Sinteza unor derivați ai 1,2,4-triazolului în baza n-[4-(3-metil-5-sulfanil-4h-1,2,4-triazol-4-il)fenil]acetamidei
Închide
Conţinutul numărului revistei
Articolul precedent
Articolul urmator
794 12
Ultima descărcare din IBN:
2024-04-12 10:51
Căutarea după subiecte
similare conform CZU
547.792.2 (1)
Chimie organică (484)
SM ISO690:2012
RUSNAC, Roman, GARBUZ, Olga, BARBĂ, Nicanor, GULEA, Aurelian, BALAN, Greta, BRUDUNIUC, Olga. Sinteza unor derivați ai 1,2,4-triazolului în baza n-[4-(3-metil-5-sulfanil-4h-1,2,4-triazol-4-il)fenil]acetamidei. In: Studia Universitatis Moldaviae (Seria Ştiinţe Reale şi ale Naturii), 2018, nr. 1(111), pp. 133-143. ISSN 1814-3237.
EXPORT metadate:
Google Scholar
Crossref
CERIF

DataCite
Dublin Core
Studia Universitatis Moldaviae (Seria Ştiinţe Reale şi ale Naturii)
Numărul 1(111) / 2018 / ISSN 1814-3237 /ISSNe 1857-498X

Sinteza unor derivați ai 1,2,4-triazolului în baza n-[4-(3-metil-5-sulfanil-4h-1,2,4-triazol-4-il)fenil]acetamidei

Ynthesis of derivatives of 1,2,4-triazol based on n-[4-(3-methyl-5-sulfanyl-4h-1,2,4-triazol-4-yl)phenyl]acetamide

CZU: 547.792.2

Pag. 133-143

Rusnac Roman1, Garbuz Olga1, Barbă Nicanor1, Gulea Aurelian1, Balan Greta2, Bruduniuc Olga3
 
1 Universitatea de Stat din Moldova,
2 Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu“,
3 Agenţia Naţională pentru Sănătate Publică
 
 
Disponibil în IBN: 30 septembrie 2018


Rezumat

În articol sunt descrise metodele de sinteză a 8 compuși organici din seria 1,2,4-triazol-3-tiolilor, dintre care 7 compuși sunt noi, a căror structură a fost confirmată prin sinteză și cu ajutorul metodelor spectrale: 1H-RMN, 13C-RMN și IR (FTIR). Compușii (2) și (3) au fost investigați cu ajutorul difracției razelor X pe monocristal. Unii compuși obținuți au demonstrat proprietăți antiproliferative moderate: inhibă creșterea celulelor de HEp-2 și BxPC-3. Activitate antifungică au demonstrat compușii (2) și (7), cu o valoare a CMI de 0,125 μg/mL. Proprietățile antioxidative au fost studiate cu ajutorul metodei ABTS și DPPH; astfel, cel mai bun atioxidant s-a dovedit a fi 2-[(2- hidroxifenil)metiliden]-N-[4-(3-metil-5-sulfanil-4H-1,2,4-triazol-4-il)fenil]hidrazin-1-carbotioamida (7)..  

The article describes the synthesis methods of 8 organic compounds from the 1,2,4-triazole-3-thiol series, of which 7 compounds are new. The structure of compounds was confirmed by spectral methods: 1H-NMR, 13C -RMN and IR (FTIR). The triazoles (2) and (3) were investigated by X-ray diffraction on monocrystal. Some compounds have demonstrated moderate antiproliferative properties, in growth of HEp-2 and BxPC-3 cells. Antifungal activity is characteristic far compounds (2) and (7) with a MIC of 0.125 μg/mL. Antioxidative properties were studied using the ABTS and DPPH method where the best one was found to be 2-[(2-hydroxyphenyl)methylidene]-N-[4-(3-methyl-5- sulfanyl-4-triazol-4-yl)phenyl]hydrazine-1-carbothioamide (7).

Cuvinte-cheie
1, 2, anticancer,

4-triazol, tiosemicarbazone,

antioxidativ, N-fenil-acetamidă.

