氨三乙酸、缬氨酸、亮氨酸的三元过渡金属配合物:合成和生物学应用

Mostafa M H Khalil Eglal R Souaya Eman H Ismail Eman Rabie

引用本文: Mostafa M H Khalil, Eglal R Souaya, Eman H Ismail, Eman Rabie. 氨三乙酸、缬氨酸、亮氨酸的三元过渡金属配合物:合成和生物学应用[J]. 无机化学学报, 2013, 29(9): 1969-1978. doi: 10.3969/j.issn.1001-4861.2013.00.319 shu
Citation:  Mostafa M H Khalil, Eglal R Souaya, Eman H Ismail, Eman Rabie. Ternary Transition Metal Complexes of Nitrilotriacetic Acid and Valine or Leucine:Synthesis and Biological Applications[J]. Chinese Journal of Inorganic Chemistry, 2013, 29(9): 1969-1978. doi: 10.3969/j.issn.1001-4861.2013.00.319 shu

氨三乙酸、缬氨酸、亮氨酸的三元过渡金属配合物:合成和生物学应用

摘要: 以氨三乙酸HNTA2-为主要配体,缬氨酸(valine)或亮氨酸(leucine)为次要配体在微酸性介质中合成了Ni(Ⅱ),Cu(Ⅱ),and Zn(Ⅱ)的三元配合物。用元素分析、热分析、FTIR,UV-Vis分光光度法,磁性测量和质谱法表征了合成的三元配合物。结果表明,三元配合物可在金属(M):氨三乙酸(HNTA):缬氨酸(valine)或亮氨酸(leucine)=1:1:1时制得,其分子结构为[M(HNTA)(valine)(H2O)2]·1.5H2O and[M(HNTA)(leucine)(H2O)2]·1.5H2O(其中M=Ni(Ⅱ) or Cu(Ⅱ))和H2[Zn(NTA)(valine)(H2O)]H2O。标题三元过渡金属配合物为八面体对称构型。同时研究了该三元配合物对大肠杆菌,金黄色葡萄球菌,白色念珠菌,黄曲霉菌(菌株从开罗大学理学院微分析中心获得)的抗菌活性。根据推荐的知名方法用标准的抗菌和抗真菌剂进行体外测试(in vitro)以评估我们的新制备的配合物对细菌和真菌物种的生长抑制活性。

English

  • 
    1. [1] Charlot M F, Kahn O, Jeannin S, et al. Inorg. Chem., 1980, 19:1411-1416[1] Charlot M F, Kahn O, Jeannin S, et al. Inorg. Chem., 1980, 19:1411-1416

    2. [2] Sigel H, Operschall B P, Massoud S S, et al. Dalton Trans., 2006,46:5521-5529[2] Sigel H, Operschall B P, Massoud S S, et al. Dalton Trans., 2006,46:5521-5529

    3. [3] Czakis-Sulikowska D, Czylkowska A, Radwanska D, et al. J. Therm. Anal. Cal., 2007,90:557-564.[3] Czakis-Sulikowska D, Czylkowska A, Radwanska D, et al. J. Therm. Anal. Cal., 2007,90:557-564.

    4. [4] Bocarsly J R, Barton J K. Inorg. Chem., 1992,31:2827-2832[4] Bocarsly J R, Barton J K. Inorg. Chem., 1992,31:2827-2832

    5. [5] Farver O, Pecht I. Coord. Chem. Rev., 1989,95:17-23[5] Farver O, Pecht I. Coord. Chem. Rev., 1989,95:17-23

    6. [6] Crowe J, Dobeli H, Gentz R, et al. Methods Mol. Bio., 1994, 31:371-387[6] Crowe J, Dobeli H, Gentz R, et al. Methods Mol. Bio., 1994, 31:371-387

    7. [7] Nieba-Axmann S E, Persson A, Hamalainen M, et al. Anal. Biochem., 1997,252:217-222[7] Nieba-Axmann S E, Persson A, Hamalainen M, et al. Anal. Biochem., 1997,252:217-222

