CAS: 146897-68-9; Lactoferricin B

该化合物是一种来自包括牛奶在内的各种秘诀液中发现的甘蓝蛋白素,一种来自紫色ferrin(一种甘蓝蛋白素)的浸泡物,以其抗微生物特性而著称,展示了各种细菌,真菌和病毒的抗菌活动.蓝石棉素B的结构由一系列氨基酸组成,有助于其破坏微生物膜的能力,导致细胞分解.这种浸泡物还因其免疫分子作用而得到承认,加强了免疫反应,并有可能在炎症调中发挥作用.此外,对Lactoferricin B进行了研究,以其潜在的食品保存应用和作为治疗感染的治疗剂,在各种pH条件下的稳定性和对蛋白酶的抗药性进一步增强了其在临床和食品工业环境中的效用.

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    专利信息


    专利号:US-6063919-A
    优先权日:1998-08-14
    标题:Process for the synthesis of exochelins
    发明人:GAUDIOSO LARRY A; WEGLARZ MICHAEL A
    权利人:KEYSTONE BIOMEDICAL INC
    摘要:A process for the synthesis of an Exochelin comprising the steps of generating L-N-[(2-benzyloxy-(benzoyl)] serine or L-N-[2-benzyloxy (benzoyl)] threonine, creating L-N-t-Boc- epsilon -hydroxynorleucine and reacting same to produce L-N-Boc- epsilon -bromonorleucine trimethylsilylethyl ester, providing a dicarboxylic acid and forming an O-benzyl methyl hydroxamate from the dicarboxylic acid, coupling the O-benzyl methyl hydroxamate with the L-N-Boc- epsilon -bromonorleucine trimethylsilylethyl ester to give an L-N2-Boc-N6-methyl,N6-(benzyloxy) lysine 2-trimethylsilylethyl ester which incorporates the dicarboxylic acid as modified above, removing the N-tert-butoxycarbonyl protecting group from the L-N2-Boc-N6-methyl, N6-(benzyloxy) lysine 2-trimethylsilylethyl ester to yield a substituted lysine, and coupling the same with the L-N-[2-benzyloxy (benzoyl) serine or -threonine to yield a 2-trimethyl silylethyl ester of dibenzyl Exochelic acid, transforming the 2-trimethyl silylethyl ester of dibenzyl Exochelic acid to dibenzyl Exochelic acid, preparing benzyl epi-cobactin, forming an ester bond between the dibenzyl Exochelic acid and benzyl epi-cobactin to form an intermediate, and, hydrogenolytically removing three benzyl groups from said intermediate, resulting in the synthesized Exochelin. More particularly, a synthesis for Exochelin 786SM (R) is disclosed wherein the dicarboxylic acid is suberic acid and the serine form is utilized.

    专利号:US-8742013-B2
    优先权日:2009-04-24
    标 题:Synthesis of lipoamide-grafted high molecular compound and method therefor
    发明人:NOH INSUP; JO SEONGYEUN; KIM DOYEON; WOO JUNGHOON
    权利人:NOH INSUP; JO SEONGYEUN; KIM DOYEON; WOO JUNGHOON; NAT UNIV SEOUL TECH CTENTER
    摘要:The present disclosure provides polymer compounds binding with lipoamide produced by the reaction of the primary amine group of lipoamide with the carboxy group of polysaccharide compounds such as chondroitin sulfates, carboxymethyl celluloses, or hyaluronic acids; functional compounds such as peptides, proteins, growth factors; or drugs; or biocompatible polymers such as poly(ethylene oxide), poly(vinyl alcohol), or poly(vinyl pyrrolidone). The present disclosure also provides their synthesis methods, products of hydrogels and films using the same as and methods for manufacturing the products.

