CAS: 4696-76-8; (2R,3S,4R,5R,6R)-5-Amino-2-(Aminomethyl)-6-(((1R,2S,3S,4R,6S)-4,6-Diamino-3-(((2S,3R,4S,5S,6R)-4-Amino-3,5-Dihydroxy-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-2-yl)Oxy)-2-Hydroxycyclohexyl)Oxy)Tetrahydro-2H-Pyran-3,4-Diol

该化合物是一种来自Streptomices kanamyceticus的微粒球菌抗生素,在结构上与卡纳米氏菌相似;它通过与30S 脊髓膜炎分管结合,抑制蛋白合成,从而对克格朗阴性细菌和一些克格伦阳性细菌进行广泛监测;Bekanamycin对Mycobactium Turus和其他抗药性菌株特别有效,使其在结核病治疗和兽医应用中具有价值;其各种配方的稳定性和跨抗病率低提高了其在临床和农业环境中的效用;然而,它与其他微粒色色色相相比,由于潜在的肾毒性和毒性,它需要仔细监测.

结构式图片

上下游产品

CAS号2037-48-1 2-脱氧链胺,二氢溴化物 | CAS号60183-25-7 3-Amino-3-deoxy... | CAS号59433-00-0 2,6-Diamino-2,6... | CAS号3847-27-6 kanamycin A sulphate

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    海关参考信息

    专利信息


    专利号:US-RE28647-E
    优先权日:1971-06-02
    标 题:Preparation of 3-4 dideoxykanamycin B active against resistant bacteria
    摘要:Synthesis of 3''-4''-dideoxykanamycin B which comprises protecting the amino and all or a part of the hydroxyl groups other than 3'' and 4''-hydroxyl groups of kanamycin B, sulfonylating 3''- and 4''hydroxyl groups to give a derivative having disulfonic ester groups, removing said ester groups to give 3''-4''-unsaturated compound, reducing said compound and finally removing the residual protecting groups.

    专利号:US-4337336-A
    优先权日:1980-02-25
    标 题:Derivative of kanamycin A and a process for the preparation thereof
    发明人:UMEZAWA HAMAO; UMEZAWA SUMIO; FUKATSU SHUNZO; YONETA TOSHIO; WAKAZAWA TADASHI
    权利人:MICROBIAL CHEM RES FOUND
    摘要:There are provided new compounds, 3',4'-anhydro-4'-epi derivatives of kanamycin A of the formula: ##STR1## wherein R represents an alkyl, aralkyl or aryl group and Y represents an alkylidene, aralkylidene, cycloalkylidene or tetrahydropyranylidene group which are useful as an intermediate for the synthesis of 3',4'-dideoxykanamycin A and 4'-deoxykanamycin A from kanamycin A. The compounds of formula (I) can be prepared by treating the corresponding 4'-O-sulfonyl derivative with an alkali metal alcoholate in a lower alkanol under an alkaline condition.

    专利号:US-4156078-A
    优先权日:1975-12-11
    标 题:Process for the synthesis of 3',4'-dideoxykanamycin B and products
    发明人:TSUCHIYA TSUTOMU; UMEZAWA HAMAO; UMEZAWA SUMIO
    权利人:MICROBIAL CHEM RES FOUND
    摘要:A useful antibiotic, 3',4'-dideoxykanamycin B can be prepared in shortened steps and in an improved overall yield by a new process starting from kanamycin B via new intermediate derivatives of kanamycin B in which all the amino groups and possibly the 2'-hydroxyl group are protected with sulfonyl-type protecting groups selected from lower alkyl-, aryl- and aralkyl-sulfonyl groups.

    专利号:US-6833445-B2
    优先权日:2000-01-21
    标题:Guanidinylation, guanidinoglycosides, uses, and methods of assaying their activity
    发明人:GOODMAN MURRAY; TOR YITZHAK; BAKER TRACY; LUEDTKE NATHAN
    权利人:UNIV CALIFORNIA
    摘要:Provided are reagents and methods useful for the synthesis of guanidinylated compounds. Also provided are methods for assaying molecules, including guanidinylated molecules that modulate viral infection and replication.

