Cancer cell Cytotoxicities of 1-(4-substitutedbenzoyl)-4-(4-chlorobenzhydryl)piperazine derivatives

A series of novel 1-(4-substitutedbenzoyl)-4-(4-chlorobenzhydryl)piperazine derivatives 5a-g was designed by a nucleophilic substitution reaction of 1-(4-chlorobenzhydryl)piperazine with various benzoyl chlorides and characterized by elemental analyses, IR and 1H nuclear magnetic resonance spectra. Cytotoxicity of the compounds was demonstrated on cancer cell lines from liver (HUH7, FOCUS, MAHLAVU, HEPG2, HEP3B), breast (MCF7, BT20, T47D, CAMA-1), colon (HCT-116), gastric (KATO-3) and endometrial (MFE-296) cancer cell lines. Time-dependent cytotoxicity analysis of compound 5a indicated the long-term in situ stability of this compound. All compounds showed significant cell growth inhibitory activity on the selected cancer cell lines. © 2012 by the authors; licensee MDPI, Basel, Switzerland.

Dergi Adı International Journal of Molecular Sciences
Cild 13
Dergi Sayısı 7
Sayfalar 8071 - 8085
Yayın Tarihi 2012
Eser Adı
[dc.title]
Cancer cell Cytotoxicities of 1-(4-substitutedbenzoyl)-4-(4-chlorobenzhydryl)piperazine derivatives
Yazar
[dc.contributor.author]
Yarim, M.
Yazar
[dc.contributor.author]
Koksal, M.
Yazar
[dc.contributor.author]
Durmaz, I.
Yazar
[dc.contributor.author]
Atalay, R.
Yayın Türü
[dc.type]
article
Özet
[dc.description.abstract]
A series of novel 1-(4-substitutedbenzoyl)-4-(4-chlorobenzhydryl)piperazine derivatives 5a-g was designed by a nucleophilic substitution reaction of 1-(4-chlorobenzhydryl)piperazine with various benzoyl chlorides and characterized by elemental analyses, IR and 1H nuclear magnetic resonance spectra. Cytotoxicity of the compounds was demonstrated on cancer cell lines from liver (HUH7, FOCUS, MAHLAVU, HEPG2, HEP3B), breast (MCF7, BT20, T47D, CAMA-1), colon (HCT-116), gastric (KATO-3) and endometrial (MFE-296) cancer cell lines. Time-dependent cytotoxicity analysis of compound 5a indicated the long-term in situ stability of this compound. All compounds showed significant cell growth inhibitory activity on the selected cancer cell lines. © 2012 by the authors; licensee MDPI, Basel, Switzerland.
Kayıt Giriş Tarihi
[dc.date.accessioned]
2020-03-17
Yayın Tarihi
[dc.date.issued]
2012
Açık Erişim Tarihi
[dc.date.available]
2020-03-17
Dil
[dc.language.iso]
eng
Konu Başlıkları
[dc.subject]
1-(4-chlorobenzhydryl)piperazine derivatives
Konu Başlıkları
[dc.subject]
Benzoyl chlorides
Konu Başlıkları
[dc.subject]
Cancer
Konu Başlıkları
[dc.subject]
Cell proliferation
Konu Başlıkları
[dc.subject]
Cytotoxicity
Haklar
[dc.rights]
info:eu-repo/semantics/openAccess
ISSN
[dc.identifier.issn]
16616596
Yayının ilk sayfa sayısı
[dc.identifier.startpage]
8071
Yayının son sayfa sayısı
[dc.identifier.endpage]
8085
Dergi Adı
[dc.relation.journal]
International Journal of Molecular Sciences
Dergi Sayısı
[dc.identifier.issue]
7
Cild
[dc.identifier.volume]
13
Tek Biçim Adres
[dc.identifier.uri]
https://hdl.handle.net/20.500.11831/2973
Pubmed Id
[dc.identifier.pubmed]
PubMed ID: 22942690
Görüntülenme Sayısı ( Şehir )
Görüntülenme Sayısı ( Ülke )
Görüntülenme Sayısı ( Zaman Dağılımı )
Görüntülenme
21
20.03.2023 tarihinden bu yana
İndirme
1
20.03.2023 tarihinden bu yana
Son Erişim Tarihi
29 Eylül 2023 03:16
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cancer compounds compound (KATO-3) endometrial (MFE-296) indicated gastric (HCT-116) Time-dependent CAMA-1) cytotoxicity analysis long-term activity Switzerland licensee authors selected inhibitory growth significant showed stability substitution chlorides benzoyl various 1-(4-chlorobenzhydryl)piperazine reaction nucleophilic elemental designed derivatives 1-(4-substitutedbenzoyl)-4-(4-chlorobenzhydryl)piperazine
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