C75 blocks fasting-induced c-Fos expression in the arcuate nucleus (Arc), lateral hypothalamic area (LHA), and paraventricular nucleus (PVN) 10–24 h after i.p. injection. Intraperitoneal administration of C75 at 30 mg/kg body weight inhibits food intake of mice by ≥95% within 2 h after i.p. injection[3]. C75-treated DIO mice has a 50% greater weight loss, and a 32.9% increased production of energy because of fatty acid oxidation. C75 treatment of rodent adipocytes and hepatocytes and human breast cancer cells increases fatty acid oxidation and ATP levels by increasing CPT-1 activity, even in the presence of elevated concentrations of malonyl-CoA[4].
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
C75 抑制前列腺癌细胞 PC3 的 IC50 值为35 μM。 MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务 C75 Chemical Structure CAS ...C75 | C 75 | C-75 | Fatty Acid Synthase (FASN) | Inhibitor | inhibitor | inhibitC75 是合成的脂肪酸合成酶 (FASN) 抑制剂。C75 抑制前列腺癌细胞 PC3 的 IC50 值为 35 μM。- 高纯度，全球文献引用。C75
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