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Telmisartan

Telmisartan is an angiotensin II receptor antagonist used to treat high blood pressure and heart failure.
It works by blocking the effects of angiotensin II, a hormone that narrows blood vessels and raises blood pressure.
Telmisartan may also have anti-inflammatory and metabolic effects.
Researchers can use PubCompare.ai's AI-driven platform to optimize Telmisartan research by enhanceing reproducibility and accuracy.
The intuative tool helps locate protocols from literature, pre-prints, and patents, and uses AI-driven comparisons to identify the best protocols and produts.
Streamline your Telmisartar research with PubCompare.ai.

Most cited protocols related to «Telmisartan»

Male ApoE−/−/C57BL/6J mice or wild type C57BL/6J mice at 10–12 wk of age were obtained from the Jackson Laboratory, Bar Harbor, Maine, and housed at the Stanford Animal Facility, Stanford, CA. Animal care and experimental procedures were conducted in compliance with Stanford Laboratory Animal Care Guidelines. The Administrative Panel on Laboratory Animal Care at Stanford University approved all procedures involving mice.
Two mechanistically distinct, but complementary mouse AAA models were used in this study: subcutaneous Ang II infusion in ApoE−/− mice (Ang II/ApoE−/− model) and intra-aortic PPE infusion in C57BL/6J mice (PPE model). In most experiments, ApoE−/− mice were fed chow supplemented with irbesartan (50 mg/kg), telmisartan (10 mg/kg) or bosentan (100 mg/kg), or were daily given drinking water supplemented with fluvastatin (40 mg/kg) or doxycycline (100 mg/kg). As controls, separate groups of ApoE−/− mice for individual experiments were given the standard chow and drinking water without drug supplementation. One week later, to induce AAAs, all mice were subcutaneously implanted with osmotic minipumps (Alzet model 2004, Durect Corporation, Cupertino, CA) for continuous infusion of Ang II at 1000 ng/kg/min, and treated continuously with their respective drugs for 28 days [9] (link). In additional experiments, C57BL/6J mice were fed telmisartan-supplemented chow (10 mg/kg) or the standard chow. One week thereafter, AAAs were created by transient intra-aortic infusion of PPE as described previously [93] (link), and these mice were continuously fed with the chow with or without telmisartan supplementation for additional 2 wk. In all experiments, doses for two ARBs and bosentan were selected based on published mouse studies in which each drug lowered blood pressure and/or suppressed cardiovascular pathology [94] (link)–[96] (link).
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Publication 2012
Animals Animals, Laboratory Aorta ApoE protein, human Bosentan Cardiovascular System Doxycycline Fluvastatin Irbesartan Males Mice, House Mice, Inbred C57BL Osmosis Pharmaceutical Preparations Subcutaneous Infusions Telmisartan Transients Triple-A Syndrome
The Prevention Regimen for Effectively Avoiding Second Strokes (PRoFESS) trial was a 2-by-2 factorial, double-blind, active and placebo-controlled study of the fixed combination of low-dose aspirin (25 mg) and extended-release dipyridamole (200 mg) given twice daily as compared with clopid ogrel (75 mg) given once daily, and of telmisartan (80 mg once daily) as compared with placebo, in patients with a recent ischemic stroke. This article focuses on the antiplatelet comparison within the factorial design. The antiplatelet part of the factorial design was initially intended to compare clopidogrel plus aspirin with aspirin plus extended-release dipyridamole. The design was modified, after 2027 patients were randomly assigned, when the Management of Atherothrombosis with Clopidogrel in High-Risk Patients with Recent TIA or Ischemic Stroke (MATCH) trial demonstrated an increased risk of bleeding with the combination of clopidogrel and aspirin.8 (link) Patients initially assigned to receive clopidogrel plus aspirin had been treated for up to 8 months before they were switched to clopidogrel alone at the time of the protocol amendment; 18,305 patients were subsequently randomly assigned to receive aspirin plus extended-release dipyridamole or clopidogrel alone.
Details of the trial design have been published previously.18 (link) The steering committee designed and oversaw the trial; data management was performed by the sponsor (Boehringer Ingelheim). A trial management committee, with representatives from the steering committee and the sponsor, met regularly to evaluate progress. The cochairs and the members of the steering committee had complete access to the trial data and prepared the final manuscript, and they vouch for the design, the final statistical analysis, and the completeness, accuracy, and interpretation of the data. The final statistical analyses were conducted simultaneously by the independent statisticians at the Medical University of South Carolina (who provided data and interim analysis reports to the data and safety monitoring committee) and the statisticians from Boehringer Ingelheim.
The protocol was approved by the appropriate regulatory authorities and ethics committees or institutional review boards. All patients provided written informed consent.
Publication 2008
Aspirin Aspirin, Dipyridamole Drug Combination Cerebrovascular Accident Clopidogrel Committee Members Dipyridamole Ethics Committees Ethics Committees, Research Extended-Release Dipyridamole-Aspirin Patients Placebos Safety Secondary Prevention Stroke, Ischemic Telmisartan Treatment Protocols
Detailed information about the trial design has been published previously.25 (link),26 (link) The study protocol is available with the full text of this article at NEJM.org. Eligible participants were enrolled at seven clinical sites from February 2006 through June 2009. All the participants provided written informed consent. Participants were randomly assigned in a 1:1 ratio to lisinopril plus telmisartan or lisinopril plus placebo. Randomization was performed centrally with the use of permuted blocks. In addition, participants were randomly assigned in a 1:1 ratio to a standard blood-pressure target (120/70 to 130/80 mm Hg) or a low blood-pressure target (95/60 to 110/75 mm Hg), with stratification according to age, sex, race, baseline estimated GFR, and clinical site. The last study visit was in June 2014.
