-
1
-
-
0031915368
-
Sesquiterpene lactones specifically inhibit activation of NF-κB by Preventing the Degradation of IκB-α and IκB-β
-
Hehner SP, Heinrich M, Bork PM, Vogt M, Ratter F, Lehmann V, Schulze-Osthoff K, Droge W, Schmitz ML. Sesquiterpene lactones specifically inhibit activation of NF-κB by Preventing the Degradation of IκB-α and IκB-β. J. Biol. Chem. 1998; 273: 1288-1297.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 1288-1297
-
-
Hehner, S.P.1
Heinrich, M.2
Bork, P.M.3
Vogt, M.4
Ratter, F.5
Lehmann, V.6
Schulze-Osthoff, K.7
Droge, W.8
Schmitz, M.L.9
-
2
-
-
0036676714
-
Anti-trypanosomal activity of Helenalin and some structurally related sesquiterpene lactones
-
Schmidt TJ, Brun R, Willuhn G, Khalid SA. Anti-trypanosomal activity of Helenalin and some structurally related sesquiterpene lactones. Planta Med. 2002; 68: 750-751.
-
(2002)
Planta Med.
, vol.68
, pp. 750-751
-
-
Schmidt, T.J.1
Brun, R.2
Willuhn, G.3
Khalid, S.A.4
-
3
-
-
18444367100
-
Anticancer potential of sesquiterpene lactones: bioactivity and molecular mechanisms
-
Zhang S, Won YK, Ong CN, Shen HM. Anticancer potential of sesquiterpene lactones: bioactivity and molecular mechanisms. Curr. Med. Chem. Anticancer Agents 2005; 5: 239-249.
-
(2005)
Curr. Med. Chem. Anticancer Agents
, vol.5
, pp. 239-249
-
-
Zhang, S.1
Won, Y.K.2
Ong, C.N.3
Shen, H.M.4
-
4
-
-
0031371106
-
Synthesis and evaluation of the plant growth regulatory activity of 8-oxabicyclo[3.2.1]oct-6-en-3-one derivates
-
Barbosa LCA, Demuner AJ, Borges EEL, Mann J. Synthesis and evaluation of the plant growth regulatory activity of 8-oxabicyclo[3.2.1]oct-6-en-3-one derivates. J. Braz. Chem. Soc. 1997; 8: 19-27.
-
(1997)
J. Braz. Chem. Soc.
, vol.8
, pp. 19-27
-
-
Barbosa, L.C.A.1
Demuner, A.J.2
Borges, E.E.L.3
Mann, J.4
-
5
-
-
0036519777
-
Síntese e avaliação da atividade fitotóxica de lactonas derivadas do 2,4-dimetil-8-oxabiciclo[3.2.1]oct-6-en-3-ona
-
Barbosa LCA, Maltha CRA, Borges EEL. Síntese e avaliação da atividade fitotóxica de lactonas derivadas do 2, 4-dimetil-8-oxabiciclo[3.2.1]oct-6-en-3-ona. Quím. Nova 2002; 25: 203-208.
-
(2002)
Quím. Nova
, vol.25
, pp. 203-208
-
-
Barbosa, L.C.A.1
Maltha, C.R.A.2
Borges, E.E.L.3
-
6
-
-
0033662011
-
Sesquiterpene lactones with potential use as natural herbicide models. 2. Guaianolides
-
Macías FA, Galindo JCG, Castellano D, Velasco RF. Sesquiterpene lactones with potential use as natural herbicide models. 2. Guaianolides. J. Agric. Food Chem. 2000; 48: 5288-5296.
-
(2000)
J. Agric. Food Chem.
, vol.48
, pp. 5288-5296
-
-
Macías, F.A.1
Galindo, J.C.G.2
Castellano, D.3
Velasco, R.F.4
-
7
-
-
33745792758
-
Sesquiterpene lactones as allelochemicals
-
Macías FA, Fernandez A, Varela RM, Molinillo JMG, Torres A, Alves PLCA. Sesquiterpene lactones as allelochemicals. J. Nat. Prod. 2006; 69: 795-800.
-
(2006)
J. Nat. Prod.
, vol.69
, pp. 795-800
-
-
Macías, F.A.1
Fernandez, A.2
Varela, R.M.3
Molinillo, J.M.G.4
Torres, A.5
Alves, P.L.C.A.6
-
8
-
-
11244258624
-
Phytogrowth-inhibitory lactones derivatives of glaucolide B
-
Barbosa LCA, Costa AV, Piló-Veloso D, Lopes JLC, Hernandez-Terrones MG, King-Diaz B, Lotina-Hennsen B. Phytogrowth-inhibitory lactones derivatives of glaucolide B. Z. Naturforsch. 2004; 59: 803-805.
