-
1
-
-
84874656763
-
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
-
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
-
3
-
-
84872556406
-
Anticancer steroids: Linking natural and semi-synthetic compounds
-
J.A. Salvador, J.F. Carvalho, M.A. Neves, S.M. Silvestre, A.J. Leitao, M.M. Silva, and M.L. Sa e Melo Anticancer steroids: linking natural and semi-synthetic compounds Nat. Prod. Rep. 30 2013 324 374
-
(2013)
Nat. Prod. Rep.
, vol.30
, pp. 324-374
-
-
Salvador, J.A.1
Carvalho, J.F.2
Neves, M.A.3
Silvestre, S.M.4
Leitao, A.J.5
Silva, M.M.6
Sa Melo E, M.L.7
-
4
-
-
84879209332
-
Efficient construction of novel D-ring modified steroidal dienamides and their cytotoxic activities
-
B. Yu, X.J. Shi, J.l. Ren, X.N. Sun, P.P. Qi, Y. Fang, X.W. Ye, M.M. Wang, J.W. Wang, E. Zhang, D.Q. Yu, and H.M. Liu Efficient construction of novel D-ring modified steroidal dienamides and their cytotoxic activities Eur. J. Med. Chem. 66 2013 171 179
-
(2013)
Eur. J. Med. Chem.
, vol.66
, pp. 171-179
-
-
Yu, B.1
Shi, X.J.2
Ren, L.J.3
Sun, X.N.4
Qi, P.P.5
Fang, Y.6
Ye, X.W.7
Wang, M.M.8
Wang, J.W.9
Zhang, E.10
Yu, D.Q.11
Liu, H.M.12
-
5
-
-
84884780752
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
12
-
-
33745154819
-
Structure-based design of spiro-oxindoles as potent, specific small-molecule inhibitors of the MDM2-p53 interaction
-
DOI 10.1021/jm051122a
-
K. Ding, Y. Lu, Z. Nikolovska-Coleska, G. Wang, S. Qiu, S. Shangary, W. Gao, D. Qin, J. Stuckey, K. Krajewski, P.P. Roller, and S. Wang Structure-based design of spiro-oxindoles as potent, specific small-molecule inhibitors of the MDM2-p53 interaction J. Med. Chem. 49 2006 3432 3435 (Pubitemid 43902447)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.12
, pp. 3432-3435
-
-
Ding, K.1
Lu, Y.2
Nikolovska-Coleska, Z.3
Wang, G.4
Qiu, S.5
Shangary, S.6
Gao, W.7
Qin, D.8
Stuckey, J.9
Krajewski, K.10
Roller, P.P.11
Wang, S.12
-
13
-
-
84860300994
-
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
-
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
-
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
-
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
-
17
-
-
84877695456
-
Development of novel alkene oxindole derivatives as orally efficacious AMP-activated protein kinase activators
-
L.F. Yu, Y.Y. Li, M.B. Su, M. Zhang, W. Zhang, L.N. Zhang, T. Pang, R.T. Zhang, B. Liu, J.Y. Li, J. Li, and F.J. Nan Development of novel alkene oxindole derivatives as orally efficacious AMP-activated protein kinase activators ACS Med. Chem. Lett. 4 2013 475 480
-
(2013)
ACS Med. Chem. Lett.
, vol.4
, pp. 475-480
-
-
Yu, L.F.1
Li, Y.Y.2
Su, M.B.3
Zhang, M.4
Zhang, W.5
Zhang, L.N.6
Pang, T.7
Zhang, R.T.8
Liu, B.9
Li, J.Y.10
Li, J.11
Nan, F.J.12
-
18
-
-
77956280420
-
Spiroindolones, a potent compound class for the treatment of malaria
-
M. Rottmann, C. McNamara, B.K. Yeung, M.C. Lee, B. Zou, B. Russell, P. Seitz, D.M. Plouffe, N.V. Dharia, J. Tan, S.B. Cohen, K.R. Spencer, G.E. Gonzalez-Paez, S.B. Lakshminarayana, A. Goh, R. Suwanarusk, T. Jegla, E.K. Schmitt, H.P. Beck, R. Brun, F. Nosten, L. Renia, V. Dartois, T.H. Keller, D.A. Fidock, E.A. Winzeler, and T.T. Diagana Spiroindolones, a potent compound class for the treatment of malaria Science 329 2010 1175 1180
-
(2010)
Science
, vol.329
, pp. 1175-1180
-
-
Rottmann, M.1
McNamara, C.2
Yeung, B.K.3
Lee, M.C.4
Zou, B.5
Russell, B.6
Seitz, P.7
Plouffe, D.M.8
Dharia, N.V.9
Tan, J.10
Cohen, S.B.11
Spencer, K.R.12
Gonzalez-Paez, G.E.13
Lakshminarayana, S.B.14
Goh, A.15
Suwanarusk, R.16
Jegla, T.17
Schmitt, E.K.18
Beck, H.P.19
Brun, R.20
Nosten, F.21
Renia, L.22
Dartois, V.23
Keller, T.H.24
Fidock, D.A.25
Winzeler, E.A.26
Diagana, T.T.27
more..
