2,4-dinitrophenyl carbonochloridate | 34793-93-6

• 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: 2,4-dinitrophenyl carbonochloridate
• 英文别名: 2,4-dinitrophenyl chloroformate；(2,4-Dinitrophenyl) carbonochloridate
• CAS: 34793-93-6
• 化学式: C₇H₃ClN₂O₆
• 分子量: 246.564
• InChiKey: UYABSLBMZAYXNN-UHFFFAOYSA-N

物化性质

• 沸点：
  346.3±22.0 °C(Predicted)
• 密度：
  1.693±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  118
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  2,4-dinitrophenyl carbonochloridate 、 地氯雷他定 以 二氯甲烷 为溶剂， 生成 (2,4-Dinitrophenyl) 4-(13-chloro-4-azatricyclo[9.4.0.03,8]pentadeca-1(11),3(8),4,6,12,14-hexaen-2-ylidene)piperidine-1-carboxylate
  参考文献：
  名称：

  Loratadine analogues as MAGL inhibitors

  摘要：

  Compound 12a (JZP-361) acted as a potent and reversible inhibitor of human recombinant MAGL (hMAGL, IC50 = 46 nM), and was found to have almost 150-fold higher selectivity over human recombinant fatty acid amide hydrolase (hFAAH, IC50 = 7.24 mu M) and 35-fold higher selectivity over human alpha/beta-hydrolase-6 (hABHD6, IC50 = 1.79 mu M). Additionally, compound 12a retained H-1 antagonistic affinity (pA(2) = 6.81) but did not show cannabinoid receptor activity, when tested at concentrations <= 10 mu M. Hence, compound 12a represents a novel dual-acting pharmacological tool possessing both MAGL-inhibitory and antihistaminergic activities. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2015.02.037
• 作为产物：
  描述：

  2,4-二硝基酚 、 三光气 在 potassium carbonate 作用下， 以 二氯甲烷 为溶剂， 反应 3.0h， 生成 2,4-dinitrophenyl carbonochloridate
  参考文献：
  名称：

  DNP and DNP Prodrug Treatment of Neuromuscular, Neurodegenerative, Autoimmune, Developmental, Traumatic Brain Injury, Concussion, Dry Eye Disease, Hearing Loss and/or Metabolic Diseases

  摘要：

  一种治疗神经肌肉、神经肌肉退行性、神经退行性、自身免疫、发育、创伤、与听力损失相关以及/或代谢性疾病的组合物和治疗方法，包括脊髓性肌萎缩（SMA）综合症（SMA1、SMA2、SMA3和SMA4，也称为I型、II型、III型和IV型）、创伤性脑损伤（TBI）、脑震荡、干眼症（干眼病）、青光眼、Sjogren综合症、类风湿性关节炎、LASIK手术后、抗抑郁药物使用、Wolfram综合症和Wolcott-Rallison综合症。该组合物选自包括2,3-DNP、2,4-DNP、2,5-DNP、2,6-DNP、3,4-DNP或3,5-DNP、二元2,3-二硝基苯酚、2,4-二硝基苯酚、2,5-二硝基苯酚、2,6-二硝基苯酚、3,4-二硝基苯酚或3,5-二硝基苯酚（2,3-DNP、2,4-DNP、2,5-DNP、2,6-DNP、3,4-DNP或3,5-DNP）前药；双生子前药、生物前体分子和它们的组合。治疗神经退行性疾病的组合物剂量可为患者体重约0.01毫克/千克至约50毫克/千克。治疗代谢性疾病的组合物剂量可为患者体重约1毫克/70千克至约100毫克/70千克，每日最大剂量约为患者体重约200毫克/70千克。

  公开号：

  US20170252347A1

文献信息

• [EN] CONTROLLED DRUG RELEASE FROM SOLID SUPPORTS<br/>[FR] SUPPORTS SOLIDES POUR LA LIBÉRATION CONTRÔLÉE DE MÉDICAMENTS
  申请人：PROLYNX LLC

  公开号：WO2011140392A1

  公开（公告）日：2011-11-10

  The invention relates to solid supports useful in medical applications that provide controlled release of drugs, such as peptides, nucleic acids and small molecules. The drugs are covalently coupled to the solid support through a linkage that releases the drug or a prodrug through controlled beta elimination.

