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methyl 4-amino-4-deoxy-α-D-glucopyranoside

中文名称
——
中文别名
——
英文名称
methyl 4-amino-4-deoxy-α-D-glucopyranoside
英文别名
Methyl-4-amino-4-deoxy-α-D-glucopyranosid;(2S,3R,4S,5S,6S)-5-amino-6-(hydroxymethyl)-2-methoxyoxane-3,4-diol
methyl 4-amino-4-deoxy-α-D-glucopyranoside化学式
CAS
——
化学式
C7H15NO5
mdl
——
分子量
193.2
InChiKey
LMHVHMYRVUPVRG-ZFYZTMLRSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -2.3
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    105
  • 氢给体数:
    4
  • 氢受体数:
    6

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    methyl 4-amino-4-deoxy-α-D-glucopyranosidesodium methylate 作用下, 以 甲醇 为溶剂, 反应 40.0h, 生成 Methyl-4-deoxy-4-<<(1S)-(1,5/4,6)-4,5,6-trihydroxy-3-hydroxymethyl-2-cyclohexen-1-yl->amino>-α-D-glucopyranoside
    参考文献:
    名称:
    Synthesis of some analogues of methyl dehydro-oligobiosaminide (acarviosin)
    摘要:
    DOI:
    10.1016/s0008-6215(00)90465-8
  • 作为产物:
    描述:
    methyl 4-azido-4-deoxy-α-D-glucopyranoside 在 氢气 作用下, 以 甲醇 为溶剂, 以57%的产率得到methyl 4-amino-4-deoxy-α-D-glucopyranoside
    参考文献:
    名称:
    抗生素低聚抑制剂的共同结构单元的合成
    摘要:
    甲基 N-[(1S)-(1,2,4/3,5,6)-2,3,4,6-四羟基-5-(羟甲基)环己基]-4-氨基-4,6-二脱氧- α-D-吡喃葡萄糖苷是抗生素低聚抑制素的常见结构单元,已被合成并表征为七乙酸酯。
    DOI:
    10.1246/cl.1982.1729
  • 作为试剂:
    描述:
    乙酸酐 、 (1S,2R,3R,4R,6S)-2,3-dihydroxy-7-(2,4-dinitrophenyl)-4-hydroxymethyl-7-azabicyclo<4.1.0>heptane 在 吡啶methyl 4-amino-4-deoxy-α-D-glucopyranoside 作用下, 生成 methyl 2,3,6-tri-O-acetyl-4-deoxy-4-<(1R)-(1,2/3,6)-4-acetoxymethyl-2,3-diacetoxy-6-(2,4-dinitrophenylamino)cyclohexylamino>-α-D-glucopyranoside 、 methyl 2,3,6-tri-O-acetyl-4-deoxy-4-<(1R)-(1,3,5/2,4)-5-acetoxymethyl-3,4-diacetoxy-2-(2,4-dinitrophenylamino)cyclohexylamino>-α-D-glucopyranoside 、 (1R,4S,5R,6R,7R)-5,6-diacetoxy-7-(2,4-dinitrophenylamino)-2-oxabicyclo<3.2.1>octane
    参考文献:
    名称:
    Ogawa, Seiichiro; Tsunoda, Hidetoshi, Liebigs Annalen der Chemie, 1993, # 7, p. 755 - 770
    摘要:
    DOI:
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文献信息

