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301“…As for treatment, pentamidine and suramin have historically been the drugs of choice for the treatment of blood-stage gambiense-HAT and rhodesiense-HAT, respectively. …”
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302por Lin, Hui-Chung, Chiao, Der-Jiang, Shu, Pei-Yun, Lin, Hui-Tsu, Hsiung, Chia-Chu, Lin, Chang-Chi, Kuo, Szu-Cheng“…Treatment with antivirals (suramin or 6-azauridine) or neutralizing antibodies (monoclonal antibodies [MAbs] or patient sera) was shown to inhibit mos-CHIK VRP infection in a dose-dependent manner. …”
Publicado 2023
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303por Tuly, Khanis Farhana, Hossen, Md. Bayazid, Islam, Md. Ariful, Kibria, Md. Kaderi, Alam, Md. Shahin, Harun-Or-Roshid, Md., Begum, Anjuman Ara, Hasan, Sohel, Mahumud, Rashidul Alam, Mollah, Md. Nurul Haque“…Finally, we suggested the top-ranked six drug molecules (Suramin, Rifaximin, Telmisartan, Tukysa Tucatinib, Lynparza Olaparib, and TG.02) for the treatment of BC by molecular docking analysis with the proposed HubGs-mediated receptors. …”
Publicado 2023
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304por Winquist, Eric, Waldron, Tricia, Berry, Scott, Ernst, D Scott, Hotte, Sébastien, Lukka, Himu“…Single trials reported improved disease control with estramustine-vinblastine, vinorelbine-hydrocortisone, and suramin-hydrocortisone compared to controls. Trials of non-cytotoxic agents have reported equivocal results. …”
Publicado 2006
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305por Vázquez-Cuevas, Francisco G, Zárate-Díaz, Erika P, Garay, Edith, Arellano, Rogelio O“…It was found that UTP increased MAPK phosphorylation by up to 550% with an EC50 of 3.34 +/- 0.92 and 1.41 +/- 0.67 μM, for p44 and p42, respectively; these increases were blocked by suramin. UDP also induced p44/p42 phosphorylation, but at high concentrations. …”
Publicado 2010
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306“…Conversely, whereas the P2X receptor antagonist PPADS and the P2Y antagonist reactive blue-2 partially inhibited increases in the translocation of nNOS and [Ca(2+)]i by ATP, the non-selective P2 receptor antagonist suramin completely blocked them. In addition, the increase in the nNOS translocation by ATP was blocked by NMDA receptor antagonists and inhibitors of protein kinase A, protein kinase C, and Src kinase. …”
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307por Vasconcellos, Raphael De Souza, Mariotini-Moura, Christiane, Gomes, Rodrigo Saar, Serafim, Tiago Donatelli, Firmino, Rafaela de Cássia, Silva e Bastos, Matheus, de Castro, Felipe Freitas, de Oliveira, Claudia Miranda, Borges-Pereira, Lucas, de Souza, Anna Cláudia Alves, de Souza, Ronny Francisco, Gómez, Gabriel Andres Tafur, Pinheiro, Aimara da Costa, Maciel, Talles Eduardo Ferreira, Silva-Júnior, Abelardo, Bressan, Gustavo Costa, Almeida, Márcia Rogéria, Baqui, Munira Muhammad Abdel, Afonso, Luís Carlos Crocco, Fietto, Juliana Lopes Rangel“…In addition, rLicNTPDase-2 showed stable activity over a pH range of 6.0 to 9.0 and was partially inhibited by ARL67156 and suramin. Microscopic analyses revealed the presence of this protein on cell surfaces, vesicles, flagellae, flagellar pockets, kinetoplasts, mitochondria and nuclei. …”
Publicado 2014
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308por Barnawi, Jameel, Tran, Hai, Jersmann, Hubertus, Pitson, Stuart, Roscioli, Eugene, Hodge, Greg, Meech, Robyn, Haberberger, Rainer, Hodge, Sandra“…To elucidate functional effects of increased S1PR5 on macrophage phagocytic ability, we performed the phagocytosis assay in the presence of varying concentrations of suramin, an antagonist of S1PR3 and S1PR5. The effects of cigarette smoking on the S1P system were investigated using a THP-1 macrophage cell line model. …”
Publicado 2015
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309por Huipao, Nawiya, Borwornpinyo, Suparerk, Wiboon-ut, Suwimon, Campbell, Craig R., Lee, Il-Ha, Hiranyachattada, Siriphun, Sukasem, Chonlaphat, Thitithanyanont, Arunee, Pholpramool, Chumpol, Cook, David I., Dinudom, Anuwat“…This effect of the inactivated-H5N1 was inhibited by sialic acid receptor inhibitor (α-2,3 sialidase), adenosine diphosphatase (apyrase), P2Y receptor (P2YR) inhibitor (suramin), P2Y(6)R antagonist (MRS2578), phospholipase C inhibitor (U73122), protein kinase C inhibitors (BIM and Gö6976) and cell-permeant Ca(2+) chelator (BAPTA-AM). …”
