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C75

C75
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Purity:98.84%
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C75

Catalog No. T10657Cas No. 218137-86-1
C75 is an inhibitor synthetic fatty-acid synthase (FASN) and inhibits prostate cancer cells PC3 (IC50: 35 μM).
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Pack SizePriceAvailabilityQuantity
1 mg$41In Stock
2 mg$59In Stock
5 mg$119In Stock
50 mgInquiryIn Stock
1 mL x 10 mM (in DMSO)$108In Stock
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Product Introduction

Bioactivity
Description
C75 is an inhibitor synthetic fatty-acid synthase (FASN) and inhibits prostate cancer cells PC3 (IC50: 35 μM).
Targets&IC50
PC3 cells:35 μM
In vitro
C75 (10-50 μM) reduces the growth of LNCaP spheroids in a concentration-dependent manner (IC50: 50 μM). (-)-C75 inhibits FAS activity and has a cytotoxic effect on tumor cell lines, without affecting food consumption. (+)-C75 inhibits CPT1 and produces anorexia. The differential activity of C75 enantiomers may lead to the development of potential new specific drugs for cancer and obesity [2].
In vivo
C75 (i.p.) blocks fasting-induced c-Fos expression in the arcuate nucleus, lateral hypothalamic area, and paraventricular nucleus. C75 (30 mg/kg, i.p.) inhibits the food intake of mice by ≥95% within 2 h[3]. C75-treated DIO mice have 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].
AliasC-75
Chemical Properties
Molecular Weight254.32
FormulaC14H22O4
Cas No.218137-86-1
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 75.6 mg/mL (297.3 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.9321 mL19.6603 mL39.3205 mL196.6027 mL
5 mM0.7864 mL3.9321 mL7.8641 mL39.3205 mL
10 mM0.3932 mL1.9660 mL3.9321 mL19.6603 mL
20 mM0.1966 mL0.9830 mL1.9660 mL9.8301 mL
50 mM0.0786 mL0.3932 mL0.7864 mL3.9321 mL
100 mM0.0393 mL0.1966 mL0.3932 mL1.9660 mL

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Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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