7038-74-6

Usage

Uses

Used in Pharmaceutical Industry:
6-Cyclopropyl-2-sulfanylpyrimidin-4-ol is used as a key intermediate in the synthesis of nucleic acid components and their analogs for the development of novel therapeutic agents. Its unique structure allows for the creation of new molecules with potential applications in treating various diseases and conditions.
Used in Research and Development:
In the field of research and development, 6-cyclopropyl-2-sulfanylpyrimidin-4-ol serves as a valuable compound for exploring the structure-activity relationships of nucleic acid analogs. This helps scientists understand the molecular mechanisms underlying their biological activities and optimize their therapeutic potential.
Used in Drug Design:
6-Cyclopropyl-2-sulfanylpyrimidin-4-ol is utilized in drug design to create new chemical entities with improved pharmacological properties. Its incorporation into drug candidates can lead to the development of more effective and targeted treatments for various diseases.

InChI:InChI=1/C7H8N2OS/c10-6-3-5(4-1-2-4)8-7(11)9-6/h3-4H,1-2H2,(H2,8,9,10,11)

Upstream product

• 17356-08-0 thiourea 
• 24922-02-9 Ethyl 3-cyclopropyl-3-oxopropionate 
• 32249-35-7 methyl 3-cyclopropyl-3-oxopropanoate 

Relevant academic research and scientific papers

Design, synthesis, and acaricidal activity of phenyl methoxyacrylates containing 2-alkenylthiopyrimidine

A series of novel phenyl methoxyacrylate derivatives containing a 2-alkenylthiopyrimidine substructure were designed, synthesized, and evaluated in terms of acaricidal activity. The structures of the title compounds were identified by 1H NMR, 13C NMR and high-resolution mass spectra (HRMS). Compound (E)-methyl 2-(2-((2-(3,3-dichloroallylthio)-6-(trifluoromethyl)pyrimidin-4-yloxy) methyl)phenyl)-3-methoxyacr-ylate (4j) exhibited significant acaricidal activity against Tetranychus cinnabarinus (T. cinnabarinus) in greenhouse tests possessing nearly twice the larvicidal and ovicidal activity compared to fluacrypyrim. Furthermore, the results of the field trials demonstrated that compound 4j could effectively control Panonychuscitri with long-lasting persistence and rapid action. The toxicology data in terms of LD50 value confirmed that compound 4j has a relatively low acute toxicity to mammals, birds, and honeybees.

Synthesis and evaluation of 5,6-disubstituted thiopyrimidine aryl aminothiazoles as inhibitors of the calcium-activated chloride channel TMEM16A/Ano1

Transmembrane protein 16A (TMEM16A), also called Ano1, is a Ca2+ activated Cl? channel expressed widely in mammalian epithelia, as well as in vascular smooth muscle and some tumors and electrically excitable cells. TMEM16A inhibitors have potential utility for treatment of disorders of epithelial fluid and mucus secretion, hypertension, some cancers and other diseases. 4-Aryl-2-amino thiazole T16Ainh-01 was previously identified by high-throughput screening. Here, a library of 47 compounds were prepared that explored the 5,6-disubstituted pyrimidine scaffold found in T16Ainh-01. TMEM16A inhibition activity was measured using fluorescence plate reader and short-circuit current assays. We found that very little structural variation of T16Ainh-01 was tolerated, with most compounds showing no activity at 10 μM. The most potent compound in the series, 9bo, which substitutes 4-methoxyphenyl in T16Ainh-01 with 2-thiophene, had IC50 ～1 μM for inhibition of TMEM16A chloride conductance.