메뉴 건너뛰기




Volumn 6, Issue 10, 2011, Pages 1841-1853

Synthesis and Antitumor Molecular Mechanism of Agents Based on Amino 2-(3',4',5'-Trimethoxybenzoyl)benzo[b]furan: Inhibition of Tubulin and Induction of Apoptosis

Author keywords

Antiproliferative agents; Apoptosis; Caspase activation; Colchicine binding site; Tubulin

Indexed keywords

(4 AMINOBENZO[B]FURAN 2 YL)(3,4,5 TRIMETHOXYPHENYL)METHANONE; (5 AMINO 3 METHYL 6 METHOXYBENZO[B]FURAN 2 YL)(3,4,5 TRIMETHOXYPHENYL)METHANONE; (5 AMINO 3 METHYL 7 METHOXYBENZO[B]FURAN 2 YL)(3,4,5 TRIMETHOXYPHENYL)METHANONE; (5 AMINO 3 METHYLBENZO[B]FURAN 2 YL)(3,4,5 TRIMETHOXYPHENYL)METHANONE; (5 AMINO 6 METHOXYBENZO[B]FURAN 2 YL)(3,4,5 TRIMETHOXYPHENYL)METHANONE; (5 AMINO 7 METHOXYBENZO[B]FURAN 2 YL)(3,4,5 TRIMETHOXYPHENYL)METHANONE; (5 AMINOBENZO[B]FURAN 2 YL)(3,4,5 TRIMETHOXYPHENYL)METHANONE; (6 AMINOBENZO[B]FURAN 2 YL)(3,4,5 TRIMETHOXYPHENYL)METHANONE; (7 AMINO 3 METHYL 5 METHOXYBENZO[B]FURAN 2 YL)(3,4,5 TRIMETHOXYPHENYL)METHANONE; (7 AMINOBENZO[B]FURAN 2 YL)(3,4,5 TRIMETHOXYPHENYL)METHANONE; 2 (3',4',5' TRIMETHOXYBENZOYL) 3 METHYL 5 AMINO 6 METHOXYBENZO[B]FURAN; 2 (3',4',5' TRIMETHOXYBENZOYL)BENZO[B]FURAN DERIVATIVE; 2 BROMO N [2 (3,4,5 TRIMETHOXYBENZOYL) 1 BENZO[B]FURAN 4 YL]ACRYLAMIDE; 2 BROMO N [2 (3,4,5 TRIMETHOXYBENZOYL) 1 BENZO[B]FURAN 5 YL]ACRYLAMIDE; 2 BROMO N [2 (3,4,5 TRIMETHOXYBENZOYL) 1 BENZO[B]FURAN 6 YL]ACRYLAMIDE; 2 BROMO N [2 (3,4,5 TRIMETHOXYBENZOYL) 1 BENZO[B]FURAN 7 YL]ACRYLAMIDE; 2 BROMO N [3 METHYL 2 (3,4,5 TRIMETHOXYBENZOYL) 1 BENZO[B]FURAN 5 YL]ACRYLAMIDE; 2 BROMO N [3 METHYL 5 METHOXY 2 (3,4,5 TRIMETHOXYBENZOYL) 1 BENZO[B]FURAN 7 YL]ACRYLAMIDE; 2 BROMO N [3 METHYL 6 METHOXY 2 (3,4,5 TRIMETHOXYBENZOYL) 1 BENZO[B]FURAN 5 YL]ACRYLAMIDE; 2 BROMO N [3 METHYL 7 METHOXY 2 (3,4,5 TRIMETHOXYBENZOYL) 1 BENZO[B]FURAN 5 YL]ACRYLAMIDE; 2 BROMO N [7 METHOXY 2 (3,4,5 TRIMETHOXYBENZOYL) 1 BENZO[B] FURAN 5 YL]ACRYLAMIDE; 4 BUTYL [2 [[6 METHOXY 3 METHYL 2 (3,4,5 TRIMETHOXYBENZOYL) 1 BENZO[B]FURAN 5 YL]AMINO] 2 OXOETHYL]CARBAMATE; ANTINEOPLASTIC AGENT; CASPASE 3; CASPASE 8; COLCHICINE; COMBRETASTATIN A4; N [6 METHOXY 3 METHYL 2 (3,4,5 TRIMETHOXYBENZOYL) 1 BENZO[B] FURAN 5 YL]GLYCINAMIDE HYDROCHLORIDE; TUBULIN; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 80053398841     PISSN: 18607179     EISSN: 18607187     Source Type: Journal    
DOI: 10.1002/cmdc.201100279     Document Type: Article
Times cited : (13)

