New 1,3,4-thiadiazoles derivatives : synthesis, antiproliferative activity, molecular docking and molecular dynamics
Aim: A series of 1,3,4-thiadiazole himachalene hybrids were prepared from the treatment of a himachalen-4-one thiosemicarbazone derivative with N-aryl-C-ethoxycarbonyl-nitrilimines and diarylnitrilimines via a 1,3-dipolar cycloaddition reaction. Materials & methods: The structures were confirmed by NMR, IR and high-resolution mass spectroscopy (HRMS). Results & conclusion: The newly synthesized hybrid compounds were tested for their in vitro antitumor activities against a panel of cancer cell lines including fibrosarcoma (HT-1080), lung carcinoma (A-549) and breast carcinoma (MCF-7 and MDA-MB-231). Among the tested products, 4a showed excellent activity against the HT-1080 and MCF-7 cell lines with IC50 values of 11.18 ± 0.69 and 12.38 ± 0.63 μm, comparable to that of the reference drug. Docking results confirmed that the active inhibitors were well accumulated in the mushroom tyrosinase active site. Flow cytometry analysis indicated that hybrid 4a induced apoptosis and cell cycle arrest in the G0/G1 phase. Molecular modeling studies affirmed the intercalative binding of compound 4a in the active site.
| Medienart: |
E-Artikel |
|---|
| Erscheinungsjahr: |
2022 |
|---|---|
| Erschienen: |
2022 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:14 |
|---|---|
| Enthalten in: |
Future medicinal chemistry - 14(2022), 12 vom: 15. Juni, Seite 881-897 |
| Sprache: |
Englisch |
|---|
| Beteiligte Personen: |
Bimoussa, Abdoullah [VerfasserIn] |
|---|
| Links: |
|---|
| Themen: |
1,3,4-thiadiazole |
|---|
| Anmerkungen: |
Date Completed 10.06.2022 Date Revised 06.09.2022 published: Print-Electronic Citation Status MEDLINE |
|---|
| doi: |
10.4155/fmc-2022-0016 |
|---|
| funding: |
|
|---|---|
| Förderinstitution / Projekttitel: |
|
| PPN (Katalog-ID): |
NLM341920665 |
|---|
| LEADER | 01000naa a22002652 4500 | ||
|---|---|---|---|
| 001 | NLM341920665 | ||
| 003 | DE-627 | ||
| 005 | 20231226012859.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 231226s2022 xx |||||o 00| ||eng c | ||
| 024 | 7 | |a 10.4155/fmc-2022-0016 |2 doi | |
| 028 | 5 | 2 | |a pubmed24n1139.xml |
| 035 | |a (DE-627)NLM341920665 | ||
| 035 | |a (NLM)35670219 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 100 | 1 | |a Bimoussa, Abdoullah |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a New 1,3,4-thiadiazoles derivatives |b synthesis, antiproliferative activity, molecular docking and molecular dynamics |
| 264 | 1 | |c 2022 | |
| 336 | |a Text |b txt |2 rdacontent | ||
| 337 | |a ƒaComputermedien |b c |2 rdamedia | ||
| 338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
| 500 | |a Date Completed 10.06.2022 | ||
| 500 | |a Date Revised 06.09.2022 | ||
| 500 | |a published: Print-Electronic | ||
| 500 | |a Citation Status MEDLINE | ||
| 520 | |a Aim: A series of 1,3,4-thiadiazole himachalene hybrids were prepared from the treatment of a himachalen-4-one thiosemicarbazone derivative with N-aryl-C-ethoxycarbonyl-nitrilimines and diarylnitrilimines via a 1,3-dipolar cycloaddition reaction. Materials & methods: The structures were confirmed by NMR, IR and high-resolution mass spectroscopy (HRMS). Results & conclusion: The newly synthesized hybrid compounds were tested for their in vitro antitumor activities against a panel of cancer cell lines including fibrosarcoma (HT-1080), lung carcinoma (A-549) and breast carcinoma (MCF-7 and MDA-MB-231). Among the tested products, 4a showed excellent activity against the HT-1080 and MCF-7 cell lines with IC50 values of 11.18 ± 0.69 and 12.38 ± 0.63 μm, comparable to that of the reference drug. Docking results confirmed that the active inhibitors were well accumulated in the mushroom tyrosinase active site. Flow cytometry analysis indicated that hybrid 4a induced apoptosis and cell cycle arrest in the G0/G1 phase. Molecular modeling studies affirmed the intercalative binding of compound 4a in the active site | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a 1,3,4-thiadiazole | |
| 650 | 4 | |a apoptosis | |
| 650 | 4 | |a himachalenes | |
| 650 | 4 | |a in vitro | |
| 650 | 4 | |a molecular mechanisms | |
| 650 | 7 | |a Antineoplastic Agents |2 NLM | |
| 650 | 7 | |a Thiadiazoles |2 NLM | |
| 700 | 1 | |a Oubella, Ali |e verfasserin |4 aut | |
| 700 | 1 | |a Bamou, Fatima Zahra |e verfasserin |4 aut | |
| 700 | 1 | |a Khdar, Zein Alabdeen |e verfasserin |4 aut | |
| 700 | 1 | |a Fawzi, Mourad |e verfasserin |4 aut | |
| 700 | 1 | |a Laamari, Yassine |e verfasserin |4 aut | |
| 700 | 1 | |a Ait Itto, My Youssef |e verfasserin |4 aut | |
| 700 | 1 | |a Morjani, Hamid |e verfasserin |4 aut | |
| 700 | 1 | |a Auhmani, Aziz |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Future medicinal chemistry |d 2009 |g 14(2022), 12 vom: 15. Juni, Seite 881-897 |w (DE-627)NLM194822109 |x 1756-8927 |7 nnns |
| 773 | 1 | 8 | |g volume:14 |g year:2022 |g number:12 |g day:15 |g month:06 |g pages:881-897 |
| 856 | 4 | 0 | |u http://dx.doi.org/10.4155/fmc-2022-0016 |3 Volltext |
| 912 | |a GBV_USEFLAG_A | ||
| 912 | |a GBV_NLM | ||
| 951 | |a AR | ||
| 952 | |d 14 |j 2022 |e 12 |b 15 |c 06 |h 881-897 | ||