Eudistomins W and X, two new beta-carbolines from the micronesian tunicate Eudistoma sp.J Nat Prod. 2003 Feb; 66(2):272-5.JN
Abstract
Chemical investigation of the Micronesian ascidian Eudistoma sp. afforded two new eudistomin congeners, which were designated eudistomins W (1) and X (2). The structures of the new compounds were unambiguously established on the basis of NMR spectroscopic ((1)H, (13)C, COSY, (1)H detected direct, and long-range (13)C-(1)H correlations) and mass spectrometric (EI and ESIMS) data. Compound 2 exhibited antibiotic activity toward Bacillus subtilis, Staphyloccocus aureus, and Escherichia coli and was also found to be fungicidal against Candida albicans in an agar diffusion assay. Compound 1 was selectively active against C. albicans but showed no antibacterial activity.
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
12608864
Citation
Schupp, Peter, et al. "Eudistomins W and X, Two New Beta-carbolines From the Micronesian Tunicate Eudistoma Sp." Journal of Natural Products, vol. 66, no. 2, 2003, pp. 272-5.
Schupp P, Poehner T, Edrada R, et al. Eudistomins W and X, two new beta-carbolines from the micronesian tunicate Eudistoma sp. J Nat Prod. 2003;66(2):272-5.
Schupp, P., Poehner, T., Edrada, R., Ebel, R., Berg, A., Wray, V., & Proksch, P. (2003). Eudistomins W and X, two new beta-carbolines from the micronesian tunicate Eudistoma sp. Journal of Natural Products, 66(2), 272-5.
Schupp P, et al. Eudistomins W and X, Two New Beta-carbolines From the Micronesian Tunicate Eudistoma Sp. J Nat Prod. 2003;66(2):272-5. PubMed PMID: 12608864.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Eudistomins W and X, two new beta-carbolines from the micronesian tunicate Eudistoma sp.
AU - Schupp,Peter,
AU - Poehner,Timo,
AU - Edrada,RuAngelie,
AU - Ebel,Rainer,
AU - Berg,Albrecht,
AU - Wray,Victor,
AU - Proksch,Peter,
PY - 2003/3/1/pubmed
PY - 2003/7/8/medline
PY - 2003/3/1/entrez
SP - 272
EP - 5
JF - Journal of natural products
JO - J Nat Prod
VL - 66
IS - 2
N2 - Chemical investigation of the Micronesian ascidian Eudistoma sp. afforded two new eudistomin congeners, which were designated eudistomins W (1) and X (2). The structures of the new compounds were unambiguously established on the basis of NMR spectroscopic ((1)H, (13)C, COSY, (1)H detected direct, and long-range (13)C-(1)H correlations) and mass spectrometric (EI and ESIMS) data. Compound 2 exhibited antibiotic activity toward Bacillus subtilis, Staphyloccocus aureus, and Escherichia coli and was also found to be fungicidal against Candida albicans in an agar diffusion assay. Compound 1 was selectively active against C. albicans but showed no antibacterial activity.
SN - 0163-3864
UR - https://www.unboundmedicine.com/medline/citation/12608864/Eudistomins_W_and_X_two_new_beta_carbolines_from_the_micronesian_tunicate_Eudistoma_sp_
DB - PRIME
DP - Unbound Medicine
ER -