References (59)
  • 1
    • 0028943734 scopus 로고
    • C. B. Thompson, Science 1995, 267, 1456-1462.
    • (1995) Science , vol.267 , pp. 1456-1462
    • Thompson, C.B.1
  • 28
    • 80053406409 scopus 로고    scopus 로고
    • 2-Hydroxy-3-nitrobenzaldehyde (6e), 2-hydroxy-5-nitrobenzaldehyde (6b), and 1-(2-hydroxy-5-nitrophenyl)ethanone (6c) are commercially available and were used as received; 2-hydroxy-6-nitrobenzaldehyde
    • 2-Hydroxy-3-nitrobenzaldehyde (6e), 2-hydroxy-5-nitrobenzaldehyde (6b), and 1-(2-hydroxy-5-nitrophenyl)ethanone (6c) are commercially available and were used as received; 2-hydroxy-6-nitrobenzaldehyde
  • 30
    • 61749099637 scopus 로고    scopus 로고
    • For the preparation of 1-(2-hydroxy-5-methoxy-3-nitrophenyl)ethanone
    • For the preparation of 6d, see: K. S. MacMillan, T. Nguyen, I. Hwang, D. L. Boger, J. Am. Chem. Soc. 2009, 131, 1187- 1194. For the preparation of 1-(2-hydroxy-5-methoxy-3-nitrophenyl)ethanone
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 1187-1194
    • MacMillan, K.S.1    Nguyen, T.2    Hwang, I.3    Boger, D.L.4
  • 31
    • 0028104631 scopus 로고
    • For the synthesis of 2-hydroxy-4-methoxy-5-nitrobenzaldehyde
    • (6 f), see M. Cushman, H. Zhu, R. L. Geahlen, A. J. Kraker, J. Med. Chem. 1994, 37, 3353 -3362. For the synthesis of 2-hydroxy-4-methoxy-5-nitrobenzaldehyde
    • (1994) J. Med. Chem. , vol.37 , pp. 3353-3362
    • Cushman, M.1    Zhu, H.2    Geahlen, R.L.3    Kraker, A.J.4
  • 33
    • 33947437378 scopus 로고
    • For the preparation of 1-(2-hydroxy-4-methoxy-5-nitrophenyl)ethanone (6h), see: H. Banks, J. Am. Chem. Soc. 1938, 60, 1370
    • (1938) J. Am. Chem. Soc. , vol.60 , pp. 1370
    • Banks, H.1
  • 34
    • 42749084791 scopus 로고    scopus 로고
    • For the synthesis of 2-hydroxy-3-methoxy-5-nitrobenzaldehyde (6i), see: M. Kowalewska, H. Kwiecień , Tetrahedron 2008, 64, 5085 -5090
    • (2008) Tetrahedron , vol.64 , pp. 5085-5090
    • Kowalewska, M.1    Kwiecień, H.2
  • 35
    • 1842437397 scopus 로고
    • For the synthesis of 1-(2-hydroxy-3-methoxy-5-nitrophenyl) ethanone (6j), see: W. Horton, J. T. Spence, J. Am. Chem. Soc. 1958, 80, 2453 -2456.
    • (1958) J. Am. Chem. Soc. , vol.80 , pp. 2453-2456
    • Horton, W.1    Spence, J.T.2
  • 39
    • 0028929328 scopus 로고
    • H. Steller, Science 1995, 267, 1445-1449.
    • (1995) Science , vol.267 , pp. 1445-1449
    • Steller, H.1
  • 58
    • 80053411325 scopus 로고    scopus 로고
    • Molecular Operating Environment (MOE 2010.10), Chemical Computing Group Inc., Montreal, QC (Canada): (accessed July 6, 2011).
    • Molecular Operating Environment (MOE 2010.10), Chemical Computing Group Inc., Montreal, QC (Canada): (accessed July 6, 2011).
  • 59
    • 33751358567 scopus 로고    scopus 로고
    • PLANTS: Application of Ant Colony Optimization to Structure-Based Drug Design", in Ant Colony Optimization and Swarm Intelligence, 5th International Workshop, ANTS 2006, Brussels (Belgium), September 4-7, (Eds.: M. Dorigo, L.M. Gambardella, M. Birattari, A. Martinoli, R. Poli, T. Stützle), Springer, Berlin, 2006, LNCS 4150247-258.
    • O. Korb, T. Stützle, T.E. Exner, "PLANTS: Application of Ant Colony Optimization to Structure-Based Drug Design", in Ant Colony Optimization and Swarm Intelligence, 5th International Workshop, ANTS 2006, Brussels (Belgium), September 4-7, 2006 (Eds.: M. Dorigo, L.M. Gambardella, M. Birattari, A. Martinoli, R. Poli, T. Stützle), Springer, Berlin, 2006, LNCS 4150, pp.247-258.
    • (2006)
    • Korb, O.1    Stützle, T.2    Exner, T.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.