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Volumn 51, Issue 46, 2012, Pages 11606-11610

The first generation of β-galactosidase-responsive prodrugs designed for the selective treatment of solid tumors in prodrug monotherapy

Author keywords

auristatin; cancer; galactoside; prodrugs; self immolative linkers

Indexed keywords

AURISTATIN; CANCER; GALACTOSIDE; PRODRUGS; SELF-IMMOLATIVE LINKERS;

EID: 84868560034     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201204935     Document Type: Article
Times cited : (97)

References (46)
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    • For the successful application of ADEPT, Tietze proposed the following requirements: 1)-the cytotoxic agent derived from the prodrug should achieve an IC50 value of <10-n M; and 2)-the toxicity ratio between the prodrug and the drug should exceed 1000. For more details, see.
    • For the successful application of ADEPT, Tietze proposed the following requirements: 1)-the cytotoxic agent derived from the prodrug should achieve an IC50 value of <10-n M; and 2)-the toxicity ratio between the prodrug and the drug should exceed 1000. For more details, see:, L. F. Tietze, T. Herzig, T. Feuerstein, I. Schuberth, Eur. J. Org. Chem. 2002, 1634-1645.
    • (2002) Eur. J. Org. Chem. , pp. 1634-1645
    • Tietze, L.F.1    Herzig, T.2    Feuerstein, T.3    Schuberth, I.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.