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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 124 (1993), S. 83-102 
    ISSN: 1434-4475
    Keywords: Estradiol derivatives ; Platinum(II) complexes ; Human mammary carcinoma cell lines MDA-MB 231 and MCF-7 ; Antitumor activity ; Estrogen-receptor binding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Estrogen-receptor binding moieties were introduced into Pt(II) complexes in order to facilitate the selective transport into cancer cells. Estradiol esters of 2,3-diaminopropionic acid and estradiol ethers of 1,2-diamino-2-methyl-3-(p-hydroxyphenyl)propane were attached to Pt(II) complexes. The antitumor activity of the compounds was tested towards the human mammary carcinoma cell lines MDA-MB 231 and MCF-7, respectively, and the estrogen-receptor binding affinity of the Pt(II) complexes was determined. The steroidal Pt(II) complexes gave a maximum growth inhibition of 80% and a maximum estrogen-receptor binding affinity of 5.18.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 1029-1038 
    ISSN: 0009-2940
    Keywords: Antitumor activity ; 1, 2-Diaminoethanes ; P388 Leukemia ; Platinum(II) complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Twelve new diamine ligands are synthesized and characterized in which a benzyl group and another vicinal substituent or a benzyl group, a 4-Cl-benzyl group, and a 4-MeO-benzyl group, respectively, and two other geminal substituents are attached to the 1,2-diaminoethane skeleton. The diamine ligands are transformed into the dichloroplatinum(II) complexes. The chloride ligands of four complexes are replaced by the lactate anion, α-Cyclodextrin and polyvinylpyrrolidone are used to increase the water solubility of the Pt(II) complexes. The antitumor activity of the Pt(II) complexes is tested towards the P388 leukemia. The compounds with small alkyl substituents show antitumor activities which are much higher than the antitumor activity of cis-platinum. Compared to the insoluble dichloro complexes, the lactate complexes and the formulations with α-cyclodextrin and polyvinylpyrrolidone exhibit good water solubility, and no decrease of the antitumor activity is observed.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 128 (1995), S. 173-181 
    ISSN: 0009-2940
    Keywords: Porphyrins ; Platinum(II) complexes ; Photodynamic therapy ; Antitumor activity ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Platinum(II) Complexes with Porphyrin Ligands: Synthesis and Synergisms in the Photodynamic Tumor TherapyTwelve porphyrin ligands (2-5, 8, 13-16, 19, 27, 28) and their platinum(II) complexes (29-40) were synthesized and characterized. Nine of the porphyrins are derived from hemin, and three are based on tetraphenylporphyrin. The ligands were transformed into diammine-dicarboxylatoplatinum(II) complexes and diamine-dichloroplatinum(II) complexes. The antitumor activity in the photodynamic therapy of the ligands and their complexes was tested in vitro towards the MDA-MB-231 mammary carcinoma cell line. The results obtained showed an additive effect of the photodynamic activity of the porphyrin skeleton when irradiated with visible red light and the cytotoxic activity of the platinum moiety in the complexes.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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