-
(2004)
Z. Naturforsch.
, vol.59
, pp. 803-805
-
-
Barbosa, L.C.A.1
Costa, A.V.2
Piló-Veloso, D.3
Lopes, J.L.C.4
Hernandez-Terrones, M.G.5
King-Diaz, B.6
Lotina-Hennsen, B.7
-
9
-
-
66749092954
-
Síntese e avaliação da atividade fitotóxica de derivados da α-Santonina
-
Alvarenga ES, Barbosa LCA, Saliba WA, Arantes FFP, Demuner AJ. Síntese e avaliação da atividade fitotóxica de derivados da α-Santonina. Quím. Nova 2009; 32: 401-406.
-
(2009)
Quím. Nova
, vol.32
, pp. 401-406
-
-
Alvarenga, E.S.1
Barbosa, L.C.A.2
Saliba, W.A.3
Arantes, F.F.P.4
Demuner, A.J.5
-
10
-
-
33846066297
-
11,13-Dihydro-dehydroleucodine, a derivative of dehydroleucodine with an inactivated alkylating function conserves the anti-proliferative activity in G2 but does not cause cytotoxicity
-
Polo LM, Castro CM, Cruzado MC, Collino CJG, Cuello-Carrión FD, Ciocca DR, Giordano OS, Ferrari M, López LA. 11, 13-Dihydro-dehydroleucodine, a derivative of dehydroleucodine with an inactivated alkylating function conserves the anti-proliferative activity in G2 but does not cause cytotoxicity. Eur. J. Pharmacol. 2007; 556: 19-26.
-
(2007)
Eur. J. Pharmacol.
, vol.556
, pp. 19-26
-
-
Polo, L.M.1
Castro, C.M.2
Cruzado, M.C.3
Collino, C.J.G.4
Cuello-Carrión, F.D.5
Ciocca, D.R.6
Giordano, O.S.7
Ferrari, M.8
López, L.A.9
-
11
-
-
0015165481
-
Tumor inhibitors. 69. Structure-cytotoxicity relations among the sesquiterpene lactones
-
Kupchan SM, Eakin MA, Thomas AM. Tumor inhibitors. 69. Structure-cytotoxicity relations among the sesquiterpene lactones. J. Med. Chem. 1971; 14: 1147-1152.
-
(1971)
J. Med. Chem.
, vol.14
, pp. 1147-1152
-
-
Kupchan, S.M.1
Eakin, M.A.2
Thomas, A.M.3
-
12
-
-
0017756246
-
Antitumor agents. 25. Synthesis and antitumor activity of uracil and thymine alpha-methylene-gamma-lactones and related derivatives
-
Lee KH, Wu YS, Hall IH. Antitumor agents. 25. Synthesis and antitumor activity of uracil and thymine alpha-methylene-gamma-lactones and related derivatives. J. Med. Chem. 1977; 20: 911-914.
-
(1977)
J. Med. Chem.
, vol.20
, pp. 911-914
-
-
Lee, K.H.1
Wu, Y.S.2
Hall, I.H.3
-
13
-
-
15744396281
-
A potent apoptosis-inducing activity of a sesquiterpene lactone, arucanolide, in HL60 Cells: a crucial role of apoptosis-inducing factor
-
Nakagawa Y, Iinuma M, Matsuura N, Yi K, Naoi M, Nakayama T, Nozawa Y, Akao Y. A potent apoptosis-inducing activity of a sesquiterpene lactone, arucanolide, in HL60 Cells: a crucial role of apoptosis-inducing factor. J. Pharmacol. Sci. 2005; 97: 242-252.
-
(2005)
J. Pharmacol. Sci.
, vol.97
, pp. 242-252
-
-
Nakagawa, Y.1
Iinuma, M.2
Matsuura, N.3
Yi, K.4
Naoi, M.5
Nakayama, T.6
Nozawa, Y.7
Akao, Y.8
-
14
-
-
33847166620
-
Synthesis and biological evaluation of 4-methylideneisoxazolidin-5-ones-A new class of highly cytotoxic α-methylidene-γ-lactones
-
Rozalski M, Krajewska U, Panczyk M, Mirowski M, Rozalska B, Wasek T, Janecki T. Synthesis and biological evaluation of 4-methylideneisoxazolidin-5-ones-A new class of highly cytotoxic α-methylidene-γ-lactones. Eur. J. Med. Chem. 2007; 42: 248-255.
