methyl 140-Cyclohexyl-2,2-dimethylspiro[1,3-dioxane-5,70-indolo[1,2-e][1,5]benzoxazocine]-11-carboxylate | 956580-04-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: methyl 140-Cyclohexyl-2,2-dimethylspiro[1,3-dioxane-5,70-indolo[1,2-e][1,5]benzoxazocine]-11-carboxylate
• 英文别名: methyl 14'-cyclohexyl-2,2-dimethylspiro[1,3-dioxane-5,7'-indolo[1,2-e][1,5]benzoxazocine]-11'-carboxylate；methyl 14'-cyclohexyl-2.2-dimethylspiro[1,3-dioxane-5,7'-indolo[1,2-e][1,5]benzoxazocine]-11'-carboxylate；methyl 19'-cyclohexyl-2,2-dimethylspiro[1,3-dioxane-5,10'-8-oxa-12-azatetracyclo[10.7.0.02,7.013,18]nonadeca-1(19),2,4,6,13(18),14,16-heptaene]-15'-carboxylate
• CAS: 956580-04-4
• 化学式: C₃₀H₃₅NO₅
• 分子量: 489.612
• InChiKey: CFIBPPDATQTIAZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6
• 重原子数：
  36
• 可旋转键数：
  3
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  58.9
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  methyl 140-Cyclohexyl-2,2-dimethylspiro[1,3-dioxane-5,70-indolo[1,2-e][1,5]benzoxazocine]-11-carboxylate 在 甲醇 、 对甲苯磺酸 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 乙腈 为溶剂， 反应 3.25h， 生成
  参考文献：
  名称：

  Discovery of (7R)-14-Cyclohexyl-7-{[2-(dimethylamino)ethyl](methyl) amino}-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylic Acid (MK-3281), a Potent and Orally Bioavailable Finger-Loop Inhibitor of the Hepatitis C Virus NS5B Polymerase

  摘要：

  Infections caused by hepatitis C virus (HCV) are a significant world health problem for which novel therapies are in urgent demand. The polymerase of HCV is responsible for the replication of viral genome and has been a prime target for drug discovery efforts. Here, we report on the further development of tetracyclic indole inhibitors, binding to an allosteric site on the thumb domain. Structure-activity relationship (SAR) studies around an indolo-benzoxazocine scaffold led to the identification of compound 33 (MK-3281), an inhibitor with good potency in the HCV subgenomic replication assay and attractive molecular properties suitable for a clinical candidate. The compound caused a consistent decrease in viremia in vivo using the chimeric mouse model of HCV infection.

  DOI：

  10.1021/jm1013105
• 作为产物：
  描述：

  5,5-双(溴甲基)-2,2-二甲基-1,3-二氧六环 在 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 4.33h， 以50%的产率得到methyl 140-Cyclohexyl-2,2-dimethylspiro[1,3-dioxane-5,70-indolo[1,2-e][1,5]benzoxazocine]-11-carboxylate
  参考文献：
  名称：

  WO2007/129119

  摘要：

  公开号：

文献信息

• [EN] MACROCYCLIC INDOLE DERIVATIVES FOR THE TREATMENT OF HEPATITIS C INFECTIONS<br/>[FR] DÉRIVÉS MACROCYCLIQUES D'INDOLE POUR LE TRAITEMENT DES INFECTIONS D'HÉPATITE C
  申请人：ANGELETTI P IST RICHERCHE BIO

  公开号：WO2009010783A1

  公开（公告）日：2009-01-22

  A class of macrocyclic compounds of formula (I), wherein R7, R9, B, F, M, Q, W, Y and Z are defined herein, that are useful as inhibitors of viral proteases, particularly the hepatitis C virus (HCV) NS3 protease, are provided. Also provided are processes for the synthesis and use of such 5 macrocyclic compounds for treating or preventing HCV infection.

  提供一类宏环化合物的化学式(I)，其中R7、R9、B、F、M、Q、W、Y和Z的定义如下，这些化合物可用作病毒蛋白酶抑制剂，特别是对乙型肝炎病毒（HCV）NS3蛋白酶的抑制剂。还提供了合成和使用这些5种宏环化合物的方法，用于治疗或预防HCV感染。
• Pentacyclic Indole Derivatives as Antiviral Agents
  申请人：Capito Elena

  公开号：US20100009959A1

  公开（公告）日：2010-01-14

  The present invention relates to pentacyclic indole derivatives of formula (I): wherein A, Ar, R 1 , R 2 , W, X, Y and Z are defined herein, and pharmaceutically acceptable salts thereof, pharmaceutical compositions comprising them, and their use for the treatment or prevention of infection by hepatitis C virus.

  本发明涉及公式（I）的五环吲哚衍生物：其中A，Ar，R1，R2，W，X，Y和Z在此定义，并且其药学上可接受的盐，包括它们的制药组合物，以及它们用于治疗或预防丙型肝炎病毒感染的用途。
• Therapeutic compounds
  申请人：Conte Immacolata

  公开号：US20090048239A1

  公开（公告）日：2009-02-19

  A class of macrocyclic compounds of formula (I), wherein R 7 , A, Ar, B, D, F, M, Q 1 , Q 2 , W, X, Y and Z are defined herein, that are useful as inhibitors of viral proteases, particularly the hepatitis C virus (HCV) NS3 protease, are provided. Also provided are processes for the synthesis and use of such macrocyclic compounds for treating or preventing HCV infection.

  提供一类宏环化合物(I)的公式，其中R7、A、Ar、B、D、F、M、Q1、Q2、W、X、Y和Z在此定义，可用作病毒蛋白酶的抑制剂，特别是乙型肝炎病毒（HCV）NS3蛋白酶的抑制剂。同时提供了合成和使用这种宏环化合物治疗或预防HCV感染的方法。
• Pentacyclic indole derivatives as antiviral agents
  申请人：Istituto di Richerche di Biologia Molecolare P. Angeletti SpA

  公开号：US08232390B2

  公开（公告）日：2012-07-31

  The present invention relates to pentacyclic indole derivatives of formula (I): wherein A, Ar, R1, R2, W, X, Y and Z are defined herein, and pharmaceutically acceptable salts thereof, pharmaceutical compositions comprising them, and their use for the treatment or prevention of infection by hepatitis C virus.

  本发明涉及公式（I）的五环吲哚衍生物，其中A，Ar，R1，R2，W，X，Y和Z在此定义，并且其药学上可接受的盐，包括它们的制药组合物，以及它们用于治疗或预防乙型肝炎病毒感染的用途。
• MACROCYCLIC INDOLE DERIVATIVES FOR THE TREATMENT OF HEPATITIS C INFECTIONS
  申请人：Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A.

  公开号：EP2178886A1

  公开（公告）日：2010-04-28