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别名 | N/A | 储存条件 (自收到货起) |
3年 / -20°C / 粉状 1年 / -80°C / 溶于溶剂 |
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化学式 | C21H21ClF2O4S |
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分子量 | 442.9 | CAS号 | 471905-41-6 | ||||||||
Solubility (25°C)* | 体外 | DMSO | 89 mg/mL (200.94 mM) | ||||||||
Water | Insoluble | ||||||||||
Ethanol | Insoluble | ||||||||||
体内(现配现用) |
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* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
产品描述 | MK-0752是一种适度有效的γ-secretase(γ-分泌酶)抑制剂,降低Aβ40产量,IC50为5 nM。Phase 1/2。 | ||
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靶点 |
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体外研究 | MK-0752是一种适度有效的γ-分泌抑制剂,其剂量依赖性减少人SH-SY5Y 细胞中Aβ40,IC50为5 nM。[1]在体外,MK-0752阻断凹槽胞内结构域(ICD)裂解,以及随后的核易位。[2] | ||
体内研究 | 在猕猴大脑中,MK-0752(240 mg/kg)使新产生的Aβ生成减少,AUV下降90%。此外,MK-0752治疗增加Aβ 1-14,Aβ 1-15,和Aβ 1-16水平,而减少Aβ 1-17水平。[1]在豚鼠体内,MK-0752 (10 mg/kg -30 mg/kg)口服给药导致Aβ40在血浆,大脑和脑脊液(CSF)中剂量依赖性减少,在大脑中IC50为440 nM。[2] | ||
特征 | 一种适度有效的γ-分泌酶抑制剂。 |
动物实验 | 动物模型 | 小脑延髓池移植的(CMP)猕猴模型。 |
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剂量 | ≤240 mg/kg | |
给药处理 | p.o. |
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数据来源于[Data independently produced by Oncotarget, 2014, 5(2), 363-74]
数据来源于[Data independently produced by , , Neoplasia, 2018, 21(1):93-105]
数据来源于[Data independently produced by , , Cancer Biol Ther, 2014, 15(5):633-42]
数据来源于[Data independently produced by , , Oncol Lett, 2016, 12(4):2900-2905]
Distinct pathways drive anterior hypoblast specification in the implanting human embryo [ Nat Cell Biol, 2024, 26(3):353-365] | PubMed: 38443567 |
Simultaneous Inhibition of Ceramide Hydrolysis and Glycosylation Synergizes to Corrupt Mitochondrial Respiration and Signal Caspase Driven Cell Death in Drug-Resistant Acute Myeloid Leukemia [ Cancers (Basel), 2023, 15(6)1883] | PubMed: 36980769 |
In vitro antineoplastic effects of MK0752 in HPV-positive head and neck squamous cell carcinoma [ J Cancer Res Clin Oncol, 2023, 149(16):14691-14699] | PubMed: 37587308 |
Prediction of drug candidates for clear cell renal cell carcinoma using a systems biology-based drug repositioning approach [ EBioMedicine, 2022, 78:103963] | PubMed: 35339898 |
Establishment and characterization of immortalized sweat gland myoepithelial cells [ Sci Rep, 2022, 12(1):7] | PubMed: 34997030 |
Delta/Jagged-mediated Notch signaling induces the differentiation of agr2-positive epidermal mucous cells in zebrafish embryos [ PLoS Genet, 2021, 17(12):e1009969] | PubMed: 34962934 |
PLK1 and NOTCH Positively Correlate in Melanoma and their Combined Inhibition Results in Synergistic Modulations of Key Melanoma Pathways [ Mol Cancer Ther, 2020, molcanther.0654.2020] | PubMed: 33177155 |
A novel human colon signet-ring cell carcinoma organoid line: establishment, characterization and application [ Carcinogenesis, 2020, 41(7):993-1004] | PubMed: 31740922 |
DRUGPATH - a novel bioinformatic approach identifies DNA-damage pathway as a regulator of size maintenance in human ESCs and iPSCs [ Sci Rep, 2019, 9(1):1897] | PubMed: 30760778 |
IL6 blockade potentiates the anti-tumor effects of γ-secretase inhibitors in Notch3-expressing breast cancer. [ Cell Death Differ, 2018, 25(2):330-339] | PubMed: 29027990 |
特定的存储和包装每个产品的信息在产品说明书上都有注明。大多数Selleck产品,在推荐的条件下存储可稳定保存两年。产品有时建议的储存温度不同,大多数建议储存在-20°C,抑制剂属于化学试剂,可在常温下运输储存两周左右。即使如此,我们保证产品的出货量将保持产品质量的条件下,一般都会放入冰袋。望阁下收到产品后,请按照产品数据表建议适当存储。
如果需要长期保存,请于零下二十度低温保存。禁止用于人体及治疗!
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