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- 详细信息
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 英文名:
(±)-C75
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- 规格:
1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 1 mg | 产品价格: | ¥395.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥790.0 |
| 规格: | 10 mg | 产品价格: | ¥1540.0 |
| 规格: | 25 mg | 产品价格: | ¥3080.0 |
| 规格: | 50 mg | 产品价格: | ¥5000.0 |
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trans-C75
CAS No. : 191282-48-1
MCE 国际站:trans-C75
产品活性:trans-C75 ((±)-C75) 是 C75 的对映异构体,C75 是脂肪酸合成酶 (FASN) 的抑制剂。
研究领域:Metabolic Enzyme/Protease
作用靶点:Fatty Acid Synthase (FASN)
In Vitro: trans-C75 ((±)-C75) inhibits PC3 cell growht with an IC50 of 35 μM at 24 h.
trans-C75 ((±)-C75)(10-50 μM) also reduces the growth of LNCaP spheroids in a concentration-dependent manner with an IC50 of 50 μM.
trans-C75 ((±)-C75) inhibits FAS activity and has a cytotoxic effect on tumor cell lines, without affecting food consumption.
trans-C75 ((±)-C75) inhibits CPT1 and its administration produces anorexia, suggesting that central inhibition of CPT1 is essential for the anorectic effect of C75. The differential activity of C75 enantiomers may lead to the development of potential new specific drugs for cancer and obesity.
In Vivo: 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.
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.
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