    专利号:US-10472663-B2
    优先权日:2015-01-21
    标 题:Procedure for the rapid determination of bacterial susceptibility to antibiotics that inhibit protein synthesis
    发明人:FERNÃ?NDEZ GARCÃ?A JOSÉ LUIS; GOSÃ?LVEZ BERENGUER JAIME; BOU ARÉVALO GERMÃ?N; TAMAYO NOVAS MARIA; SANTISO BRANDARIZ REBECA; OTERO FARIÑA FÃ?TIMA MARÃ?A
    权利人:ABM TECH LLC
    摘要:The present invention relates to a method for the rapid evaluation of bacterial susceptibility or non-susceptibility of bacteria to antibiotics that inhibit protein synthesis. The rationale is to identify bacterial responses that depend or are influenced by protein synthesis. If this response is prevented or reduced by the antibiotic that inhibits the protein synthesis, the bacteria are susceptible to this antibiotic. Otherwise, if the response keeps similar despite the incubation with the antibiotic, the bacteria are not susceptible or resistant to this antibiotic. These responses could be determined at the DNA lev-el, cell wall level, morphological level or any other experimental approach, including metabolic, bio-chemical, physiological or genetic processes.

    专利号:US-2008206803-A1
    优先权日:2001-09-28
    标题:Metabolic genes and related methods and compositions
    发明人:GALLIVAN JUSTIN
    权利人:CALIFORNIA INST OF TECHN
    摘要:Certain aspects of the invention provide nucleic acid constructs that can be used to cause a cell to be dependent on a particular enzymatic activity or on the presence of a particular small molecule. Certain aspects of the invention also provide methods for cloning genes involved in the synthesis, modification or degradation of a given molecule and for the directed evolution of proteins that perform a specified enzymatic function. Certain methods of the invention can be used to isolate the genes responsible for directing the biosynthesis, modification or degradation of a particular target molecule and to isolate polypeptide variants having new or improved enzymatic activity.
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    主要参考文献


    1: Zhang Y, He HM, Zhang J, Liu FJ, Li C, Wang BW, Qiao RZ. HPLC-ELSD determination of kanamycin B in the presence of kanamycin A in fermentation broth. Biomed Chromatogr. 2015 Mar;29(3):396-401. doi: 10.1002/bmc.3289. Epub 2014 Jul 17. doi: 10.1021/acs.jmedchem.5b01375. Epub 2015 Dec 1.
    3: Truitt AR, Choi BE, Li J, Soto AM. Effect of Mutations on the Binding of Kanamycin-B to RNA Hairpins Derived from the Mycobacterium tuberculosis Ribosomal A-Site. Biochemistry. 2015 Dec 29;54(51):7425-37. doi: 10.1021/acs.biochem.5b00710. Epub 2015 Dec 17. doi: 10.1007/s00253-010-2908-5. Epub 2010 Oct 9. doi: 10.1021/acs.joc.5b00248. Epub 2015 Apr 13. doi: 10.1371/journal.pone.0181971. eCollection 2017.
    10: Mingeot-Leclercq MP, Van Schepdael A, Brasseur R, Busson R, Vanderhaeghe HJ, Claes PJ, Tulkens PM. New derivatives of kanamycin B obtained by modifications and substitutions in position 6''. 2. In vitro and computer-aided toxicological evaluation with respect to interactions with phosphatidylinositol. J Med Chem. 1991 Apr;34(4):1476-82. doi: 10.1016/j.ab.2011.04.007. Epub 2011 Apr 15. doi: 10.1021/acsinfecdis.5b00069. Epub 2015 Aug 6. Russian. Russian. French.

    合成参考文献


    参考文献:10.1016/j.bmc.2011.06.049
    摘要:Li ZL, Li QS, Zhang HJ, Hu Y, Zhu DD, Zhu HL. Design, synthesis and biological evaluation of urea derivatives from o-hydroxybenzylamines and phenylisocyanate as potential FabH inhibitors. Bioorg Med Chem. 2011 Aug 01;19(15):4413–20. doi: 10.1016/j.bmc.2011.06.049.
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