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3β-(1,1-dimethylethoxy)-5-androsten-17-one | 1167-53-9

中文名称
——
中文别名
——
英文名称
3β-(1,1-dimethylethoxy)-5-androsten-17-one
英文别名
3β-tert-butoxyandrost-5-en-17-one;3β-t-butoxyandrost-5-ene-17-one;3β-t-Butoxyandrost-5-en-17-on;3beta-(1,1-Dimethylethoxy)-5-androsten-17-one;(3S,8R,9S,10R,13S,14S)-10,13-dimethyl-3-[(2-methylpropan-2-yl)oxy]-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-one
3β-(1,1-dimethylethoxy)-5-androsten-17-one化学式
CAS
1167-53-9
化学式
C23H36O2
mdl
——
分子量
344.538
InChiKey
XRQMGIQLKOIPKU-VYAQIDIUSA-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:
    174-179 °C
  • 沸点:
    438.8±45.0 °C(Predicted)
  • 密度:
    1.04±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.8
  • 重原子数:
    25
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.87
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 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
    醋酸去氢表雄酮 prasterone acetate 853-23-6 C21H30O3 330.467
    去氢表雄酮 dehydroepiandrosterone 53-43-0 C19H28O2 288.43
    16-脱氢孕烯醇酮乙酸酯 16-dehydropregnenolone acetate 979-02-2 C23H32O3 356.505
    —— 3β-tosyloxyandrost-5-ene-17-one 2719-96-2 C26H34O4S 442.62
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量
    —— 3β-t-Butoxy-18-carbonitrilpregn-5-en-20-on —— C26H39NO2 397.601
    —— 3β-t-Butoxy-20-carbonitrilpregn-5-en 62623-47-6 C26H41NO 383.618
    —— 3β-t-Butoxy-20-carbonitril-20-peracetoxypregn-5-en 62623-48-7 C28H43NO4 457.654

反应信息

  • 作为反应物:
    参考文献:
    名称:
    α-过乙酰氧基腈的光解。2.1两种合成方法对18-氰基-20-酮类固醇的比较。
    摘要:
    DOI:
    10.1021/ja00447a041
  • 作为产物:
    描述:
    醋酸去氢表雄酮吡啶 、 potassium hydroxide 作用下, 以 甲醇 为溶剂, 反应 8.0h, 生成 3β-(1,1-dimethylethoxy)-5-androsten-17-one
    参考文献:
    名称:
    Synthesis, antiproliferative activity, acute toxicity and assessment of the antiandrogenic activities of new androstane derivatives
    摘要:
    以市售的(25R)-5-螺烯-3β-醇(薯蓣皂苷)(4)为起始原料,合成了一些 17-氧代-5-雄烯-3β-基酯(9a-9f)和 3β-烷氧基-5-雄烯-17-酮(11a-11e)。评估了合成化合物对前列腺癌细胞株 DU-145 的抗增殖活性、急性毒性和对血清雄激素水平的影响,并与作为阳性对照的非那雄胺进行了比较。其中一些化合物的细胞毒性和抗雄激素活性优于阳性对照。报告了合成化合物的详细合成、光谱数据和生物活性。
    DOI:
    10.1007/s12272-011-0702-2
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文献信息

