Selumetinib Sulfate
A sulfate salt form of selumetinib with the same therapeutic properties. This oral medication targets a specific signaling pathway called MEK that cancer cells rely on to grow and divide uncontrollably.
आणविक भार
555.8000 g/mol
TPSA
171.00 Ų
चिकित्सीय क्षेत्र
क्रिया का तंत्र
Inhibits MEK1 and/or MEK2 kinases in the RAS/MAPK signaling pathway, blocking the transmission of growth signals that promote cancer cell proliferation and survival.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits MEK1 and/or MEK2 kinases in the RAS/MAPK signaling pathway, blocking the transmission of growth signals that promote cancer cell proliferation and survival.
2D संरचना
Cite this structure
Embed this structure
SMILES
Cn1cnc2c(F)c(Nc3ccc(Br)cc3Cl)c(C(=O)NOCCO)cc21.O=S(=O)(O)O
InChI
InChI=1S/C17H15BrClFN4O3.H2O4S/c1-24-8-21-16-13(24)7-10(17(26)23-27-5-4-25)15(14(16)20)22-12-3-2-9(18)6-11(12)19;1-5(2,3)4/h2-3,6-8,22,25H,4-5H2,1H3,(H,23,26);(H2,1,2,3,4)
Molecular Formula
C17H17BrClFN4O7S
HBD / HBA
5 / 10
घूर्णनीय बंधन
6
भारी परमाणु
32
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
अक्सर पूछे जाने वाले प्रश्न
A sulfate salt form of selumetinib with the same therapeutic properties. This oral medication targets a specific signaling pathway called MEK that cancer cells rely on to grow and divide uncontrollably.
Inhibits MEK1 and/or MEK2 kinases in the RAS/MAPK signaling pathway, blocking the transmission of growth signals that promote cancer cell proliferation and survival.
Yes, Selumetinib Sulfate is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2105684. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 16214875. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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