Recent advancements in organotin (IV) complexes as potential anticancer agents

J Devi, J Yadav - Anti-Cancer Agents in Medicinal Chemistry …, 2018 - ingentaconnect.com
Cancer is a multistep disease incorporating physical, chemical, environmental, metabolic
and genetic factors, which play direct or indirect role in the induction and deterioration of …

Medicinal chemistry and the molecular operating environment (MOE): application of QSAR and molecular docking to drug discovery

S Vilar, G Cozza, S Moro - Current topics in medicinal chemistry, 2008 - ingentaconnect.com
The search for new compounds with a given biological activity requires enormous effort in
terms of manpower and cost. This effort arises from the large number of compounds that …

Synthesis of novel derivatives of oxindole, their urease inhibition and molecular docking studies

M Taha, NH Ismail, A Khan, SAA Shah, A Anwar… - Bioorganic & Medicinal …, 2015 - Elsevier
We synthesized a series of novel 5–24 derivatives of oxindole. The synthesis started from 5-
chlorooxindole, which was condensed with methyl 4-carboxybezoate and result in the …

New thioxothiazolidinyl-acetamides derivatives as potent urease inhibitors: Design, synthesis, in vitro inhibition, and molecular dynamic simulation

N Dastyafteh, M Noori, M Nazari Montazer… - Scientific Reports, 2023 - nature.com
To identify potent urease inhibitors, in the current study, a series of thioxothiazolidinyl-
acetamides were designed and synthesized. The prepared compounds were characterized …

Design, synthesis, and evaluation of novel organophosphorus inhibitors of bacterial ureases

S Vassiliou, A Grabowiecka… - Journal of Medicinal …, 2008 - ACS Publications
A new group of organophosphorus inhibitors of urease, P-methyl phosphinic acids was
discovered by using the structure based inhibitor design approach. Several derivatives of …

A patent update on therapeutic applications of urease inhibitors (2012–2018)

A Hameed, M Al-Rashida, M Uroos… - Expert opinion on …, 2019 - Taylor & Francis
Introduction: Urease is a nickel-containing metalloenzyme that is commonly found in
different bacteria, plants, algae, and fungi and mediates the growth of many pathogenic …

QSAR studies on hydroxamic acids: a fascinating family of chemicals with a wide spectrum of activities

SP Gupta - Chemical reviews, 2015 - ACS Publications
Hydroxamic acids constitute a unique family of chemicals with multiple biological activities,
because they act as potent and selective inhibitors of a large number of enzymes, such as …

Evaluation of allicin as soil urease inhibitor

R Mathialagan, N Mansor, B Al-Khateeb… - Procedia …, 2017 - Elsevier
Urea is the most widely used form of N fertilizer in agriculture. However, if it is not
incorporated into soil soon after application, urea has the disadvantage of undergoing …

In Silico study of the active site of Helicobacter pylori urease and its inhibition by hydroxamic acids

R Arora, U Issar, R Kakkar - Journal of Molecular Graphics and Modelling, 2018 - Elsevier
Hydroxamic acids have emerged as the most promising candidates from among the different
classes of inhibitors of urease. In order to understand the mechanism of their action, we …

[PDF][PDF] A review on hydroxamic acids: Widespectrum chemotherapeutic agents

Z Syed, K Sonu, A Dongre, G Sharma… - Int. J. Biol. Biomed, 2020 - researchgate.net
Recent developments in drug discovery have highlighted the ability of hydroxamic acids to
form complexes with various metal ions, in particular iron, zinc, magnesium and calcium …