STAT5-IN-2 - ≥99% , CAS No.2111834-61-6

CAS: 2111834-61-6 Cat. No.: S649601 Peso molecular: 397.51 PubChem CID: 137628635

GRADE & PURITY ≥99%

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Descripción general

STAT5-IN-2 is a STAT5 inhibitor,STAT5-IN-2 has potent antileukemic effect

In Vitro

STAT5-IN-2 has EC 50 values of 9 μM and 5 μM in K562 and KU812 cells, respectively. STAT5-IN-2 (100 nM-50 µM; 48 hours) has EC 50 values of 2.6 µM and 3.5 µM in KG1a and MV-4-11 cells, respectively. STAT5-IN-2 (10 µM; 48 hours) induces apoptosis in all cell lines (K562, KU812, KG1a and MV-4-11 cells). STAT5-IN-2 (10 µM; 24 hours) blocks phosphorylation of STAT5. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability AssayCell Line: KG1a and MV-4-11 cell lines Concentration: 100 nM, 10 µM, 20 µM, 30 µM, 40 µM, 50 µM Incubation Time: 48 hours Result: Inhibited cell growth in KG1a and MV-4-11 cell lines Apoptosis AnalysisCell Line: K562, KU812, KG1a and MV-4-11 cells Concentration: 10 µM Incubation Time: 48 hours Result: Significantly increased the number of apoptotic cells. Western Blot AnalysisCell Line: KG1a, MV-4-11 and KU812 cells Concentration: 10 µM Incubation Time: 24 hours Result: Inhibited phosphorylation of STAT5 compared to no influence on phosphorylation level of STAT3, Akt and Erk1/2.

Form:Solid

IC50& Target:STAT5 9 μM (EC 50 , in K562 cells) STAT5 5 μM (EC 50 , in KU812 cells )

Specifications

Especificaciones y pureza

≥99%

Mecanismos bioquímicos y fisiológicos

STAT5-IN-2 is a STAT5 inhibitor, extracted from reference 1, example 17f. STAT5-IN-2 has potent antileukemic effect.

Condiciones de almacenamiento de almacenamiento

Store at -20°C

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥99%

Nombres e identificadores

• Sonrisas canónicas: CC1(CCN(C2=C1C=C(C=C2)C3=CN=CC=C3)CCOC4=CC5=C(C=C4)NC=C5)C
• IUPAC Name: 1-[2-(1H-indol-5-yloxy)ethyl]-4,4-dimethyl-6-pyridin-3-yl-2,3-dihydroquinoline
• InChIKey: BELIZDRKUICBJC-UHFFFAOYSA-N
• INCHI: 1S/C26H27N3O/c1-26(2)10-13-29(14-15-30-22-6-7-24-20(16-22)9-12-28-24)25-8-5-19(17-23(25)26)21-4-3-11-27-18-21/h3-9,11-12,16-18,28H,10,13-15H2,1-2H3
• PubChem CID: 137628635
• Peso molecular: 397.51

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Quinolines and derivatives
      • Subclass Hydroquinolines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Quinolines and derivatives
• Subclass: Hydroquinolines
• Intermediate Tree Nodes: Not available
• Direct Parent: Hydroquinolines
• Alternative Parents: Indoles Dialkylarylamines Methylpyridines Alkyl aryl ethers Benzenoids Pyrroles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Tetrahydroquinoline - Indole or derivatives - Indole - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Methylpyridine - Alkyl aryl ether - Benzenoid - Pyridine - Heteroaromatic compound - Pyrrole - Tertiary amine - Azacycle - Ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as hydroquinolines. These are derivatives of quinoline in which in which at least one double bond in the quinoline moiety are reduced by adding two hydrogen atoms.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Solubilidad: DMSO : 100 mg/mL (251.57 mM; Need ultrasonic)