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    Dexamethasone

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      Dexamethasone

      SKU
      D0359

      Category: Antibiotics

      Synonyms
      MK-125, NSC 34521, 9&alpha,-Fluoro-16&alpha,-methylprednisolone,
      50-02-2
      CAS-Number
      C22H29FO5
      Molecular Formula
      392.46
      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
      Soluble in DMSO (25mg/ml), ethanol (20mg/ml) or chloroform.
      Melting Point
      262-264 °C (lit.)
      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.
      Hazard statements
      H360FD
      Precautionary statements
      P201 - P202 - P280 - P308 + P313 - P405 - P501
      GHS Symbol
      GHS08
      Signal word
      Danger
      Transportation
      Not dangerous goods
      Description
      Dexamethasone is a potent anti-inflammatory and immunosuppressive agent useful in a variety of inflammatory and autoimmune conditions. This synthetic glucocorticoid acts as an agonist of human glucocorticoid receptor (GR) and binds with a higher affinity than the natural ligand cortisol. Through GR activation, dexamethasone has both transactivating and transrepressing effects on gene expression, resulting in anti-inflammatory properties. The anti-inflammatory effects are complex, but primarily via inhibition of inflammatory cells and suppression of expression of inflammatory mediators.
      Smiles
      O=C1C=C[C@@]2(C)C(CC[C@]3([H])[C@]2(F)[C@@H](O)C[C@@]4(C)[C@@]3([H])C[C@@H](C)[C@]4(O)C(CO)=O)=C1
      InChi Key
      UREBDLICKHMUKA-CXSFZGCWSA-N
      References
      (1) M.A. Clark, et al.; Prostaglandins 32, 703 (1986) , (2) R. Matasic, et al.; J. Leukoc. Biol. 66, 909 (1999) , (3) I. Rahman; Biochem. Pharmacol. 60, 1041 (2000) , (4) I.M. Beck, et al.; Endocr. Rev. 30, 830 (2009) , (5) C. van Kooten, et al.; Handb. Exp. Pharmacol. 2009, 233 (2009) , (6) I.S. Okoye, et al.; Cancer Immunol. Immunother. (Epub ahead of print) (2020)
      InChi
      InChI=1S/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3/t12-,15+,16+,17+,19+,20+,21+,22+/m1/s1

      Dexamethasone is a potent anti-inflammatory and immunosuppressive agent useful in a variety of inflammatory and autoimmune conditions. This synthetic glucocorticoid acts as an agonist of human glucocorticoid receptor (GR) and binds with a higher affinity than the natural ligand cortisol. Through GR activation, dexamethasone has both transactivating and transrepressing effects on gene expression, resulting in anti-inflammatory properties. The anti-inflammatory effects are complex, but primarily via inhibition of inflammatory cells and suppression of expression of inflammatory mediators.

      SKU: D0359 Category: Antibiotics
      • Additional information

      Additional information

      Synonyms

      MK-125, NSC 34521, 9&alpha,-Fluoro-16&alpha,-methylprednisolone,

      Purity

      ≥98% (HPLC)

      Appearance

      White to off-white powder

      CAS-Number

      50-02-2

      Molecular Formula

      C22H29FO5

      Molecular Weight

      392.46

      Identity

      1H-NMR

      Solvents

      Soluble in DMSO (25mg/ml), ethanol (20mg/ml) or chloroform.

      Melting Point

      262-264 °C (lit.)

      Smiles

      O=C1C=C[C@@]2(C)C(CC[C@]3([H])[C@]2(F)[C@@H](O)C[C@@]4(C)[C@@]3([H])C[C@@H](C)[C@]4(O)C(CO)=O)=C1

      InChi Key

      UREBDLICKHMUKA-CXSFZGCWSA-N

      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.

      Hazard statements

      H360FD

      Precautionary statements

      P201 – P202 – P280 – P308 + P313 – P405 – P501

      GHS Symbol

      GHS08

      Signal word

      Danger

      Transportation

      Not dangerous goods

      References

      (1) M.A. Clark, et al.; Prostaglandins 32, 703 (1986), (2) R. Matasic, et al.; J. Leukoc. Biol. 66, 909 (1999), (3) I. Rahman; Biochem. Pharmacol. 60, 1041 (2000), (4) I.M. Beck, et al.; Endocr. Rev. 30, 830 (2009), (5) C. van Kooten, et al.; Handb. Exp. Pharmacol. 2009, 233 (2009), (6) I.S. Okoye, et al.; Cancer Immunol. Immunother. (Epub ahead of print) (2020)

      InChi

      InChI=1S/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3/t12-,15+,16+,17+,19+,20+,21+,22+/m1/s1

      Quantity

      500 mg, 1 g, Bulk

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