FEN1-IN-1
Based on 8 publication(s) in Google Scholar
FEN1-IN-1 (compound 1) is a small molecule flap endonuclease 1 (FEN1) inhibitor with antitumor activity. FEN1-IN-1 binds to the active site of FEN1 and partly achieves inhibition by the co-ordination of Mg2+ ions. FEN1-IN-1 initiaties a DNA damage response and activates the ATM checkpoint signalling pathway, the phosphorylation of histone H2AX and the ubiquitination of FANCD2 in mammalian cells. FEN1-IN-1 is promising for research of cancers.
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- Pureté: 99.85%
- CAS No.: 824983-91-7
- Formule: C15H12N2O5S
- Masse moléculaire:332.33
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Stockage: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) FEN1-IN-1
More- Chem Eng J. 2023 Aug 15, 470, 144407.
- Biosens Bioelectron. 2025 Oct 25:293:118160. [Abstract]
- Adv Healthc Mater. 2025 Mar;14(6):e2404411. [Abstract]
- ACS Appl Mater Interfaces. 2024 Oct 16;16(41):55181-55188. [Abstract]
- Sens Actuators B Chem. 2023 Oct 15, 393, 134265.
- Anal Chem. 2021 Feb 16;93(6):3287-3294. [Abstract]
- ChemElectroChem. 2023 Mar 16.
- University of Alberta. 2025.
Activité biologique
FEN1[1]
FEN1-IN-1 (0-30 μM, 3 days) inhibits 212 cell-lines growth with a mean GI 50 of 15.5 μM[1].
FEN1-IN-1 (0.2-20 μM, 24 h) induces Hela cells disrupted for MRE11A more sensitive and decreasea the survival of the MRE11A deficient cell-lines due to cytotoxicity[1].
FEN1-IN-1 (0-10 μM, 24 h) inhibits both FEN1 and EXO1 function and induces a DNA damage response to activate the signalling pathways in SW620 and HCT-116 cells[1].
FEN1-IN-1 (10 μM, 24 h) leads to replication fork instabilities that, if left unrepaired, can lead to cell death[1].
Tissue-specific sensitivity to FEN1-IN-1 (GI50: μM)[1]
| FEN1-IN-1 | Bladder | Breast | Colorectal | Gastric | Liver | Lung | Pancreatic | Prostate | Gynae | Head & Neck |
| Cell-lines screened | 19 | 22 | 21 | 25 | 21 | 37- | 24 | 7 | 21 | 15 |