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Volumn 13, Issue 3, 2003, Pages 475-478

Synthesis and SAR of α-acylaminoketone ligands for control of gene expression

Author keywords

[No Author keywords available]

Indexed keywords

ECDYSONE; HYDRAZINE DERIVATIVE; KETONE DERIVATIVE; RH 5849;

EID: 0037330768     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(02)00980-0     Document Type: Article
Times cited : (40)

References (24)
  • 11
    • 0031709954 scopus 로고    scopus 로고
    • For other orthogonal systems see: (a) Moradpour D., Englert C., Blum H.E. Biol. Chem. 379:1998;1189 (b) Shi Y., Koh J.T. Chemistry & Biology. 8:2001;501 (c) Tedesco R., Thomas J.A., Katzenellenbogen B.S., Katzenellenbogen J.A. Chemistry & Biology. 8:2001;277 (d) Doyle D.F., Braasch D.A., Jackson L.K., Weiss H.E., Boehm M.F., Mangelsdorf D.J., Corey D.R. J. Am. Chem. Soc. 123:2001;11367.
    • (1998) Biol. Chem. , vol.379 , pp. 1189
    • Moradpour, D.1    Englert, C.2    Blum, H.E.3
  • 12
    • 0035006293 scopus 로고    scopus 로고
    • For other orthogonal systems see: (a) Moradpour D., Englert C., Blum H.E. Biol. Chem. 379:1998;1189 (b) Shi Y., Koh J.T. Chemistry & Biology. 8:2001;501 (c) Tedesco R., Thomas J.A., Katzenellenbogen B.S., Katzenellenbogen J.A. Chemistry & Biology. 8:2001;277 (d) Doyle D.F., Braasch D.A., Jackson L.K., Weiss H.E., Boehm M.F., Mangelsdorf D.J., Corey D.R. J. Am. Chem. Soc. 123:2001;11367.
    • (2001) Chemistry & Biology , vol.8 , pp. 501
    • Shi, Y.1    Koh, J.T.2
  • 13
    • 0035068096 scopus 로고    scopus 로고
    • For other orthogonal systems see: (a) Moradpour D., Englert C., Blum H.E. Biol. Chem. 379:1998;1189 (b) Shi Y., Koh J.T. Chemistry & Biology. 8:2001;501 (c) Tedesco R., Thomas J.A., Katzenellenbogen B.S., Katzenellenbogen J.A. Chemistry & Biology. 8:2001;277 (d) Doyle D.F., Braasch D.A., Jackson L.K., Weiss H.E., Boehm M.F., Mangelsdorf D.J., Corey D.R. J. Am. Chem. Soc. 123:2001;11367.
    • (2001) Chemistry & Biology , vol.8 , pp. 277
    • Tedesco, R.1    Thomas, J.A.2    Katzenellenbogen, B.S.3    Katzenellenbogen, J.A.4
  • 14
    • 0035930028 scopus 로고    scopus 로고
    • For other orthogonal systems see: (a)
    • For other orthogonal systems see: (a) Moradpour D., Englert C., Blum H.E. Biol. Chem. 379:1998;1189 (b) Shi Y., Koh J.T. Chemistry & Biology. 8:2001;501 (c) Tedesco R., Thomas J.A., Katzenellenbogen B.S., Katzenellenbogen J.A. Chemistry & Biology. 8:2001;277 (d) Doyle D.F., Braasch D.A., Jackson L.K., Weiss H.E., Boehm M.F., Mangelsdorf D.J., Corey D.R. J. Am. Chem. Soc. 123:2001;11367.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 11367
    • Doyle, D.F.1    Braasch, D.A.2    Jackson, L.K.3    Weiss, H.E.4    Boehm, M.F.5    Mangelsdorf, D.J.6    Corey, D.R.7
  • 18
    • 0013446931 scopus 로고    scopus 로고
    • 2 for 24 h. Ligand stock solutions were prepared (10 mM in DMSO) and diluted 100-fold in media. 50 μL of diluted ligand solution was added to each well. The final concentration of DMSO was maintained at 0.03% in both controls and treatments. β-Galactosidase reporter gene expression was measured 48 h after treatment of the cells using Gal Screen™ bioluminescent reporter gene assay system from Tropix (GSY1000). Luminescence was detected at room temperature using a Dynex MLX microtiter plate luminometer. Fold inductions were calculated by dividing relative light units (RLU) in ligand treated cells with RLU in DMSO treated cells.
  • 22
    • 0013459663 scopus 로고    scopus 로고
    • 3) δ 12.1, 17.1, 17.4, 17.5, 21.5, 34.3, 55.6, 67.5, 111.3, 118.3, 125.0, 125.1, 126.5, 127.7, 129.2, 132.5, 136.7, 137.6, 137.9, 158.0, 168.9, 201.0. The 3rd fraction (50% ether in hexanes) contained additional 2di (34.5 mg, 20%) of lower purity.
  • 24
    • 0013408411 scopus 로고    scopus 로고
    • -1. MS (ESI, +ve ion) m/z 366 (M+1).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.