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fructose 1,6-diphosphate | 34693-15-7

中文名称
——
中文别名
——
英文名称
fructose 1,6-diphosphate
英文别名
fructose-1,6-bisphosphate;FBP;D-fructose 1,6-bisphosphate;FDP;Fosfructose;1,6-di-O-phosphono-beta-D-fructofuranose;[(2R,3S,4S,5R)-2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methyl dihydrogen phosphate
fructose 1,6-diphosphate化学式
CAS
34693-15-7
化学式
C6H14O12P2
mdl
——
分子量
340.117
InChiKey
RNBGYGVWRKECFJ-ARQDHWQXSA-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

物化性质

  • 沸点:
    722.6±70.0 °C(Predicted)
  • 密度:
    2.095±0.06 g/cm3(Predicted)
  • 物理描述:
    Solid
  • 溶解度:
    94 mg/mL
  • 碰撞截面:
    157.51 Ų [M-H]- [CCS Type: DT, Method: stepped-field]

计算性质

  • 辛醇/水分配系数(LogP):
    -5.6
  • 重原子数:
    20
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    203
  • 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
  • 下游产品
    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

  • [EN] PYRROLOPYRROLE COMPOSITIONS AS PYRUVATE KINASE (PKR) ACTIVATORS<br/>[FR] COMPOSITIONS DE PYRROLOPYRROLE EN TANT QU'ACTIVATEURS DE LA PYRUVATE KINASE (PKR)
    申请人:FORMA THERAPEUTICS INC
    公开号:WO2018175474A1
    公开(公告)日:2018-09-27
    The disclosure relates to modulating pyruvate kinase and provides novel chemical compounds of formula (I) useful as activators of PKR, as well as various uses of these compounds. PKR activating compounds are useful in the treatment of diseases and disorders associated with PKR and/or PKM2, such as pyruvate kinase deficiency (PKD), sickle cell disease (SCD), and thalassemia.
    该披露涉及调节丙酮酸激酶,并提供了化学式(I)的新型化合物,可用作PKR的激活剂,以及这些化合物的各种用途。激活PKR的化合物在治疗与PKR和/或PKM2相关的疾病和障碍方面非常有用,如丙酮酸激酶缺乏症(PKD)、镰状细胞病(SCD)和地中海贫血。
  • Diisopropylethylamine/hexafluoroisopropanol-mediated ion-pairing ultra-high-performance liquid chromatography/mass spectrometry for phosphate and carboxylate metabolite analysis: utility for studying cellular metabolism
    作者:Lili Guo、Andrew J. Worth、Clementina Mesaros、Nathaniel W. Snyder、Jerry D. Glickson、Ian A. Blair
    DOI:10.1002/rcm.7667
    日期:2016.8.30
    acid-containing metabolites was developed. Diisopropylethylamine (DIPEA) was used as an IP reagent in combination with reversed-phase liquid chromatography (RP-LC) and a triple quadrupole mass spectrometer using selected reaction monitoring (SRM) and negative electrospray ionization (NESI). An additional reagent, hexafluoroisopropanol (HFIP), which has been previously used to improve sensitivity of nucleotide
    理性分析低分子量极性代谢物的质谱(MS)分析可能具有挑战性,因为异构体的色谱分离度差且电离效率不足。这些代谢物包括关键代谢途径(如糖酵解,磷酸戊糖途径和克雷布斯循环)的中间体。因此,对生物流体或细胞培养模型中这些代谢物的敏感,特异和全面的定量分析,可以洞察扰动的新陈代谢起作用的多种疾病状态。方法建立了离子对反相超高效液相色谱(IP-RP-UHPLC)/ MS方法,以分离和分析与生化相关的含磷酸盐和羧酸的代谢物。二异丙基乙胺(DIPEA)用作IP试剂,结合反相液相色谱(RP-LC)和三重四极杆质谱仪,使用选定的反应监测(SRM)和负电喷雾电离(NESI)。以前已使用附加试剂六氟异丙醇(HFIP)来提高通过UHPLC / MS进行核苷酸分析的灵敏度,以提高灵敏度。结果当与IP碱一起添加时,HFIP与乙酸相比,对某些分析物(包括1,6-6-磷酸二氢果糖,磷酸烯醇丙酮酸和6-磷酸葡萄糖酸)的IP-RP-UHPLC
  • Phosphonic derivatives of carbohydrates: chemoenzymatic synthesis
    作者:Giuseppe Guanti、Luca Banfi、Maria Teresa Zannetti
    DOI:10.1016/s0040-4039(00)00326-9
    日期:2000.4
    racemic β-hydroxyaldehydes bearing a phosphonate group in the ω-position were synthesised and allowed to react with dihydroxyacetone phosphate (DHAP) via an enzymatic aldol addition catalysed by fructose 1,6-bisphosphate aldolase (FruA). After enzymatic dephosphorylation, a set of unnatural ω-phosphonic deoxysugars was obtained.
    合成了一系列在ω-位带有膦酸酯基的同源外消旋β-羟醛,并通过果糖1,6-双磷酸醛缩酶(FruA)催化的醛醇加成反应,使其与磷酸二羟基丙酮(DHAP)反应。酶促脱磷酸作用后,获得了一组非天然的ω-膦酸脱氧糖。
  • [EN] METHOD FOR PRODUCING CARBOHYDRATES FROM DIHYDROXYACETONE<br/>[FR] PROCÉDÉ DE PRODUCTION DE GLUCIDES À PARTIR DE DIHYDROXYACÉTONE
    申请人:KEMBIOTIX LLC
    公开号:WO2016201110A1
    公开(公告)日:2016-12-15
    The present invention relates to the use of dihydroxyacetone ("DHA") in the preparation of a number of natural and rare carbohydrates. The present invention comprises three stages. In the first stage of the present invention, syngas and formaldehyde are produced from natural gas, biogas, biomass and C02 from industrial plants including electricity generating plants, steel mills, cement factories and bio refineries. In the second stage of the present invention, formaldehyde and syngas from first stage are condensed to produce DHA. In the third stage of the present invention, DHA serves as a starting material for the synthesis of natural and rare carbohydrates using enzymes belonging to isomerase, aldolases, epimerase and transketolase groups.
    本发明涉及二羟基乙酮("DHA")在制备多种天然和稀有碳水化合物中的应用。本发明包括三个阶段。在本发明的第一阶段中,从天然气、沼气、生物质和工业厂房(包括发电厂、钢铁厂、水泥厂和生物精炼厂)的C02中生产合成气和甲醛。在本发明的第二阶段中,从第一阶段得到的甲醛和合成气被凝结以产生DHA。在本发明的第三阶段中,DHA作为合成天然和稀有碳水化合物的起始物质,使用属于异构酶、醛缩酶、差向异构酶和转酮酶等酶类的酶。
  • Preparation of pharmaceutical salts of piperazine compounds
    申请人:Wu Wenxue
    公开号:US20060241295A1
    公开(公告)日:2006-10-26
    The present invention is generally directed to a process to directly prepare pharmaceutically acceptable salts enriched with respect to selected rotameric salts of a basic compound, by creative choice of an acid and a solvent medium. The process is particularly useful in preparing specific rotamers of pharmaceutically useful salts in desired preponderance of a rotamer.
    本发明通常涉及一种直接制备药用可接受盐的过程,该过程通过创造性地选择酸和溶剂介质,使其富集于一种基本化合物的选择性转构盐。该过程特别适用于在所需的转构体的优势下制备具有药用价值的盐的特定转构体。
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