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Artigo de periodico
Design of Inhibitors for Glyceraldehyde-3-phosphate Dehydrogenase (GAPDH) Enzyme of Leishmania mexicana (2020)
Alves, Krisnna M.A. ; Cardoso, Fábio José Bonfim ; Honório, Káthia Maria ; Molfetta, Fábio A. de
Source: Medicinal Chemistry. Unidade: EACH
Subjects: LEISHMANIA MEXICANA, ENZIMAS, QUÍMICA MÉDICA
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ABNT
ALVES, Krisnna M.A. et al. Design of Inhibitors for Glyceraldehyde-3-phosphate Dehydrogenase (GAPDH) Enzyme of Leishmania mexicana. Medicinal Chemistry, v. 16, n. 6, p. 784-795, 2020Tradução . . Disponível em: https://doi.org/10.2174/1573406415666190712111139. Acesso em: 18 nov. 2024.
APA
Alves, K. M. A., Cardoso, F. J. B., Honório, K. M., & Molfetta, F. A. de. (2020). Design of Inhibitors for Glyceraldehyde-3-phosphate Dehydrogenase (GAPDH) Enzyme of Leishmania mexicana. Medicinal Chemistry, 16( 6), 784-795. doi:10.2174/1573406415666190712111139
NLM
Alves KMA, Cardoso FJB, Honório KM, Molfetta FA de. Design of Inhibitors for Glyceraldehyde-3-phosphate Dehydrogenase (GAPDH) Enzyme of Leishmania mexicana [Internet]. Medicinal Chemistry. 2020 ; 16( 6): 784-795.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406415666190712111139
Vancouver
Alves KMA, Cardoso FJB, Honório KM, Molfetta FA de. Design of Inhibitors for Glyceraldehyde-3-phosphate Dehydrogenase (GAPDH) Enzyme of Leishmania mexicana [Internet]. Medicinal Chemistry. 2020 ; 16( 6): 784-795.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406415666190712111139
Artigo de periodico
Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells (2018)
Vasconcelos, Stanley Nunes Siqueira ; Sciani, Juliana Mozer ; Lisboa, Nicole Mambeli; Stefani, Hélio Alexandre
Source: Medicinal Chemistry. Unidade: FCF
Subjects: MOLÉCULA, ANTINEOPLÁSICOS
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ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells. Medicinal Chemistry, v. 14, n. 7, p. 709-714, 2018Tradução . . Disponível em: https://doi.org/10.2174/1573406414666180309153142. Acesso em: 18 nov. 2024.
APA
Vasconcelos, S. N. S., Sciani, J. M., Lisboa, N. M., & Stefani, H. A. (2018). Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells. Medicinal Chemistry, 14( 7), 709-714. doi:10.2174/1573406414666180309153142
NLM
Vasconcelos SNS, Sciani JM, Lisboa NM, Stefani HA. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells [Internet]. Medicinal Chemistry. 2018 ; 14( 7): 709-714.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406414666180309153142
Vancouver
Vasconcelos SNS, Sciani JM, Lisboa NM, Stefani HA. Synthesis of a Tyr-Tyr dipeptide library and evaluation against tumor cells [Internet]. Medicinal Chemistry. 2018 ; 14( 7): 709-714.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406414666180309153142
Artigo de periodico
Nitric oxide signaling and the cross talk with prostanoids pathways in vascular system (2017)
Silva, Bruno R; Paula, Tiago D; Paulo, Michele; Bendhack, Lusiane Maria
Source: Medicinal Chemistry. Unidade: FCFRP
Subjects: ÓXIDO NÍTRICO, DOENÇAS CARDIOVASCULARES, VASODILATAÇÃO
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ABNT
SILVA, Bruno R et al. Nitric oxide signaling and the cross talk with prostanoids pathways in vascular system. Medicinal Chemistry, v. 13, n. 4, p. 319-333, 2017Tradução . . Disponível em: https://doi.org/10.2174/1573406412666161228115627. Acesso em: 18 nov. 2024.