-
(2007)
Eur. J. Med. Chem.
, vol.42
, pp. 248-255
-
-
Rozalski, M.1
Krajewska, U.2
Panczyk, M.3
Mirowski, M.4
Rozalska, B.5
Wasek, T.6
Janecki, T.7
-
15
-
-
0001317795
-
Potential allelopathic activity of several sesquiterpene lactone models
-
Macías FA, Galindo JCG, Massanet GM. Potential allelopathic activity of several sesquiterpene lactone models. Phytochemistry 1992; 31: 1969-1977.
-
(1992)
Phytochemistry
, vol.31
, pp. 1969-1977
-
-
Macías, F.A.1
Galindo, J.C.G.2
Massanet, G.M.3
-
16
-
-
67650383493
-
Synthesis and cytotoxic activity of α-santonin derivatives
-
Arantes FFP, Barbosa LCA, Alvarenga ES, Demuner AJ, Bezerra DP, Ferreira JRO, Costa-Lotufo LV, Pessoa C, Moraes MO. Synthesis and cytotoxic activity of α-santonin derivatives. Eur. J. Med. Chem. 2009; 44: 3739-3745.
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 3739-3745
-
-
Arantes, F.F.P.1
Barbosa, L.C.A.2
Alvarenga, E.S.3
Demuner, A.J.4
Bezerra, D.P.5
Ferreira, J.R.O.6
Costa-Lotufo, L.V.7
Pessoa, C.8
Moraes, M.O.9
-
17
-
-
0000165694
-
SAR analysis of synthetic neolignans and related compounds which are anti-leishmaniasis active compounds using pattern recognition methods
-
Costa MCA, Barata LES, Takahata Y. SAR analysis of synthetic neolignans and related compounds which are anti-leishmaniasis active compounds using pattern recognition methods. J. Mol. Struct. (Theochem.) 1995; 340: 185-192.
-
(1995)
J. Mol. Struct. (Theochem.)
, vol.340
, pp. 185-192
-
-
Costa, M.C.A.1
Barata, L.E.S.2
Takahata, Y.3
-
18
-
-
78650678396
-
2 from Bothrops jararacussu
-
2 from Bothrops jararacussu. Toxicon 2011; 57: 100-108.
-
(2011)
Toxicon
, vol.57
, pp. 100-108
-
-
Alvarenga, E.S.1
Silva, S.A.2
Barbosa, L.C.A.3
Demuner, A.J.4
Parreira, A.G.5
Ribeiro, R.I.M.A.6
Marcussi, A.7
Ferreirea, J.M.S.8
Resende, R.R.9
Granjeiro, P.A.10
Silva, J.A.11
Soares, A.M.12
Marangoni, S.13
Silva, S.L.D.14
-
19
-
-
0037133996
-
A structure-activity relationship (SAR) study of synthetic neolignans and related compounds with biological activity against Escherichia coli
-
Camargo AJ, Mercadante R, Honório KM, Alves CN, Da Silva ABF. A structure-activity relationship (SAR) study of synthetic neolignans and related compounds with biological activity against Escherichia coli. J. Mol. Struct. (Theochem.) 2002; 583: 105-116.
-
(2002)
J. Mol. Struct. (Theochem.)
, vol.583
, pp. 105-116
-
-
Camargo, A.J.1
Mercadante, R.2
Honório, K.M.3
Alves, C.N.4
Da Silva, A.B.F.5
-
20
-
-
0344826535
-
A quantum chemical and statistical study of flavonoid compounds (flavones) with anti-HIV activity
-
Souza J, Santos RHA, Ferreira MMC, Molfetta FA, Camargo AJ, Honório KM, Da Silva ABF. A quantum chemical and statistical study of flavonoid compounds (flavones) with anti-HIV activity. Eur. J. Med. Chem. 2003; 38: 929-938.
-
(2003)
Eur. J. Med. Chem.
