Fumarate hydratase-IN-1
Based on 20 publication(s) in Google Scholar
Fumarate hydratase-IN-1 (compound 2) is a cell-permeable fumarate hydratase inhibitor. Fumarate hydratase-IN-1 has antiproliferative activity against several cancer cell lines with a mean IC50 of 2.2 μM.
For research use only. We do not sell to patients.
- Purity: 99.58%
- CAS No.: 1644060-37-6
- Formula: C27H30N2O4
- Molecular Weight:446.54
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Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
Publications Citing Use of MedChemExpress (MCE) Fumarate hydratase-IN-1
More- Signal Transduct Target Ther. 2024 Dec 30;9(1):367. [Abstract]
- Nature. 2023 Mar;615(7952):490-498. [Abstract]
- Cell Metab. 2026 Feb 23:S1550-4131(26)00016-1. [Abstract]
- Mol Cell. 2025 Jun 19;85(12):2287-2302.e9. [Abstract]
- Adv Sci (Weinh). 2025 Nov 9:e07524. [Abstract]
- Nat Chem Biol. 2022 Sep;18(9):954-962. [Abstract]
- Small. 2023 Apr;19(16):e2207194. [Abstract]
- Pharmacol Res. 2023 Mar:189:106697. [Abstract]
- Cell Death Dis. 2025 Jun 3;16(1):432. [Abstract]
- EMBO J. 2024 Jun;43(12):2337-2367. [Abstract]
- J Transl Med. 2023 Aug 18;21(1):553. [Abstract]
- Aging Cell. 2026 Apr;25(4):e70451. [Abstract]
- Cell Rep. 2023 Oct 12;42(10):113246. [Abstract]
- JCI Insight. 2026 Feb 10:e195866. [Abstract]
- J Inflamm Res. 2025 Apr 21:18:5399-5413. [Abstract]
- J Asia Pac Entomol. 2024 Dec.
- bioRxiv. 2026 Apr 7:2026.04.03.716311. [Abstract]
- bioRxiv. 2025 Dec 10:2025.12.08.692638. [Abstract]
- Res Sq. 2025 Feb 16.
- Patent. US20250018019A1.
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WB
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RT-PCR
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IF
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WB
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Histological Imaging/Staining
Biological Activity
Fumarate hydratase[1]
Fumarate hydratase-IN-1 inhibits SW620, ACHN, HCT-116, PC3, and SK-MEL-28 cell lines with a mean IC50 of 2.2 μM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 1644060-37-6
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Appearance Solid
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Molecular Weight 446.54
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Formula C27H30N2O4
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Color Off-white to yellow
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SMILES
O=C(OCC)[C@]1([C@H](CC(NC)=O)C2=O)C(N2CC(C=C3)=CC=C3C4=CC=CC=C4)=CCCC1
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year
Publications (20)
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Journal Impact Factor
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Most Recent
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Signal Transduct Target Ther
2024 Dec 30;9(1):367. PMID: 39737965 -
Nature
2023 Mar;615(7952):490-498. PMID: 36890227
Fumarate hydratase-IN-1 purchased from MedChemExpress. Usage Cited in: Nature. 2023 Mar;615(7952):490-498. [Abstract]
Both Fumarate hydratase-IN-1 (FHIN1) and Dimethyl fumarate (DMF) treatment limit IFNβ-induced STAT1 and JAK1 phosphorylation in BMDMs.
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Cell Metab
Lack of PCK1 in hepatic stellate cells causes liver fibrosis by fueling tricarboxylic acid cycle and increasing glycolysis. [Abstract]2026 Feb 23:S1550-4131(26)00016-1. PMID: 41734768 -
Mol Cell
2025 Jun 19;85(12):2287-2302.e9. PMID: 40505663 -
Adv Sci (Weinh)
Amphiregulin and Epiregulin Confer Radioresistance in Esophageal Squamous Cell Carcinoma Through Oxidative Phosphorylation. [Abstract]2025 Nov 9:e07524. PMID: 41208199 -
Nat Chem Biol
2022 Sep;18(9):954-962. PMID: 35710616 -
Small
2023 Apr;19(16):e2207194. PMID: 36634971 -
Pharmacol Res
Dimethyl fumarate inhibits necroptosis and alleviates systemic inflammatory response syndrome by blocking the RIPK1-RIPK3-MLKL axis. [Abstract]2023 Mar:189:106697. PMID: 36796462
Fumarate hydratase-IN-1 purchased from MedChemExpress. Usage Cited in: Pharmacol Res. 2023 Mar:189:106697. [Abstract]
Fumarate hydratase-IN-1 (FHIN1, 6.25-25 μM; 1 h) attenuates TSI (2 h)-induced necroptosis in a dose-dependent manner in BMDMs.
Fumarate hydratase-IN-1 purchased from MedChemExpress. Usage Cited in: Pharmacol Res. 2023 Mar:189:106697. [Abstract]
Fumarate hydratase-IN-1 (FHIN1, 6.25-25 μM; 1 h) inhibits the RIPK1-RIPK3-MLKL signaling pathway in BMDMs after stimulation with TSI (2 h).
