Substitued (E)-β-(benzoyl)acrylic acids suppressed survival of neoplastic human HeLa cells
Umanjeno preživljavanje neoplastičkih humanih HeLa ćelija supstituisanim (E)-b-(benzoil) akrilnim kiselinama
Autori
Juranić, ZoricaStevović, Lj.
Drakulić, Branko
Stanojković, Tatjana
Radulović, Siniša
Juranić, Ivan
Članak u časopisu (Objavljena verzija)
Metapodaci
Prikaz svih podataka o dokumentuApstrakt
The bacteriostatic activity of some of alkyl substituted (E)-β-(benzoyl)acrylic acids was shown earlier. The aim of this study was to investigate the antiproliferative action of 19 alkyl-, or halogeno-, or methoxy-, or acetamido-substituted (E)-β-(benzoyl)acrylic acids, against human cervix carcinoma, HeLa, cells. Target HeLa cells were continuously treated with increasing concentrations of substituted (E)-β-(benzoyl)acrylic acids during two days. The MTT test was used for assessment of the antiproliferative action of this group of compounds. Treatment of HeLa cells with 4-methyl-, 4-fluoro-, 4-chloro-, 4-bromo-and 4-methoxy-derivatives of (E)-β-(benzoyl) acrylic acid leads to the expression of cytostatic activity against HeLa cells (IC50 were in the range from 31-40 μM). Their antiproliferative action was less than that of the basic compound (E)-β-(benzoyl)acrylic acid whose IC50 was 28.5 μM. The 3,4-dimethyl-, 2,4-dimethyl-and 2,5-dimethyl-derivatives as well as the 4-ethyl-and 3,4-d...ichloro-and 2,4-dichloro-derivatives, have stronger cytostatic activity than the correspoding monosubstituted and parent compound. Their IC50 were 18.5 μM; 17.5 μM; 17.0 μM; 17.5 μM; 22.0 μM and 18 μM, respectively. The 4-iso-propyl-and 4-n-butyl-derivatives excited higher cytostatic activity than the compounds with a lower number of methylene -CH2-groups in the substitutent. Their IC50 were 14.5 μM and 6.5 μM respectively. The 2,5-di-iso-propyl-and 4-tert-butyl-derivatives expressed the most strong antiproliferative action against the investigated HeLa cells, IC50 being 4.5 μM and 5.5 μM, respectively. The investigated compounds affected the survival of HeLa cells, expressing a strong structure-activity relationship of the Hansch type.
Još ranije je pokazana bakteriostatska aktivnost nekih alkil supstituisanih
(E)-b-(benzoil)akrilnih kiselina. Cilj ovog rada je bio proučavanje antiproliferativnog dejstva 19 (E)-b-(benzoil)akrilnih kiselina, alkil-, ili halogeno-, ili metoksi-, ili acetamido-supstituisnaih, na ćelije humnog karcinoma grlića materice,
HeLa ćelije. Ciljne HeLa ćelije, su kontinualno tretirane rastućim koncentracijama
supstituisanih (E)-b-(benzoil)akrilnih kiselina tokom dva dana. MTT test je
korišćen za utvrđanje antiproliferativnog dejstva ovog jedinjenja. Tretiranje HeLa
ćelija 4-metil-, 4-fluoro, 4-hloro-, 4-bromo- i 4-metoksi-derivatima (E)-b-(benzoil)akrilne kiseline dovelo je do ispoljavanja citostatske aktivnosti prema HeLa
ćelijama (IC50 su između 31.40 mM). Njihovo antiproliferativno dejstvo je bilo manje
nego kod osnovnog jedinjenja, (E)-b-(benzoil)akrilne kiseline, čije IC50 je bilo 28,5 mM.
