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lonaprisan | 211254-73-8

中文名称
——
中文别名
——
英文名称
lonaprisan
英文别名
11β-(4-acetylphenyl)-17β-hydroxy-17α-(1,1,2,2,2-pentafluoroethyl)-estra-4,9-dien-3-one;(8S,11R,13S,14S,17S)-11-(4-acetylphenyl)-17-hydroxy-13-methyl-17-(1,1,2,2,2-pentafluoroethyl)-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one
lonaprisan化学式
CAS
211254-73-8
化学式
C28H29F5O3
mdl
——
分子量
508.528
InChiKey
VHZPUDNSVGRVMB-RXDLHWJPSA-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:
    601.0±55.0 °C(Predicted)
  • 密度:
    1.34±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.5
  • 重原子数:
    36
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    54.4
  • 氢给体数:
    1
  • 氢受体数:
    8

SDS

SDS:cdbb94d51dc3608a2a2c780f41cfa3da
查看

反应信息

  • 作为反应物:
    描述:
    甲醇lonaprisan 生成 11β-(4-acetylphenyl)-20,20,21,21,21-pentafluoro-17-hydroxy-19-nor-17α-pregna-4,9-dien-3-one methanol solvate
    参考文献:
    名称:
    CRYSTALLINE FORMS OF 11SS-(4-ACETYLPHENYL)-20,20,21,21,21-PENTAFLUORO-17-HYDROXY-19-NOR-17A-PREGNA-4,9-DIEN-3-ONE
    摘要:
    本发明涉及11β-(4-乙酰基苯基)-20,20,21,21,21-五氟-17-羟基-19-去-17α-孕-4,9-二烯-3-酮的晶体形式。本发明特别涉及该化合物的两种晶体无溶剂型/无水型多晶形态,即I型和II型。然而,本发明还涉及该化合物的晶体溶剂型,例如11β-(4-乙酰基苯基)-20,20,21,21,21-五氟-17-羟基-19-去-17α-孕-4,9-二烯-3-酮的甲醇和乙醇溶剂型,作为制备这两种I型和II型多晶形态的前体。本发明还描述了通过置换结晶或研磨法制备I型的过程。在形成无溶剂型之前选择最后的溶剂可以基于11β-(4-乙酰基苯基)-20,20,21,21,21-五氟-17-羟基-19-去-17α-孕-4,9-二烯-3-酮的各个溶剂型的纯化行为的差异。本发明的I型多晶形态特别适用于制造药品。
    公开号:
    US20080085875A1
  • 作为产物:
    描述:
    11β-(4-acetylphenyl)-20,20,21,21,21-pentafluoro-17-hydroxy-19-nor-17α-pregna-4,9-dien-3-one methanol solvate 以 为溶剂, 反应 4.6h, 生成 lonaprisan
    参考文献:
    名称:
    CRYSTALLINE FORMS OF 11SS-(4-ACETYLPHENYL)-20,20,21,21,21-PENTAFLUORO-17-HYDROXY-19-NOR-17A-PREGNA-4,9-DIEN-3-ONE
    摘要:
    本发明涉及11β-(4-乙酰基苯基)-20,20,21,21,21-五氟-17-羟基-19-去-17α-孕-4,9-二烯-3-酮的晶体形式。本发明特别涉及该化合物的两种晶体无溶剂型/无水型多晶形态,即I型和II型。然而,本发明还涉及该化合物的晶体溶剂型,例如11β-(4-乙酰基苯基)-20,20,21,21,21-五氟-17-羟基-19-去-17α-孕-4,9-二烯-3-酮的甲醇和乙醇溶剂型,作为制备这两种I型和II型多晶形态的前体。本发明还描述了通过置换结晶或研磨法制备I型的过程。在形成无溶剂型之前选择最后的溶剂可以基于11β-(4-乙酰基苯基)-20,20,21,21,21-五氟-17-羟基-19-去-17α-孕-4,9-二烯-3-酮的各个溶剂型的纯化行为的差异。本发明的I型多晶形态特别适用于制造药品。
    公开号:
    US20080085875A1
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文献信息

