N-substituted tetrahydro-2,4-dioxoquinazolin-1-yl acetic acids as aldose reductase inhibitors
Novel N-substituted tetrahydro-2,4-dioxoquinazolin-1-yl acetic acids characterized by formal replacement of the substituted benzyl moiety by cyclohexylmethyl and n-heptyl residues, respectively, were synthesized and evaluated as aldose reductase inhibitors.
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Published in: | Pharmazie Vol. 62; no. 8; p. 636 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
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01-08-2007
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Abstract | Novel N-substituted tetrahydro-2,4-dioxoquinazolin-1-yl acetic acids characterized by formal replacement of the substituted benzyl moiety by cyclohexylmethyl and n-heptyl residues, respectively, were synthesized and evaluated as aldose reductase inhibitors. |
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AbstractList | Novel N-substituted tetrahydro-2,4-dioxoquinazolin-1-yl acetic acids characterized by formal replacement of the substituted benzyl moiety by cyclohexylmethyl and n-heptyl residues, respectively, were synthesized and evaluated as aldose reductase inhibitors. |
Author | Matuszczak, B Rakowitz, D Gmeiner, A |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/17867563$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Acetates - chemical synthesis Acetates - pharmacology Aldehyde Reductase - antagonists & inhibitors Animals Cattle Dimethyl Sulfoxide Enzyme Inhibitors - chemical synthesis Enzyme Inhibitors - pharmacology Lens, Crystalline - enzymology Magnetic Resonance Spectroscopy Quinazolines - chemical synthesis Quinazolines - pharmacology Solvents Spectrometry, Mass, Electrospray Ionization |
Title | N-substituted tetrahydro-2,4-dioxoquinazolin-1-yl acetic acids as aldose reductase inhibitors |
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