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      Pravastatin sodium

      SKU
      P0933

      Category: API's & Intermediates

      Synonyms
      Eptastatin sodium salt hydrate, 3&beta,-Hydroxycompactin, Mevalothin
      81131-70-6
      CAS-Number
      C23H35O7Na · xH2O
      Molecular Formula
      446.51 (anhydrous basis)
      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 crystalline solid
      Identity
      1H-NMR

      Properties

      Solvents
      Soluble in water (30mg/ml) or DMSO (30mg/ml).
      Shipping
      AMBIENT
      Short Term Storage
      RT
      Long Term Storage
      +4°C
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at +4°C.
      Transportation
      Not dangerous goods
      Description
      Pravastatin is a water-soluble, orally effective, competitive inhibitor of Hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase (Ki = 2.3nM), the rate-limiting enzyme in the cholesterol biosynthetic pathway and the target of the “statin” class of cholesterol-lowering/regulating compounds. Pravastatin potently blocks cholesterol synthesis in vivo (Ki~ 1 nM) and displays cardioprotective properties. Pravastatin reduces LDL cholesterol and triglyceride levels and increase HDL cholesterol in the prevention of cardiovascular disease. Pravastatin also acts as an immunomodulator and as an inhibitor of p21ras isoprenylation.
      Smiles
      O[C@H]1C[C@H](OC([C@@H](C)CC)=O)[C@@]2([H])C(C=C[C@H](C)[C@@H]2CC[C@](O)([H])C[C@H](O)CC(O[Na])=O)=C1
      InChi Key
      VWBQYTRBTXKKOG-BAWPFLGFSA-M
      References
      (1) T. Koga, et al., Biochim. Biophys. Acta 1045, 115 (1990) , (2) S.M. Singhvi, et al., Br. J. Clin. Pharmacol. 29, 239 (1990) , (3) A. Corsini, et al., Pharmacol. Res. 31, 9 (1995) , (4) B.A. Hamelin & J. Turgeon, Trends Pharmacol. Sci. 19, 26 (1998) , (5) M. Tatsuta, et al., Br. J. Cancer 77, 581 (1998) , (6) W.H. Kaesemeyer, et al., J. Am. Coll. Cardiol. 33, 234 (1999) , (7) B. Kwak, et al., Nat Med. 6, 1399 (2000) , (8) J.A. Tobert, Nat. Rev. Drug Discov. 2, 517 (2003) , (9) A.A. Al-Badr, et al., Prof. Drug Subst. Excip. Rel. Methodol. 39, 433 (2014)

      Pravastatin is a water-soluble, orally effective, competitive inhibitor of Hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase (Ki = 2.3nM), the rate-limiting enzyme in the cholesterol biosynthetic pathway and the target of the “statin” class of cholesterol-lowering/regulating compounds. Pravastatin potently blocks cholesterol synthesis in vivo (Ki~ 1 nM) and displays cardioprotective properties. Pravastatin reduces LDL cholesterol and triglyceride levels and increase HDL cholesterol in the prevention of cardiovascular disease. Pravastatin also acts as an immunomodulator and as an inhibitor of p21ras isoprenylation.

      SKU: P0933 Category: API's & Intermediates
      • Additional information

      Additional information

      Synonyms

      Eptastatin sodium salt hydrate, 3&beta,-Hydroxycompactin, Mevalothin

      Purity

      ≥98% (HPLC)

      Appearance

      White crystalline solid

      CAS-Number

      81131-70-6

      Molecular Formula

      C23H35O7Na · xH2O

      Molecular Weight

      446.51 (anhydrous basis)

      Identity

      1H-NMR

      Solvents

      Soluble in water (30mg/ml) or DMSO (30mg/ml).

      Smiles

      O[C@H]1C[C@H](OC([C@@H](C)CC)=O)[C@@]2([H])C(C=C[C@H](C)[C@@H]2CC[C@](O)([H])C[C@H](O)CC(O[Na])=O)=C1

      InChi Key

      VWBQYTRBTXKKOG-BAWPFLGFSA-M

      Shipping

      AMBIENT

      Short Term Storage

      RT

      Long Term Storage

      +4°C

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at +4°C.

      Transportation

      Not dangerous goods

      References

      (1) T. Koga, et al., Biochim. Biophys. Acta 1045, 115 (1990), (2) S.M. Singhvi, et al., Br. J. Clin. Pharmacol. 29, 239 (1990), (3) A. Corsini, et al., Pharmacol. Res. 31, 9 (1995), (4) B.A. Hamelin & J. Turgeon, Trends Pharmacol. Sci. 19, 26 (1998), (5) M. Tatsuta, et al., Br. J. Cancer 77, 581 (1998), (6) W.H. Kaesemeyer, et al., J. Am. Coll. Cardiol. 33, 234 (1999), (7) B. Kwak, et al., Nat Med. 6, 1399 (2000), (8) J.A. Tobert, Nat. Rev. Drug Discov. 2, 517 (2003), (9) A.A. Al-Badr, et al., Prof. Drug Subst. Excip. Rel. Methodol. 39, 433 (2014)

      Quantity

      50 mg, Bulk

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