, 50, and 100 nM, Givinostat reduced IL-1β secretion more than 70%. Givinostat (ITF-2357) suppresses the production of IL-6 in PBMCs stimulated with TLR agonists as well as the combination of IL-12 plus IL-18. IL-6 secretion decreases to 50% at 50 nM Givinostat, but at 1... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN3056 | 4-O-Galloylbergenin | Others | Others |
4-O-Galloylbergenin shows significant 2,2-diphenyl-1-picrylhydrazyl (DPPH) free-radical scavenging activity with EC50 7.8 uM, it shows more antioxidant activity than the positive control vitamin C (EC50 = 28.3 uM). | |||
TN5154 | Torilolone | Others | Others |
Torilin and torilolone show hepatoprotective effects on tacrine-induced cytotoxicity in human liver-derived Hep G2 cells,the EC50 values are 20.6 +/- 1.86 and 3.6 +/- 0.1 microM, respectively; and silybin as a positive control shows an EC50 value of 69.0 | |||
TN1606 |
(-)-Epiafzelechin
(-)-表阿夫儿茶精,表阿夫儿茶精 |
COX | Immunology/Inflammation; Neuroscience |
(-)-Epiafzelechin exhibits significant anti-inflammatory activity on carrageenin-induced mouse paw edema, it exhibits a dose-dependent inhibition on the COX activity with an IC50 value of 15 microM, it exhibits about 3-fold weaker inhibitory potency on th |