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Bioactive pyrrole-based compounds with target selectivity
GL Petri, V Spano, R Spatola, R Holl… - European journal of …, 2020 - Elsevier
The discovery of novel synthetic compounds with drug-like properties is an ongoing
challenge in medicinal chemistry. Natural products have inspired the synthesis of …
challenge in medicinal chemistry. Natural products have inspired the synthesis of …
Pyrrole: A Decisive Scaffold for the Development of Therapeutic Agents and Structure‐Activity Relationship
An overview of pyrroles as distinct scaffolds with therapeutic potential and the significance of
pyrrole derivatives for drug development are provided in this article. It lists instances of …
pyrrole derivatives for drug development are provided in this article. It lists instances of …
Recent advances in nitrogen-containing heterocyclic compounds as receptor tyrosine kinase inhibitors for the treatment of cancer: Biological activity and structural …
Erratic cell proliferation is the initial symptom of cancer, which can eventually metastasize to
other organs. Before cancer becomes metastatic, its spread is triggered by pro-angiogenic …
other organs. Before cancer becomes metastatic, its spread is triggered by pro-angiogenic …
Pyrrolo [2, 3-d] pyrimidines as potential kinase inhibitors in cancer drug discovery: A critical review
MS Madhurya, V Thakur, S Dastari, N Shankaraiah - Bioorganic Chemistry, 2024 - Elsevier
Abstract Pyrrolo [2, 3-d] pyrimidine-based kinase inhibitors have emerged as an important
class of targeted therapeutics to combat various types of cancer. The distinctive structural …
class of targeted therapeutics to combat various types of cancer. The distinctive structural …
[HTML][HTML] Selective type II TRK inhibitors overcome xDFG mutation mediated acquired resistance to the second-generation inhibitors selitrectinib and repotrectinib
S **ang, X Lu - Acta Pharmaceutica Sinica B, 2024 - Elsevier
Neurotrophic receptor kinase (NTRK) fusions are actionable oncogenic drivers of multiple
pediatric and adult solid tumors, and tropomyosin receptor kinase (TRK) has been …
pediatric and adult solid tumors, and tropomyosin receptor kinase (TRK) has been …
Anticancer activity of Mannich bases: a review of recent literature
G Roman - ChemMedChem, 2022 - Wiley Online Library
This report summarizes the latest published data on the antiproliferative action and cytotoxic
activity of Mannich bases, a structurally heterogeneous category of chemical entities that …
activity of Mannich bases, a structurally heterogeneous category of chemical entities that …
Identification of ureidocoumarin-based selective discoidin domain receptor 1 (DDR1) inhibitors via drug repurposing approach, biological evaluation, and in silico …
Discoidin domain receptor 1 (DDR1) kinase has emerged as a promising target for cancer
therapy, and selective DDR1 inhibitors have shown promise as effective therapeutic …
therapy, and selective DDR1 inhibitors have shown promise as effective therapeutic …
Synthesis strategies and medicinal value of pyrrole and its fused heterocyclic compounds
SS Fatahala, MS Mohamed, JY Sabry… - Medicinal …, 2022 - benthamdirect.com
In the last several decades, interest in pyrrole and pyrrolopyrimidine derivatives has
increased owing to their biological importance, such as anti-tumor, anti-microbial, anti …
increased owing to their biological importance, such as anti-tumor, anti-microbial, anti …
Synthesis and Biological Evaluation of 12-Aryl-11-hydroxy-5,6-dihydropyrrolo[2″,1″:3′,4′]pyrazino[1′,2′:1,5]pyrrolo[2,3-d]pyridazine-8(9H)-one Derivatives …
In the present paper, a facile and efficient synthetic procedure has been applied to obtain
dihydrodipyrrolo [1, 2-a: 2′, 1′-c] pyrazine-2, 3-dicarboxylates (5a–s), which have …
dihydrodipyrrolo [1, 2-a: 2′, 1′-c] pyrazine-2, 3-dicarboxylates (5a–s), which have …
Design and synthesis of new 4-(3, 4, 5-trimethoxyphenyl) thiazole–pyrimidine derivatives as potential antiproliferative agents
A new series of 3, 4, 5-trimethoxyphenyl thiazole pyrimidines has been synthesized and
biologically evaluated for its in vitro anticancer activity. Compounds 4a, 4b, and 4h with …
biologically evaluated for its in vitro anticancer activity. Compounds 4a, 4b, and 4h with …