N-[[4-(p-Toluoylamino)phenyl]sulfonyl]-D-phenylalanine

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: N-[[4-(p-Toluoylamino)phenyl]sulfonyl]-D-phenylalanine
• 英文别名: (R)-2-[4-(4-Methyl-benzoylamino)-benzenesulfonylamino]-3-phenyl-propionic acid；(2R)-2-[[4-[(4-methylbenzoyl)amino]phenyl]sulfonylamino]-3-phenylpropanoic acid
• 化学式: C₂₃H₂₂N₂O₅S
• 分子量: 438.504
• InChiKey: WUMGWKJNFKXXRX-OAQYLSRUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  31
• 可旋转键数：
  8
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.13
• 拓扑面积：
  121
• 氢给体数：
  3
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  D-phenylalanine tert-butyl ester 在 palladium on activated charcoal N-甲基吗啉 、 氢气 、 三氟乙酸 作用下， 以 甲醇 、 二氯甲烷 、 乙酸乙酯 为溶剂， 反应 2.0h， 生成 N-[[4-(p-Toluoylamino)phenyl]sulfonyl]-D-phenylalanine
  参考文献：
  名称：

  Highly Selective and Orally Active Inhibitors of Type IV Collagenase (MMP-9 and MMP-2):  N-Sulfonylamino Acid Derivatives

  摘要：

  Various N-sulfonylamino acid derivatives were synthesized and evaluated for their in vitro and in vivo activities to inhibit type IV collagenase (MMP-9 and MMP-2). When the amino acid residue and the sulfonamide moiety were modified, their inhibitory activities were greatly affected by the structure of the sulfonamide moiety. A series of aryl sulfonamide derivatives containing biaryl, tetrazole, amide, and triple bond were found to be potent and highly selective inhibitors of MMP-9 and MMP-2 In addition, these compounds were orally active in animal models of tumor growth and metastasis. These results revealed the potential of the N-sulfonylamino acid derivatives as a new type of candidate drug for the treatment of cancer.

  DOI：

  10.1021/jm9707582

文献信息

• Sulfonylamino acid derivatives as metalloproteinase inhibitors
  申请人：ONO PHARMACEUTICAL CO., LTD.

  公开号：EP0757037A2

  公开（公告）日：1997-02-05

  The present invention relates to: (i) matrix metalloproteinase (MMP) inhibitors containing sulfonylamino acid derivatives of the formula (Ia): wherein R1 is hydrogen, C1-4 alkyl; R2 is hydrogen, C1-8 alkyl etc.; E is -CONR3-, in which R3 is hydrogen, C1-4 alkyl etc., -NR3CO-, -CO-O-, -O-CO- etc.; A is hydrogen, C1-8 alkyl, C3-7 cycloalkyl, or Ar; J is bond, C2-4 alkylene etc.; G is -(CH2)m-, in which m is 2, 3 or 4, or in which R6 and R7 is hydrogen, C1-8 alkyl etc.; and non-toxic salts thereof, (ii) novel sulfonylamino acid derivatives of the formula (Ib): wherein all the symbols are as defined for formula (Ia), with the exclusion of certain compounds; and non-toxic salts thereof, and (iii) processes for the preparation of the compounds of formula (Ib). The compounds of formulae (Ia) and (Ib) are useful for prevention and/or treatment of diseases induced by overexpression or excess activity of MMP, such as rheumatoid diseases, arthrosteitis, unusual bone resorption, osteoporosis, periodontitis, interstitial nephritis, arteriosclerosis, pulmonary emphysema, cirrhosis, cornea injury, metastasis, invasion or growth of tumor cells, autoimmune diseases (Crohn's disease, Sjogren's syndrome etc.), diseases caused by vascular emigration or infiltration of leukocytes, or arterialization.

  本发明涉及 (i) 含式(Ia)的磺酰基氨基酸衍生物的基质金属蛋白酶(MMP)抑制剂： 其中R1是氢、C1-4烷基；R2是氢、C1-8烷基等；E是-CONR3-，其中R3是氢、C1-4烷基等、-NR3CO-、-CO-O-、-O-CO-等；A是氢、C1-8烷基、C3-7环烷基或Ar；J是键、C2-4亚烷基等；G是-(CH2)m-，其中m是2、3或4，或 其中 R6 和 R7 是氢、C1-8 烷基等；以及它们的无毒盐、 (ii) 式(Ib)的新型磺酰基氨基酸衍生物： 其中所有符号与式 (Ia) 所定义的相同，但某些化合物除外；及其无毒盐，以及 (iii) 式(Ib)化合物的制备工艺。 式(Ia)和(Ib)化合物可用于预防和/或治疗因 MMP 过度表达或活性过强而诱发的疾病，如类风湿病、关节炎、异常骨吸收、骨质疏松症、牙周炎、间质性肾炎、动脉硬化、肺气肿、肝硬化、角膜损伤、肿瘤细胞转移、侵袭或生长、自身免疫性疾病（克罗恩病、Sjogren 综合征等）、血管外流引起的疾病。白细胞的血管迁移或浸润或动脉化引起的疾病。
• US6177466B1
  申请人：——

  公开号：US6177466B1

  公开（公告）日：2001-01-23
• US6403644B1
  申请人：——

  公开号：US6403644B1

  公开（公告）日：2002-06-11
• Highly Selective and Orally Active Inhibitors of Type IV Collagenase (MMP-9 and MMP-2):  <i>N</i>-Sulfonylamino Acid Derivatives
  作者：Yoshinori Tamura、Fumihiko Watanabe、Takuji Nakatani、Ken Yasui、Masahiro Fuji、Tadafumi Komurasaki、Hiroshige Tsuzuki、Ryuji Maekawa、Takayuki Yoshioka、Kenji Kawada、Kenji Sugita、Mitsuaki Ohtani

  DOI：10.1021/jm9707582

  日期：1998.2.1

  Various N-sulfonylamino acid derivatives were synthesized and evaluated for their in vitro and in vivo activities to inhibit type IV collagenase (MMP-9 and MMP-2). When the amino acid residue and the sulfonamide moiety were modified, their inhibitory activities were greatly affected by the structure of the sulfonamide moiety. A series of aryl sulfonamide derivatives containing biaryl, tetrazole, amide, and triple bond were found to be potent and highly selective inhibitors of MMP-9 and MMP-2 In addition, these compounds were orally active in animal models of tumor growth and metastasis. These results revealed the potential of the N-sulfonylamino acid derivatives as a new type of candidate drug for the treatment of cancer.