montgomery, deanna anand, jessica p. baber, mason a. twarozynski, jack j. hartman, joshua g. delong, lennon j. traynor, john r. mosberg, henry i.
The opioid receptors modulate a variety of biological functions, including pain, mood, and reward. As a result, opioid ligands are being explored as potential therapeutics for a variety of indications. Multifunctional opioid ligands, which act simultaneously at more than one type of opioid receptor, show promise for use in the treatment of addictio...
Ehexige, Ehexige Ganbold, Tsogzolmaa Yu, Xiang Han, Shuqin Baigude, Huricha
Published in
Molecules
Lipid nanoparticles (LNP) are the most potent carriers for the delivery of nucleic acid-based therapeutics. The first FDA approved a short interfering RNA (siRNA) drug that uses a cationic LNP system for the delivery of siRNA against human transthyretin (hTTR). However, preparation of such LNP involves tedious multi-step synthesis with relatively l...
Chen, He Ding, Yuan Yang, Qian Barnych, Bogdan González-Sapienza, Gualberto Hammock, Bruce D. Wang, Minghua Hua, Xiude
Published in
ACS applied materials & interfaces
Shao, Changxuan Zhu, Yongjie Lai, Zhenheng Tan, Peng Shan, Anshan
Published in
Future medicinal chemistry
Baker, Kristin R. Jana, Bimal Hansen, Anna Mette Nielsen, Hanne Mørck Franzyk, Henrik Guardabassi, Luca
Published in
Frontiers in Cellular and Infection Microbiology
Synthetic peptidomimetics may be designed to mimic functions of antimicrobial peptides, including potentiation of antibiotics, yet possessing improved pharmacological properties. Pairwise screening of 42 synthetic peptidomimetics combined with the antibiotics azithromycin and rifampicin in multidrug-resistant (MDR) Escherichia coli ST131 and Klebsi...
Rai, Jagdish
Published in
Chemical biology & drug design
Retroinverso analog of a natural polypeptide can sometimes mimic the structure and function of the natural peptide. The additional advantage of using retroinverso analog is that it is resistant to proteolysis. The retroinverso analogs have peptide sequence in reverse direction with respect to natural peptide and also have chirality of amino acid in...
Oliva, Francesco Bucci, Raffaella Tamborini, Lucia Pieraccini, Stefano Pinto, Andrea Pellegrino, Sara
Published in
Frontiers in Chemistry
Unnatural amino acids have tremendously expanded the folding possibilities of peptides and peptide mimics. While α,α-disubstituted and β-amino acids are widely studied, γ-derivatives have been less exploited. Here we report the conformational study on the bicyclic unnatural γ amino acid, 4,5,6,6a-tetrahydro-3a H -pyrrolo[3,4-d]isoxazole-3-carboxyli...
Vasquez, Joseph K. Blackwell, Helen E.
Published in
ACS infectious diseases
Molchanova, Natalia Wang, Hengzhuang Hansen, Paul R. Høiby, Niels Nielsen, Hanne M. Franzyk, Henrik
Published in
Frontiers in Microbiology
Pseudomonas aeruginosa infection is a predominant cause of morbidity and mortality in patients with cystic fibrosis infection and with a compromised immune system. Emergence of bacterial resistance renders existing antibiotics inefficient, and therefore discovery of new antimicrobial agents is highly warranted. In recent years, numerous studies hav...
Liu, Bee Hui Jobichen, Chacko Chia, C S Brian Chan, Tim Hon Man Tang, Jing Ping Chung, Theodora X Y Li, Jia Poulsen, Anders Hung, Alvin W Koh-Stenta, Xiaoying
...
Published in
Proceedings of the National Academy of Sciences of the United States of America
Sal-like 4 (SALL4) is a nuclear factor central to the maintenance of stem cell pluripotency and is a key component in hepatocellular carcinoma, a malignancy with no effective treatment. In cancer cells, SALL4 associates with nucleosome remodeling deacetylase (NuRD) to silence tumor-suppressor genes, such as PTEN. Here, we determined the crystal str...