APA
Silva, B. R., Paula, T. D., Paulo, M., & Bendhack, L. M. (2017). Nitric oxide signaling and the cross talk with prostanoids pathways in vascular system. Medicinal Chemistry, 13( 4), 319-333. doi:10.2174/1573406412666161228115627
NLM
Silva BR, Paula TD, Paulo M, Bendhack LM. Nitric oxide signaling and the cross talk with prostanoids pathways in vascular system [Internet]. Medicinal Chemistry. 2017 ; 13( 4): 319-333.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406412666161228115627
Vancouver
Silva BR, Paula TD, Paulo M, Bendhack LM. Nitric oxide signaling and the cross talk with prostanoids pathways in vascular system [Internet]. Medicinal Chemistry. 2017 ; 13( 4): 319-333.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406412666161228115627
Artigo de periodico
The role of QSAR and virtual screening studies in type 2 diabetes drug discovery (2017)
Pantaleão, Simone Queiroz; Fujii, Drielli Gomes Vital; Maltarollo, Vinicius Gonçalves; Silva, Danielle da C; Trossini, Gustavo Henrique Goulart ; Weber, Karen C; Honório, Káthia Maria
Source: Medicinal Chemistry. Unidades: FCF, EACH
Subjects: FÁRMACOS, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA
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ABNT
PANTALEÃO, Simone Queiroz et al. The role of QSAR and virtual screening studies in type 2 diabetes drug discovery. Medicinal Chemistry, v. 13, p. 706-720, 2017Tradução . . Disponível em: https://doi.org/10.2174/1573406413666170522152102. Acesso em: 18 nov. 2024.
APA
Pantaleão, S. Q., Fujii, D. G. V., Maltarollo, V. G., Silva, D. da C., Trossini, G. H. G., Weber, K. C., & Honório, K. M. (2017). The role of QSAR and virtual screening studies in type 2 diabetes drug discovery. Medicinal Chemistry, 13, 706-720. doi:10.2174/1573406413666170522152102
NLM
Pantaleão SQ, Fujii DGV, Maltarollo VG, Silva D da C, Trossini GHG, Weber KC, Honório KM. The role of QSAR and virtual screening studies in type 2 diabetes drug discovery [Internet]. Medicinal Chemistry. 2017 ; 13 706-720.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406413666170522152102
Vancouver
Pantaleão SQ, Fujii DGV, Maltarollo VG, Silva D da C, Trossini GHG, Weber KC, Honório KM. The role of QSAR and virtual screening studies in type 2 diabetes drug discovery [Internet]. Medicinal Chemistry. 2017 ; 13 706-720.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406413666170522152102
Artigo de periodico
Bergenin from peltophorum dubium: isolation, characterization, and antioxidant activities in non-biological systems and erythrocytes (2017)
Oliveira, Guilherme A. L.; Oliveira, George L. da Silva; Nicolau, Lucas A. D.; Mafud, Ana Carolina; Batista, Larissa F.; Mascarenhas, Yvonne Primerano ; Souza, Luan K. M.; David, Jorge M.; Pinto, Larissa S.; Alves, Clayton Q.; Medeiros, Jand V. R.
Source: Medicinal Chemistry. Unidade: IFSC
Subjects: PROTEÍNAS, FÍSICA DA MATÉRIA CONDENSADA
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ABNT
OLIVEIRA, Guilherme A. L. et al. Bergenin from peltophorum dubium: isolation, characterization, and antioxidant activities in non-biological systems and erythrocytes. Medicinal Chemistry, v. 13, n. 6, p. 592-603, 2017Tradução . . Disponível em: https://doi.org/10.2174/1573406413666170306120152. Acesso em: 18 nov. 2024.
APA
Oliveira, G. A. L., Oliveira, G. L. da S., Nicolau, L. A. D., Mafud, A. C., Batista, L. F., Mascarenhas, Y. P., et al. (2017). Bergenin from peltophorum dubium: isolation, characterization, and antioxidant activities in non-biological systems and erythrocytes. Medicinal Chemistry, 13( 6), 592-603. doi:10.2174/1573406413666170306120152
NLM
Oliveira GAL, Oliveira GL da S, Nicolau LAD, Mafud AC, Batista LF, Mascarenhas YP, Souza LKM, David JM, Pinto LS, Alves CQ, Medeiros JVR. Bergenin from peltophorum dubium: isolation, characterization, and antioxidant activities in non-biological systems and erythrocytes [Internet]. Medicinal Chemistry. 2017 ; 13( 6): 592-603.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406413666170306120152
Vancouver
Oliveira GAL, Oliveira GL da S, Nicolau LAD, Mafud AC, Batista LF, Mascarenhas YP, Souza LKM, David JM, Pinto LS, Alves CQ, Medeiros JVR. Bergenin from peltophorum dubium: isolation, characterization, and antioxidant activities in non-biological systems and erythrocytes [Internet]. Medicinal Chemistry. 2017 ; 13( 6): 592-603.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406413666170306120152
Artigo de periodico
Molecular design, synthesis and evaluation of 2,3-diarylquinoxalines as estrogen receptor ligands (2015)
Sangi, Diego P.; Cominetti, Márcia Regina; Becceneri, Amanda B.; Resende, Flavia A.; Varanda, Eliana Aparecida; Montanari, Carlos Alberto ; Paixão, Márcio Weber; Corrêa, Arlene Gonçalves
Source: Medicinal Chemistry. Unidade: IQSC
Subjects: QUÍMICA MÉDICA, ESTRÓGENOS
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ABNT
SANGI, Diego P. et al. Molecular design, synthesis and evaluation of 2,3-diarylquinoxalines as estrogen receptor ligands. Medicinal Chemistry, v. 11, n. 8, p. 736-746, 2015Tradução . . Disponível em: https://doi.org/10.2174/1573406411666150513093039. Acesso em: 18 nov. 2024.
