3-(1-benzothiophen-3-yl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid | 1236271-20-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 芴
• 英文名称: 3-(1-benzothiophen-3-yl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid
• CAS: 1236271-20-7
• 化学式: C₂₆H₂₁NO₄S
• 分子量: 443.5
• InChiKey: BQIZNDWONIMCGM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  32
• 可旋转键数：
  7
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  104
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  3-(1-benzothiophen-3-yl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid 、 {2-Amino-3-[2-(1-carbamoyl-2-naphthalen-2-yl-ethylcarbamoyl)-piperidin-1-yl]-3-oxo-propylsulfanylmethyl}-phosphonic acid 、 亚磷酸二乙酯 生成 {2-(2-Acetylamino-3-benzo[b]thiophen-3-yl-propionylamino)-3-[2-(1-carbamoyl-2-naphthalen-2-yl-ethylcarbamoyl)-piperidin-1-yl]-3-oxo-propylsulfanylmethyl}-phosphonic acid
  参考文献：
  名称：

  Compounds For the Inhibition of Undesired Cell Proliferation and Use Thereof

  摘要：

  本发明涉及具有式（I）的化合物，其中虚线表示单键或双键或不存在，A1-A9，Q，R1-R11，T，U，V，W1-W3，X1，X2，Y和Z如权利要求和说明书所定义，包括该化合物的制药组合物和用于制造治疗涉及异常细胞增殖、不良细胞增殖、异常有丝分裂和/或不良有丝分裂疾病药物的化合物的用途。

  公开号：

  US20080194524A1

文献信息

• Arylmethylene substituted N-acyl-beta-amino alcohols
  申请人：Bayer Schering Pharma Aktiengesellschaft

  公开号：EP2018859A1

  公开（公告）日：2009-01-28

  The present invention relates to arylmethylene substituted N-Acyl-β-amino alcohols of the formula I in which Y is selected from the aryl or heteroaryl groups: and R1, R2, R3, R4, R5, Q, X and W have the meaning as defined in the description. The compounds according to the invention are effective FSH antagonists and can be used for example for fertility control in men or in women, or for the prevention and/or treatment of osteoporosis.

  本发明涉及式I的芳基亚甲基取代的N-酰基-β-氨基醇 其中 Y 从芳基或杂芳基中选择: 和 R1、R2、R3、R4、R5、Q、X和W的含义如描述中所定义。 根据本发明的化合物是有效的FSH拮抗剂，例如可用于男性或女性的生育控制，或用于骨质疏松症的预防和/或治疗。
• [EN] COMPOUNDS FOR THE INHIBITION OF UNDESIRED CELL PROLIFERATION AND USE THEREOF<br/>[FR] COMPOSES POUR L'INHIBITION DE LA PROLIFERATION CELLULAIRE INDESIRABLE ET LEUR UTILISATION
  申请人：JERINI AG

  公开号：WO2005063259A1

  公开（公告）日：2005-07-14

  The present invention is related to compounds having formula (I), wherein the dashed line indicates a single or double bond or is absent and wherein A1-A9, Q, R1-R11, T, U, V, W1-W3, X1, X2, Y and Z are as defined in the claims and description, pharmaceutical compositions comprising the compounds and the use of the compounds for the manufacture of a medicament for the treatment of deseases involving abnormal cell proliferation, undesired cell proliferation, abnormal mitosis and/or undesired mitosis.

  本发明涉及具有式（I）的化合物，其中虚线表示单键或双键或不存在，A1-A9、Q、R1-R11、T、U、V、W1-W3、X1、X2、Y和Z的定义如权利要求和描述中所定义，包括这些化合物的药物组合物以及利用这些化合物制备用于治疗涉及异常细胞增殖、不良细胞增殖、异常有丝分裂和/或不良有丝分裂的药物的用途。
• Identification of Compounds Modifying A Cellular Response
  申请人：Thastrup Ole

  公开号：US20090239755A1

  公开（公告）日：2009-09-24

  The present invention relates to methods for identifying compounds capable of modulating a cellular response. The methods involve attaching living cells to solid supports comprising a library of test compounds. The test compounds are linked to the solid support via cleavable linkers and may thus be released from the solid supports. Solid supports comprising cells, wherein the cellular response of interest has been modulated are selected and the test compound of the solid support can then be identified. The cellular response may for example be changes in complex formation between proteins.

  本发明涉及识别能够调节细胞反应的化合物的方法。该方法涉及将活细胞附着在包含测试化合物库的固体支撑体上。测试化合物通过可切割的连接剂与固体支撑体连接，因此可以从固体支撑体释放出来。选择细胞被固体支撑体调节了感兴趣的细胞反应的固体支撑体，并且可以鉴定固体支撑体上的测试化合物。细胞反应可以是蛋白质复合物形成的变化，例如。
• Arylmethylene Substituted N-Acyl-Beta-Amino Alcohols
  申请人：WORTMANN Lars

  公开号：US20090082372A1

  公开（公告）日：2009-03-26

  The present invention relates to arylmethylene substituted N-Acyl-β-amino alcohols of the formula I in which Y is selected from the aryl or heteroaryl groups: and R1, R2, R3, R4, R5, Q, X and W have the meaning as defined in the description. The compounds according to the invention are effective FSH antagonists and can be used for example for fertility control in men or in women, or for the prevention and/or treatment of osteoporosis.

  本发明涉及公式I的芳基亚甲基取代的N-酰基-β-氨基醇化合物，其中Y选自芳基或杂芳基基团：R1，R2，R3，R4，R5，Q，X和W的含义如描述中所定义。本发明的化合物是有效的FSH拮抗剂，例如可用于男性或女性的生育控制，或用于骨质疏松症的预防和/或治疗。
• MACROCYCLIC COMPOUNDS FOR INHIBITION OF TUMOR NECROSIS FACTOR ALPHA
  申请人：Lee Jinbo

  公开号：US20100152099A1

  公开（公告）日：2010-06-17

  The invention provides macrocyclic compounds and methods for their synthesis and use. In particular, the invention provides macrocyclic compounds that modulate the activity of tumor necrosis factor alpha and/or are useful in the treatment of medical conditions, such as, rheumatoid arthritis, psoriasis, and asthma.

  该发明提供了大环化合物及其合成和使用方法。具体而言，该发明提供了调节肿瘤坏死因子α活性和/或用于治疗医学状况（如类风湿性关节炎、银屑病和哮喘）的大环化合物。