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Volumn 88, Issue , 2014, Pages 44-52

Discovery of novel steroidal pyran-oxindole hybrids as cytotoxic agents

Author keywords

Apoptosis; Cell cycle arrest; Cytotoxicity; Pyran oxindole hybrids

Indexed keywords

3BETA ACETYL DEHYDROEPIANDROSTERONE; ANTINEOPLASTIC AGENT; FLUOROURACIL; STEROIDAL ALPHA, ALPHA DICYANOALKENE; STEROIDAL PYRAN OXINDOLE HYBRID; UNCLASSIFIED DRUG; INDOLE DERIVATIVE; OXINDOLE; PYRAN DERIVATIVE; STEROID;

EID: 84904582012     PISSN: 0039128X     EISSN: 18785867     Source Type: Journal    
DOI: 10.1016/j.steroids.2014.05.022     Document Type: Article
Times cited : (24)

References (28)
  • 1
    • 84874656763 scopus 로고    scopus 로고
    • An overview of synthetic approaches for heterocyclic steroids
    • R. Singh, and G. Panda An overview of synthetic approaches for heterocyclic steroids Tetrahedron 69 2013 2853 2884
    • (2013) Tetrahedron , vol.69 , pp. 2853-2884
    • Singh, R.1    Panda, G.2
  • 2
    • 84886728610 scopus 로고    scopus 로고
    • Synthesis of sex hormone-derived modified steroids possessing antiproliferative activity
    • É. Frank, and G. Schneider Synthesis of sex hormone-derived modified steroids possessing antiproliferative activity J. Steroid Biochem. Mol. Biol. 137 2013 301 315
    • (2013) J. Steroid Biochem. Mol. Biol. , vol.137 , pp. 301-315
    • Frank, É.1    Schneider, G.2
  • 5
    • 84884780752 scopus 로고    scopus 로고
    • Stereoselective synthesis of novel antiproliferative steroidal (E, E) dienamides through a cascade aldol/cyclization process
    • B. Yu, X.N. Sun, X.J. Shi, P.P. Qi, Y. Fang, E. Zhang, D.Q. Yu, and H.M. Liu Stereoselective synthesis of novel antiproliferative steroidal (E, E) dienamides through a cascade aldol/cyclization process Steroids 78 2013 1134 1140
    • (2013) Steroids , vol.78 , pp. 1134-1140
    • Yu, B.1    Sun, X.N.2    Shi, X.J.3    Qi, P.P.4    Fang, Y.5    Zhang, E.6    Yu, D.Q.7    Liu, H.M.8
  • 6
    • 84875191834 scopus 로고    scopus 로고
    • Facile synthesis of novel D-ring modified steroidal dienamides via rearrangement of 2H-pyrans
    • B. Yu, E. Zhang, X.N. Sun, J.L. Ren, Y. Fang, B.L. Zhang, D.Q. Yu, and H.M. Liu Facile synthesis of novel D-ring modified steroidal dienamides via rearrangement of 2H-pyrans Steroids 78 2013 494 499
    • (2013) Steroids , vol.78 , pp. 494-499
    • Yu, B.1    Zhang, E.2    Sun, X.N.3    Ren, J.L.4    Fang, Y.5    Zhang, B.L.6    Yu, D.Q.7    Liu, H.M.8
  • 7
    • 84866859500 scopus 로고    scopus 로고
    • Mineralocorticoid receptor antagonists for the treatment of hypertension and diabetic nephropathy
    • D.W. Piotrowski Mineralocorticoid receptor antagonists for the treatment of hypertension and diabetic nephropathy J. Med. Chem. 55 2012 7957 7966
    • (2012) J. Med. Chem. , vol.55 , pp. 7957-7966
    • Piotrowski, D.W.1
  • 8
    • 84879579619 scopus 로고    scopus 로고
    • Systematic structure modifications of multitarget prostate cancer drug candidate galeterone to produce novel androgen receptor down-regulating agents as an approach to treatment of advanced prostate cancer
    • P. Purushottamachar, A.M. Godbole, L.K. Gediya, M.S. Martin, T.S. Vasaitis, A.K. Kwegyir-Afful, S. Ramalingam, Z. Ates-Alagoz, and V.C.O. Njar Systematic structure modifications of multitarget prostate cancer drug candidate galeterone to produce novel androgen receptor down-regulating agents as an approach to treatment of advanced prostate cancer J. Med. Chem. 56 2013 4880 4898
