Enasidenib (AG-221)

99%

  • Product Code: 56892
  CAS:    1446502-11-9
Molecular Weight: 473.38 g./mol Molecular Formula: C₁₉H₁₇F₆N₇O
EC Number: MDL Number: MFCD29472245
Melting Point: Boiling Point:
Density: Storage Condition: -20℃
Product Description: Enasidenib is primarily used in the treatment of relapsed or refractory acute myeloid leukemia (AML) with a specific genetic mutation. It targets the IDH2 enzyme, which is often mutated in certain cancers, including AML. By inhibiting this mutated enzyme, enasidenib helps to restore normal cell differentiation, reducing the growth of cancerous cells. It is particularly beneficial for patients who have not responded well to other treatments, offering a targeted therapy option. The drug is administered orally, making it convenient for long-term use. Clinical studies have shown that enasidenib can improve overall survival and reduce the need for blood transfusions in some patients. It represents a significant advancement in personalized medicine for AML patients with IDH2 mutations.
Product Specification:
Test Specification
APPEARANCE White to Off-White Solid
PURITY 98.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.005 10-20 days ฿5,500.00
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-
0.025 10-20 days ฿12,600.00
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-
0.100 10-20 days ฿36,800.00
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Enasidenib (AG-221)
Enasidenib is primarily used in the treatment of relapsed or refractory acute myeloid leukemia (AML) with a specific genetic mutation. It targets the IDH2 enzyme, which is often mutated in certain cancers, including AML. By inhibiting this mutated enzyme, enasidenib helps to restore normal cell differentiation, reducing the growth of cancerous cells. It is particularly beneficial for patients who have not responded well to other treatments, offering a targeted therapy option. The drug is administered orally, making it convenient for long-term use. Clinical studies have shown that enasidenib can improve overall survival and reduce the need for blood transfusions in some patients. It represents a significant advancement in personalized medicine for AML patients with IDH2 mutations.
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