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Batzelladine D and norbatzelladine L purified from marine sponge Monanchora arbuscula induce the reversal of fluconazole
Batzelladine D and norbatzelladine L purified from marine sponge Monanchora arbuscula induce the reversal of fluconazole
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Batzelladine D and norbatzelladine L purified from marine sponge Monanchora arbuscula induce the reversal of fluconazole

Levy T.S. Domingos Mario F. C Santos; Daniel C. de Moraes; Leandro Figueira Reis de Sá; Vinicius A.D. da Silva; Lana M Meuren; Roberto Gomes de Souza Berlinck; Antonio Ferreira Pereira

Bioorganic Chemistry Maryland Heights: Academic Press v. 105, art.104402, Dec. 2020

Maryland Heights 2020

Localização: IQSC - Inst. Química de São Carlos    (P19068 )(Acessar)

2
N-phosphonomethylglycine utilization by the psychrotolerant yeast Solicoccozyma terricola M 3.1.4
N-phosphonomethylglycine utilization by the psychrotolerant yeast Solicoccozyma terricola M 3.1.4
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N-phosphonomethylglycine utilization by the psychrotolerant yeast Solicoccozyma terricola M 3.1.4

Stosiek, Natalia ; Terebieniec, Agata ; Ząbek, Adam ; Młynarz, Piotr ; Cieśliński, Hubert ; Klimek-Ochab, Magdalena

Bioorganic chemistry, 2019-12, Vol.93, p.102866-102866, Article 102866 [Periódico revisado por pares]

United States: Elsevier Inc

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3
Antioxidant activity and inhibition of ultraviolet radiation-induced skin damage of Selenium-rich peptide fraction from selenium-rich yeast protein hydrolysate
Antioxidant activity and inhibition of ultraviolet radiation-induced skin damage of Selenium-rich peptide fraction from selenium-rich yeast protein hydrolysate
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Antioxidant activity and inhibition of ultraviolet radiation-induced skin damage of Selenium-rich peptide fraction from selenium-rich yeast protein hydrolysate

Guo, Hengke ; Guo, Siyu ; Liu, Hongmei

Bioorganic chemistry, 2020-12, Vol.105, p.104431-104431, Article 104431 [Periódico revisado por pares]

United States: Elsevier Inc

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4
Organocatalyzed solvent free an efficient novel synthesis of 2,4,5-trisubstituted imidazoles for α-glucosidase inhibition to treat diabetes
Organocatalyzed solvent free an efficient novel synthesis of 2,4,5-trisubstituted imidazoles for α-glucosidase inhibition to treat diabetes
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Organocatalyzed solvent free an efficient novel synthesis of 2,4,5-trisubstituted imidazoles for α-glucosidase inhibition to treat diabetes

Yar, Muhammad ; Bajda, Marek ; Shahzad, Sohail ; Ullah, Nisar ; Gilani, Mazhar Amjad ; Ashraf, Muhammad ; Rauf, Abdul ; Shaukat, Ayesha

Bioorganic chemistry, 2015-02, Vol.58, p.65-71 [Periódico revisado por pares]

United States: Elsevier Inc

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5
Batzelladine D and norbatzelladine L purified from marine sponge Monanchora arbuscula induce the reversal of fluconazole
Batzelladine D and norbatzelladine L purified from marine sponge Monanchora arbuscula induce the reversal of fluconazole
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Artigo 		Adicionar ao Meu Espaço

Batzelladine D and norbatzelladine L purified from marine sponge Monanchora arbuscula induce the reversal of fluconazole

Domingos, Levy T.S. ; Santos, Mário F.C. ; de Moraes, Daniel C. ; de Sá, Leandro F.R. ; da Silva, Vinicius A.D. ; Meuren, Lana M. ; Berlinck, Roberto G.S. ; Ferreira-Pereira, Antonio

Bioorganic chemistry, 2020-12, Vol.105, p.104402-104402, Article 104402 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Deciphering the biotransformation mechanism of dialkylresorcinols by CYP4F11
Deciphering the biotransformation mechanism of dialkylresorcinols by CYP4F11
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Deciphering the biotransformation mechanism of dialkylresorcinols by CYP4F11

Shi, Yue ; Wolf, Clemens A. ; Lotfy, Rowaa ; Sharma, Sangeeta S. ; Tesfa, Abel Fekadu ; Wolber, Gerhard ; Bureik, Matthias ; Clark, Benjamin R.

Bioorganic chemistry, 2023-02, Vol.131, p.106330-106330, Article 106330 [Periódico revisado por pares]

United States: Elsevier Inc

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7
The anti-cancer compound Schweinfurthin A targets Osh2 and disrupts lipid metabolism in the yeast model
The anti-cancer compound Schweinfurthin A targets Osh2 and disrupts lipid metabolism in the yeast model
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The anti-cancer compound Schweinfurthin A targets Osh2 and disrupts lipid metabolism in the yeast model

Moosavi, Behrooz ; Gao, Mengqi ; Zhu, Xiao-Lei ; Yang, Guang-Fu

Bioorganic chemistry, 2020-01, Vol.94, p.103471, Article 103471 [Periódico revisado por pares]

United States: Elsevier Inc

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8
1,8-Substituted anthraquinones, anthrones and bianthrones as potential non-azole leads against fungal infections
1,8-Substituted anthraquinones, anthrones and bianthrones as potential non-azole leads against fungal infections
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1,8-Substituted anthraquinones, anthrones and bianthrones as potential non-azole leads against fungal infections

Jalab, Murhaf ; Critchley, Megan E. ; Taylor, Charlotte M. ; Lawrence, Clare L. ; Smith, Robert B.

Bioorganic chemistry, 2019-10, Vol.91, p.103151-103151, Article 103151 [Periódico revisado por pares]

United States: Elsevier Inc

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9
Hopane-type triterpenes from Cnidoscolus spinosus and their bioactivities
Hopane-type triterpenes from Cnidoscolus spinosus and their bioactivities
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Hopane-type triterpenes from Cnidoscolus spinosus and their bioactivities

López-Huerta, Fabiola A. ; Nieto-Camacho, Antonio ; Morales-Flores, Félix ; Hernández-Ortega, Simón ; Chávez, María Isabel ; Méndez Cuesta, Carlos A. ; Martínez, Ignacio ; Espinoza, Bertha ; Espinosa-García, Francisco J. ; Delgado, Guillermo

Bioorganic chemistry, 2020-07, Vol.100, p.103919-103919, Article 103919 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Benzo[a]phenoxazinium chlorides: Synthesis, antifungal activity, in silico studies and evaluation as fluorescent probes
Benzo[a]phenoxazinium chlorides: Synthesis, antifungal activity, in silico studies and evaluation as fluorescent probes
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Benzo[a]phenoxazinium chlorides: Synthesis, antifungal activity, in silico studies and evaluation as fluorescent probes

Leitão, Maria Inês P.S. ; Rama Raju, B. ; Cerqueira, Nuno M.F.S.A. ; Sousa, Maria João ; Gonçalves, M. Sameiro T.

Bioorganic chemistry, 2020-05, Vol.98, p.103730, Article 103730 [Periódico revisado por pares]

United States: Elsevier Inc

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Deste Autor:

  1. Sá, L
  2. Domingos, L
  3. Moraes, D
  4. Silva, V
  5. Pereira, A

Neste Assunto:

  1. Biochemistry & Molecular Biology
  2. Life Sciences & Biomedicine
  3. Physical Sciences
  4. Chemistry, Organic
  5. Chemistry

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

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