Skip To Main Content
Valdet Uka on Muck Rack

Valdet Uka

As seen in: Wiley Online Library, BioRxiv
Is this you? As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work. Claim your profile

Get in touch with Valdet

Contact Valdet, search articles and posts on X, monitor coverage, and track replies from one place.

Learn more about Muck Rack

Actions

Share this page

Is this you?

As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.
Claim your profile

Articles

Unveiling the Chemical Space of Astin‐Type Peptides in Aster Tataricus, Cyanodermella Asteris, and Talaromyces Islandicus

|
By Valdet Uka, Shen Tang, Jonas F. Ohlrogge, Angela Sester
| Wiley Online Library Verified
Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement The data that support the findings of this study are available in the supplementary material of this article. Supporting Information Filename Description chem70669-sup-0001-SuppMat.pdf22.3 MB The authors have cited additional references within the Supporting Information [30-34].
Open in Who Shared Issue with article?

Unveiling the Chemical Space of Astin-Type Peptides in Aster Tataricus, Cyanodermella Asteris, and Talaromyces Islandicus

|
By Valdet Uka, universiteti i prishtines, Shen Tang, Professur für Biochemie
| tu-dresden.de
Abstract Externe IDs PubMed 41518250 Schlagworte Astins, Cyclochlorotines, Fungi, high-resolution MS, Molecular networking, Plant
Open in Who Shared Issue with article?

The Maculalactone Biosynthetic Gene Cluster, a Cryptic Furanolide Pathway Revealed in Nodularia sp. NIES-3585

|
By Paul D'Agostino, Kumar Saurav, Tobias M. Milzarek, Valdet Uka
| BioRxiv
Abstract Cyanobacteria have long been known as a prolific source of bioactive natural products (NPs). One such group of NPs are the furanolides, whose first congeners were discovered in the 1980s and 1990s. A structural characteristic of furanolides is a γ-butyrolactone moiety with aromatic or aliphatic substituents at the α- and β-positions and an aromatic substituent at its γ-position.
Open in Who Shared Issue with article?
See all 3 articles