[HTML][HTML] The use of spirocyclic scaffolds in drug discovery

Y Zheng, CM Tice, SB Singh - Bioorganic & Medicinal Chemistry Letters, 2014 - Elsevier
Owing to their inherent three-dimensionality and structural novelty, spiro scaffolds have
been increasingly utilized in drug discovery. In this brief review, we highlight selected …

Spirooxindoles: Promising scaffolds for anticancer agents

B Yu, DQ Yu, HM Liu - European journal of medicinal chemistry, 2015 - Elsevier
The search for novel anticancer agents with more selectivity and lower toxicity continues to
be an area of intensive investigation. The unique structural features of spirooxindoles …

Pyrazoline hybrids as promising anticancer agents: An up-to-date overview

D Matiadis, M Sagnou - International Journal of Molecular Sciences, 2020 - mdpi.com
Pyrazolines are five-membered heterocycles possessing two adjacent nitrogens. They have
attracted significant attention from organic and medicinal chemists due to their potent …

Oxindole: A chemical prism carrying plethora of therapeutic benefits

M Kaur, M Singh, N Chadha, O Silakari - European Journal of Medicinal …, 2016 - Elsevier
Oxindole has emerged as a valuable scaffold in medicinal chemistry possessing diverse
range of pharmacological activities. Its value has further been increased by its natural …

Recent advances in the synthesis of biologically active spirooxindoles

MMM Santos - Tetrahedron, 2014 - Elsevier
The spirooxindole system is the core structure of a variety of medicinal agents and natural
products. 1, 2 In fact, spirooxindole derivatives have been described with different biological …

[HTML][HTML] Synthesis of ruthenium complexes and their catalytic applications: A review

J Hafeez, M Bilal, N Rasool, U Hafeez… - Arabian Journal of …, 2022 - Elsevier
Ruthenium complexes are an important class that has multiple catalytic and biological
applications. Ruthenium has a remarkably broad and diversified chemical spectrum. In the …

Metalloporphyrin catalyzed C–H amination

R Singh, A Mukherjee - ACS Catalysis, 2019 - ACS Publications
Direct C–H bond functionalization to form C–N bonds via nitrenoid insertion is one of the
most effective strategies to construct N-functionalized molecules of importance. In this …

Discovery of Novel Spiro[3H-indole-3,2′-pyrrolidin]-2(1H)-one Compounds as Chemically Stable and Orally Active Inhibitors of the MDM2–p53 Interaction

A Gollner, D Rudolph, H Arnhof, M Bauer… - Journal of medicinal …, 2016 - ACS Publications
Scaffold modification based on Wang's pioneering MDM2–p53 inhibitors led to novel,
chemically stable spiro-oxindole compounds bearing a spiro [3 H-indole-3, 2′-pyrrolidin]-2 …

Spiro-oxindoles as a promising class of small molecule inhibitors of p53–MDM2 interaction useful in targeted cancer therapy

AK Gupta, M Bharadwaj, A Kumar… - Topics in Current …, 2017 - Springer
As a result of the toxicity of currently available anticancer drugs and the inefficiency of
chemotherapeutic treatments, the design and discovery of effective and selective antitumor …

Recent in vivo advances of spirocyclic scaffolds for drug discovery

VF Batista, DCGA Pinto, AMS Silva - Expert Opinion on Drug …, 2022 - Taylor & Francis
Introduction Spirocyclic scaffolds are an exceptional tool in drug design, allowing fine-tuning
of a molecule's conformational and physicochemical properties. As it expands and …