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1
Pyrodysinoic acid derivatives from the marine sponge dysidea robusta
Pyrodysinoic acid derivatives from the marine sponge dysidea robusta
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Pyrodysinoic acid derivatives from the marine sponge dysidea robusta

David E. Williams Suzi O Marques; Eduardo Hadju; Solange Peixinho; Raymond J Andersen; Roberto Gomes de Souza Berlinck

Journal of Natural Products Washington v. 72, n. 9, p. 1691-1694, 20078

Washington 2009

Localização: IQSC - Inst. Química de São Carlos    (P11702 )(Acessar)

2
Pyrodysinoic acid derivatives from the marine sponge dysidea robusta
Pyrodysinoic acid derivatives from the marine sponge dysidea robusta
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Pyrodysinoic acid derivatives from the marine sponge dysidea robusta

David E. Williams Suzi O Marques; Eduardo Hadju; Solange Peixinho; Raymond J Andersen; Roberto Gomes de Souza Berlinck

Journal of Natural Products Washington v. 72, n. 9, p. 1691-1694, 20078

Washington 2009

Localização: IQSC - Inst. Química de São Carlos    (P11702 )(Acessar)

3
Use of experimental design for the optimization of the production of new secondary metabolites by two penicillium species
Use of experimental design for the optimization of the production of new secondary metabolites by two penicillium species
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Use of experimental design for the optimization of the production of new secondary metabolites by two penicillium species

Eli Fernando Pimenta Aline Maria Vita-Marques; Aristeu Tininis; Mirna Helena Regali Seleghim; Lara Durães Sette; Katyuscya Veloso; Antonio G Ferreira; David E Williams; Brian o Patrick; Doralyn S Dalisay; Raymond J Andersen; Roberto Gomes de Souza Berlinck

Journal of Natural Products Washington v. 73, n. 11, p. 1821-1832, 2010

Washington 2010

Localização: IQSC - Inst. Química de São Carlos    (P12903 )(Acessar)

4
Use of experimental design for the optimization of the production of new secondary metabolites by two penicillium species
Use of experimental design for the optimization of the production of new secondary metabolites by two penicillium species
Material Type:
Artigo 		Adicionar ao Meu Espaço

Use of experimental design for the optimization of the production of new secondary metabolites by two penicillium species

Eli Fernando Pimenta Aline Maria Vita-Marques; Aristeu Tininis; Mirna Helena Regali Seleghim; Lara Durães Sette; Katyuscya Veloso; Antonio G Ferreira; David E Williams; Brian o Patrick; Doralyn S Dalisay; Raymond J Andersen; Roberto Gomes de Souza Berlinck

Journal of Natural Products Washington v. 73, n. 11, p. 1821-1832, 2010

Washington 2010

Localização: IQSC - Inst. Química de São Carlos    (P12903 )(Acessar)

5
Cultures of the marine bacterium Pseudovibrio dentrificans Ab134 produce bromotyrosine-derived alkaloids previously only isolated from marine sponges
Cultures of the marine bacterium Pseudovibrio dentrificans Ab134 produce bromotyrosine-derived alkaloids previously only isolated from marine sponges
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Cultures of the marine bacterium Pseudovibrio dentrificans Ab134 produce bromotyrosine-derived alkaloids previously only isolated from marine sponges

Karen J Nicacio Laura P Ióca; Adriana M Fróes; Luciana Leomil; Luciana R Appolinario; Christiane C Thompson; Fabiano L Thompson; Antonio G Ferreira; David E Williams; Raymond J Andersen; Alessandra S Eustaquio; Roberto Gomes de Souza Berlinck

Journal of Natural Products Wahington v. 80, n. 2, p.235-240, 2017

Washington 2017

Localização: IQSC - Inst. Química de São Carlos    (P16742 )(Acessar)

6
Rearranged terpenoids from the marine sponge Darwinella cf. oxeata and its predador, the Nudibranch Felimida grahami
Rearranged terpenoids from the marine sponge Darwinella cf. oxeata and its predador, the Nudibranch Felimida grahami
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Rearranged terpenoids from the marine sponge Darwinella cf. oxeata and its predador, the Nudibranch Felimida grahami

Maria Camila Acevedo Ramírez David E Williams; Juliana R Gubiani; Lizbeth Lorena López Parra; Mario Ferreira Conceição Santos; Daiane D Ferreira; Juliana T Mesquita; André Gustavo Tempone; Antonio G Ferreira; Vinicius Padula; Eduardo Hajdu; Raymond J Andersen; Roberto Gomes de Souza Berlinck

Journal of Natural Products Wahington v. 80, n. 3, p. 720-725, 2017

Wahington 2017

Localização: IQSC - Inst. Química de São Carlos    (P16775 )(Acessar)

