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2 000 new building blocks are synthesized monthly. Here is an important update to our MedChem Highlights from March 2024
Recent News
11 April 2024
Press Release
Cambridge, UK and Kyiv, Ukraine, 11 April 2024: Metrion Biosciences Limited (“Metrion”), the specialist ion channel and cardiac safety screening contract research organisation (CRO) and drug discovery company, and Enamine Ltd (“Enamine”), the global leader in supplying small molecules and early drug discovery services, announced that Metrion has enhanced its High Throughput Screening (HTS) services with the addition of access to Enamine’s compound libraries.
27 March 2024
Press Release
March, 2024, Kyiv, Ukraine. Enamine Ltd, the global leader in supplying small molecules and early drug discovery services, announces the expansion of its library synthesis capabilities with a focus on Enamine REAL compounds to further support the growing demands of agricultural and pharmaceutical companies, research institutes, and drug discovery centers.
01 March 2024
News
We are excited to announce a strategic collaboration between Enamine, the world's leading provider of chemical building blocks, compound libraries, and biology services, and Genez International, a prominent enterprise with 15 years of experience in cross-border supply management, biopharmaceutical research and development, semiconductor equipment, and high-definition digital imaging systems.
Synthesis , 2010, 15, 2588-2598
DOI: 10.1055/s-0029-1218840
Khodachenko A. N.; Shivanyuk A. N.; Shishkina S. V.; Shishkin O. V.; Nazarenko K. G.; Tolmachev A. A.
The reactions of five-, six-, seven-, and eight-membered cyclic imido ethers with one equivalent of sulfamide lead to the corresponding sulfamoylamidines in 70-80% yields. Sulfamoylamidines undergo condensations with aliphatic and aromatic aldehydes as well as aliphatic ketones to give thiatriazine dioxides in 50-95% yields. The NMR spectroscopic studies reveal ring-chain tautomerism of some thiatriazine dioxides in solution. The ratio between the tautomers depends on the temperature, solvent polarity, and electronic properties of the substituents of the pendant aryl rings. Thiatriazine dioxides are readily alkylated and acylated at position 2.
Khodachenko A. N.; Shivanyuk A. N.; Shishkina S. V.; Shishkin O. V.; Nazarenko K. G.; Tolmachev A. A.
Synthesis 2010, 15, 2588-2598
DOI: 10.1055/s-0029-1218840