3,4-Dimetil-, 2,4-dimetil- i 2,5-dimetil- supstituisani, kao i 4-etil- te 3,4-dihloro-i
2,4- ...dihloro- derivati, imaju jaču citostatsku aktivnost od odgovarajućeg monosupstituisanog i osnovnog jedinjenja.Njihove IC50 vrednosti su 18,5 mM; 17,5 mM, 17,0 mM; 17,5
mM; 22,0 mMi18mM, u navedenom redosledu. 4-iso-Propil- i 4-n-butil-derivati pokazuju
višu citostatsku aktivnost od jedinjenja sa manjim brojem metilenskih –CH2. grupa u
supstituentu. Wihove IC50 vrednosti su 14,5 mM odnosno 6,5 mM. 2,5-Di-iso-propil- i
4-tert-butil- derivati ispoqavaju najjače antiproliferativno dejstvo prema ispitivanim HeLa ćelijama, IC50 su 4,5 mM i 5,5 mM u navedenom redosledu. Proučavana
jedinjenja utiču na pre.ivqavawe HeLa ćelija, ispoljavajunji izrazitu relaciju Hanschovog tipa između strukture i biološke aktivnosti.
Ključne reči:
Benzoylacrylic acids / Cytotoxicity / HeLa cells / QSARIzvor:
Journal of the Serbian Chemical Society, 1999, 64, 9, 505-512Izdavač:
- Belgrade : Serbian Chemical Society
Finansiranje / projekti:
- The Serbian Ministry of Sciences and Technology
- Boehringer Ingelheim Pharma
Institucija/grupa
IHTMTY - JOUR AU - Juranić, Zorica AU - Stevović, Lj. AU - Drakulić, Branko AU - Stanojković, Tatjana AU - Radulović, Siniša AU - Juranić, Ivan PY - 1999 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/4403 AB - The bacteriostatic activity of some of alkyl substituted (E)-β-(benzoyl)acrylic acids was shown earlier. The aim of this study was to investigate the antiproliferative action of 19 alkyl-, or halogeno-, or methoxy-, or acetamido-substituted (E)-β-(benzoyl)acrylic acids, against human cervix carcinoma, HeLa, cells. Target HeLa cells were continuously treated with increasing concentrations of substituted (E)-β-(benzoyl)acrylic acids during two days. The MTT test was used for assessment of the antiproliferative action of this group of compounds. Treatment of HeLa cells with 4-methyl-, 4-fluoro-, 4-chloro-, 4-bromo-and 4-methoxy-derivatives of (E)-β-(benzoyl) acrylic acid leads to the expression of cytostatic activity against HeLa cells (IC50 were in the range from 31-40 μM). Their antiproliferative action was less than that of the basic compound (E)-β-(benzoyl)acrylic acid whose IC50 was 28.5 μM. The 3,4-dimethyl-, 2,4-dimethyl-and 2,5-dimethyl-derivatives as well as the 4-ethyl-and 3,4-dichloro-and 2,4-dichloro-derivatives, have stronger cytostatic activity than the correspoding monosubstituted and parent compound. Their IC50 were 18.5 μM; 17.5 μM; 17.0 μM; 17.5 μM; 22.0 μM and 18 μM, respectively. The 4-iso-propyl-and 4-n-butyl-derivatives excited higher cytostatic activity than the compounds with a lower number of methylene -CH2-groups in the substitutent. Their IC50 were 14.5 μM and 6.5 μM respectively. The 2,5-di-iso-propyl-and 4-tert-butyl-derivatives expressed the most strong antiproliferative action against the investigated HeLa cells, IC50 being 4.5 μM and 5.5 μM, respectively. The investigated compounds affected the survival of HeLa cells, expressing a strong structure-activity relationship of the Hansch type. AB - Još ranije je pokazana bakteriostatska aktivnost nekih alkil supstituisanih (E)-b-(benzoil)akrilnih kiselina. Cilj ovog rada je bio proučavanje antiproliferativnog dejstva 19 (E)-b-(benzoil)akrilnih kiselina, alkil-, ili halogeno-, ili metoksi-, ili