1-(2-Iodoethyl)-3,5-dimethylbenzene | 928775-73-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 1-(2-Iodoethyl)-3,5-dimethylbenzene
• CAS: 928775-73-9
• 化学式: C₁₀H₁₃I
• 分子量: 260.118
• InChiKey: KWWYUKAGESJMLX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  1-(2-Iodoethyl)-3,5-dimethylbenzene 在 苄基三乙基氯化铵 、 potassium carbonate 、 ethylenediamine Tetraacetic Acid 作用下， 以 甲醇 、 乙腈 为溶剂， 生成 4-[2-(3,5-dimethylphenyl)ethyl]-6-{[(5Z)-4-oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene]methyl}-3,4-dihydro-2H-1,4-benzoxazin-3-one
  参考文献：
  名称：

  Design and synthesis of phenethyl benzo[1,4]oxazine-3-ones as potent inhibitors of PI3Kinaseγ

  摘要：

  The Type 1 PI3Kinases comprise a family of enzymes, which primarily phosphorylate PIP2 to give the second messenger PIP3, a key player in many intracellular signaling processes [Science, 2002, 296, 1655; Trends Pharmacol. Sci. 2003, 24, 366]. Of the four type 1 PI3Ks, the gamma-isoform, which is expressed almost exclusively in leukocytes [Curr. Biol., 1997, 7, R470], is of particular interest with respect to its role in inflammatory diseases such as rheumatoid arthritis (RA) and chronic obstructive pulmonary disease (COPD) [Mol. Med. Today, 2000, 6, 347]. Investigation of a series of 4,6-disubstituted-4H-benzo[1,4]oxazin-3-ones has led to the identification of single-digit nanomolar inhibitors of PI3K gamma, several of which had good cell based activity and were shown to be active in vivo in an aspectic peritonitis model of inflammatory cell migration. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.10.080
• 作为产物：
  描述：

  β-(3,5-Dimethylphenyl)ethyl alcohol 在 咪唑 、 碘 、 三苯基膦 作用下， 以 二氯甲烷 为溶剂， 生成 1-(2-Iodoethyl)-3,5-dimethylbenzene
  参考文献：
  名称：

  Design and synthesis of phenethyl benzo[1,4]oxazine-3-ones as potent inhibitors of PI3Kinaseγ

  摘要：

  The Type 1 PI3Kinases comprise a family of enzymes, which primarily phosphorylate PIP2 to give the second messenger PIP3, a key player in many intracellular signaling processes [Science, 2002, 296, 1655; Trends Pharmacol. Sci. 2003, 24, 366]. Of the four type 1 PI3Ks, the gamma-isoform, which is expressed almost exclusively in leukocytes [Curr. Biol., 1997, 7, R470], is of particular interest with respect to its role in inflammatory diseases such as rheumatoid arthritis (RA) and chronic obstructive pulmonary disease (COPD) [Mol. Med. Today, 2000, 6, 347]. Investigation of a series of 4,6-disubstituted-4H-benzo[1,4]oxazin-3-ones has led to the identification of single-digit nanomolar inhibitors of PI3K gamma, several of which had good cell based activity and were shown to be active in vivo in an aspectic peritonitis model of inflammatory cell migration. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.10.080

文献信息

• [EN] POLYMER CONJUGATE COMPRISING A BIOACTIVE AGENT<br/>[FR] CONJUGUÉ DE POLYMÈRE COMPRENANT UN AGENT BIOACTIF
  申请人：POLYACTIVA PTY LTD

  公开号：WO2017041142A1

  公开（公告）日：2017-03-16

  The present invention relates in general to polymer-bioactive agent conjugates for delivering a bioactive agent to a subject. The polymer-bioactive agent conjugates contain triazole moieties in the polymer backbone and a bioactive moiety selected from quinolones, NSAIDs and mixtures thereof. The present invention also relates to methods for preparing the polymer conjugates using click cycloaddition chemical reactions, to monomer-bioactive agent conjugates suitable for preparing the polymer conjugates, and to pharmaceutical products comprising the polymer conjugates for the post-surgical care to treat or prevent infections, provide analgesia and treat inflammation.