7
Bromopyrrole alkaloid inhibitors of the proteasome isolated from a dictyonella sp. Marine Sponge collected at the Amazon river mouth
Bromopyrrole alkaloid inhibitors of the proteasome isolated from a dictyonella sp. Marine Sponge collected at the Amazon river mouth
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Bromopyrrole alkaloid inhibitors of the proteasome isolated from a dictyonella sp. Marine Sponge collected at the Amazon river mouth

Renata Torres Mattos Paschoalino de Souza Vitor F Freire; Juliana R Gubiani; Raquel O Ferreira; Daniela B. B Trivella; Fernando C Moraes; Wladimir C Paradas; Leonardo Tavares Salgado; Renato C Pereira; Gilberto M Amado Filho; Antonio G Ferreira; David E Williams; Raymond J Andersen; Tadeusz F Molinski; Roberto Gomes de Souza Berlinck

Journal of Natural Products Washington, DC : American Chemical Society - ACS v.81, p.2296-2300,2019

Washington, DC 2019

Localização: IQSC - Inst. Química de São Carlos    (P17829 )(Acessar)

8
Anti-parasitic guanidine and pyrimidine alkaloids from the Marine Sponge Monanchora arbuscula
Anti-parasitic guanidine and pyrimidine alkaloids from the Marine Sponge Monanchora arbuscula
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Anti-parasitic guanidine and pyrimidine alkaloids from the Marine Sponge Monanchora arbuscula

Mário Ferreira dos Santos Philip M Harper; David Williams; Juliana T Mesquita; Érika Gracielle Pinto; Thaís A da Costa-Silva; Eduardo Hadju; Antonio G Ferreira; Raquel A Santos; Patrick J Murphy; Raymond J Andersen; André Gustavo Tempone; Roberto Gomes de Souza Berlinck

Journal of Natural Products v. 78, n. 5, p. 1721-1731, 2015

Washington 2015

Localização: IQSC - Inst. Química de São Carlos    (P15671 )(Acessar)

9
Condensation of macrocyclic polyketides produced by penicullium sp.DRF2 with mercaptopyruvate represents a new fungal detoxification pathway
Condensation of macrocyclic polyketides produced by penicullium sp.DRF2 with mercaptopyruvate represents a new fungal detoxification pathway
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Condensation of macrocyclic polyketides produced by penicullium sp.DRF2 with mercaptopyruvate represents a new fungal detoxification pathway

Marcos V Castro Laura Pavan Ióca; David E Williams; Bruna Z Costa; Carolina Megumi Mizuno; Mario F. C Santos; Karen de Jesus; Everton Lucena F Ferreira; Mirna Helena Regali Seleghim; Lara Durães Sette; Edenir Rodrigues Pereira Filho; Antonio G Ferreira; Natália S Gonçalves; Raquel A Santos; Brian O Patrick; Raymond J Andersen; Roberto Gomes de Souza Berlinck

Journal of Natural Products v. 79, n. 6, p. 1668-1678, 2016

Washington 2016

Localização: IQSC - Inst. Química de São Carlos    (P16276 )(Acessar)

10
Analogues of Marine Guanidine alkaloids are in vitro effective against Trypanosoma cruzi and selectively eliminate Leishmania (L.) infantum intracellular Amastigotes
Analogues of Marine Guanidine alkaloids are in vitro effective against Trypanosoma cruzi and selectively eliminate Leishmania (L.) infantum intracellular Amastigotes
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Analogues of Marine Guanidine alkaloids are in vitro effective against Trypanosoma cruzi and selectively eliminate Leishmania (L.) infantum intracellular Amastigotes

Ligia M Martins Juiana T Mesquita; Érika G Pinto; Thaís A da Costa-Silva; Samanta Etel Treiger Borborema; Andres J Galisteo Junior; Bruno J Neves; Carolina H Andrade; Zainab Al Shuhaib; Elliot L Bennett; Gregory P Black; Philip M Harper; Daniel M Evans; Hisham S Fituri; John P Leyland; Claire Martin; Terence D Roberts; Andrew J Thornhill; Stephen A Vale; Andrew Howard-Jones; Dafydd A Thomas; Harri L Williams; Larry E Overman; Roberto Gomes de Souza Berlinck; Patrick J Murphy; André G Tempone

Journal of Natural Products Washington v. 79, n. 9. p.2202-2210, 2016

Washington 2016

Localização: IQSC - Inst. Química de São Carlos    (P16530 )(Acessar)

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Deste Autor:

  1. Berlinck, R
  2. Andersen, R
  3. Williams, D
  4. Ferreira, A
  5. Seleghim, M

Neste Assunto:

  1. Produtos Naturais
  2. Química Orgânica
  3. Biologia Marinha
  4. Proteínas
  5. Biologia Molecular

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

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