Metal chelates of dl-penicillamine
Other investigators have reported that the administration of penicillamine (β,β-dimethylcysteine) to patients with Wilson's disease results in a marked urinary excretion of Cu. Also, the toxic effects of Hg and Pb are reduced by treatments with penicillamine. These observations suggest that pen...
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Veröffentlicht in: | Archives of biochemistry and biophysics 1962-05, Vol.97 (2), p.370-372 |
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description | Other investigators have reported that the administration of penicillamine (β,β-dimethylcysteine) to patients with Wilson's disease results in a marked urinary excretion of Cu. Also, the toxic effects of Hg and Pb are reduced by treatments with penicillamine. These observations suggest that penicillamine has an exceptional ability to bind with metals. Hence, in the present investigation, the formation constants of penicillamine chelates were determined by the potentiometric titration method of Bjerrum. Affinity of bivalent metals for penicillamine results in the following decreasing order: Hg > Ni > Cu > Zn > Cd > Pb. The over-all formation constants (log
K
1
K
2) for the 2:1 chelates for Hg, Ni, and Cu are 23.5, 22.3, and 21.7, respectively, placing penicillamine among the most potent chelating agents for the heavier metals. The structure of the chelates was deduced as a combination of the metal between the NH
2 and SH groups as is the case with cysteine. |
doi_str_mv | 10.1016/0003-9861(62)90090-5 |
format | Article |
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K
1
K
2) for the 2:1 chelates for Hg, Ni, and Cu are 23.5, 22.3, and 21.7, respectively, placing penicillamine among the most potent chelating agents for the heavier metals. The structure of the chelates was deduced as a combination of the metal between the NH
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K
1
K
2) for the 2:1 chelates for Hg, Ni, and Cu are 23.5, 22.3, and 21.7, respectively, placing penicillamine among the most potent chelating agents for the heavier metals. The structure of the chelates was deduced as a combination of the metal between the NH
2 and SH groups as is the case with cysteine.</description><subject>Chelating Agents - chemistry</subject><subject>Metals - chemistry</subject><subject>Old Medline</subject><subject>Penicillamine</subject><subject>Penicillins - chemistry</subject><issn>0003-9861</issn><issn>1096-0384</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1962</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtPwzAQhC0EoqXwDxCqOCA4BNbxI_YFCVW8pCIucLac9UYYJU2JUyT-PSmt4MZpL9_M7AxjxxwuOXB9BQAis0bzc51fWAALmdphYw5WZyCM3GXjX2TEDlJ6B-Bc6nyfjbiUevBQY3b6RL2vp_hGte8pTdtqGupsSYuIsa59Exd0yPYqXyc62t4Je727fZk9ZPPn-8fZzTxDoUyfYalMFWTgBcdCoS8FKMypACnAYgjG-6qwtjJeeRPKQkJhA2pVBiQQZSEm7Gzju-zajxWl3jUxIQ1fLKhdJWcECCXzfADlBsSuTamjyi272Pjuy3Fw623curhbF3c6dz_bODXITrb-q7Kh8CfajjEA1xuAhpafkTqXMNICKcSOsHehjf8nfAMDWXHd</recordid><startdate>196205</startdate><enddate>196205</enddate><creator>Kuchinskas, Edward J.</creator><creator>Rosen, Yale</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>196205</creationdate><title>Metal chelates of dl-penicillamine</title><author>Kuchinskas, Edward J. ; Rosen, Yale</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-cb58fd4d171c75cab305c2e704309cdd8aaf799f8a5a8db74079dc65bdce03b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1962</creationdate><topic>Chelating Agents - chemistry</topic><topic>Metals - chemistry</topic><topic>Old Medline</topic><topic>Penicillamine</topic><topic>Penicillins - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kuchinskas, Edward J.</creatorcontrib><creatorcontrib>Rosen, Yale</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of biochemistry and biophysics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kuchinskas, Edward J.</au><au>Rosen, Yale</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metal chelates of dl-penicillamine</atitle><jtitle>Archives of biochemistry and biophysics</jtitle><addtitle>Arch Biochem Biophys</addtitle><date>1962-05</date><risdate>1962</risdate><volume>97</volume><issue>2</issue><spage>370</spage><epage>372</epage><pages>370-372</pages><issn>0003-9861</issn><eissn>1096-0384</eissn><abstract>Other investigators have reported that the administration of penicillamine (β,β-dimethylcysteine) to patients with Wilson's disease results in a marked urinary excretion of Cu. Also, the toxic effects of Hg and Pb are reduced by treatments with penicillamine. These observations suggest that penicillamine has an exceptional ability to bind with metals. Hence, in the present investigation, the formation constants of penicillamine chelates were determined by the potentiometric titration method of Bjerrum. Affinity of bivalent metals for penicillamine results in the following decreasing order: Hg > Ni > Cu > Zn > Cd > Pb. The over-all formation constants (log
K
1
K
2) for the 2:1 chelates for Hg, Ni, and Cu are 23.5, 22.3, and 21.7, respectively, placing penicillamine among the most potent chelating agents for the heavier metals. The structure of the chelates was deduced as a combination of the metal between the NH
2 and SH groups as is the case with cysteine.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>14460165</pmid><doi>10.1016/0003-9861(62)90090-5</doi><tpages>3</tpages></addata></record> |
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subjects | Chelating Agents - chemistry Metals - chemistry Old Medline Penicillamine Penicillins - chemistry |
title | Metal chelates of dl-penicillamine |
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