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Mavacamten

Catalog No. T7134Cas No. 1642288-47-8
Alias SAR439152, MYK-461

Mavacamten (MYK-461) is an orally bioavailable inhibitor of cardiac myosin ATPase,( IC50s of 490, 711 nM for bovine cardiac and human cardiac, respectively)

Mavacamten

Mavacamten

Purity: 99.53%
Catalog No. T7134Alias SAR439152, MYK-461Cas No. 1642288-47-8
Mavacamten (MYK-461) is an orally bioavailable inhibitor of cardiac myosin ATPase,( IC50s of 490, 711 nM for bovine cardiac and human cardiac, respectively)
Pack SizePriceAvailabilityQuantity
1 mg$40In Stock
5 mg$73In Stock
10 mg$108In Stock
25 mg$189In Stock
50 mg$268In Stock
100 mg$376In Stock
1 mL x 10 mM (in DMSO)$80In Stock
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Purity:99.53%
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Product Introduction

Bioactivity
Description
Mavacamten (MYK-461) is an orally bioavailable inhibitor of cardiac myosin ATPase,( IC50s of 490, 711 nM for bovine cardiac and human cardiac, respectively)
Targets&IC50
ATPase (human cardiac myosin):711 nM, ATPase (Bovine cardiac myosin):490 nM
In vitro
MYK-461 is found to have an IC50 value of 490 nM in the bovine system, 711 nM in the human system, and 2140 nM in the rabbit system, indicating selectivity of >4-fold for cardiac myosin[1]
In vivo
MYK-461 reduces cardiac contractility, prevents left ventricular hypertrophy, and reverses pathologic remodeling. In cats, it relieves left ventricular outflow tract obstruction[2]
Animal Research
Five?cats received a combination of alfaxalone and midazolam for anesthetic induction, followed by inhaled isoflurane and oxygen maintenance.?Blood pressure was measured via an automated blood pressure cuff at five-minute intervals with supplementary continuous monitoring by arterial line when arterial access could be obtained.?Following induction of anesthesia, a complete baseline echocardiogram was performed (timepoint #1).?Cats were then treated with atropine 0.04 mg/kg IV, followed by an infusion of isoproterenol 0.04 μg/kg/min IV to elevate heart rate back to pre-anesthetized values and induce the previously observed LVOT obstruction.?After five to seven minutes, a stable heart rate of 200–220 bpm was reached and a complete echocardiogram was performed (timepoint #2).?At the completion of imaging, a ten-minute intravenous infusion of MYK-461 (n = 5) at 0.3 mg/kg/hr IV was started.?Focused echocardiography was performed after five minutes (timepoint #3).?After ten minutes, the MYK-461 infusion rate was lowered to 0.12 mg/kg/hr IV, a blood sample was drawn and an echocardiogram performed (timepoint #4).?If ventricular function remained hypercontractile or within normal limits by visual inspection, another blood sample was obtained and the MYK-461infusion rate was increased to 0.36 mg/kg/hr IV for ten minutes.?Focused echocardiography was performed after five minutes (timepoint #5).?After ten minutes, the MYK-461 infusion rate was lowered to 0.15 mg/kg/hr IV, a blood sample was drawn and an echocardiogram performed (timepoint #6).?Following imaging, the isoproterenol infusion was discontinued.?When heart rate returned to baseline levels (five to seven minutes), a complete echocardiogram was performed on MYK-461 alone (timepoint #7).?Study drug was then discontinued, and animals were awakened, extubated and moved to recovery.?Three of five cats were available to return for a control arm of this experiment after a 6-week washout period.The experiment was completed with identical methodology with the exception that MYK-461 was substituted for vehicle (control) at matched volumes/infusion rates[2].
AliasSAR439152, MYK-461
Chemical Properties
Molecular Weight273.33
FormulaC15H19N3O2
Cas No.1642288-47-8
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 150 mg/mL (548.79 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.6586 mL18.2929 mL36.5858 mL182.9291 mL
5 mM0.7317 mL3.6586 mL7.3172 mL36.5858 mL
10 mM0.3659 mL1.8293 mL3.6586 mL18.2929 mL
20 mM0.1829 mL0.9146 mL1.8293 mL9.1465 mL
50 mM0.0732 mL0.3659 mL0.7317 mL3.6586 mL
100 mM0.0366 mL0.1829 mL0.3659 mL1.8293 mL

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