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cedrelone | 1254-85-9

中文名称
——
中文别名
——
英文名称
cedrelone
英文别名
Cedrelon;(1R,2R,4R,6S,7S,10R,11R)-6-(furan-3-yl)-17-hydroxy-1,7,11,15,15-pentamethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadeca-12,16-diene-14,18-dione
cedrelone化学式
CAS
1254-85-9
化学式
C26H30O5
mdl
——
分子量
422.521
InChiKey
OQMUOVSEPOBWMK-BWLMZZBKSA-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

  • 熔点:
    204 °C
  • 沸点:
    584.2±50.0 °C(Predicted)
  • 密度:
    1.30±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    31
  • 可旋转键数:
    1
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    80
  • 氢给体数:
    1
  • 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

反应信息

  • 作为反应物:
    描述:
    cedrelone 为溶剂, 反应 6.0h, 以30%的产率得到14β,15β,22β,23β-diepoxy-6-hydroxy-1,5,20(22)-meliatriene-2,7,21-trione
    参考文献:
    名称:
    Cedrelone 的光氧化,来自香椿的四萜类化合物¶
    摘要:
    摘要 Cedrelone 是一种四降三萜类化合物,通过紫外线光解产生真正的光氧化产物 3 [14 β,15β,22β,23β-diepoxy-6-hydroxy-1,5,20(22)-meliatriene-2,7,21-trione ] 其结构已通过 NMR 研究确定并通过 X 射线晶体学证实,以及产物 4 [14 β,15β-epoxy-6,23-dihydroxy-1,5,20(22)-meliatriene-2,7, 21-trione]。添加玫瑰红会增加光氧化速率,而 DABCO 会降低光解速率,证明单线态氧参与了光氧化。两种光产品都表现出拒食活性。
    DOI:
    10.1562/0031-8655(2000)072<0464:pocatf>2.0.co;2
  • 作为产物:
    描述:
    Cedrelon-acetat乙二胺 作用下, 以 甲醇 为溶剂, 反应 0.08h, 以82%的产率得到cedrelone
    参考文献:
    名称:
    Ethylenediamine: an effective reagent for deacetylation of natural products
    摘要:
    The use of ethylenediamine in methanol is described for the selective cleavage of the acetate group in nimbin (1) to 6-deacetyl nimbin (1a) under microwave irradiation. This method enables to deacetylate without affecting other functional groups such as ,-unsaturated ketone, ester, ether, etc. in certain tetranortriterpenoids and other acetate-containing natural compounds.
    DOI:
    10.1080/10286020.2010.507545
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文献信息