Participants underwent standardized imaging27 (link) in a 1.5-T MRI scanner to determine total kidney volume, left-ventricular-mass index, and renal blood flow at baseline and at 24, 48, and 60 months. Renal vascular resistance was calculated on the basis of blood flow and mean arterial pressure.28 Image analysis was performed,27 (link) and strict quality-control measures were maintained throughout the study.
After randomization, treatment with lisinopril and the masked study medication (telmisartan or placebo) was initiated, and the doses were adjusted in a stepwise fashion to achieve the desired blood-pressure targets (with the use of home blood-pressure measures) while the plasma levels of creatinine and potassium were monitored. Second-, third-, and fourth-line antihypertensive agents were added as needed (Table S1 in the Supplementary Appendix, available at NEJM .org). Central measurements of the serum creati-nine level and local measurements of blood urea nitrogen and electrolytes were obtained at all clinical-site visits, and 24-hour urine collections were obtained for central measurements of albumin, sodium, potassium, creatinine, and aldosterone excretion annually. Adherence to therapy was calculated as the number of drug cards (32 pills per card) given to patients minus the number returned unused during the study period, divided by the number of months of study participation.
Publication 2014
Albumins Aldosterone Antihypertensive Agents Blood Circulation Blood Pressure Contraceptives, Oral Creatinine Electrolytes Kidney Left Ventricles Lisinopril Patients Pharmaceutical Preparations Placebos Plasma Potassium Renal Circulation Serum Sodium Telmisartan Therapeutics Urea Nitrogen, Blood Urine Specimen Collection Vascular Resistance
This randomized, double-blind, placebo-controlled clinical trial was designed to assess the efficacy of a combination of an ACE inhibitor (lisinopril) and an ARB (telmisartan), as compared with lisinopril and placebo, in reducing disease progression in patients with moderately advanced ADPKD. A steering committee of investigators designed the trial. An external advisory committee selected by the National Institute of Diabetes and Digestive and Kidney Diseases and the National Institutes of Health reviewed the protocol and served as the data and safety monitoring board. The institutional review board at each site approved the study protocol, which is available with the full text of this article at NEJM.org and has been published previously.16 (link),17 (link)Data collected by site investigative teams were managed by the data coordinating center and analyzed by study statisticians. The first author wrote the first draft of the manuscript, with substantial contributions from the coauthors, and all the authors jointly decided to submit the manuscript for publication. All the authors vouch for the accuracy and completeness of the data and analyses and for the fidelity of this report to the protocol. The study drugs were donated by Boehringer Ingelheim Pharmaceuticals (telmisartan and matched placebo) and Merck (lisinopril). Neither company had any role in the design of the study, accrual or analysis of data, the preparation of the manuscript, or the decision to submit the manuscript for publication.
Publication 2014
Angiotensin-Converting Enzyme Inhibitors Clinical Trials Data Monitoring Committees Diabetes Mellitus Digestive System Disease Progression Ethics Committees, Research Kidney Diseases Lisinopril Patients Pharmaceutical Preparations Placebos Polycystic Kidney, Autosomal Dominant Telmisartan
The trial was initially designed to enroll 15,500 patients, a sample size that was considered sufficient to accrue 2170 patients with recurrent stroke during a 4-year trial. On the basis of this assumption, the trial would have a power of more than 99% to detect a relative risk reduction of 25% in the telmisartan group, as compared with the placebo group, given the evidence at the time.6 (link),10 (link) However, despite a subsequent increase in sample size to more than 20,000 patients and a 6-month extension of the trial, only 1715 patients with recurrent stroke were projected. This revised event rate provided a power of 91% to detect a relative risk reduction of 15% in the telmisartan group, as compared with the placebo group.
The primary analysis was the time to recurrent stroke. A Cox proportional-hazards regression model with baseline age, diabetes status, ACE-inhibitor use, and modified Rankin Scale as covariates was the prespecified model intended to be used for the analysis of outcomes. However, the assumption of proportional hazards was not satisfied, and we therefore explored whether the treatment effect varied according to time (after an inspection of the Kaplan–Meier curves), with additional analyses describing the results separately within and beyond 6 months. All analyses of the outcomes were conducted under the intention-to-treat principle with the use of a time-to-event approach and included all randomized patients.
Subgroup analyses for the primary outcome and for major cardiovascular events were evaluated with the use of tests for interaction for prespecified baseline features. These included the use of ACE inhibitors, systolic blood pressure, history of diabetes mellitus, and a stroke risk score generated from the overall data of the trial, which included age, sex, physical activity level, baseline systolic blood pressure, history of hypertension, diabetes status, previous myocardial infarction, atrial fibrillation, peripheral arterial disease, and stroke before qualifying event (for details, see the Supplementary Appendix, available with the full text of this article at www.nejm.org).
Publication 2008
Angiotensin-Converting Enzyme Inhibitors Atrial Fibrillation Cardiovascular System Cerebrovascular Accident Diabetes Mellitus High Blood Pressures Myocardial Infarction Patients Peripheral Vascular Diseases Placebos Systolic Pressure Telmisartan

