(2S,3S)-3-Hydroxy-2-[3-[6-(2-methylpropoxy)-2-naphthalenyl]-1,2,4-oxadiazol-5-yl]-1-pyrrolidinecarboximidamide | 1870811-02-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: (2S,3S)-3-Hydroxy-2-[3-[6-(2-methylpropoxy)-2-naphthalenyl]-1,2,4-oxadiazol-5-yl]-1-pyrrolidinecarboximidamide
• 英文别名: (2S,3S)-3-hydroxy-2-[3-[6-(2-methylpropoxy)naphthalen-2-yl]-1,2,4-oxadiazol-5-yl]pyrrolidine-1-carboximidamide
• CAS: 1870811-02-1
• 化学式: C₂₁H₂₅N₅O₃
• 分子量: 395.5
• InChiKey: UKWLYAISZGNWAH-ROUUACIJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  29
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  122
• 氢给体数：
  3
• 氢受体数：
  6

文献信息

• [EN] SPHINGOSINE KINASE INHIBITOR AMIDOXIME PRODRUGS<br/>[FR] PROMÉDICAMENTS D'AMIDOXINE INHIBITEURS DE LA SPHINGOSINE KINASE
  申请人：THORPE STEVEN BRANDON

  公开号：WO2017172989A1

  公开（公告）日：2017-10-05

  Sphingosine kinases are enzymes that catalyze the biosynthesis of sphingosine-1-phosphate. The invention provides prodrugs of compounds that are effective for inhibition of sphingosine kinase type 1, sphingosine kinase type 2, or both, according to formula (I) as described herein. Formula I compounds are useful in the treatment of a range of diseases wherein increasing the level of sphingosine-1-phosphate in blood is medically indicated. The invention also provides pharmaceutical compositions of Formula I compounds.

  鞘氨醇激酶是催化鞘氨醇-1-磷酸酯生物合成的酶。本发明提供了根据本文所述的公式(I)有效抑制鞘氨醇激酶1型、鞘氨醇激酶2型或两者的化合物的前药。公式I化合物在治疗一系列疾病中是有用的，其中在血液中增加鞘氨醇-1-磷酸酯水平在医学上是指示的。本发明还提供了公式I化合物的药物组合物。
• Sphingosine kinase inhibitor amidoxime prodrugs
  申请人：University of Virginia Patent Foundation

  公开号：US11180489B2

  公开（公告）日：2021-11-23

  Sphingosine kinases are enzymes that catalyze the biosynthesis of sphingosine-1-phosphate. The invention provides prodrugs of compounds that are effective for inhibition of sphingosine kinase type 1, sphingosine kinase type 2, or both, according to formula (I) as described herein. Formula I compounds are useful in the treatment of a range of diseases wherein increasing the level of sphingosine-1-phosphate in blood is medically indicated. The invention also provides pharmaceutical compositions of Formula I compounds.

  鞘氨醇激酶是催化鞘氨醇-1-磷酸的生物合成的酶。本发明提供了有效抑制鞘氨醇激酶 1 型、鞘氨醇激酶 2 型或二者的化合物原药，如本文所述的式 (I)。式 I 化合物可用于治疗一系列疾病，在这些疾病中，提高血液中鞘磷脂-1-磷酸的水平具有医学指征。本发明还提供了式 I 化合物的药物组合物。
• SPHINGOSINE KINASE INHIBITOR AMIDOXIME PRODRUGS
  申请人：University Of Virginia Patent Foundation

  公开号：EP3436451B1

  公开（公告）日：2021-09-29
• SPHINGOSINE KINASE INHIBITORS
  申请人：LYNCH Kevin R.

  公开号：US20170298032A1

  公开（公告）日：2017-10-19

  Sphingosine kinases are enzymes that catalyze the biosynthesis of sphingosine-1-phosphate. The invention provides compounds that are effective for inhibition of sphingosine kinase type 1, sphingosine kinase type 2, or both. Certain compounds are selective for sphingosine kinase type 2 relative to sphingosine kinase type 1. Compounds of the invention can be used in treatment of a range of diseases wherein increasing the level of sphingosine-1-phosphate in blood is medically indicated. Diseases that can be treated by administration of an effective dose of a compound of the invention include a neoplastic disease that involves excess vascular growth; macular degeneration or diabetic retinopathy; an allergic disease such as asthma, an inflammatory disease of the eye such as uveitis, scleritis, or vitritis; an inflammatory disease of the kidney; a fibrotic disease; atherosclerosis; or pulmonary arterial hypertension. A compound of the invention can be used to improve the integrity of a vascular barrier in a disease where the vascular barrier is disrupted, such as cancer or Alzheimer's disease.