  这项发明涉及在医疗应用中有用的固体支持物，可提供药物的控制释放，如肽、核酸和小分子。这些药物通过一个通过受控β消除释放药物或前药的连接与固体支持物共价偶联。
• GLYCOPEPTIDE AND LIPOGLYCOPEPTIDE ANTIBIOTICS WITH IMPROVED SOLUBILITY
  申请人：Rafai Far Adel

  公开号：US20120149632A1

  公开（公告）日：2012-06-14

  The invention relates to derivatives of glycopeptide and lipoglycopeptide antibiotics possessing an altered ionization state with respect to the parent glycopeptide or lipoglycopeptide antibiotic, and having the ability to be regenerated as the parent glycopeptide or lipoglycopeptide antibiotic under physiological conditions. These compounds are useful as antibiotics for the prevention and/or the treatment of bacterial infections.

  这项发明涉及具有与母体糖肽或脂质糖肽抗生素相比具有改变的电离状态的糖肽和脂质糖肽抗生素衍生物，并且具有在生理条件下能够再生为母体糖肽或脂质糖肽抗生素的能力。这些化合物可用作预防和/或治疗细菌感染的抗生素。
• [EN] SUBSTITUTED BENZIMIDAZOLE CARBOXAMIDES AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS<br/>[FR] BENZIMIDAZOLE CARBOXAMIDES SUBSTITUÉS ET LEUR UTILISATION DANS LE TRAITEMENT DE TROUBLES MÉDICAUX
  申请人：BIAL BIOTECH INVEST INC

  公开号：WO2021055591A1

  公开（公告）日：2021-03-25

  The invention provides substituted benzimidazole carboxamides and related compounds, compositions containing such compounds, medical kits, and methods for using such compounds and compositions to treat a medical disorder, e.g., cancer, lysosomal storage disorder, neurodegenerative disorder, inflammatory disorder, in a patient.

  这项发明提供了替代苯并咪唑羧酰胺及相关化合物，含有这些化合物的组合物，医疗工具包，以及使用这些化合物和组合物治疗患者的医疗疾病的方法，例如癌症、溶酶体贮积症、神经退行性疾病、炎症性疾病。
• Novel physiologically active substances
  申请人：Kotake Yoshihiko

  公开号：US20050245514A1

  公开（公告）日：2005-11-03

  Compounds represented by the following general formula (I), pharmacologically acceptable salts thereof or hydrates of the same: (I) wherein W represents and R 3 , R 7 , R 16 , R 17 , R 20 , R 21 and R 21′ are the same or different and each represents hydrogen, etc. Because of inhibiting angiogenesis and inhibiting the production of VEGF particularly in hypoxia, the compounds (I) are useful as remedies for solid cancer.

  具有下述通式(I)表示的化合物、其药理学上可接受的盐或水合物：(I)其中W代表，R3、R7、R16、R17、R20、R21及R21'相同或不同，各自代表氢等。由于能抑制血管生成及在缺氧条件下抑制VEGF的产生，化合物(I)可作为实体癌症的治疗药物。
• 12 MEMBERED-RING MACROLACTAM DERIVATIVES
  申请人：Miyano Masayuki

  公开号：US20080312317A1

  公开（公告）日：2008-12-18

  There provided a 12-membered-ring macrolactam derivative having antitumor activity: A compound represented by Formula (1) or a salt thereof. In this Formula, R 1 is a hydrogen atom, a C 1-6 alkyl group, a C 1-6 alkylcarbonyl group or a C 6-14 arylcarbonyl group; R 2 is a hydrogen atom or a C 1-6 alkyl group; R 3 is a hydrogen atom or a hydroxyl group; R 4 is a hydrogen atom or a hydroxyl group; R 5 is a hydrogen atom or a C 1-6 alkyl group; R 6 is a hydrogen atom or a hydroxyl group; and R 7 is an acetyl group or the like.

  提供了一种具有抗肿瘤活性的12-成员环大环内酰胺衍生物：由化学式（1）表示的化合物或其盐。在该化学式中，R1是氢原子、C1-6烷基基团、C1-6烷基羰基基团或C6-14芳基羰基基团；R2是氢原子或C1-6烷基基团；R3是氢原子或羟基；R4是氢原子或羟基；R5是氢原子或C1-6烷基基团；R6是氢原子或羟基；R7是乙酰基或类似物。