Recent advancement in pyrrolidine moiety for the management of cancer: A review
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- Type
- review
- Published
- 2024-01-01
- Cited by
- 24
- References
- 122
- Access
- Open access
- OpenAlex
- https://openalex.org/W4390606968
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:266806198
Keywords
Pyrrolidine, Pharmacophore, Cancer, Medicine, Pharmacology
References
- BH3‐only proteins: The death‐puppeteer's wires
- Matrix metalloproteinases (MMPs), the main extracellular matrix (ECM) enzymes in collagen degradation, as a target for anticancer drugs
- Synthesis and anticancer activity of novel 4-morpholino-7,8-dihydro-5H-thiopyrano[4,3-d]pyrimidine derivatives bearing chromone moiety.
- Apoptosis in development
- Sphingosine Kinase 2 Inhibition and Blood Sphingosine 1-Phosphate Levels
- A potential therapeutic strategy for chronic lymphocytic leukemia by combining Idelalisib and GS-9973, a novel spleen tyrosine kinase (Syk) inhibitor
- A New Type of Pyrrolidine Biosynthesis Is Involved in the Late Steps of Xenocoumacin Production in Xenorhabdus nematophila
- Conformational Analysis of the DFG-out Kinase Motif and Biochemical Profiling of Structurally Validated Type II Inhibitors
- Drug development: Raise standards for preclinical cancer research
- Imaging matrix metalloproteinases in cancer
- Molecular Cloning and Functional Characterization of a Novel Mammalian Sphingosine Kinase Type 2 Isoform*
- Regulation of Histone Acetylation in the Nucleus by Sphingosine-1-Phosphate
- A brain serine/threonine protein kinase activated by Cdc42 and Rac1
- Sphingosine Kinase 2 Is a Nuclear Protein and Inhibits DNA Synthesis*
- Synthesis, cytotoxicity and structure-activity relationship study of terpyridines
- Requirement for PAK4 in the Anchorage-independent Growth of Human Cancer Cell Lines*
- PAK4–6 in cancer and neuronal development
- Strategies for overcoming ABC-transporters-mediated multidrug resistance (MDR) of tumor cells.
- Azetidine, pyrrolidine and hexamethyleneimine at 170 K.
- Crystal structure of Pyrococcus horikoshii tryptophanyl-tRNA synthetase and structure-based phylogenetic analysis suggest an archaeal origin of tryptophanyl-tRNA synthetase
Cited by
- Synthesis and computational insights of hybrid heterocyclic bis-chalcone compounds and their cytotoxic effects against breast cancer cells
- Unleashing the potential of cyclodextrin-based nanosponges in management of colon cancer: A review
- Navigating the future of cancer management through carbon nanodots: A review
- Formation of All-Carbon Quaternary Centers via Enantioselective Pd-Catalyzed α-Vinylation of γ-Lactams
- Progress in the Stereoselective Synthesis Methods of Pyrrolidine-Containing Drugs and Their Precursors
- Therapeutic approaches of nanostructure metallic materials in management of colorectal cancer: Recent advancement
- Demystifying the management of cancer through smart nano-biomedicine via regulation of reactive oxygen species.
- Acid ionization constant of potential bioactive functionalized N benzoylthiourea/ 2-thiohydantoin-pyrrolidine derivatives by potentiometric titration in acetonitrile-water
- Antibacterial Activity and Antifungal Activity of Monomeric Alkaloids
- A review on recent progress in synthesis and biological activities of spiropyrrolidine and its derivatives
- Evaluation of Pyrrolone‐Fused Benzosuberene MK2 Inhibitors as Promising Therapeutic Agents for HNSCC: In Vitro Efficacy, In‐Vivo Safety, and Pharmacokinetic Profiling
- BB-SAR: An Application for Data-driven Analysis and Rational Design of Medicinal Chemistry Series
- Brønsted Acid-Assisted Lewis Acid Mediated Intramolecular Trapping of Aminoenol with Activated Alkenes and Ketones.
- The aroma evolution in lotus (Nelumbo nucifera Gaertn.) seed juice: A comprehensive analysis of processing and low-temperature storage effects.
- Unveiling the research directions for pyrrolidine-based small molecules as versatile antidiabetic and anticancer agents.
- Overcoming Clusterin-Induced Chemoresistance in Cancer: A Computational Study Using a Fragment-Based Drug Discovery Approach
- Chiral 1,3,5‐Triazines as Potential EGFR Inhibitors: Pharmacophore Modeling, Synthesis, Molecular Docking, Molecular Dynamics Simulation, and Anticancer Evaluation
- Design, Synthesis, and Bioevaluation of Novel Spiro[indoline‐pyrrolidin]‐pyrazole Hybrids as Potential Bioactive Scaffolds
- Reactions of 2-aryl-1-(vinylsulfonyl)pyrrolidines with diamines
- Water-Soluble Piperazine Phosphates as Greener and more Sustainable Heterogeneous Organocatalysts for Preparing Pyrrolidinones
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