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Refinado por: Nome da Publicação: Bioorganic And Medicinal Chemistry remover
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1
1,12-Substituted tetracyclines as antioxidant agents
1,12-Substituted tetracyclines as antioxidant agents
Material Type:
Artigo 		Adicionar ao Meu Espaço

1,12-Substituted tetracyclines as antioxidant agents

Lertvorachon, Jittiwud ; Kim, Jong-Pyung ; Soldatov, Dmitriy V. ; Boyd, Jason ; Roman, Gheorghe ; Cho, Sung Ju ; Popek, Tomasz ; Jung, Young-Sik ; Lau, Peter C.K. ; Konishi, Yasuo

Bioorganic & medicinal chemistry, 2005-08, Vol.13 (15), p.4627-4637 [Periódico revisado por pares]

Oxford: Elsevier Ltd

Texto completo disponível

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2
16-bromoepiandrosterone, an activator of the mammalian immune system, inhibits glucose 6-phosphate dehydrogenase from Trypanosoma cruzi and is toxic to these parasites grown in culture
16-bromoepiandrosterone, an activator of the mammalian immune system, inhibits glucose 6-phosphate dehydrogenase from Trypanosoma cruzi and is toxic to these parasites grown in culture
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16-bromoepiandrosterone, an activator of the mammalian immune system, inhibits glucose 6-phosphate dehydrogenase from Trypanosoma cruzi and is toxic to these parasites grown in culture

Artur T. Cordeiro Otávio Henrique Thiemann

Bioorganic and Medicinal Chemistry Oxford : Pergamon-Elsevier Science v. 18, n. 13, p. 4762-4768, July 2010

Oxford 2010

Localização: IFSC - Inst. Física de São Carlos    (PROD011998 )(Acessar)

3
16-bromoepiandrosterone, an activator of the mammalian immune system, inhibits glucose 6-phosphate dehydrogenase from Trypanosoma cruzi and is toxic to these parasites grown in culture
16-bromoepiandrosterone, an activator of the mammalian immune system, inhibits glucose 6-phosphate dehydrogenase from Trypanosoma cruzi and is toxic to these parasites grown in culture
Material Type:
Artigo 		Adicionar ao Meu Espaço

16-bromoepiandrosterone, an activator of the mammalian immune system, inhibits glucose 6-phosphate dehydrogenase from Trypanosoma cruzi and is toxic to these parasites grown in culture

Artur T. Cordeiro Otávio Henrique Thiemann

Bioorganic and Medicinal Chemistry Oxford : Pergamon-Elsevier Science v. 18, n. 13, p. 4762-4768, July 2010

Oxford 2010

Localização: IFSC - Inst. Física de São Carlos    (PROD011998 )(Acessar)

4
2D QSAR and similarity studies on cruzain inhibitors aimed at improving selectivity over cathepsin L
2D QSAR and similarity studies on cruzain inhibitors aimed at improving selectivity over cathepsin L
Material Type:
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2D QSAR and similarity studies on cruzain inhibitors aimed at improving selectivity over cathepsin L

Renato F. Freitas Tudor I Oprea; Carlos Alberto Montanari

Bioorganic and Medicinal Chemistry Oxford v. 16, n.12, p. 838-853, 2008

Oxford 2008

Acesso online. A biblioteca também possui exemplares impressos.

5
2D QSAR and similarity studies on cruzain inhibitors aimed at improving selectivity over cathepsin L
2D QSAR and similarity studies on cruzain inhibitors aimed at improving selectivity over cathepsin L
Material Type:
Artigo 		Adicionar ao Meu Espaço

2D QSAR and similarity studies on cruzain inhibitors aimed at improving selectivity over cathepsin L

Renato F. Freitas Tudor I Oprea; Carlos Alberto Montanari

Bioorganic and Medicinal Chemistry Oxford v. 16, n.12, p. 838-853, 2008

Oxford 2008

Acesso online. A biblioteca também possui exemplares impressos.

6
2D QSAR studies on tyroid hormone receptor ligands
2D QSAR studies on tyroid hormone receptor ligands
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2D QSAR studies on tyroid hormone receptor ligands

Napoleão Fonseca Valadares Marcelo S Castilho; Igor Polikarpov; Richard Charles Garratt

Bioorganic and Medicinal Chemistry Oxford v. 15, n. 13, p. 4609-4617, Jul. 2007

Oxford 2007

Localização: IFSC - Inst. Física de São Carlos    (PROD013708 )(Acessar)

7
2D QSAR studies on tyroid hormone receptor ligands
2D QSAR studies on tyroid hormone receptor ligands
Material Type:
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2D QSAR studies on tyroid hormone receptor ligands

Napoleão Fonseca Valadares Marcelo S Castilho; Igor Polikarpov; Richard Charles Garratt

Bioorganic and Medicinal Chemistry Oxford v. 15, n. 13, p. 4609-4617, Jul. 2007

Oxford 2007

Localização: IFSC - Inst. Física de São Carlos    (PROD013708 )(Acessar)

8
2D quantitative structure-activity relationship studies on a series of cholesteryl ester preotein inhibitors
2D quantitative structure-activity relationship studies on a series of cholesteryl ester preotein inhibitors
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2D quantitative structure-activity relationship studies on a series of cholesteryl ester preotein inhibitors

Marcelo S. Castilho Rafael Victorio Carvalho Guido; Adriano Defini Andricopulo

Bioorganic and Medicinal Chemistry Oxford v. 15, n. 18, p. 6242-6252, Sep. 2007

Oxford 2007

Localização: IFSC - Inst. Física de São Carlos    (PROD013867 )(Acessar)

9
2D quantitative structure-activity relationship studies on a series of cholesteryl ester preotein inhibitors
2D quantitative structure-activity relationship studies on a series of cholesteryl ester preotein inhibitors
Material Type:
Artigo 		Adicionar ao Meu Espaço

2D quantitative structure-activity relationship studies on a series of cholesteryl ester preotein inhibitors

Marcelo S. Castilho Rafael Victorio Carvalho Guido; Adriano Defini Andricopulo

Bioorganic and Medicinal Chemistry Oxford v. 15, n. 18, p. 6242-6252, Sep. 2007

Oxford 2007

Localização: IFSC - Inst. Física de São Carlos    (PROD013867 )(Acessar)

10
Ability of higenamine and related compounds to enhance glucose uptake in L6 cells
Ability of higenamine and related compounds to enhance glucose uptake in L6 cells
Material Type:
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Ability of higenamine and related compounds to enhance glucose uptake in L6 cells

Kato, Eisuke ; Kimura, Shunsuke ; Kawabata, Jun

Bioorganic & medicinal chemistry, 2017-12, Vol.25 (24), p.6412-6416 [Periódico revisado por pares]

England: Elsevier Ltd

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Deste Autor:

  1. Andricopulo, A
  2. Carvalho, I
  3. Guido, R
  4. Montanari, C
  5. Silva, J

Neste Assunto:

  1. Trypanosoma Cruzi
  2. Pharmacology & Pharmacy
  3. Chemistry, Medicinal
  4. Chemistry
  5. Life Sciences & Biomedicine

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.