CAS: 14108-60-2; H-Dl-2-Nal-Oh

该化合物是一种氨酸衍生物,其特征是带有环烷结构的乙碳的环烷基体,该化合物是D型和L型手性分子,可影响其生物活动和相互作用,通常用于生化研究,并作为合成peptides和其他复杂分子的一个构件.该环烷基组有助于其盐酸性特征,可影响溶性以及与生物膜的相互作用.此外,该化合物可能因其有色性质而具有独特的光学特性,使其对立体化学学和药物设计的研究感兴趣,其应用可能扩大到医药化学和材料科学等领域,其中纳入芳香系统可增强由此产生的化合物的特性.在处理和使用时,应参考安全数据,如任何化学物质一样.

结构式图片

相似化合物

112883-43-9 138774-94-4 143218-10-4

上下游产品

CAS号6960-34-5 L-3-(2-萘)-丙氨酸 | CAS号111726-64-8 3-(萘-2-基)-2-氧代丙酸

合成工艺路线路线简述

    2-Benzoylamino-3-[2]Naphthyl-Acrylic Acid置于盐酸,氢氧化钾,Sodium Amalgam体系中,化学反应生成Dl-3-(2-萘基)丙氨酸
    参考文献:Kikkoji,Biochemische Zeitschrift,1911,Vol. 35,P. 67
    标题:Kikkoji,Biochemische Zeitschrift,1911,Vol. 35,P. 67

    海关参考信息

    专利信息


    专利号:US-11753440-B2
    优先权日:2018-06-05
    标题 :Methods for the synthesis of arginine-containing peptides
    发明人:HEIDL MARC; GEOTTI-BIANCHINI PIERO
    权利人:DSM IP ASSETS BV
    摘要:Methods for the synthesis of arginine-containing peptides are provided. The methods include a deprotection step that minimizes the transfer of by-products deriving from cleaved sulfonyl-5 based side chain protecting groups from arginine to amino acids carrying electron rich side chains.

    专利号:US-7122628-B2
    优先权日:2000-12-22
    标 题:Process for the synthesis of a peptide having a Trp residue
    发明人:JACKSON STEVEN ALLEN
    权利人:IPSEN MFG IRELAND LTD
    摘要:A process for the solid phase synthesis of a peptide having at least one thyptophan residue, wherein said method comprises temporarily protecting the indole ring of said tryptophan residue with a side chain protecting group which is labile to a base wherein said protecting group is removed during cleavage of said peptide from the solid support.

    专利号:US-9475837-B2
    优先权日:2011-12-23
    标题 :Process for the synthesis of therapeutic peptides
    发明人:HURLEY FIONN; WEGNER KATARZYNA; FOLEY PATRICK
    权利人:IPSEN MFG IRELAND LTD
    摘要:The present invention relates to a process for the large-scale synthesis of therapeutic peptides using a Sieber Amide resin, which comprises solid-phase Fmoc-chemistry.

    专利号:US-2024209029-A1
    优先权日:2021-04-21
    标题:Adiponectin glycopeptides and compositions and methods of use thereof
    发明人:WANG YU; LI XUECHEN; XU AIMIN; WU HONGXIANG; ZHANG YIWEI; LI YUANXIN
    权利人:UNIV HONG KONG
    摘要:An improved method for the chemical synthesis of glycosylated peptides has been developed. The method uses stereoselective glycan synthesis and chemical peptide ligation to produce glycopeptides at lower-cost and with higher efficiency/yield compared to conventional methods. In particular, a method for the large-scale, chemical synthesis of hydroxylated amino acid building blocks and glycosylated amino acids suitable for solid phase peptide synthesis (SPPS) are disclosed. SPPS-based methods using the glycosylated amino acids to chemically synthesize adiponectin-like peptides are also described. In vivo studies show that the adiponectin mimicking glycopeptides exhibit significant anticancer, anti-obesity and insulin sensitizing effects. Pharmaceutical compositions of the synthetic glycopeptides and methods of use thereof in treating diseases associated with deficient adiponectin are also described.

    专利号:WO-2020031179-A1
    优先权日:2018-08-06
    标题:Methods for synthesis of cannabinoid compounds
    发明人:JAGTAP PRAKASH; MUSA SANAA
    权利人:BEETLEBUNG PHARMA LTD
    摘要:The present invention provides simple synthetic routes for the preparation of cannabinoid compounds such as CBD, CBDV, THC, THCV, CBN, HU-308, CBG, CBC, and derivatives thereof, which are stereoselective and provide the desired cannabinoid compound in high yield.

    专利号:US-7067554-B2
    优先权日:2000-05-30
    标 题 :Method for the synthesis of compounds of formula I and their uses thereof
    发明人:MJALLI ADNAN M M; GOPALASWAMY RAMESH; AVOR KWASI A; WYSONG CHRISTOPHER L; ANDREW PATRON
    权利人:TRANSTECH PHARMA INC
    摘要:This invention provides certain compounds, methods of their preparation, pharmaceutical compositions comprising the compounds, their use in treating human or animal disorders. The compounds of the invention are useful as modulators of the interaction between the receptor for advanced glycated end products (RAGE) and its ligands, such as advanced glycated end products (AGEs), S100/calgranulin/EN-RAGE, β-amyloid and amphoterin, and for the management, treatment, control, or as an adjunct treatment for diseases in humans caused by RAGE. Such diseases or disease states include acute and chronic inflammation, the development of diabetic late complications such as increased vascular permeability, nephropathy, atherosclerosis, and retinopathy, the development of Alzheimer's disease, erectile dysfunction, and tumor invasion and metastasis.
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    主要参考文献

    [参考文献]: Lei Wang, Et Al. Adding L-3-(2-Naphthyl)Alanine To The Genetic Code Of E. Coli. J Am Chem Soc. 2002 Mar 6;124(9):1836-7.

    合成参考文献


    摘要:Pollegioni, L.; Molla, G., Science of Synthesis: Biocatalysis in Organic Synthesis, (2015) 3, 267.
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