Pseudoxylallemycins A-F, cyclic tetrapeptides with rare allenyl modifications isolated from Pseudoxylaria sp. X802: a competitor of fungus-growing termite cultivars
Research output: Contribution to journal › Letter › Research › peer-review
Standard
Pseudoxylallemycins A-F, cyclic tetrapeptides with rare allenyl modifications isolated from Pseudoxylaria sp. X802 : a competitor of fungus-growing termite cultivars. / Guo, Huijuan; Kreuzenbeck, Nina B.; Otani, Saria; Garcia-Altares, Maria; Dahse, Hans-Martin; Weigel, Christiane; Aanen, Duur K.; Hertweck, Christian; Thomas-Poulsen, Michael; Beemelmanns, Christine.
In: Organic Letters, Vol. 18, No. 14, 2016, p. 3338-3341.Research output: Contribution to journal › Letter › Research › peer-review
Harvard
APA
Vancouver
Author
Bibtex
}
RIS
TY - JOUR
T1 - Pseudoxylallemycins A-F, cyclic tetrapeptides with rare allenyl modifications isolated from Pseudoxylaria sp. X802
T2 - a competitor of fungus-growing termite cultivars
AU - Guo, Huijuan
AU - Kreuzenbeck, Nina B.
AU - Otani, Saria
AU - Garcia-Altares, Maria
AU - Dahse, Hans-Martin
AU - Weigel, Christiane
AU - Aanen, Duur K.
AU - Hertweck, Christian
AU - Thomas-Poulsen, Michael
AU - Beemelmanns, Christine
PY - 2016
Y1 - 2016
N2 - Based on fungus-fungus pairing assays and HRMS-based dereplication strategy, six new cyclic tetrapeptides, pseudoxylallemycins A-F (1-6), were isolated from the termite-associated fungus Pseudoxylaria sp. X802. Structures were characterized using NMR spectroscopy, HRMS, and Marfey's reaction. Pseudoxylallemycins B-D (2-4) possess a rare and chemically accessible allene moiety amenable for synthetic modifications, and derivatives A-D showed antimicrobial activity against Gram-negative human-pathogenic Pseudomonas aeruginosa and antiproliferative activity against human umbilical vein endothelial cells and K-562 cell lines.
AB - Based on fungus-fungus pairing assays and HRMS-based dereplication strategy, six new cyclic tetrapeptides, pseudoxylallemycins A-F (1-6), were isolated from the termite-associated fungus Pseudoxylaria sp. X802. Structures were characterized using NMR spectroscopy, HRMS, and Marfey's reaction. Pseudoxylallemycins B-D (2-4) possess a rare and chemically accessible allene moiety amenable for synthetic modifications, and derivatives A-D showed antimicrobial activity against Gram-negative human-pathogenic Pseudomonas aeruginosa and antiproliferative activity against human umbilical vein endothelial cells and K-562 cell lines.
KW - Journal Article
U2 - 10.1021/acs.orglett.6b01437
DO - 10.1021/acs.orglett.6b01437
M3 - Letter
C2 - 27341414
VL - 18
SP - 3338
EP - 3341
JO - Organic Letters
JF - Organic Letters
SN - 1523-7060
IS - 14
ER -
ID: 169945955