CAS: 1695-77-8; (2R,4Ar,5Ar,6S,7S,8R,9S,9Ar,10As)-4A,7,9-Trihydroxy-2-Methyl-6,8-Bis(Methylamino)Decahydro-4H-Benzo[b]Pyrano[2,3-E][1,4]Dioxin-4-One

该化合物是一种氨基环球球抗生素抗生共素,主要用于治疗细菌感染,尤其是由克氏阴性生物引起的感染,其功能是约束30S血清亚元素,抑制蛋白合成,而不会导致对氨基甲酸酯的误读. 血清素对Nesisseria gonorrhoeae(包括抗青霉素菌菌菌株)特别有效,使它成为治疗淋病的宝贵替代物,它与其他抗生酶的交叉抗药率低,副作用最小,进一步提高其临床效用.该化合物稳定在水溶液中,呈现出良好的组织渗透,确保可靠的药用基因突变素,其特性和安全性使它成为定向抗微生物疗法的首选.

结构式图片

上下游产品

1,3-bis(N-benzyloxycarbonyl)-spectinomycin 2'-O-benzoyl-N,N-bis(benzyloxycarbonyl)-spectinomycin (+)-spectinomycin dihydr°Chloride spectinomycinN,N'-(benzyloxy)carbonylspectinomycin

合成工艺路线路线简述

  • 合成目标产物 Spectinomycin 主要起始原料 Carbamic Acid, [(2R,4Ar,5Ar,6S,7S,8R,9S,9Ar,10As)-Decahydro-4A,7,9-Trihydroxy-2-Methyl-4-Oxo-2H-Pyrano[2,3-B][1,4]Benzodioxin-6,8-Diyl]Bis[n-Methyl-, C,C'-Bis(Phenylmethyl) Ester
  • (文献来源)合成步骤主要原料 Carbamic Acid, [(2R,4Ar,5Ar,6S,7S,8R,9S,9Ar,10As)-Decahydro-4A,7,9-Trihydroxy-2-Methyl-4-Oxo-2H-Pyrano[2,3-B][1,4]Benzodioxin-6,8-Diyl]Bis[n-Methyl-, C,C'-Bis(Phenylmethyl) Ester
Bis-Cbz-Spectinomycin置于palladium On Activated Charcoal 氢气体系中,用 异丙醇 用作溶剂,化学反应 12.0H,以90%的收率获得大观霉素
参考文献:一种将2-酮戊二酸双键连接到糖苷二醇上的简洁通用方法:合成高比糖苷和大观霉素.
标题:一种将2-酮戊二酸双键连接到糖苷二醇上的简洁通用方法:合成高比糖苷和大观霉素.
摘要:
Doi:10.1002/anie.200500434

海关参考信息

专利信息


专利号:US-11046978-B2
优先权日:2016-03-16
标 题:Synthesis of isoprenoids and derivatives
发明人:GONZALEZ RAMON; CLOMBURG JAMES M; CHEONG SEOKJUNG
权利人:UNIV RICE WILLIAM M
摘要:This disclosure generally relates to the use of enzyme combinations or recombinant microbes comprising same to make isoprenoid precursors, isoprenoids and derivatives thereof including prenylated aromatic compounds. Novel metabolic pathways exploiting Claisen, aldol, and acyioin condensations are used instead of the natural mevalonate (MVA) pathway or 1-deoxy-d-xylulose 5-phosphate (DXP) pathways for generating isoprenoid precursors such as isopentenyl pyrophosphate (IPP), dimethylallyl pyrophosphate (DMAPP), and geranyl pyrophosphate (GPP). These pathways have the potential for better carbon and or energy efficiency than native pathways. Both decarboxylative and non-carboxylative condensations are utilized, enabling product synthesis from a number of different starting compounds. These condensation reactions serve as a platform for the synthesis of isoprenoid precursors when utilized in combination with a variety of metabolic pathways and enzymes for carbon rearrangement and the addition/removal of functional groups. Isoprenoid alcohols are key intermediary products for the production of isoprenoid precursors in these novel synthetic metabolic pathways.

