40142-92-5

Upstream product

• 18774-49-7 benzo[4,5]thieno[2,3-d]pyrimidin-4(3H)-one 
• 34761-09-6 ethyl 3-aminobenzothiophene-2-carboxylate 
• 108-94-1 cyclohexanone 
• 4506-71-2 ethyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate 
• 14346-24-8 8-thia-4,6-diazatricyclo[7.4.0.0[2,7]]trideca-1⁽⁹⁾,2⁽⁷⁾,3,5-tetraen-3-ol 
• 18774-49-7 8-thia-4,6-diazatricyclo[7.4.0.0[2,7]]trideca-1⁽⁹⁾,2⁽⁷⁾,3,5,10,12-hexaen-3-ol 
• 7311-95-7 ethyl 2-amino-1-benzothiophene-3-carboxylate 

Downstream Products

• 1228939-88-5 4-(2-methoxyanilino)-[1]benzothieno[2,3-d]pyrimidine 
• 1228939-90-9 4-(4-methoxyanilino)-[1]benzothieno[2,3-d]pyrimidine 
• 1228939-85-2 4-anilino[1]benzothieno[2,3-d]pyrimidine 
• 1066435-07-1 4-(2-methylanilino)-[1]benzothieno[2,3-d]pyrimidine 
• 1414524-17-6 N-benzylbenzo[4,5]thieno[2,3-d]pyrimidin-4-amine 
• 1414524-19-8 N-(2-methylbenzyl)benzo[4,5]thieno[2,3-d]pyrimidin-4-amine 

Relevant academic research and scientific papers

Computer-aided identification, synthesis and evaluation of substituted thienopyrimidines as novel inhibitors of HCV replication

A structure-based virtual screening technique was applied to the study of the HCV NS3 helicase, with the aim to find novel inhibitors of the HCV replication. A library of ～450000 commercially available compounds was analysed in silico and 21 structures were selected for biological evaluation in the HCV replicon assay. One hit characterized by a substituted thieno-pyrimidine scaffold was found to inhibit the viral replication with an EC50value in the sub-micromolar range and a good selectivity index. Different series of novel thieno-pyrimidine derivatives were designed and synthesised; several new structures showed antiviral activity in the low or sub-micromolar range.

FLT3 INHIBITORS AND USES THEREOF

The present invention provides methods of using compounds of formula I: or compositions thereof for the inhibition of FLT3, and the treatment of FLT3-mediated disorders.

IRAK INHIBITORS AND USES THEREOF

The present invention provides arylo-fused thienopyrimidine compounds, compositions thereof, and methods of using the same.

Synthesis and evaluation of apoptosis induction of thienopyrimidine compounds on KRAS and BRAF mutated colorectal cancer cell lines

Monoclonal antibodies (MoAb) and tyrosine kinase inhibitors (TKI) targeting the EGFR (Epidermal Growth Factor Receptor) pathways are currently used in colorectal cancer treatment. Despite the improvement of median overall survival, resistance is observed

Synthesis and study of antiproliferative activity of novel thienopyrimidines on glioblastoma cells

The receptor tyrosine kinases (for example EGFR, PDGFR, VEGFR) are a transmembrane protein family which plays a crucial role in tumor growth, survival, metastasis dissemination and angiogenesis. During the past 10 years, many tyrosine kinase inhibitors (T