1-Benzyl-purin | 14671-20-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 咪唑并嘧啶类
• 英文名称: 1-Benzyl-purin
• 英文别名: 1-Benzylpurine
• CAS: 14671-20-6
• 化学式: C₁₂H₁₀N₄
• 分子量: 210.238
• InChiKey: LQTMKPZRKXYOLG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  43.6
• 氢给体数：
  0
• 氢受体数：
  3

文献信息

• [EN] HIV REPLICATION INHIBITORS<br/>[FR] INHIBITEURS DE LA RÉPLICATION DU VIH
  申请人：SOUTHERN RES INST

  公开号：WO2013033003A1

  公开（公告）日：2013-03-07

  Compounds of Formula (I) wherein B is selected from the group consisting of substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl; Y is a linker moiety selected from the group consisting of a direct bond. R, R1, R2, and R3 are each individually selected from the group consisting substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, or heterocycle.

  式（I）中的化合物，其中B选自取代或未取代的芳基，取代或未取代的杂环基；Y是选自直接键等的连接子基团。R、R1、R2和R3分别选自取代或未取代的芳基，取代或未取代的杂环基或杂环烃基。
• [EN] PEPTIDOMIMETICS FOR THE TREATMENT OF NOROVIRUS INFECTION<br/>[FR] PEPTIDOMIMÉTIQUES POUR LE TRAITEMENT D'UNE INFECTION À NOROVIRUS
  申请人：UNIV EMORY

  公开号：WO2017197377A1

  公开（公告）日：2017-11-16

  The present invention is directed to compounds, compositions and methods for preventing, treating or curing Norovirus infection in human subjects or other animal hosts.

  本发明涉及用于预防、治疗或治愈人类主体或其他动物宿主中的诺如病毒感染的化合物、组合物和方法。
• Cobalamin mediated delivery of nucleic acids, analogs and derivatives thereof
  申请人：Collins A. Douglas

  公开号：US20060074034A1

  公开（公告）日：2006-04-06

  This invention is in the area of cobalamin-mediated delivery of nucleic acids and analogs and derivatives thereof to a host to affect gene expression.

  这项发明涉及钴胺素介导的核酸及其类似物和衍生物的传递到宿主以影响基因表达。
• Phenylindoles for the treatment of HIV
  申请人：——

  公开号：US20020193415A1

  公开（公告）日：2002-12-19

  The invention as disclosed herein is a method and composition for the treatment of HIV in humans and other host animals, that includes the administration of an effective HIV treatment amount of a phenylindole as described herein or a pharmaceutically acceptable salt or prodrug thereof, optionally in a pharmaceutically acceptable carrier. The compounds of this invention either possess antiviral (i.e., anti-HIV) activity, or are metabolized to a compound that exhibits such activity.

  本发明公开了一种用于治疗人类和其他宿主动物体内的HIV的方法和组合物，包括根据本文所述的给予有效的HIV治疗量的苯基吲哚或其药学上可接受的盐或前药，可选地在药学上可接受的载体中。本发明的化合物具有抗病毒（即抗HIV）活性，或者经代谢后形成具有该活性的化合物。
• [EN] QUINAZOLINONE ANALOGS AND USE OF QUINAZOLINONE ANALOGS FOR TREATING OR PREVENTING CERTAIN VIRAL INFECTIONS<br/>[FR] ANALOGUES DE QUINAZOLINONE ET UTILISATION D'ANALOGUES DE QUINAZOLINONE POUR LE TRAITEMENT OU LA PRÉVENTION DE CERTAINES INFECTIONS VIRALES
  申请人：SOUTHERN RES INST

  公开号：WO2013025508A1

  公开（公告）日：2013-02-21

  Provided is a process for treating or preventing a viral infection in a subject, wherein the viral infection is from a flavivirus selected from the group consisting of Hepatitis C Virus (genotypes 1-7) and Japanese Encephalitis Virus. The process includes administering to the subject a therapeutically effective amount of at least one compound represented by the formula:(Formula (I))

  提供了一种用于治疗或预防受试者体内来自黄病毒组中选定的黄色病毒感染的方法，所述黄色病毒包括丙型肝炎病毒（基因型1-7）和日本脑炎病毒。该过程包括向受试者施用至少一种由公式（I）表示的化合物的治疗有效量。