APA
Sangi, D. P., Cominetti, M. R., Becceneri, A. B., Resende, F. A., Varanda, E. A., Montanari, C. A., et al. (2015). Molecular design, synthesis and evaluation of 2,3-diarylquinoxalines as estrogen receptor ligands. Medicinal Chemistry, 11( 8), 736-746. doi:10.2174/1573406411666150513093039
NLM
Sangi DP, Cominetti MR, Becceneri AB, Resende FA, Varanda EA, Montanari CA, Paixão MW, Corrêa AG. Molecular design, synthesis and evaluation of 2,3-diarylquinoxalines as estrogen receptor ligands [Internet]. Medicinal Chemistry. 2015 ; 11( 8): 736-746.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406411666150513093039
Vancouver
Sangi DP, Cominetti MR, Becceneri AB, Resende FA, Varanda EA, Montanari CA, Paixão MW, Corrêa AG. Molecular design, synthesis and evaluation of 2,3-diarylquinoxalines as estrogen receptor ligands [Internet]. Medicinal Chemistry. 2015 ; 11( 8): 736-746.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406411666150513093039
Artigo de periodico
The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design (2014)
Silva, Fredson Torres; Trossini, Gustavo Henrique Goulart
Source: Medicinal Chemistry. Unidade: FCF
Subjects: BIODISPONIBILIDADE, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA
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ABNT
SILVA, Fredson Torres e TROSSINI, Gustavo Henrique Goulart. The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design. Medicinal Chemistry, v. 10, n. 5, p. 441-448, 2014Tradução . . Acesso em: 18 nov. 2024.
APA
Silva, F. T., & Trossini, G. H. G. (2014). The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design. Medicinal Chemistry, 10( 5), 441-448.
NLM
Silva FT, Trossini GHG. The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design. Medicinal Chemistry. 2014 ; 10( 5): 441-448.[citado 2024 nov. 18 ]
Vancouver
Silva FT, Trossini GHG. The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design. Medicinal Chemistry. 2014 ; 10( 5): 441-448.[citado 2024 nov. 18 ]
Artigo de periodico
Identification of structural and electronic features for a series of MCH1R antagonists (2013)
Silva, Danielle C.; Andricopulo, Adriano Defini ; Lima, Emmanuela F.; Honório, Káthia Maria
Source: Medicinal Chemistry. Unidades: IFSC, EACH
Subjects: MODELAGEM MOLECULAR, RECEPTORES HORMONAIS, QUÍMICA MÉDICA
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ABNT
SILVA, Danielle C. et al. Identification of structural and electronic features for a series of MCH1R antagonists. Medicinal Chemistry, v. 9, n. 1, p. 22-31, 2013Tradução . . Disponível em: https://doi.org/10.2174/157340613804488305. Acesso em: 18 nov. 2024.
APA
Silva, D. C., Andricopulo, A. D., Lima, E. F., & Honório, K. M. (2013). Identification of structural and electronic features for a series of MCH1R antagonists. Medicinal Chemistry, 9( 1), 22-31. doi:10.2174/157340613804488305
NLM
Silva DC, Andricopulo AD, Lima EF, Honório KM. Identification of structural and electronic features for a series of MCH1R antagonists [Internet]. Medicinal Chemistry. 2013 ; 9( 1): 22-31.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/157340613804488305
Vancouver
Silva DC, Andricopulo AD, Lima EF, Honório KM. Identification of structural and electronic features for a series of MCH1R antagonists [Internet]. Medicinal Chemistry. 2013 ; 9( 1): 22-31.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/157340613804488305
Artigo de periodico
Pharmacokinetic properties and in silico ADME modeling in drug discovery (2013)
Honório, Kathia Maria; Moda, Tiago L.; Andricopulo, Adriano Defini
Source: Medicinal Chemistry. Unidades: IFSC, EACH
Subjects: PLANEJAMENTO DE FÁRMACOS, QUÍMICA MÉDICA, FARMACOCINÉTICA
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ABNT
HONÓRIO, Kathia Maria e MODA, Tiago L. e ANDRICOPULO, Adriano Defini. Pharmacokinetic properties and in silico ADME modeling in drug discovery. Medicinal Chemistry, v. 9, n. 2, p. 163-176, 2013Tradução . . Disponível em: https://doi.org/10.2174/1573406411309020002. Acesso em: 18 nov. 2024.
