메뉴 건너뛰기




Volumn 68, Issue 11, 2004, Pages 2341-2345

Enzymatic synthesis of dehydro cyclo(His-Phe)s, analogs of the potent cell cycle inhibitor, dehydrophenylahistin, and their inhibitory activities toward cell division

Author keywords

Albonoursin; Dehydro cyclic dipeptide; Diketopiperazine; Enzymatic conversion; Inhibitor for cell division

Indexed keywords

AROMATIC COMPOUNDS; BIOSYNTHESIS; CONCENTRATION (PROCESS); DERIVATIVES; ENZYME INHIBITION; POLYPEPTIDES; REACTION KINETICS;

EID: 11144309625     PISSN: 09168451     EISSN: None     Source Type: Journal    
DOI: 10.1271/bbb.68.2341     Document Type: Article
Times cited : (15)

References (9)
  • 1
    • 0016593869 scopus 로고
    • Naturally occurring 2,5-diketopiperazines and related compounds
    • Sammes, P. G., Naturally occurring 2,5-diketopiperazines and related compounds. Fortschr. Chrm. Org. Naturst., 32, 51-118 (1975).
    • (1975) Fortschr. Chrm. Org. Naturst. , vol.32 , pp. 51-118
    • Sammes, P.G.1
  • 2
    • 0033545547 scopus 로고    scopus 로고
    • Enzymatic dehydrogenation of cyclo(L-Leu-L-Phe) to a bioactive derivative, albonoursin
    • Kanzaki, H., Imura, D., Nitoda, T., and Kawazu, K., Enzymatic dehydrogenation of cyclo(L-Leu-L-Phe) to a bioactive derivative, albonoursin. J. Mol. Cat. B: Enzymatic, 6, 265-270 (1999).
    • (1999) J. Mol. Cat. B: Enzymatic , vol.6 , pp. 265-270
    • Kanzaki, H.1    Imura, D.2    Nitoda, T.3    Kawazu, K.4
  • 3
    • 0033980537 scopus 로고    scopus 로고
    • Effective production of a dehydro cyclic dipeptide albonoursin with pronuclear fusion inhibitory activity. II. Biosynthetic and bioconversion studies
    • Kanzaki, H., Imura, D., Nitoda, T., and Kawazu, K., Effective production of a dehydro cyclic dipeptide albonoursin with pronuclear fusion inhibitory activity. II. Biosynthetic and bioconversion studies. J. Antibiotics, 53, 58-62 (2000).
    • (2000) J. Antibiotics , vol.53 , pp. 58-62
    • Kanzaki, H.1    Imura, D.2    Nitoda, T.3    Kawazu, K.4
  • 4
    • 0034233052 scopus 로고    scopus 로고
    • Enzymatic conversion of cyclic dipeptides to dehydro derivatives that inhibit cell division
    • Kanzaki, H., Imura, D., Nitoda, T., and Kawazu, K., Enzymatic conversion of cyclic dipeptides to dehydro derivatives that inhibit cell division. J. Biosci. Bioeng., 90, 86-89 (2000).
    • (2000) J. Biosci. Bioeng. , vol.90 , pp. 86-89
    • Kanzaki, H.1    Imura, D.2    Nitoda, T.3    Kawazu, K.4
  • 5
    • 0036956924 scopus 로고    scopus 로고
    • A novel potent cell cycle inhibitor dehydrophenylahistin: Enzymatic synthesis and inhibitory activity toward sea urchin embryo
    • Kanzaki, H., Yanagisawa, S., Kanoh, K., and Nitoda, T., A novel potent cell cycle inhibitor dehydrophenylahistin: enzymatic synthesis and inhibitory activity toward sea urchin embryo. J. Antibiotics, 55, 1042-1047 (2002).
    • (2002) J. Antibiotics , vol.55 , pp. 1042-1047
    • Kanzaki, H.1    Yanagisawa, S.2    Kanoh, K.3    Nitoda, T.4
  • 7
    • 0033676367 scopus 로고    scopus 로고
    • Biosynthetic intermediates of tetradehydro cyclic dipeptide albonoursin produced by Streptomyces albulus KO-23
    • Kanzaki, H., Yanagisawa, S., and Nitoda, T., Biosynthetic intermediates of tetradehydro cyclic dipeptide albonoursin produced by Streptomyces albulus KO-23. J. Antibiotics, 53, 1257-1264 (2000).
    • (2000) J. Antibiotics , vol.53 , pp. 1257-1264
    • Kanzaki, H.1    Yanagisawa, S.2    Nitoda, T.3
  • 8
    • 11144296887 scopus 로고    scopus 로고
    • Preparation of piperazinedione derivative inhibitors of plasminogen activator inhibitor. PCT Int. Appl. 94 pp. WO 9521832, A1 19950817 (1995)
    • Brocchini, S. J., Bryans, J. S., Justin, S., Folkes, A. J., Latham, C. J., and Brumwell, J. E. (Xenova Ltd., UK), Preparation of piperazinedione derivative inhibitors of plasminogen activator inhibitor. PCT Int. Appl. 94 pp. WO 9521832, A1 19950817 (1995).
    • Brocchini, S.J.1    Bryans, J.S.2    Justin, S.3    Folkes, A.J.4    Latham, C.J.5    Brumwell, J.E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.