诺米林 T3672
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
5 mg | 1063-77-0 | ¥413.00 | 询底价 |
1 mg | 1063-77-0 | ¥185.00 | 询底价 |
500 mg | 1063-77-0 | ¥6,590.00 | 询底价 |
50 mg | 1063-77-0 | ¥1,960.00 | 询底价 |
25 mg | 1063-77-0 | ¥1,320.00 | 询底价 |
10 mg | 1063-77-0 | ¥663.00 | 询底价 |
100 mg | 1063-77-0 | ¥2,920.00 | 询底价 |
Product Introduction
Bioactivity
英文名: Nomilin
描述: Nomilin 是一种柠檬苦素类化合物,从柑桔类提取物中获得,是抗肥胖症和降糖药。
细胞实验: Cell lines: HUVECs. Concentrations: 5 μg-500 μg/ml. Incubation Time: 48 h. Method:. HUVECs were seeded (5000 cells/well) in 96-well flat-bottomed titer plate and incubated for 24 h at 37 °C in 5% CO2 atmosphere. Different concentrations of Nomilin (5 μg-500 μg/ml) were added and incubated further for 48 h. Before 4 h completion of incubation, 20 μl MTT (5 mg/ml) was added. Percentage of dead cells was determined using an ELISA plate reader set to record absorbance at 570 nm.
动物实验: Animal Models: Four to six week old male C57BL/6 mice. Formulation: light paraffin oil. Dosages: 6 mg/kg, I.P.
体外活性: Administration of Nomilin significantly retarded endothelial cell proliferation, invasion, migration and tube formation. It also possesses anti-proliferative activity against the number of human cancer cell lines including leukemia (HL-60), ovary (SKOV-3), liver (Hep G2), cervix (HeLa), stomach (NCI-SNU-1), and breast (MCF-7)[2]. Nomilin significantly decreased TRAP-positive multinucleated cell numbers compared with the control and exhibited no cytotoxicity. It decreases bone resorption activity and downregulates osteoclast-specific genes, NFATc1 and TRAP mRNA levels. Furthermore, Nomilin suppressed MAPK signaling pathways. Thus, Nomilin has inhibitory effects on osteoclastic differentiation in vitro[3].
体内活性: Nomilin is an effective inducer of gluthathione S-transferase activity in mice and to inhibit carcinogenesis in the hamster buccal pouch assay. Nomilin can shorten anaesthetic-induced sleeping time in mice, probably through a stimulant action on the central nervous system [1]. Nomilin significantly inhibited tumour-directed capillary formation. Serum proinflammatory cytokines such as IL-1β, IL-6, TNF-α and GM-CSF and also serum NO levels were significantly reduced by the treatment of nomilin. Administration of Nomilin significantly reduced the serum level of VEGF, a proangiogenic factor and increased the antiangiogenic factors TIMP-1 and IL-2 [2].
存储条件: keep away from direct sunlightPowder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: H2O : Insoluble
Ethanol : Insoluble
DMSO : 50 mg/mL (97.17 mM)
关键字: inhibit | anti-hyperglycemic | limonoid | Nomilin | ischemia-reperfusion | anti-obesity | Inhibitor | compound
相关产品: 3',4',7-Trihydroxyisoflavone | Ganoderic acid X | PF-06260933 | Isojacareubin | HS-276 | 6,4'-Dihydroxy-7-methoxyflavanone | MAP4K4-IN-3 | Dehydrogeijerin | SKLB-163 | Isonardosinone
相关库: Anti-Tumor Natural Product Library | Anti-Aging Compound Library | Anti-Prostate Cancer Compound Library | Anti-Liver Cancer Compound Library | Covalent Natural Product Library | Kinase Inhibitor Library | Anti-Colorectal Cancer Compound Library | Traditional Chinese Medicine Monomer Library | Natural Product Library for HTS | Anti-Pancreatic Cancer Compound Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途