Synthesis, Sunscreen, and Toxicity <i>In Vitro</i> Test of C-Styrylcalix[4]resorcinaryl Octacinnamate and C-Phenylcalix[4]resorcinaryl Dodecacinnamate

The need for qualified sunscreen materials has increased from year to year. This prompt researchers to find new sunscreen ingredients that have good activity. In this study, new C-styrylcalix[4]resorcinaryl octacinnamate 1 and C-phenylcalix[4]resorcinaryl dodecacinnamate 2 have been synthesized via...

Full description

Bibliographic Details
Main Authors: Budiana I Gusti Made Ngurah, Paulus Taek
Format: Article
Language:English
Published: Department of Chemistry, Universitas Gadjah Mada 2022-08-01
Series:Indonesian Journal of Chemistry
Subjects:
Online Access:https://jurnal.ugm.ac.id/ijc/article/view/70019
_version_ 1811321281103003648
author Budiana I Gusti Made Ngurah
Paulus Taek
author_facet Budiana I Gusti Made Ngurah
Paulus Taek
author_sort Budiana I Gusti Made Ngurah
collection DOAJ
description The need for qualified sunscreen materials has increased from year to year. This prompt researchers to find new sunscreen ingredients that have good activity. In this study, new C-styrylcalix[4]resorcinaryl octacinnamate 1 and C-phenylcalix[4]resorcinaryl dodecacinnamate 2 have been synthesized via esterification reaction. The target molecules were characterized by FTIR, 1H-NMR and LC-MS spectrometers. The sunscreen activity was evaluated using an ultraviolet spectrophotometer and the cytotoxicity assay was tested on kidney Vero cells using the cell culture method. Compound 1 was obtained as light brown solid in 68% yield with the melting point of 247 °C. Compound 2 was obtained as light yellow solid in 69% yield with melting point of 268°C. The sunscreen test shows that 1 and 2 can absorb UV-B radiation with the SPF values of 67.45 and 70.85, respectively. The cytotoxicity assay shows that the IC50 values of 1, 2, and parasol are 1468.2, 676.1 and 758.7 μg/mL, respectively. Based on the sunscreen activity test and toxicity assay, it can be said that calix[4]resorcinarenes 1 and 2 have potential to be developed as sunscreen ingredients.
first_indexed 2024-04-13T13:15:15Z
format Article
id doaj.art-7aef4235f11d4918ba702381c8f112f2
institution Directory Open Access Journal
issn 1411-9420
2460-1578
language English
last_indexed 2024-04-13T13:15:15Z
publishDate 2022-08-01
publisher Department of Chemistry, Universitas Gadjah Mada
record_format Article
series Indonesian Journal of Chemistry
spelling doaj.art-7aef4235f11d4918ba702381c8f112f22022-12-22T02:45:30ZengDepartment of Chemistry, Universitas Gadjah MadaIndonesian Journal of Chemistry1411-94202460-15782022-08-012241155116210.22146/ijc.7001932221Synthesis, Sunscreen, and Toxicity <i>In Vitro</i> Test of C-Styrylcalix[4]resorcinaryl Octacinnamate and C-Phenylcalix[4]resorcinaryl DodecacinnamateBudiana I Gusti Made Ngurah0Paulus Taek1Department of Chemistry, Faculty of Education, Universitas Nusa Cendana, Kupang 85001, East Nusa Tenggara, IndonesiaDepartment of Biology, Faculty of Education, Universitas Nusa Cendana, Kupang 85001, East Nusa Tenggara, IndonesiaThe need for qualified sunscreen materials has increased from year to year. This prompt researchers to find new sunscreen ingredients that have good activity. In this study, new C-styrylcalix[4]resorcinaryl octacinnamate 1 and C-phenylcalix[4]resorcinaryl dodecacinnamate 2 have been synthesized via esterification reaction. The target molecules were characterized by FTIR, 1H-NMR and LC-MS spectrometers. The sunscreen activity was evaluated using an ultraviolet spectrophotometer and the cytotoxicity assay was tested on kidney Vero cells using the cell culture method. Compound 1 was obtained as light brown solid in 68% yield with the melting point of 247 °C. Compound 2 was obtained as light yellow solid in 69% yield with melting point of 268°C. The sunscreen test shows that 1 and 2 can absorb UV-B radiation with the SPF values of 67.45 and 70.85, respectively. The cytotoxicity assay shows that the IC50 values of 1, 2, and parasol are 1468.2, 676.1 and 758.7 μg/mL, respectively. Based on the sunscreen activity test and toxicity assay, it can be said that calix[4]resorcinarenes 1 and 2 have potential to be developed as sunscreen ingredients.https://jurnal.ugm.ac.id/ijc/article/view/70019synthesissunscreentoxicityesterification
spellingShingle Budiana I Gusti Made Ngurah
Paulus Taek
Synthesis, Sunscreen, and Toxicity <i>In Vitro</i> Test of C-Styrylcalix[4]resorcinaryl Octacinnamate and C-Phenylcalix[4]resorcinaryl Dodecacinnamate
Indonesian Journal of Chemistry
synthesis
sunscreen
toxicity
esterification
title Synthesis, Sunscreen, and Toxicity <i>In Vitro</i> Test of C-Styrylcalix[4]resorcinaryl Octacinnamate and C-Phenylcalix[4]resorcinaryl Dodecacinnamate
title_full Synthesis, Sunscreen, and Toxicity <i>In Vitro</i> Test of C-Styrylcalix[4]resorcinaryl Octacinnamate and C-Phenylcalix[4]resorcinaryl Dodecacinnamate
title_fullStr Synthesis, Sunscreen, and Toxicity <i>In Vitro</i> Test of C-Styrylcalix[4]resorcinaryl Octacinnamate and C-Phenylcalix[4]resorcinaryl Dodecacinnamate
title_full_unstemmed Synthesis, Sunscreen, and Toxicity <i>In Vitro</i> Test of C-Styrylcalix[4]resorcinaryl Octacinnamate and C-Phenylcalix[4]resorcinaryl Dodecacinnamate
title_short Synthesis, Sunscreen, and Toxicity <i>In Vitro</i> Test of C-Styrylcalix[4]resorcinaryl Octacinnamate and C-Phenylcalix[4]resorcinaryl Dodecacinnamate
title_sort synthesis sunscreen and toxicity i in vitro i test of c styrylcalix 4 resorcinaryl octacinnamate and c phenylcalix 4 resorcinaryl dodecacinnamate
topic synthesis
sunscreen
toxicity
esterification
url https://jurnal.ugm.ac.id/ijc/article/view/70019
work_keys_str_mv AT budianaigustimadengurah synthesissunscreenandtoxicityiinvitroitestofcstyrylcalix4resorcinaryloctacinnamateandcphenylcalix4resorcinaryldodecacinnamate
AT paulustaek synthesissunscreenandtoxicityiinvitroitestofcstyrylcalix4resorcinaryloctacinnamateandcphenylcalix4resorcinaryldodecacinnamate