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epiandrosterone | 20120-08-5

中文名称
——
中文别名
——
英文名称
epiandrosterone
英文别名
d-Epiandrosterone;(3S,8R,9S,10S,13S,14S)-3-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one
epiandrosterone化学式
CAS
20120-08-5
化学式
C19H30O2
mdl
——
分子量
290.446
InChiKey
QGXBDMJGAMFCBF-QRIARFFBSA-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:
    177-179 °C(Solv: ethyl ether (60-29-7); benzene (71-43-2))
  • 沸点:
    413.1±45.0 °C(Predicted)
  • 密度:
    1.085±0.06 g/cm3(Predicted)
  • 物理描述:
    Solid
  • 溶解度:
    0.0202 mg/mL at 23 °C

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    21
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.95
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

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:
    epiandrosterone 在 Jones reagent 作用下, 生成 5a-雄甾烷二酮
    参考文献:
    名称:
    Hydroxylation of steroids by Fusarium oxysporum, Exophiala jeanselmei and Ceratocystis paradoxa
    摘要:
    The potential of Fusarium oxysporum var. cubense UAMH 9013 to perform steroid biotransformations was reinvestigated using single phase and pulse feed conditions. The following natural steroids served as substrates: dehydroepiandrosterone (1), pregnenolone (2), testosterone (3), progesterone (4), cortisone (5), prednisone (6), estrone (7) and sarsasapogenin (8). The results showed the possible presence of C-7 and C-15 hydroxylase enzymes. This hypothesis was explored using three synthetic androstanes: androstane-3,17-dione (9), androsta-4,6-diene-3,17-dione (10) and 3 alpha,5 alpha-cycloandrost-6-en-17-one (11). These fermentations of non-natural steroids showed that C-7 hydroxylation was as a result of that position being allylic. The evidence also pointed towards the presence of a C-15 hydroxylase enzyme.The eleven steroids were also fed to Exophiala jeanselmei var. lecanii-corni UAMH 8783. The results showed that the fungus appears to have very active 5 alpha and 14 alpha-hydroxylase enzymes, and is also capable of carrying out allylic oxidations.Ceratocystis paradoxa UAMH 8784 was grown in the presence of the above-mentioned steroids. The results showed that monooxygenases which effect allylic hydroxylation and Baeyer-Villiger rearrangement were active. However, redox reactions predominated. (C) 2011 Elsevier Inc. All rights reserved.
    DOI:
    10.1016/j.steroids.2011.06.010
  • 作为产物:
    描述:
    去氢表雄酮 在 palladium on activated charcoal 、 氢气 作用下, 生成 epiandrosterone
    参考文献:
    名称:
    Hydroxylation of steroids by Fusarium oxysporum, Exophiala jeanselmei and Ceratocystis paradoxa
    摘要:
    The potential of Fusarium oxysporum var. cubense UAMH 9013 to perform steroid biotransformations was reinvestigated using single phase and pulse feed conditions. The following natural steroids served as substrates: dehydroepiandrosterone (1), pregnenolone (2), testosterone (3), progesterone (4), cortisone (5), prednisone (6), estrone (7) and sarsasapogenin (8). The results showed the possible presence of C-7 and C-15 hydroxylase enzymes. This hypothesis was explored using three synthetic androstanes: androstane-3,17-dione (9), androsta-4,6-diene-3,17-dione (10) and 3 alpha,5 alpha-cycloandrost-6-en-17-one (11). These fermentations of non-natural steroids showed that C-7 hydroxylation was as a result of that position being allylic. The evidence also pointed towards the presence of a C-15 hydroxylase enzyme.The eleven steroids were also fed to Exophiala jeanselmei var. lecanii-corni UAMH 8783. The results showed that the fungus appears to have very active 5 alpha and 14 alpha-hydroxylase enzymes, and is also capable of carrying out allylic oxidations.Ceratocystis paradoxa UAMH 8784 was grown in the presence of the above-mentioned steroids. The results showed that monooxygenases which effect allylic hydroxylation and Baeyer-Villiger rearrangement were active. However, redox reactions predominated. (C) 2011 Elsevier Inc. All rights reserved.
    DOI:
    10.1016/j.steroids.2011.06.010
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文献信息

  • [EN] IMIDAZOLIUM REAGENT FOR MASS SPECTROMETRY<br/>[FR] RÉACTIF D'IMIDAZOLIUM POUR SPECTROMÉTRIE DE MASSE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2021234004A1
    公开(公告)日:2021-11-25
    The present invention relates to compounds which are suitable to be used in mass spectrometry as well as methods of mass spectrometric determination of analyte molecules using said compounds.
    本发明涉及适用于质谱的化合物,以及利用该化合物进行分析物分子的质谱测定方法。
  • [EN] EPIANDROSTERONE AND/OR ANDROSTERONE DERIVATIVES AND METHOD OF USE THEREOF<br/>[FR] DÉRIVÉS D'ÉPIANDROSTÉRONE ET/OU D'ANDROSTÉRONE ET LEUR PROCÉDÉ D'UTILISATION
    申请人:SUTTER WEST BAY HOSPITALS DOING BUSINESS AS CALIFORNIA PACIFIC MEDICAL CT
    公开号:WO2012134446A1
    公开(公告)日:2012-10-04
    Disclosed herein are epiandrosterone and androsterone derivatives of Formula (II), process of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.
    本文揭示了式(II)的雄烯酮和雄甾酮衍生物,其制备方法,药物组合物以及使用方法。
  • 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'-位置用酰胺基团取代的核糖核苷。在某些实施例中,酰胺基团是烷基酰胺基团。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硫酸酯二硫酸酯键替代。在一个首选实施例中,配体胆固醇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硫酸酯二硫酸酯键替代。在一个首选实施例中,配体胆固醇5β-胆烷酸配体改善了寡核苷酸的药代动力学性能。
  • [EN] PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS<br/>[FR] COMPOSÉS PHARMACEUTIQUES POUR LE TRAITEMENT DE TROUBLES MÉDIÉS PAR LE COMPLÉMENT
    申请人:ACHILLION PHARMACEUTICALS INC
    公开号:WO2020198062A1
    公开(公告)日:2020-10-01
    This disclosure provides pharmaceutical compounds to treat medical disorders, such as complement-mediated disorders, including complement Cl -mediated disorders.
    这份披露提供了用于治疗医学疾病的药物化合物,例如包括补体介导的疾病在内的补体Cl-介导的疾病。
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