Olumacostat glasaretil
CAS No. 1261491-89-7
Olumacostat glasaretil ( Olumacostat glasaretil | DRM01B | DRM-01B )
产品货号. M11083 CAS No. 1261491-89-7
乙酰辅酶 A (CoA) 羧化酶 (ACC) 的小分子抑制剂;抑制原代和转化的人类皮脂细胞中的从头脂质合成。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥494 | 有现货 |
|
5MG | ¥786 | 有现货 |
|
10MG | ¥1191 | 有现货 |
|
25MG | ¥2260 | 有现货 |
|
50MG | ¥3872 | 有现货 |
|
100MG | ¥5646 | 有现货 |
|
200MG | ¥8035 | 有现货 |
|
500MG | 获取报价 | 有现货 |
|
1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Olumacostat glasaretil
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述乙酰辅酶 A (CoA) 羧化酶 (ACC) 的小分子抑制剂;抑制原代和转化的人类皮脂细胞中的从头脂质合成。
-
产品描述A small molecule inhibitor of acetyl coenzyme A (CoA) carboxylase (ACC); inhibits de novo lipid synthesis in primary and transformed human sebocytes; reduces saturated and monounsaturated fatty acyl chains across lipid species, including di- and triacylglycerols, phospholipids, cholesteryl esters, and wax esters; significantly reduces hamster ear sebaceous gland size; a pro-drug of TOFA with enhance delivery in vivo.Other Indication Phase 3 Clinical(In Vitro):Acetyl coenzyme A carboxylase controls the first, rate limiting step in fatty acid biosynthesis. Olumacostat glasaretil inhibits de novo lipid synthesis in primary and transformed human sebocytes. At 3 μM, olumacostat glasaretil reduces fatty acid synthesis to at or below baseline levels. 14C-acetate incorporation levels are 85%-90% lower for SEB-1 cultures treated with olumacostat glasaretil at 20 μM compared to control samples. At 3 μM, olumacostat glasaretil reduces sebocyte triacylglycerol, cholesteryl/wax ester, diacylglycerol, cholesterol and phospholipid levels from control values on average by approximately 86%, 57%, 51%, 39% and 37%, respectively. (In Vivo):Olumacostat glasaretil is a pro-drug of the ACC inhibitor 5-(tetradecyloxy)-2-furoic acid (TOFA) and is designed to enhance delivery in vivo. Topical application of olumacostat glasaretil but not TOFA significantly reduces hamster ear sebaceous gland size. HPLC analyses of hamster ear extracts shows that olumacostat glasaretil treatment increases ACC levels and the ratio of acetyl-CoA to free CoA in tested animals, indicating increased fatty acid oxidation. These changes are consistent with ACC inhibition. Matrix-assisted laser desorption/ionization (MALDI) imaging reveals that OG applied onto Yorkshire pig ears accumulates in sebaceous glands relative to the surrounding dermis. At week 12, OG treatment shows greater reductions from baseline in inflammatory lesions and noninflammatory lesions, and more patients with greater than or equal to 2-grade improvement in investigator global assessment score than vehicle.
-
体外实验Acetyl coenzyme A carboxylase controls the first, rate limiting step in fatty acid biosynthesis. Olumacostat glasaretil inhibits de novo lipid synthesis in primary and transformed human sebocytes. At 3 μM, olumacostat glasaretil reduces fatty acid synthesis to at or below baseline levels. 14C-acetate incorporation levels are 85%-90% lower for SEB-1 cultures treated with olumacostat glasaretil at 20 μM compared to control samples. At 3 μM, olumacostat glasaretil reduces sebocyte triacylglycerol, cholesteryl/wax ester, diacylglycerol, cholesterol and phospholipid levels from control values on average by approximately 86%, 57%, 51%, 39% and 37%, respectively.
-
体内实验Olumacostat glasaretil is a pro-drug of the ACC inhibitor 5-(tetradecyloxy)-2-furoic acid (TOFA) and is designed to enhance delivery in vivo. Topical application of olumacostat glasaretil but not TOFA significantly reduces hamster ear sebaceous gland size. HPLC analyses of hamster ear extracts shows that olumacostat glasaretil treatment increases ACC levels and the ratio of acetyl-CoA to free CoA in tested animals, indicating increased fatty acid oxidation. These changes are consistent with ACC inhibition. Matrix-assisted laser desorption/ionization (MALDI) imaging reveals that OG applied onto Yorkshire pig ears accumulates in sebaceous glands relative to the surrounding dermis. At week 12, OG treatment shows greater reductions from baseline in inflammatory lesions and noninflammatory lesions, and more patients with greater than or equal to 2-grade improvement in investigator global assessment score than vehicle.
-
同义词Olumacostat glasaretil | DRM01B | DRM-01B
-
通路Others
-
靶点Other Targets
-
受体Others
-
研究领域Other Indications
-
适应症Other Disease
化学信息
-
CAS Number1261491-89-7
-
分子量481.6221
-
分子式C26H43NO7
-
纯度>98% (HPLC)
-
溶解度10 mM in DMSO
-
SMILESO=C(C1=CC=C(OCCCCCCCCCCCCCC)O1)OCC(N(CC(OCC)=O)C)=O
-
化学全称2-Furancarboxylic acid, 5-(tetradecyloxy)-, 2-[(2-ethoxy-2-oxoethyl)methylamino]-2-oxoethyl ester
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Bissonnette R, et al. J Am Acad Dermatol. 2017 Jan;76(1):33-39.
2. Hunt DW, et al. J Invest Dermatol. 2017 Jul;137(7):1415-1423.
3. Melnik BC. J Invest Dermatol. 2017 Jul;137(7):1405-1408.
产品手册
关联产品
-
Kaempferol 7-O-rhamn...
Kaempferol 7-O-rhamnoside is a natural product from Maytenus hookeri.
-
Tri-Salicylic Acid
三水杨酸是阿司匹林热分解的产物,是一种用于蛋白质组学研究的化合物。
-
DTDCI
3,3'-二乙基硫二碳花青碘化物是电位敏感探针。可用于可转移膜孔的荧光分析以及膜电位对鳗鱼肠刷状缘膜囊泡中 Na 共转运的影响。