[HTML][HTML] Synthesis of Novel Suramin Analogs With Anti-Proliferative Activity via FGF1 and FGFRD2 Blockade

N Parveen, YL Lin, RH Chou, CM Sun, C Yu - Frontiers in Chemistry, 2022 - frontiersin.org
A promising approach in cancer therapy is the inhibition of cell proliferation using small
molecules. In this study, we report the synthesis of suramin derivatives and their …

[HTML][HTML] Suramin derivatives play an important role in blocking the interaction between FGF1 and FGFRD2 to inhibit cell proliferation

N Parveen, YL Lin, MI Khan, RH Chou, CM Sun… - European Journal of …, 2020 - Elsevier
The inhibition of protein function by small compounds plays a critical role in controlling cell
proliferation. We report on a new class of small molecule (NCTU-Alan-2026) inhibitors for …

Synthesis and binding mode of heterocyclic analogues of suramin inhibiting the human basic fibroblast growth factor

F Manetti, V Cappello, M Botta, F Corelli… - Bioorganic & medicinal …, 1998 - Elsevier
The design, synthesis, and biological evaluation of a series of pyrrole and pyrazole
congeners 2 of suramin, directed toward the development and identification of new ligands …

[PDF][PDF] Pharmaceutical and Biological Effects of Suramin and Potential of Its Derivatives and Analogues

SC Tsay, JR Hwu - Org. Med. Chem. Int. J, 2017 - researchgate.net
As a popular drug, suramin has attracted much attention for a century. It has an extensive
record of clinical trials. This review article gives a brief introduction of its wide biological …

New heterocyclic analogs of suramin with bFGF inhibiting activity. Synthesis, sar and possible mode of action

G Biasoli, M Botta, M Ciomei, F Corelli… - Medicinal Chemistry …, 1994 - usiena-air.unisi.it
Some heterocyclic analogs of suramin with potent and selective basic fibroblast growth
factor (bFGF) complexing activity have been synthesized. The possible mode of action of …

Suramin blocks interaction between human FGF1 and FGFR2 D2 domain and reduces downstream signaling activity

ZS Wu, CF Liu, B Fu, RH Chou, C Yu - Biochemical and biophysical …, 2016 - Elsevier
The extracellular portion of the human fibroblast growth factor receptor2 D2 domain (FGFR2
D2) interacts with human fibroblast growth factor 1 (hFGF1) to activate a downstream …

Antitumour activity of suramin analogues in human tumour cell lines and primary cultures of tumour cells from patients

S Dhar, J Gullbo, K Csoka, E Eriksson, K Nilsson… - European Journal of …, 2000 - Elsevier
Suramin has shown promising antitumour activity against several tumour types, both in vitro
and in vivo, but the clinical utility of this compound is hampered by its unfavourable toxicity …

[HTML][HTML] Suramin inhibits the growth of nasopharyngeal carcinoma cells via the downregulation of osteopontin

S Jiang, X Chen, C Li, X Zhang… - Molecular …, 2012 - spandidos-publications.com
Radiotherapy is the principal therapy for nasopharyngeal carcinoma (NPC) at early stages.
A number of chemotherapeutic methods have been used to inhibit the progression of NPC at …

[引用][C] Suramin awakes?

HM Pinedo, RE van Rijswijk - Journal of clinical oncology, 1992 - ascopubs.org
ADVANCES IN molecular biology and the concept of autocrine-stimulated tumor growth
have provided many novel targets for cancer therapy. Suramin may be regarded as the …

[引用][C] Suramin

MA Eisenberger, LM Reyno - Cancer treatment reviews, 1994 - Elsevier
Suramin is a polysulfonated naphthylurea with demonstrable activity against cancer of the
prostate. While its precise mechanism of antitumor activity is uncertain, it is likely to be …