2-naphthylmethyl (4-nitrophenyl) carbonate | 158951-86-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 2-naphthylmethyl (4-nitrophenyl) carbonate
• 英文别名: carbonic acid naphthalen-2-ylmethyl ester 4-nitro-phenyl ester；Naphthalen-2-ylmethyl (4-nitrophenyl) carbonate
• CAS: 158951-86-1
• 化学式: C₁₈H₁₃NO₅
• 分子量: 323.305
• InChiKey: KSOJGWOMZGWJHF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  24
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  81.4
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-naphthylmethyl (4-nitrophenyl) carbonate 在 N-甲基吗啉 、 sodium azide 、 sodium carbonate 作用下， 以 四氢呋喃 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 0.83h， 生成
  参考文献：
  名称：

  从5H-噻唑-4-酮和硝基烯烃催化合成对叔硫醇：双官能基于脲肽的布朗斯台德碱催化

  摘要：

  满载：基于脲肽的双官能布朗斯台德碱1有效促进α-巯基羧酸盐替代物与硝基烯烃的第一个直接催化迈克尔反应，该反应涉及完全取代的α-碳原子结构。

  DOI：

  10.1002/anie.201305644
• 作为产物：
  描述：

  2-萘甲醇 、 对硝基苯基氯甲酸酯 在 吡啶 作用下， 以 二氯甲烷 为溶剂， 生成 2-naphthylmethyl (4-nitrophenyl) carbonate
  参考文献：
  名称：

  从5H-噻唑-4-酮和硝基烯烃催化合成对叔硫醇：双官能基于脲肽的布朗斯台德碱催化

  摘要：

  满载：基于脲肽的双官能布朗斯台德碱1有效促进α-巯基羧酸盐替代物与硝基烯烃的第一个直接催化迈克尔反应，该反应涉及完全取代的α-碳原子结构。

  DOI：

  10.1002/anie.201305644

文献信息

• [EN] ACYLPIPERAZINES AS INHIBITORS OF TRANSGLUTAMINASE AND THEIR USE IN MEDICINE<br/>[FR] ACYL-PIPERAZINES EN TANT QU'INHIBITEURS DE LA TRANSGLUTAMINASE ET LEUR UTILISATION EN MÉDECINE
  申请人：UNIV ASTON

  公开号：WO2014057266A1

  公开（公告）日：2014-04-17

  The present invention relates to novel compounds of Formula I capable of inhibiting tissue transglutaminase, and uses of the same in medicine. In particular, the invention provides compounds for use in the treatment of prevention of disease and conditions such as fibrosis (e.g. cystic fibrosis), scarring, neurodegenerative diseases (e.g. Alzheimer's disease, Huntington's disease and Parkinson's disease), autoimmune diseases (e.g. multiple sclerosis and coeliac disease), thrombosis, proliferative disorders (e.g. cancers), AIDS, psoriasis and inflammation (e.g. chronic inflammatory diseases).

  本发明涉及一种能够抑制组织转谷氨酰胺酶的化合物I式新化合物，以及在医学上的用途。具体而言，该发明提供了用于治疗或预防疾病和病况的化合物，如纤维化（例如囊性纤维化）、瘢痕形成、神经退行性疾病（例如阿尔茨海默病、亨廷顿病和帕金森病）、自身免疫疾病（例如多发性硬化症和乳糜泻）、血栓形成、增生性疾病（例如癌症）、艾滋病、银屑病和炎症（例如慢性炎症性疾病）的化合物。
• Synthesis of β-Hydroxy α-Amino Acids Through Brønsted Base-Catalyzed <i>syn</i>-Selective Direct Aldol Reaction of Schiff Bases of Glycine <i>o</i>-Nitroanilide
  作者：Silvia Vera、Ana Vázquez、Ricardo Rodriguez、Sandra del Pozo、Iñaki Urruzuno、Abel de Cózar、Antonia Mielgo、Claudio Palomo

  DOI：10.1021/acs.joc.1c00406

  日期：2021.6.4

  Here we report the highly enantio- and syn-selective synthesis of β-hydroxy α-amino acids from glycine imine derivatives under Brønsted base (BB) catalysis. The key of this approach is the use of benzophenone-derived imine of glycine o-nitroanilide as a pronucleophile, where the o-nitroanilide framework provides an efficient hydrogen-bonding platform that accounts for nucleophile reactivity and diastereoselectivity

  在这里，我们报告了在 Brønsted 碱 (BB) 催化下从甘氨酸亚胺衍生物合成 β-羟基 α-氨基酸的高度对映选择性和顺选择性合成。该方法的关键是使用二苯甲酮衍生的甘氨酸邻硝基苯胺亚胺作为亲核试剂，其中邻硝基苯胺框架提供了一个有效的氢键平台，可解释亲核试剂的反应性和非对映选择性。
• Acylpiperazines as Inhibitors of Transglutaminase and Their Use in Medicine
  申请人：ASTON UNIVERSITY

  公开号：US20150259310A1

  公开（公告）日：2015-09-17

  The present invention relates to novel compounds of Formula I capable of inhibiting tissue transglutaminase, and uses of the same in medicine. In particular, the invention provides compounds for use in the treatment of prevention of disease and conditions such as fibrosis (e.g. cystic fibrosis), scarring, neurodegenerative diseases (e.g. Alzheimer's disease, Huntington's disease and Parkinson's disease), autoimmune diseases (e.g. multiple sclerosis and coeliac disease), thrombosis, proliferative disorders (e.g. cancers), AIDS, psoriasis and inflammation (e.g. chronic inflammatory diseases).

