Applications of π-π stacking interactions in the design of drug-delivery systems

WR Zhuang, Y Wang, PF Cui, L **ng, J Lee… - Journal of controlled …, 2019‏ - Elsevier
Noncovalent forces are of considerable importance in the formation of self-assembled drug-
delivery systems. In addition to non-destructively linking the delivery vehicle and guest drug …

Nitro-group-containing drugs

K Nepali, HY Lee, JP Liou - Journal of medicinal chemistry, 2018‏ - ACS Publications
The nitro group is considered to be a versatile and unique functional group in medicinal
chemistry. Despite a long history of use in therapeutics, the nitro group has toxicity issues …

[HTML][HTML] Azo dyes in clothing textiles can be cleaved into a series of mutagenic aromatic amines which are not regulated yet

BJ Brüschweiler, C Merlot - Regulatory Toxicology and Pharmacology, 2017‏ - Elsevier
Azo dyes represent the by far most important class of textile dyes. Their biotransformation by
various skin bacteria may release aromatic amines (AAs) which might be dermally absorbed …

Reactive metabolites of the anticonvulsant drugs and approaches to minimize the adverse drug reaction

R Pal, K Singh, SA Khan, P Chawla, B Kumar… - European Journal of …, 2021‏ - Elsevier
Several generations of antiepileptic drugs (AEDs) are available in the market for the
treatment of seizures, but these are amalgamated with acute to chronic side effects. The …

Predicting toxicities of reactive metabolite–positive drug candidates

AS Kalgutkar, D Dalvie - Annual review of pharmacology and …, 2015‏ - annualreviews.org
Because of the inability to predict and quantify the risk of idiosyncratic adverse drug
reactions (IADRs) and because reactive metabolites (RMs) are thought to be responsible for …

Discovery and early clinical development of an inhibitor of 5-lipoxygenase activating protein (AZD5718) for treatment of coronary artery disease

D Pettersen, J Broddefalk, H Emtenäs, MA Hayes… - 2019‏ - ACS Publications
5-Lipoxygenase activating protein (FLAP) inhibitors attenuate 5-lipoxygenase pathway
activity and reduce the production of proinflammatory and vasoactive leukotrienes. As such …

Mechanism-based insights into removing the mutagenicity of aromatic amines by small structural alterations

I Shamovsky, L Ripa, F Narjes, B Bonn… - Journal of Medicinal …, 2021‏ - ACS Publications
Aromatic and heteroaromatic amines (ArNH2) are activated by cytochrome P450
monooxygenases, primarily CYP1A2, into reactive N-arylhydroxylamines that can lead to …

Role of human sulfotransferase 1A1 and N-acetyltransferase 2 in the metabolic activation of 16 heterocyclic amines and related heterocyclics to genotoxicants in …

M Chevereau, H Glatt, D Zalko, JP Cravedi… - Archives of …, 2017‏ - Springer
Heterocyclic aromatic amines (HAAs) are primarily produced during the heating of meat or
fish. HAAs are mutagenic and carcinogenic, and their toxicity in model systems depend on …

Should the incorporation of structural alerts be restricted in drug design? An analysis of structure-toxicity trends with aniline-based drugs

AS Kalgutkar - Current Medicinal Chemistry, 2015‏ - ingentaconnect.com
Certain idiosyncratic adverse drug reactions (IADRs) can be triggered by electrophilic
protein-reactive metabolites that are formed in the process of drug metabolism. While …

Cascade Reaction of Arylboronic Acids and 2′-Cyano-biaryl-2-aldehyde N-Tosylhydrazones: Access to Functionalized 9-Amino-10-arylphenanthrenes

Y Liu, L Chen, Z Wang, P Liu, Y Liu… - The Journal of Organic …, 2018‏ - ACS Publications
An efficient, general, and convenient protocol for the synthesis of functionalized 9-amino-10-
arylphenanthrene derivatives using a catalyst-free cascade reaction of arylboronic acids and …