17326-27-1

Usage

Uses

Used in Pharmaceutical Industry:
2-chloro-9-methyl-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbaldehyde (SALTDATA: FREE) is used as a novel hepatitis C virus inhibitor for its potential antiviral properties. It targets the hepatitis C virus by interfering with essential viral processes, thereby inhibiting the virus's ability to replicate and spread within the host.
The compound's unique structure allows it to interact with specific viral components, making it a promising candidate for the development of new antiviral drugs. Its use in the pharmaceutical industry is focused on combating hepatitis C, a viral infection that affects the liver and can lead to severe health complications if left untreated.

InChI:InChI=1/C10H7ClN2O2/c1-6-3-2-4-13-9(6)12-8(11)7(5-14)10(13)15/h2-5H,1H3

Upstream product

• 68-12-2 N,N-dimethyl-formamide 
• 17326-09-9 2-hydroxy-9-methyl-4H-pyrido[1,2-a]pyrimidin-4-one 

Downstream Products

• 519047-18-8 9-Methyl-4-oxo-2-(phenylamino)-4H-pyrido[1,2-a]pyrimidine-3-carbaldehyde 
• 1204419-57-7 9-Methyl-4-oxo-2-(phenylamino)-4H-pyrido[1,2-a]pyrimidine-3-carboxylic acid 
• 303024-37-5 (E)-2-(benzylamino)-3-((benzylimino)methyl)-9-methyl-4H-pyrido[1,2-a]pyrimidin-4-one 

Relevant academic research and scientific papers

Structure-activity relationship of spop inhibitors against kidney cancer

Speckle-type POZ protein (SPOP) is overexpressed in the nucleus and misallocated in the cytoplasm in almost all the clear-cell renal cell carcinomas (ccRCCs), which leads to kidney tumorigenesis. Previously, we elucidated that the oncogenic SPOP-signaling pathway in ccRCC could be suppressed by 6b that inhibits SPOP-mediated protein interactions. Herein, we have established a structure-activity relationship for 6b analogues as SPOP inhibitors. Compound 6lc suppresses the viability and inhibits the colony formation of ccRCC cell lines driven by cytoplasmic SPOP, superior to 6b. Compound 6lc binds to the SPOP protein in vitro and disrupts SPOP binding to phosphatase-and-tensin homologue (PTEN) in HEK293T cells, which causes the observable phenomena: a decline in the ubiquitination of PTEN, elevated levels of both PTEN and dual-specificity phosphatase 7, and decreased levels of phosphorylated AKT and ERK when ccRCC cell lines are exposed to 6lc in a dose-response manner. Taken together, compound 6lc is a potent candidate against kidney tumorigenesis.

X-ray Structure and Molecular Docking Guided Discovery of Novel Chitinase Inhibitors with a Scaffold of Dipyridopyrimidine-3-carboxamide

Chitinases are the glycosyl hydrolase for catalyzing the degradation of chitin and play an indispensable role in bacterial pathogenesis, fungal cell wall remodeling, and insect molting. Thus, chitinases are attractive targets for therapeutic drugs and pes

2-imine-5-keto-2,5-dihydro-1-H-dipyridylpyrimidine compound

The invention provides synthesis and purpose of a 2-imine-5-keto-2,5-dihydro-1-H-dipyrido [3,4-C: 1 ', 2'-F] pyrimidine compound. Specifically, the invention discloses a compound shown as a following general formula (I) and pharmaceutically-acceptable salt or a pharmaceutically-acceptable solvate, and the definitions of various genes are shown in the Specification. The compound can be taken as an inhibitor taking SPOP as a target or prepared into a drug for treating and/or preventing a disease (such as a kidney cancer and the like) taking the SPOP as the target.

Characterization and structure-activity relationship study of iminodipyridinopyrimidines as novel hepatitis C virus inhibitor

Upon high-throughput screening of synthetic small molecule libraries with the infectious hepatitis C virus (HCV) cell culture system, we identified an iminodipyridinopyrimidine (IDPP) scaffold. IDPP did not inhibit HCV replication, but exhibited very potent inhibitory activity on early and late steps of HCV life cycle. Applying an intensive structure-activity relationship (SAR) study, a promising IDPP Lead compound (12c) with excellent potency (EC50 = 10 nM), high safety margin (SI > 2000), and an acceptable stability in human and rat liver microsomes (t1/2 >60 min) was identified. Overall, our results suggest that the IDPP scaffold could be used for the development of novel HCV interventions.

ANTI - INFECTIVE PYRIDO (1,2 -A) PYRIMIDINES

The present invention relates to small molecule compounds and their use in the treatment of bacterial infections, in particular Tuberculosis.

Anti-infective compounds

The present invention relates to small molecule compounds and their use in the treatment of bacterial infections, in particular Tuberculosis.