    • (2013) J. Med. Chem. , vol.56 , pp. 4880-4898
    • Purushottamachar, P.1    Godbole, A.M.2    Gediya, L.K.3    Martin, M.S.4    Vasaitis, T.S.5    Kwegyir-Afful, A.K.6    Ramalingam, S.7    Ates-Alagoz, Z.8    Njar, V.C.O.9
  • 9
    • 84884373879 scopus 로고    scopus 로고
    • A novel [1,2,4] triazolo [1,5-A] pyrimidine-based phenyl-linked steroid dimer: Synthesis and its cytotoxic activity
    • B. Yu, X.J. Shi, Y.F. Zheng, Y. Fang, E. Zhang, D.Q. Yu, and H.M. Liu A novel [1,2,4] triazolo [1,5-a] pyrimidine-based phenyl-linked steroid dimer: Synthesis and its cytotoxic activity Eur. J. Med. Chem. 69 2013 323 330
    • (2013) Eur. J. Med. Chem. , vol.69 , pp. 323-330
    • Yu, B.1    Shi, X.J.2    Zheng, Y.F.3    Fang, Y.4    Zhang, E.5    Yu, D.Q.6    Liu, H.M.7
  • 10
    • 36749025633 scopus 로고    scopus 로고
    • Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents
    • DOI 10.1002/anie.200701342
    • C.V. Galliford, and K.A. Scheidt Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents Angew. Chem. Int. Ed. 46 2007 8748 8758 (Pubitemid 350207923)
    • (2007) Angewandte Chemie - International Edition , vol.46 , Issue.46 , pp. 8748-8758
    • Galliford, C.V.1    Scheidt, K.A.2
  • 11
    • 84869188848 scopus 로고    scopus 로고
    • Isatins as privileged molecules in design and synthesis of spiro-fused cyclic frameworks
    • G.S. Singh, and Z.Y. Desta Isatins as privileged molecules in design and synthesis of spiro-fused cyclic frameworks Chem. Rev. 112 2012 6104 6155
    • (2012) Chem. Rev. , vol.112 , pp. 6104-6155
    • Singh, G.S.1    Desta, Z.Y.2
  • 13
    • 84860300994 scopus 로고    scopus 로고
    • Synthesis of novel spirooxindole derivatives by one pot multicomponent reaction and their antimicrobial activity
    • G. Bhaskar, Y. Arun, C. Balachandran, C. Saikumar, and P.T. Perumal Synthesis of novel spirooxindole derivatives by one pot multicomponent reaction and their antimicrobial activity Eur. J. Med. Chem. 51 2012 79 91
    • (2012) Eur. J. Med. Chem. , vol.51 , pp. 79-91
    • Bhaskar, G.1    Arun, Y.2    Balachandran, C.3    Saikumar, C.4    Perumal, P.T.5
  • 14
    • 84875229746 scopus 로고    scopus 로고
    • Synthesis and discovery of novel piperidone-grafted mono- and bis- spirooxindole-hexahydropyrrolizines as potent cholinesterase inhibitors
    • Y. Kia, H. Osman, R.S. Kumar, V. Murugaiyah, A. Basiri, S. Perumal, H.A. Wahab, and C.S. Bing Synthesis and discovery of novel piperidone-grafted mono- and bis- spirooxindole-hexahydropyrrolizines as potent cholinesterase inhibitors Biorg. Med. Chem. 21 2013 1696 1707
    • (2013) Biorg. Med. Chem. , vol.21 , pp. 1696-1707
    • Kia, Y.1    Osman, H.2    Kumar, R.S.3    Murugaiyah, V.4    Basiri, A.5    Perumal, S.6    Wahab, H.A.7    Bing, C.S.8
  • 15
    • 84876692727 scopus 로고    scopus 로고
    • A facile chemo-, regio- and stereoselective synthesis and cholinesterase inhibitory activity of spirooxindole-pyrrolizine-piperidine hybrids
    • Y. kia, H. Osman, R.S. Kumar, V. Murugaiyah, A. Basiri, S. Perumal, and I.A. Razak A facile chemo-, regio- and stereoselective synthesis and cholinesterase inhibitory activity of spirooxindole-pyrrolizine-piperidine hybrids Bioorg. Med. Chem. Lett. 23 2013 2979 2983
    • (2013) Bioorg. Med. Chem. Lett. , vol.23 , pp. 2979-2983
    • Kia, Y.1    Osman, H.2    Kumar, R.S.3    Murugaiyah, V.4    Basiri, A.5    Perumal, S.6    Razak, I.A.7
