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Volumn 56, Issue 4, 2001, Pages 319-324

Synthesis and biological activity of glycosyl conjugates of N-(4-hydroxyphenyl)retinamide

Author keywords

Antiproliferative compounds; Glycolipids; Glycosylation; Retinoid

Indexed keywords

4 RETINAMIDOPHENYL BETA D MANNOPYRANOSIDE; ANTILEUKEMIC AGENT; FENRETINIDE; RETINOID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0035305646     PISSN: 0014827X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-827X(01)01074-6     Document Type: Article
Times cited : (11)

References (18)
  • 4
    • 0029816269 scopus 로고    scopus 로고
    • Bioactivities of N-(4-hydroxyphenyl)retinamide and retinoyl β-glucuronide
    • (and references therein)
    • Formelli F., Barua A.B., Olson J.A. Bioactivities of N-(4-hydroxyphenyl)retinamide and retinoyl β-glucuronide. FASEB J. 9:1996;1014. (and references therein).
    • (1996) FASEB J. , vol.9 , pp. 1014
    • Formelli, F.1    Barua, A.B.2    Olson, J.A.3
  • 5
    • 0025964195 scopus 로고
    • Growth suppression of human breast carcinoma cells in cultures by N-(4-hydroxyphenyl)retinamide and its glucuronide and through synergism with glutarate
    • Bhatnagar R., Abou-Issa H., Curley R.W., Koolemans-Beynen A., Moeschberger M.L., Webb T.E. Growth suppression of human breast carcinoma cells in cultures by N-(4-hydroxyphenyl)retinamide and its glucuronide and through synergism with glutarate. Biochem. Pharmacol. 41:1991;1471.
    • (1991) Biochem. Pharmacol. , vol.41 , pp. 1471
    • Bhatnagar, R.1    Abou-Issa, H.2    Curley, R.W.3    Koolemans-Beynen, A.4    Moeschberger, M.L.5    Webb, T.E.6
  • 7
    • 0027365618 scopus 로고
    • In vivo use of N-(4-hydroxyphenylretinamide)-O-glucuronide as a breast cancer chemopreventive agent
    • (and references therein)
    • Abou-Issa H., Curley R.W., Panigot M.J., Wilcox K.A., Webb T.E. In vivo use of N-(4-hydroxyphenylretinamide)-O-glucuronide as a breast cancer chemopreventive agent. Anticancer Res. 13:1993;1431. (and references therein).
    • (1993) Anticancer Res. , vol.13 , pp. 1431
    • Abou-Issa, H.1    Curley, R.W.2    Panigot, M.J.3    Wilcox, K.A.4    Webb, T.E.5
  • 8
  • 10
    • 0032997176 scopus 로고    scopus 로고
    • Alkylating agents from sugars. Alkyl hexopyranoside derivatives as carrier systems for chlorambucyl
    • (and references therein)
    • Iglesias-Gerra F., Candela J.I., Bautista J., Alcudia F., Vega-Perez J. Alkylating agents from sugars. Alkyl hexopyranoside derivatives as carrier systems for chlorambucyl. Carbohydr. Res. 316:1999;71. (and references therein).
    • (1999) Carbohydr. Res. , vol.316 , pp. 71
    • Iglesias-Gerra, F.1    Candela, J.I.2    Bautista, J.3    Alcudia, F.4    Vega-Perez, J.5
  • 11
    • 0031022634 scopus 로고    scopus 로고
    • A convenient synthesis of peracetylated glycosyl halides using bismuth (III) halides as catalysts
    • Montero J.-L., Winum J.-Y., Leydet A., Kamal M., Pavia A.A., Roque J-P. A convenient synthesis of peracetylated glycosyl halides using bismuth (III) halides as catalysts. Carbohydr. Res. 297:1997;175.
    • (1997) Carbohydr. Res. , vol.297 , pp. 175
    • Montero, J.-L.1    Winum, J.-Y.2    Leydet, A.3    Kamal, M.4    Pavia, A.A.5    Roque, J.-P.6
  • 12
    • 85007898424 scopus 로고
    • Synthesis of p-nitrophenyl β-D-glucopyranosiduronic acid and its utilization as a substrate for the assay of β-glucuronidase activity
    • Kato K., Yashida K., Tsukamoto H., Nobugana M., Masuya T., Sawada T. Synthesis of p-nitrophenyl β-D-glucopyranosiduronic acid and its utilization as a substrate for the assay of β-glucuronidase activity. Chem. Pharm. Bull. 8:1960;239.
    • (1960) Chem. Pharm. Bull. , vol.8 , pp. 239
    • Kato, K.1    Yashida, K.2    Tsukamoto, H.3    Nobugana, M.4    Masuya, T.5    Sawada, T.6
  • 13
    • 0021110855 scopus 로고
    • P-Nitrophenyl β-D-glucopyranoside, a new substrate for glucansucrases
    • Binder T.P., Robyt J.F. p-Nitrophenyl β-D-glucopyranoside, a new substrate for glucansucrases. Carbohydr. Res. 124:1983;287.
    • (1983) Carbohydr. Res. , vol.124 , pp. 287
    • Binder, T.P.1    Robyt, J.F.2
  • 14
    • 0001665967 scopus 로고
    • Phase-transfer catalysed synthesis of 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosides
    • Kleine H.P., Weinberg D.V., Kaufman R.J., Sidhu R.S. Phase-transfer catalysed synthesis of 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosides. Carbohydr. Res. 142:1985;333.
    • (1985) Carbohydr. Res. , vol.142 , pp. 333
    • Kleine, H.P.1    Weinberg, D.V.2    Kaufman, R.J.3    Sidhu, R.S.4
  • 15
    • 0343819303 scopus 로고
    • Improved preparative methods for p-nitrophenyl α-D-mannopyranoside tetraacetate and p-nitrophenyl α-L-rhamnopyranoside triacetate
    • Garegg P.J., Hultberg H., Iversen T. Improved preparative methods for p-nitrophenyl α-D-mannopyranoside tetraacetate and p-nitrophenyl α-L-rhamnopyranoside triacetate. Carbohydr. Res. 62:1978;173.
    • (1978) Carbohydr. Res. , vol.62 , pp. 173
    • Garegg, P.J.1    Hultberg, H.2    Iversen, T.3
  • 16
    • 0031880119 scopus 로고    scopus 로고
    • A simple, general and efficient method for O and N-retinoylation. Application to the synthesis of 2-retinoyl-lecithin
    • Sangmam C., Winum J.-Y., Lucas M., Montero J.-L., Chavis C. A simple, general and efficient method for O and N-retinoylation. Application to the synthesis of 2-retinoyl-lecithin. Synth. Commun. 28:1998;2945.
    • (1998) Synth. Commun. , vol.28 , pp. 2945
    • Sangmam, C.1    Winum, J.-Y.2    Lucas, M.3    Montero, J.-L.4    Chavis, C.5
  • 18
    • 0030008514 scopus 로고    scopus 로고
    • Chemopreventive activities of C-glucuronide/glycoside analogs of retinoid-O-glucuronides against breast cancer development and growth
    • Curley R.W., Abou-Issa H., Panigot M.J., Repa J.J., Clagett-Dame M., Alshafie G. Chemopreventive activities of C-glucuronide/glycoside analogs of retinoid-O-glucuronides against breast cancer development and growth. Anticancer Res. 16:1996;757.
    • (1996) Anticancer Res. , vol.16 , pp. 757
    • Curley, R.W.1    Abou-Issa, H.2    Panigot, M.J.3    Repa, J.J.4    Clagett-Dame, M.5    Alshafie, G.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.