Cerif XML Export

<?xml version='1.0' encoding='utf-8'?>
<CERIF xmlns='urn:xmlns:org:eurocris:cerif-1.5-1' xsi:schemaLocation='urn:xmlns:org:eurocris:cerif-1.5-1 http://www.eurocris.org/Uploads/Web%20pages/CERIF-1.5/CERIF_1.5_1.xsd' xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance' release='1.5' date='2012-10-07' sourceDatabase='Output Profile'>
<cfResPubl>
<cfResPublId>ibn-ResPubl-66268</cfResPublId>
<cfResPublDate>2018-09-15</cfResPublDate>
<cfVol>111</cfVol>
<cfIssue>1</cfIssue>
<cfStartPage>133</cfStartPage>
<cfISSN>1814-3237</cfISSN>
<cfURI>https://ibn.idsi.md/ro/vizualizare_articol/66268</cfURI>
<cfTitle cfLangCode='RO' cfTrans='o'>Sinteza unor derivați ai 1,2,4-triazolului &icirc;n baza n-[4-(3-metil-5-sulfanil-4h-1,2,4-triazol-4-il)fenil]acetamidei</cfTitle>
<cfKeyw cfLangCode='RO' cfTrans='o'>1; 2; 4-triazol; tiosemicarbazone; anticancer; antioxidativ; N-fenil-acetamidă.</cfKeyw>
<cfAbstr cfLangCode='RO' cfTrans='o'><p>&Icirc;n articol sunt descrise metodele de sinteză a 8 compuși organici din seria 1,2,4-triazol-3-tiolilor, dintre care 7 compuși sunt noi, a căror structură a fost confirmată prin sinteză și cu ajutorul metodelor spectrale: <sup>1</sup>H-RMN, <sup>13</sup>C-RMN și IR (FTIR). Compușii (2) și (3) au fost investigați cu ajutorul difracției razelor X pe monocristal. Unii compuși obținuți au demonstrat proprietăți antiproliferative moderate: inhibă creșterea celulelor de HEp-2 și BxPC-3. Activitate antifungică au demonstrat compușii (2) și (7), cu o valoare a CMI de 0,125 &mu;g/mL. Proprietățile antioxidative au fost studiate cu ajutorul metodei ABTS și DPPH; astfel, cel mai bun atioxidant s-a dovedit a fi 2-[(2- hidroxifenil)metiliden]-N-[4-(3-metil-5-sulfanil-4<em>H</em>-1,2,4-triazol-4-il)fenil]hidrazin-1-carbotioamida (7).. &nbsp;</p></cfAbstr>
<cfAbstr cfLangCode='EN' cfTrans='o'><p>The article describes the synthesis methods of 8 organic compounds from the 1,2,4-triazole-3-thiol series, of which 7 compounds are new. The structure of compounds was confirmed by spectral methods: <sup>1</sup>H-NMR, <sup>13</sup>C -RMN and IR (FTIR). The triazoles (2) and (3) were investigated by X-ray diffraction on monocrystal. Some compounds have demonstrated moderate antiproliferative properties, in growth of HEp-2 and BxPC-3 cells. Antifungal activity is characteristic far compounds (2) and (7) with a MIC of 0.125 &mu;g/mL. Antioxidative properties were studied using the ABTS and DPPH method where the best one was found to be 2-[(2-hydroxyphenyl)methylidene]-N-[4-(3-methyl-5- sulfanyl-4-triazol-4-yl)phenyl]hydrazine-1-carbothioamide (7).</p></cfAbstr>
<cfResPubl_Class>
<cfClassId>eda2d9e9-34c5-11e1-b86c-0800200c9a66</cfClassId>
<cfClassSchemeId>759af938-34ae-11e1-b86c-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
</cfResPubl_Class>
<cfResPubl_Class>
<cfClassId>e601872f-4b7e-4d88-929f-7df027b226c9</cfClassId>
<cfClassSchemeId>40e90e2f-446d-460a-98e5-5dce57550c48</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
</cfResPubl_Class>
<cfPers_ResPubl>
<cfPersId>ibn-person-42837</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-42831</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-15791</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-499</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-43478</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-58708</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
</cfPers_ResPubl>
</cfResPubl>
<cfPers>
<cfPersId>ibn-Pers-42837</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-42837-2</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
<cfFamilyNames>Rusnac</cfFamilyNames>
<cfFirstNames>Roman</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-42831</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-42831-2</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
<cfFamilyNames>Garbuz</cfFamilyNames>
<cfFirstNames>Olga</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-15791</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-15791-2</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
<cfFamilyNames>Barba</cfFamilyNames>
<cfFirstNames>Nicanor</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-499</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-499-2</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
<cfFamilyNames>Gulya</cfFamilyNames>
<cfFirstNames>Aurelian</cfFirstNames>
<cfFamilyNames>Гуля</cfFamilyNames>
<cfFirstNames>Аурелиан</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-43478</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-43478-2</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
<cfFamilyNames>Balan</cfFamilyNames>
<cfFirstNames>Greta</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-58708</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-58708-2</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2018-09-15T24:00:00</cfStartDate>
<cfFamilyNames>Бурдунюк</cfFamilyNames>
<cfFirstNames>Ольга</cfFirstNames>
</cfPersName_Pers>
</cfPers>
</CERIF>