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6-O-linoleyl-α-D-glucopyranosyl-β-D-fructofuranoside | 101686-99-1

中文名称
——
中文别名
——
英文名称
6-O-linoleyl-α-D-glucopyranosyl-β-D-fructofuranoside
英文别名
β-D-fructofuranosyl-(O6-octadeca-9c,12c-dienoyl-α-D-glucopyranoside);β-D-Fructofuranosyl-(O6-octadeca-9c,12c-dienoyl-α-D-glucopyranosid);[(2R,3S,4S,5R,6R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (9Z,12Z)-octadeca-9,12-dienoate
6-O-linoleyl-α-D-glucopyranosyl-β-D-fructofuranoside化学式
CAS
101686-99-1
化学式
C30H52O12
mdl
——
分子量
604.736
InChiKey
HYOLCVBYZVOUNB-MVIOKFNFSA-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):
    3.1
  • 重原子数:
    42
  • 可旋转键数:
    21
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    196
  • 氢给体数:
    7
  • 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

反应信息

点击查看最新优质反应信息

文献信息

  • Reactive diluents and coatings comprising them
    申请人:Oostveen Arnoldus Evarardus
    公开号:US20050042379A1
    公开(公告)日:2005-02-24
    The invention relates to the use of a fatty acid modified carbohydrate obtainable by reaction of: (i) at least one carbohydrate or an acyl ester thereof; and (ii) a fatty acid, an alkyl ester thereof or a derivative thereof as a reactive diluent in a coating. The invention further relates to a coating which includes at least one binder and, as a reactive diluent, a fatty acid modified carbohydrate obtainable by reaction of (i) at least one carbohydrate or an acyl ester thereof; and (ii) a fatty acid, an alkyl ester thereof or a derivative thereof.
    该发明涉及使用一种脂肪酸改性的碳水化合物,其可通过以下反应获得:(i)至少一种碳水化合物或其酰基;和(ii)脂肪酸、其烷基或其衍生物作为涂层中的反应稀释剂。该发明还涉及一种涂层,其中包括至少一种粘合剂和作为反应稀释剂的脂肪酸改性的碳水化合物,其可通过以下反应获得:(i)至少一种碳水化合物或其酰基;和(ii)脂肪酸、其烷基或其衍生物
  • PERORAL IMMUNOGEN COMPOSITION AND PROCESS FOR PRODUCING THE SAME
    申请人:THE NISSHIN OIL MILLS, LTD.
    公开号:EP0775494A1
    公开(公告)日:1997-05-28
    The invention provides an immunogen composition for oral administration comprising an immunogen and one or more fatty acid esters of sucrose wherein the fatty acid has 6 to 18 carbons.
    本发明提供了一种用于口服的免疫原组合物,该组合物包含一种免疫原和一种或多种蔗糖脂肪酸,其中脂肪酸具有 6 至 18 个原子。
  • Compositions containing aliphatic monocarboxylic acid esters or amides for the treatment of skin diseases
    申请人:CELLEGY PHARMACEUTICALS, INC.
    公开号:EP0839529A2
    公开(公告)日:1998-05-06
    Skin conditions characterized by hyperactive mitochondria including inflammatory, hyperproliferative, hyperplastic, and dysplastic skin cells are treated with topical formulations of 5 to 19 carbon atom length aliphatic monocarboxylic acid esters or amides, as well as 5 to 19 carbon atom length monoaliphatic amines or their pharmaceutically acceptable salts.
    以线粒体功能亢进为特征的皮肤病,包括炎症性、增生性、增生性和发育不良性皮肤细胞,可使用 5 至 19 个原子长度的脂肪族单羧酸酰胺,以及 5 至 19 个原子长度的单脂肪胺或它们的药学上可接受的盐类的外用制剂进行治疗。
  • LEUKOCYTE ANALYSIS METHOD AND ANALYSIS REAGENT FOR USE IN THE METHOD
    申请人:ARKRAY, Inc.
    公开号:EP2278331A1
    公开(公告)日:2011-01-26
    The present invention provides a method for analyzing leukocytes, by which the leukocytes can be classified and measured stably with high accuracy even when a dilution ratio of a sample containing the leukocytes is low or a flow velocity during the analysis is slow, and an analysis reagent used for the analysis method. The analysis method of the present invention includes the steps of mixing a sample containing leukocytes and erythrocytes and an analysis reagent containing a surfactant that reacts with leukocytes; and measuring the leukocytes by passing a mixed solution of the sample and the analysis reagent through a fine through-hole, measuring a signal detected when the mixed solution passes through the fine through-hole, and classifying and counting the leukocytes in the sample. The analysis reagent further contains a nonionic surfactant, and the nonionic surfactant has a sugar residue as a hydrophilic region and an aliphatic chain as a hydrophobic region.
    本发明提供了一种分析白细胞的方法,通过该方法,即使含有白细胞的样品的稀释率较低或分析过程中流速较慢,也能稳定地对白细胞进行分类和测量,且准确度高;本发明还提供了一种用于该分析方法的分析试剂。本发明的分析方法包括以下步骤:将含有白细胞和红细胞的样品与含有能与白细胞反应的表面活性剂分析试剂混合;通过将样品和分析试剂的混合溶液通过细通孔,测量混合溶液通过细通孔时检测到的信号,并对样品中的白细胞进行分类和计数,从而测量白细胞。分析试剂还含有非离子表面活性剂非离子表面活性剂的亲区域为糖残基,疏区域为脂肪族链。
  • Method for treating a blood component containing sample
    申请人:ARKRAY, Inc.
    公开号:EP2677317A1
    公开(公告)日:2013-12-25
    Provided is a treatment method for damaging an erythrocyte and a leukocyte while suppressing damage to cells other than blood cells present in blood. In an embodiment, the disclosure relates to a method for treating a sample containing blood components, the method including mixing a sample containing blood components with a surfactant A, where the surfactant A is a nonionic surfactant represented by General formula R1-O-(EO)n-R2 (I).
    本发明提供了一种在抑制对血液中血细胞以外的细胞造成损伤的同时,对红细胞和白细胞造成损伤的处理方法。在一个实施方案中,本公开涉及一种处理含有血液成分的样品的方法,该方法包括将含有血液成分的样品与表面活性剂 A 混合,其中表面活性剂 A 是通式 R1-O-(EO)n-R2 (I) 所代表的非离子表面活性剂
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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 纤维素二糖八壬烷酸酯 硫脂I 石斛碱;青藤碱 甲基6-O-(2-十四烷基-3-羟基十八碳酰基)-alpha-D-吡喃葡萄糖苷 环戊羧酸,1-氨基-2-甲基-,(1R,2S)-rel- 特女贞苷 海藻糖6,6'-二甲藻酸酯 海藻糖 6,6'-二山嵛酸酯 水螅毒素 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-吡喃葡萄糖苷, 6-O-(1-氧代癸基)-alpha-D-吡喃葡萄糖基, 6-癸酸酯 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-吡喃葡糖酐-2,6-双油酸酯与聚环氧乙烷(2:1)的醚化物 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