3-氨基-n-[2-(4-吗啉)乙基]苯甲酰胺 | 746570-90-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 3-氨基-n-[2-(4-吗啉)乙基]苯甲酰胺
• 英文名称: 3-amino-N-(2-morpholinoethyl)benzamide
• 英文别名: 3-amino-N-[2-(morpholin-4-yl)ethyl]benzamide；3-amino-N-(2-morpholin-4-ylethyl)benzamide
• CAS: 746570-90-1
• 化学式: C₁₃H₁₉N₃O₂
• mdl: MFCD09741241
• 分子量: 249.313
• InChiKey: MZBSDNLQCYWGGQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.2
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.461
• 拓扑面积：
  67.6
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-氨基-n-[2-(4-吗啉)乙基]苯甲酰胺 、 (E)-3-(4-(adamantan-1-yl)phenoxy)acrylic acid 在 N,N-二异丙基乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 以40.5%的产率得到(E)-3-[3-(4-adamantan-1-yl-phenoxy)-acryloylamino]-N-(2-morpholine-4-yl-ethyl)-benzamide
  参考文献：
  名称：

  Synthesis and Structure–Activity Relationship of (E)-Phenoxyacrylic Amide Derivatives as Hypoxia-Inducible Factor (HIF) 1α Inhibitors

  摘要：

  A series of (E)-phenoxyacrylic amide derivatives were synthesized and evaluated as hypoxia inducible factor (HIF) la inhibitors. The present structure activity relationship study on this series identified the morpholinoethyl containing ester 4p as a potent inhibitor of HIF-1 alpha under hypoxic conditions (IC50 = 0.12 mu M in a cell-based HRE reporter assay) in HCT116 cells. The representative compound 4p suppressed hypoxia-induced HIF-1 alpha accumulation and targeted gene expression in a dose-dependent manner. The effect of HIF-l alpha inhibition by 4p was further demonstrated by its inhibitory activity on in vitro tube formation and migration of cells, which may be valuable for development of novel therapeutics for cancer and tumor angiogenesis.

  DOI：

  10.1021/jm301419d
• 作为产物：
  描述：

  N-(2-morpholinoethyl)-3-nitrobenzamide 在 palladium 10% on activated carbon 氢气 作用下， 以 乙醇 为溶剂， 反应 2.0h， 生成 3-氨基-n-[2-(4-吗啉)乙基]苯甲酰胺
  参考文献：
  名称：

  5-OXO-5,8-DIHYDRO-PYRIDO-PYRIMIDINES AS INHIBITORS OF C-FMS KINASE

  摘要：

  本发明针对当前对选择性和强效蛋白酪氨酸激酶抑制剂的需求，提供对c-fms激酶的强效抑制剂。本发明涉及以下式I的新化合物： 或其盐、对映体、互变异构体、结晶、多晶型、无定形、溶剂化物、水合物、酯、前药或代谢物形式，其中A、Y、Z、R 101 和R 200 在说明书中有描述。

  公开号：

  US20080114007A1

文献信息

• 5-OXO-5,8-DIHYDRO-PYRIDO-PYRIMIDINES AS INHIBITORS OF C-FMS KINASE
  申请人：Player R. Mark

  公开号：US20080114007A1

  公开（公告）日：2008-05-15

  The invention addresses the current need for selective and potent protein tyrosine kinase inhibitors by providing potent inhibitors of c-fms kinase. The invention is directed to the novel compounds of Formula I: or a salt, stereoisomer, tautomer, crystalline, polymorph, amorphous, solvate, hydrate, ester, prodrug or metabolite form thereof, wherein A, Y, Z, R 101 and R 200 are described in the specification.