  • Synthesis of carbasugar-containing non-glycosidically linked pseudodisaccharides and higher pseudooligosaccharides
    作者:Ian Cumpstey
    DOI:10.1016/j.carres.2009.09.008
    日期:2009.11
    This minireview covers synthetic methods towards carbasugar-containing non-glycosidically linked pseudodisaccharides or higher pseudooligosaccharides. Carbocyclic pyranose mimetics (saturated or unsaturated between C-5 and C-5a) are linked by ether, thioether or amine bridges to carbohydrates or other carbasugars.
    这份简短的综述涵盖了针对含碳水化合物的非糖苷键连接的假二糖或高级假寡糖的合成方法。碳环吡喃糖模拟物(在C-5和C-5a之间饱和或不饱和)通过醚桥,硫醚桥或胺桥连接到碳水化合物或其他Carcarbugars。
  • Generalized Anomeric Effect in <i>gem</i>-Diamines: Stereoselective Synthesis of α-<i>N</i>-Linked Disaccharide Mimics
    作者:Elena M. Sánchez-Fernández、Rocío Rísquez-Cuadro、Matilde Aguilar-Moncayo、M. Isabel García-Moreno、Carmen Ortiz Mellet、José M. García Fernández
    DOI:10.1021/ol901125n
    日期:2009.8.6
    The orbital (negative hyperconjugation) contribution to the generalized anomeric effect is highly increased in bicyclic gem-diamines with a pseudoamide-type endocyclic nitrogen atom, which has been exploited for the stereoselective synthesis of configurationally stable α-N-linked azadisaccharide heteroanalogues of the natural disaccharides maltose and isomaltose as aglycon-sensitive inhibitors of isomaltase
    在具有假酰胺型内环氮原子的双环宝石-二胺中,轨道(负超共轭)对广义异头作用的贡献大大增加,已被用于立体选择性合成天然构型稳定的α- N-连接的氮杂二糖杂类似物二糖麦芽糖和异麦芽糖作为糖异糖苷酶的糖苷配基敏感抑制剂。
  • Synthesis and biological activities of methyl oligobiosaminide and some deoxy isomers thereof
    作者:Yasushi Shibata、Yasuhiro Kosuge、Seiichiro Ogawa
    DOI:10.1016/0008-6215(90)84091-8
    日期:1990.5
    Methyl oligobiosaminide (1) the core structure of oligostatin C, and five analogues, the 6-hydroxy-(2), 2-deoxy- (3), 2-deoxy-6-hydroxy- (4), 3-deoxy- (5), and 3-deoxy-6-hydroxy derivatives (6), were synthesized by coupling the protected pseudo-sugar epoxide 46 with suitable methyl 4-amino-4-deoxy-alpha-D-hexopyranoside derivatives. Compounds 3 and 6 showed notable inhibitory activity against alpha-D-glucosidase
    甲基oligobiosaminide(1)的核心结构是oligostatin C和5个类似物,即6-羟基-(2),2-脱氧-(3),2-脱氧-6-羟基-(4),3-脱氧-( 5)和3-脱氧-6-羟基衍生物(6)是通过将保护的假糖环氧化物46与合适的甲基4-氨基-4-脱氧-α-D-己吡喃糖苷衍生物偶联而合成的。化合物3和6分别显示出对α-D-葡糖苷酶和α-D-甘露糖苷酶的显着抑制活性,而化合物1几乎没有活性。
  • SYNTHESIS OF A COMMON STRUCTURAL UNIT OF THE ANTIBIOTIC OLIGOSTATINS
    作者:Seiichiro Ogawa、Yoshikazu Iwasawa、Tatsushi Toyokuni、Tetsuo Suami
    DOI:10.1246/cl.1982.1729
    日期:1982.11.5
    Methyl N-[(1S)-(1,2,4/3,5,6)-2,3,4,6-tetrahydroxy-5-(hydroxymethyl)cyclohexyl]-4-amino-4,6-dideoxy-α-D-glucopyranoside, a common structural unit of the antibiotic oligostatins, has been synthesized and characterized as the heptaacetate.
    甲基 N-[(1S)-(1,2,4/3,5,6)-2,3,4,6-四羟基-5-(羟甲基)环己基]-4-氨基-4,6-二脱氧- α-D-吡喃葡萄糖苷是抗生素低聚抑制素的常见结构单元,已被合成并表征为七乙酸酯。
  • Sorbistin, a new aminoglycoside antibiotic complex of bacterial origin. III. Structure determination.
    作者:MASATAKA KONISHI、SACHIKO KAMATA、TAKASHI TSUNO、KEI-ICHI NUMATA、HIROSHI TSUKIURA、TAKAYUKI NAITO、HIROSHI KAWAGUCHI
    DOI:10.7164/antibiotics.29.1152
    日期:——
    The structures of sorbistins A1, A2, B, C and D have been determined including stereochemistry. Sorbistins A1, A2 and B are composed of a 4-acyl-amino-4-deoxy-D-glucose and 1, 4-diamino-1, 4-dideoxy-D-sorbitol, the latter compound being hitherto undescribed in literature. Sorbistins C and D have the same aglycone of 1, 4-diamino-1, 4-dideoxy-D-sorbitol, which is linked with D-glucose and 4-amino-4-deoxy-D-glucose, respectively, through a glycosidic bond.
    已经确定了sorbistins A1、A2、B、C和D的结构,包括立体化学。sorbistins A1、A2和B由4-酰氨基-4-脱氧-D-葡萄糖和1,4-二氨基-1,4-二脱氧-D-山梨醇组成,后者在文献中尚未描述。sorbistins C和D具有相同的苷元1,4-二氨基-1,4-二脱氧-D-山梨醇,分别通过糖苷键与D-葡萄糖和4-氨基-4-脱氧-D-葡萄糖相连。
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