ChemicalBook--->CAS DataBase List--->2243736-45-8

2243736-45-8

2243736-45-8 Structure

2243736-45-8 Structure
IdentificationBack Directory
[Name]

FB23-2
[CAS]

2243736-45-8
[Synonyms]

FB23-2
FB23-2,1.5g
FB23-2(FTO Demethylase inhibitor FB23-2)
2-[[2,6-Dichloro-4-(3,5-dimethyl-4-isoxazolyl)phenyl]amino]-N-hydroxybenzamide
Benzamide, 2-[[2,6-dichloro-4-(3,5-dimethyl-4-isoxazolyl)phenyl]amino]-N-hydroxy-
[Molecular Formula]

C18H15Cl2N3O3
[MDL Number]

MFCD32174281
[MOL File]

2243736-45-8.mol
[Molecular Weight]

392.24
Chemical PropertiesBack Directory
[density ]

1.428±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

DMSO:70.25(Max Conc. mg/mL);179.1(Max Conc. mM)
[form ]

A solid
[pka]

8.72±0.40(Predicted)
[color ]

White to light yellow
[InChI]

1S/C18H15Cl2N3O3/c1-9-16(10(2)26-23-9)11-7-13(19)17(14(20)8-11)21-15-6-4-3-5-12(15)18(24)22-25/h3-8,21,25H,1-2H3,(H,22,24)
[InChIKey]

ILHNIWOZZKIBNW-UHFFFAOYSA-N
[SMILES]

ClC1=C(NC2=C(C(NO)=O)C=CC=C2)C(Cl)=CC(C3=C(C)ON=C3C)=C1
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

FB23-2 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
Spectrum DetailBack Directory
[Spectrum Detail]

FB23-2(2243736-45-8)1HNMR
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