acetamido-supstituisnaih, na ćelije humnog karcinoma grlića materice, HeLa ćelije. Ciljne HeLa ćelije, su kontinualno tretirane rastućim koncentracijama supstituisanih (E)-b-(benzoil)akrilnih kiselina tokom dva dana. MTT test je korišćen za utvrđanje antiproliferativnog dejstva ovog jedinjenja. Tretiranje HeLa ćelija 4-metil-, 4-fluoro, 4-hloro-, 4-bromo- i 4-metoksi-derivatima (E)-b-(benzoil)akrilne kiseline dovelo je do ispoljavanja citostatske aktivnosti prema HeLa ćelijama (IC50 su između 31.40 mM). Njihovo antiproliferativno dejstvo je bilo manje nego kod osnovnog jedinjenja, (E)-b-(benzoil)akrilne kiseline, čije IC50 je bilo 28,5 mM. 3,4-Dimetil-, 2,4-dimetil- i 2,5-dimetil- supstituisani, kao i 4-etil- te 3,4-dihloro-i 2,4- dihloro- derivati, imaju jaču citostatsku aktivnost od odgovarajućeg monosupstituisanog i osnovnog jedinjenja.Njihove IC50 vrednosti su 18,5 mM; 17,5 mM, 17,0 mM; 17,5 mM; 22,0 mMi18mM, u navedenom redosledu. 4-iso-Propil- i 4-n-butil-derivati pokazuju višu citostatsku aktivnost od jedinjenja sa manjim brojem metilenskih –CH2. grupa u supstituentu. Wihove IC50 vrednosti su 14,5 mM odnosno 6,5 mM. 2,5-Di-iso-propil- i 4-tert-butil- derivati ispoqavaju najjače antiproliferativno dejstvo prema ispitivanim HeLa ćelijama, IC50 su 4,5 mM i 5,5 mM u navedenom redosledu. Proučavana jedinjenja utiču na pre.ivqavawe HeLa ćelija, ispoljavajunji izrazitu relaciju Hanschovog tipa između strukture i biološke aktivnosti. PB - Belgrade : Serbian Chemical Society T2 - Journal of the Serbian Chemical Society T1 - Substitued (E)-β-(benzoyl)acrylic acids suppressed survival of neoplastic human HeLa cells T1 - Umanjeno preživljavanje neoplastičkih humanih HeLa ćelija supstituisanim (E)-b-(benzoil) akrilnim kiselinama VL - 64 IS - 9 SP - 505 EP - 512 DO - 10.2298/jsc9909505j ER -
@article{ author = "Juranić, Zorica and Stevović, Lj. and Drakulić, Branko and Stanojković, Tatjana and Radulović, Siniša and Juranić, Ivan", year = "1999", abstract = "The bacteriostatic activity of some of alkyl substituted (E)-β-(benzoyl)acrylic acids was shown earlier. The aim of this study was to investigate the antiproliferative action of 19 alkyl-, or halogeno-, or methoxy-, or acetamido-substituted (E)-β-(benzoyl)acrylic acids, against human cervix carcinoma, HeLa, cells. Target HeLa cells were continuously treated with increasing concentrations of substituted (E)-β-(benzoyl)acrylic acids during two days. The MTT test was used for assessment of the antiproliferative action of this group of compounds. Treatment of HeLa cells with 4-methyl-, 4-fluoro-, 4-chloro-, 4-bromo-and 4-methoxy-derivatives of (E)-β-(benzoyl) acrylic acid leads to the expression of cytostatic activity against HeLa cells (IC50 were in the range from 31-40 μM). Their antiproliferative action was less than that of the basic compound (E)-β-(benzoyl)acrylic acid whose IC50 was 28.5 μM. The 3,4-dimethyl-, 2,4-dimethyl-and 2,5-dimethyl-derivatives as well as the 4-ethyl-and 3,4-dichloro-and 2,4-dichloro-derivatives, have stronger cytostatic activity than the correspoding monosubstituted and parent compound. Their IC50 were 18.5 μM; 17.5 μM; 17.0 μM; 17.5 μM; 22.0 μM and 18 μM, respectively. The 4-iso-propyl-and 4-n-butyl-derivatives excited higher cytostatic activity than the compounds with a lower number of methylene -CH2-groups in the substitutent. Their