CAS: 1758-80-1; (S)-2,4-Diaminobutanoic Acid

该化合物是一种化学化合物,其特点是氨基酸结构,包括两个矿类和一个碳球酸组,通常被作为氢溴化盐,它能提高其水中的溶性,使其在各种生物化学应用中发挥作用.该化合物因其在氨基酸新陈代谢研究中的作用而著称,可以作为合成peptides和其他生物相关分子的建筑块.L-DAB HBr经常用于...

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1883-09-6 73143-97-2 125238-99-5

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CAS号7729-30-8 D-吖啶-2-羧酸 | CAS号10270-94-7 (S)-2-氨基-4-((叔丁... | CAS号34404-27-8 (2S)-2,4-二({[(2... | CAS号3350-20-7 (S)-4-(((苄氧基)羰基... | CAS号14191-90-3 L-去甲精氨酸盐酸盐 | CAS号107-95-9 β-丙氨酸 | CAS号4219-23-2 4-amino-2-chlor... | CAS号4128-00-1 (3s)-3-氨基-2-吡咯烷酮

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  • 687998-39-6 = 1758-80-1 + 4128-00-1
    反应条件:1.1 Solvents: Water; Ph 7.4
    标题:Triggered Degradation Of Poly(Ester Amide)S Via Cyclization Of Pendant Functional Groups Of Amino Acid Monomers
    作者:Mejia,Jose S.; Gillies,Elizabeth R.
    参考文献:Polymer Chemistry 日期:2013 卷标:4(6) 页码:1969-1982
L-谷氨酸置于sodium Azide,硫酸体系中,用 氯仿 用作溶剂,化学反应生成L-2,4-二氨基丁酸氢溴酸盐
参考文献:一种合成选择性保护 (2S)-1,2,4-三氨基丁烷衍生物的新方法
标题:一种合成选择性保护 (2S)-1,2,4-三氨基丁烷衍生物的新方法
摘要:描述了通过 (25)-N 4-Benzyloxy-Carbonyl-2,4-Diaminobutanamid 由 L-谷氨酸选择性保护的 (25)-1,2,4-三氨基丁烷的有效合成.
Doi:10.1055/s-2005-869989

海关参考信息

专利信息


专利号:US-12188072-B2
优先权日:2018-03-19
标题 :Compositions and methods for rapid in vitro synthesis of bioconjugate vaccines in vitro via production and N-glycosylation of protein carriers in detoxified prokaryotic cell lysates
发明人:JEWETT MICHAEL CHRISTOPHER; STARK JESSICA CAROL; DELISA MATTHEW P; JAROENTOMEECHAI THAPAKORN
权利人:UNIV NORTHWESTERN; UNIV CORNELL
摘要:Disclosed are methods, systems, components, and compositions for cell-free synthesis of glycosylated carrier proteins. The glycosylated carrier proteins may be utilized in vaccines, including anti-bacterial vaccines. The glycosylated carrier proteins may include a bacterial polysaccharide conjugated to a carrier, which may be utilized to generate an immune response in an immunized host against the polysaccharide conjugated to the carrier. The glycosylated carrier proteins may be synthesized in cell-free glycoprotein synthesis (CFGpS) systems using prokaryote cell lysates that are enriched in components for glycoprotein synthesis such as oligosaccharyltransferases (OSTs) and lipid-linked oligosaccharides (LLOs) including OSTs and LLOs associated with synthesis of bacterial O antigens.

专利号:US-12365930-B2
优先权日:2016-07-14
标题:Method for rapid in vitro synthesis of glycoproteins via recombinant production of N-glycosylated proteins in prokaryotic cell lysates
发明人:JEWETT MICHAEL CHRISTOPHER; STARK JESSICA CAROL; DELISA MATTHEW P; JAROENTOMEECHAI THAPAKORN
权利人:UNIV NORTHWESTERN; UNIV CORNELL
摘要:Disclosed are methods, systems, components, and compositions for cell-free synthesis of glycosylated proteins. The glycosylated proteins may be utilized in vaccines, including anti-bacterial vaccines. The glycosylated proteins may include a bacterial polysaccharide conjugated to a carrier, which may be utilized to generate an immune response in an immunized host against the polysaccharide conjugated to the carrier. The glycosylated proteins may be synthesized in cell-free glycoprotein synthesis (CFGpS) systems using prokaryote cell lysates that are enriched in components for glycoprotein synthesis such as oligosaccharyltransferases (OSTs) and lipid-linked oligosaccharides (LLOs) including OSTs and LLOs associated with synthesis of bacterial O antigens.

专利号:US-8598346-B2
优先权日:2008-07-16
标 题 :Synthesis of cyclic amidines
发明人:LENTZEN GEORG; NEUHAUS THORSTEN
权利人:LENTZEN GEORG; NEUHAUS THORSTEN; BITOP AG
摘要:The invention relates to an innovative method for synthesis of cyclic amidines. The synthesis starts from a β-, γ- or δ-lactone which is twofold brominated. After esterification of the carboxyl function, the bromine atoms are nucleophilically substituted and the corresponding diamino compound is obtained. The ring closure to the cyclic amidine is accomplished subsequently by reaction with orthoester, imidate or thioimidate. Owing to interposing additional steps for recovery of the diamino compound in enantiomerically pure form, the enantiomers of the cyclic amidines can be stereoselectively synthesized.