    8. [8] Maloriery K M, Shnek D R, Sasaki D Y, et al. Chem. Biol., 1996,3:185-192[8] Maloriery K M, Shnek D R, Sasaki D Y, et al. Chem. Biol., 1996,3:185-192

    9. [9] Bumba L, Tichy M, Dobakova M, et al. J. Struct. Bio., 2005, 152:28-35[9] Bumba L, Tichy M, Dobakova M, et al. J. Struct. Bio., 2005, 152:28-35

    10. [10] Hu Q H, Li X F, Du G C, et al. J. Chem. Engin., 2008,143: 111-116[10] Hu Q H, Li X F, Du G C, et al. J. Chem. Engin., 2008,143: 111-116

    11. [11] Ben Hander G M. Res. J. Chem. Sci., 2012,2(3):12-20[11] Ben Hander G M. Res. J. Chem. Sci., 2012,2(3):12-20

    12. [12] Anderson R L, Bishop W E, Campbell R L. Crit. Re. Toxicol.,1985,15(1):1-102[12] Anderson R L, Bishop W E, Campbell R L. Crit. Re. Toxicol.,1985,15(1):1-102

    13. [13] IARC: Nitrilotriacetic Acid and Its Salts. In: "IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Humans", IARC, Lyons. 1990,48:181-214[13] IARC: Nitrilotriacetic Acid and Its Salts. In: "IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Humans", IARC, Lyons. 1990,48:181-214

    14. [14] Evangelou M W H, Ebel M, Schaeffer A. Chemosphere, 2007,68(6):989-1003[14] Evangelou M W H, Ebel M, Schaeffer A. Chemosphere, 2007,68(6):989-1003

    15. [15] Kaur G, Hasan S K, Srivastava R C. Archives of toxicology, 1980,45:203-206[15] Kaur G, Hasan S K, Srivastava R C. Archives of toxicology, 1980,45:203-206

    16. [16] Pollack S, Ruocco S. in vivo. Blood., 1981,57(6):1117-1118[16] Pollack S, Ruocco S. in vivo. Blood., 1981,57(6):1117-1118

    17. [17] Mendola M E, Paul T, Strathmann T J, et al. Polyhedron, 2009,28:269-78[17] Mendola M E, Paul T, Strathmann T J, et al. Polyhedron, 2009,28:269-78

    18. [18] Kumita H, Jitsukawa K, Masuda H, et al. Inorg. Chim. Acta, 1998,283:160-166[18] Kumita H, Jitsukawa K, Masuda H, et al. Inorg. Chim. Acta, 1998,283:160-166

    19. [19] Anderegg G, Komplexone X L, Helv. Chim. Acta, 1967,50: 2333-40[19] Anderegg G, Komplexone X L, Helv. Chim. Acta, 1967,50: 2333-40

    20. [20] Hopgood D, Augelici R J. J. Am. Chem. Soc., 1968,90: 2508-13[20] Hopgood D, Augelici R J. J. Am. Chem. Soc., 1968,90: 2508-13

    21. [21] Chohan H Z, Arif M, Akhtar M A, et al. Bioinorg. Chem. Appl., 2006,1:83131 DOI: 10.1155/BCA/2006/83131[21] Chohan H Z, Arif M, Akhtar M A, et al. Bioinorg. Chem. Appl., 2006,1:83131 DOI: 10.1155/BCA/2006/83131

    22. [22] Sakyan I, Logoglu E, Arslan S, et al. Biometals, 2004,17(2): 115-120[22] Sakyan I, Logoglu E, Arslan S, et al. Biometals, 2004,17(2): 115-120

    23. [23] Chohan H Z, Arif M, Sarfraz M. Appl. Organomet. Chem., 2007,21(4):294-302[23] Chohan H Z, Arif M, Sarfraz M. Appl. Organomet. Chem., 2007,21(4):294-302

