C75 | Fatty Acid Synthase Inhibitor - MedChemExpress
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C75 is a synthetic fatty-acid synthase (FASN) inhibitor; inhibits prostate cancer cells PC3 with an IC50 of 35 μM. C75 is a potent CPT1A activator.
For research use only. We do not sell to patients.
C75 Chemical Structure
CAS No. : 218137-86-1
Size | Price | Stock | Quantity |
---|---|---|---|
Free Sample (0.1 - 0.5 mg) | Apply Now | ||
Solid + Solvent (Highly Recommended) | |||
10 mM * 1 mL in DMSO ready for reconstitution | USD 132 | In-stock | 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31 |
Solution | |||
10 mM * 1 mL in DMSO | USD 132 | In-stock | 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31 |
Solid | |||
5 mg | USD 120 | In-stock | 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31 |
10 mg | USD 199 | In-stock | 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31 |
25 mg | USD 400 | In-stock | 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31 |
50 mg | USD 640 | In-stock | 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31 |
100 mg | USD 1020 | In-stock | 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31 |
200 mg | Get quote | ||
500 mg | Get quote |
* Please select Quantity before adding items.
This product is a controlled substance and not for sale in your territory.
Customer Review
Based on 29 publication(s) in Google Scholar
Other Forms of C75:
- trans-C75 In-stock
- (−)-C75 Get quote
- (+)-trans-C75 Get quote
C75 Related Antibodies
26 Publications Citing Use of MCE C75
- •Nature. 2023 Jun;618(7964):374-382. [Abstract]
- •Gastroenterology. 2024 Jan 24:S0016-5085(24)00064-7. [Abstract]
- •Cell Metab. 2021 Jan 5;33(1):51-64.e9. [Abstract]
- •J Hepatol. 2020 May;72(5):976-989. [Abstract]
- •Nat Commun. 2024 Sep 27;15(1):8273. [Abstract]
- •Bioact Mater. 2024 Mar, 33, 85-99.
- •Cell Rep Med. 2024 May 29:101592. [Abstract]
- •J Immunother Cancer. 2021 Aug;9(8):e003093. [Abstract]
- •Cell Mol Biol Lett. 2024 Aug 21;29(1):112. [Abstract]
- •Mol Metab. 2024 May 4:101953. [Abstract]
- •J Neuroinflammation. 2023 Nov 15;20(1):264. [Abstract]
- •Cell Rep. 2023 Jan 31.
- •Cell Rep. 2022 Nov 8;41(6):111591. [Abstract]
- •Cell Death Dis. 2021 Oct 12;12(10):934. [Abstract]
- •Cell Death Dis. 2020 Jan 13;11(1):25. [Abstract]
- •Cell Death Discov. 2022 Oct 28;8(1):431. [Abstract]
- •Biochim Biophys Acta Mol Basis Dis. 2022 Sep 20;166550. [Abstract]
- •Anal Chem. 2020 Mar 17;92(6):4419-4426. [Abstract]
- •Cancers (Basel). 2024 Apr 25;16(9):1651. [Abstract]
- •Lipids Health Dis. 2024 Feb 3;23(1):37. [Abstract]
- •Respir Res. 2023 Mar 15;24(1):81. [Abstract]
- •Food Chem Toxicol. 2022 Oct 5;113450. [Abstract]
- •Am J Cancer Res. 2020 Feb 1;10(2):595-609. [Abstract]
- •Vet Microbiol. 2023 Jan 24;278:109668. [Abstract]
- •J Cell Sci. 2022 Jul 1;jcs.259090. [Abstract]
- •SSRN. 2023 May 24.
C75 purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2022 Oct 28;8(1):431. [Abstract]
Transwell migration assay. C75 reduces the migration ability of NUPR1-overexpressing SK-Hep1 cells.C75 purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2022 Oct 28;8(1):431. [Abstract]
Cell Counting Kit-8 (CCK8) assay. NUPR1 overexpression-induced proliferation of MHCC-97H and SK-Hep1 cells can be reversed by C75 (50 μM; 48 h).C75 purchased from MedChemExpress. Usage Cited in: Am J Cancer Res. 2020 Feb 1;10(2):595-609. [Abstract]
Of the transcription of spliced X-box-binding protein 1 (sXBP1) and phosphorylated translational initiation factor 2 in eukaryotes (eIF2α) are higher in ANGTPL4-/- macrophages but are restored to normal levels following C75 treatment. Powered by Bioz See more details on BiozFeatured Recommendations
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Customer Review
Description | C75 is a synthetic fatty-acid synthase (FASN) inhibitor; inhibits prostate cancer cells PC3 with an IC50 of 35 μM[1][2][3]. C75 is a potent CPT1A activator[5]. | IC50 & Target | IC50: 35 μM (PC3 cell)[1] | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
In Vitro | C75 inhibits PC3 cell growht with an IC50 of 35 μM at 24 h. C75 (10-50 μM) also reduces the growth of LNCaP spheroids in a concentration-dependent manner with an IC50 of 50 μM[1]. (-)-C75 inhibits FAS activity and has a cytotoxic effect on tumor cell lines, without affecting food consumption. (+)-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[2]. MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. C75 Related Antibodies | ||||||||||||
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[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]. MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||
Molecular Weight | 254.32 | ||||||||||||
Formula | C14H22O4 | ||||||||||||
CAS No. | 218137-86-1 | ||||||||||||
Appearance | Solid | ||||||||||||
Color | White to off-white | ||||||||||||
SMILES | O=C(C(C1=C)C(CCCCCCCC)OC1=O)O | ||||||||||||
Shipping | Room temperature in continental US; may vary elsewhere. | ||||||||||||
Storage |
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Solvent & Solubility | In Vitro: DMSO : 100 mg/mL (393.21 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO) H2O : < 0.1 mg/mL (insoluble) Preparing Stock Solutions
* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol) Mass kg g mg μg ng pg = Concentration M mM μM nM pM × Volume L mL μL × Molecular Weight *Concentration (start) × Volume (start) = Concentration (final) × Volume (final) This equation is commonly abbreviated as: C1V1 = C2V2 Concentration (start) M mM μM nM pMC1 × Volume (start) L mL μLV1 = Concentration (final) M mM μM nM pMC2 × Volume (final) L mL μLV2 In Vivo:Select the appropriate dissolution method based on your experimental animal and administration route. For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents: To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day. The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Dosage mg/kgAnimal weight (per animal) gDosing volume (per animal) μLNumber of animals Recommended: Prepare an additional quantity of animals to account for potential losses during experiments. Please enter your animal formula composition: % DMSO + % + % Tween-80 + % Saline Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak. The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE). Calculation results: Working solution concentration: mg/mL Method for preparing stock solution: mg drug dissolved in μL DMSO (Stock solution concentration: mg/mL). The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only. If necessary, please contact MedChemExpress (MCE). Tel: 609-228-6898 E-mail: [email protected] Technical Support: [email protected] Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline. Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution If the continuous dosing period exceeds half a month, please choose this protocol carefully. Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution. | ||||||||||||
Purity & Documentation | Purity: 99.91% Select Batch: HY-12364-88905 HY-12364-100761 HY-12364-127282 HY-12364-168217 HY-12364-241938 HY-12364-479372 HY-12364-28130 HY-12364-287466 HY-12364-86787 HY-12364-288587 HY-12364-80650 Data Sheet (278 KB) SDS (393 KB)COA (246 KB) LCMS (91 KB) Handling Instructions (2659 KB) | ||||||||||||
References |
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Cell Assay [1] | Cells are seeded in 96-well plates and incubated for 2 days to allow exponential phase growth. Cells are then ished twice with PBS and treated with C75. After 24 or 48 h incubation, MTT is added to a final concentration of 0.5 mg/ml and cultures are incubated for 2 h. Cells are then solubilized with DMSO before measuring absorbance at 570 nm. Cell growth is also measured, using MTT assay, every 24 h up to 96 h[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
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Animal Administration [3] | Mice: C75 is administered either by i.p. (i.p.; 30 mg/kg of body weight) or i.c.v. (10 μg in 3 μL of RPMI medium 1640) injection. One, 11.5, and 24 h after i.p. injection, cumulative food intake is measured, mice are killed, brains are sectioned, and slices are subjected to immunohistochemical staining for c-Fos. All i.p. injections are given 1 h before the start of the dark cycle. For i.c.v. injection, mice are anesthetized with metofane and given 3 μl of RPMI medium 1640 (control) or C75 in RPMI medium 1640 into the lateral ventricle with a calibrated 10-μl Hamilton syringe[3]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
References |
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[1]. Rae C, et al. Inhibition of Fatty Acid Synthase Sensitizes Prostate Cancer Cells to Radiotherapy.
[2]. Makowski K, et al. Differential pharmacologic properties of the two C75 enantiomers: (+)-C75 is a strong anorectic drug; (-)-C75 has antitumor activity. Chirality. 2013 May;25(5):281-7.
[3]. Gao S, et al. Effect of the anorectic fatty acid synthase inhibitor C75 on neuronal activity in the hypothalamus and brainstem. Proc Natl Acad Sci U S A. 2003 May 13;100(10):5628-33.
[4]. Thupari JN, et al. C75 increases peripheral energy utilization and fatty acid oxidation in diet-induced obesity. Proc Natl Acad Sci U S A. 2002 Jul 9;99(14):9498-502.
[5]. Yan Xue, et al. Inhibition of Carnitine Palmitoyltransferase 1A Aggravates Fatty Liver Graft Injury via Promoting Mitochondrial Permeability Transition. Transplantation. 2021 Mar 1;105(3):550-560.
Complete Stock Solution Preparation Table
* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
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DMSO | 1 mM | 3.9321 mL | 19.6603 mL | 39.3205 mL | 98.3013 mL |
5 mM | 0.7864 mL | 3.9321 mL | 7.8641 mL | 19.6603 mL | |
10 mM | 0.3932 mL | 1.9660 mL | 3.9321 mL | 9.8301 mL | |
15 mM | 0.2621 mL | 1.3107 mL | 2.6214 mL | 6.5534 mL | |
20 mM | 0.1966 mL | 0.9830 mL | 1.9660 mL | 4.9151 mL | |
25 mM | 0.1573 mL | 0.7864 mL | 1.5728 mL | 3.9321 mL | |
30 mM | 0.1311 mL | 0.6553 mL | 1.3107 mL | 3.2767 mL | |
40 mM | 0.0983 mL | 0.4915 mL | 0.9830 mL | 2.4575 mL | |
50 mM | 0.0786 mL | 0.3932 mL | 0.7864 mL | 1.9660 mL | |
60 mM | 0.0655 mL | 0.3277 mL | 0.6553 mL | 1.6384 mL | |
80 mM | 0.0492 mL | 0.2458 mL | 0.4915 mL | 1.2288 mL | |
100 mM | 0.0393 mL | 0.1966 mL | 0.3932 mL | 0.9830 mL |
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C75 Related Classifications
- Cancer
- Cancer Targeted Therapy Cancer Metabolism and Metastasis
- Metabolic Enzyme/Protease
- Fatty Acid Synthase (FASN)
- Do most proteins show cross-species activity?
Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.
Keywords:
C75218137-86-1C 75C-75Fatty Acid Synthase (FASN)Inhibitorinhibitorinhibit
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