专利号:US-8809553-B2 优先权日:2010-06-15 标题:Process for the preparation of pteridine derivatives 发明人:ATTOLINO EMANUELE; MICHIELETTI MARIO; ROSSI DAVIDE; ALLEGRINI PIETRO 权利人:ATTOLINO EMANUELE; MICHIELETTI MARIO; ROSSI DAVIDE; ALLEGRINI PIETRO; DIPHARMA FRANCIS SRL 摘要:The application discloses a process for the preparation of 5-deoxy-L-arabinose of formula (VI); comprising the conversion of a compound of formula (XII); wherein n is 0, 1 or 2; which can be used as intermediate for the synthesis of sapropterin.
专利号:WO-2011000481-A1 优先权日:2009-07-02 标 题 :Synthesis of pyrazine derivates 发明人:IGNATYEV NIKOLAI MYKOLA; SHEREMETEV ALEXEI B; ALEXANDROVA NATALIA S 权利人:MERCK PATENT GMBH; IGNATYEV NIKOLAI MYKOLA; SHEREMETEV ALEXEI B; ALEXANDROVA NATALIA S 摘要:The present invention relates to a method for producing pyrazine derivates, wherein the reaction medium comprises at least one ionic liquid, and to the use of ionic liquids for producing pyrazine derivates.
专利号:US-2012184724-A1 优先权日:2009-09-22 标 题 :Protected monomers and methods of deprotection for rna synthesis 发明人:SIERZCHALA AGNIESZKA B; SMART BRIAN PHILLIP; DELLINGER DOUGLAS J; DELLINGER GERALDINE; MYERSON JOEL; TIMAR ZOLTAN 权利人:SIERZCHALA AGNIESZKA B; SMART BRIAN PHILLIP; DELLINGER DOUGLAS J; DELLINGER GERALDINE; MYERSON JOEL; TIMAR ZOLTAN; AGILENT TECHNOLOGIES INC 摘要:A nucleoside monomer that is protected by a thionocarbamate protecting group and contains one or more 2 H, 13 C, or 15 N isotopes in the ribose and/or base part is provided, as well as a method for making a polynucleotide that uses the same. Also provided is a polynucleotide synthesis method that employs a diamine to deprotect a protected polynucleotide.
专利号:US-9266889-B2 优先权日:2011-03-25 标题:Composition, synthesis, and use of new substituted pyran and pterin compounds 发明人:BASU PARTHA; PIMKOV IGOR 权利人:UNIV HOLY GHOST DUQUESNE 摘要:The present invention relates to substituted pterin compounds, their synthesis and use. In particular, the present invention relates to a new precursor compound and its analogs for synthesizing a new substituted pterin compound and its analogs. These new compounds are particularly suitable for treating molybdenum cofactor deficiency.
专利号:US-2007243147-A1 优先权日:2004-07-24 标 题:Skin and/or Hair Composition Containing Compounds for Increasing The Tanning of Skin 发明人:WOLBER RAINER; TOM DIECK KAREN; SCHERNER CATHRIN; SCHLENZ KATHRIN; KRUSE INGE 权利人:BEIERSDORF AG 摘要:The invention relates to agents that are to be applied to the skin or hair and contain compounds for intensifying tanning of the skin and increasing melanin synthesis in skin or hair. The invention particularly relates to cosmetic or dermatological preparations. Using said preparations results in inducing and intensifying the tanning mechanisms of the skin, intensifying the hair color, and thus also increasing intrinsic protection of the skin or hair.
专利号:US-9943809-B2 优先权日:2014-02-27 标题 :Solvent resistant thin film composite membrane and its preparation 发明人:DOM ELKE; HERMANS SANNE; KOECKELBERGHS GUY; VANKELECOM IVO 权利人:KATHOLIEKE UNIV LEUVEN KU LEUVEN RESEARCH & DEVELOPMENT; UNIV LEUVEN KATH 摘要:The present invention relates to improved methods for synthesis of thin film composite membranes by interfacial polymerization. More in particular, the method of the present invention comprises the impregnation of an ultrafiltration porous support membrane with an aqueous solution containing a polyfunctional nucleophilic monomer, and contacting the impregnated support membrane with a second largely water-immiscible solvent containing a polyfunctional epoxide monomer.
参考标题:Structure-Based Design Of Highly Potent Toll-Like Receptor 7/8 Dual Agonists For Cancer Immunotherapy 作者:Zhisong Wang,Yan Gao,Lei He,Shuhao Sun,Tingting Xia,Lu Hu,Licheng Yao,Liangliang Wang,Dan Li,Hui Shi,Xuebin Liao |发布日期:2021.6.10 摘要:Activation Of The Toll-Like Receptors 7 And 8 Has Emerged As A Promising Strategy For Cancer Immunotherapy. Herein, We Report The Design And Synthesis Of A Series Of Pyrido[3,2-D]Pyrimidine-Based Toll-Like Receptor 7/8 Dual Agonists That Exhibited Potent And Near-Equivalent Agonistic Activities Toward Tlr7 And Tlr8. In Vitro, Compounds 24E And 25A Significantly Induced The Secretion Of Ifn-α, Ifn-γ