(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-bromophenyl)propanoic acid

• 分子结构分类: 有机化合物 - 苯类化合物 - 芴
• 英文名称: (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-bromophenyl)propanoic acid
• 英文别名: (3S)-3-(4-bromophenyl)-3-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid
• 化学式: C₂₄H₂₀BrNO₄
• 分子量: 466.3
• InChiKey: GVCLAQFMSVKNKH-QFIPXVFZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.8
• 重原子数：
  30
• 可旋转键数：
  7
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  75.6
• 氢给体数：
  2
• 氢受体数：
  4

文献信息

• Biphenyl and biphenyl-analogous compounds as integrin antagonists
  申请人：——

  公开号：US20020016461A1

  公开（公告）日：2002-02-07

  The present invention relates to biphenyl and biphenyl-analogous compounds, their preparation and use as pharmaceutical compositions, as integrin antagonists and in particular for the production of pharmaceutical compositions for the treatment and prophylaxis of cancer, arteriosclerosis, restenosis, osteolytic disorders such as osteoporosis and ophthalmic diseases. The compounds according to the invention have the formula ( 1 ) 1 wherein R 1 , R 2 , U, V, A, B, W, R 3 , C and R 4 have the meaning as defined in the claims.

  本发明涉及联苯和类联苯化合物，它们的制备和用作药物组合物，作为整合素拮抗剂，特别用于生产用于治疗和预防癌症、动脉硬化、再狭窄、骨溶解性疾病如骨质疏松和眼科疾病的药物组合物。根据本发明的化合物具有以下式(1)其中R1、R2、U、V、A、B、W、R3、C和R4的含义如权利要求中所定义。
• [EN] NEW BIPHENYL AND BIPHENYL-ANALOGOUS COMPOUNDS AS INTEGRIN ANTAGONISTS<br/>[FR] NOUVEAUX COMPOSES DE BIPHENYLE ET D'ANALOGUES DE BIPHENYLE UTILISES EN TANT QU'ANTAGONISTES D'INTEGRINES
  申请人：BAYER AG

  公开号：WO2000035864A1

  公开（公告）日：2000-06-22

  The present invention relates to biphenyl and biphenyl-analogous compounds, their preparation and use as pharmaceutical compositions, as integrin antagonists and in particular for the production of pharmaceutical compositions for the treatment and prophylaxis of cancer, arteriosclerosis, restenosis, osteolytic disorders such as osteoporosis and ophthalmic diseases. The compounds according to the invention have formula (1) wherein R1, R2, U, V, A, B, W, R3, C and R4 have the meaning as defined in the claims.

  本发明涉及二苯基和二苯基类似化合物，它们的制备和用作药物组成物，作为整合素拮抗剂，特别是用于制备用于治疗和预防癌症、动脉硬化、再狭窄、骨质疏松等骨骼疾病和眼科疾病的药物组成物。根据本发明，所述化合物具有式（1），其中R1、R2、U、V、A、B、W、R3、C和R4的含义如权利要求所定义。
• New biphenyl and biphenyl-analogous compounds as integrin antagonists
  申请人：——

  公开号：US20040030132A1

  公开（公告）日：2004-02-12

  The present invention relates to biphenyl and biphenyl-analogous compounds, their preparation and use as pharmaceutical compositions, as integrin antagonists and in particular for the production of pharmaceutical compositions for the treatment and prophylaxis of cancer, arteriosclerosis, restenosis, osteolytic disorders such as osteoporosis and ophthalmic diseases. The compounds according to the invention have the formula (1) 1 wherein R 1 , R 2 , U, V, A, B, W, R 3 , C and R 4 have the meaning as defined in the claims.

  本发明涉及联苯和联苯类似化合物，其制备和用作药物组成物，作为整合素拮抗剂，特别是用于制备用于治疗和预防癌症、动脉硬化、再狭窄、骨质疏松等骨溶解性疾病和眼科疾病的药物组成物。本发明的化合物具有式（1）其中R1、R2、U、V、A、B、W、R3、C和R4的含义如权利要求中所定义。
• 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。
• NEW BIPHENYL AND BIPHENYL-ANALOGOUS COMPOUNDS AS INTEGRIN ANTAGONISTS
  申请人：Bayer HealthCare AG

  公开号：EP1140809B1

  公开（公告）日：2005-08-31