C75 | Fatty Acid Synthase Inhibitor - MedChemExpress

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                                  1. Metabolic Enzyme/Protease
                                  2. Fatty Acid Synthase (FASN)
                                  3. C75
                                  C75 Cat. No.: HY-12364 Purity: 99.91% Data Sheet COA SDS Handling Instructions FAQs Technical Support

                                  Solubility

                                  In Vivo Dissolution Calculator

                                  Help & FAQs

                                  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
                                  1. C75

                                  CAS No. : 218137-86-1

                                  Size Price Stock Quantity
                                  Free Sample (0.1 - 0.2 mg) Apply Now
                                  Solid + Solvent (Highly Recommended)
                                  10 mM * 1 mL in DMSO ready for reconstitution In-stock 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31
                                  Solution
                                  10 mM * 1 mL in DMSO In-stock 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31
                                  Solid
                                  5 mg In-stock 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31
                                  10 mg In-stock 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31
                                  25 mg In-stock 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31
                                  50 mg In-stock 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31
                                  100 mg In-stock 0 1 2 3 4 5 6 7 Estimated Time of Arrival: December 31
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                                  Customer Review

                                  Based on 42 publication(s) in Google Scholar

                                  Other Forms of C75:

                                  • trans-C75 In-stock
                                  • (−)-C75 Get quote
                                  • (+)-trans-C75 Get quote
                                  • C75 (Standard) Get quote

                                  C75 Related Antibodies

                                  Top Publications Citing Use of Products

                                  39 Publications Citing Use of MCE C75

                                  • Nat Genet. 2025 Mar;57(3):680-693.
                                  • Gastroenterology. 2024 Jan 24:S0016-5085(24)00064-7. [Abstract]
                                  • Bioact Mater. 2023 Nov 9:33:85-99.
                                  • Nature. 2023 Jun;618(7964):374-382. [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]
                                  • Cell Mol Biol Lett. 2024 Aug 21;29(1):112. [Abstract]
                                  • Cell Rep Med. 2024 May 29:101592. [Abstract]
                                  • J Neuroinflammation. 2023 Nov 15;20(1):264. [Abstract]
                                  • J Immunother Cancer. 2021 Aug;9(8):e003093. [Abstract]
                                  • Cell Death Dis. 2025 Oct 7;16(1):715. [Abstract]
                                  • Regen Biomater. 2025 Jun 16:12:rbaf056. [Abstract]
                                  • Cell Death Dis. 2021 Oct 12;12(10):934. [Abstract]
                                  • Cell Death Dis. 2020 Jan 13;11(1):25. [Abstract]
                                  • Hepatol Int. 2025 Nov 12. [Abstract]
                                  • Mol Metab. 2024 Jun:84:101953. [Abstract]
                                  • Cell Rep. 2023 Jan 31;42(1):112027.
                                  • Cell Rep. 2022 Nov 8;41(6):111591. [Abstract]
                                  • Cell Death Discov. 2022 Oct 28;8(1):431. [Abstract]
                                  • Anal Chem. 2020 Mar 17;92(6):4419-4426. [Abstract]
                                  • J Ethnopharmacol. 2026 Feb 28:357:120890. [Abstract]
                                  • PLoS Pathog. 2025 May 6;21(5):e1013068. [Abstract]
                                  • Mol Neurobiol. 2025 Apr 8. [Abstract]
                                  • Pharmaceuticals (Basel). 2025 Jan 31;18(2):194.
                                  • 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]
                                  • Biochim Biophys Acta Mol Basis Dis. 2022 Dec 1;1868(12):166550. [Abstract]
                                  • Eur J Immunol. 2025 Dec;55(12):e70087. [Abstract]
                                  • Eur J Immunol. 2025 Oct;55(10):e70068. [Abstract]
                                  • Anticancer Drugs. 2025 Jul 1;36(6):459-467. [Abstract]
                                  • Vet Microbiol. 2023 Mar:278:109668. [Abstract]
                                  • Food Chem Toxicol. 2022 Nov:169:113450. [Abstract]
                                  • J Cell Sci. 2022 Aug 1;135(15):jcs259090. [Abstract]
                                  • Am J Cancer Res. 2020 Feb 1;10(2):595-609. [Abstract]
                                  • SSRN. 2025 Dec 23.
                                  • bioRxiv. 2025 February 08.
                                  • SSRN. 2023 May 24.
                                  WB Cell Proliferation/Viability Assay

