Design and synthesis of potent, non-peptidic inhibitors of HPTPbeta.

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Citation

Amarasinghe KK, Evdokimov AG, Xu K, Clark CM, Maier MB, Srivastava A, Colson AO, Gerwe GS, Stake GE, Howard BW, Pokross ME, Gray JL, Peters KG

Design and synthesis of potent, non-peptidic inhibitors of HPTPbeta.

Bioorg Med Chem Lett. 2006 Aug 15;16(16):4252-6. Epub 2006 Jun 12.

PubMed ID
16759857 [ View in PubMed
]
Abstract

The sulfamic acid phosphotyrosine mimetic was coupled with a previously known malonate template to obtain highly selective and potent inhibitors of HPTPbeta. Potentially hydrolyzable malonate ester functionalities were replaced with 1,2,4-oxadiazoles without a significant effect on HPTPbeta potency.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Receptor-type tyrosine-protein phosphatase betaP23467Details