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Volumn 16, Issue 7-9, 1997, Pages 1229-1233

Beta-L-(-)-dioxolane cytidine (β-L-(-)-OddC) as a potent compound for the treatment of cancer

Author keywords

[No Author keywords available]

Indexed keywords

CYTARABINE; DIOXOLANE CYTIDINE; NUCLEOSIDE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 9844262797     PISSN: 07328311     EISSN: None     Source Type: Journal    
DOI: 10.1080/07328319708006164     Document Type: Conference Paper
Times cited : (9)

References (11)
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    • Bridges, E.G. and Cheng, Y-C. Use of novel beta-L-nucleoside analogues for treatment and prevention of chronic hepatitis B virus infection and hepatocellular carcinoma. Advances in Liver Disease. 13: 231-245, 1995.
    • (1995) Advances in Liver Disease , vol.13 , pp. 231-245
    • Bridges, E.G.1    Cheng, Y.-C.2
  • 3
    • 0028047132 scopus 로고
    • Antiviral activity of 2′,3′-dideoxy-beta-L-5-fluorocytidine and 2′,3′-dideoxy-betaL-cytidine against hepatitis B virus and human immunodeficiency virus type 1 in vitro
    • Lin, T-S., Luo, M.Z., Liu, M.C., Pai, S.B., Dutschman, G.E. and Cheng, Y-C. Antiviral activity of 2′,3′-dideoxy-beta-L-5-fluorocytidine and 2′,3′-dideoxy-betaL-cytidine against hepatitis B virus and human immunodeficiency virus type 1 in vitro. Biochem. Pharm, 47: 171-174, 1993.
    • (1993) Biochem. Pharm , vol.47 , pp. 171-174
    • Lin, T.-S.1    Luo, M.Z.2    Liu, M.C.3    Pai, S.B.4    Dutschman, G.E.5    Cheng, Y.-C.6
  • 4
    • 0026697262 scopus 로고
    • Deoxycytidine deaminase resistant stereoisomer is the active form of (±)-2′,3′-dideoxy-3′-thiacytidine in the inhibition of hepatitis B virus replication
    • Chang, C.N., Doong, S.L., Zhou, J.H., Beach, J.W., Jeong, L.S., Chu, C.K. Tsai, C.H. and Cheng, Y-C. Deoxycytidine deaminase resistant stereoisomer is the active form of (±)-2′,3′-dideoxy-3′-thiacytidine in the inhibition of hepatitis B virus replication. J. Biol. Chem., 267: 13939-13942, 1992.
    • (1992) J. Biol. Chem. , vol.267 , pp. 13939-13942
    • Chang, C.N.1    Doong, S.L.2    Zhou, J.H.3    Beach, J.W.4    Jeong, L.S.5    Chu, C.K.6    Tsai, C.H.7    Cheng, Y.-C.8
  • 7
    • 0029836284 scopus 로고    scopus 로고
    • Uptake and metabolism of the new anticancer compound beta-L-(-)-dioxolane cytidine in human prostate carcinoma DU-145 cells
    • Grove, K.L. and Cheng, Y-C. Uptake and metabolism of the new anticancer compound beta-L-(-)-dioxolane cytidine in human prostate carcinoma DU-145 cells. Cancer Res., 56: 4187-4191, 1996.
    • (1996) Cancer Res. , vol.56 , pp. 4187-4191
    • Grove, K.L.1    Cheng, Y.-C.2
  • 8
    • 0028982940 scopus 로고
    • Anticancer activity of beta-L-(-)-dioxolane cytidine, a novel nucleoside analogue with the unnatural L configuration
    • Grove, K.L., Quo, X., Liu, S-H., Gao, Z., Chu, C.K. and Cheng, Y-C. Anticancer activity of beta-L-(-)-dioxolane cytidine, a novel nucleoside analogue with the unnatural L configuration. Cancer Res., 55: 3008-3011, 1995.
    • (1995) Cancer Res. , vol.55 , pp. 3008-3011
    • Grove, K.L.1    Quo, X.2    Liu, S.-H.3    Gao, Z.4    Chu, C.K.5    Cheng, Y.-C.6
  • 9
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    • 0029088833 scopus 로고
    • L- And D-enantiomers of 2′,3′-dideoxycytidine 5′-triphosphate analogs as substrates for human DNA polymerases
    • Kukhanova, M., Liu, S-H., Mozzherin, D., Lin, T-S., Chu, C.K. and Cheng, Y-C. L- and D-enantiomers of 2′,3′-dideoxycytidine 5′-triphosphate analogs as substrates for human DNA polymerases. J. Biol. Chem., 39: 23055-23059, 1995.
    • (1995) J. Biol. Chem. , vol.39 , pp. 23055-23059
    • Kukhanova, M.1    Liu, S.-H.2    Mozzherin, D.3    Lin, T.-S.4    Chu, C.K.5    Cheng, Y.-C.6
  • 11
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    • Enzymatic assay for the quantification of deoxynucleoside triphosphates in human cells exposed to antiretroviral 2′,3′-dideoxy nucleosides
    • Gao, W.Y., Johns, D.G. and Mitsoya, H. Enzymatic assay for the quantification of deoxynucleoside triphosphates in human cells exposed to antiretroviral 2′,3′-dideoxy nucleosides. Analyt. Biochem., 222: 116, 122.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.