Most recents protocols related to «Telmisartan»


Nebivolol HCl (NEB, 99.4% purity), was kindly supplied by Sigma Company for Pharmaceutical Industries, Quesna, Egypt.

Telmisartan (TEL,99.91% purity) was gently given by International Drug Agency for Pharmaceutical Industry (IDI), Cairo, Egypt

Pharmaceutical Preparations

Nevilob Tablets (Batch No. 2033518) labeled to include 5 mg NEB per tablet, a product of Marcyrl Pharmaceutical Industries, Cairo, Egypt.

Micardis Tablets (Batch No. 906949) are labeled to include 40 mg TEL per tablet, a product of Boehringer Ingelheim Pharma, Germany.

Both preparations were purchased from a local Pharmacy in the Egyptian market.

Methanol, acetonitrile, ethanol, Phenol, hexane, Tween-80, 99% cetrimide, 95% sodium dodecyl sulphate, methylcellulose, and β-cyclodextrin were bought from Sigma-Aldrich, Germany. All surfactants were prepared in distilled water at a concentration of 1% w/v or v/v.

Also, 96%acetic acid, sodium acetate trihydrate, sodium hydroxide, and boric acid were bought from the same source.

Acetate buffer (0.2 M) was prepared using sodium acetate trihydrate and acetic acid and its pH was adjusted at 3.7 − 5.5, while borate buffer (0.2 M) was composed of boric acid and potassium chloride, and pH was adjusted to cover the range of (6–9) using sodium hydroxide.

Human plasma samples were obtained from Blood Bank, Mansoura University Hospital (Mansoura, Egypt), and kept frozen at − 20 °C until use after gentle thawing.