APA
Honório, K. M., Moda, T. L., & Andricopulo, A. D. (2013). Pharmacokinetic properties and in silico ADME modeling in drug discovery. Medicinal Chemistry, 9( 2), 163-176. doi:10.2174/1573406411309020002
NLM
Honório KM, Moda TL, Andricopulo AD. Pharmacokinetic properties and in silico ADME modeling in drug discovery [Internet]. Medicinal Chemistry. 2013 ; 9( 2): 163-176.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406411309020002
Vancouver
Honório KM, Moda TL, Andricopulo AD. Pharmacokinetic properties and in silico ADME modeling in drug discovery [Internet]. Medicinal Chemistry. 2013 ; 9( 2): 163-176.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/1573406411309020002
Artigo de periodico
Molecular features for antitrypanosomal activity of thiosemicarbazones revealed by OPS-PLS QSAR studies (2012)
Lozano, Norka Beatriz Huamán; Maltarollo, Vinícius Gonçalves; Weber, Karen Cacilda; Honório, Káthia Maria; Guido, Rafael Victorio Carvalho ; Andricopulo, Adriano Defini ; Silva, Alberico Borges Ferreira da
Source: Medicinal Chemistry. Unidades: EACH, IFSC, IQSC
Subjects: QUÍMICA MÉDICA, TRIPANOSSOMICIDAS, MODELAGEM MOLECULAR
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ABNT
LOZANO, Norka Beatriz Huamán et al. Molecular features for antitrypanosomal activity of thiosemicarbazones revealed by OPS-PLS QSAR studies. Medicinal Chemistry, v. No 2012, n. 6, p. 1045-1056, 2012Tradução . . Disponível em: https://doi.org/10.2174/157340612804075043. Acesso em: 18 nov. 2024.
APA
Lozano, N. B. H., Maltarollo, V. G., Weber, K. C., Honório, K. M., Guido, R. V. C., Andricopulo, A. D., & Silva, A. B. F. da. (2012). Molecular features for antitrypanosomal activity of thiosemicarbazones revealed by OPS-PLS QSAR studies. Medicinal Chemistry, No 2012( 6), 1045-1056. doi:10.2174/157340612804075043
NLM
Lozano NBH, Maltarollo VG, Weber KC, Honório KM, Guido RVC, Andricopulo AD, Silva ABF da. Molecular features for antitrypanosomal activity of thiosemicarbazones revealed by OPS-PLS QSAR studies [Internet]. Medicinal Chemistry. 2012 ; No 2012( 6): 1045-1056.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/157340612804075043
Vancouver
Lozano NBH, Maltarollo VG, Weber KC, Honório KM, Guido RVC, Andricopulo AD, Silva ABF da. Molecular features for antitrypanosomal activity of thiosemicarbazones revealed by OPS-PLS QSAR studies [Internet]. Medicinal Chemistry. 2012 ; No 2012( 6): 1045-1056.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/157340612804075043
Artigo de periodico
Comparative molecular field analysis of a series of inhibitors of HIV-1 protease (2011)
Ferreira, Leonardo Luiz Gomes ; Leitão, Andrei ; Montanari, Carlos Alberto ; Andricopulo, Adriano Defini
Source: Medicinal Chemistry. Unidades: IQSC, IFSC
Subjects: NUCLEOSÍDEOS, PLANEJAMENTO DE FÁRMACOS, TRYPANOSOMA CRUZI, INIBIDORES DE ENZIMAS
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ABNT
FERREIRA, Leonardo Luiz Gomes et al. Comparative molecular field analysis of a series of inhibitors of HIV-1 protease. Medicinal Chemistry, v. 7, n. 2, p. 71-79, 2011Tradução . . Disponível em: https://doi.org/10.2174/157340611794859370. Acesso em: 18 nov. 2024.
