CAS: 25912-50-9; 3-Aminocyclohexanecarboxylicacid

该化合物是有机化合物,其特点是环氧环状结构,有氨基氨基酸组和一个碳酸功能组;该化合物是无色的,可溶于水中的黄黄色固体,反映了其极性,因为氨基和碳基酸类都有,它具有包括碳和氮在内的分子公式,表明其作为氨基硫的作用;氨基化合物组的存在使该化合物具有基本性,而碳基硫酸组则助长了其酸性,使其能够参与各种化学反应,包括浸泡物结层的形成. 3-亚米诺-甲基酸基酸经常用于生物化学研究,并用作合成制药和农用化学的建筑块,其结构特征也表明该化合物在材料科学和聚合化学中的潜在用途.总体而言,该化合物对于生物和合成化学环境都具有重大意义.

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81131-40-0 334932-13-7 222530-39-4

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上下游产品

meta-aminobenzoic acid i-Amyl alcohol 3-[(tert-butoxycarbonyl)amino]cyclo-hexanecarboxylic acid trans rac-cyclohexyl 1,3-dicarboxylic acid ethyl 3-amin°Cyclohexanecarboxylate 3-[(tert-butoxycarbonyl)amino]cyclo-hexanecarboxylic acid 3-amin°Cyclohexanecarboxylic acid dimethyl amide tert-butyl ester(3-dimethylcarbamoyl-cyclohexyl)-carbamic acid tert-butyl ester

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    专利信息


    专利号:US-9206222-B2
    优先权日:2009-06-29
    标题:Solid phase peptide synthesis of peptide alcohols
    发明人:CAUSSIL-AMBLARD MURIEL; MARTINEZ JEAN; TAILHADES JULIEN
    权利人:CAUSSIL-AMBLARD MURIEL; MARTINEZ JEAN; TAILHADES JULIEN; CENTRE NAT RECH SCIENT
    摘要:The present invention relates to the synthesis of depsipeptides on solid phase support. Said depsipeptides are then implicated in a solution phase O—N acyl shift enabling to obtain the corresponding peptide alcohols.

    专利号:US-2023364251-A1
    优先权日:2020-08-06
    标 题:Methods for the synthesis of protein-drug conjugates
    发明人:BORCHARDT ALLEN; HUGHES ROBERT MICHAEL
    权利人:CIDARA THERAPEUTICS INC
    摘要:The present invention relates to intermediates and methods for synthesizing protein-drug conjugates that can be used for the treatment of diseases and related conditions.

    专利号:US-8546533-B2
    优先权日:2008-08-29
    标 题:Pipecolic linker and its use for chemistry on solid support
    发明人:MARTINEZ JEAN; ZAJDEL PAWEL; PAWLOWSKI MACIEJ; SUBRA GILLES
    权利人:MARTINEZ JEAN; ZAJDEL PAWEL; PAWLOWSKI MACIEJ; SUBRA GILLES; CENTRE NAT RECH SCIENT; UNIV MONTPELLIER 1; UNIV JAGELLONE; UNIV MONTPELLIER II
    摘要:The present invention relates to a pipecolic linker and its use as a solid-phase linker in organic synthesis. Said pipecolic solid-phase linker may be used for coupling functional groups chosen between primary amines, secondary amines, aromatic amines, alcohols, phenols and thiols. In particular, said pipecolic solid-phase linker may be used for peptide or pseudopeptide synthesis, such as the reverse N to C peptide synthesis or the retro-inverso peptide synthesis, or for the synthesis of small organic molecules.

    专利号:US-5892038-A
    优先权日:1997-12-08
    标 题 :Hydroxy-amino acid amides
    发明人:DOLLE III ROLAND ELLWOOD; PATEL HITESH K
    权利人:PHARMACOPEIA INC
    摘要:Compounds of Formula I I are disclosed as inhibitors of plasmepsin and cathepsin D. The compounds are therefore useful to treat diseases such as malaria. In preferred compounds of formula I, Y is the residue of an N-acylated amino acid, a substituted 4-aminoproline or a substituted piperazinealkanoic acid. Intermediates in the solid phase synthesis of compounds of formula I, in which the compounds are attached to a solid support, are also disclosed.

    专利号:TW-202220698-A
    优先权日:2020-08-06
    标题:Methods for the synthesis of protein-drug conjugates

    专利号:WO-2011000848-A1
    优先权日:2009-06-29
    标题 :Solid phase peptide synthesis of peptide alcohols

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    合成参考文献


    参考文献:10.1007/bf01243878
    摘要:Pycock CJ, Horton RW. Dopamine-dependent hyperactivity in the rat following manipulation of GABA mechanisms in the region of the nucleus accumbens. Journal of Neural Transmission. 1979 Mar;45(1):17–33. doi: 10.1007/bf01243878.
    参考文献:10.1111/j.1471-4159.1986.tb00624.x
    摘要:Limberger N, Späth L, Starke K. Release of Previously Incorporated γ‐[3H]Aminobutyric Acid in Rabbit Caudate Nucleus Slices. Journal of Neurochemistry. 1986 Apr;46(4):1102–8. doi: 10.1111/j.1471-4159.1986.tb00624.x.
    参考文献:10.1016/j.bbamem.2010.07.032
    摘要:Edwards N, Anderson CMH, Gatfield KM, Jevons MP, Ganapathy V, Thwaites DT. Amino acid derivatives are substrates or non-transported inhibitors of the amino acid transporter PAT2 (slc36a2). Biochimica et Biophysica Acta (BBA) - Biomembranes. 2011 Jan;1808(1):260–70. doi: 10.1016/j.bbamem.2010.07.032.
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