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Publication 2023
Acetate Acetic Acid acetonitrile Borates boric acid Buffers Cetrimide Cyclodextrins Ethanol Freezing Hexanes Homo sapiens Methanol Methylcellulose Micardis Nebivolol Pharmaceutical Preparations Phenol Plasma Potassium Chloride Sodium Acetate Trihydrate Sodium Hydroxide Sulfate, Sodium Dodecyl Surfactants Tablet Telmisartan Tween 80
The animals were divided into two groups. Group 1 (6 animals) received pure telmisartan (1 mg/kg) with 0.5% w/v sodium carboxymethylcellulose, and Group 2 (6 animals) received optimized cocrystals (equivalent to 1 mg/kg pure telmisartan) with 0.5% w/v sodium carboxymethylcellulose. Blood samples were collected at predetermined time intervals from the retro-orbital venous plexus of the rats and centrifuged for 5 min at 10,000 rpm. The plasma was separated and drug analysis was carried out by RP-HPLC method [47 ] using the software ‘Class-Vp series version 5.03 (Shimadzu)’. The in vivo pharmacokinetic parameters such as peak plasma concentration (Cmax), total area under the plasma concentration-time curve (AUC0–∞), elimination rate constant (KE), and relative bioavailability (%) were calculated by using Kinetica software (version 4.4.1; Thermo Fisher Scientific, Waltham, MA, USA).
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Publication 2023
Animals BLOOD High-Performance Liquid Chromatographies Pharmaceutical Preparations Plasma Rattus norvegicus Sodium Carboxymethylcellulose Telmisartan Veins
Telmisartan-maleic acid cocrystals were prepared using different stoichiometric amounts of telmisartan and maleic acid (Table 1). The molar ratios of the pure drug as well as the coformer were varied to observe the impact of drug:coformer ratio on crystallization. The specific molar ratio of telmisartan (514 mg, 1 mmoL) and maleic acid (116 mg, 1 mmoL) was mixed physically using an ointment slab. Then the drug-coformer powder blend was slowly added to a solvent mixture (i.e., distilled water: ethanol; 1:1) and stirred continuously, using a magnetic stirrer until the ethanol was evaporated out. Then it was transferred into a petri dish and kept at 50 °C for complete drying. Finally, the formed crystalline material was scrapped and stored in a desiccator for further use.
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Publication 2023
Crystallization Ethanol Hyperostosis, Diffuse Idiopathic Skeletal maleic acid Molar Ointments Pharmaceutical Preparations Powder Solvents Telmisartan
The docking of telmisartan (drug) and maleic acid (coformer) was performed in AutoDock Vina using standard Monte Carlo algorithms [45 (link)]. Dry-state docking was performed to avoid any interference of water molecules or other solvents during docking. Thus, in this stage of docking, a non-ionic form of maleic acid was undertaken, where the ionic state of the same was taken and docked in Avogadro and UCSF Chimera. Telmisartan was caged in a Grid Box of dimension 50 Å × 40 Å × 40 Å with the centers of the x, y, and z coordinates set at 6.847, −2.774, and −0.147.
Since maleic acid is a weak acid and may partially ionize in these solvents, the ionized form of the maleic acid was also taken in a separate docking, and subsequent bonding interactions were monitored in UCSF Chimera. For studying the interaction of the maleate anion, the anionic structure was further prepared in Chem Draw Ultra, the energy minimized in Avogadro and saved in .mol2 format, and subsequently docked on the maleic-telmisartan system. For tracking the cocrystal formation at the seeding stage, the telmisartan and maleic acid were taken at different molar ratios, where 50% of maleic acid was assumed to be ionized, since it is a weak acid.
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Publication 2023
Acids Anions Chimera Debility Ions maleate maleic acid Molar Pharmaceutical Preparations Solvents Telmisartan
An XRD study was performed to assess the physico-chemical state of telmisartan in prepared telmisartan-maleic acid cocrystals. The XRD study was performed by X-Ray Diffractometer (X’Pert Pro, Panalytical, Almelo, The Netherlands) using monochromatized Cu Kα radiation (λ = 1.54 Å) at a voltage of 45 kV and a current of 40 mA. Measurements were carried out in the angular scan range from 5° to 50° (2θ) at a scan speed of 1°/min. This study also helps to determine the size of the formed crystallite using Scherrer’s formula.
Crystallite size Dp=K λBcosθ,
where Dp is average crystallite size (nm), K is Scherrer constant, λ is X-ray wavelength, B is FWHM (Full Width at Half Maximum) of XRD peak, and θ is XRD peak position.
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Publication 2023
maleic acid Radiation Radiography Radionuclide Imaging Telmisartan