APA
Ferreira, L. L. G., Leitão, A., Montanari, C. A., & Andricopulo, A. D. (2011). Comparative molecular field analysis of a series of inhibitors of HIV-1 protease. Medicinal Chemistry, 7( 2), 71-79. doi:10.2174/157340611794859370
NLM
Ferreira LLG, Leitão A, Montanari CA, Andricopulo AD. Comparative molecular field analysis of a series of inhibitors of HIV-1 protease [Internet]. Medicinal Chemistry. 2011 ; 7( 2): 71-79.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/157340611794859370
Vancouver
Ferreira LLG, Leitão A, Montanari CA, Andricopulo AD. Comparative molecular field analysis of a series of inhibitors of HIV-1 protease [Internet]. Medicinal Chemistry. 2011 ; 7( 2): 71-79.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/157340611794859370
Artigo de periodico
Quantitative structure-activity studies on a series of migrastatin analogs as inhibitors of cancer cell metastasis (2011)
Santos, Ricardo N.; Guido, Rafael Victorio Carvalho ; Oliva, Glaucius ; Dias, Luiz C.; Andricopulo, Adriano Defini
Source: Medicinal Chemistry. Unidade: IFSC
Subjects: NEOPLASIAS (TRATAMENTO), METÁSTASE NEOPLÁSICA, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURAS QUÍMICAS E ATIVIDADES BIOLÓGICAS (ESTUDO), PLANEJAMENTO DE FÁRMACOS
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ABNT
SANTOS, Ricardo N. et al. Quantitative structure-activity studies on a series of migrastatin analogs as inhibitors of cancer cell metastasis. Medicinal Chemistry, v. 7, n. 3, p. 155-164, 2011Tradução . . Disponível em: https://doi.org/10.2174/157340611795564240. Acesso em: 18 nov. 2024.
APA
Santos, R. N., Guido, R. V. C., Oliva, G., Dias, L. C., & Andricopulo, A. D. (2011). Quantitative structure-activity studies on a series of migrastatin analogs as inhibitors of cancer cell metastasis. Medicinal Chemistry, 7( 3), 155-164. doi:10.2174/157340611795564240
NLM
Santos RN, Guido RVC, Oliva G, Dias LC, Andricopulo AD. Quantitative structure-activity studies on a series of migrastatin analogs as inhibitors of cancer cell metastasis [Internet]. Medicinal Chemistry. 2011 ; 7( 3): 155-164.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/157340611795564240
Vancouver
Santos RN, Guido RVC, Oliva G, Dias LC, Andricopulo AD. Quantitative structure-activity studies on a series of migrastatin analogs as inhibitors of cancer cell metastasis [Internet]. Medicinal Chemistry. 2011 ; 7( 3): 155-164.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/157340611795564240
Artigo de periodico
CoMFA and CoMSIA 3D QSAR models for a series of cyclic imides with analgesic activity (2009)
Borchhardt, D. M.; Andricopulo, Adriano Defini
Source: Medicinal Chemistry. Unidade: IFSC
Subjects: RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, PLANEJAMENTO DE FÁRMACOS, FARMACODINÂMICA, ANALGÉSICOS (ATIVIDADE), QUÍMICA MÉDICA
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ABNT
BORCHHARDT, D. M. e ANDRICOPULO, Adriano Defini. CoMFA and CoMSIA 3D QSAR models for a series of cyclic imides with analgesic activity. Medicinal Chemistry, v. 5, n. Ja 2009, p. 66-73, 2009Tradução . . Disponível em: https://doi.org/10.2174/157340609787049299. Acesso em: 18 nov. 2024.
APA
Borchhardt, D. M., & Andricopulo, A. D. (2009). CoMFA and CoMSIA 3D QSAR models for a series of cyclic imides with analgesic activity. Medicinal Chemistry, 5( Ja 2009), 66-73. doi:10.2174/157340609787049299
NLM
Borchhardt DM, Andricopulo AD. CoMFA and CoMSIA 3D QSAR models for a series of cyclic imides with analgesic activity [Internet]. Medicinal Chemistry. 2009 ; 5( Ja 2009): 66-73.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/157340609787049299
Vancouver
Borchhardt DM, Andricopulo AD. CoMFA and CoMSIA 3D QSAR models for a series of cyclic imides with analgesic activity [Internet]. Medicinal Chemistry. 2009 ; 5( Ja 2009): 66-73.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/157340609787049299
Artigo de periodico
CDK9 a potential target for drug development (2008)
Canduri, Fernanda ; Peres, Patrícia Cardoso; Caceres, Rafael Andrade; Azevedo Junior, Walter Filgiueira
Source: Medicinal Chemistry. Unidade: IQSC
Subjects: FÁRMACOS, MODELAGEM MOLECULAR, CÉLULAS, PROTEÍNAS
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ABNT
CANDURI, Fernanda et al. CDK9 a potential target for drug development. Medicinal Chemistry, v. 4, n. 3, p. 210-218, 2008Tradução . . Acesso em: 18 nov. 2024.
