摘要:
Immunologic adjuvants are obtained by the synthesis of 6-(5-cholesten-3#-yloxy)hexyl 6-amino-6-deoxy-1-thio-β-D-galactopyranoside and its 6-deoxy-6-oleamido derivative.
摘要:
Compounds of the formulae Y-R wherein Y is 1-thio-B-L-fucose, 1-thio-B-D-galactose or 1-thio-B-lactose and R is 2-(1- adamantyl) ethyt, 3- [(p-tetrafluorophenethyl) phenyl] propyl, 6-(5-cholesten-3B-yloxy) hex-3-ynl, oleyl, or hexadecyl are useful immunologic adjuvants in vaccines.
摘要:
The present disclosure provides compositions comprising an oligosaccharide composition of formula I, wherein said compositions are useful for delivery of certain agents, including, for example, nucleic acids.
摘要:
The present disclosure provides compositions comprising an oligosaccharide composition of formula I, wherein said compositions are useful for delivery of certain agents, including, for example, nucleic acids.
摘要:
Provided are a compound that inhibits sodium-glucose co-transporter 1, and a pharmaceutically acceptable salt and stereoisomer thereof. The compound is used in a pharmaceutical composition and preparation and usage methods, which comprise an application of a drug and composition thereof in the preparation for treating and improving diabetes, cardiovascular and cerebrovascular diseases, weight loss, fatty liver disease, constipation, metabolism-related diseases and tumor treatment.
摘要:
The present invention provides novel processes for the preparation of Fondaparinux sodium by using the compound of formula ABC5. In some embodiments, the intermediates for the synthesis of Fondaparinux sodium, are also provided.