  • Oligonucleotides comprising a non-phosphate backbone linkage
    申请人:Manoharan Muthiah
    公开号:US20060287260A1
    公开(公告)日:2006-12-21
    One aspect of the present invention relates to a ribonucleoside substituted with a phosphonamidite group at the 3′-position. In certain embodiments, the phosphonamidite is an alkyl phosphonamidite. Another aspect of the present invention relates to a double-stranded oligonucleotide comprising at least one non-phosphate linkage. Representative non-phosphate linkages include phosphonate, hydroxylamine, hydroxylhydrazinyl, amide, and carbamate linkages. In certain embodiments, the non-phosphate linkage is a phosphonate linkage. In certain embodiments, a non-phosphate linkage occurs in only one strand. In certain embodiments, a non-phosphate linkage occurs in both strands. In certain embodiments, a ligand is bound to one of the oligonucleotide strands comprising the double-stranded oligonucleotide. In certain embodiments, a ligand is bound to both of the oligonucleotide strands comprising the double-stranded oligonucleotide. In certain embodiments, the oligonucleotide strands comprise at least one modified sugar moiety. Another aspect of the present invention relates to a single-stranded oligonucleotide comprising at least one non-phosphate linkage. Representative non-phosphate linkages include phosphonate, hydroxylamine, hydroxylhydrazinyl, amide, and carbamate linkages. In certain embodiments, the non-phosphate linkage is a phosphonate linkage. In certain embodiments, a ligand is bound to the oligonucleotide strand. In certain embodiments, the oligonucleotide comprises at least one modified sugar moiety.
    本发明的一个方面涉及在3'-位置用磷酰胺基团取代的核糖核苷。在某些实施例中,磷酰胺基团是烷基磷酰胺基团。本发明的另一个方面涉及包含至少一个非磷酸酯连接的双链寡核苷酸。代表性的非磷酸酯连接包括磷酸酯、羟胺、羟基肼基、酰胺和碳酸酯连接。在某些实施例中,非磷酸酯连接是磷酸酯连接。在某些实施例中,非磷酸酯连接仅出现在一条链中。在某些实施例中,非磷酸酯连接出现在两条链中。在某些实施例中,配体结合到包含双链寡核苷酸的寡核苷酸链中的一条链上。在某些实施例中,配体结合到包含双链寡核苷酸的寡核苷酸链中的两条链上。在某些实施例中,寡核苷酸链包含至少一个修饰的糖基团。本发明的另一个方面涉及包含至少一个非磷酸酯连接的单链寡核苷酸。代表性的非磷酸酯连接包括磷酸酯、羟胺、羟基肼基、酰胺和碳酸酯连接。在某些实施例中,非磷酸酯连接是磷酸酯连接。在某些实施例中,配体结合到寡核苷酸链上。在某些实施例中,寡核苷酸包含至少一个修饰的糖基团。
  • Oligonucleotides comprising a C5-modified pyrimidine
    申请人:Manoharan Muthiah
    公开号:US20050288244A1
    公开(公告)日:2005-12-29
    One aspect of the present invention relates to a double-stranded oligonucleotide comprising at least one ligand. In certain embodiments, a ligand is bound to only one of the two oligonucleotide strands comprising the double-stranded oligonucleotide. In certain embodiments, both of the oligonucleotide strands of the double-stranded oligonucleotide independently comprise a bound ligand. In certain embodiments, the oligonucleotide strands comprise at least one modified sugar moiety. In certain embodiments, a phosphate linkage in one or both of the strands of the oligonucleotide has been replaced with a phosphorothioate or phosphorodithioate linkage. In a preferred embodiment, the ligand is cholesterol or 5β-cholanic acid. Another aspect of the present invention relates to a single-stranded oligonucleotide comprising at least one ligand. In certain embodiments, the oligonucleotide comprises at least one modified sugar moiety. In certain embodiments, a phosphate linkage of the oligonucleotide has been replaced with a phosphorothioate or phosphorodithioate linkage. In a preferred embodiment, the ligand is cholesterol or 5β-cholanic acid. The ligand improves the pharmacokinetic properties of the oligonucleotide.
    本发明的一个方面涉及包含至少一个配体的双链寡核苷酸。在某些实施例中,配体仅结合到构成双链寡核苷酸的两个核苷酸链中的一个。在某些实施例中,双链寡核苷酸的两个核苷酸链都独立地包含一个结合的配体。在某些实施例中,核苷酸链包含至少一个修饰的糖基。在某些实施例中,核苷酸链的一个或两个链中的磷酸酯键已被磷硫酸酯或磷二硫酸酯键替代。在一个首选实施例中,配体是胆固醇或5β-胆烷酸。本发明的另一个方面涉及包含至少一个配体的单链寡核苷酸。在某些实施例中,核苷酸包含至少一个修饰的糖基。在某些实施例中,核苷酸的磷酸酯键已被磷硫酸酯或磷二硫酸酯键替代。在一个首选实施例中,配体是胆固醇或5β-胆烷酸。配体改善了寡核苷酸的药代动力学性能。
  • [EN] METHODS AND COMPOSITIONS FOR TREATING CANCER<br/>[FR] MÉTHODES ET COMPOSITIONS POUR LE TRAITEMENT DU CANCER
    申请人:UNIV HEALTH NETWORK
    公开号:WO2015051447A1
    公开(公告)日:2015-04-16
    A compound of Formula I and/or II and/or a composition comprising a compound of Formula I and/or II is described as well as uses of said compounds and compositions for inhibiting microtubule polymerization, inducing lysosome disruption and/or treating a cancer, including a hematological cancer such as leukemia.
