6933-26-2Relevant academic research and scientific papers
Time-resolved spectroscopic study of the photochemistry of tiaprofenic acid in a neutral phosphate buffered aqueous solution from femtoseconds to final products
Su, Tao,Ma, Jiani,Li, Ming-De,Guan, Xiangguo,Yu, Lihong,Phillips, David Lee
, p. 811 - 824 (2013)
The photo-decarboxylation and overall reaction mechanism of tiaprofenic acid (TPA) was investigated by femtosecond transient absorption (fs-TA), nanosecond transient absorption (ns-TA), and nanosecond time-resolved resonance Raman (ns-TR3) spec
Mechanism of lipid peroxidation photosensitized by tiaprofenic acid: Product studies using linoleic acid and 1,4-Cyclohexadienes as model substrates
Samadi, Abdelouahid,Martinez, Luis A.,Miranda, Miguel A.,Morera, Isabel M.
, p. 359 - 365 (2007/10/03)
A careful study of the linoleic acid hydroperoxide (LOOH) profile obtained upon peroxidation of linoleic acid (LA) photosensitized by tiaprofenic acid (TPA) and analogous ketones has been undertaken to distinguish between type-I and type-II photoperoxidation mechanisms. 1,4-Cyclohexadiene and 1,2-dimethylcyclohexa-2,5-diene-carboxylic acid (CHDCA) have also been used as models for LA since they also have double allylic systems. Coir-radiation of LA with TPA and decarboxytiaprofenic acid (DTPA) in acetonitrile and micellar media produced significant amounts of conjugated dienic LOOH. The cis,trans to trans,trans ratio depended on the irradiation time; thus, this parameter is an ambiguous tool for mechanistic assignment. An interesting finding was the decrease of the LOOH level after long irradiation times in mixtures photooxidized by DTPA, which is attributed to quenching of the DTPA triplet by the generated dienic LOOH. High-performance liquid chromatography analyses confirmed that the main pathway operating in photodynamic lipid peroxidation sensitized by (D)TPA is a type-I mechanism. However, product studies using CHDCA have clearly shown that a type-II mechanism is also operating and might contribute to the overall photooxidation process in a significant way.
Structure and photochemical behavior of the cyclodextrin inclusion complexes of the benzoylthiophene-derived drugs tiaprofenic acid (= 5-benzoyl-α-methylthiophene-2-acetic acid) and suprofen (=α-methyl-4-(2-thienylcarbonyl)benzeneacetic acid)
Monti, Sandra,Encinas, Susana,Lahoz, Agustin,Marconi, Giancarlo,Sortino, Salvatore,Perez-Prieto, Julia,Miranda, Miguel A.
, p. 2452 - 2466 (2007/10/03)
The effect of β-cyclodextrin (β-CD) on the excited-state reactivity of the two benzoylthiophene derivatives, tiaprofenic acid (TPA; 2) and suprofen (SPF; 3) in their carboxylate forms is studied. The presence of βcyclodextrin does not affect the nature of the photoproduced transients and the photoproducts, but increases the photodegradation quantum yields of both drugs. The efficiency of the photodecarboxylation process is enhanced. This effect is rationalized in the light of the inclusion of 2 and 3 in the β-CD cavity, affecting the energy of the lowest excited states of the drugs. The structure of the complexes is determined by induced circular dichroism, and molecular-mechanics and dynamic Monte Carlo calculations. The photoreactivity of the decarboxylated photoproduct 7 of tiaprofenic acid (2) in presence of β-CD is also examined.
Antibodies directed to drug epitopes to investigate the structure of drug-protein photoadducts. Recognition of a common photobound substructure in tiaprofenic acid/ketoprofen cross-photoreactivity
Lahoz,Hernandez,Miranda,Perez-Prieto,Morera,Castell
, p. 1486 - 1491 (2007/10/03)
Drug-induced photoallergy is an immune adverse reaction to the combined effect of drugs and light. From the mechanistic point of view, it first involves covalent binding of drug to protein resulting in the formation of a photoantigen. Hence, determination of the structures of drug-protein photoadducts is of great relevance to understand the molecular basis of photoallergy and cross-immunoreactivity among drugs. Looking for new strategies to investigate the covalent photobinding of drugs to proteins, we generated highly specific antibodies to drug chemical substructures. The availability of such antibodies has allowed us to discriminate between the different modes by which tiaprofenic acid (TPA), suprofen (SUP), and ketoprofen (KTP) photobind to proteins. The finding that the vast majority of the TPA photoadduct can be accounted for by means of antibody anti-benzoyl strongly supports the view that the drug binds preferentially via the thiophene ring, leaving the benzene ring more accessible. By contrast, selective recognition of SUP-protein photoadducts by antibody anti-thenoyl evidences a preferential coupling via the benzene ring leaving the thiophene moiety more distant from the protein matrix. In the case of KTP, photoadducts are exclusively recognized by antibody anti-benzoyl, indicating that the benzene ring is again more accessible. As a result of this research, we have been able to identify a common substructure that is present in TPA-albumin and KTP-albumin photoadducts. This is remarkable since, at a first sight, the greatest structural similarities can be found between TPA and SUP as they share the same benzoylthiophene chromophore. These findings can explain the previously reported observations of cross-reactivity to KTP (or TPA) in patients photosensitized to TPA (or KTP).
Photochemistry of tiaprofenic acid, a nonsteroidal anti-inflammatory drug with phototoxic side effects
Bosca,Miranda,Vargas
, p. 181 - 182 (2007/10/02)
The phototoxic nonsteroidal anti-inflammatory drug tiaprofenic acid (1) is photolabile under aerobic conditions. Irradiation of a methanol solution of 1 under oxygen produces the photoproducts 2, 3, 4, and 5, and also produces a singlet oxygen as evidenced by trapping with 2,5-dimethylfuran.
Synthesis of some Thiophenium Bis(t-butoxycarbonyl)methylides
Bowles, Timothy,Jones, Ray,Porter, Alexander E. A.,Rechka, Josef A.,Rzepa, Henry S.,Williams, David J.
, p. 1023 - 1028 (2007/10/02)
Thiophene derivatives react with di-t-butyl diazomalonate in the presence of rhodium(II) carboxylates to yield thiophenium bis(t-butoxycarbonyl)methylides.Rhodium(II) hexanoate is a more efficient catalyst than rhodium(II) acetate, shortening reaction times and increasing yields of the ylides.Series of 2-halogeno-, 2-alkyl-, 2-benzyl-5-halogeno-, and 2-benzyl-5-alkyl-thiophenium ylides are described.Whilst 2-methyl-, 2-ethyl-, and 2-isopropyl-thiophenes readily form the ylides in good yield, 2-t-butylthiophene appears to undergo further reaction to yield 1,3-bis-t-butoxycarbonyl-2-(3-t-butyl-6,6-bis-t-butoxycarbonyl-2-thioniabicyclohex-3-en-2-yl)methanide (2) whose structure has been confirmed by X-ray crystallography.
