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Volumn 105, Issue , 2014, Pages 49-57
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Novel l-amino acid ester prodrugs of azacitidine: Design, enzymatic synthesis and the investigation of release behavior
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Author keywords
Amino acid ester prodrug; Amino acid azacitidine conjugates; Azacitidine; Enzymatic synthesis; Regioselectivity
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Indexed keywords
ESTERIFICATION;
ESTERS;
REGIOSELECTIVITY;
AMINO ACID ESTERS;
AMINO ACID-AZACITIDINE CONJUGATES;
AMINO-CARBOXYLATES;
AZACITIDINE;
CATALYTIC EFFICIENCIES;
ENZYMATIC SYNTHESIS;
RELEASE BEHAVIORS;
SUSTAINED RELEASE;
AMINO ACIDS;
5' O L ALANYL AZACITIDINE;
5' O L LEUCYL AZACITIDINE;
5' O L PHENYLALANYL AZACITIDINE;
5' O L VALYL AZACITIDINE;
AMINO ACID DERIVATIVE;
AZACITIDINE;
L AMINO ACID ESTER AZACITIDINE PRODRUG;
NUCLEOSIDE DERIVATIVE;
PYRIDINE;
SUBTILISIN;
UNCLASSIFIED DRUG;
ARTICLE;
CONTROLLED STUDY;
DEPROTECTION REACTION;
DRUG DESIGN;
DRUG HYDROLYSIS;
DRUG SELECTIVITY;
DRUG SYNTHESIS;
ENZYME SYNTHESIS;
IN VITRO STUDY;
PH;
REGIOSELECTIVITY;
SUSTAINED DRUG RELEASE;
TRANSESTERIFICATION;
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EID: 84899445533
PISSN: 13811177
EISSN: 18733158
Source Type: Journal
DOI: 10.1016/j.molcatb.2014.03.018 Document Type: Article |
Times cited : (6)
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References (34)
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