Results 1 to 10 of about 4,105 (201)

Terfenadine, a histamine H1 receptor antagonist, induces apoptosis by suppressing STAT3 signaling in human colorectal cancer HCT116 cells [PDF]

open access: yesFrontiers in Pharmacology
IntroductionColorectal cancer is a highly aggressive and metastatic cancer with inadequate clinical outcomes. Given the crucial role of histamine and histamine receptors in colorectal carcinogenesis, this study aimed at exploring the anticancer effects ...
Manoj Kumar Baniya   +2 more
doaj   +4 more sources

Inhibitory effect of terfenadine on Kir2.1 and Kir2.3 channels [PDF]

open access: yesActa Pharmaceutica, 2021
Terfenadine is a second-generation H1-antihistamine that despite potentially can produce severe side effects it has recently gained attention due to its anticancer properties. Lately, the subfamily 2 of inward rectifier potassium channels (Kir2) has been
Delgado-Ramírez Mayra   +5 more
doaj   +3 more sources

Antihistamine drug terfenadine suppressed the cycle progression of gastric cancer cells by targeting PI3K/AKT/mTOR signaling [PDF]

open access: yesFrontiers in Pharmacology
BackgroundGastric cancer (GC) remains a leading cause of cancer-related mortality worldwide, highlighting the urgent need for effective and accessible therapies. Drug repurposing offers a cost-effective strategy to identify novel candidates from approved
Yanping Zhu   +11 more
doaj   +2 more sources

Repurposing terfenadine and domperidone for inhibition of apoptotic gene association in colorectal cancer: A system pharmacology approach integrated with molecular docking, MD simulations, and post-MD simulation analysis [PDF]

open access: yesBioinformatics and Biology Insights
Colorectal cancer (CRC) remains a leading cause of global cancer mortality, underscoring the need for novel therapeutic strategies. This study used a systems pharmacology approach integrated with molecular docking and molecular dynamics (MD) simulations ...
Pushpaveni C   +7 more
doaj   +2 more sources

Repurposing Terfenadine as a Novel Antigiardial Compound

open access: yesPharmaceuticals, 2023
Giardia lamblia is a highly infectious protozoan that causes giardiasis, a gastrointestinal disease with short-term and long-lasting symptoms. The currently available drugs for giardiasis treatment have limitations such as side effects and drug ...
Daniel Osmar Suárez-Rico   +6 more
doaj   +2 more sources

In vivo visualization of cardiac extracellular adenosine dynamics and its pharmacological modulation in zebrafish heart failure models [PDF]

open access: yesScientific Reports
Heart failure (HF) remains a major clinical challenge with poor prognosis despite extensive research and established treatments. Extracellular ATP and adenosine (Ado), as damage-associated molecular patterns (DAMPs), contribute to HF pathogenesis through
Phurpa Phurpa   +12 more
doaj   +2 more sources

Proteomic and functional profiling of suspended jejunal enteroids reveals pharmacokinetic fidelity to native intestine [PDF]

open access: yesiScience
Summary: Intestinal enteroids are “mini-guts” that recapitulate essential features of the intestinal epithelium in vitro . We developed and characterized native basal-out (BO) and morphogenically everted apical-out (AO) jejunal enteroids cultured in ...
Foteini Tzioufa   +17 more
doaj   +2 more sources

In silico exploration of anti-prostate cancer compounds from differential expressed genes [PDF]

open access: yesBMC Urology
Prostate cancer (PCa) is a complex and biologically diverse disease with no curative treatment options at present. This study aims to utilize computational methods to explore potential anti-PCa compounds based on differentially expressed genes (DEGs ...
Basiru Olaitan Ajiboye   +7 more
doaj   +2 more sources

Fimasartan, an angiotensin II receptor antagonist, ameliorates an in vivo zebrafish model of heart failure [PDF]

open access: yesThe Korean Journal of Internal Medicine, 2020
Background/Aims Angiotensin II in the failing heart initially helps to maintain cardiac output and blood pressure, but ultimately accelerates its deterioration.
Hailian Quan   +3 more
doaj   +1 more source

Terfenadine resensitizes doxorubicin activity in drug-resistant ovarian cancer cells via an inhibition of CaMKII/CREB1 mediated ABCB1 expression

open access: yesFrontiers in Oncology, 2022
Ovarian cancer is one of the most lethal gynecological malignancies. Recurrence or acquired chemoresistance is the leading cause of ovarian cancer therapy failure.
Wei Huang   +10 more
doaj   +1 more source

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