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1-N-tert-butyloxycarbonyl-3,4-O-isopropylidene-phytosphingosine | 799267-98-4

中文名称
——
中文别名
——
英文名称
1-N-tert-butyloxycarbonyl-3,4-O-isopropylidene-phytosphingosine
英文别名
tert-butyl N-[(1S)-1-[(4S,5R)-2,2-dimethyl-5-tetradecyl-1,3-dioxolan-4-yl]-2-hydroxyethyl]carbamate
1-N-tert-butyloxycarbonyl-3,4-O-isopropylidene-phytosphingosine化学式
CAS
799267-98-4
化学式
C26H51NO5
mdl
——
分子量
457.695
InChiKey
BAIXVBWGYFERDF-ZRBLBEILSA-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):
    7.8
  • 重原子数:
    32
  • 可旋转键数:
    18
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.96
  • 拓扑面积:
    77
  • 氢给体数:
    2
  • 氢受体数:
    5

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:
    描述:
    1-N-tert-butyloxycarbonyl-3,4-O-isopropylidene-phytosphingosine 在 PhCH=Ru[1,3-bis(2,4,6-Me3C6H2)-2-imidazolidinylidene]Cl2 2,2,6,6-tetramethyl-piperidine-N-oxyl 、 polymer-NMe3*Br(OAc)2 、 三环己基膦 作用下, 以 四氢呋喃二氯甲烷甲苯 为溶剂, 反应 4.5h, 生成 [(E)-(S)-1-((4S,5R)-2,2-Dimethyl-5-tetradecyl-[1,3]dioxolan-4-yl)-3-((2R,3S,4R,5S,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-allyl]-carbamic acid tert-butyl ester
    参考文献:
    名称:
    Efficient Synthesis of α-C-Galactosyl Ceramide Immunostimulants: Use of Ethylene-Promoted Olefin Cross-Metathesis
    摘要:
    Olefin cross-metathesis has been used to prepare alpha-C-galactosylceramide derivatives. The metathesis process merged vinyl and propenyl glycosides with vinyl derivatives of phytosphingosine. The use of ethylene enhanced the yield of the methathesis step.
    DOI:
    10.1021/ol0482137
  • 作为产物:
    描述:
    参考文献:
    名称:
    作为低毒抗癌剂的新型合成硫代秋水仙碱衍生物
    摘要:
    新的硫代秋水仙碱衍生物 (1-8) 被设计为毒性较低的抗癌剂,具有秋水仙碱的强大抗癌活性。描述了这些化合物的合成和生物学评价。作为体外生物学研究的初步结果,化合物 1、6 和 7 显示出比秋水仙碱更低的毒性和有效的抗癌活性。
    DOI:
    10.1002/ardp.200500148
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文献信息

