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ChemicalBook--->CAS DataBase List--->62004-35-7

62004-35-7

62004-35-7 Structure

62004-35-7 Structure
IdentificationBack Directory
[Name]

LFM-A13
[CAS]

62004-35-7
[Synonyms]

LFM-A13
2-CYANO-N-(2,5-DIBROMOPHENYL)-3-HYDROXY-2-BUTENAMIDE
2-Cyano-N-(2,5-dibromophenyl)-3-hydroxybut-2-enamide
2-Cyano-N-(2,5-dibromophenyl)-3-hydroxy-2-buteneamide
2-Butenamide, 2-cyano-N-(2,5-dibromophenyl)-3-hydroxy-
2-Cyano-3-hydroxy-but-2-enoic acid (2,5-dibromo-phenyl)-amide
ALPHA-CYANO-BETA-HYDROXY-BETA-METHYL-N-(2,5-DIBROMOPHENYL)PROPENAMIDE
[Molecular Formula]

C11H8Br2N2O2
[MDL Number]

MFCD02179204
[MOL File]

62004-35-7.mol
[Molecular Weight]

360
Chemical PropertiesBack Directory
[storage temp. ]

−20°C
[solubility ]

DMSO: 15 mg/mL
[form ]

powder
[color ]

white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312+P362+P364-P304+P340+P312-P305+P351+P338+P337+P313-P501
[Hazard Codes ]

Xn
[Risk Statements ]

20/21/22
[Safety Statements ]

36/37
[WGK Germany ]

3
[HS Code ]

2926.90.4801
Hazard InformationBack Directory
[Uses]

LFM-A13 is a novel anti-leukemic agent targeting Bruton''s tyrosine kinase (BTK). LFM-A13 is a BTK inhibitor.
[Biological Activity]

Potent and selective inhibitor of Bruton's tyrosine kinase (BTK). Inhibits recombinant BTK with an IC 50 value of 2.5 μ M and has no activity on other protein kinases ( including JAK1, JAK3, HCK, EGFR kinase and insulin receptor kinase) at concentrations of up to 278 μ M.
[in vivo]

LFM-A13 (10 or 50 mg/kg; i.p.) exhibits anti-tumor effects dose dependently in the MMTV/Neu transgenic mouse model of breast cancer[3]. FM-A13 (50 mg/kg; tiw; i.p.) attenuates DMBA-induced mammary tumorigenesis in mice by modulating a variety of factors associated with cell cycle, survival and apoptosis[4].

Animal Model:MMTV/neu transgenic mouse model[3]
Dosage:50 or 100 mg/kg
Administration:Intraperitoneal injection (i.p.); twice a day for 5 consecutive days a week
Result:Attenuated mammary tumor formation in mice.
Animal Model:DMBA-induced breast cancer mouse model[4]
Dosage:50 mg/kg (or combinated with Paclitaxel (HY-B0015) (10 mg/kg; once per week intraperitoneally))
Administration:Intraperitoneal injection (i.p.); 3 times a week
Result:Inhibited DMBA-induced mammary tumor incidence, average tumor number, average tumor weight, and size in BALB/c mice.
Significantly decreased PLK1, cyclin D1, CDK-4, P53 and Bcl-2 expression, but increased the expression of p21, IκB, Bax and caspase 3 expression in mice.
[IC 50]

Plx1: 10 μM (IC50); PLK3: 61 μM (IC50); BRK: 267 μM (IC50); BMX: 281 μM (IC50); FYN: 240 μM (IC50); Met: 215 μM (IC50); Btk: 2.5 μM (IC50)
[storage]

Store at RT
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