专利号:US-2024240209-A1
优先权日:2021-04-20
标 题:Synthesis of enantiopure cis-a-irone from a renewable carbon source
发明人:CHEN XIXIAN; ZHANG CONGQIANG; T REHKA; SHUKAL SUDHA; SMITH DEREK; ANDRÉ ISABELLE; JEREMY ESQUE
权利人:AGENCY SCIENCE TECH & RES; INSTITUT NATIONAL DE RECH POUR L AGRICULTURE LALIMENTATION ET LENVIRONMENT; CENTRE NAT RECH SCIENT; INSTITUT NAT DES SCIENCES APPLIQUEES DE TOULOUSE
摘要:Synthesis of enantiopure cis-α-irone from a renewable carbon source Disclosed herein are natural and synthetic enzymes capable of performing a method of producing cis-α-irone. The method comprises providing an enzyme capable of converting psi-ionone to cis-α-irone; and contacting the enzyme and psi-ionone under suitable conditions to produce cis-α-irone. The enzyme may be a methyltransferase from Streptomyces albireticuli (SaMT), a promiscuous bifunctional methyltransferase/cyclase (pMT1) enzyme from Streptomyces, or a modified pMT1 enzyme with at least one substitution. The enzymes allow the in-vivo and in-vitro production of cis-α-irone including the use of glucose as feedstock for the biotransformation into cis-α-irone.

专利号:US-10925977-B2
优先权日:2006-10-05
标 题 :Efficient synthesis of chelators for nuclear imaging and radiotherapy: compositions and applications
发明人:YANG DAVID J; YU DONGFANG; THOMPSON ANDREW S
权利人:YANG DAVID J; YU DONGFANG; THOMPSON ANDREW S; CEIL POINT LLC; UNIV TEXAS
摘要:Novel methods of synthesis of chelator-targeting ligand conjugates, compositions comprising such conjugates, and therapeutic and diagnostic applications of such conjugates are disclosed. The compositions include chelator-targeting ligand conjugates optionally chelated to one or more metal ions. Methods of synthesizing these compositions in high purity are also presented. Also disclosed are methods of imaging, treating and diagnosing disease in a subject using these novel compositions, such as methods of imaging a tumor within a subject and methods of diagnosing myocardial ischemia.

专利号:US-2024197774-A1
优先权日:2021-04-16
标 题:Synthesis of Antimicrobial PVP-coated Bismuth Nanoparticles
发明人:LOPEZ-RIBOT JOSE; VAZQUEZ-MUNOZ ROBERTO
权利人:UNIV TEXAS
摘要:Described herein is a facile, fast, and economical method for the synthesis of BAL-mediated PVP-BiNPs, using basic laboratory instruments and reagents readily available in most laboratories.

专利号:WO-2024165611-A1
优先权日:2023-02-07
标题:Production of a disaccharide and/or milk oligosaccharide by a cell with reduced synthesis of udp-glcnac
发明人:BEAUPREZ JOERI; DECOENE THOMAS; VERCAUTEREN ANNELIES
权利人:INBIOSE NV
摘要:The present invention is in the technical field of synthetic biology, metabolic engineering and cell cultivation. The invention provides a cell for production of a disaccharide and/or an oligosaccharide like a milk oligosaccharide wherein synthesis of UDP-N-acetylglucosamine in said cell is rendered less functional. The invention further provides use of said cell in a cultivation or incubation. The invention also describes methods for the production of a disaccharide and/or an oligosaccharide like a milk oligosaccharide using said cell as well as the purification of said disaccharide and/or oligosaccharide like a milk oligosaccharide.

专利号:WO-2024165524-A1
优先权日:2023-02-06
标 题:Production of a saccharide by a cell with reduced synthesis of lactobionic acid
发明人:BEAUPREZ JOERI; DECOENE THOMAS; VERCAUTEREN ANNELIES
权利人:INBIOSE NV
摘要:The present invention is in the technical field of synthetic biology, metabolic engineering and cell cultivation. The invention provides a cell for production of a saccharide wherein synthesis of lactobionic acid in said cell is rendered less functional or is knocked out. The invention further provides use of said cell in a cultivation or incubation. The invention also describes methods for the production of a saccharide using said cell as well as the purification of said saccharide.
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✅ COA系统入驻 | 共享模式

主要参考文献


1: Holloway WJ. Spectinomycin. Med Clin North Am. 1982 Jan;66(1):169-73.
59:1-46. doi: 10.1007/BFb0102295. 74(5):1311-1316. doi: 10.1093/jac/dkz012.
4: McCormack WM, Finland M. Drugs five years later. Spectinomycin. Ann Intern Med. 1976 Jun;84(6):712-6. doi: 10.7326/0003-4819-84-6-712. 287(6408):1827-9. doi: 10.1136/bmj.287.6408.1827.

合成参考文献


参考文献:10.1021/cr100444b
摘要:Lichtenthaler FW. 2-Oxoglycosyl (“Ulosyl”) and 2-Oximinoglycosyl Bromides: Versatile Donors for the Expedient Assembly of Oligosaccharides with β-d-Mannose, β-l-Rhamnose, N-Acetyl-β-d-mannosamine, and N-Acetyl-β-d-mannosaminuronic Acid Units. Chem. Rev. 2011 Jul 13;111(9):5569–609. doi: 10.1021/cr100444b.
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