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    Cabozantinib S-malate

    Available from stock

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      Cabozantinib S-malate

      SKU
      C0698

      Categories:

      Synonyms
      XL184 malate , BMS907351 malate , N-(4-((6,7-dimethoxyquinolin-4-yl)oxy)phenyl)-N-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide (S)-2-hydroxysuccinate
      1140909-48-3
      CAS-Number
      C32H30FN3O10
      Molecular Formula
      635.59
      Molecular Weight

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

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥99% (HPLC)
      Appearance
      White to off white crystalline powder
      Identity
      1H-NMR

      Properties

      Solvents
      DMSO, methanol, DMF
      Melting Point
      166 - 169°C

      Documentation

      Safety Data Sheet (SDS)
      CDX C0698 MSDS.pdf
      Shipping
      AMBIENT
      Short Term Storage
      +4°C
      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
      Precautionary statements
      P264, P280, P301+P312, P302+P352, P305+P351+P338, P332+P313, P337+P313
      GHS Symbol
      GHS07
      Transportation
      Not dangerous goods
      Description
      The s-malate salt form of Cabozantinib is very potent orally available inhibitor of multiple receptor tyrosine kinases (RTK), specifically MET and VEGFR2. It also inhibits KIT, FLT3, Tie-2, RET and AXL. Cabozantinib shows dose-dependent inhibition of tumor growth and tumor regression, associated with disruption of the tumor vasculature, angiogenesis and extensive tumor cell apoptosis.
      Smiles
      O[C@@H](CC(O)=O)C(O)=O.COC1=CC2=C(C=C1OC)C(OC1=CC=C(NC(=O)C3(CC3)C(=O)NC3=CC=C(F)C=C3)C=C1)=CC=N2
      InChi Key
      HFCFMRYTXDINDK-WNQIDUERSA-N
      References
      (1) R. Kurzrock, et al., J. Clin. Oncol. 29, 2660 (2011) , (2) M. Yakes, et al., Mol. Cancer Ther. 10, 2298 (2011) , (3) C. Hage, et al., Cell Death Dis. 4, e627 (2013) , (4) F. Bentzien, et al., Thyroid. 23, 1569 (2013) , (5) Y. Sun, et al., Med. Sci. Monit. 21, 2316 (2015) , (6) J.N. Markowitz & K.M. Fancher, Pharmacotherapy 38, 357 (2018) , (7) C. Gruellich, Recent Results Cancer Res. 211, 67 (2018)

      The s-malate salt form of Cabozantinib is very potent orally available inhibitor of multiple receptor tyrosine kinases (RTK), specifically MET and VEGFR2. It also inhibits KIT, FLT3, Tie-2, RET and AXL. Cabozantinib shows dose-dependent inhibition of tumor growth and tumor regression, associated with disruption of the tumor vasculature, angiogenesis and extensive tumor cell apoptosis.

      SKU: C0698
      • Additional information

      Additional information

      Synonyms

      XL184 malate, BMS907351 malate, N-(4-((6,7-dimethoxyquinolin-4-yl)oxy)phenyl)-N-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide (S)-2-hydroxysuccinate

      Purity

      ≥99% (HPLC)

      Appearance

      White to off white crystalline powder

      CAS-Number

      1140909-48-3

      Molecular Formula

      C32H30FN3O10

      Molecular Weight

      635.59

      Identity

      1H-NMR

      Solvents

      DMSO, methanol, DMF

      Melting Point

      166 – 169°C

      Smiles

      O[C@@H](CC(O)=O)C(O)=O.COC1=CC2=C(C=C1OC)C(OC1=CC=C(NC(=O)C3(CC3)C(=O)NC3=CC=C(F)C=C3)C=C1)=CC=N2

      InChi Key

      HFCFMRYTXDINDK-WNQIDUERSA-N

      Shipping

      AMBIENT

      Short Term Storage

      +4°C

      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

      Precautionary statements

      P264, P280, P301+P312, P302+P352, P305+P351+P338, P332+P313, P337+P313

      GHS Symbol

      GHS07

      Transportation

      Not dangerous goods

      References

      (1) R. Kurzrock, et al., J. Clin. Oncol. 29, 2660 (2011), (2) M. Yakes, et al., Mol. Cancer Ther. 10, 2298 (2011), (3) C. Hage, et al., Cell Death Dis. 4, e627 (2013), (4) F. Bentzien, et al., Thyroid. 23, 1569 (2013), (5) Y. Sun, et al., Med. Sci. Monit. 21, 2316 (2015), (6) J.N. Markowitz & K.M. Fancher, Pharmacotherapy 38, 357 (2018), (7) C. Gruellich, Recent Results Cancer Res. 211, 67 (2018)

      Quantity

      100 mg, 500 mg, 1 g, Bulk

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