7-氨基-4-甲基-2H-1,4-苯并噁嗪 | 220844-82-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并恶嗪类
• 中文名称: 7-氨基-4-甲基-2H-1,4-苯并噁嗪
• 英文名称: 4-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-7-amine
• 英文别名: 4-methyl-3,4-dihydro-2H-benzo[1,4]oxazin-7-ylamine；7-amino-4-methyl-2H-1,4-benzoxazine；4-methyl-2,3-dihydro-1,4-benzoxazin-7-amine
• CAS: 220844-82-6
• 化学式: C₉H₁₂N₂O
• mdl: MFCD11599197
• 分子量: 164.207
• InChiKey: FSIRYCPDUFGICB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  12
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.333
• 拓扑面积：
  38.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  7-氨基-4-甲基-2H-1,4-苯并噁嗪 在 硫酸 作用下， 以 苯 为溶剂， 生成 1,2,3,6-Tetrahydro-1-methyl-9-(trifluoromethyl)-7H-[1,4]oxazino[3,2-g]quinolin-7-one
  参考文献：
  名称：

  Novel Series of Potent, Nonsteroidal, Selective Androgen Receptor Modulators Based on 7H-[1,4]Oxazino[3,2-g]quinolin-7-ones

  摘要：

  Recent interest in orally available androgens has fueled the search for new androgens for use in hormone replacement therapy and as anabolic agents. In pursuit of this, we have discovered a series of novel androgen receptor modulators derived from 7H-[1,4]oxazino[3,2-g]quinolin-7-ones. These compounds were synthesized and evaluated in competitive binding assays and an androgen receptor transcriptional activation assay. A number of compounds from the series demonstrated single-digit nanomolar agonist activity in vitro. In addition, lead compound (R)-16e was orally active in established rodent models that measure androgenic and anabolic properties of these agents. In this assay, (R)-16e demonstrated full efficacy in muscle and only partially stimulated the prostate at 100 mg/kg. These data suggest that these compounds may be utilized as selective androgen receptor modulators or SARMs. This series represents a novel class of compounds for use in androgen replacement therapy.

  DOI：

  10.1021/jm061329j
• 作为产物：
  描述：

  7-硝基-3,4-二氢-2H-1,4-苯并噁嗪 在 palladium 10% on activated carbon 、 氢气 、 sodium hydride 作用下， 以 乙酸乙酯 、 mineral oil 为溶剂， 反应 2.5h， 生成 7-氨基-4-甲基-2H-1,4-苯并噁嗪
  参考文献：
  名称：

  [EN] INHIBITORS OF MYCOBACTERIUM TUBERCULOSIS LIPOAMIDE DEHYDROGENASE
  [FR] INHIBITEURS DE LA LIPOAMIDE DÉSHYDROGÉNASE DE MYCOBACTERIUM TUBERCULOSIS

  摘要：

  本发明涉及用于抑制脂肪酰胺脱氢酶（Lpd）的化合物和治疗结核病的方法。

  公开号：

  WO2022150574A1

文献信息

• 预防和治疗慢性疼痛药物的胍类化合物
  申请人：绍兴从零医药科技有限公司

  公开号：CN111548313A

  公开（公告）日：2020-08-18

  本发明涉及通式(Ⅰ)所示的涉及作为防治慢性疼痛疾病的胍类化合物、其药学上可接受的盐、其前体药物、其溶剂化物、氘代物或其立体异构体，其中R1、R2、R3、R4、R5、Ar1、Ar2、p和q的定义同说明书中所述定义；本发明还涉及所述化合物的制备方法，含有所述化合物的药物组合物和药物制剂，以及所述化合物在用于预防或治疗哺乳动物治疗带状疱疹疼，三叉神经疼，偏头痛等神经病理性疼痛，胰腺炎，关节炎疼等在内的急慢性炎性疼痛等疼痛症状和疼痛引起的及其他因素引起的睡眠失调等疾病的药物中的应用。
• [EN] QUINAZOLINE DERIVATIVES FOR USE AGAINST CANCER<br/>[FR] DERIVES DE QUINAZOLINE A UTILISER CONTRE LE CANCER
  申请人：ASTRAZENECA AB

  公开号：WO2006040526A1

  公开（公告）日：2006-04-20

  The invention concerns quinazoline derivatives of Formula (I) or a pharmaceutically-acceptable salt, solvate or pro-drug thereof, wherein each of p, R1, q, R2, R3, R4, R5, Ring A, X1, R6, r and R7 has any of the meanings defined in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use in the treatment of cell proliferative disorders or in the treatment of disease states associated with angiogenesis and/or vascular permeability.