    24. [24] Ramakrishna R, Ashis K, Patra P, et al. Polyhedron, 2008, 27:1343-1352[24] Ramakrishna R, Ashis K, Patra P, et al. Polyhedron, 2008, 27:1343-1352

    25. [25] Jian fang D, Lianzhi L, Guihua L, et al. J. Mol. Struc., 2011, 986:57-63[25] Jian fang D, Lianzhi L, Guihua L, et al. J. Mol. Struc., 2011, 986:57-63

    26. [26] Jian L, Tingting L, Sulan C, et al. J. Inorg. Biochem., 2006, 100:1888-1896[26] Jian L, Tingting L, Sulan C, et al. J. Inorg. Biochem., 2006, 100:1888-1896

    27. [27] Khalil M, Hamed E, Abdel Azim S et al. J. Therm. Anal. Calorim., 2010,101:129-135[27] Khalil M, Hamed E, Abdel Azim S et al. J. Therm. Anal. Calorim., 2010,101:129-135

    28. [28] Dawson R M C. Data for Biochemical Research, Oxford: Clarendon Press, 1959.[28] Dawson R M C. Data for Biochemical Research, Oxford: Clarendon Press, 1959.

    29. [29] Santi E, Torre M H, Kremer E, et al. J. Vib. Spectrosc., 1993,5:285-93[29] Santi E, Torre M H, Kremer E, et al. J. Vib. Spectrosc., 1993,5:285-93

    30. [30] Ismail E H, Souaya E R, Amr A M. J. Appl. Poly. Sci., 2012,124(3):1976-1980[30] Ismail E H, Souaya E R, Amr A M. J. Appl. Poly. Sci., 2012,124(3):1976-1980

    31. [31] Souaya E R, Ismail E H, Mohamed A A, et al. J. Therm. Anal. Calorim., 2009,95:553-558[31] Souaya E R, Ismail E H, Mohamed A A, et al. J. Therm. Anal. Calorim., 2009,95:553-558

    32. [32] Gabbott P. Principles and Applications of Thermal Analysis. 1st ed. UK: Blackwell Publishing Ltd., 2008.[32] Gabbott P. Principles and Applications of Thermal Analysis. 1st ed. UK: Blackwell Publishing Ltd., 2008.

    33. [33] Shengli J, Mian J, Sanping C, et al. J. Therm. Anal. Calorim., 2001,66:423-429.[33] Shengli J, Mian J, Sanping C, et al. J. Therm. Anal. Calorim., 2001,66:423-429.

    34. [34] Chartone-Souza E, Loyola T L, Rodriguez M B, et al. J. Inorg. Biochem., 2005,99:1001-1008[34] Chartone-Souza E, Loyola T L, Rodriguez M B, et al. J. Inorg. Biochem., 2005,99:1001-1008

    35. [35] Gordon A S, Howell L D, Harwood V C. J. Microbiol., 1994, 40:408-411[35] Gordon A S, Howell L D, Harwood V C. J. Microbiol., 1994, 40:408-411

    36. [36] Jawetz E, Melnick J L, Adelberg E A. Review of Medical Microbiology, 16th Ed., Los Anglos, CA: Lang Medical Publications1979.[36] Jawetz E, Melnick J L, Adelberg E A. Review of Medical Microbiology, 16th Ed., Los Anglos, CA: Lang Medical Publications1979.

    37. [37] Hughes W H, Stewart H C. Concise Antibiotic Treatment Butter Worth, London 1970.[37] Hughes W H, Stewart H C. Concise Antibiotic Treatment Butter Worth, London 1970.

  • 加载中
计量
  • PDF下载量:  0
  • 文章访问数:  852
  • HTML全文浏览量:  173
文章相关
  • 收稿日期:  2013-02-16
  • 网络出版日期:  2013-05-28
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

/

返回文章