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    Temozolomide

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      Temozolomide

      SKU
      T0072

      Category: API's & Intermediates

      Synonyms
      3,4-Dihydro-3-methyl-4-oxoimidazo[5,1-d]-1,2,3,5-tetrazine-8-carboxamide , CCRG 81045 , MB 39831 , Methazolastone , NSC 362856 , Temodal
      85622-93-1
      CAS-Number
      C6H6N6O2
      Molecular Formula
      194.15
      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 light pink powder
      Identity
      1H-NMR

      Properties

      Solvents
      DMSO (5 mg/ml), DMF (5 mg/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.
      Hazard statements
      H302-H315-H319-H335-H350-H360
      Precautionary statements
      P201-P261-P305 + P351 + P338-P308 + P313
      GHS Symbol
      GHS07+GHS08
      Signal word
      Danger
      Transportation
      Not dangerous goods
      Description
      Temozolomide is a DNA methylating agent and drug resistance-modifying agent with antitumor and antiangiogenic properties. Temozolomide induces G2/M arrest and apoptosis through adduction of a methyl group to O6 position of guanine in genomic DNA and interfering with DNA replication and leading to cytotoxicity in proliferating cells. It has been shown to induce autophagy in malignant glioma cells. It is effective in a variety of types of cancer, including aggressive brain cancers.
      Smiles
      O=C1N(C)N=NC2=C(C(N)=O)N=CN21
      InChi Key
      BPEGJWRSRHCHSN-UHFFFAOYSA-N
      References
      (1) A.S. Clark, et al., J. Med. Chem. 38, 1493 (1995) , (2) E.S. Newlands, et al., Cancer Treat. Rev. 23, 35 (1997) (Review) , (3) S.S. Agarwala & J.M. Kirkwood, Oncologist 5, 144 (2000) (Review) , (4) S.J. Danson & M.R. Middleton, Expert Rev. Anticancer Ther. 1, 13 (2001) (Review) , (5) T. Kanzawa, et al., Cell Death Differ. 11, 448 (2004) , (6) F. Marchesi, et al., Pharmacol. Res. 56, 275 (2007) , (7) G. Jiang, et al., Curr. Med. Chem. 19, 3886 (2012) (Review)
      InChi
      InChI=1S/C6H6N6O2/c1-11-6(14)12-2-8-3(4(7)13)5(12)9-10-11/h2H,1H3,(H2,7,13)

      Temozolomide is a DNA methylating agent and drug resistance-modifying agent with antitumor and antiangiogenic properties. Temozolomide induces G2/M arrest and apoptosis through adduction of a methyl group to O6 position of guanine in genomic DNA and interfering with DNA replication and leading to cytotoxicity in proliferating cells. It has been shown to induce autophagy in malignant glioma cells. It is effective in a variety of types of cancer, including aggressive brain cancers.

      SKU: T0072 Category: API's & Intermediates
      • Additional information

      Additional information

      Synonyms

      3,4-Dihydro-3-methyl-4-oxoimidazo[5,1-d]-1,2,3,5-tetrazine-8-carboxamide, CCRG 81045, MB 39831, Methazolastone, NSC 362856, Temodal

      Purity

      ≥98% (HPLC)

      Appearance

      White to light pink powder

      CAS-Number

      85622-93-1

      Molecular Formula

      C6H6N6O2

      Molecular Weight

      194.15

      Identity

      1H-NMR

      Solvents

      DMSO (5 mg/ml), DMF (5 mg/ml)

      Smiles

      O=C1N(C)N=NC2=C(C(N)=O)N=CN21

      InChi Key

      BPEGJWRSRHCHSN-UHFFFAOYSA-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

      H302-H315-H319-H335-H350-H360

      Precautionary statements

      P201-P261-P305 + P351 + P338-P308 + P313

      GHS Symbol

      GHS07+GHS08

      Signal word

      Danger

      Transportation

      Not dangerous goods

      References

      (1) A.S. Clark, et al., J. Med. Chem. 38, 1493 (1995), (2) E.S. Newlands, et al., Cancer Treat. Rev. 23, 35 (1997) (Review), (3) S.S. Agarwala & J.M. Kirkwood, Oncologist 5, 144 (2000) (Review), (4) S.J. Danson & M.R. Middleton, Expert Rev. Anticancer Ther. 1, 13 (2001) (Review), (5) T. Kanzawa, et al., Cell Death Differ. 11, 448 (2004), (6) F. Marchesi, et al., Pharmacol. Res. 56, 275 (2007), (7) G. Jiang, et al., Curr. Med. Chem. 19, 3886 (2012) (Review)

      InChi

      InChI=1S/C6H6N6O2/c1-11-6(14)12-2-8-3(4(7)13)5(12)9-10-11/h2H,1H3,(H2,7,13)

      Quantity

      250 mg, 1 g, Bulk

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