Top products related to «Telmisartan»

Sourced in United States, Germany
Telmisartan is a laboratory equipment product manufactured by Merck Group. It is a pharmaceutical ingredient used in the development and testing of various medical treatments. The core function of Telmisartan is to serve as a reference standard for analytical and quality control purposes.
Sourced in Germany, United States
Telmisartan is a pharmaceutical product manufactured by Boehringer Ingelheim. It is a laboratory equipment used for research and development purposes.
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DMSO is a versatile organic solvent commonly used in laboratory settings. It has a high boiling point, low viscosity, and the ability to dissolve a wide range of polar and non-polar compounds. DMSO's core function is as a solvent, allowing for the effective dissolution and handling of various chemical substances during research and experimentation.
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Ang II is a peptide hormone that is involved in the regulation of blood pressure and fluid balance in the body. It is a key component of the renin-angiotensin-aldosterone system (RAAS), which plays a central role in the homeostatic control of blood pressure, fluid, and electrolyte balance. Ang II acts on specific receptors to exert its physiological effects.
Sourced in United States, Germany, United Kingdom, China
Valsartan is a pharmaceutical ingredient used in the production of various medications. It functions as an angiotensin II receptor blocker, which helps regulate blood pressure. Valsartan is a white to practically white, crystalline powder with specific physicochemical properties.
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STZ is a laboratory equipment product manufactured by Merck Group. It is designed for use in scientific research and experiments. The core function of STZ is to serve as a tool for carrying out specific tasks or procedures in a laboratory setting. No further details or interpretation of its intended use are provided.
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Telmisartan is a white to yellowish-white crystalline powder used in the manufacture of pharmaceutical products. It is a lab equipment product designed for use in chemical research and analysis.
Sourced in United States
Telmisartan is a synthetic organic compound used as a reference standard in analytical testing. It is a white to off-white crystalline powder.
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Streptomycin is a broad-spectrum antibiotic used in laboratory settings. It functions as a protein synthesis inhibitor, targeting the 30S subunit of bacterial ribosomes, which plays a crucial role in the translation of genetic information into proteins. Streptomycin is commonly used in microbiological research and applications that require selective inhibition of bacterial growth.
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Fetal Bovine Serum (FBS) is a cell culture supplement derived from the blood of bovine fetuses. FBS provides a source of proteins, growth factors, and other components that support the growth and maintenance of various cell types in in vitro cell culture applications.

More about "Telmisartan"

Telmisartan, an angiotensin II receptor antagonist (AIIRA), is a powerful medication used to treat high blood pressure (hypertension) and heart failure.
It works by blocking the effects of angiotensin II, a hormone that narrows blood vessels and increases blood pressure.
Telmisartan may also possess anti-inflammatory and metabolic properties, making it a versatile therapeutic option.
Researchers can leverage PubCompare.ai's innovative AI-driven platform to optimize their Telmisartan research and enhance reproducibility and accuracy.
This intuitive tool helps locate relevant protocols from scientific literature, preprints, and patents, and utilizes AI-driven comparisons to identify the best protocols and products for your research needs.
When investigating Telmisartan, researchers may also encounter related terms and compounds, such as DMSO (dimethyl sulfoxide), a common solvent used in Telmisartan studies, Ang II (angiotensin II), the target of Telmisartan's mechanism of action, Valsartan, another AIIRA, STZ (streptozotocin), a compound used to induce diabetes in animal models, and FBS (fetal bovine serum), a commonly used cell culture supplement.
By streamlining your Telmisartan research with PubCompare.ai's AI-powered tools, you can ensure your experiments are well-designed, reproducible, and yield accurate results, advancing our understanding of this important cardiovascular and metabolic therapeutic agent.