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    Mildronate dihydrate

    Available from stock

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      Mildronate dihydrate

      SKU
      M0558

      Categories:

      Synonyms
      Meldonium , MET 88 , Quaterin , THP
      86426-17-7
      CAS-Number
      C6H14N2O2 . 2H2O
      Molecular Formula
      182.22
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥98% (HPLC)
      Appearance
      White to off-white powder
      Identity
      1H-NMR

      Properties

      Solvents
      water (20 mg/ml), ethanol (20 mg/ml)
      Shipping
      AMBIENT
      Short Term Storage
      +4°C
      Long Term Storage
      -20°C
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at -20°C.
      Hazard statements
      H315-H319-H335
      Precautionary statements
      P261-P305 + P351 + P338
      GHS Symbol
      GHS07
      Signal word
      Warning
      Transportation
      Packing Group III
      Description
      Mildronate is a structural analog of γ,-butyrobetaine (γ,BB), an intermediate in the biosynthesis of carnitine and a modulator of energy metabolism. It blocks carnitine synthesis by inhibiting γ,BB hydroxylase (BBOX) and, less potently, carnitine acetyltransferase (CrAT). Through these actions, mildronate reduces the levels of free carnitine and long chain acyl carnitine. This leads to suppressed fatty acid metabolism and mitochondrial uncoupling during oxidative conditions, resulting in cardioprotective, antidiabetic and neuroprotective effects. Mildronate also improves cognition and reduces amyloid-β, pathology in a mouse model of Alzheimer’s disease.
      Smiles
      [O-]C(CCN[N+](C)(C)C)=O
      InChi Key
      PVBQYTCFVWZSJK-UHFFFAOYSA-N
      References
      (1) B.Z. Simkhovich, et al., Biochem. Pharmacol. 37, 195 (1988) , (2) M. Dambrova, et al., Trends Cardiovasc. Med. 12, 275 (2002) (Review) , (3) E. Liepinsh, et al., J. Cardiovasc. Pharmacol. 48, 314 (2006) , (4) R. Vilskersts, et al., Pharmacology 83, 287 (2009) , (5) K. Jaudzems, et al., J. Enzyme Inhib. Med. Chem. 24, 1269 (2009) , (6) J. Pupure, et al., Neurosci. Lett. 470, 100 (2010) , (7) V.Z. Klusa, et al., Int. J. Mol. Sci. 11, 4465 (2010) , (8) I.K. Leung, et al., Chem. Biol. 17, 1316 (2010) , (9) E. Liepinsh, et al., Eur. J. Pharmacol. 658, 277 (2011) , (10) K. Tars, et al., J. Med. Chem. 57, 2213 (2014) , (11) U. Beitnere, et al., J. Neurosci. Res. 92, 338 (2014) , (12) M. Makrecka, et al., Eur. J. Pharmacol. 723, 55 (2014)
      InChi
      InChI=1S/C6H14N2O2/c1-8(2,3)7-5-4-6(9)10/h7H,4-5H2,1-3H3

      Mildronate is a structural analog of γ,-butyrobetaine (γ,BB), an intermediate in the biosynthesis of carnitine and a modulator of energy metabolism. It blocks carnitine synthesis by inhibiting γ,BB hydroxylase (BBOX) and, less potently, carnitine acetyltransferase (CrAT). Through these actions, mildronate reduces the levels of free carnitine and long chain acyl carnitine. This leads to suppressed fatty acid metabolism and mitochondrial uncoupling during oxidative conditions, resulting in cardioprotective, antidiabetic and neuroprotective effects. Mildronate also improves cognition and reduces amyloid-β, pathology in a mouse model of Alzheimer’s disease.

      SKU: M0558
      • Additional information

      Additional information

      Synonyms

      Meldonium, MET 88, Quaterin, THP

      Purity

      ≥98% (HPLC)

      Appearance

      White to off-white powder

      CAS-Number

      86426-17-7

      Molecular Formula

      C6H14N2O2 . 2H2O

      Molecular Weight

      182.22

      Identity

      1H-NMR

      Solvents

      water (20 mg/ml), ethanol (20 mg/ml)

      Smiles

      [O-]C(CCN[N+](C)(C)C)=O

      InChi Key

      PVBQYTCFVWZSJK-UHFFFAOYSA-N

      Shipping

      AMBIENT

      Short Term Storage

      +4°C

      Long Term Storage

      -20°C

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at -20°C.

      Hazard statements

      H315-H319-H335

      Precautionary statements

      P261-P305 + P351 + P338

      GHS Symbol

      GHS07

      Signal word

      Warning

      Transportation

      Packing Group III

      References

      (1) B.Z. Simkhovich, et al., Biochem. Pharmacol. 37, 195 (1988), (2) M. Dambrova, et al., Trends Cardiovasc. Med. 12, 275 (2002) (Review), (3) E. Liepinsh, et al., J. Cardiovasc. Pharmacol. 48, 314 (2006), (4) R. Vilskersts, et al., Pharmacology 83, 287 (2009), (5) K. Jaudzems, et al., J. Enzyme Inhib. Med. Chem. 24, 1269 (2009), (6) J. Pupure, et al., Neurosci. Lett. 470, 100 (2010), (7) V.Z. Klusa, et al., Int. J. Mol. Sci. 11, 4465 (2010), (8) I.K. Leung, et al., Chem. Biol. 17, 1316 (2010), (9) E. Liepinsh, et al., Eur. J. Pharmacol. 658, 277 (2011), (10) K. Tars, et al., J. Med. Chem. 57, 2213 (2014), (11) U. Beitnere, et al., J. Neurosci. Res. 92, 338 (2014), (12) M. Makrecka, et al., Eur. J. Pharmacol. 723, 55 (2014)

      InChi

      InChI=1S/C6H14N2O2/c1-8(2,3)7-5-4-6(9)10/h7H,4-5H2,1-3H3

      Quantity

      10 mg, 25 mg, Bulk

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