专利号:US-5144073-A 优先权日:1988-08-31 标 题 :Process for preparation of dipeptides 发明人:HUBBS JOHN C 权利人:HUBBS JOHN C 摘要:Disclosed is a process for synthesis of a dipeptide such as N-acetyl-L- alpha -aspartyl-L-phenylalanine methyl ester wherein one amino acid serves as a chiral template which allows for synthesis of a second amino acid residue to form said dipeptide. The process involves several novel steps such as a nucleophile addition step. In addition, several novel intermediates are described.
专利号:US-6664282-B2 优先权日:1999-09-17 标 题:Synthesis of [3,5,7]-1H-imidazo [1,5-a]imidazol-2 (3H)- one compounds 发明人:ELABDELLAOUI HASSAN M; OSTRESH JOHN M; HOUGHTEN RICHARD A 权利人:TORREY PINES INST 摘要:Individual substituted [3,5,7]-1H-imidazo[1,5-a]imidazol-2(3H)-one compounds and their pharmaceutically-acceptable salts are disclosed, as are libraries of such compounds. Methods of preparing and using the libraries of compounds as well as individual compounds of the libraries are also disclosed.
专利号:EP-2588602-A1 优先权日:2010-07-01 标题:Variants of glucoamylase 发明人:DEGN PETER EDVARD; BOTT RICHARD R; VROEMEN CASPER WILLEM; SCHEFFERS MARTIJN SILVAN; AEHLE WOLFGANG; PETERSEN ELIN 权利人:DUPONT NUTRITION BIOSCI APS; DANISCO US INC 摘要:The present invention relates to combinatorial variants of a parent glucoamylase that have altered properties for reducing the synthesis of condensation products during hydrolysis of starch. Accordingly the variants of a parent glucoamylase are suitable such as for use within brewing and glucose syrup production. Also disclosed are DMA constructs encoding the variants and methods of producing the glucoamylase variants in host cells.
专利号:US-2006217788-A1 优先权日:2004-07-09 标 题:Method of using laser induced injury to activate topical prodrugs 发明人:HERRON G S; BOMMANNAN D B 权利人:HERRON G S; BOMMANNAN D B 摘要:Methods and compositions are disclosed for improving the wound healing process and increasing collagen synthesis following laser induced thermal injury. The method comprises delivering prodrugs to a target site before the target site is injured and taking advantage of those enzymes that are physiologically-expressed to promote wound healing to convert the prodrugs to active drugs. The claimed invention has the advantage of the prodrugs being readily available to immediately participate in the wound healing process, but not have any negative side-effects of the active drug being present before injury occurs.
专利号:WO-2009056901-A1 优先权日:2007-10-31 标题:Cyclodipeptide synthases (cdss) and their use in the synthesis of linear dipeptides
专利号:WO-0119783-A1 优先权日:1999-09-17 标 题:Synthesis of [3,5,7]-1h-imidazo[1,5-a]imidazol-2(3h)-one compounds
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