In connection to our previously reported phosphine compounds as antitumor agents, this article describes the preparation of ferrocenyl amino-phosphine and their possible cytotoxic potential towards the human hepatocellular carcinoma cell line Hep3B. The preliminary results suggested that ferrocenyl amino-phosphines can be potential anti-tumour agents which might be considered as novel cancer chemotherapeutic agents. In particular, compounds 4b, 4d and 4f exhibit strong cytotoxicity with IC 50 < 5 μg ml -1. These compounds possess more promising cytotoxic activities than their precursor non-substituted ferrocene as well as the reference metallodrug cisplatin.Institute of Textiles and ClothingDepartment of Applied Biology and Chemical Tech...
Molecular compounds containing organometallic tags have been found to be potential therapeutics agai...
One cyclopalladated ferrocene compound CP was synthesized, which showed a good cell cytotoxicity. As...
A series of ferrocenyl ester complexes, varying the lipophilic character of the pendant groups, was ...
A series of planar chiral ferrocene cydopalladated compounds were synthesized and characterized. The...
The discovery of ferrocene in 1951 and subsequent structure elucidation essentially founded the fiel...
Ferrocene, a stable 18-electron metallocene, has been readily modified to include other functionalit...
Ferrocene, a stable 18-electron metallocene, has been readily modified to include other functionalit...
A series of planar chiral ferrocene cyclopalladated compounds were synthesized and characterized. Th...
Since the discovery of ferrocene in 1951 and subsequent structure elucidation in the following years...
Examples of organometallic compounds as nucleoside analogues are rare within the field of medicinal ...
Earlier in vitro studies have shown that ferrocenyl amino acid and dipeptide bioconjugates exhibit a...
The development of new organometallic compounds as anticancer agents is currently an active area of ...
The development of new organometallic compounds as anticancer agents is currently an active area of ...
Cisplatin, the first successful metallotherapy, has been utilized over the past four decades as chem...
Cisplatin, the first successful metallotherapy, has been utilized over the past four decades as chem...
Molecular compounds containing organometallic tags have been found to be potential therapeutics agai...
One cyclopalladated ferrocene compound CP was synthesized, which showed a good cell cytotoxicity. As...
A series of ferrocenyl ester complexes, varying the lipophilic character of the pendant groups, was ...
A series of planar chiral ferrocene cydopalladated compounds were synthesized and characterized. The...
The discovery of ferrocene in 1951 and subsequent structure elucidation essentially founded the fiel...
Ferrocene, a stable 18-electron metallocene, has been readily modified to include other functionalit...
Ferrocene, a stable 18-electron metallocene, has been readily modified to include other functionalit...
A series of planar chiral ferrocene cyclopalladated compounds were synthesized and characterized. Th...
Since the discovery of ferrocene in 1951 and subsequent structure elucidation in the following years...
Examples of organometallic compounds as nucleoside analogues are rare within the field of medicinal ...
Earlier in vitro studies have shown that ferrocenyl amino acid and dipeptide bioconjugates exhibit a...
The development of new organometallic compounds as anticancer agents is currently an active area of ...
The development of new organometallic compounds as anticancer agents is currently an active area of ...
Cisplatin, the first successful metallotherapy, has been utilized over the past four decades as chem...
Cisplatin, the first successful metallotherapy, has been utilized over the past four decades as chem...
Molecular compounds containing organometallic tags have been found to be potential therapeutics agai...
One cyclopalladated ferrocene compound CP was synthesized, which showed a good cell cytotoxicity. As...
A series of ferrocenyl ester complexes, varying the lipophilic character of the pendant groups, was ...