FB23-2

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Products Intro: Product Name:FB23-2
CAS:2243736-45-8
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
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Products Intro: Product Name:FB23-2
CAS:2243736-45-8
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Company Name: Zhejiang J&C Biological Technology Co.,Limited
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Products Intro: Product Name:FB23-2
CAS:2243736-45-8
Purity:99% Package:5KG;1KG Remarks:FB23-2
Company Name: CR Corporation Limited
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CAS:2243736-45-8
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Products Intro: Product Name:FB23-2
CAS:2243736-45-8
Purity:98% Package:1mg Remarks:V31465

FB23-2 manufacturers

  • FB23-2
  • FB23-2 pictures
  • $32.00 / 1mg
  • 2025-11-11
  • CAS:2243736-45-8
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  • Purity: 98.00%
  • Supply Ability: 10g
FB23-2 Basic information
Product Name:FB23-2
Synonyms:FB23-2;FB23-2(FTO Demethylase inhibitor FB23-2);Benzamide, 2-[[2,6-dichloro-4-(3,5-dimethyl-4-isoxazolyl)phenyl]amino]-N-hydroxy-;FB23-2,1.5g;2-[[2,6-Dichloro-4-(3,5-dimethyl-4-isoxazolyl)phenyl]amino]-N-hydroxybenzamide;FB23 2,AML,Apoptosis,leukemia,acute,anti-proliferation,Inhibitor,FB232,m6A,myeloid,mRNA,inhibit,FB23-2,demethylase,FB-23-2;2-((2,6-Dichloro-4-(3,5-dimethylisoxazol-4-yl)phenyl)amino)-N-hydroxybenzamide;FB23-2, 10 mM in DMSO
CAS:2243736-45-8
MF:C18H15Cl2N3O3
MW:392.24
EINECS:
Product Categories:
Mol File:2243736-45-8.mol
FB23-2 Structure
FB23-2 Chemical Properties
density 1.428±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility DMSO:70.25(Max Conc. mg/mL);179.1(Max Conc. mM)
form A solid
pka8.72±0.40(Predicted)
color White to light yellow
Safety Information
MSDS Information
FB23-2 Usage And Synthesis
UsesFB23-2 is a potent and selective inhibitor of mRNA N6-methyladenosine (m6A) demethylase FTO, with an IC50 of 2.6 μM. FB23-2 has anti-proliferation activity. FB23-2 can be used for the research of acute myeloid leukemia (AML)[1].
in vivo

FB23-2 (2 mg/kg; i.p.; daily; for 10 days) substantially suppresses leukemia progression and prolongs survival[1].
FB23-2 exhibits elimination half-life (rat 6.7 h) and Cmax (rat 2421.3 ng/mL) following intraperitoneal injection (rat 3 mg/kg)[1].

Animal Model:NOD/LtSz-scid IL2RG-SGM3 (NSGS) mice, xeno-transplanted with MONOMAC6 AML cells[1]
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[1]
Dosage:3 mg/kg (Pharmacokinetic Analysis)
Administration:Intraperitoneal injection
Result:T1/2 (6.7 hours), Cmax (2421.3 ng/mL).
References[1] Huang Y, et al. Small-Molecule Targeting of Oncogenic FTO Demethylase in Acute Myeloid Leukemia. Cancer Cell. 2019 Apr 15;35(4):677-691.e10. DOI:10.1016/j.ccell.2019.03.006
FB23-2 Preparation Products And Raw materials
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