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Formula | C20H24FN5O3 |
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Molecular Weight | 401.43 | CAS No. | 873697-71-3 | |
Solubility (25°C)* | In vitro | DMSO | 80 mg/mL (199.28 mM) | |
Ethanol | 80 mg/mL (199.28 mM) | |||
Water | Insoluble | |||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
Description | Omecamtiv mecarbil (CK-1827452) is a specific cardiac myosin activator and a clinical drug for left ventricular systolic heart failure. Phase 2. | |
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In vitro | In vitro, Omecamtiv mecarbil selectively activates cardiac myosin by increasing the myosin ATPase rate. [1] In isolated cardiac myocytes, Omecamtiv mecarbil results in increase of myocyte contractility and overcomes of the myosin inhibitor BDM without increasing the calcium transient or inhibiting the PDE pathway. [1] | |
In vivo | Omecamtiv mecarbil significantly increases fractional shortening starting at 0.4 mM plasma concentrations in SD rats, sham animals and in rats with heart failure. [1] In conscious dogs with myocardial infarction (MI-sHF), Omecamtiv mecarbil leads to a significant increase in wall thickening (25%), stroke volume (44%), cardiac output (22%) and left ventricular (LV) systolic ejection time (26%). In addition, Omecamtiv mecarbil also results in the decreases of some hemodynamic parameters including heart rate, mean left atrial pressure, and LV end-diastolic pressure. In conscious dogs with left ventricular hypertrophy (LVH-sHF), Omecamtiv mecarbil leads to similar and not statistically different effects on hemodynamic parameters. [2] |
Animal Study:[1] |
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Data from [Data independently produced by University of Illinois at Chicago, 2014]
Data from [Data independently produced by , , J Physiol, 2018, 596(1):31-46]
The force of the myosin motor sets cooperativity in thin filament activation of skeletal muscles [ Commun Biol, 2022, 5(1):1266] | PubMed: 36400920 |
Effects of omecamtiv mecarbil and mavacamten in isolated human atrium [ Naunyn Schmiedebergs Arch Pharmacol, 2022, 10.1007/s00210-022-02333-0] | PubMed: 36399186 |
Myosin with hypertrophic cardiac mutation R712L has a decreased working stroke which is rescued by omecamtiv mecarbil [ Elife, 2021, 10e63691] | PubMed: 33605878 |
Mechanistic analysis of actin-binding compounds that affect the kinetics of cardiac myosin-actin interaction [ J Biol Chem, 2021, S0021-9258(21)00245-3] | PubMed: 33639160 |
Generative adversarial networks for construction of virtual populations of mechanistic models: simulations to study Omecamtiv Mecarbil action [ J Pharmacokinet Pharmacodyn, 2021, 10.1007/s10928-021-09787-4] | PubMed: 34716531 |
Development and Application of NovelIn VitroAssays to Advance Drug Discovery for Arrhythmogenic Cardiomyopathy and Respiratory Syncytial Virus Infection [ ProQuest , 2021, 28718834] | PubMed: none |
Orthophosphate increases the efficiency of slow muscle-myosin isoform in the presence of omecamtiv mecarbil [ Nat Commun, 2020, 11(1):3405] | PubMed: 32636378 |
Sarcomere integrated biosensor detects myofilament-activating ligands in real time during twitch contractions in live cardiac muscle [ J Mol Cell Cardiol, 2020, 147:49-61] | PubMed: 32791214 |
Phosphorylation of Cardiac Myosin-Binding protein-C Contributes to Calcium Homeostasis [ J Biol Chem, 2020, jbc.RA120.13296] | PubMed: 32554466 |
SarcTrack: An Adaptable Software Tool for Efficient Large-Scale Analysis of Sarcomere Function in hiPSC-Cardiomyocytes [Toepfer CN, et al. Circ Res, 2019, 10.1161/CIRCRESAHA.118.314505] | PubMed: 30700234 |
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