IC50 were 14.5 μM and 6.5 μM respectively. The 2,5-di-iso-propyl-and 4-tert-butyl-derivatives expressed the most strong antiproliferative action against the investigated HeLa cells, IC50 being 4.5 μM and 5.5 μM, respectively. The investigated compounds affected the survival of HeLa cells, expressing a strong structure-activity relationship of the Hansch type., Još ranije je pokazana bakteriostatska aktivnost nekih alkil supstituisanih (E)-b-(benzoil)akrilnih kiselina. Cilj ovog rada je bio proučavanje antiproliferativnog dejstva 19 (E)-b-(benzoil)akrilnih kiselina, alkil-, ili halogeno-, ili metoksi-, ili acetamido-supstituisnaih, na ćelije humnog karcinoma grlića materice, HeLa ćelije. Ciljne HeLa ćelije, su kontinualno tretirane rastućim koncentracijama supstituisanih (E)-b-(benzoil)akrilnih kiselina tokom dva dana. MTT test je korišćen za utvrđanje antiproliferativnog dejstva ovog jedinjenja. Tretiranje HeLa ćelija 4-metil-, 4-fluoro, 4-hloro-, 4-bromo- i 4-metoksi-derivatima (E)-b-(benzoil)akrilne kiseline dovelo je do ispoljavanja citostatske aktivnosti prema HeLa ćelijama (IC50 su između 31.40 mM). Njihovo antiproliferativno dejstvo je bilo manje nego kod osnovnog jedinjenja, (E)-b-(benzoil)akrilne kiseline, čije IC50 je bilo 28,5 mM. 3,4-Dimetil-, 2,4-dimetil- i 2,5-dimetil- supstituisani, kao i 4-etil- te 3,4-dihloro-i 2,4- dihloro- derivati, imaju jaču citostatsku aktivnost od odgovarajućeg monosupstituisanog i osnovnog jedinjenja.Njihove IC50 vrednosti su 18,5 mM; 17,5 mM, 17,0 mM; 17,5 mM; 22,0 mMi18mM, u navedenom redosledu. 4-iso-Propil- i 4-n-butil-derivati pokazuju višu citostatsku aktivnost od jedinjenja sa manjim brojem metilenskih –CH2. grupa u supstituentu. Wihove IC50 vrednosti su 14,5 mM odnosno 6,5 mM. 2,5-Di-iso-propil- i 4-tert-butil- derivati ispoqavaju najjače antiproliferativno dejstvo prema ispitivanim HeLa ćelijama, IC50 su 4,5 mM i 5,5 mM u navedenom redosledu. Proučavana jedinjenja utiču na pre.ivqavawe HeLa ćelija, ispoljavajunji izrazitu relaciju Hanschovog tipa između strukture i biološke aktivnosti.", publisher = "Belgrade : Serbian Chemical Society", journal = "Journal of the Serbian Chemical Society", title = "Substitued (E)-β-(benzoyl)acrylic acids suppressed survival of neoplastic human HeLa cells, Umanjeno preživljavanje neoplastičkih humanih HeLa ćelija supstituisanim (E)-b-(benzoil) akrilnim kiselinama", volume = "64", number = "9", pages = "505-512", doi = "10.2298/jsc9909505j" }
Juranić, Z., Stevović, Lj., Drakulić, B., Stanojković, T., Radulović, S.,& Juranić, I.. (1999). Substitued (E)-β-(benzoyl)acrylic acids suppressed survival of neoplastic human HeLa cells. in Journal of the Serbian Chemical Society Belgrade : Serbian Chemical Society., 64(9), 505-512. https://doi.org/10.2298/jsc9909505j
Juranić Z, Stevović L, Drakulić B, Stanojković T, Radulović S, Juranić I. Substitued (E)-β-(benzoyl)acrylic acids suppressed survival of neoplastic human HeLa cells. in Journal of the Serbian Chemical Society. 1999;64(9):505-512. doi:10.2298/jsc9909505j .
Juranić, Zorica, Stevović, Lj., Drakulić, Branko, Stanojković, Tatjana, Radulović, Siniša, Juranić, Ivan, "Substitued (E)-β-(benzoyl)acrylic acids suppressed survival of neoplastic human HeLa cells" in Journal of the Serbian Chemical Society, 64, no. 9 (1999):505-512, https://doi.org/10.2298/jsc9909505j . .