-
19
-
-
81255211335
-
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
-
20
-
-
77953129713
-
Design and synthesis of spirotryprostatin-inspired diketopiperazine systems from prolyl spirooxoindolethiazolidine derivatives
-
A. Bertamino, C. Aquino, M. Sala, N.D. Simone, C.A. Mattia, L. Erra, S. Musella, P. Iannelli, A. Carotenuto, P. Grieco, E. Novellino, P. Campiglia, and I. Gomez-Monterrey Design and synthesis of spirotryprostatin-inspired diketopiperazine systems from prolyl spirooxoindolethiazolidine derivatives Bioorg. Med. Chem. 18 2010 4328 4337
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 4328-4337
-
-
Bertamino, A.1
Aquino, C.2
Sala, M.3
Simone, N.D.4
Mattia, C.A.5
Erra, L.6
Musella, S.7
Iannelli, P.8
Carotenuto, A.9
Grieco, P.10
Novellino, E.11
Campiglia, P.12
Gomez-Monterrey, I.13
-
21
-
-
22944473048
-
Structure-based design of potent non-peptide MDM2 inhibitors
-
DOI 10.1021/ja051147z
-
K. Ding, Y. Lu, Z. Nikolovska-Coleska, S. Qiu, Y. Ding, W. Gao, J. Stuckey, K. Krajewski, P.P. Roller, Y. Tomita, D.A. Parrish, J.R. Deschamps, and S. Wang Structure-based design of potent non-peptide MDM2 inhibitors J. Am. Chem. Soc. 127 2005 10130 10131 (Pubitemid 41045454)
-
(2005)
Journal of the American Chemical Society
, vol.127
, Issue.29
, pp. 10130-10131
-
-
Ding, K.1
Lu, Y.2
Nikolovska-Coleska, Z.3
Qiu, S.4
Ding, Y.5
Gao, W.6
Stuckey, J.7
Krajewski, K.8
Roller, P.P.9
Tomita, Y.10
Parrish, D.A.11
Deschamps, J.R.12
Wang, S.13
-
22
-
-
0027345554
-
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
-
23
-
-
53349165559
-
Discovery of 4-aryl-2-oxo-2H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay
-
W. Kemnitzer, S. Jiang, H. Zhang, S. Kasibhatla, C. Crogan-Grundy, C. Blais, G. Attardo, R. Denis, S. Lamothe, H. Gourdeau, B. Tseng, J. Drewe, and S.X. Cai Discovery of 4-aryl-2-oxo-2H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay Biorg. Med. Chem. Lett. 18 2008 5571 5575
-
(2008)
Biorg. Med. Chem. Lett.
, vol.18
, pp. 5571-5575
-
-
Kemnitzer, W.1
Jiang, S.2
Zhang, H.3
Kasibhatla, S.4
Crogan-Grundy, C.5
Blais, C.6
Attardo, G.7
Denis, R.8
Lamothe, S.9
Gourdeau, H.10
Tseng, B.11
Drewe, J.12
Cai, S.X.13
-
24
-
-
9744248288
-
Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 1. Structure-activity relationships of the 4-aryl group
-
DOI 10.1021/jm049640t
-
W. Kemnitzer, J. Drewe, S. Jiang, H. Zhang, Y. Wang, J. Zhao, S. Jia, J. Herich, D. Labreque, R. Storer, K. Meerovitch, D. Bouffard, R. Rej, R. Denis, C. Blais, S. Lamothe, G. Attardo, H. Gourdeau, B. Tseng, S. Kasibhatla, and S.X. Cai Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 1. Structure-activity relationships of the 4-aryl group J. Med. Chem. 47 2004 6299 6310 (Pubitemid 39587254)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.25
, pp. 6299-6310
-
-
Kemnitzer, W.1
Drewe, J.2
Jiang, S.3
Zhang, H.4
Wang, Y.5
Zhao, J.6
Jia, S.7
Herich, J.8
Labreque, D.9
Storer, R.10
Meerovitch, K.11
Bouffard, D.12
Rej, R.13
Denis, R.14
Blais, C.15
Lamothe, S.16
Attardo, G.17
Gourdeau, H.18
Tseng, B.19
Kasibhatla, S.20
Cai, S.X.21
more..
-
25
-
-
84896737743
-
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
-
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
-
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
-
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
|