  • 16
    • 84876106505 scopus 로고    scopus 로고
    • Cu(OTf) catalyzed three component reaction: Efficient synthesis of spiro[indoline-3,4'-pyrano[3,2-b] pyran derivatives and their anticancer potency towards A549 human lung cancer cell lines
    • K. Parthasarathy, C. Praveen, C. Balachandran, P. Senthil Kumar, S. Ignacimuthu, and P.T. Perumal Cu(OTf) catalyzed three component reaction: Efficient synthesis of spiro[indoline-3,4'-pyrano[3,2-b] pyran derivatives and their anticancer potency towards A549 human lung cancer cell lines Bioorg. Med. Chem. Lett. 23 2013 2708 2713
    • (2013) Bioorg. Med. Chem. Lett. , vol.23 , pp. 2708-2713
    • Parthasarathy, K.1    Praveen, C.2    Balachandran, C.3    Senthil Kumar, P.4    Ignacimuthu, S.5    Perumal, P.T.6
  • 19
    • 81255211335 scopus 로고    scopus 로고
    • Brønsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles
    • J. Yu, F. Shi, and L.Z. Gong Brønsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles Acc. Chem. Res. 44 2011 1156 1171
    • (2011) Acc. Chem. Res. , vol.44 , pp. 1156-1171
    • Yu, J.1    Shi, F.2    Gong, L.Z.3
  • 22
    • 0027345554 scopus 로고
    • Microbial pyran-2-ones and dihydropyran-2-ones
    • J.M. Dickinson Microbial pyran-2-ones and dihydropyran-2-ones Nat. Prod. Rep. 10 1993 71 98
    • (1993) Nat. Prod. Rep. , vol.10 , pp. 71-98
    • Dickinson, J.M.1
  • 25
    • 84896737743 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of novel steroidal spiro-oxindoles as potent antiproliferative agents
    • B. Yu, X.J. Shi, P.P. Qi, D.Q. Yu, and H.M. Liu Design, synthesis and biological evaluation of novel steroidal spiro-oxindoles as potent antiproliferative agents J. Steroid Biochem. Mol. Biol. 141 2014 121 134
    • (2014) J. Steroid Biochem. Mol. Biol. , vol.141 , pp. 121-134
    • Yu, B.1    Shi, X.J.2    Qi, P.P.3    Yu, D.Q.4    Liu, H.M.5
  • 26
    • 77951131263 scopus 로고    scopus 로고
    • A Facile, one-pot synthesis of functionalized spiro-oxindoles via vinylogous aldol reaction of vinyl malononitriles with isatin derivatives in aqueous media
    • T.H. Babu, K. Karthik, and P.T. Perumal A Facile, one-pot synthesis of functionalized spiro-oxindoles via vinylogous aldol reaction of vinyl malononitriles with isatin derivatives in aqueous media Synlett 2010 2010 1128 1132
    • (2010) Synlett , vol.2010 , pp. 1128-1132
    • Babu, T.H.1    Karthik, K.2    Perumal, P.T.3
  • 27
    • 84886086001 scopus 로고    scopus 로고
    • Recent advances in diversity oriented synthesis through isatin-based multicomponent reactions
    • Y. Liu, H. Wang, and J. Wan Recent advances in diversity oriented synthesis through isatin-based multicomponent reactions Asian J. Org. Chem. 2 2013 374 386
    • (2013) Asian J. Org. Chem. , vol.2 , pp. 374-386
    • Liu, Y.1    Wang, H.2    Wan, J.3
  • 28
    • 84862908937 scopus 로고    scopus 로고
    • Highly efficient and stereoselective construction of dispiro- [oxazolidine-2-thione] bisoxindoles and dispiro[imidazolidine-2-thione] bisoxindoles
    • Y.Y. Han, W.B. Chen, W.Y. Han, Z.J. Wu, X.M. Zhang, and W.C. Yuan Highly efficient and stereoselective construction of dispiro-[oxazolidine-2-thione] bisoxindoles and dispiro[imidazolidine-2-thione] bisoxindoles Org. Lett. 14 2013 490 493
    • (2013) Org. Lett. , vol.14 , pp. 490-493
    • Han, Y.Y.1    Chen, W.B.2    Han, W.Y.3    Wu, Z.J.4    Zhang, X.M.5    Yuan, W.C.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.