    专利号:US-12377186-B2
    优先权日:2018-01-19
    标 题:Antimicrobial biopolymer compositions, methods of synthesis, and applications of use
    发明人:KIM MINKYU; CAMP CHRISTOPHER P
    权利人:UNIV ARIZONA
    摘要:Biopolymer compositions comprising antimicrobial peptides (AMPs) for treating infections such as bacterial infections, viral infections, fungal infections, and parasitic infections. The compositions herein may also be used for treating infections associated with antibiotic-resistant bacteria, antifungal-resistant fungi, antiviral-resistant viruses, or for treating biological warfare agents (BWAs) such as Bacillus anthracis and Yersenia pestis. The present invention also provides methods of synthesis of said biopolymer compositions, wherein AMP biopolymers can be synthesized as an artificially engineered protein by genetically fusing an AMP; a protein that behaves similarly to polymer tethers; and a protein as a modifiable material platform that can transform to self-assembled nanoparticles, self-standing films, or adhesives to easily attach tethered AMPs onto any biomaterial surface for various clinical applications.

    专利号:WO-9108220-A1
    优先权日:1989-12-01
    标 题:A method for the stepwise, controlled synthesis of chemical species, particularly peptides, coupled products obtained by the method and the use of these coupled products, e.g. as vaccines
    发明人:HOUEN GUNNAR; HOLM ARNE
    权利人:HOUEN GUNNAR; HOLM ARNE
    摘要:Chemical species, particularly peptides, are synthesized by a stepwise, controlled process, in which a proteinaceous substance such as a protein is used as the synthesis substrate. The products obtained by the process can be used e.g. as vaccines against various diseases and as matrix materials or carrier molecules.

    专利号:US-9005895-B2
    优先权日:2010-06-21
    标题:Compositions, methods and kits for nucleic acid synthesis and amplification
    发明人:WOO CORA L; BERKMAN JENNIFER; YIM PRISCILLA W
    权利人:WOO CORA L; BERKMAN JENNIFER; YIM PRISCILLA W; LIFE TECHNOLOGIES CORP
    摘要:The present invention is directed to compositions, methods and kits useful for the synthesis of nucleic acid molecules. More specifically, compositions, methods and kits are provided for the amplification of nucleic acid molecules in a one-step RT-PCR procedure comprising one or more agents used to increase tolerance to PCR inhibitors.

    专利号:EP-1382327-A1
    优先权日:2002-07-17
    标 题 :Method of protection of the skin against ageing
    发明人:DANOUX LOUIS; FREIS OLGA; PAULY GILLES
    权利人:COGNIS FRANCE SA
    摘要:A method for the production of means for the stimulation of human is proposednSkin cells as well as to protect against skin aging and damaging influencesnEnvironmental toxins and UV radiation, characterized in that the means at least onenSubstance containing the synthesis of energy donors of the mitochondrial respiratory chainnincreases while at the same time the rate of reactive oxygen species (ROS) innCell metabolism lowers.n n n Furthermore, the use of cosmetic and / or pharmaceutical preparations,ncontaining at least one substance which the synthesis of energy donorsnthe mitochondrial respiratory chain increases while at the same time the rate of reactive oxygen speciesn(ROS) in cell metabolism, to stimulate human skin cellsnas well as to the protection against skin aging and damaging influences by environmental poisons andnUV radiation proposed.

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    合成参考文献


    参考文献:10.1128/aac.43.1.1
    摘要:De Lucca AJ, Walsh TJ. Antifungal peptides: novel therapeutic compounds against emerging pathogens. Antimicrob Agents Chemother. 1999 Jan;43(1):1–11.
    参考文献:10.1128/aac.42.7.1587
    摘要:Wakabayashi H, Abe S, Teraguchi S, Hayasawa H, Yamaguchi H. Inhibition of Hyphal Growth of Azole-Resistant Strains of Candida albicans by Triazole Antifungal Agents in the Presence of Lactoferrin-Related Compounds. Antimicrob Agents Chemother. 1998 Jul;42(7):1587–91. doi: 10.1128/aac.42.7.1587.
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