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- W2430361736 abstract "Replacement of key structural or binding elements of a peptide lead with nonpeptide components can improve affinity and metabolic stability (1-5). Such a strategy was successfully applied to the generation of potent, cell-permeable inhibitors of Ras famesyltransferase (FTase) (6,7). The central pair of amino acids in the CAAX tetrapeptide was replaced with the nonpeptide scaffold 3-methylamino-1-carboxymethyl-2,3-dihydro-5-phenyl-1H-1,4-benzodiazepin-2-one, (N-Me)BZA, shown below." @default.
- W2430361736 created "2016-06-24" @default.
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- W2430361736 date "2003-11-14" @default.
- W2430361736 modified "2023-09-25" @default.
- W2430361736 title "Synthesis of 3-Amino-1-Carboxymethyl- Benzodiazepine (BZA) Peptidomimetics" @default.
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- W2430361736 doi "https://doi.org/10.1385/0-89603-517-4:385" @default.
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