
FB23-2
CAS No. 2243736-45-8
FB23-2( FTO Demethylase inhibitor FB23-2 )
Catalog No. M13595 CAS No. 2243736-45-8
FB23-2 is a potent, selective inhibitor of the mRNA N 6-methyladenosine (m 6A) demethylase FTO.
Purity : >98% (HPLC)






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2MG | 53 | In Stock |
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5MG | 87 | In Stock |
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10MG | 151 | In Stock |
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25MG | 255 | In Stock |
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50MG | 376 | In Stock |
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500MG | 1197 | In Stock |
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Biological Information
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Product NameFB23-2
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NoteResearch use only, not for human use.
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Brief DescriptionFB23-2 is a potent, selective inhibitor of the mRNA N 6-methyladenosine (m 6A) demethylase FTO.
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DescriptionFB23-2 is a potent, selective inhibitor of the mRNA N 6-methyladenosine (m 6A) demethylase FTO, directly bind to FTO, inhibits FTO demethylation of m6 A in RNA in vitro with IC50 of 2.6 uM; demonstrates significantly improved anti-proliferative activity on NB4 and MONOMAC6 cells with IC50 of 0.8-1.5 uM, compared with parental compound FB23; dramatically suppresses proliferation and promotes the differentiation/apoptosis of human acute myeloid leukemia (AML) cell line cells and primary blast AML cells in vitro; FB23-2 significantly inhibits the progression of human AML cell lines and primary cells in xeno-transplanted mice.
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In VitroCell Proliferation Assay Cell Line:MA9 cells, FLT3ITD/NPM1 cells (mouse BM cells)Concentration:0.5 μM, 2 μM, 5 μMIncubation Time:24 hours, 48 hours, 72 hours Result:Suppressed the proliferation of BM cells.RT-PCRCell Line:NB4 cells, MONOMAC6 cells Concentration:1 μM, 5 μM , 20 μM Incubation Time:72 hours Result:Significantly increased ASB2 and RARA mRNA levels.Apoptosis Analysis Cell Line:NB4 cells, MONOMAC6 cells Concentration:1 μM, 5 μM , 20 μM Incubation Time:48 hours (NB4 cells),72 hours (MONOMAC6 cells)Result:Induced apoptosis.Cell Cycle Analysis Cell Line:MONOMAC6 cells Concentration:5 μM , 20 μM Incubation Time:24 hours Result:Induced cell cycle arrest at G1 stage.
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In VivoAnimal Model:NOD/LtSz-scid IL2RG-SGM3 (NSGS) mice, xeno-transplanted with MONOMAC6 AML cells Dosage:2 mg/kg Administration:Intraperitoneal injection, daily, for 10 days Result:Delayed the onset of full-blown leukemic symptoms and significantly prolonged survival by almost doubling the median survival.Animal Model:Sprague Dawley (SD) rats Dosage:3 mg/kg (Pharmacokinetic Analysis)Administration:Intraperitoneal injection Result:T1/2 (6.7 hours), Cmax (2421.3 ng/mL).
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SynonymsFTO Demethylase inhibitor FB23-2
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PathwayChromatin/Epigenetic
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TargetHistone Demethylase
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RecptorHistone Demethylase
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Research Area——
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Indication——
Chemical Information
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CAS Number2243736-45-8
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Formula Weight392.236
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Molecular FormulaC18H15Cl2N3O3
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Purity>98% (HPLC)
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SolubilityDMSO : 62.5 mg/mL 159.34 mM
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SMILESO=C(NO)C1=CC=CC=C1NC2=C(Cl)C=C(C3=C(C)ON=C3C)C=C2Cl
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Chemical Name2-((2,6-dichloro-4-(3,5-dimethylisoxazol-4-yl)phenyl)amino)-N-hydroxybenzamide
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Huang Y, et al. Cancer Cell. 2019 Apr 15;35(4):677-691.e10.
molnova catalog



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