  本发明一般涉及聚合物-生物活性剂共轭物，用于向受试者递送生物活性剂。该聚合物-生物活性剂共轭物在聚合物骨架中含有三唑基团和从喹诺酮、非甾体类抗炎药和二者混合物中选择的生物活性基团。本发明还涉及使用点击环加成化学反应制备聚合物共轭物的方法，适用于制备聚合物共轭物的单体-生物活性剂共轭物，以及包含聚合物共轭物的药品产品，用于术后护理以治疗或预防感染、提供镇痛和治疗炎症。
• [EN] RORY MODULATORS<br/>[FR] MODULATEURS DU RÉCEPTEUR GAMMA ORPHELIN ASSOCIÉ AUX RÉTINOÏDES (RORY)
  申请人：BRISTOL MYERS SQUIBB CO

  公开号：WO2014062938A1

  公开（公告）日：2014-04-24

  Described are RORy modulators of the formula (I), and N-oxides thereof, and pharmaceutically acceptable salts thereof, and solvates and hydrates thereof, wherein R1, R2, R3, R4, R5, R6, Ra, x, y, L, G, Z, the bond denoted by "q", the ring system denoted by "A" and the ring system denoted by "B" are defined herein. Also provided are pharmaceutical compositions comprising the same. Such compounds and compositions are useful in methods for modulating RORy activity in a cell and methods for treating a subject suffering from a disease or disorder in which the subject would therapeutically benefit from modulation of RORy activity, for example, autoimmune and/or inflammatory disorders.

  描述了化学式(I)中的RORy调节剂，以及其N-氧化物、药用可接受的盐、溶剂和水合物，其中R1、R2、R3、R4、R5、R6、Ra、x、y、L、G、Z、由“q”表示的键，由“A”表示的环系统和由“B”表示的环系统在此处进行了定义。还提供了包含这些化合物的药物组合物。这些化合物和组合物在调节细胞中的RORy活性的方法和治疗患有需要从RORy活性调节中获益的疾病或紊乱的受试者的方法中是有用的，例如自身免疫和/或炎症性疾病。
• RORGamma Modulators
  申请人：BRISTOL-MYERS SQUIBB COMPANY

  公开号：US20150266856A1

  公开（公告）日：2015-09-24

  Described are RORy modulators of the formula (I), and N-oxides thereof, and pharmaceutically acceptable salts thereof, and solvates and hydrates thereof, wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R a , x, y, L, G, Z, the bond denoted by “q”, the ring system denoted by “A” and the ring system denoted by “B” are defined herein. Also provided are pharmaceutical compositions comprising the same. Such compounds and compositions are useful in methods for modulating RORy activity in a cell and methods for treating a subject suffering from a disease or disorder in which the subject would therapeutically benefit from modulation of RORy activity, for example, autoimmune and/or inflammatory disorders.

  本文描述了公式（I）的RORy调节剂及其N-氧化物、药学上可接受的盐、溶剂和水合物，其中R1、R2、R3、R4、R5、R6、Ra、x、y、L、G、Z、“q”表示的键、表示的环系统“A”和表示的环系统“B”在此定义。还提供了包含这些化合物的制药组合物。这些化合物和组合物在调节细胞中的RORy活性的方法和治疗患有疾病或障碍的受试者中是有用的，其中该受试者在调节RORy活性方面具有治疗益处，例如自身免疫和/或炎症性疾病。
• RORγ modulators
  申请人：BRISTOL-MYERS SQUIBB COMPANY

  公开号：US10035790B2

  公开（公告）日：2018-07-31

  Described are RORy modulators of the formula (I), and N-oxides thereof, and pharmaceutically acceptable salts thereof, and solvates and hydrates thereof, wherein R1, R2, R3, R4, R5, R6, Ra, x, y, L, G, Z, the bond denoted by “q”, the ring system denoted by “A” and the ring system denoted by “B” are defined herein. Also provided are pharmaceutical compositions comprising the same. Such compounds and compositions are useful in methods for modulating RORy activity in a cell and methods for treating a subject suffering from a disease or disorder in which the subject would therapeutically benefit from modulation of RORy activity, for example, autoimmune and/or inflammatory disorders.

  描述了式 (I) 的 RORy 调节剂、其 N-氧化物、其药学上可接受的盐、其溶液和水合物，其中 R1、R2、R3、R4、R5、R6、Ra、x、y、L、G、Z、用 "q "表示的键、用 "A "表示的环系和用 "B "表示的环系在本文中定义。此外，还提供了包含这些化合物的药物组合物。此类化合物和组合物可用于调节细胞中 RORy 活性的方法和治疗患有疾病或失调的受试者的方法，其中受试者将从调节 RORy 活性中获得治疗上的益处，例如自身免疫和/或炎症性失调。