SYNTHESIS AND CHARACTERIZATION OF ZN(II)-OXIDOBENZYLIDENE AMINOPROPANOATE AND ZN(II)-OXIDOBENZYLIDENE AMINOACETATE COMPLEXES, AND ITS INHIBITION STUDIES ON Α- AMYLASE
Nowadays, the potential of complex compounds in medical applications has been studied by <br /> <br /> many researchers. Many complexes of Zn(II) with Schiff base derivative have been synthesized <br /> <br /> and its potential as antidiabetic type 2 have been studied. In thi...
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id-itb.:289062018-10-04T15:10:03ZSYNTHESIS AND CHARACTERIZATION OF ZN(II)-OXIDOBENZYLIDENE AMINOPROPANOATE AND ZN(II)-OXIDOBENZYLIDENE AMINOACETATE COMPLEXES, AND ITS INHIBITION STUDIES ON Α- AMYLASE YONATHAN SURYANA (NIM:10514017), MICHAEL Indonesia Final Project INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/28906 Nowadays, the potential of complex compounds in medical applications has been studied by <br /> <br /> many researchers. Many complexes of Zn(II) with Schiff base derivative have been synthesized <br /> <br /> and its potential as antidiabetic type 2 have been studied. In this research, synthesis of Zn(II)- <br /> <br /> (E)-2-((2-oxidobenzylidene)amino)propanoate complex (Zn(II)-OBAP complex) and Zn(II)-(E)- <br /> <br /> 2-((2-oxidobenzylidene)amino)acetate complex (Zn(II)-OBAA complex) have been conducted. <br /> <br /> Both complexes were synthesized with stoichiometry ratio Zn(II):salicylaldehyde:amino acid = <br /> <br /> 1,0:1,0:1,1. Both complexes were synthesized in situ. 1H-NMR analysis result of Zn(II)-OBAP <br /> <br /> complex showed a singlet signal at chemical shift of 8,38 ppm, while a singlet signal at chemical <br /> <br /> shift of 8,37 ppm visible in 1H-NMR spectrum of Zn(II)-OBAA. Those singlet signals originated <br /> <br /> from H atom in the imine functional group, which is present in each ligand. FTIR spectrum of <br /> <br /> Zn(II)-OBAP complex showed an imine peak at wavenumber 1623 cm-1, while imine peak at <br /> <br /> wavenumber 1644 cm-1 was observed on FTIR spectrum of Zn(II)-OBAA. Furthermore, on both <br /> <br /> spectra, no aldehyde vibration peak was observed. This indicated that the salicylaldehyde have <br /> <br /> reacted with the amino acid. Based on the analysis of Zn content by AAS, Zn(II)-OBAP <br /> <br /> complex was predicted to have the molecular formula [ZnL1(H2O)].4H2O (L1 = OBAP Ligand), <br /> <br /> while the Zn(II)-OBAA complex was predicted to have the molecular formula <br /> <br /> [ZnL2(H2O)].4H2O (L2 = OBAA Ligand). Bioactivity assay using -amylase showed that both of <br /> <br /> complexes cannot inhibit -amylase activity in vitro.n vitro. text |
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Nowadays, the potential of complex compounds in medical applications has been studied by <br />
<br />
many researchers. Many complexes of Zn(II) with Schiff base derivative have been synthesized <br />
<br />
and its potential as antidiabetic type 2 have been studied. In this research, synthesis of Zn(II)- <br />
<br />