  • Blood cell deficiency treatment method
    申请人:——
    公开号:US20030083231A1
    公开(公告)日:2003-05-01
    The invention relates to the use of compounds to treat a number of conditions, such as thrombocytopenia, neutropenia or the delayed effects of radiation therapy. Compounds that can be used in the invention include methyl-2,3,4-trihydroxy-1-O-(7,17-dioxoandrost-5-ene-3&bgr;-yl)-&bgr;-D-glucopyranosiduronate, 16&agr;,3&agr;-dihydroxy-5&agr;-androstan-17-one or 3,7,16,17-tetrahydroxyandrost-5-ene, 3,7,16,17-tetrahydroxyandrost-4-ene,3,7,16,17-tetrahydroxyandrost-1-ene or 3,7,16,17-tetrahydroxyandrostane that can be used in the treatment method.
    该发明涉及使用化合物治疗多种疾病,如血小板减少症、中性粒细胞减少症或放疗延迟效应。可以用于该发明的化合物包括甲基-2,3,4-三羟基-1-O-(7,17-二氧代雄烯-3β-基)-β-D-葡糖吡喃糖醛酸酯、16α,3α-二羟基-5α-雄甾酮-17-酮或3,7,16,17-四羟基雄烷-5-烯、3,7,16,17-四羟基雄烷-4-烯、3,7,16,17-四羟基雄烷-1-烯或3,7,16,17-四羟基雄烷可用于治疗方法中。
  • Compositions and treatment methods
    申请人:Ahlem N. Clarence
    公开号:US20060079492A1
    公开(公告)日:2006-04-13
    The invention relates to the use of compounds to treat a number of conditions, such as thrombocytopenia, neutropenia or the delayed effects of radiation therapy. Compounds that can be used in the invention include methyl-2,3,4-trihydroxy-1-O-(7,17-dioxoandrost-5-ene-3β-yl)-β-D-glucopyranosiduronate, 16α,3α-dihydroxy-5α-androstan-17-one or 3,7,16,17-tetrahydroxyandrost-5-ene, 3,7,16,17-tetrahydroxyandrost-4-ene, 3,7,16,17-tetrahydroxyandrost-1-ene or 3,7,16,17-tetrahydroxyandrostane that can be used in the treatment method.
    本发明涉及使用化合物治疗多种疾病,例如血小板减少症、中性粒细胞减少症或放射治疗的延迟影响。可用于本发明的化合物包括甲基-2,3,4-三羟基-1-O-(7,17-二氧代雄烯-5-烯-3β-基)-β-D-葡萄糖吡喃糖醇酸酯、16α,3α-二羟基-5α-雄甾烷-17-酮或3,7,16,17-四羟基雄烯-5-烯、3,7,16,17-四羟基雄烯-4-烯、3,7,16,17-四羟基雄烯-1-烯或3,7,16,17-四羟基雄甾烷可用于治疗方法。
  • COMPOSITIONS AND TREATMENT METHODS-2
    申请人:Frincke James M.
    公开号:US20100222425A1
    公开(公告)日:2010-09-02
    The invention relates to the use of compounds to treat a number of conditions, such as thrombocytopenia, neutropenia or the delayed effects of radiation therapy. Compounds that can be used in the invention include methyl-2,3,4-trihydroxy-1-O-(7,17-dioxoandrost-5-ene-3β-yl)-β-D-glucopyranosiduronate, 16α,3α-dihydroxy-5α-androstan-17-one or 3,7,16,17-tetrahydroxyandrost-5-ene, 3,7,16,17-tetrahydroxyandrost-4-ene, 3,7,16,17-tetrahydroxyandrost-1-ene or 3,7,16,17-tetrahydroxyandrostane that can be used in the treatment method.
    本发明涉及使用化合物治疗多种疾病,例如血小板减少症、中性粒细胞减少症或放射治疗的延迟影响。可以在本发明中使用的化合物包括甲基-2,3,4-三羟基-1-O-(7,17-二氧代雄烯-5-烯-3β-基)-β-D-葡萄糖吡喃糖醇酸酯、16α,3α-二羟基-5α-雄甾烷-17-酮或3,7,16,17-四羟基雄烯-5-烯、3,7,16,17-四羟基雄烯-4-烯、3,7,16,17-四羟基雄烯-1-烯或3,7,16,17-四羟基雄烷。这些化合物可以用于治疗方法中。
  • 15-THIA STEROID COMPOUNDS AND COMPOSITIONS
    申请人:Frincke James M.
    公开号:US20110218162A1
    公开(公告)日:2011-09-08
    The invention relates to the use of compounds to treat a number of conditions, such as thrombocytopenia, neutropenia or the delayed effects of radiation therapy. Compounds that can be used in the invention include methyl-2,3,4-trihydroxy-1-O-(7,17-dioxoandrost-5-ene-3β-yl)-β-D-glucopyranosiduronate, 16α,3α-dihydroxy-5α-androstan-17-one or 3,7,16,17-tetrahydroxyandrost-5-ene, 3,7,16,17-tetrahydroxyandrost-4-ene, 3,7,16,17-tetrahydroxyandrost-1-ene or 3,7,16,17-tetrahydroxyandrostane that can be used in the treatment method.
    本发明涉及使用化合物治疗多种疾病,例如血小板减少症、中性粒细胞减少症或放射治疗的延迟效应。可用于本发明的化合物包括甲基-2,3,4-三羟基-1-O-(7,17-二氧代雄烯-5-烯-3β-基)-β-D-葡萄糖吡喃糖醇、16α,3α-二羟基-5α-雄甾酮-17-酮或3,7,16,17-四羟基雄烯-5-烯、3,7,16,17-四羟基雄烯-4-烯、3,7,16,17-四羟基雄烯-1-烯或3,7,16,17-四羟基雄烷,可用于治疗方法。
  • Pregn-5-en-20-yne-3,7,17-triol derivatives for use in therapy
    申请人:Hollis-Eden Pharmaceuticals Inc.
    公开号:EP2135611A1
    公开(公告)日:2009-12-23
    The invention relates to the use of compounds to treat a number of conditions, such as thrombocytopenia, neutropenia or the delayed effects of radiation therapy. Compounds that can be used in the invention include methyl-2,3,4-trihydroxy-1-O-(7,17-dioxoandrost-5-ene-3β-yl)-β-D-glucopyranosiduronate.
    本发明涉及使用化合物治疗多种疾病,如血小板减少症、中性粒细胞减少症或放射治疗的延迟效应。可用于本发明的化合物包括 2,3,4-三羟基-1-O-(7,17-二氧代雄甾烷-5-烯-3β-基)-β-D-吡喃葡萄糖苷酸甲酯。
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