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Revision as of 20:04, 19 April 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'UNII_Ref', 'ChemSpiderID_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEMBL_Ref', 'KEGG_Ref') per Chem/Drugbox validation (← Previous edit Latest revision as of 08:59, 23 June 2023 edit undoGraeme Bartlett (talk | contribs)Administrators249,716 edits caps for c in carboxylate in SMILES 
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{{Orphan|date=April 2011}}

{{chembox {{chembox
| Watchedfields = changed
| verifiedrevid = 355707858 | verifiedrevid = 424908581
| ImageFile =Copper ibuprofenate.png
| ImageSize = 200px | Name =
| ImageFile = Copper(II) Ibuprofenate.jpg
| IUPACName = biscopper(II)
| ImageFile1 = IBPCOP.jpg
| OtherNames =
| IUPACName = biscopper(II)
| Section1 = {{Chembox Identifiers
| OtherNames =
| SystematicName =
| Section1 = {{Chembox Identifiers
| Abbreviations = | Abbreviations =
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 66840-44-6 | CASNo = 66840-44-6
| EINECS = | EINECS =
| PubChem = | PubChem =
| SMILES = C(C(C)C1=CC=C(CC(C)C)C=C1)=O.C(C(C)C1=CC=C(CC(C)C)C=C1)=O. | SMILES = c0cc(CC(C)C)ccc0C(C)(O123)O(O(O1)C(C)c0ccc(CC(C)C)cc0)(O(O2)C(C)c0ccc(CC(C)C)cc0)O(O3)C(C)c0ccc(CC(C)C)cc0
| StdInChI=1S/4C13H17O2.2Cu/c4*1-9(2)8-11-4-6-12(7-5-11)10(3)13(14)15;;/h4*4-7,9-10H,8H2,1-3H3;;/q4*-3;2*+6
| InChI =
| StdInChIKey=HEFOJHHJEKPEDO-UHFFFAOYSA-N
| RTECS = | RTECS =
| MeSHName = | MeSHName =
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| KEGG_Ref = {{keggcite|correct|kegg}} | KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = | KEGG =
}}
| ATCCode_prefix =
| Section2 = {{Chembox Properties
| ATCCode_suffix =
| C=52 | H=68 | O=8 | Cu=2
| ATC_Supplemental =}}
| Section2 = {{Chembox Properties
| C=26 | H=36 | O=4 | Cu=1
| Appearance = Green powder | Appearance = Green powder
| Density = | Density =
| MeltingPt = | MeltingPt =
| Melting_notes = | MeltingPt_notes =
| BoilingPt = | BoilingPt =
| Boiling_notes = | BoilingPt_notes =
| Solubility = Slightly soluble | Solubility = Slightly soluble
| SolubleOther = Slightly soluble | SolubleOther = Slightly soluble
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| pKa = | pKa =
| pKb = }} | pKb = }}
| Section3 = {{Chembox Structure | Section3 = {{Chembox Structure
| CrystalStruct = | CrystalStruct =
| Coordination = | Coordination =
| MolShape = }} | MolShape = }}
| Section4 = {{Chembox Thermochemistry | Section4 = {{Chembox Thermochemistry
| DeltaHf = | DeltaHf =
| DeltaHc = | DeltaHc =
| Entropy = | Entropy =
| HeatCapacity = }} | HeatCapacity = }}
| Section5 = {{Chembox Pharmacology | Section5 = {{Chembox Pharmacology
| AdminRoutes = | AdminRoutes =
| Bioavail = | Bioavail =
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| Legal_AU = | Legal_AU =
| Legal_CA = | Legal_CA =
| PregCat = | Pregnancy_category =
| PregCat_AU = | Pregnancy_AU =
| PregCat_US = }} | Pregnancy_US = }}
| Section6 = {{Chembox Explosive | Section6 = {{Chembox Explosive
| ShockSens = | ShockSens =
| FrictionSens = | FrictionSens =
| ExplosiveV = | DetonationV =
| REFactor = }} | REFactor = }}
| Section7 = {{Chembox Hazards | Section7 = {{Chembox Hazards
| EUClass =
| EUIndex =
| MainHazards = | MainHazards =
| NFPA-H = | NFPA-H =
| NFPA-F = | NFPA-F =
| NFPA-R = | NFPA-R =
| NFPA-O = | NFPA-S =
| RPhrases =
| SPhrases =
| RSPhrases =
| FlashPt = | FlashPt =
| Autoignition = | AutoignitionPt =
| ExploLimits = | ExploLimits =
| PEL = }} | PEL = }}
| Section8 = {{Chembox Related | Section8 = {{Chembox Related
| OtherAnions = | OtherAnions =
| OtherCations = | OtherCations =
| OtherFunctn = | OtherFunction =
| Function = | OtherFunction_label =
| OtherCpds = ] | OtherCompounds = ]
]}} ]}}
}} }}
'''Copper ibuprofenate''' is a ] consisting of ] and the ] form of the ] ].<ref name="latif">{{cite journal|last=A. Latif |first=Abuhijleh|year=1997|title=Synthesis and characterization of copper-ibuprofenate complexes with 2,2'-bipyridine and 1,10-phenanthrolines and their hydrolytic activities in phosphate diester cleavage|journal=Polyhedron|volume=16|issue=4|pages=733–740| doi = 10.1016/0277-5387(96)00214-8}}</ref><ref name="Frazier">{{cite journal|last=Frazier|first=D. R. |coauthors= S. K. Lynch and G. O. Carlisle|year=1981|title=Synthesis and magnetic properties of biscopper(II) |journal=Journal of Inorganic and Nuclear Chemistry|volume=43|issue=11| doi = 10.1016/0022-1902(81)80610-0}}</ref><ref name="Abu">{{cite journal |author=Abuhijleh AL |title=Mononuclear and binuclear copper(II) complexes of the antiinflammatory drug ibuprofen: synthesis, characterization, and catecholase-mimetic activity |journal=J. Inorg. Biochem. |volume=55 |issue=4 |pages=255–62 |year=1994 |month=September |pmid=7964714 |doi= 10.1016/0162-0134(94)85010-0}}</ref> '''Copper ibuprofenate''' is a ] consisting of ] and the ] form of the ] ].<ref name="Frazier">{{cite journal|last=Frazier|first=D. R. |author2=S. K. Lynch |author3=G. O. Carlisle|year=1981|title=Synthesis and magnetic properties of biscopper(II) |journal=Journal of Inorganic and Nuclear Chemistry|volume=43|issue=11|pages=2747–2748 | doi = 10.1016/0022-1902(81)80610-0}}</ref><ref name="Abu">{{cite journal |author=Abuhijleh AL |title=Mononuclear and binuclear copper(II) complexes of the antiinflammatory drug ibuprofen: synthesis, characterization, and catecholase-mimetic activity |journal=J. Inorg. Biochem. |volume=55 |issue=4 |pages=255–62 |date=September 1994 |pmid=7964714 |doi= 10.1016/0162-0134(94)85010-0}}</ref> The compound is prepared by the reaction of sodium ibuprofenate with ].


