CAS: 21788-37-4; L-Biotin

该化合物是化学化合物,其独特的双环结构,包含thieno和imidazole环.该化合物具有五氟酸味,有助于其作为生物活性分子的潜力.(3aR,4R,6aS)所显示的立体化学学表明原子的具体空间安排,可显著影响该化合物的生物活动和相互作用.这种性质的化合物通常可能具有与药用化学有关的特性,包括药物开发中的潜在作用或合成过程中的中间作用.六氢-2-氧组的存在表明它可能参与各种化学反应,包括涉及核糖类或电药类.

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    (+/-)-biotin R)-1( oder !3)-benzyl-2-oxo-(3ar,6ac)-hexahydro-thieno[3,4-d]imidazol-4t-yl]-valeric acid5-[(3aR)-1( oder !3)-benzyl-2-oxo-(3ar,6ac)-hexahydro-thieno[3,4-d]imidazol-4t-yl]-valeric acid H-thieno[3,4-d]imidazol-4-yl)-pentanoic acid5-(2-oxo-2,3-dihydro-1H-thieno[3,4-d]imidazol-4-yl)-pentanoic acid phosgene biotin vitamin H (+/-)-biotin methyl ester 5-((3aS,6R,6aR)-2-Oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoic acid (3-phenyl-propyl)-amide

    合成工艺路线路线简述

      📜1'N-Benzyl Biotin置于氨,Sodium,Xylene体系中,化学反应生成生物素杂质27
      参考文献:Synthesis Of Biotin
      标题:Synthesis Of Biotin

      海关参考信息

      专利信息


      专利号:US-2005009055-A1
      优先权日:2002-07-12
      标 题 :System and method for examination of microarrays using scanning electron microscope
      发明人:CICCOLELLA PAUL C; HOZBOR MARIA A
      权利人:AFFYMETRIX INC
      摘要:The present invention provides methods to detect biomolecules on a microarray using a scanning electron microscope. In one embodiment of the invention, errors in oligonucleotide synthesis during manufacturing of microarrays are detected by monitoring synthesis of control probes on the chips. In another embodiment, misalignment of features on the chip is determined. In yet another embodiment, the size, shape and edge definition of features on the chip is determined. In further embodiments, methods are provided for analyzing interactions between an oligonucleotide target and an oligonucleotide probe on a microarray and methods for testing conditions in a microarray manufacturing process.

      专利号:US-2007249024-A1
      优先权日:2004-06-03
      标 题:Novel Dna Synthesis Technology with 3'-Beaded Oligo Dna and Dna Polymerase
      发明人:MURAISO KANAE
      权利人:BISO INFO DESIGN INC
      摘要:A method of synthesizing a desired DNA having a predetermined sequence, comprising the steps of (a) preparing, based on the desired DNA, a plurality of 3′-biotin-immobilized oligo DNA having a fixed length; (b) preparing a starting DNA which has a complementary sequence to a 3′ end of a first immobilized oligo DNA of the plurality of oligo DNA, and wherein the starting DNA has a length shorter than the length of the first immobilized oligo DNA; (c) annealing the starting DNA with the first immobilized oligo DNA, extending the starting DNA to complement the first immobilized oligo DNA, thereby making a newly extended DNA; (d) denaturing a first double strand DNA consisting of the newly extended DNA and the first immobilized oligo DNA; (e) collecting the extended DNA by removing the first immobilized oligo DNA from the extended DNA; (f) annealing the collected, extended DNA with a second immobilized oligo DNA from the plurality of oligo DNA, further extending the extended DNA to complement the second oligo DNA, thereby making a further extended DNA; (g) denaturing a second double stranded DNA consisting of the second immobilized oligo DNA and the further extended DNA; (h) collecting the further extended DNA by removing the second immobilized oligo DNA from the extended DNA; and (i) repeating steps (f) through (h) until the further extended DNA becomes the predetermined sequence thereby completing synthesis of the desired DNA.