, vol.38
, pp. 929-938
-
-
Souza, J.1
Santos, R.H.A.2
Ferreira, M.M.C.3
Molfetta, F.A.4
Camargo, A.J.5
Honório, K.M.6
Da Silva, A.B.F.7
-
21
-
-
26444569267
-
A quantum chemical and statistical study of ganoderic acids with cytotoxicity against tumor cell
-
Yang H, Chen G, Li Y. A quantum chemical and statistical study of ganoderic acids with cytotoxicity against tumor cell. Eur. J. Med. Chem. 2005; 40: 972-976.
-
(2005)
Eur. J. Med. Chem.
, vol.40
, pp. 972-976
-
-
Yang, H.1
Chen, G.2
Li, Y.3
-
22
-
-
16244364387
-
A structure-activity relationship study of quinone compounds with trypanocidal activity
-
Molfetta FA, Bruni AT, Honório KM, Da Silva ABF. A structure-activity relationship study of quinone compounds with trypanocidal activity. Eur. J. Med. Chem. 2005; 40: 329-338.
-
(2005)
Eur. J. Med. Chem.
, vol.40
, pp. 329-338
-
-
Molfetta, F.A.1
Bruni, A.T.2
Honório, K.M.3
Da Silva, A.B.F.4
-
23
-
-
34249871693
-
Synthesis and cytotoxic activity of some 3-benzyl-5-arylidenefuran-2(5H)-ones
-
Teixeira RR, Barbosa LCA, Maltha CRA, Rocha ME, Bezerra DP, Costa-Lotufo LV, Pessoa C, Moraes MO. Synthesis and cytotoxic activity of some 3-benzyl-5-arylidenefuran-2(5H)-ones. Molecules 2007; 12: 1101-1116.
-
(2007)
Molecules
, vol.12
, pp. 1101-1116
-
-
Teixeira, R.R.1
Barbosa, L.C.A.2
Maltha, C.R.A.3
Rocha, M.E.4
Bezerra, D.P.5
Costa-Lotufo, L.V.6
Pessoa, C.7
Moraes, M.O.8
-
24
-
-
0034034172
-
Antiproliferative effects of compounds derived from plants of Northeast Brazil
-
Pessoa C, Silveira ER, Lemos TL, Wetmore LA, Moraes MO, Leyva A. Antiproliferative effects of compounds derived from plants of Northeast Brazil. Phytother. Res. 2000; 14: 187-191.
-
(2000)
Phytother. Res.
, vol.14
, pp. 187-191
-
-
Pessoa, C.1
Silveira, E.R.2
Lemos, T.L.3
Wetmore, L.A.4
Moraes, M.O.5
Leyva, A.6
-
25
-
-
1542314403
-
Antiproliferative effects of Abietane Diterpenes from Aegiphila lhotzkyana
-
Costa-Lotufo LV, Silveira ER, Barros MC, Lima MA, De Moraes ME, De Moraes MO, Pessoa C. Antiproliferative effects of Abietane Diterpenes from Aegiphila lhotzkyana. Planta Med. 2004; 70: 180-182.
-
(2004)
Planta Med.
, vol.70
, pp. 180-182
-
-
Costa-Lotufo, L.V.1
Silveira, E.R.2
Barros, M.C.3
Lima, M.A.4
De Moraes, M.E.5
De Moraes, M.O.6
Pessoa, C.7
-
26
-
-
47549098276
-
In vivo growth inhibition of sarcoma 180 by piperlonguminine, an alkaloid amide from the Piper species
-
Bezerra DP, Pessoa C, Moraes MO, Alencar NM, Mesquita RO, Lima MW, Alves AP, Pessoa OD, Chaves JH, Silveira ER, Costa-Lotufo LV. In vivo growth inhibition of sarcoma 180 by piperlonguminine, an alkaloid amide from the Piper species. J. Appl. Toxicol. 2008; 28: 599-607.
-
(2008)
J. Appl. Toxicol.
, vol.28
, pp. 599-607
-
-
Bezerra, D.P.1
Pessoa, C.2
Moraes, M.O.3
Alencar, N.M.4
Mesquita, R.O.5
Lima, M.W.6
Alves, A.P.7
Pessoa, O.D.8
Chaves, J.H.9
Silveira, E.R.10
Costa-Lotufo, L.V.11
-
27
-
-
41249085021
-
Synthesis and anticancer activity of new class of bisphosphonates/phosphanamidates
-
Kiran YB, Reddy CD, Gunasekar D, Reddy CS, Leon A, Barbosa LCA. Synthesis and anticancer activity of new class of bisphosphonates/phosphanamidates. Eur. J. Med. Chem. 2008; 43: 885-892.