  • [EN] NUCLEOTIDE AND NUCLEOSIDE THERAPEUTIC COMPOSITIONS AND USES RELATED THERETO<br/>[FR] COMPOSITIONS THÉRAPEUTIQUES À BASE DE NUCLÉOTIDES ET NUCLÉOSIDES ET UTILISATIONS ASSOCIÉES
    申请人:UNIV EMORY
    公开号:WO2017155923A1
    公开(公告)日:2017-09-14
    This disclosure relates to nucleotide and nucleoside therapeutic compositions and uses in treating infectious diseases, viral infections, and cancer, where the base of the nucleotide or nucleoside contains at least one thiol, thione or thioether.
    这份披露涉及到核苷酸和核苷类治疗组合物,用于治疗传染病、病毒感染和癌症,在这些组合物中,核苷酸或核苷的碱基至少含有一个硫醇、硫酮或硫醚。
  • [EN] ALKYNE CONTAINING NUCLEOTIDE AND NUCLEOSIDE THERAPEUTIC COMPOSITIONS AND USES RELATED THERETO<br/>[FR] COMPOSITIONS THÉRAPEUTIQUES À BASE DE NUCLÉOTIDES ET NUCLÉOSIDES CONTENANT UN ALCYNE ET UTILISATIONS ASSOCIÉES
    申请人:UNIV EMORY
    公开号:WO2017189978A1
    公开(公告)日:2017-11-02
    This disclosure relates to nucleotide and nucleoside therapeutic compositions and uses in treating infectious diseases, viral infections, and cancer, where the base of the nucleotide or nucleoside contains at least one thiol, thione or thioether.
    这份披露涉及到核苷酸和核苷类治疗组合物,用于治疗传染病、病毒感染和癌症,其中核苷酸或核苷的碱基至少含有一个硫醇、硫酮或硫醚。
  • [EN] NUCLEOTIDE AND NUCLEOSIDE COMPOSITIONS AND USES RELATED THERETO<br/>[FR] COMPOSITIONS À BASE DE NUCLÉOTIDE ET DE NUCLÉOSIDE ET UTILISATIONS CORRESPONDANTES
    申请人:UNIV EMORY
    公开号:WO2015038596A1
    公开(公告)日:2015-03-19
    This disclosure relates to nucleotide and nucleoside therapeutic compositions and uses in treating infectious diseases, viral infections, and cancer, where the base of the nucleotide or nucleoside contains at least one thiol, thione or thioether.
    这份披露涉及到核苷酸和核苷类治疗组合物,用于治疗传染病、病毒感染和癌症,在这些组合物中,核苷酸或核苷的碱基至少含有一个硫醇、硫酮或硫醚。
  • [EN] NUCLEOTIDE AND NUCLEOSIDE THERAPEUTIC COMPOSITIONS AND USES RELATED THERETO<br/>[FR] COMPOSITIONS THÉRAPEUTIQUES RENFERMANT DES NUCLÉOTIDES ET DES NUCLÉOSIDES ET UTILISATIONS ASSOCIÉES
    申请人:UNIV EMORY
    公开号:WO2014124430A1
    公开(公告)日:2014-08-14
    This disclosure relates to nucleotide and nucleoside therapeutic compositions and uses related thereto. In certain embodiments, the disclosure relates to halogenated nucleosides optionally conjugated to a phosphorus oxide or pharmaceutically acceptable salts thereof. In certain embodiments, the disclosure relates to conjugate compounds or pharmaceutically acceptable salts thereof comprising an amino acid ester or a sphingolipid or derivative linked by a phosphorus oxide to a nucleotide or nucleoside. In certain embodiments, the disclosure contemplates pharmaceutical compositions comprising these compounds for uses in treating infectious diseases, viral infections, and cancer.
    这项披露涉及核苷酸和核苷类治疗组合物及其相关用途。在某些实施例中,该披露涉及卤代核苷,可选择地与磷氧化物或其药用可接受盐结合。在某些实施例中,该披露涉及结合物或其药用可接受盐,包括通过磷氧化物与核苷酸或核苷相连的氨基酸酯或鞘脂类或衍生物。在某些实施例中,该披露考虑了包括这些化合物的药用组合物,用于治疗传染病、病毒感染和癌症。
  • Novel synthetic C-glycolipids, their synthesis and use to treat infections, cancer and autoimmune diseases
    申请人:Tsuji Moriya
    公开号:US20050222048A1
    公开(公告)日:2005-10-06
    The invention is directed to novel compounds of formulae (I), (II) and (III): wherein X is O or NH; R 3 is OH or a monosaccharide and R 4 is hydrogen, or R 3 is hydrogen and R 4 is OH or a monosaccharide; R 5 is hydrogen or a monosaccharide; and pharmaceutically acceptable salts or esters thereof. The invention is also directed to the use of the compounds both directly and as immune adjuvants for treating cancer, infectious diseases and autoimmune diseases. The invention is also directed to syntheses of the intermediates which can be used to make these novel compounds.
    该发明涉及以下化合物的新颖化合物:其中X为O或NH;R3为OH或单糖,R4为氢,或R3为氢,R4为OH或单糖;R5为氢或单糖;以及其药用盐或酯。该发明还涉及这些化合物的直接使用以及作为免疫佐剂用于治疗癌症、传染病和自身免疫疾病。该发明还涉及合成这些中间体的方法,这些中间体可用于制备这些新颖化合物。
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