Abstract:
:An efficient synthesis of dialkylsubstituted maleic anhydrides 1a-j is described. The inhibitory potential of these original anhydride derivatives was tested toward the three human isoforms A, B and C of dual specific phosphatases Cdc25. A micromolar range inhibition of Cdc25s was observed with the maleic anhydrides bearing simple alkyl side chains longer than C(9), to reach the optimal activity with a C(17) chain length.
journal_name
Eur J Med Chemjournal_title
European journal of medicinal chemistryauthors
Brault L,Denancé M,Banaszak E,El Maadidi S,Battaglia E,Bagrel D,Samadi Mdoi
10.1016/j.ejmech.2006.09.014subject
Has Abstractpub_date
2007-02-01 00:00:00pages
243-7issue
2eissn
0223-5234issn
1768-3254pii
S0223-5234(06)00349-7journal_volume
42pub_type
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