Your English writing platform
Discover LudwigExact(1)
CYP2D6 and CYP2D8 in the cynomolgus monkey metabolize the same compounds as humans, namely bufuralol and dextromethorphan, although their drug-metabolizing activity levels are different from those in humans (Uno et al. 2010).
Similar(59)
A better understanding of the mechanisms of alkylaniline genotoxicity is probably to provide important insights into the environmental and genetic origins of one or more human cancers and may reveal a substantial role for this group of compounds as human chemical carcinogens.
The use of metal chaperones, such as PBT2, as novel therapeutic compounds for the treatment of both 'normal' and 'pathological' cognitive decline is strongly endorsed by these findings and warrants further mechanistic investigation into the precise mechanism of action of this class of compound, as well as human clinical trials to validate these rodent data.
A comparative analysis was carried out of the anti-tumour activity of the four compounds as well as vintriptol in four human ovarian cancer xenografts different in histology, growth rate and chemosensitivity.
IARC classified Cr VI) compounds as Group 1 and they are carcinogenic to humans [ 98].
In this paper, we reported the isolation and structural elucidation of new compounds, as well as cytotoxicities of all the compounds against five human cancer cell lines.
Coal tar and coal-tar pitch are listed as Group 1 (carcinogenic to humans) carcinogens, and the U.S. EPA currently classifies seven PAH compounds as probable human carcinogens (Group B2): benz[ a]anthracene, benzo[ a]pyrene, benzo[ b]fluoranthene, benzo[ k]fluoranthene, chrysene, dibenz[ a, h]anthracene, and indeno[1,2,3- cd]pyrene.
A fuller understanding of the mechanisms of alkylaniline genotoxicity is expected to provide important insights into the environmental and genetic origins of one or more human cancers and may reveal a substantial role for this group of compounds as potential human chemical carcinogens.
In order to carry out more rational design, based on structure-based drug design, several series of N-substituted-dihydropyrazole derivatives, totally 78 compounds as potential human telomerase inhibitors were designed and synthesized.
More recently, S. cerevisiae has also been used in the bioethanol industry and for the production of heterologous compounds, such as human insulin, hepatitis vaccines, and human papillomavirus vaccines (Hou et al., 2012).
This is generally attributed to unique bioactive compounds such as human milk oligosaccharides that serve as metabolic substrates for a limited number of microbes (19), although breast milk itself also harbors a transferrable microbiota (20).
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com