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3′-O-benzyl-4,6;4′,6′-di-O-benzylidene-2′-O-tert-butyldimethylsilyl-2-O-palmitoyl-α,α-D-trehalose | 1450826-92-2

中文名称
——
中文别名
——
英文名称
3′-O-benzyl-4,6;4′,6′-di-O-benzylidene-2′-O-tert-butyldimethylsilyl-2-O-palmitoyl-α,α-D-trehalose
英文别名
[(2R,4aR,6R,7R,8S,8aS)-6-[[(2R,4aR,6R,7R,8S,8aR)-7-[tert-butyl(dimethyl)silyl]oxy-2-phenyl-8-phenylmethoxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-6-yl]oxy]-8-hydroxy-2-phenyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-7-yl] hexadecanoate
3′-O-benzyl-4,6;4′,6′-di-O-benzylidene-2′-O-tert-butyldimethylsilyl-2-O-palmitoyl-α,α-D-trehalose化学式
CAS
1450826-92-2
化学式
C55H80O12Si
mdl
——
分子量
961.318
InChiKey
KIKGZRNYUMUKGE-KHWKEZTQSA-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):
    11.41
  • 重原子数:
    68
  • 可旋转键数:
    26
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    130
  • 氢给体数:
    1
  • 氢受体数:
    12

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 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:
    参考文献:
    名称:
    结核分枝杆菌磺基糖脂类似物的简化的脱氧丙酸酯酰基链:链长是高抗原性必不可少的
    摘要:
    越长越好:分枝杆菌二酰基磺化糖脂(酰基2 SGL)类似物中1,3-甲基支链脂肪酰基链单元长度的增加导致其抗原性显着改善,并且产品比天然抗原酰基更有效2个SGL。
    DOI:
    10.1002/cbic.201300482
  • 作为产物:
    描述:
    海藻糖吡啶2,6-二甲基吡啶三乙基硅烷4-二甲氨基吡啶 、 iron(III) chloride hexahydrate 、 palladium 10% on activated carbon 、 甲酸铵N,N'-二环己基碳二亚胺 作用下, 以 甲醇二氯甲烷乙腈 为溶剂, 反应 11.75h, 生成 3′-O-benzyl-4,6;4′,6′-di-O-benzylidene-2′-O-tert-butyldimethylsilyl-2-O-palmitoyl-α,α-D-trehalose
    参考文献:
    名称:
    Synthesis of a Mycobacterium tuberculosis Tetra-acylated Sulfolipid Analogue and Characterization of the Chiral Acyl Chains Using Anisotropic NAD 2D-NMR Spectroscopy
    摘要:
    Tetra-O-acylated sulfolipids are metabolites found in the cell wall of Mycobacterium tuberculosis, the causative agent of tuberculosis. Their role in pathogenesis remains, however, undefined. Here we describe a novel access to model tetra-O-acylated trehalose sulfate derivatives having simple acyl chains. The trehalose core was regioselectively protected using a tandem procedure with catalytic iron(III) chloride hexahydrate and further desymmetrized. Model chiral fatty acids, prepared by a zinc-mediated cross-coupling, were incorporated into the trehalose core. The enantiomeric excess of the chiral fatty acids has been measured by natural abundance deuterium (NAD) 2D-NMR spectroscopy in a polypeptide based chiral liquid crystal. The synthetic approach established for the model compounds can easily be developed for the preparation of other analogues and natural sulfolipids.
    DOI:
    10.1021/jo4012255
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文献信息

  • Synthesis of a <i>Mycobacterium tuberculosis</i> Tetra-acylated Sulfolipid Analogue and Characterization of the Chiral Acyl Chains Using Anisotropic NAD 2D-NMR Spectroscopy
    作者:Aurélie Lemétais、Yann Bourdreux、Philippe Lesot、Jonathan Farjon、Jean-Marie Beau
    DOI:10.1021/jo4012255
    日期:2013.8.2
    Tetra-O-acylated sulfolipids are metabolites found in the cell wall of Mycobacterium tuberculosis, the causative agent of tuberculosis. Their role in pathogenesis remains, however, undefined. Here we describe a novel access to model tetra-O-acylated trehalose sulfate derivatives having simple acyl chains. The trehalose core was regioselectively protected using a tandem procedure with catalytic iron(III) chloride hexahydrate and further desymmetrized. Model chiral fatty acids, prepared by a zinc-mediated cross-coupling, were incorporated into the trehalose core. The enantiomeric excess of the chiral fatty acids has been measured by natural abundance deuterium (NAD) 2D-NMR spectroscopy in a polypeptide based chiral liquid crystal. The synthetic approach established for the model compounds can easily be developed for the preparation of other analogues and natural sulfolipids.