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Cell Death Dis
Oncometabolite fumarate facilitates PD-L1 expression and immune evasion in clear cell renal cell carcinoma. [Abstract]2025 Jun 3;16(1):432. PMID: 40461489
Fumarate hydratase-IN-1 purchased from MedChemExpress. Usage Cited in: Cell Death Dis. 2025 Jun 3;16(1):432. [Abstract]
Fumarate hydratase-IN-1 (FHIN1, 20 μM, 24 h) upregulates the protein and mRNA levels of PD-L1 in RCC10 and RCC4 cells.
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EMBO J
SUCLG1 restricts POLRMT succinylation to enhance mitochondrial biogenesis and leukemia progression. [Abstract]2024 Jun;43(12):2337-2367. PMID: 38649537 -
J Transl Med
Rutaecarpine induces the differentiation of triple-negative breast cancer cells through inhibiting fumarate hydratase. [Abstract]2023 Aug 18;21(1):553. PMID: 37592347 -
Aging Cell
2026 Apr;25(4):e70451. PMID: 41874464 -
Cell Rep
Allosterically inhibited PFKL via prostaglandin E2 withholds glucose metabolism and ovarian cancer invasiveness. [Abstract]2023 Oct 12;42(10):113246. PMID: 37831605 -
JCI Insight
IFN-γ-induced trained immunity enhances killing of priority pathogens in healthy and genetically vulnerable individuals. [Abstract]2026 Feb 10:e195866. PMID: 41665962 -
J Inflamm Res
Fumarate Hydratase Restrains mtDNA Attenuates LPS-Induced Acute Lung Injury Through cGAS-STING Pathways. [Abstract]2025 Apr 21:18:5399-5413. PMID: 40291460
Fumarate hydratase-IN-1 purchased from MedChemExpress. Usage Cited in: J Inflamm Res. 2025 Apr 21:18:5399-5413. [Abstract]
Fumarate level in lung tissue after Fumarate hydratase-IN-1 (FHIN1, 50 mg/kg; i.p.; Single dose) treatment (n=6).
Fumarate hydratase-IN-1 purchased from MedChemExpress. Usage Cited in: J Inflamm Res. 2025 Apr 21:18:5399-5413. [Abstract]
Fumarate hydratase-IN-1 (FHIN1, 10-20 μM; 3 h). Typical JC-1 immunofluorescence staining and statistical results in THP-1.
Fumarate hydratase-IN-1 purchased from MedChemExpress. Usage Cited in: J Inflamm Res. 2025 Apr 21:18:5399-5413. [Abstract]
Fumarate hydratase-IN-1 (FHIN1, 10-20 μM; 3 h). Western blots for cGAS, STING, IRF3 and p-IRF3 (n=6).
Fumarate hydratase-IN-1 purchased from MedChemExpress. Usage Cited in: J Inflamm Res. 2025 Apr 21:18:5399-5413. [Abstract]
Fumarate hydratase-IN-1 (FHIN1, 50 mg/kg; i.p.; Single dose). Typical H&E staining for mice lung tissues.
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bioRxiv
2026 Apr 7:2026.04.03.716311. PMID: 41993415 -
bioRxiv
Oncometabolite fumarate impairs ATR-CHK1 signaling by succinating RPA1 in Fumarate Hydratase-deficient renal cell carcinoma cells. [Abstract]2025 Dec 10:2025.12.08.692638. PMID: 41427347 -
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Solvent & Solubility
DMSO : 50 mg/mL (111.97 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
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.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 2.5 mg/mL (5.60 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.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 2.5 mg/mL (5.60 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.
Please enter the basic information of animal experiments:
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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%+
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+%Tween-80 + +
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%Saline +
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).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
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
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Data Sheet (275 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
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| DMSO | 1 mM | 2.2394 mL | 11.1972 mL | 22.3944 mL | 55.9860 mL |
| 5 mM | 0.4479 mL | 2.2394 mL | 4.4789 mL | 11.1972 mL | |
| 10 mM | 0.2239 mL | 1.1197 mL | 2.2394 mL | 5.5986 mL | |
| 15 mM | 0.1493 mL | 0.7465 mL | 1.4930 mL | 3.7324 mL | |
| 20 mM | 0.1120 mL | 0.5599 mL | 1.1197 mL | 2.7993 mL | |
| 25 mM | 0.0896 mL | 0.4479 mL | 0.8958 mL | 2.2394 mL | |
| 30 mM | 0.0746 mL | 0.3732 mL | 0.7465 mL | 1.8662 mL | |
| 40 mM | 0.0560 mL | 0.2799 mL | 0.5599 mL | 1.3997 mL | |
| 50 mM | 0.0448 mL | 0.2239 mL | 0.4479 mL | 1.1197 mL | |
| 60 mM | 0.0373 mL | 0.1866 mL | 0.3732 mL | 0.9331 mL | |
| 80 mM | 0.0280 mL | 0.1400 mL | 0.2799 mL | 0.6998 mL | |
| 100 mM | 0.0224 mL | 0.1120 mL | 0.2239 mL | 0.5599 mL |