ChemicalBook > Product Catalog >Biochemical Engineering >Biochemical Reagents >Agonist Inhibitors >CGP 57380

CGP 57380

CGP 57380 Suppliers list
Company Name: 3B Pharmachem (Wuhan) International Co.,Ltd.  
Tel: 18930552037
Email: 3bsc@sina.com
Company Name: Shanghai Ennopharm Co., Ltd.  
Tel: +86 (21) 6435-5022
Email:
Company Name: Haoyuan Chemexpress Co., Ltd.  
Tel: 021-58950125
Email: info@chemexpress.com
Company Name: Guangzhou Isun Pharmaceutical Co., Ltd  
Tel: 020-39119399 18927568969
Email: isunpharm@qq.com
Company Name: AdooQ BioScience, LLC   
Tel: +1 (866) 930-6790
Email: info@adooq.com

CGP 57380 manufacturers

  • CGP 57380
  • CGP 57380 pictures
  • $33.00
  • 2026-07-27
  • CAS:522629-08-9
  • Purity: 99.89%
  • Supply Ability: 10g
  • CGP 57380
  • CGP 57380 pictures
  • $1.00
  • 2019-12-26
  • CAS:522629-08-9
  • Min. Order: 1g
  • Purity: 99%
  • Supply Ability: 200kg
CGP 57380 Basic information
Product Name:CGP 57380
Synonyms:CGP 57380;CGP57380, N3-(4-fluorophenyl)-1h-pyrazolo[3,4-d]pyrimidine-3,4-diamine;MNK1 Inhibitor;N3-(4-Fluorophenyl)-1H-pyrazolo[3,4-d]pyrimidine-3,4-diamine;CGP57380; CGP-57380;CS-1420;MNK1 Inhibitor - CAS 522629-08-9 - Calbiochem;P 57380
CAS:522629-08-9
MF:C11H9FN6
MW:244.23
EINECS:
Product Categories:Inhibitors
Mol File:522629-08-9.mol
CGP 57380 Structure
CGP 57380 Chemical Properties
storage temp. 2-8°C
solubility DMSO: soluble10mg/mL, clear
form powder
color white to beige
InChI1S/C11H9FN6/c12-6-1-3-7(4-2-6)16-11-8-9(13)14-5-15-10(8)17-18-11/h1-5H,(H4,13,14,15,16,17,18)
InChIKeyUQPMANVRZYYQMD-UHFFFAOYSA-N
SMILESNc1ncnc2[nH]nc(Nc3ccc(F)cc3)c12
Safety Information
WGK Germany 3
HS Code 2933599590
Storage Class11 - Combustible Solids
MSDS Information
CGP 57380 Usage And Synthesis
UsesCGP 57380 has been used:
  • as a mitogen-activated protein kinase-interacting kinase 1 (MNK1) inhibitor to investigate the role of Mnk1 on eukaryotic translation initiation factor 4F (eIF4F) assembly and Newcastle disease virus (NDV) replication in HeLa cells
  • as an MNK1 inhibitor to block eIF4 complex to evaluate the contribution of interferon (IFN-γ) translation during m157- transgenic (Tg) stimulation
  • as a β-catenin nuclear translocation inhibitor to analyze its effects on cytoplasmic and nuclear fractions of cells

DefinitionChEBI: N3-(4-fluorophenyl)-2H-pyrazolo[3,4-d]pyrimidine-3,4-diamine is a pyrazolopyrimidine.
Biological ActivityInhibitor of MAP-kinase interacting kinase-1 (Mnk1, MKNK1) (IC 50 = 2.2 μ M) that displays selectivity over p38, JNK1, ERK1, ERK2, PKC and c-src family kinases. Blocks phosphorylation of eIF4E in cellular assays (IC 50 = 3 μ M) and inhibits LPS-induced TNF α expression in macrophages.
Biochem/physiol ActionsCGP 57380 is a β-catenin nuclear translocation inhibitor, which prevents the proliferation of severalcancers. It enhances radiation-induced apoptosis in nasopharyngeal carcinoma (NPC). CGP 57380 upregulates β-catenin in the cytoplasm and inhibits epithelial-mesenchymal transition (EMT).
storageStore at +4°C
references[1]. knauf u, tschopp c, gram h. negative regulation of protein translation by mitogen-activated protein kinase-interacting kinases 1 and 2. mol cell biol, 2001, 21(16): 5500-5511.
[2]. ishida m, ishida t, nakashima h, et al. mnk1 is required for angiotensin ii-induced protein synthesis in vascular smooth muscle cells. circ res, 2003, 93(12): 1218-1224.
[3]. andersson k, sundler r. posttranscriptional regulation of tnfalpha expression via eukaryotic initiation factor 4e (eif4e) phosphorylation in mouse macrophages. cytokine, 2006, 33(1): 52-57.
[4]. rowlett rm, chrestensen ca, nyce m, et al. mnk kinases regulate multiple tlr pathways and innate proinflammatory cytokines in macrophages. am j physiol gastrointest liver physiol, 2008, 294(2): g452-459.
CGP 57380 Preparation Products And Raw materials
Tag:CGP 57380(522629-08-9) Related Product Information
Gemcitabine 1H-Benzotriazole Sorafenib tosylate Fludarabine Vorinostat Erlotinib hydrochloride CGP 57380