-
(2008)
Eur. J. Med. Chem.
, vol.43
, pp. 885-892
-
-
Kiran, Y.B.1
Reddy, C.D.2
Gunasekar, D.3
Reddy, C.S.4
Leon, A.5
Barbosa, L.C.A.6
-
28
-
-
78649328995
-
Synthesis of novel α-santonin derivatives as potential cytotoxic agents
-
Arantes FFP, Barbosa LCA, Maltha CRA, Demuner AJ, Costa PM, Ferreira JRO, Costa-Lotufo LV, Moraes MO, Pessoa C. Synthesis of novel α-santonin derivatives as potential cytotoxic agents. Eur. J. Med. Chem. 2010; 45: 6045-6051.
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 6045-6051
-
-
Arantes, F.F.P.1
Barbosa, L.C.A.2
Maltha, C.R.A.3
Demuner, A.J.4
Costa, P.M.5
Ferreira, J.R.O.6
Costa-Lotufo, L.V.7
Moraes, M.O.8
Pessoa, C.9
-
29
-
-
0037571112
-
Merck molecular force field. I. Basis, form, scope, parameterization, and performance of MMFF94
-
Halgren TA. Merck molecular force field. I. Basis, form, scope, parameterization, and performance of MMFF94. J. Comput. Chem. 1996; 17: 490-519.
-
(1996)
J. Comput. Chem.
, vol.17
, pp. 490-519
-
-
Halgren, T.A.1
-
30
-
-
35448937584
-
Optimization of parameters for semiempirical methods V: modification of NDDO approximations and application to 70 elements
-
Stewart JJP. Optimization of parameters for semiempirical methods V: modification of NDDO approximations and application to 70 elements. J. Mol. Model. 2007; 13: 1173-1212.
-
(2007)
J. Mol. Model.
, vol.13
, pp. 1173-1212
-
-
Stewart, J.J.P.1
-
31
-
-
85153548766
-
-
Spartan PC Pro. Wavefunction, Inc., Irvine, CA, USA.
-
Spartan PC Pro. Wavefunction, Inc., Irvine, CA, USA.
-
-
-
-
32
-
-
85153556094
-
-
MOPAC2009, Stewart Computational Chemistry, version 9.327W.
-
Stewart JJP. MOPAC2009, Stewart Computational Chemistry, version 9.327W.
-
-
-
Stewart, J.J.P.1
-
33
-
-
85153555973
-
-
PLS Toolbox Ver. 2.0.1c, for use with MATLAB 6.0
-
Wise M, Gallagher NB. PLS Toolbox Ver. 2.0.1c, for use with MATLAB 6.0, 1999.
-
(1999)
-
-
Wise, M.1
Gallagher, N.B.2
-
34
-
-
0035960239
-
Systematic study of the quality of various quantum similarity descriptors. Use of the autocorrelation function and principal component analysis
-
Boon G, Langenaeker W, De Proft F, Hans DeWinter JP, Tollenaere P. Systematic study of the quality of various quantum similarity descriptors. Use of the autocorrelation function and principal component analysis. J. Phys. Chem. A 2001; 105: 8805-8814.
-
(2001)
J. Phys. Chem. A
, vol.105
, pp. 8805-8814
-
-
Boon, G.1
Langenaeker, W.2
De Proft, F.3
Hans DeWinter, J.P.4
Tollenaere, P.5
-
35
-
-
0035903890
-
Antimalarial activity of dihydroartemisinin derivatives against P. falciparum resistant to mefloquine: a quantum chemical and multivariate study
-
Pinheiro JC, Ferreira MMC, Romero OAS. Antimalarial activity of dihydroartemisinin derivatives against P. falciparum resistant to mefloquine: a quantum chemical and multivariate study. J. Mol. Struct. (Theochem) 2001; 572: 35-44.
-
(2001)
J. Mol. Struct. (Theochem)
, vol.572
, pp. 35-44
-
-
Pinheiro, J.C.1
Ferreira, M.M.C.2
Romero, O.A.S.3
-
36
-
-
0345859602
-
Aspectos Mecanísticos da Adição de Michael
-
Mattos MC, Marzorati L. Aspectos Mecanísticos da Adição de Michael. Quím. Nova 1999; 22: 710-714.
-
(1999)
Quím. Nova
, vol.22
, pp. 710-714
-
-
Mattos, M.C.1
Marzorati, L.2
|