专利号:US-9938509-B2
优先权日:2010-12-08
标 题 :Biocatalysts and methods for the synthesis of armodafinil
发明人:ANG EE LUI; ALVIZO OSCAR; BEHROUZIAN BEHNAZ; CLAY MICHAEL D; COLLIER STEVEN J; EBERHARD ELLEN D; FAN FU; SONG SHIWEI; SMITH DEREK J; WIDEGREN MAGNUS; WILSON ROBERT; XU JUNYE; ZHU JUN
权利人:CODEXIS INC
摘要:The present invention relates to non-naturally occurring polypeptides useful for preparing armodafinil, polynucleotides encoding the polypeptides, and methods of using the polypeptides. The non-naturally occurring polypeptides of the present invention are effective in carrying out biocatalytic conversion of the (i) 2-(benzhydrylsulfinyl)acetamide to (−)-2-[(R)-(diphenylmethyl)sulfinyl]acetamide (armodafinil), or (ii) benzhydryl-thioacetic acid to (R)-2-(benzhydrylsulfinyl)acetic acid, which is a pivotal intermediate in the synthesis of armodafinil, in enantiomeric excess.

专利号:US-2006211083-A1
优先权日:2005-01-21
标题:Products and processes for in vitro synthesis of biomolecules
发明人:KATZEN FEDERICO; KUDLICKI WIESLAW; FLETCHER JULIA
权利人:KATZEN FEDERICO; KUDLICKI WIESLAW; FLETCHER JULIA
摘要:Provided herein are products and processes for efficiently synthesizing biomolecules in vitro using cell-free extracts derived from mammalian cells and insect cells. In an embodiment, provided is a process for preparing a cell-free extract from insect cells and mammalian cells that efficiently synthesizes post-translationally modified target proteins (e.g., glycosylated target proteins). In some embodiments, a ribonucleic acid is synthesized in vitro that comprises a cap, a 5′ untranslated region comprising an 18S rRNA binding ribonucleotide sequence, and a target ribonucleotide sequence. It has been determined that such ribonucleic acids result in efficient in vitro synthesis of a target protein using cell-free extracts derived from non-rabbit mammalian cells and insect cells.

专利号:US-8722852-B2
优先权日:2006-04-28
标 题 :Cosmetic composition for stimulating the synthesis of proteins of the basement membrane
发明人:ZIEGLER HUGO; IMFELD DOMINIK; STOCKLI MARTIN; HEIDL MARC
权利人:ZIEGLER HUGO; IMFELD DOMINIK; STOCKLI MARTIN; HEIDL MARC; DSM IP ASSETS BV
摘要:Cosmetic composition which can be applied topically, comprising at least one compound of the general formula (I) in which R 1 is H, C 1 -C 20 -alkyl, cycloalkyl or aryl-C 1 -C 4 -alkyl, n is 1-4, X is —O—, —NH— or —NR 2 — and R 2 H or C 1 -C 20 -alkyl; and at least one compound corresponding to the above formula (I) but in which XR 1 with X having the possible meaning of —NH— is the residue of an alpha-amino acid; use of these compounds and of the composition for stimulating the synthesis of the proteins of the basement membrane; and also both those compounds of the formula (I) in which X is —NR 2 — and both R 1 and R 2 are different from H, and the compounds corresponding to formula (I) but in which XR 1 with X having the possible meaning of —NH— is the residue of an alpha-amino acid, as such.
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主要参考文献

[参考文献]: Beart Pm, Et Al. L-2,4-Diaminobutyric Acid And The Gaba System. Neurosci Lett. 1977 Jul;5(3-4):193-8.
[参考文献]: Panasci L, Et Al. The Cytolytic Effect Of L-2,4 Diaminobutyric Acid With Malignant Glioma Cells And Fibroblasts. Cancer Chemother Pharmacol. 1988;21(2):143-4.
[参考文献]: Ronquist G, Et Al. Antitumor Activity Of L-2,4 Diaminobuturic Acid Against Mouse Fibrosarcoma Cells In Vitro And In Vivo. J Cancer Res Clin Oncol. 1980;96(3):259-68.

合成参考文献


摘要:W. Schaeg and F. Schneider. Z. Physiol. Chem. 326, 40 (1961).
参考文献:10.1007/s11060-006-9186-1
摘要:Bergenheim AT, Roslin M, Ungerstedt U, Waldenström A, Henriksson R, Ronquist G. Metabolic Manipulation of Glioblastoma in Vivo by Retrograde Microdialysis of L-2, 4 Diaminobutyric Acid (DAB). Journal of Neuro-Oncology. 2006 Jun 14;80(3):285–93. doi: 10.1007/s11060-006-9186-1.
参考文献:10.1099/00221287-138-7-1461
摘要:YAMAMOTO S, TSUZAKI Y, TOUGOU K, SHINODA S. Purification and characterization of L-2,4-diaminobutyrate decarboxylase from Acinetobacter calcoaceticus. Journal of General Microbiology. 1992 Jul 01;138(7):1461–5. doi: 10.1099/00221287-138-7-1461.
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