  • Simplified Deoxypropionate Acyl Chains for<i>Mycobacterium tuberculosis</i>Sulfoglycolipid Analogues: Chain Length is Essential for High Antigenicity
    作者:Benjamin Gau、Aurélie Lemétais、Marco Lepore、Luis Fernando Garcia-Alles、Yann Bourdreux、Lucia Mori、Martine Gilleron、Gennaro De Libero、Germain Puzo、Jean-Marie Beau、Jacques Prandi
    DOI:10.1002/cbic.201300482
    日期:2013.12.16
    The longer, the better: Increasing the lengths of the 1,3‐methyl‐branched fatty acyl chain units in mycobacterial diacylated sulfoglycolipid (Acyl2SGL) analogues led to dramatic improvements in their antigenic properties and gave products more potent than the natural antigen Acyl2SGLs.
    越长越好:分枝杆菌二酰基磺化糖脂(酰基2 SGL)类似物中1,3-甲基支链脂肪酰基链单元长度的增加导致其抗原性显着改善,并且产品比天然抗原酰基更有效2个SGL。
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同类化合物

霉酚酸苯酚beta-D-葡糖苷 阜孢霉素B 阜孢杀菌素 蔗糖棕榈酸酯 蔗糖四异硬脂酸酯 蔗糖七月桂酸酯 药喇叭(IPOMOEAPURGA)树脂 硫脂I 石斛碱;青藤碱 环戊羧酸,1-氨基-2-甲基-,(1R,2S)-rel- 海藻糖 6,6'-二山嵛酸酯 木松香II 木松香I 单岩藻糖基乳糖-N-四糖 二唾液酸乳-N-四糖 乳糖醛酸 乙醋化己二酸双淀粉 中文名称暂缺 β-D-呋喃果糖基-α-D-吡喃葡萄苷二硬脂酸酯 Β-D-呋喃果糖基-Α-D-吡喃葡糖苷十二酸双酯 alpha-D-吡喃葡萄糖基-alpha-D-吡喃葡萄糖苷 6-(3-羟基-2-十四烷基十八烷酸酯) [(3aR,5R,5aR,8aS,8bR)-2,2,7,7-四甲基四氢-3aH-二[1,3]二噁唑并[4,5-b:4',5'-d]吡喃-5-基]甲基丁酸酯(non-preferredname) [(2R,3S,4S,5R,6R)-6-[(2R,3R,4S,5S,6R)-6-(十六烷酰氧基甲基)-3,4,5-三羟基四氢吡喃-2-基]氧基-3,4,5-三羟基四氢吡喃-2-基]甲基十六烷酸酯 [(2R,3S,4S,5R)-3,4-二羟基-2,5-二(羟基甲基)四氢呋喃-2-基][(2R,3S,4S,5R,6S)-3,4,5,6-四羟基四氢吡喃-2-基]甲基2-甲基-4-(2-甲基癸-1-烯-4-基)己二酸酯 [(2R,3R,4S,5R,6R)-6-[[(1R,2R,3R,4R,6R)-2,3-二羟基-5,8-二氧杂双环[4.2.0]辛烷-4-基]氧基]-3,4,5-三羟基四氢吡喃-2-基]甲基3-羟基-2-十四烷基十八烷酸酯 N-乙酰基-硫代胞壁酰-丙氨酰-异谷氨酰胺 N-(O-alpha-D-甘露糖基-(1-3)-O-(O-alpha-D-甘露糖基-(1->3)-O-(alpha-D-甘露糖基-(1-6))-alpha-D-甘露糖基-(1-6))-O-beta-D-甘露糖基-(1->4)-O-2-(乙酰氨基)-2-脱氧-beta-D-吡喃葡萄糖基-(1->4)-2-(乙酰氨基)-2-脱氧-beta-D-吡喃葡萄糖基)-L-天冬氨酰胺 L-缬氨酰-L-丙氨酰-L-缬氨酰甘氨酰-L-α-谷氨酰-L-α-谷氨酰-L-脯氨酰甘氨酰-L-脯氨酰-N~5~-(二氨基甲亚基)-L-鸟氨酸酰胺 D-甘露糖基-(1-6)-D-甘露糖基-(1-4)-2-乙酰氨基-2-脱氧-D-吡喃葡萄糖基-(1-4)-2-乙酰氨基-1-N-(4'-L-天冬氨酰)-2-脱氧-beta-D-吡喃葡萄糖基胺 D-(+)-海藻糖6-单油酸酯 9,10-二氯-2,6-二甲基蒽 8-甲氧基羰基辛基2-O-(aL-呋喃基呋喃糖基)-3-O-(aD-吡喃半乳糖基)-bD-吡喃半乳糖苷 6-山慈菇甙A 6-O-alpha-D-吡喃半乳糖基-D-葡萄糖酸 6,6'-二((2R,3R)-3-羟基-2-十四烷基十八烷酸酯)-海藻糖 4H-吡咯并[3,2,1-脱]蝶啶,5,6-二氢-4,5-二甲基-(9CI) 4-嘧啶甲腈,2-苯基- 4-[[(2R)-2-羟基-3,3-二甲基-4-[(2R,3R,4S,5S,6R)-3,4,5-三羟基-6-(羟基甲基)四氢吡喃-2-基]氧基丁酰基]氨基]丁酸 4-[6-(1,2-二羟基乙基)-3,4,5-三羟基-四氢吡喃-2-基]氧基-2,3,5-三羟基-7,8-二氧代-辛酸 3-O-棕榈酰-beta-D-呋喃果糖基2,3-二-O-棕榈酰-alpha-D-吡喃葡萄糖苷 3-(6H-苯并[b][1,5]苯并噁噻庚英-6-基)丙基-二甲基-铵2-羟基-2-羰基-乙酸酯 2-脱氧-3-O-[(3R)-3-羟基十四烷酰基]-2-{[(3R)-3-羟基十四烷酰基]氨基}-1-O-膦酰-alpha-D-吡喃葡萄糖 2-氨基-6-[[3,5,6-三羟基-2-氧代-4-[3,4,5-三羟基-6-(羟基甲基)四氢吡喃-2-基]氧基己基]氨基]己酸 2-氨基-4-氧代-4-[[3,4,5-三羟基-6-[[3,4,5-三羟基-6-[[3,4,5-三羟基-6-(羟基甲基)四氢吡喃-2-基]氧基甲基]四氢吡喃-2-基]氧基甲基]四氢吡喃-2-基]氨基]丁酸 2-N-(羧基丙基氨基)-2-脱氧葡萄吡喃糖 2,6-二甲基-6-(3-O-(beta-吡喃葡萄糖基)-4-O-(2-甲基丁酰基)alpha-阿拉伯吡喃糖基氧基)-2,7-辛二烯酸 1-二甲胺基萘-5-磺酰-甘氨酰-赖氨酰-酪氨酰-丙氨酰-脯氨酰-色氨酰-缬氨酸 1-O,2-O,3-O-三(3-硝基丙酰基)-alpha-D-吡喃葡萄糖 1,1-O-(4,6-二羟基-1,2-亚苯亚甲基)-4-O-[6-O-(1-氧代-2,4-癸二烯基)-beta-D-吡喃半乳糖基]-alpha-D-吡喃葡萄糖3-(7-羟基-8,14-二甲基十六碳-2,4,8,10-四烯酸酯) (Z,Z)-甲基-D-吡喃葡糖苷-2,6-二油酸酯