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Lipofermata

Chemical Structure : Lipofermata

CAS No.: 297180-15-5

Lipofermata (CB16.2 aka)

货号: PC-35366Not For Human Use, Lab Use Only.

Lipofermata (CB16.2 aka) is a specific fatty acid transport (FATP) inhibitor, blocks human FATP2-mediated fatty acid uptake (IC50=4.84 uM in Caco-2 cells) without impacting other cellular functions.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

Lipofermata (CB16.2 aka) is a specific fatty acid transport (FATP) inhibitor, blocks human FATP2-mediated fatty acid uptake (IC50=4.84 uM in Caco-2 cells) without impacting other cellular functions.
Lipofermata demonstrates cellualr transport inhibition activity models for myocytes (mmC2C12), pancreatic β-cells (rnINS-1E), intestinal epithelial cells (hsCaco-2), and hepatocytes (hsHepG2), as well as primary human adipocytes, which is specific for long and very long chain fatty acids but has no effect on medium chain fatty acids (C6-C10).
Lipofermata also abrogates lipid transport into melanoma cells and reduces melanoma growth and invasion.

物理化学性质&存储条件

分子量 360.229
分子式 C15H10BrN3OS
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

5-bromo-5'-phenylspiro[1H-indole-3,2'-3H-1,3,4-thiadiazole]-2-one

参考文献

1. Ahowesso C, et al. Biochem Pharmacol. 2015 Nov 1;98(1):167-81.

2. Black PN, et al. Medchemcomm. 2016 Apr 1;7(4):612-622.

3. Zhang M, et al. Cancer Discov. 2018 Jun 14. pii: CD-17-1371.

4. Sandoval A, et al. Biochem Pharmacol. 2010 Apr 1;79(7):990-9.

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