Salbutamol, also known as albuterol, is a bronchodilator medication commonly used to treat asthma and chronic obstructive pulmonary disease (COPD). It works by relaxing the muscles in the airways, making it easier to breathe. Salbutamol is available in various forms, including inhalers, nebulizers, tablets, and syrups.
14100 mg/L 0.06 M Soluble in ethanol, sparingly soluble in water, and very soluble in chlorform. Soluble in most organic solvents. In water, 1.43X10+4 mg/L, temp not specified 2.15e+00 g/L
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Albuterol hydrochloride is the HCl salt of Albuterol -- a β2-AR agonist. Albuterol hydrochloride is a short-acting, selective beta2-adrenergic receptor agonist used in the treatment of asthma and COPD. It is 29 times more selective for beta2 receptors than beta1 receptors giving it higher specificity for pulmonary beta receptors versus beta1-adrenergic receptors located in the heart.
Sulfamerazine sodium is a sulfonamide antibiotic that is commonly used in the treatment of bacterial infections. It is a white crystalline powder that is soluble in water and has a molecular weight of 264.28 g/mol. Sulfamerazine sodium is a derivative of sulfanilamide and is known for its broad-spectrum antibacterial activity.
Rosuvastatin (D3 Sodium) is a lipid-lowering drug that belongs to the class of statins. It is used to treat hypercholesterolemia and prevent cardiovascular diseases. Rosuvastatin works by inhibiting the enzyme HMG-CoA reductase, which is responsible for the production of cholesterol in the liver. This paper will discuss the method of synthesis or extraction, chemical structure and biological activity, biological effects, applications, future perspectives, and challenges of Rosuvastatin (D3 Sodium).
Verubecestat is a small molecule inhibitor that targets beta-secretase 1 (BACE1), an enzyme that plays a crucial role in the production of amyloid beta (Aβ) peptides. Aβ peptides are known to accumulate in the brains of Alzheimer's disease patients, leading to the formation of plaques and neurodegeneration. Verubecestat has been developed as a potential therapeutic agent for Alzheimer's disease, and its chemical structure, biological activity, and potential applications have been extensively studied.
MK8033 Hcl is a novel and specific dual ATP competitive c-Met/Ron inhibitor (IC50=1 nM Wt c-Met) under investigation as a treatment for cancer.IC50 Value: 1 nM (Wt c-Met); 2.0 nM (c-Met N1100Y) [1]Target: c-Metin vitro: MK-8033 binds 3-fold more tightly to phosphorylated c-Met kinase domain (Kd= 3.2 nM) than to its unphosphorylated counterpart (Kd = 10.4 nM). Signigicantly, MK-8033 potently inhibits kinase activity of three oncogenic c-Met activation loop mutants, Y1230C, Y1230H, and Y1235D (IC50s ranging from 0.6 to 1 nM at 50 uM ATP) in addition to other c-Met activating mutants N1100Y and M1250T. MK-8033 potently inhibited GTL-16 proliferation with an IC50 of 582 ± 30 nM. By contrast the HCT116 cell line, which does not harbor basal c-Met activation, was not inhibited by MK-8033 (IC50 > 10000 nM) [1]. MK-8033 radiosensitized the high-c-Met-expressing EBC-1 and H1993 cells but not the low-c-Met-expressing cell lines A549 and H460. However, irradiation of A549 and H460 cells increased the expression of c-Met protein at 30 minutes after the irradiation. Subsequent targeting of this up-regulated c-Met by using MK-8033 followed by a second radiation dose reduced the clonogenic survival of both A549 and H460 cells. MK-8033reduced the levels of radiation-induced phosphorylated (activated) c-Met in A549 cells [2].in vivo: MK-8033 was orally dosed in GTL-16 tumor xenograft bearing mice. Mice were euthanized 1 h after dosing and tested for p-Met (Y1349) in tumors and MK-8033 concentrations in plasma. At 100 mg/kg,essentially complete inhibition of p-Met (Y1349) was achieved. An in vivo IC50 of 1.3 uM was deduced from the relationship between plasma MK-8033 level and Met pY1349. Treatment with escalating dosed of MK-8033 for 21 days lead to antitumor efficacies in a dose-dependent manner. Dosing at 3, 10, 30, and 100 mg/kg resulted in 22, 18, 57, and 86% tumor growth inhibition, respectively, relative to tumor from vehicle-treated mice.
MUT056399 is a highly potent inhibitor of the FabI enzyme of both S. aureus and E. coli with 50% inhibitory concentration IC50s of 12 nM and 58 nM, respectively.IC50 value: 12 nM (for S. aureus), 58 nM (for E. coli) [1]Target: FabI enzymein vitro: MUT056399 is a highly potent new inhibitor of the FabI enzyme of both Staphylococcus aureus and Escherichia coli. MUT056399 is very active against S. aureus strains, including methicillin-susceptible S. aureus (MSSA), methicillin-resistant S. aureus (MRSA), linezolid-resistant, and multidrug-resistant strains, with MIC90s between 0.03 and 0.12 μg/ml. MUT056399 is also active against coagulase-negative staphylococci, with MIC90s between 0.12 and 4 μg/ml. MUT056399 is very active against the 118 S. aureus strains tested, including MSSA and MRSA isolates and linezolid-resistant and multidrug-resistant strains, with MIC90s between ≤0.03 and 0.12 μg/ml.In vivo: MUT056399, administered subcutaneously, protected mice from a lethal systemic infection induced by MSSA, MRSA, and vancomycin-intermediate S. aureus strains (50% effective doses ranging from 19.3 mg/kg/day to 49.6 mg/kg/day). In the nonneutropenic murine thigh infection model, the same treatment with MUT056399 reduced the bacterial multiplication of MSSA and MRSA in the thighs of immunocompetent mice.
Saquinavir is a protease inhibitor that is used in the treatment of HIV/AIDS. It was the first drug of its kind to be approved by the FDA in 1995. Saquinavir is a synthetic compound that is derived from a natural product, and it has been shown to be effective in reducing viral load and improving the quality of life for patients with HIV/AIDS.
Rimegepant is a small molecule drug that belongs to the class of calcitonin gene-related peptide (CGRP) receptor antagonists. It is used for the treatment of acute migraine attacks in adults. Rimegepant is a promising drug due to its high potency, selectivity, and favorable pharmacokinetic properties.