CYCLIC DINUCLEOTIDES CONTAINING BENZIMIDAZOLE, METHOD FOR THE PRODUCTION OF SAME, AND USE OF SAME TO ACTIVATE STIMULATOR OF INTERFERON GENES (STING)-DEPENDENT SIGNALING PATHWAYS
[EN] NOVEL PHOSPHOROUS (V)-BASED REAGENTS, PROCESSES FOR THE PREPARATION THEREOF, AND THEIR USE IN MAKING STEREO-DEFINED ORGANOPHOSHOROUS (V) COMPOUNDS<br/>[FR] NOUVEAUX RÉACTIFS À BASE DE PHOSPHORE (V), LEURS PROCÉDÉS DE PRÉPARATION ET LEUR UTILISATION DANS LA FABRICATION DE COMPOSÉS ORGANOPHOSHOREUX (V) STÉRÉODÉFINIS
申请人:BRISTOL MYERS SQUIBB CO
公开号:WO2019200273A1
公开(公告)日:2019-10-17
The present invention relates to novel phosphorous (V) (P(V)) reagents, methods for preparing thereof, and methods for preparing organophosphorous (V) compounds by using the novel reagents.
Enzymatic shortcut: Cyclicdinucleotides, which are of great interest to study immunology and immune oncology, can be synthesized in a one‐step biotransformation significantly shortening the chemical synthesis route. The enzyme displays a surprisingly large substrate scope.
AGENT FOR TREATMENT OF DRY EYE CHARACTERIZED BY COMBINING P2Y² RECEPTOR AGONIST WITH HYALURONIC ACID OR SALT THEREOF, METHOD FOR TREATING DRY EYE, AND USE OF THE P2Y² RECEPTOR AGONIST AND HYALURONIC ACID OR SALT THEREOF
申请人:Santen Pharmaceutical Co., Ltd
公开号:EP2614838A1
公开(公告)日:2013-07-17
An agent for treatment of dry eye comprising a combination of a P2Y2 receptor agonist at a therapeutically effective concentration and hyaluronic acid or a salt thereof at a therapeutically effective concentration, which agent has a dosage form of an ophthalmic agent, can promote the secretion of tear remarkably and can improve corneal epithelial disorders remarkably, and is therefore expected to be a novel agent for treatment of dry eye.
Cyclic dinucleotides containing benzimidazole, method for the production of same, and use of same to activate stimulator of interferon genes (sting)-dependent signaling pathways
申请人:BIOLOG LIFE SCIENCE INSTITUTE GmbH & Co. KG
公开号:US11001605B2
公开(公告)日:2021-05-11
Cyclic dinucleotides are described, which in contrast to their natural congeners carry lipophilic nucleobases and have higher membrane permeability and increased biological activity.