SYNTHESIS OF SOME CHALCONE DERIVATIVES, IN VITRO AND IN SILICO TOXICITY EVALUATION

A. N. Kristanti, .- and H. Suwito, .- and N.S. Aminah, .- and K.U. Haq, .- and H. D. Hardiyanti, .- and H. Anggraeni, .- and N. Faiza, .- and R.S. Anto, .- and S. Muharromah, .- (2020) SYNTHESIS OF SOME CHALCONE DERIVATIVES, IN VITRO AND IN SILICO TOXICITY EVALUATION. Rasayan Journal of Chemistry, 13 (1). pp. 654-662. ISSN 0974-1496 | e-ISSN: 0976-0083

[img] Text (Fulltext)
C01. Fulltext.pdf

Download (7MB)
[img] Text (Review dan Validasi)
C01. Validasi dan Review.pdf

Download (4MB)
[img] Text (Similarity)
C01. Similarity.pdf

Download (3MB)
[img] Text (Bukti Submission)
C01. Bukti Submission.pdf

Download (2MB)
Official URL: http://rasayanjournal.co.in/admin/php/upload/917_p...

Abstract

Chalcone can be synthesized using some methods, but conventional Claisen-Schmidt condensation is still the best method. The objevtives of this study were to synthesize some chalcone derivatives using conventional ClaisenSchmidt condensation by reacting 2-hydroxyacetophenone and some substituted benzaldehydes using NaOH 40%, followed by evaluating their cytotoxicity in vitro against HeLa cancer cells line using MTT method and analyzing molecular docking on p53 and MDM2 interaction. Cytotoxicity test exhibited that 2,5-dimethoxy-2´- hydroxychalcone and 4-chloro-2'-hydroxychalcone gave very low IC50, but both did not show potential apoptosis activity, while in docking analysis 4-chloro-2'-hydroxychalcone showing the best results.

Item Type: Article
Uncontrolled Keywords: 2-Hydroxychalcone Derivatives, Claisen-Schmidt Condensation, HeLa Cell, Apoptosis, MDM2 Protein
Subjects: Q Science
Q Science > QD Chemistry
Divisions: 08. Fakultas Sains dan Teknologi > Kimia
Creators:
CreatorsNIM
A. N. Kristanti, .-UNSPECIFIED
H. Suwito, .-UNSPECIFIED
N.S. Aminah, .-UNSPECIFIED
K.U. Haq, .-UNSPECIFIED
H. D. Hardiyanti, .-UNSPECIFIED
H. Anggraeni, .-UNSPECIFIED
N. Faiza, .-UNSPECIFIED
R.S. Anto, .-UNSPECIFIED
S. Muharromah, .-UNSPECIFIED
Depositing User: Mr Vega Andi Budiman
Date Deposited: 17 Mar 2022 02:40
Last Modified: 17 Mar 2022 02:40
URI: http://repository.unair.ac.id/id/eprint/113576
Sosial Share:

Actions (login required)

View Item View Item