Mavacamten

Mavacamten

Product Name MYK-461
CAS Number 1642288-47-8
Molecular Formula C₁₈H₁₆FN₃O₃S
Molecular Weight 373.40 g/mol
Appearance White to off-white powder
Assay (HPLC) ≥ 98.0%
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 10 ppm
Storage Store in a cool, dry place, protected from light
Solubility Soluble in DMSO, DMF; slightly soluble in ethanol

 

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What is Mavacamten?

Mavacamten (development code MYK-461) is a first-in-class, selective, allosteric inhibitor of cardiac myosin. It is the first pharmacological agent approved to target the underlying pathophysiology of hypertrophic cardiomyopathy (HCM) —a condition characterized by excessive cardiac muscle contraction, hypercontractility, and impaired relaxation (diastolic dysfunction).

Mechanism of action: Mavacamten binds selectively to the catalytic domain of cardiac myosin ATPase, reducing the number of myosin heads available for actin binding. This decreases cardiac contractility, reduces left ventricular outflow tract (LVOT) gradient, and improves diastolic filling.

Chemical structure highlights:

  • Small molecule (MW 273.33)

  • Allosteric modulator (not ATP-competitive)

  • Highly selective for cardiac myosin (vs. smooth muscle or skeletal myosin)

  • Oral bioavailability (well-absorbed)

Synonym:MYK-461(SAR-439152);SAR439152;SAR439152;SAR-439152;SAR-439152;SAR439152;SAR439152;MYK-461;MYK461;MYK461;MAVACAMTEN;MYK-461-Mavacamten|SAR439152;Mavacamten(MYK-461;2,4(1H,3H)-Pyrimidinedione,3-(1-methylethyl)-6-[[(1S)-1-phenylethyl]amino]-

 

Specifications

Parameter Specification
MYK‑461 Content (HPLC) ≥ 98.0%
Identification IR / MS / NMR conforms to reference
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%
Heavy Metals (as Pb) ≤ 10 ppm
Arsenic (As) ≤ 1 ppm
Residual Solvents Meets USP requirements

Source & Purity

  • Source: Synthetic chemical synthesis

  • Standardization: ≥98.0% MYK-461 (HPLC)

  • Forms: White to off‑white powder

  • Applications: Pharmaceutical research, formulation development, analytical standards, preclinical studies

Documentation & Supply

  • Monthly capacity: 5+ kg

  • Lead time: 3–5 days (samples), 10–15 days (bulk)

  • Documentation: COA, MSDS,HPLC chromatogram, stability data, NMR (upon request)

  • Packaging: 1 kg, 5 kg, 10 kg, 25 kg (double‑layer PE bag inside, fiber drum outside)

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