  本发明涉及式(I)喹唑啉衍生物或其药物可接受的盐、溶剂化物或前药，其中p、R1、q、R2、R3、R4、R5、环A、X1、R6、r和R7各自具有说明书中定义的任何含义；其制备方法、含有它们的药物组合物以及它们在制造用于治疗细胞增殖障碍或治疗与血管生成和/或血管通透性相关的疾病状态的药物中的应用。
• Bicycloheteroarylamine compounds as ion channel ligands and uses thereof
  申请人：Kelly G. Michael

  公开号：US20050277643A1

  公开（公告）日：2005-12-15

  Amine compounds are disclosed that have a formula represented by the following: The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, traumatic injury, and others.

  抗氨化合物的公开披露，其化学式如下所示： 这些化合物可以制备成药物组合物，并可用于预防和治疗包括人类在内的哺乳动物的各种疾病，例如疼痛、炎症、创伤等。
• Amide derivatives as ion-channel ligands and pharmaceutical compositions and methods of using the same
  申请人：Kelly G. Michael

  公开号：US20060194801A1

  公开（公告）日：2006-08-31

  Compounds are disclosed that have a formula represented by the following: The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, traumatic injury, and others.

  抱歉，我无法直接提供翻译结果。但我可以帮助您翻译这段文字。这段文字的中文翻译如下： 揭示了具有以下表示的公式的化合物： 这些化合物可以制备为药物组合物，并可用于预防和治疗包括人类在内的哺乳动物的各种疾病，例如疼痛、炎症、创伤性损伤等。
• A Druglike Small Molecule that Targets r(CCUG) Repeats in Myotonic Dystrophy Type 2 Facilitates Degradation by RNA Quality Control Pathways
  作者：Sarah Wagner-Griffin、Masahito Abe、Raphael I. Benhamou、Alicia J. Angelbello、Kamalakannan Vishnu、Jonathan L. Chen、Jessica L. Childs-Disney、Matthew D. Disney

  DOI：10.1021/acs.jmedchem.1c00414

  日期：2021.6.24

  Myotonic dystrophy type 2 (DM2) is one of >40 microsatellite disorders caused by RNA repeat expansions. The DM2 repeat expansion, r(CCUG)exp (where “exp” denotes expanded repeating nucleotides), is harbored in intron 1 of the CCHC-type zinc finger nucleic acid binding protein (CNBP). The expanded RNA repeat causes disease by a gain-of-function mechanism, sequestering various RNA-binding proteins including

  2 型强直性肌营养不良 (DM2) 是由 RNA 重复扩增引起的 >40 种微卫星疾病之一。DM2 重复扩增 r(CCUG) exp（其中“exp”表示扩增的重复核苷酸）包含在 CCHC 型锌指核酸结合蛋白 (CNBP) 的内含子 1 中。扩展的 RNA 重复通过功能获得机制引起疾病，隔离各种 RNA 结合蛋白，包括前 mRNA 剪接调节因子 MBNL1。MBNL1 的隔离导致其功能丧失和随之而来的天然底物选择性剪接的失调。值得注意的是，该 r(CCUG) exp导致成熟 CNBP mRNA 中内含子 1 的保留。在此，我们报告了与 r(CCUG) exp采用的结构结合的药物样小分子并改善 DM2 相关缺陷。这些小分子通过筛选来自以 RNA 为重点的小分子文库的命中进行优化，以提供一种化合物，该化合物可特异性结合 r(CCUG) exp并具有纳摩尔亲和力，促进其所在的异常保留内含子的内源性降解，并拯救选择性剪接缺陷。