Publicado 2017
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310por Salem, Mabrouka, Tremblay, Alain, Pelletier, Julie, Robaye, Bernard, Sévigny, Jean“…CXCL10 expression and secretion induced by poly(I:C) in both P2ry6(-/-) and WT IEC were inhibited by general P2 antagonists (suramin and Reactive-Blue-2), by apyrase, and by specific antagonists of P2Y(1), P2Y(2), P2Y(6) (only in WT), and P2X4. …”
Publicado 2018
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311por Harcha, Paloma A., López, Ximena, Sáez, Pablo J., Fernández, Paola, Barría, Iván, Martínez, Agustín D., Sáez, Juan C.“…Interestingly, the increase in membrane permeability of WT MCs was also prevented by suramin, a P2 purinergic inhibitor, suggesting that Panx1 Chs act as ATP-releasing channels impermeable to Ca(2+). …”
Publicado 2019
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312“…We also found that pre-treatment with the purinergic P2R antagonist suramin inhibits HRV-enhanced MUC5AC expression and protein release, implicating involvement of purinergic signaling by extracellular ATP. …”
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313por Tian, Jianbo, Lu, Zequn, Niu, Siyuan, Zhang, Shanshan, Ying, Pingting, Wang, Lu, Zhang, Ming, Cai, Yimin, Dong, Tianyi, Zhu, Ying, Zhong, Rong, Wang, Zhihua, Chang, Jiang, Miao, Xiaoping“…Finally, MCM10 inhibitors Suramin and its analogues were revealed to effectively block the metastasis of ESCC cells. …”
Publicado 2021
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314por Yamaguchi, Akihiro, Teratani, Toshiaki, Chu, Po‐sung, Suzuki, Takahiro, Taniki, Nobuhito, Mikami, Yohei, Shiba, Shunsuke, Morikawa, Rei, Amiya, Takeru, Aoki, Ryo, Kanai, Takanori, Nakamoto, Nobuhiro“…Preconditioning with an inulin‐supplemented diet for 2 weeks significantly reduced hepatic adenosine triphosphate (ATP) content; suramin, a purinergic P2 receptor antagonist, abolished the protective effect. …”
Publicado 2021
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315“…The inhibition of these toxins by natural (2S albumin and flocculating proteins from Moringa oleifera seeds) and synthetic inhibitors (suramin) was also carried out in this study. The results from docking indicate that the inhibitors bind near the C-terminal domain which may restrict the movement of this domain and may halt the access of the substrate to the active site of this enzyme. …”
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316por Marriott, Amy E., Furlong Silva, Julio, Pionnier, Nicolas, Sjoberg, Hanna, Archer, John, Steven, Andrew, Kempf, Dale, Taylor, Mark J., Turner, Joseph D.“…A selected culture system was validated as a drug screen using reference anti-Wolbachia (doxycycline, ABBV-4083 / flubentylosin) or direct-acting compounds (flubendazole, suramin). BALB/c IL-4Rα(-/-)IL-5(-/-) or CB.17 SCID mice were superior to Mongolian gerbils in generating adult worms and supporting in vivo persistence for periods of up to 52 weeks. …”
Publicado 2022
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317por Gruenbacher, Georg, Gander, Hubert, Dobler, Gabriele, Rahm, Andrea, Klaver, Dominik, Thurnher, Martin“…Findings were validated in human monocyte‐derived M2 macrophages. The suramin analogue NF340 and P2Y(11) receptor‐knockout cells confirmed that agonist‐mediated responses were specific to P2Y(11) receptor stimulation. …”
Publicado 2021
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318por Angelico, Patrizia, Velasco, Cristina, Guarneri, Luciano, Sironi, Giorgio, Leonardi, Amedeo, Testa, Rodolfo“…Also, experiments were performed in rats in which bladders were infused with suramin (3 and 10 μM) in order to block the non-adrenergic, non-cholinergic component of bladder contraction. …”
Publicado 2005
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319“…HdP2X is antagonised by pyridoxal-phosphate-6-azophenyl-2',4' disulfonic acid (IC(50 )15.0 μM) and suramin (IC(50 )22.6 μM) and zinc and copper inhibit ATP-evoked currents with IC(50 )values of 62.8 μM and 19.9 μM respectively. …”
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320por Wang, De-Ping, Wang, Mei-Yue, Li, Yong-Mei, Shu, Wen, Cui, Wen, Jiang, Fang-Ying, Zhou, Xin, Wang, Wen-Ming, Cao, Ji-Min“…Moreover, we docked two small molecule inhibitors of DENV helicase (ST-610 and suramin) to the ILHV helicase and found that these two molecules had the potential to inhibit the activity of ILHV helicase as well. …”
Publicado 2022
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