
STAT5-IN-1
CAS No. 285986-31-4
STAT5-IN-1( Signal Transducers and Activators of Transcription 5 )
Catalog No. M13870 CAS No. 285986-31-4
A selective, small molecule inhibitor of the transcription factor STAT5 with IC50 of 47±17 uM in FP assays.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 42 | In Stock |
![]() ![]() |
10MG | 77 | In Stock |
![]() ![]() |
25MG | 165 | In Stock |
![]() ![]() |
50MG | 290 | In Stock |
![]() ![]() |
100MG | 492 | In Stock |
![]() ![]() |
200MG | Get Quote | In Stock |
![]() ![]() |
500MG | Get Quote | In Stock |
![]() ![]() |
1G | Get Quote | In Stock |
![]() ![]() |
Biological Information
-
Product NameSTAT5-IN-1
-
NoteResearch use only, not for human use.
-
Brief DescriptionA selective, small molecule inhibitor of the transcription factor STAT5 with IC50 of 47±17 uM in FP assays.
-
DescriptionA selective, small molecule inhibitor of the transcription factor STAT5 with IC50 of 47±17 uM in FP assays; shows little to no inhibition for STAT1, STAT3 and Lck (<40% inhibition at 500 uM); selectively inhibits the function of the STAT5b domain and STAT5 DNA binding in vitro, and selectively inhibits activation of STAT5 in K562 cells.
-
In VitroThe 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 extent (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.
-
In Vivo——
-
SynonymsSignal Transducers and Activators of Transcription 5
-
PathwayJAK/STAT Signaling
-
TargetSTAT
-
RecptorSTAT5β
-
Research AreaOther Indications
-
Indication——
Chemical Information
-
CAS Number285986-31-4
-
Formula Weight293.28
-
Molecular FormulaC16H11N3O3
-
Purity>98% (HPLC)
-
SolubilityDMSO: ≥23.0 mg/mL ( < 1 mg/ml refers to the product slightly soluble or insoluble )
-
SMILESO=C(N/N=C/C1=COC2=C(C=CC=C2)C1=O)C3=CN=CC=C3
-
Chemical Name3-Pyridinecarboxylic acid, [(4-oxo-4H-1-benzopyran-3-yl)methylene]hydrazide (9CI)
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Müller J, et al. Chembiochem. 2008 Mar 25; 9(5):723-7.
molnova catalog



related products
-
S3I-M2001
S3I-M2001 (Bromohydroxyacetone phosphate) is an oxazole-based peptidomimetic of the STAT3 SH2 domain-binding phosphotyrosine peptide that selectively disrupts active STAT3:STAT3 dimers.
-
AS1517499
A novel potent STAT6 inhibitor with IC50 of 21 nM in STAT6-dependent promoter reporter assay.
-
Corosolic acid
Corosolic acid contains anti-angiogenic activity that can suppress FAK signaling induced by angiopoietin-1.