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2-acetylamino-O6-phosphono-2-deoxy-D-galactose | 22332-12-3

中文名称
——
中文别名
——
英文名称
2-acetylamino-O6-phosphono-2-deoxy-D-galactose
英文别名
2-Acetylamino-O6-phosphono-2-desoxy-D-galactose;[(2R,3R,4R,5R)-5-acetamido-2,3,4-trihydroxy-6-oxohexyl] dihydrogen phosphate
2-acetylamino-<i>O</i><sup>6</sup>-phosphono-2-deoxy-D-galactose化学式
CAS
22332-12-3
化学式
C8H16NO9P
mdl
——
分子量
301.19
InChiKey
QDSLHWJDSQGPEE-OSMVPFSASA-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):
    -4.5
  • 重原子数:
    19
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    174
  • 氢给体数:
    6
  • 氢受体数:
    9

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

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文献信息

  • Oligonucleotide compounds, their production and use
    申请人:TAKEDA CHEMICAL INDUSTRIES, LTD.
    公开号:EP0653438A2
    公开(公告)日:1995-05-17
    An oligonucleotide compound or a salt thereof, which has a nucleotide sequence represented by formula (I): wherein W represents hydrogen or a protective group; B1, B2 and B3 each represent nucleic acid residues, wherein each B2 may be the same or different when n is 2 or more; X1, X2 and X3 each represent OH, SH, C1-5 alkyl, C1 -5 alkoxy, C1 -5 monoalkylamino or an aromatic ring group which may be substituted or unsubstituted, wherein each X3 may be the same or different when n is 2 or more; R1, R2 and R3 each represent hydrogen, OH, halogen, C1 -5 alkoxy or C1 -5 alkoxyalkyloxy, wherein each R2 may be the same or different when n is 2 or more; and n represents an integer from 1 to 98 is disclosed. The oligonucleotides (I) of the present invention or the salts thereof can (1) inhibit expression of genes associated with the development of malignant tumors in malignant tumor cells, (2) inhibit expression of viral genes derived from viruses, (3) inhibit expression of genes producing proteins which contribute to the development of inflammations, (4) control expression of drug-resistant genes which cause complications in chemotherapy of malignant tumors, and (5) inhibit production of cell growth factors related to reangiostenosis after PCTA (percutaneous transluminal coronary angioplasty) by complementation to DNAs or mRNAs of genes inducing various diseases. They can be therefore used as antitumor agents, antiviral agents, antiinflammatory agents and drugs for controlling expression of specific genes such as resistance genes. These oligonucleotides can also be used as probes. Further, these oligonucleotides can be used in novel drug screening assays.
    一种寡核苷酸化合物或其盐,其核苷酸序列由式 (I) 表示: 其中 W 代表氢或保护基团;B1、B2 和 B3 各自代表核酸残基,其中当 n 为 2 或更多时,每个 B2 可相同或不同;X1、X2 和 X3 各自代表 OH、SH、C1-5 烷基、C1-5 烷氧基、C1-5 单烷基氨基或可被取代或未被取代的芳环基团,其中当 n 为 2 或更多时,每个 X3 可相同或不同;R1、R2 和 R3 各自代表氢、OH、卤素、C1 -5 烷氧基或 C1 -5 烷氧基,其中当 n 为 2 或更多时,每个 R2 可以相同或不同;n 代表 1 至 98 的整数。 本发明的寡核苷酸(I)或其盐类可以:(1) 抑制恶性肿瘤细胞中与恶性肿瘤发展有关的基因的表达;(2) 抑制来自病毒的病毒基因的表达;(3) 抑制产生有助于炎症发展的蛋白质的基因的表达、(4) 控制导致恶性肿瘤化疗并发症的耐药基因的表达,以及 (5) 通过与诱发各种疾病的基因的 DNA 或 mRNA 互补,抑制与经皮冠状动脉成形术(PCTA)后再狭窄有关的细胞生长因子的产生。因此,这些寡核苷酸可用作抗肿瘤药、抗病毒药、消炎药和控制特定基因(如抗性基因)表达的药物。这些寡核苷酸还可用作探针。此外,这些寡核苷酸还可用于新型药物筛选试验。
  • [EN] COMPOSITION FOR LOWERING BLOOD GLUCOSE COMPRISING HEXOSE MONOPHOSPHATE<br/>[FR] COMPOSITION A BASE D'HEXOSE MONOPHOSPHATE PERMETTANT DE REDUIRE LA GLYCEMIE
    申请人:KOREA RES INST OF BIOSCIENCE
    公开号:WO2006006757A1
    公开(公告)日:2006-01-19
    Disclosed is a composition comprising a hexose monophosphate for lowering blood glucose by the action of orally administered hexose monophosphate of stimulating insulin production by the pancreatic beta cells and increasing serum insulin levels.
  • Distler et al., Journal of Biological Chemistry, 1958, vol. 230, p. 497,503,504
    作者:Distler et al.
    DOI:——
    日期:——
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