                                  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: 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: 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 Bioz

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                                  Related Small Molecules:

                                  Related Proteins:

                                  • Biological Activity

                                  • Protocol

                                  • Purity & Documentation

                                  • References

                                  • 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]

                                  Cellular Effect
                                  Cell Line Type Value Description References
                                  Fibroblast IC50 63.2 μM Compound: (+/-)-C-75 Antiproliferative activity against fibroblasts (unknown origin) after 72 hrs by MTT assay Antiproliferative activity against fibroblasts (unknown origin) after 72 hrs by MTT assay [PMID: 28324785]
                                  HCT-116 IC50 46.4 μM Compound: (+/-)-C-75 Antiproliferative activity against human HCT116 cells after 72 hrs by MTT assay Antiproliferative activity against human HCT116 cells after 72 hrs by MTT assay [PMID: 28324785]
                                  HepG2 IC50 7.4 ng/mL Compound: C75 Inhibition of fatty acid synthase type 1 in human HepG2 cells assessed as [1-14C]acetate incorporation into cellular fatty acid Inhibition of fatty acid synthase type 1 in human HepG2 cells assessed as [1-14C]acetate incorporation into cellular fatty acid [PMID: 18805004]
                                  Huh-7 CC50 > 100 μM Compound: 68 Cytotoxicity against human HuH7 cells assessed as cell viability after 48 hrs by CellTiter Glo assay Cytotoxicity against human HuH7 cells assessed as cell viability after 48 hrs by CellTiter Glo assay [PMID: 26771861]
                                  MCF7 IC50 27.3 μM Compound: (+/-)-C-75 Antiproliferative activity against human MCF7 cells after 72 hrs by MTT assay Antiproliferative activity against human MCF7 cells after 72 hrs by MTT assay [PMID: 28324785]
                                  MDA-MB-231 IC50 43.8 μM Compound: (+/-)-C-75 Antiproliferative activity against human MDA-MB-231 cells after 72 hrs by MTT assay Antiproliferative activity against human MDA-MB-231 cells after 72 hrs by MTT assay [PMID: 28324785]
                                  MIA PaCa-2 IC50 21.8 μM Compound: (+/-)-C-75 Antiproliferative activity against human MIAPaCa2 cells after 72 hrs by MTT assay Antiproliferative activity against human MIAPaCa2 cells after 72 hrs by MTT assay [PMID: 28324785]
                                  OVCAR-3 IC50 21.9 μM Compound: (+/-)-C-75 Antiproliferative activity against human OVCAR3 cells after 72 hrs by MTT assay Antiproliferative activity against human OVCAR3 cells after 72 hrs by MTT assay [PMID: 28324785]
                                  PC-3 IC50 26.8 μM Compound: (+/-)-C-75 Antiproliferative activity against human PC3 cells after 72 hrs by MTT assay Antiproliferative activity against human PC3 cells after 72 hrs by MTT assay [PMID: 28324785]
                                  SK-BR-3 IC50 19.8 μM Compound: (+/-)-C-75 Antiproliferative activity against human SKBR3 cells after 72 hrs by MTT assay Antiproliferative activity against human SKBR3 cells after 72 hrs by MTT assay [PMID: 28324785]
                                  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
                                  Powder -20°C 3 years
                                  4°C 2 years
                                  In solvent -80°C 6 months
                                  -20°C 1 month
                                  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
                                  Concentration Solvent Mass 1 mg 5 mg 10 mg
                                  1 mM 3.9321 mL 19.6603 mL 39.3205 mL
                                  5 mM 0.7864 mL 3.9321 mL 7.8641 mL
                                  10 mM 0.3932 mL 1.9660 mL 3.9321 mL
                                  View the 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.

