87515-27-3Relevant academic research and scientific papers
Heteroaryl-substituted deoxy glycerols and antibacterial and antiviral compositions containing the same
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, (2008/06/13)
Heteroaryl-substituted deoxy glycerols represented by the general Formulas Ia, Ib and Ic: STR1 wherein: X is oxygen (--O--) or sulfur (--S--); R is substituted or unsubstituted straight or branched chain C1-30 alkyl or alkenyl, provided that a double bond of the alkenyl does not originate at the carbon atom bound to the X substituent; Het is a 5- to 9-membered heteroaryl mono- or bicyclic ring system having no more than 1 carbonyl carbon in the ring system, with 1 to 4 nitrogen atoms as the sole heteroatoms, one of which nitrogens is bonded to the glycero carbon; and Y is hydroxyl (--OH) or thiol (--SH), pharmaceutical compositions containing the same, and methods of using the compounds, are disclosed. The compounds exhibit antiviral and antibacterial activities.
Heteroaryl-Substituted Deoxy Glycero-Phosphoethanolamines
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, (2008/06/13)
Therapeutically active, heteroaryl-substituted deoxy glycero-phosphoethanolamines are disclosed having the general Formula I: STR1 wherein one of X, Y or Z is a fatty ether substituent, one is a heteroaryl ring substituent with 1-4 nitrogens as the only heteroatoms, one of which is bonded to a carbon of the glyceryl backbone, and one is a phosphoethanolamine substituent substituted at the nitrogen, provided that each of X, Y and Z is a different substituent, and the pharmaceutical compositions comprising the therapeutically active compounds and methods of using the therapetically active compounds to treat cancerous tumors, psoriasis and inflammation are also disclosed.
1,3(R):4,6(R)-DI-O-BENZYLIDEN-D-MANNIT ALS AUSGANGSPRODUKT FUER DIE SYNTHESE OPTISCH AKTIVER GLYCERIN-DERIVATE
Schubert, Thomas,Kunisch, Franz,Welzel, Peter
, p. 2211 - 2217 (2007/10/02)
Starting from the di-O-benzylidene-D-mannitol derivative 11, certain types of optically active glycerol derivatives can be prepared with a minimum of protecting group chemistry.This is exemplified by an efficient synthesis of 2-O-alkyl glyceric acid derivatives 22 and 23.
