Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Pornvichai Temboot"'
Publikováno v:
Heliyon, Vol 7, Iss 8, Pp e07749- (2021)
RAPTA-EA1 is a promising glutathione transferase (GSTP-1) inhibitor that has previously been shown to inhibit the growth of various breast cancer cells. We studied the anticancer activity of RAPTA-EA1 on triple-negative BRCA1 competent breast cancer
Externí odkaz:
https://doaj.org/article/7c68895adc8f43e2aa613f158827392b
Publikováno v:
Colloids and Surfaces A: Physicochemical and Engineering Aspects. 660:130816
Publikováno v:
Heliyon, Vol 7, Iss 8, Pp e07749-(2021)
Heliyon
Heliyon
RAPTA-EA1 is a promising glutathione transferase (GSTP-1) inhibitor that has previously been shown to inhibit the growth of various breast cancer cells. We studied the anticancer activity of RAPTA-EA1 on triple-negative BRCA1 competent breast cancer
Publikováno v:
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 205:442-456
In this work, we investigated the interaction of amphotericin B (AmB) nanomicelles on the binding affinity and conformational change of human serum albumin (HSA) in comparison with bovine serum albumin (BSA) under physiological conditions by conducti
Autor:
Pornvichai Temboot, Kittiya Tinpun, Teerapol Srichana, Roongnapa Suedee, Titpawan Nakpheng, Sreenu Madhumanchi
Publikováno v:
Colloids and surfaces. B, Biointerfaces. 182
This work presents the outcomes of a comparative study of molecular interactions of polymyxin B (PMB) and F12 and F13 formulations in the mole ratios of 1:2 and 1:3 of PMB:sodium deoxycholate sulfate (SDCS), respectively, and a commercial PMB formula
Autor:
Teerapol Srichana, Sunisa Kaewpaiboon, Surapee Tiengrim, Zaheer Ul-Haq, Titpawan Nakpeng, Ruqaiya Khalil, Visanu Thamlikitkul, Kittiya Tinpun, Pornvichai Temboot
Publikováno v:
Journal of Drug Delivery Science and Technology. 58:101779
Polymyxin B (PMB) is used as the last line therapy for multidrug-resistant Gram-negative bacterial infections; however, nephrotoxicity is still a concern. Here, PMB carried with sodium deoxycholate sulfate (SDCS) was developed, which aimed to improve
Autor:
Laure Menin, Pornvichai Temboot, Ronald F. S. Lee, Luc Patiny, Paul J. Dyson, Adisorn Ratanaphan
Publikováno v:
Biochemical and biophysical research communications. 488(2)
RAPTA compounds, ([Ru(eta(6)-arene)(PTA)Cl-2], PTA = 1,3,5-triaza-7-phosphaadamantane), have been reported to overcome drug resistance in cisplatin resistant cells. However, the exact mechanism of these complexes is still largely unexplored. In this
Publikováno v:
Transition Metal Chemistry. 37:207-214
A bidentate ligand, 5-chloro-2-(phenylazo)pyridine (Clazpy), and its two polypyridyl ruthenium(II) complexes, [Ru(Clazpy)2bpy]Cl2·7H2O (1) and [Ru(Clazpy)2phen]Cl2·8H2O (2), were synthesized and characterized. The DNA-binding properties of these co
Publikováno v:
BMC Cancer
Background Triple-negative breast cancer (TNBC) is defined by the absence of expression of estrogen receptor, progesterone receptor and human epidermal growth factor receptor 2. Breast cancers with a BRCA1 mutation are also frequently triple-negative
The interaction of two ruthenium-arene-1,3,5-triaza-7-phosphaadamantane compounds ([Ru(eta(6)-p-cymene)Cl(2)(pta)] and [Ru(eta(6)-p-cymene)(C(6)H(6)O(4))(pta)], termed RAPTA-C (3) and carboRAPTA-C (4), resp.) with the DNA sequence of the human breast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6c1dde49efc107739d1f57c9f467040
https://infoscience.epfl.ch/record/161657
https://infoscience.epfl.ch/record/161657