      专利号:US-2004081985-A1
      优先权日:2002-07-12
      标题:Systems and method for examination of microarrays using scanning electron microscope
      发明人:CICCOLELLA PAUL C; HOZBOR MARIA A
      权利人:AFFYMETRIX INC
      摘要:The present invention provides methods to detect biomolecules on a microarray using a scanning electron microscope. In one embodiment of the invention, errors in oligonucleotide synthesis during manufacturing of microarrays are detected by monitoring synthesis of control probes on the chips. In another embodiment, misalignment of features on the chip is determined. In yet another embodiment, the size, shape and edge definition of features on the chip is determined. In further embodiments, methods are provided for analyzing interactions between an oligonucleotide target and an oligonucleotide probe on a microarray and methods for testing conditions in a microarray manufacturing process.

      专利号:US-2009118140-A1
      优先权日:2007-03-15
      标 题 :Method and system for assembly of macromolecules and nanostructures
      发明人:SUZARA VINCENT
      权利人:SUZARA VINCENT
      摘要:A template-based system enables the assembly of macromolecules and nanostructures. The template system comprises a plurality of single strand DNA molecules which are substantially parallel, substantially inline each from one end, and substantially equally spaced apart, wherein each DNA molecule has a distinguishable length and a known sequence. The system can be used for the precise, accurate, and efficient synthesis of peptides, proteins and enzymes.

      专利号:US-4656289-A
      优先权日:1984-10-25
      标 题 :1,3-dibenzyl-4-halohexahydro-1H-thieno[3,4-d]imidazol-2(3H)-one intermediates
      发明人:BATES HANS A; ROSENBLUM STUART
      权利人:RES FOUNDATION OF STATE UNIV O
      摘要:Novel synthetic routes to (3aα,6aα)-1,3-dibenzyl hexahydro-1H-thieno[3,4-d]imidazol-2(3H)-one 5,5-dioxide, a known intermediate in the synthesis of biotin are provided. n A novel synthetic route from this intermediate to biotin is also disclosed.

      专利号:US-8541569-B2
      优先权日:2008-09-06
      标题:Phosphoramidites for synthetic RNA in the reverse direction, efficient RNA synthesis and convenient introduction of 3'-end ligands, chromophores and modifications of synthetic RNA
      发明人:SRIVASTAVA SURESH C; SRIVASTAVA NAVEEN P
      权利人:SRIVASTAVA SURESH C; SRIVASTAVA NAVEEN P; CHEMGENES CORP
      摘要:The present invention provides building blocks and methods for synthesizing very pure RNA in a form that can efficiently be modified at the 3′ end. Reverse RNA monomer phosphoramidites have been developed for RNA synthesis in 5′→3′ direction, leading to very clean oligo synthesis that allows for the introduction of various modifications at the 3′-end cleanly and efficiently. Higher coupling efficiency per step have been observed during automated oligo synthesis with the reverse RNA amidites disclosed herein, resulting in a greater ability to achieve higher purity and produce very long oligonucleotides. The use of the reverse RNA phosphoramidites in the synthetic process of this invention leads to oligonucleotides free of N+1 species.

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      ✅ COA系统入驻 | 共享模式

      主要参考文献

      [参考文献]: Said Hm. Biotin: Biochemical, Physiological And Clinical Aspects. Subcell Biochem. 2012;56:1-19.

      合成参考文献


      参考文献:10.1007/bf00178614|10.1007/s002530050628
      摘要:Guan X, Wurtele ES. Reduction of growth and acetyl-CoA carboxylase activity by expression of a chimeric streptavidin gene in Escherichia coli. Applied Microbiology and Biotechnology. 1996 Feb 20;44(6):753–8. doi: 10.1007/s002530050628.
      参考文献:10.1007/bf01799109
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      参考文献:10.1007/s00253-011-3336-x
      摘要:Hidese R, Mihara H, Esaki N. Bacterial cysteine desulfurases: versatile key players in biosynthetic pathways of sulfur-containing biofactors. Applied Microbiology and Biotechnology. 2011 May 21;91(1):47–61. doi: 10.1007/s00253-011-3336-x.
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