It has been suggested that copper complexes of anti-inflammatory drugs are more active than the parent drug<ref name="Sorenson">{{cite journal |author=Sorenson JR |title=Copper complexes offer a physiological approach to treatment of chronic diseases |journal=Prog Med Chem |series=Progress in Medicinal Chemistry |volume=26 |pages=437–568 |year=1989 |pmid=2690187 |doi= 10.1016/s0079-6468(08)70246-7|isbn=9780444810380 }}<!--|accessdate=2010-02-01--></ref> and produce fewer gastrointestinal ].<ref name="Gordijo">{{cite journal |vauthors=Gordijo CR, Barbosa CA, Da Costa Ferreira AM, Constantino VR, de Oliveira Silva D |title=Immobilization of ibuprofen and copper-ibuprofen drugs on layered double hydroxides |journal=J Pharm Sci |volume=94 |issue=5 |pages=1135–48 |date=May 2005 |pmid=15793807 |doi=10.1002/jps.20336 }}</ref> In 2008, a ] was issued for the utilization of ibuprofenate complexes (including copper ibuprofenate) as a ].<ref>{{US patent reference
==Usage==
| number = 7462227
Research has suggested that copper complexes of anti-inflammatory drugs are more active than the drug by itself,<ref name="latif" /><ref name="Sorenson">{{cite journal |author=Sorenson JR |title=Copper complexes offer a physiological approach to treatment of chronic diseases |journal=Prog Med Chem |volume=26 |issue= |pages=437–568 |year=1989 |pmid=2690187 |doi= |url= |accessdate=2010-02-01}}</ref> and produce fewer gastrointestinal ].<ref name="Gordijo">{{cite journal |author=Gordijo CR, Barbosa CA, Da Costa Ferreira AM, Constantino VR, de Oliveira Silva D |title=Immobilization of ibuprofen and copper-ibuprofen drugs on layered double hydroxides |journal=J Pharm Sci |volume=94 |issue=5 |pages=1135–48 |year=2005 |month=May |pmid=15793807 |doi=10.1002/jps.20336 }}</ref> In 2008, a ] was issued for the utilization of ibuprofenate complexes (including copper ibuprofenate) as a ].<ref name="uspto">{{cite web|url=http://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO2&Sect2=HITOFF&p=1&u=/netahtml/PTO/search-bool.html&r=1&f=G&l=50&co1=AND&d=PTXT&s1=7462227&OS=7462227&RS=7462227|title=Ibuprofen complexes as wood preservatives - US pat. no, 7,462,227|publisher=US Patent Office|accessdate=1 February 2010}}</ref><ref name="patentstorm">{{cite web|url=http://www.patentstorm.us/patents/7462227/fulltext.html|title=US Patent 7462227 - Ibuprofen complexes as wood preservatives|publisher=Patent Storm|accessdate=1 February 2010}}</ref>
| issue-date = 2007-07-26
| inventor = Anderson, Albert Gordon; Feaster, John; Patel, Damini; Scialdone, Mark
| title = Ibuprofen complexes as wood preservatives
}}</ref>


==References== ==References==
{{reflist}} {{reflist}}


==Further reading==
]
*{{cite journal|last=A. Latif |first=Abuhijleh|year=1997|title=Synthesis and characterization of copper-ibuprofenate complexes with 2,2'-bipyridine and 1,10-phenanthrolines and their hydrolytic activities in phosphate diester cleavage|journal=Polyhedron|volume=16|issue=4|pages=733–740| doi = 10.1016/0277-5387(96)00214-8}}
]

]
]