  • 6,7-Dihydro-5H-benzo[7]annulene derivatives, processes for their preparation, pharmaceutical products comprising them and their use for preparing medicaments
    申请人:Bayer Intellectual Property GmbH
    公开号:US20150080438A1
    公开(公告)日:2015-03-19
    The invention relates to selective oestrogen receptor modulators (SERMs) and to processes for their preparation, to their use for the treatment and/or prophylaxis of diseases and to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular of bleeding disorders, osteoporosis, endometriosis, myomata, hormone-dependent tumours, for hormone replacement therapy and for contraception.
    该发明涉及选择性雌激素受体调节剂(SERMs),以及它们的制备方法,它们用于治疗和/或预防疾病的用途,以及它们用于制备用于治疗和/或预防疾病的药物,特别是用于治疗出血障碍、骨质疏松症、子宫内膜异位症、子宫肌瘤、激素依赖性肿瘤、激素替代疗法和避孕的用途。
  • 6,7-DIHYDRO-5H-BENZO[7]ANNULENE DERIVATIVES, PROCESS FOR PREPARATION THEREOF, PHARMACEUTICAL PREPARATIONS COMPRISING THEM, AND THE USE THEREOF FOR PRODUCTION OF MEDICAMENTS
    申请人:Wintermantel Tim
    公开号:US20130252890A1
    公开(公告)日:2013-09-26
    The invention relates to selective oestrogen receptor modulators (SERM) and methods of production thereof, use thereof for the treatment and/or prophylaxis of diseases and use thereof for the production of medicinal products for the treatment and/or prophylaxis of diseases, in particular of bleeding disorders, osteoporosis, endometriosis, myomata, hormone-dependent tumours, for hormone replacement therapy and for contraception.
    该发明涉及选择性雌激素受体调节剂(SERM)及其生产方法,以及将其用于治疗和/或预防疾病以及将其用于生产用于治疗和/或预防疾病的药物产品,特别是用于出血性疾病、骨质疏松症、子宫内膜异位症、子宫肌瘤、激素依赖性肿瘤、激素替代疗法和避孕。
  • 17-HYDROXY-17-PENTAFLUORETHYL-ESTRA-4,9(10)-DIEN-11-ARYL DERIVATIVES, METHODS FOR THE PRODUCTION THEREOF AND THE USE THEREOF FOR TREATING DISEASES
    申请人:Klar Ulrich
    公开号:US20120258941A1
    公开(公告)日:2012-10-11
    The invention relates to 17-hydroxy-17-pentafluoroethylestra-4,9(10)-diene 11-aryl derivatives of the formula I with progesterone-antagonising action and to processes for preparation thereof, to use thereof for treatment and/or prophylaxis of disorders and to the use thereof for production of medicaments for treatment and/or prophylaxis of disorders, especially of fibroids of the uterus (myomas, uterine leiomyomas), endometriosis, heavy menstrual bleeds, meningiomas, hormone-dependent breast cancers and complaints associated with the menopause, or for fertility control and emergency contraception.
    该发明涉及具有孕酮拮抗作用的式I的17-羟基-17-五氟乙基雌二烯-4,9(10)-二烯-11-芳基衍生物,以及其制备方法,用于治疗和/或预防疾病的用途,以及用于制备治疗和/或预防疾病的药物,特别是用于子宫纤维瘤(子宫肌瘤、子宫平滑肌瘤)、子宫内膜异位症、月经过多、脑膜瘤、激素依赖性乳腺癌和与绝经期相关的不适症状,或用于生育控制和紧急避孕。
  • [EN] AMIDO COMPOUNDS AND THEIR USE AS PHARMACEUTICALS<br/>[FR] COMPOSÉS AMIDO ET LEUR UTILISATION COMME PRODUITS PHARMACEUTIQUES
    申请人:INCYTE CORP
    公开号:WO2005110992A1
    公开(公告)日:2005-11-24
    The present invention relates to inhibitors of 11-ß hydroxyl steroid dehydrogenase type 1, antagonists of the mineralocorticoid receptor (MR), and pharmaceutical compositions thereof. The compounds of the invention can be useful in the treatment of various diseases associated with expression or activity of 11-ß hydroxyl steroid dehydrogenase type 1 and/or diseases associated with aldosterone excess.
    本发明涉及11-ß羟基类固醇脱氢酶类型1的抑制剂、矿皮质激素受体(MR)拮抗剂以及其药物组合物。该发明的化合物可用于治疗与11-ß羟基类固醇脱氢酶类型1的表达或活性以及醛固酮过量相关的各种疾病。
  • PROGESTERONE RECEPTOR ANTAGONISTS
    申请人:Schwede Wolfgang
    公开号:US20130072464A1
    公开(公告)日:2013-03-21
    The invention relates to 17-hydroxy-17-pentafluoroethyl-estra-4,9(10)-dien-11-aryl derivatives of formula I with progesterone-antagonizing action and methods of production thereof, use thereof for the treatment and/or prevention of diseases and use thereof for producing medicinal products for the treatment and/or prevention of diseases, in particular uterine fibroids (myomata, uterine leiomyomata), endometriosis, heavy menstrual bleeding, meningiomata, hormone-dependent breast cancers and menopause-associated complaints or for fertility control and emergency contraception.
    该发明涉及公式I的17-羟基-17-五氟乙基-雌甾-4,9(10)-二烯-11-芳基衍生物,具有孕酮拮抗作用及其生产方法,用于治疗和/或预防疾病以及用于生产用于治疗和/或预防疾病的药品,特别是子宫肌瘤(肌瘤、子宫平滑肌瘤)、子宫内膜异位症、月经过多、脑膜瘤、激素依赖性乳腺癌和更年期相关的不适或用于生育控制和紧急避孕。
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