CAS: 515-94-6; 2,3-Diaminopropanoic Acid

该化合物是一种非蛋白性氨基酸,其特点是结构中存在两个氨基组(-NH2)和一个箱状酸组(-COOH),该化合物是丙基酸的衍生物,氨基氨基酸组位于三碳链的第二和第三个碳原子上,它是一种在水中溶解的白色晶体,反映了氨基和碳箱体功能组的极性. 2,3-二氨基丙基丙基酸在各种生物化学过程中发挥作用,并有兴趣参与与丙基酸合成和氨基酸新陈代谢研究有关的研究,其独特结构使其能够参与形成peptides和蛋白质,并可能展示在药理学方面正在探索的生物活动.此外,它可以作为有机化学中更复杂的分子合成的建筑材料.

结构式图片

相似化合物

54897-59-5 18635-45-5 122235-70-5

上下游产品

CAS号600-05-5 2,3-二溴丙酸 | CAS号54897-59-5 DL-2,3-二氨基丙酸盐酸盐 | CAS号75452-33-4 tert-butyl (S)-... | CAS号78228-82-7 2-acetamido-3-a... | CAS号101087-39-2 acetylamino-(be... | CAS号18635-43-3 2-(S)-benzyloxy... | CAS号83855-20-3 Neopeptin A | CAS号3981-36-0 3-chloroalanine | CAS号7664-41-7 氨 | CAS号56012-66-9 (2,4-dioxo-hexa... | CAS号565-64-0 2,3-二氯丙酸 | CAS号473-81-4 DL-甘油酸 | CAS号107-15-3 乙二胺 | CAS号13368-86-0 1,2,5-噻唑-3-羧酸 | CAS号13515-06-5 5,6-二甲基吡嗪-2-羧酸 | CAS号1483-07-4 L-脲基丙氨酸 | CAS号6542-88-7 2-氨基乙醛 | CAS号88971-40-8 (S)-2,3-双((丁氧基羰... | CAS号62634-84-8 3-氨基-2-氮杂啶酮

合成工艺路线路线简述

    📜Boc-Dap(Nh2)-Conh2置于盐酸体系中,化学反应 5.0H,以315 Mg的收率获得产物2,3-二氨基丙酸
    参考文献:抗肿瘤抗生素博来霉素的合成研究.十二.制备l-2,3-二氨基丙酸衍生物作为合成中间体.
    标题:抗肿瘤抗生素博来霉素的合成研究.十二.制备l-2,3-二氨基丙酸衍生物作为合成中间体.
    摘要:已经开发了三种方法来制备为全合成博来霉素而适当保护的(S)-3-氨基-2-特丁氧羰基氨基丙酰胺.
    DOI:10.1248/cpb.33.509

    海关参考信息

    专利信息


    专利号:US-2008287649-A1
    优先权日:2006-12-29
    标 题 :Methods for the synthesis of cyclic peptides
    发明人:CHEN LIN; HAN YEUN-KWEI; ROBERTS CHRISTOPHER R
    权利人:CHEN LIN; HAN YEUN-KWEI; ROBERTS CHRISTOPHER R
    摘要:Methods for the synthesis of cyclic peptides are provided, as well as novel dipeptide compounds. The methods include the solid phase synthesis of a dipeptide, which is the coupled to a second peptide in a solid phase reaction. The peptide is then cyclized following the coupling reaction. The methods and dipeptides are particularly useful for the synthesis of MC-4 receptor agonist peptides.

    专利号:US-6376649-B1
    优先权日:1998-12-18
    标题 :Methods for the synthesis of α- hydroxy-β-amino acid and amide derivatives
    发明人:SEMPLE JOSEPH E; LEVY ODILE E
    权利人:CORVAS INT INC
    摘要:Methods for the synthesis of alpha-hydroxy-beta-amino acid and amide derivatives and alpha-ketoamide derivatives and novel derivatives made by these methods are provided. These methods involve reacting a N-terminally blocked (protected) aminoaldehyde with an isonitrile and a carboxylic acid to give an amino-alpha-acyloxy carboxamide. The acyloxy group may be removed to give the derivative. Alternatively the protecting group is removed and acyl shift occurs to give the derivative. These derivatives are useful in the synthesis of compounds such as peptidyl alpha-ketoamides and alpha-hydroxy-beta-carboxylic acid and amide derivatives. Certain of these compounds have been reported to have activity as inhibitors of proteases, such as serine proteases and cysteine proteases.

    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-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.

    专利号:US-6133409-A
    优先权日:1996-12-19
    标 题:Process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and αβ-unsaturated carboxylic acid and aldehyde compounds
    发明人:SALVINO JOSEPH M; MORTON GEORGE C; MASON HELEN J; LABAUDINIERE RICHARD F
    权利人:AVENTIS PHARM PROD INC
    摘要:This invention is directed to a process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and alpha , beta -unsaturated carboxylic acid and aldehyde compounds and to polymeric hydroxylamine resin compounds useful therefor.

    专利号:US-2007179279-A1
    优先权日:2005-12-30
    标题:Methods for the synthesis of arginine-containing peptides
    发明人:CHEN LIN; ROBERTS CHRISTOPHER R
    权利人:CHEN LIN; ROBERTS CHRISTOPHER R
    摘要:Methods for the synthesis of arginine-containing peptides are provided. The methods include a step that minimizes contact of side chain protected arginine with base prior to the coupling step.

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    ✅ COA系统入驻 | 共享模式

    合成参考文献

    参考DOI号:10.3390/MD18080396
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