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  2. Chelation therapy - Wikipedia

    en.wikipedia.org/wiki/Chelation_therapy

    Chelation therapy is a medical procedure that involves the administration of chelating agents to remove heavy metals from the body. [1] Chelation therapy has a long history of use in clinical toxicology [2] and remains in use for some very specific medical treatments, although it is administered under very careful medical supervision due to various inherent risks, including the mobilization of ...

  3. Ethylenediaminetetraacetic acid - Wikipedia

    en.wikipedia.org/wiki/Ethylenediaminetetraacetic...

    Ethylenediaminetetraacetic acid (EDTA), also called EDTA acid, is an aminopolycarboxylic acid with the formula [CH 2 N(CH 2 CO 2 H) 2] 2. This white, slightly water-soluble solid is widely used to bind to iron (Fe 2+ /Fe 3+) and calcium ions (Ca 2+), forming water-soluble complexes even at neutral pH. It is thus used to dissolve Fe- and Ca ...

  4. Metalloprotease inhibitor - Wikipedia

    en.wikipedia.org/wiki/Metalloprotease_inhibitor

    In vitro, EDTA, 1,10-phenanthroline and other chelating compounds lower the concentration of metal to the point where the metal is removed from the enzyme active site. Classical lock and key inhibitors such as phosphoramidon and bestatin bind tightly by approximating the transition state of the hydrolysis of the peptide, preventing it from ...

  5. Category:Chelating agents - Wikipedia

    en.wikipedia.org/wiki/Category:Chelating_agents

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  6. Chelated platinum - Wikipedia

    en.wikipedia.org/wiki/Chelated_platinum

    Although the concept and practical use of metal chelation is common, chelation of inert metals, such as platinum, has been rarely reported and the yield was extremely low. [2] To produce chelated platinum solution, tetraammonium EDTA, NTA, DTPA or HEDTA type chelating agent was mixed with platinum or platinum chemical compounds. The resulting ...

  7. DOTA (chelator) - Wikipedia

    en.wikipedia.org/wiki/DOTA_(chelator)

    DOTA is derived from the macrocycle known as cyclen.The four secondary amine groups are modified by replacement of the N-H centers with N-CH 2 CO 2 H groups. The resulting aminopolycarboxylic acid, upon ionization of the carboxylic acid groups, is a high affinity chelating agent for di- and trivalent cations.

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