Results 131 to 140 of about 27,936 (236)

Aspergillus triggers phenazine production in Pseudomonas aeruginosa [PDF]

, 2011
Objectives: Pseudomonas aeruginosa is an opportunistic human pathogen, commonly infecting cystic fibrosis (CF) patients. Aspergilli, especially Aspergillus fumigatus, are also frequently isolated from CF patients.
Pedersen, Mona Højgaard, Nielsen, Kristian Fog, Frisvad, Jens Christian, Jensen, Britt Guillaume, Søndergaard, Ib, Jelsbak, Lars   +5 more
core  

VIBRONIC SPIN-ORBIT INTERACTIONS IN PHENAZINE

, 1968
Author Institution: Naval Electronics Laboratory CenterThe $\pi-\pi$ phosphorescence spectrum (PS) of N-heterocyclic molecules is generally negative-polarized, i.e. the emitting oscillator is oriented perpendicularly to the molecular plane.
Pavlopoulos, T. G.
core   +1 more source

Push–Pull Phenazine Fluorophores: Substituent‐Position Effects on Emission and Intermolecular Organization Modulated by Hydrogen Bonding and Molecular Symmetry

ChemistryEurope
Phenazines have attracted considerable interest due to their distinctive redox and photophysical properties. However, systematic structure–property relationships for directly core‐substituted phenazines as tunable fluorophores remain underexplored.
Hiroki Sato, Masato Kudo, Jun Kumagai, Kohei Tsujimura, Nanami Hoshino, Yuito Abe, Hayato Sakai, Hiroshi Katagiri   +7 more
doaj   +1 more source

Studies on Phenazines. XXI. Bromination of Phenazine Derivatives.

Chemical and Pharmaceutical Bulletin, 1959
Yosioka, Itiro, Arafune, Shizue
openaire   +2 more sources

Identification of Phenazines with Potential Inhibitory Activity against OXA-48 Carbapenemase by Using Molecular Docking Approach to Combat Antibiotic Resistance [PDF]

Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd
Introduction: Antibiotic resistance, particularly carbapenem resistance, poses a serious global health challenge, with the OXA-48 carbapenemase being a key factor in providing this resistance.
Hourieh Kalhor, Maryam Siroosi
doaj  

Studies on Phenazines. VII. : Nitration of Phenazine and its Derivatives.

Pharmaceutical Bulletin, 1954
openaire   +4 more sources

Discovery of a phenazine-thiol conjugase from sparse data using genome-informed machine learning. [PDF]

Proc Natl Acad Sci U S A
Shan X, Trindade IB, Glasser NR, Thalhammer KO, Scurria M, Mora A, Conway SJ, Newman DK.   +7 more
europepmc   +1 more source

Modular integration of nanopore sequencing, alphafold modeling, and statistical design boosts 1-hydroxyphenazine yield in Pseudomonas aeruginosa strain KAEH25. [PDF]

BMC Microbiol
El-Mongy MA, Abuelhaded K, AbdelKhalek A, Faraag AHI.   +3 more
europepmc   +1 more source

Nitric Oxide Tunes Secreted Metabolite Bioactivity. [PDF]

Mol Microbiol
Lonergan ZR, Weisflog SL, Scurria M, Li J, Thalhammer K, Gutierrez O, Conway SJ, Newman DK.   +7 more
europepmc   +1 more source

Development of a Regioselective Synthetic Strategy and Cytotoxicity Examination of Alkoxy-Substituted Phenazine Derivatives That Disrupt G‑Quadruplex Structure. [PDF]

ACS Omega
Ręka P, Glac J, Głuszyńska A, Grolik J, Obłoza M, Ostrowska K.   +5 more
europepmc   +1 more source