E-viri
Recenzirano
Odprti dostop
-
Penthala, Narsimha Reddy; Yerramreddy, Thirupathi Reddy; Crooks, Peter A.
Bioorganic & medicinal chemistry letters, 03/2011, Letnik: 21, Številka: 5Journal Article
A series of novel substituted ( Z)-5-((1-benzyl-1 H-indol-3-yl)methylene) imidazolidin-2,4-diones ( 3a– f) and ( Z)-5-((1-benzyl-1 H-indol-3-yl)methylene)-2-iminothiazolidin-4-ones ( 3g– o) have been synthesized and evaluated for in vitro cytotoxicity against a panel of 60 human tumor cell lines . Compound 3i exhibits potent growth inhibition against melanoma UACC-257 (GI 50 = 13.3 nM) and ovarian OVCAR-8 (GI 50 = 19.5 nM) cancer cells and significant cytotoxicity (LC 50 = 308 and 851 nM, respectively) against the same cell lines within this series of compounds. A second analog, 3a, had GI 50 values of 307 and 557 nM against SK-MEL-2 melanoma and A498 renal cancer cell lines, and exhibited GI 50 values ranging from 0.30 to 6 μM against 98% of the cancer cell lines in the 60-cell panel. A series of novel substituted ( Z)-5-((1-benzyl-1 H-indol-3-yl)methylene)imidazolidin-2,4-diones ( 3a– f) and ( Z)-5-((1-benzyl-1 H-indol-3-yl)methylene)-2-iminothiazolidin-4-ones ( 3g– o) have been synthesized utilizing microwave irradiation. These analogs were evaluated for in vitro cytotoxicity against a panel of 60 human tumor cell lines . Compound 3i exhibits potent growth inhibition against melanoma UACC-257 (GI 50 = 13.3 nM) and OVCAR-8 ovarian (GI 50 = 19.5 nM) cancer cells while possessing significant cytotoxicity (LC 50 = 308 nM and LC 50 = 851 nM, respectively) against the same cell lines within this series of compounds. A second analog, 3a, had GI 50 values of 307 and 557 nM against SK-MEL-2 melanoma and A498 renal cancer cell lines, and exhibited GI 50 values ranging from 0.30 to 6 μM against 98% of all cancer cell lines in the 60-cell panel. Thus, ( Z)-5-((5-chloro-1-(4-fluorobenzyl)-1 H-indol-3-yl)methylene)-2-iminothiazolidin-4-one ( 3i) and ( Z)-methyl 1-(4-cyanobenzyl)-3-((2,5-dioxoimidazolidin-4-ylidene)methyl)-1 H-indole-6-carboxylate ( 3a) can be regarded as useful lead compounds for further structural optimization as antitumor agents.
![loading ... loading ...](themes/default/img/ajax-loading.gif)
Vnos na polico
Trajna povezava
- URL:
Faktor vpliva
Dostop do baze podatkov JCR je dovoljen samo uporabnikom iz Slovenije. Vaš trenutni IP-naslov ni na seznamu dovoljenih za dostop, zato je potrebna avtentikacija z ustreznim računom AAI.
Leto | Faktor vpliva | Izdaja | Kategorija | Razvrstitev | ||||
---|---|---|---|---|---|---|---|---|
JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
Baze podatkov, v katerih je revija indeksirana
Ime baze podatkov | Področje | Leto |
---|
Povezave do osebnih bibliografij avtorjev | Povezave do podatkov o raziskovalcih v sistemu SICRIS |
---|
Vir: Osebne bibliografije
in: SICRIS
To gradivo vam je dostopno v celotnem besedilu. Če kljub temu želite naročiti gradivo, kliknite gumb Nadaljuj.