                                  • Molarity Calculator

                                  • Dilution Calculator

                                  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 pM

                                  C1

                                  × Volume (start) L mL μL

                                  V1

                                  = Concentration (final) M mM μM nM pM

                                  C2

                                  × Volume (final) L mL μL

                                  V2

                                  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.

                                  • Protocol 1

                                    Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline

                                    Solubility: ≥ 2.5 mg/mL (9.83 mM); Clear solution

                                    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

                                    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

                                    Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
                                  • Protocol 2

                                    Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)

                                    Solubility: ≥ 2.5 mg/mL (9.83 mM); Clear solution

                                    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

                                    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

                                    Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
                                  • Protocol 3

                                    Add each solvent one by one: 10% DMSO 90% Corn Oil

                                    Solubility: ≥ 2.5 mg/mL (9.83 mM); Clear solution

                                    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

                                    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL Corn oil, and mix evenly.

                                  • Protocol 4

                                    Add each solvent one by one: 5% DMSO 40% PEG300 5% Tween-80 50% Saline

                                    Solubility: ≥ 1.25 mg/mL (4.92 mM); Clear solution

                                  • Protocol 5

                                    Add each solvent one by one: 5% DMSO 95% (20% SBE-β-CD in Saline)

                                    Solubility: ≥ 1.25 mg/mL (4.92 mM); Clear solution

                                  • Protocol 6

                                    Add each solvent one by one: 5% DMSO 95% Corn Oil

                                    Solubility: ≥ 1.25 mg/mL (4.92 mM); Clear solution

                                  In Vivo Dissolution Calculator Please enter the basic information of animal experiments:

                                  Dosage

                                  mg/kg

                                  Animal weight (per animal)

                                  g

                                  Dosing volume (per animal)

                                  μL

                                  Number 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-12364-28130 HY-12364-479372 HY-12364-845049 HY-12364-86787 HY-12364-80650 HY-12364-287466 HY-12364-288587 Data Sheet (278 KB) SDS (393 KB)

                                  COA (246 KB) LCMS (90 KB)

                                  Handling Instructions (2659 KB)
                                  References
                                  • [1]. Rae C, et al. Inhibition of Fatty Acid Synthase Sensitizes Prostate Cancer Cells to Radiotherapy. [Content Brief]

                                    [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. [Content Brief]

                                    [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. [Content Brief]

                                    [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. [Content Brief]

                                    [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. [Content Brief]

                                  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.

                                  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
                                  • [1]. Rae C, et al. Inhibition of Fatty Acid Synthase Sensitizes Prostate Cancer Cells to Radiotherapy. [Content Brief]

                                    [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. [Content Brief]

                                    [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. [Content Brief]

                                    [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. [Content Brief]

                                    [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. [Content Brief]

                                  • [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
                                  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

                                  • Disease Areas
                                  • Cancer Inflammation or Immune System Disease Metabolic or Endocrine Disease Urogenital Disease Digestive System Disease
                                  • Lipid Metabolism Breast Cancer Prostate Cancer Urogenital Cancer Digestive System Inflammation
                                  • Obesity
                                  • Cancer
                                  • Cancer Targeted Therapy Cancer Metabolism and Metastasis
                                  • Metabolic Enzyme/Protease
                                  • Fatty Acid Synthase (FASN)
                                  Help & FAQs
                                  • 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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                                  • C75 1/16
                                  • 1/16

                                    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).
                                  • 1/16

                                    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.
                                  • 1/16

                                    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.
                                  • C75
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