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Dopamine-Derived Guanidine Alkaloids from a Didemnidae Tunicate: Isolation, Synthesis, and Biological Activities.
Sakai, Ryuichi; Matsumura, Ken; Uchimasu, Hajime; Miyako, Kei; Taniguchi, Tohru; Kovvuri, V Raghavendra Rao; Acharige, Anjana Delpe; Hull, Kenneth G; Romo, Daniel; Thaveepornkul, Lakkana; Chimnaronk, Sarin; Miyamoto, Hiroko; Takada, Ayato; Watari, Hiromi; Fujita, Masaki J; Sakaue, Jiro.
Afiliação
  • Sakai R; Faculty and Graduate School of Fisheries Sciences, Hokkaido University, 3-1-1 Minato-Cho, Hakodate, Hokkaido 041-8611, Japan.
  • Matsumura K; Graduate School of Fisheries Sciences, Hokkaido University, 3-1-1 Minato-Cho, Hakodate, Hokkaido 041-8611, Japan.
  • Uchimasu H; Graduate School of Fisheries Sciences, Hokkaido University, 3-1-1 Minato-Cho, Hakodate, Hokkaido 041-8611, Japan.
  • Miyako K; Graduate School of Fisheries Sciences, Hokkaido University, 3-1-1 Minato-Cho, Hakodate, Hokkaido 041-8611, Japan.
  • Taniguchi T; Frontier Research Center for Advanced Material and Life Science, Faculty of Advanced Life Science, Hokkaido University, Kita 21 Nishi 11, Sapporo 001-0021, Japan.
  • Kovvuri VRR; Department of Chemistry and Biochemistry & The Baylor Synthesis and Drug Lead Discovery Laboratory, Baylor University, 101 Bagby Avenue, Waco, Texas 76798-7348, United States.
  • Acharige AD; Department of Chemistry and Biochemistry & The Baylor Synthesis and Drug Lead Discovery Laboratory, Baylor University, 101 Bagby Avenue, Waco, Texas 76798-7348, United States.
  • Hull KG; Department of Chemistry and Biochemistry & The Baylor Synthesis and Drug Lead Discovery Laboratory, Baylor University, 101 Bagby Avenue, Waco, Texas 76798-7348, United States.
  • Romo D; Department of Chemistry and Biochemistry & The Baylor Synthesis and Drug Lead Discovery Laboratory, Baylor University, 101 Bagby Avenue, Waco, Texas 76798-7348, United States.
  • Thaveepornkul L; Institute of Molecular Biosciences, Mahidol University, 25/25 Phutthamonthon 4 Road, Salaya, Nakhon Pathom 73170, Thailand.
  • Chimnaronk S; Institute of Molecular Biosciences, Mahidol University, 25/25 Phutthamonthon 4 Road, Salaya, Nakhon Pathom 73170, Thailand.
  • Miyamoto H; Division of Global Epidemiology, International Institute for Zoonosis Control, Hokkaido University, Kita 20 Nishi 10, Sapporo 001-0020, Japan.
  • Takada A; Division of Global Epidemiology, International Institute for Zoonosis Control, Hokkaido University, Kita 20 Nishi 10, Sapporo 001-0020, Japan.
  • Watari H; International Collaboration Unit, International Institute for Zoonosis Control, Hokkaido University, Kita 20 Nishi 10, Sapporo 001-0020, Japan.
  • Fujita MJ; One Health Research Center, Hokkaido University, Kita 20 Nishi 10, Sapporo 001-0020, Japan.
  • Sakaue J; Faculty and Graduate School of Fisheries Sciences, Hokkaido University, 3-1-1 Minato-Cho, Hakodate, Hokkaido 041-8611, Japan.
J Org Chem ; 89(9): 5977-5987, 2024 May 03.
Article em En | MEDLINE | ID: mdl-38557022
ABSTRACT
Mellpaladines A-C (1-3) and dopargimine (4) are dopamine-derived guanidine alkaloids isolated from a specimen of Palauan Didemnidae tunicate as possible modulators of neuronal receptors. In this study, we isolated the dopargimine derivative 1-carboxydopargimine (5), three additional mellpaladines D-F (6-8), and serotodopalgimine (9), along with a dimer of serotonin, 5,5'-dihydroxy-4,4'-bistryptamine (10). The structures of these compounds were determined based on spectrometric and spectroscopic analyses. Compound 4 and its congeners dopargine (11), nordopargimine (15), and 2-(6,7-dimethoxy-3,4-dihydroisoquinolin-1-yl)ethan-1-amine (16) were synthetically prepared for biological evaluations. The biological activities of all isolated compounds were evaluated in comparison with those of 1-4 using a mouse behavioral assay upon intracerebroventricular injection, revealing key functional groups in the dopargimines and mellpaladines for in vivo behavioral toxicity. Interestingly, these alkaloids also emerged during a screen of our marine natural product library aimed at identifying antiviral activities against dengue virus, SARS-CoV-2, and vesicular stomatitis Indiana virus (VSV) pseudotyped with Ebola virus glycoprotein (VSV-ZGP).
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Urocordados / Dopamina / Alcaloides Limite: Animals / Humans Idioma: En Revista: J Org Chem Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Urocordados / Dopamina / Alcaloides Limite: Animals / Humans Idioma: En Revista: J Org Chem Ano de publicação: 2024 Tipo de documento: Article