  本发明涉及一种能够抑制组织转谷氨酰胺酶的新型化合物I，以及在医学上使用它们的方法。特别地，本发明提供了用于治疗和预防疾病和病况（如纤维化（例如囊性纤维化），瘢痕，神经退行性疾病（例如阿尔茨海默病，亨廷顿病和帕金森病），自身免疫性疾病（例如多发性硬化症和乳糜泻），血栓形成，增生性疾病（例如癌症），艾滋病，牛皮癣和炎症（例如慢性炎症性疾病））的化合物。
• Use of 2, 4diamino-3-hydroxycarboxylic acid derivatives as proteasome inhibitors
  申请人：France Dennis

  公开号：US20050026994A1

  公开（公告）日：2005-02-03

  The present invention relates to the new use of 2,4-diamino-3-hydroxycarboxylic acids of formula (I), in which A and B independently represent a bond or an unsubstituted or substituted amino acyl moiety; R 1 represents hydrogen; an amino protecting group; or a group of formula R 5 Y— wherein R 5 represents hydrogen or an unsubstituted or substituted alkyl, alkenyl, alkinyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, heterocyclyl or heterocyclylalkyl group; and Y represents —CO—; —NH—CO—; —NH—CS—; —SO 2 —; —O—CO—; or —O—CS—; R 2 represents the side chain of a natural amino acid; an alkyl, arylalkyl, heteroarylalkyl or cycloalkylalkyl group; or trimethylsilylmethyl, 2-thienylmethyl or styrylmethyl; R 3 represents halogen, alkyl, alkoxy or hydroxyalkoxy; and R 4 represents 2(R)-hydroxyindan-1(S)-yl; (S)-2-hydroxy-1-phenylethyl; or 2-hydroxy-benzyl unsubstituted or substituted in 4-position by methoxy; in the manufacture of a pharmaceutical composition for the treatment of a proliferative disease, e.g., of a solid tumor; to a method of treatment of warm-blooded animals; and to 2,4-diamino-3-hydroxycarboxylic acids of formula (I*), wherein A and B independently represent an unsubstituted or substituted amino acyl moiety; R 2 represents arylalkyl; R 3 represents halogen, alkyl, alkoxy or hydroxyalkoxy; R 4 represents 2-hydroxy-benzyl unsubstituted or substituted in 4 position by methoxy; and R 5 represents arylalkyl and Y represents —CO—; or R 5 represents alkyl substituted by cycloalkyl, naphthyl, pyridyl or phenyl in which phenyl is substituted by alkyl or amino; and Y represents —O—CO; pharmaceutically acceptable salts thereof; and the use of such compounds of formula (I*) for the therapeutic treatment of the human or animal body, especially the treatment of proliferative diseases.

  本发明涉及式（I）的 2,4-二氨基-3-羟基羧酸的新用途，其中 A 和 B 独立地代表一个键或一个未取代或取代的氨基酰基；R 1 代表氢；氨基保护基；或式 R 5 Y- 其中 R 5 代表氢或未取代或取代的烷基、烯基、炔基、芳基、芳烷基、杂芳基、杂芳烷基、杂环烷基或杂环烷基；且 Y 代表 -CO-；-NH-CO-；-NH-CS-；-SO 2 -；-O-CO-；或-O-CS-； R 2 代表天然氨基酸的侧链；烷基、芳烷基、杂芳烷基或环烷基烷基；或三甲基硅甲基、2-噻吩甲基或苯乙烯甲基； R 3 3 代表卤素、烷基、烷氧基或羟基烷氧基；以及 R 4 代表 2(R)-羟基茚满-1(S)-基；(S)-2-羟基-1-苯基乙基；或未被甲氧基取代或在 4-位被甲氧基取代的 2-羟基苄基； 用于制造治疗增殖性疾病，例如式 (I*) 的 2,4-二氨基-3-羟基羧酸，其中 A 和 B 独立地代表未取代或取代的氨基酰基； R 2 代表芳烷基 3 代表卤素、烷基、烷氧基或羟基烷氧基； R 4 代表未取代的 2-羟基苄基或在 4 位被甲氧基取代的 2-羟基苄基；以及 R 5 代表芳烷基，Y 代表-CO-；或 R 5 代表被环烷基、萘基、吡啶基或苯基取代的烷基，其中苯基被烷基或氨基取代；且 Y 代表 -O-CO；其药学上可接受的盐；以及将式 (I*) 的此类化合物用于人体或动物机体的治疗，尤其是增殖性疾病的治疗。
• Development of Potent and Selective Tissue Transglutaminase Inhibitors: Their Effect on TG2 Function and Application in Pathological Conditions
  作者：Eduard Badarau、Zhuo Wang、Dan L. Rathbone、Andrea Costanzi、Thomas Thibault、Colin E. Murdoch、Said El Alaoui、Milda Bartkeviciute、Martin Griffin

  DOI：10.1016/j.chembiol.2015.08.013

  日期：2015.10

  Potent-selective peptidomimetic inhibitors of tissue transglutaminase (TG2) were developed through a combination of protein-ligand docking and molecular dynamic techniques. Derivatives of these inhibitors were made with the aim of specific TG2 targeting to the intra-and extracellular space. A cell-permeable fluorescently labeled derivative enabled detection of in situ cellular TG2 activity in human umbilical cord endothelial cells and TG2-transduced NIH3T3 cells, which could be enhanced by treatment of cells with ionomycin. Reaction of TG2 with this fluorescent inhibitor in NIH3T3 cells resulted in loss of binding of TG2 to cell surface syndecan-4 and inhibition of translocation of the enzyme into the extracellular matrix, with a parallel reduction in fibronectin deposition. In human umbilical cord endothelial cells, this same fluorescent inhibitor also demonstrated a reduction in fibronectin deposition, cell motility, and cord formation in Matrigel. Use of the same inhibitor in a mouse model of hypertensive nephrosclerosis showed over a 40% reduction in collagen deposition.