  本发明针对当前对选择性和强效蛋白酪氨酸激酶抑制剂的需求，提供对c-fms激酶的强效抑制剂。本发明涉及以下式I的新化合物： 或其盐、对映体、互变异构体、结晶、多晶型、无定形、溶剂化物、水合物、酯、前药或代谢物形式，其中A、Y、Z、R 101 和R 200 在说明书中有描述。
• KINASE INHIBITORS
  申请人：RESPIVERT LIMITED

  公开号：US20150210722A1

  公开（公告）日：2015-07-30

  There are provided compounds of formula (I), wherein R 1 to R 5 , X 1 , X 2 , Ar, L, A, A 1 , E and G have meanings given in the description, which compounds have anti-inflammatory activity (e.g., through inhibition of one or more of members of: the family of p38 mitogen-activated protein kinase enzymes; Syk kinase; and members of the Src family of tyrosine kinases) and have use in therapy, including in pharmaceutical combinations, especially in the treatment of inflammatory diseases, including inflammatory diseases of the lung, eye and intestines.

  提供了化合物的结构式(I)，其中R1至R5，X1，X2，Ar，L，A，A1，E和G的含义如描述所示，这些化合物具有抗炎活性（例如，通过抑制p38丝裂原活化蛋白激酶家族中的一个或多个成员；Syk激酶；以及酪氨酸激酶Src家族的成员之一）并且可用于治疗，包括在药物组合中，尤其是用于治疗包括肺部、眼部和肠道炎症疾病在内的炎症性疾病。
• ARYLOXY PHENOXY ACRYLIC COMPOUND HAVING HIF-1 INHIBITION ACTIVITY, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION CONTAINING SAME AS AN ACTIVE INGREDIENT
  申请人：Lee Kyeong

  公开号：US20130237542A1

  公开（公告）日：2013-09-12

  The present invention relates to a compound inhibiting HF-1 activity, a preparation method of the same, and a pharmaceutical composition comprising the same as an active ingredient. The compound of the present invention demonstrates anticancer activity not by non-selective cytotoxicity but by inhibiting the activity of HIF-1, the transcription factor playing an important role in cancer cell growth and metastasis. Accordingly, the compound or the pharmaceutically acceptable salt thereof according to the present invention inhibits HIF-1 activity, and therefore can be used as a therapeutic agent for solid tumors such as colon cancer, liver cancer, stomach cancer and breast cancer. In addition, the compound or the pharmaceutically acceptable salt thereof according to the present invention can be used as an active ingredient for a therapeutic agent for diabetic retinopathy or arthritis which may become worse when hypoxia-induced VEGF expression by HIF-1 increases.

  本发明涉及一种抑制HF-1活性的化合物，以及该化合物的制备方法和包含该化合物作为活性成分的药物组合物。本发明的化合物通过抑制HIF-1活性而不是通过非选择性细胞毒性表现出抗癌活性，HIF-1是在癌细胞生长和转移中起重要作用的转录因子。因此，根据本发明的化合物或其药用盐抑制HIF-1活性，因此可以用作固体肿瘤如结肠癌、肝癌、胃癌和乳腺癌的治疗剂。此外，根据本发明的化合物或其药用盐还可以用作糖尿病视网膜病变或关节炎的治疗剂的活性成分，当HIF-1诱导的VEGF表达增加时，这些疾病可能会恶化。
• 二芳基酰胺类化合物及其应用
  申请人：北京龙嘉博创医药科技有限公司

  公开号：CN112107568B

  公开（公告）日：2022-03-25

  本发明公开了具有式(I)所示结构的二芳基酰胺类化合物、其药学上可接受的盐在制备作为尿素通道蛋白抑制剂的药物中的用途以及一类新型的二芳基酰胺类化合物，本发明的二芳基酰胺类化合物具有良好的尿素通道蛋白抑制剂作用，能够在体内产生尿素选择性利尿并且没有明显的毒性作用。
• [EN] DIARYLAMIDE COMPOUND AND APPLICATION THEREOF<br/>[FR] COMPOSÉ DE DIARYLAMIDE ET SON APPLICATION<br/>[ZH] 二芳基酰胺类化合物及其应用
  申请人：UNIV BEIJING

  公开号：WO2020253802A1

  公开（公告）日：2020-12-24

  具有式(I)所示结构的二芳基酰胺类化合物、其药学上可接受的盐在制备作为尿素通道蛋白抑制剂的药物中的用途以及一类新型的二芳基酰胺类化合物，所述二芳基酰胺类化合物具有尿素通道蛋白抑制剂作用，能够在体内产生尿素选择性利尿并且没有明显的毒性作用。