    本文描述了一种由式I和/或II的化合物和/或包含式I和/或II的组合物组成的化合物,以及所述化合物和组合物用于抑制微管聚合、诱导溶酶体破裂和/或治疗癌症的用途,包括像白血病这样的血液系统癌症。
  • OLIGONUCLEOTIDES COMPRISING A NON-PHOSPHATE BACKBONE LINKAGE
    申请人:MANOHARAN MUTHIAH
    公开号:US20090281299A1
    公开(公告)日:2009-11-12
    One aspect of the present invention relates to a ribonucleoside substituted with a phosphonamidite group at the 3′-position. In certain embodiments, the phosphonamidite is an alkyl phosphonamidite. Another aspect of the present invention relates to a double-stranded oligonucleotide comprising at least one non-phosphate linkage. Representative non-phosphate linkages include phosphonate, hydroxylamine, hydroxylhydrazinyl, amide, and carbamate linkages. In certain embodiments, the non-phosphate linkage is a phosphonate linkage. In certain embodiments, a non-phosphate linkage occurs in only one strand. In certain embodiments, a non-phosphate linkage occurs in both strands. In certain embodiments, a ligand is bound to one of the oligonucleotide strands comprising the double-stranded oligonucleotide. In certain embodiments, a ligand is bound to both of the oligonucleotide strands comprising the double-stranded oligonucleotide. In certain embodiments, the oligonucleotide strands comprise at least one modified sugar moiety. Another aspect of the present invention relates to a single-stranded oligonucleotide comprising at least one non-phosphate linkage. Representative non-phosphate linkages include phosphonate, hydroxylamine, hydroxylhydrazinyl, amide, and carbamate linkages. In certain embodiments, the non-phosphate linkage is a phosphonate linkage. In certain embodiments, a ligand is bound to the oligonucleotide strand. In certain embodiments, the oligonucleotide comprises at least one modified sugar moiety.
    本发明的一个方面涉及到一种在3'-位点上用磷酰胺基取代的核糖核苷。在某些实施例中,磷酰胺基是一种烷基磷酰胺基。本发明的另一个方面涉及到至少含有一种非磷酸酯连接的双链寡核苷酸。代表性的非磷酸酯连接包括磷酸酯、羟胺、羟基肼、酰胺和氨基甲酸酯连接。在某些实施例中,非磷酸酯连接是磷酸酯连接。在某些实施例中,非磷酸酯连接仅出现在一个链上。在某些实施例中,非磷酸酯连接出现在两个链上。在某些实施例中,配体与包含双链寡核苷酸的寡核苷酸链的其中一个链结合。在某些实施例中,配体与包含双链寡核苷酸的寡核苷酸链的两个链都结合。在某些实施例中,寡核苷酸链包括至少一个修饰的糖基团。本发明的另一个方面涉及到至少含有一种非磷酸酯连接的单链寡核苷酸。代表性的非磷酸酯连接包括磷酸酯、羟胺、羟基肼、酰胺和氨基甲酸酯连接。在某些实施例中,非磷酸酯连接是磷酸酯连接。在某些实施例中,配体与寡核苷酸链结合。在某些实施例中,寡核苷酸包括至少一个修饰的糖基团。
  • Oligonucleotides comprising a ligand tethered to a modified or non-natural nucleobase
    申请人:Manoharan Muthiah
    公开号:US20070054279A1
    公开(公告)日:2007-03-08
    One aspect of the present invention relates to a double-stranded oligonucleotide comprising at least one ligand tethered to an altered or non-natural nucleobase. In certain embodiments, the non-natural nucleobase is difluorotolyl, nitropyrrolyl, or nitroimidazolyl. In certain embodiments, the ligand is a steroid or aromatic compound. In certain embodiments, only one of the two oligonucleotide strands comprising the double-stranded oligonucleotide contains a ligand tethered to an altered or non-natural nucleobase. In certain embodiments, both of the oligonucleotide strands comprising the double-stranded oligonucleotide independently contain a ligand tethered to an altered or non-natural nucleobase. In certain embodiments, the oligonucleotide strands comprise at least one modified sugar moiety. Another aspect of the present invention relates to a single-stranded oligonucleotide comprising at least one ligand tethered to an altered or non-natural nucleobase. In certain embodiments, the non-natural nucleobase is difluorotolyl, nitropyrrolyl, or nitroimidazolyl. In certain embodiments, the ligand is a steroid or aromatic compound. In certain embodiments, the ribose sugar moiety that occurs naturally in nucleosides is replaced with a hexose sugar, polycyclic heteroalkyl ring, or cyclohexenyl group. In certain embodiments, at least one phosphate linkage in the oligonucleotide has been replaced with a phosphorothioate linkage.
    本发明的一个方面涉及一种双链寡核苷酸,其中至少一个配体被系在改变或非天然核碱基上。在某些实施例中,非天然核碱基是二氟基甲苯基、硝基吡咯基或硝基咪唑基。在某些实施例中,配体是类固醇或芳香化合物。在某些实施例中,只有双链寡核苷酸中的两个寡核苷酸链之一包含系在改变或非天然核碱基上的配体。在某些实施例中,双链寡核苷酸中的两个寡核苷酸链都独立地包含系在改变或非天然核碱基上的配体。在某些实施例中,寡核苷酸链包括至少一个修饰糖基。本发明的另一个方面涉及一种单链寡核苷酸,其中至少一个配体被系在改变或非天然核碱基上。在某些实施例中,非天然核碱基是二氟基甲苯基、硝基吡咯基或硝基咪唑基。在某些实施例中,配体是类固醇或芳香化合物。在某些实施例中,核苷酸中自然存在的核苷糖被替换为六糖、多环杂基烷基环或环己烯基团。在某些实施例中,寡核苷酸中至少一个磷酸酯键被磷酸硫酯键所替代。
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