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STAT5-IN-1
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
STAT5-IN-1图片
CAS NO:285986-31-4
规格:≥98%
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
250mg电议
500mg电议

产品介绍
理化性质和储存条件
Molecular Weight (MW) 293.28
Formula C16H11N3O3
CAS No. 285986-31-4
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: ≥ 20 mg/mL
Water: <1mg/mL
Ethanol: <1mg/mL
Chemical Name N′-((4-Oxo-4H-chromen-3-yl)methylene)nicotinohydrazide
Synonyms STAT5 Inhibitor; STAT5-Inhibitor; STAT5-IN-1
SMILES Code O=C(N/N=C/C1=COC2=C(C=CC=C2)C1=O)C3=CN=CC=C3
实验参考方法
In Vitro

In vitro activity: STAT5-IN-1 (also known asSTAT5 Inhibitor) is a STAT5 ( signal transducer and activator of transcription 5) inhibitor with IC50 of 47 μM for STAT5β isoform. STAT5-IN-1 is a cell permeable non-petide nicotinoyl hydrazone which suppresses STAT5 via binding to the SH2 domain. STAT5 is a member of the STAT family of proteins that is implicated in cell growth and differentiation. STAT5 functions in various biological processes such as homeostasis of hematopoietic stem cells, development of blood cells, growth hormone effects, and differentiation of mammary epithelium. STAT5 has been reported as a therapeutic target for the treatment of human cancers.


Kinase Assay: The signal transducer and activator of transcription 5 (STAT5) is a member of the STAT family of proteins, implicated in cell growth and differentiation. STAT5-IN-1 inhibits STAT5 by binding to the SH2 domain. The functions of the SH2 domains of STAT3, STAT1, and of the tyrosine kinase Lck are inhibited to a lesser degree (IC50>500 μM). STAT5-IN-1 block STAT5/STAT5 DNA binding in K562 nuclear extracts. Substitution of the hydrogen at C6 of the chromone ring by an ethyl group does not affect activity of STAT5-IN-1 against STAT5β, but leads to complete loss of selectivity against other STAT family members.


Cell Assay:

In Vivo
Animal model
Formulation & Dosage
References Chembiochem. 2008 Mar 25;9(5):723-7.