| 價(jià)格 | ¥319 | ¥453 | ¥788 |
| 包裝 | 1mg | 2mg | 5mg |
| 最小起訂量 | 1mg |
| 發(fā)貨地 | 上海 |
| 更新日期 | 2026-05-08 |
| 中文名稱:拉坦前列素 | 英文名稱:Latanoprost |
| CAS:130209-82-4 | 品牌: TargetMol |
| 產(chǎn)地: 美國(guó) | 保存條件: Keep away from moisture,Store at low temperature Pure form: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| 純度規(guī)格: 99.89% | 產(chǎn)品類別: 抑制劑 |
| 貨號(hào): T001|T2528 |
| 名稱 | Latanoprost |
| 描述 | Latanoprost (Xalatan) is a prostaglandin F2alpha analogue and a prostanoid selective FP receptor agonist with an ocular hypertensive effect. |
| 細(xì)胞實(shí)驗(yàn) | HCS cells were inoculated into a 24-well culture plate (Nunc) and cultured in 10% FBS-DMEM/F12 medium at 37°C in a humidified 5% CO2 incubator. After the cells grew into logarithmic phase, the culture medium of each culture plate well was replaced entirely with the medium containing latanoprost at concentrations varying from 50 mg/l to 0.78125 mg/l, respectively. The cells were cultured under the same condition as described earlier, and their morphology and growth status were monitored every 4 h under an Eclipse TS100 inverted microscope.(Only for Reference) |
| 體外活性 | Latanoprost functioned as both an indirect activator of AMP-activated protein kinase and a selective retinoid X receptor α (RXRα) antagonist able to selectively antagonise the transcription of a RXRα/peroxisome proliferator-activated receptor γ heterodimer[2]. Latanoprost induced morphological abnormality and viability decline of HCS cells in vitro. It induces cell cycle arrest of HCS cells. Latanoprost induces abnormal changes of plasma membrane, DNA fragmentation and ultrastructural abnormality of HCS cells. Caspase activation in HCS cells is also activated by Latanoprost treatment. Latanoprost induces MTP disruption and quantitative changes of mitochondrion-associated pro-apoptotic regulators in HCS cells[1]. Latanoprost is effective in inhibiting adipogenesis, reducing lipogenesis, promoting fatty acid oxidation and enhancing GLUT4 translocation and glucose uptake both in adipocytes and myotubes[2]. |
| 體內(nèi)活性 | Latanoprost, a clinical drug for treating primary open-angle glaucoma and intraocular hypertension, effectively ameliorates glucose and lipid disorders in two mouse models of type 2 diabetes. Its treatment improves glucose tolerance. Chronic administration of latanoprost decreases serum lipids and enhances insulin signalling in white adipose tissue and skeletal muscle. It effectually activates AMPK and regulates glucose and lipid metabolism-relevant genes in diabetic mice[2]. |
| 存儲(chǔ)條件 | Keep away from moisture,Store at low temperature Pure form: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | H2O : 125 mg/mL (288.96 mM) 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 1 mg/mL (2.31 mM), Sonication is recommended. DMSO : 4.33 mg/mL (10.01 mM), Sonication is recommended. |
| 關(guān)鍵字 | RXR | retinoid X receptor α | RAR | prostanoid selective FP receptor | ProstaglandinReceptor | Prostaglandin Receptor | PHXA-41 | PHXA 41 | Latanoprost | Inhibitor | inhibit |
| 相關(guān)產(chǎn)品 | Rutin | Benzyl nicotinate | Lornoxicam | p-Hydroxycinnamic acid | Rebamipide | Tranilast | Azathioprine | Kynurenic acid | Monomethyl fumarate | Ozagrel | Pamoic acid disodium | Pranoprofen |
| 相關(guān)庫 | 經(jīng)典已知活性庫 | 抗癌上市藥物庫 | 已知活性化合物庫 | 抗衰老化合物庫 | FDA 上市藥物庫 | GPCR靶點(diǎn)分子庫 | 免疫/炎癥分子化合物庫 | 膜蛋白靶向化合物庫 | 疼痛相關(guān)化合物庫 | 藥物功能重定位化合物庫 | 抗癌臨床化合物庫 | 神經(jīng)元分化化合物庫 |
| 成立日期 | 2013-04-18 (14年) | 注冊(cè)資本 | 566.2651萬人民幣 |
| 員工人數(shù) | 100-500人 | 年?duì)I業(yè)額 | ¥ 1億以上 |
| 主營(yíng)行業(yè) | 化學(xué)試劑,生物活性小分子 | 經(jīng)營(yíng)模式 | 貿(mào)易,試劑,定制,服務(wù) |
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