Transplatin: Difference between revisions

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{{Short description|Chemical compound}}
{{DISPLAYTITLE:Transplatin}}
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| ImageFile = TransPtCl2A2.svg
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| ImageAlt = Structure of trans-dichlorodiammineplatinum(II)
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'''Transplatin''', or '''trans-dichlorodiammineplatinum(II)''', is a chemical compound with the formula trans-[PtCl<sub>2</sub>(NH<sub>3</sub>)<sub>2</sub>]. It is an isomer of the more well-known [[cisplatin]], which is used as a chemotherapy drug. Unlike cisplatin, transplatin is not effective as an anticancer agent.
== Overview ==
[[File:TransPtCl2A2.svg|thumb|right|Structure of Transplatin]]
'''Transplatin''' is a [[platinum-based chemotherapy]] drug that is an isomer of the more widely known [[cisplatin]]. Unlike cisplatin, which is used in the treatment of various types of [[cancer]], transplatin is not effective as an anticancer agent. This difference in activity is primarily due to the distinct geometric configuration of the two compounds.


==Structure and properties==
== Chemical Structure ==
Transplatin is a [[coordination complex]] of platinum with two chloride ions and two ammonia molecules. The compound is characterized by its trans configuration, meaning that the two chloride ions are opposite each other in the molecular structure. This configuration is in contrast to the cis configuration found in cisplatin, where the chloride ions are adjacent.
Transplatin, or trans-diamminedichloroplatinum(II), has a [[square planar]] geometry with two [[ammonia]] molecules and two [[chloride]] ions arranged in a trans configuration around a central platinum atom. This configuration is in contrast to the cis configuration found in cisplatin, where the ligands are adjacent to each other.


The trans configuration of transplatin affects its chemical reactivity and biological activity. The compound is less able to form cross-links with [[DNA]], which is a key mechanism by which cisplatin exerts its anticancer effects. As a result, transplatin does not have the same therapeutic properties as cisplatin.
== Mechanism of Action ==
The lack of anticancer activity in transplatin is attributed to its inability to form the same type of [[DNA cross-links]] as cisplatin. In cisplatin, the cis configuration allows the formation of intrastrand cross-links between adjacent [[guanine]] bases on [[DNA]], which is crucial for its cytotoxic effects. Transplatin, however, forms interstrand cross-links that are less effective at disrupting DNA function.


==Synthesis==
== Clinical Use ==
Transplatin can be synthesized by the reaction of [[potassium tetrachloroplatinate(II)]] with ammonia in the presence of a chloride source. The reaction typically involves the formation of an intermediate complex, which rearranges to form the trans isomer. The synthesis of transplatin is often carried out in an aqueous solution, and the product can be isolated by crystallization.
Transplatin is not used in clinical settings for cancer treatment due to its poor efficacy. However, it has been studied for its potential use in combination with other drugs or as a scaffold for developing new platinum-based compounds with improved activity and reduced side effects.


==Applications==
== Research and Development ==
While transplatin itself is not used as a drug, it serves as a useful compound in the study of platinum-based chemotherapy agents. Researchers have investigated various derivatives of transplatin in an effort to develop new anticancer drugs with improved properties. Some of these derivatives have shown promise in preclinical studies.
Research into transplatin and its derivatives continues, as scientists seek to understand the structural and chemical properties that influence the activity of platinum-based drugs. Modifications to the transplatin structure, such as changing the ligands or altering the platinum coordination environment, are being explored to enhance its therapeutic potential.


==Related compounds==
== Related Pages ==
* [[Cisplatin]]
* [[Cisplatin]]
* [[Carboplatin]]
* [[Platinum-based chemotherapy]]
* [[Oxaliplatin]]
* [[DNA cross-linking]]
 
==References==
* {{cite journal |last1=Rosenberg |first1=B. |last2=VanCamp |first2=L. |last3=Trosko |first3=J. E. |last4=Mansour |first4=V. H. |title=Platinum compounds: a new class of potent antitumour agents |journal=Nature |volume=222 |issue=5191 |pages=385–386 |year=1969 |doi=10.1038/222385a0}}
* {{cite book |last=Keppler |first=B. K. |title=Metal Complexes in Cancer Chemotherapy |publisher=VCH |year=1993 |isbn=978-3-527-28302-4}}
 
==Related pages==
* [[Chemotherapy]]
* [[Coordination chemistry]]
* [[Platinum]]


[[Category:Chemotherapy]]
[[Category:Platinum compounds]]
[[Category:Platinum compounds]]
[[Category:Coordination complexes]]
[[Category:Antineoplastic drugs]]

Latest revision as of 03:41, 13 February 2025


Overview[edit]

Structure of Transplatin

Transplatin is a platinum-based chemotherapy drug that is an isomer of the more widely known cisplatin. Unlike cisplatin, which is used in the treatment of various types of cancer, transplatin is not effective as an anticancer agent. This difference in activity is primarily due to the distinct geometric configuration of the two compounds.

Chemical Structure[edit]

Transplatin, or trans-diamminedichloroplatinum(II), has a square planar geometry with two ammonia molecules and two chloride ions arranged in a trans configuration around a central platinum atom. This configuration is in contrast to the cis configuration found in cisplatin, where the ligands are adjacent to each other.

Mechanism of Action[edit]

The lack of anticancer activity in transplatin is attributed to its inability to form the same type of DNA cross-links as cisplatin. In cisplatin, the cis configuration allows the formation of intrastrand cross-links between adjacent guanine bases on DNA, which is crucial for its cytotoxic effects. Transplatin, however, forms interstrand cross-links that are less effective at disrupting DNA function.

Clinical Use[edit]

Transplatin is not used in clinical settings for cancer treatment due to its poor efficacy. However, it has been studied for its potential use in combination with other drugs or as a scaffold for developing new platinum-based compounds with improved activity and reduced side effects.

Research and Development[edit]

Research into transplatin and its derivatives continues, as scientists seek to understand the structural and chemical properties that influence the activity of platinum-based drugs. Modifications to the transplatin structure, such as changing the ligands or altering the platinum coordination environment, are being explored to enhance its therapeutic potential.

Related Pages[edit]