APA
Canduri, F., Peres, P. C., Caceres, R. A., & Azevedo Junior, W. F. (2008). CDK9 a potential target for drug development. Medicinal Chemistry, 4( 3), 210-218.
NLM
Canduri F, Peres PC, Caceres RA, Azevedo Junior WF. CDK9 a potential target for drug development. Medicinal Chemistry. 2008 ; 4( 3): 210-218.[citado 2024 nov. 18 ]
Vancouver
Canduri F, Peres PC, Caceres RA, Azevedo Junior WF. CDK9 a potential target for drug development. Medicinal Chemistry. 2008 ; 4( 3): 210-218.[citado 2024 nov. 18 ]
Artigo de periodico
Two-dimensional QSAR studies on arylpiperazines as high-affinity 5-HT1A receptor ligands (2008)
Weber, Karen C.; Honoria, Kathia M.; Andricopulo, Adriano Defini ; Silva, Alberico Borges Ferreira da
Source: Medicinal Chemistry. Unidades: IFSC, IQSC
Subjects: RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, PLANEJAMENTO DE FÁRMACOS, SEROTONINA, PLACEBOS, PROTEÍNAS, LIGANTES, ANTIDEPRESSIVOS
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ABNT
WEBER, Karen C. et al. Two-dimensional QSAR studies on arylpiperazines as high-affinity 5-HT1A receptor ligands. Medicinal Chemistry, v. 4, n. 4, p. 328-335, 2008Tradução . . Disponível em: https://doi.org/10.2174/157340608784872325. Acesso em: 18 nov. 2024.
APA
Weber, K. C., Honoria, K. M., Andricopulo, A. D., & Silva, A. B. F. da. (2008). Two-dimensional QSAR studies on arylpiperazines as high-affinity 5-HT1A receptor ligands. Medicinal Chemistry, 4( 4), 328-335. doi:10.2174/157340608784872325
NLM
Weber KC, Honoria KM, Andricopulo AD, Silva ABF da. Two-dimensional QSAR studies on arylpiperazines as high-affinity 5-HT1A receptor ligands [Internet]. Medicinal Chemistry. 2008 ; 4( 4): 328-335.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/157340608784872325
Vancouver
Weber KC, Honoria KM, Andricopulo AD, Silva ABF da. Two-dimensional QSAR studies on arylpiperazines as high-affinity 5-HT1A receptor ligands [Internet]. Medicinal Chemistry. 2008 ; 4( 4): 328-335.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2174/157340608784872325
Artigo de periodico
Photoperiod and testosterone modulate growth and melanogenesis of S91 murine melanoma (2008)
Allil, Paulo Alexandre Arid; Visconti, Maria Aparecida ; Castrucci, Ana Maria de Lauro ; Isoldi, Mauro César
Source: Medicinal Chemistry. Unidade: IB
Subjects: MELANOMA, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALLIL, Paulo Alexandre Arid et al. Photoperiod and testosterone modulate growth and melanogenesis of S91 murine melanoma. Medicinal Chemistry, v. 4, n. 2, p. 100-105, 2008Tradução . . Acesso em: 18 nov. 2024.
APA
Allil, P. A. A., Visconti, M. A., Castrucci, A. M. de L., & Isoldi, M. C. (2008). Photoperiod and testosterone modulate growth and melanogenesis of S91 murine melanoma. Medicinal Chemistry, 4( 2), 100-105.
NLM
Allil PAA, Visconti MA, Castrucci AM de L, Isoldi MC. Photoperiod and testosterone modulate growth and melanogenesis of S91 murine melanoma. Medicinal Chemistry. 2008 ; 4( 2): 100-105.[citado 2024 nov. 18 ]
Vancouver
Allil PAA, Visconti MA, Castrucci AM de L, Isoldi MC. Photoperiod and testosterone modulate growth and melanogenesis of S91 murine melanoma. Medicinal Chemistry. 2008 ; 4( 2): 100-105.[citado 2024 nov. 18 ]

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