Results 11 to 20 of about 160 (141)
Mutagenic potency of MMS-induced 1meA/3meC lesions in E. coli. [PDF]
The mutagenic activity of MMS in E. coli depends on the susceptibility of DNA bases to methylation and their repair by cellular defense systems. Among the lesions in methylated DNA is 1meA/3meC, which is recently recognized as being mutagenic.
Janion, Celina +15 more
core +1 more source
Lethal and mutagenic properties of MMS-generated DNA lesions in Escherichia coli cells deficient in BER and AlkB-directed DNA repair. [PDF]
Methylmethane sulphonate (MMS), an S(N)2-type alkylating agent, generates DNA methylated bases exhibiting cytotoxic and mutagenic properties. Such damaged bases can be removed by a system of base excision repair (BER) and by oxidative DNA demethylation ...
Sikora, Anna +11 more
core +1 more source
The reaction of nitrilimines (2) with 1-substituted-1-methylhydrazines (3–6) led to the formation of the respective amidrazones (7) when R = CH3, Ph, and to the acyclic adducts (8,9) when R = CHO and COCH3. The acyclic adducts underwent thermal oxidative
El-Sawi, Emtithal A +3 more
core +1 more source
Synthetic Strategies to Access Fluorinated Azoles
This review highlights recent synthetic strategies for introducing fluorine groups (mono‐, di‐, and trifluoromethylation) into 11 major azole classes, identifying research gaps to inform future innovations in materials science, medicinal chemistry, and biomedical research.
Mohammed K. Abd El‐Gaber +4 more
wiley +1 more source
Drug Discovery Applications of Nitroso (Hetero)Arene Derivatives
Nitroso (hetero)aromatic compounds are bioactive molecules with antiviral, anticancer, neuroprotective, and antimicrobial properties. This review highlights their mechanisms of action—oxidative stress, DNA damage, and enzyme inhibition—alongside synthesis, structure–activity relationships, and toxicity challenges, offering insight into their ...
Silvia Roscales, Aurelio G. Csáky
wiley +1 more source
Sequential Optimization Approach Toward an Azapeptide‐Based SARS‐CoV‐2 Main Protease Inhibitor
A series of small‐molecule azapeptides with various cysteine‐reactive electrophilic groups was designed, synthesized, and investigated for Mpro inhibition. Particularly suitable warheads were identified, and their linkage to a structurally expanded peptidomimetic scaffold afforded the potent lead compound 12, with kinac/Ki = 78,900 M–1s–1 and an ...
Rabea Voget +9 more
wiley +1 more source
The gas-phase photochemistry of the diamines monomethylhydrazine (CH3NHNH2) and unsymmetrical dimethylhydrazine ((CH3)2NNH2) has been studied in the ultraviolet (UV) at 298 K.
Ghanshyam L. Vaghjiani (1277073)
core +1 more source
Monometallic and heterobimetallic Ru‐PdL complexes were synthesized and fully characterized. Their electrochemical properties were investigated by cyclic voltammetry. The Ru‐PdL complexes catalyzed the hydroarylation of NBD and the ROMP of Ph‐NBE. One complex catalyzed both reactions via tandem catalysis in one pot, converting NBD to poly (Ph‐NBE ...
Thais R. Cruz +6 more
wiley +1 more source
The cascade Michael/intramolecular transamidation reactions of 3‐phenacylidene‐2‐indolinone derivatives bearing a trifluoromethyl group as a novel Michael acceptor with hydrazines yielded the corresponding pyrazolidin‐3‐one derivatives in good to high yields with excellent diastereoselectivity.
Ryo Tsuyusaki +4 more
wiley +1 more source
The pyrazolo[4,3‐c][1,2]benzothiazine 5,5‐dioxide class was investigated with the aim of enlarging the array of Staphylococcus aureus NorA efflux pump inhibitors. The ethidium bromide efflux assay was used as a first indication of NorA inhibition; then, the ability of compounds to synergize with ciprofloxacin (CPX) against both wild‐type and resistant ...
Giada Cernicchi +14 more
wiley +1 more source