(E)-2-((2-oxidobenzylidene)amino)propanoate complex (Zn(II)-OBAP complex) and Zn(II)-(E)- <br />
<br />
2-((2-oxidobenzylidene)amino)acetate complex (Zn(II)-OBAA complex) have been conducted. <br />
<br />
Both complexes were synthesized with stoichiometry ratio Zn(II):salicylaldehyde:amino acid = <br />
<br />
1,0:1,0:1,1. Both complexes were synthesized in situ. 1H-NMR analysis result of Zn(II)-OBAP <br />
<br />
complex showed a singlet signal at chemical shift of 8,38 ppm, while a singlet signal at chemical <br />
<br />
shift of 8,37 ppm visible in 1H-NMR spectrum of Zn(II)-OBAA. Those singlet signals originated <br />
<br />
from H atom in the imine functional group, which is present in each ligand. FTIR spectrum of <br />
<br />
Zn(II)-OBAP complex showed an imine peak at wavenumber 1623 cm-1, while imine peak at <br />
<br />
wavenumber 1644 cm-1 was observed on FTIR spectrum of Zn(II)-OBAA. Furthermore, on both <br />
<br />
spectra, no aldehyde vibration peak was observed. This indicated that the salicylaldehyde have <br />
<br />
reacted with the amino acid. Based on the analysis of Zn content by AAS, Zn(II)-OBAP <br />
<br />
complex was predicted to have the molecular formula [ZnL1(H2O)].4H2O (L1 = OBAP Ligand), <br />
<br />
while the Zn(II)-OBAA complex was predicted to have the molecular formula <br />
<br />
[ZnL2(H2O)].4H2O (L2 = OBAA Ligand). Bioactivity assay using -amylase showed that both of <br />
<br />
complexes cannot inhibit -amylase activity in vitro.n vitro. |
format |
Final Project |
author |
YONATHAN SURYANA (NIM:10514017), MICHAEL |
spellingShingle |
YONATHAN SURYANA (NIM:10514017), MICHAEL SYNTHESIS AND CHARACTERIZATION OF ZN(II)-OXIDOBENZYLIDENE AMINOPROPANOATE AND ZN(II)-OXIDOBENZYLIDENE AMINOACETATE COMPLEXES, AND ITS INHIBITION STUDIES ON Α- AMYLASE |
author_facet |
YONATHAN SURYANA (NIM:10514017), MICHAEL |
author_sort |
YONATHAN SURYANA (NIM:10514017), MICHAEL |
title |
SYNTHESIS AND CHARACTERIZATION OF ZN(II)-OXIDOBENZYLIDENE AMINOPROPANOATE AND ZN(II)-OXIDOBENZYLIDENE AMINOACETATE COMPLEXES, AND ITS INHIBITION STUDIES ON Α- AMYLASE |
title_short |
SYNTHESIS AND CHARACTERIZATION OF ZN(II)-OXIDOBENZYLIDENE AMINOPROPANOATE AND ZN(II)-OXIDOBENZYLIDENE AMINOACETATE COMPLEXES, AND ITS INHIBITION STUDIES ON Α- AMYLASE |
title_full |
SYNTHESIS AND CHARACTERIZATION OF ZN(II)-OXIDOBENZYLIDENE AMINOPROPANOATE AND ZN(II)-OXIDOBENZYLIDENE AMINOACETATE COMPLEXES, AND ITS INHIBITION STUDIES ON Α- AMYLASE |
title_fullStr |
SYNTHESIS AND CHARACTERIZATION OF ZN(II)-OXIDOBENZYLIDENE AMINOPROPANOATE AND ZN(II)-OXIDOBENZYLIDENE AMINOACETATE COMPLEXES, AND ITS INHIBITION STUDIES ON Α- AMYLASE |
title_full_unstemmed |
SYNTHESIS AND CHARACTERIZATION OF ZN(II)-OXIDOBENZYLIDENE AMINOPROPANOATE AND ZN(II)-OXIDOBENZYLIDENE AMINOACETATE COMPLEXES, AND ITS INHIBITION STUDIES ON Α- AMYLASE |
title_sort |
synthesis and characterization of zn(ii)-oxidobenzylidene aminopropanoate and zn(ii)-oxidobenzylidene aminoacetate complexes, and its inhibition studies on Α- amylase |
url |
https://digilib.itb.ac.id/gdl/view/28906 |
_version_ |
1821995218635849728 |