Larotrectinib Sulfate
The sulfate salt form of larotrectinib, a TRK kinase inhibitor used to treat cancers with NTRK gene fusions including colorectal and breast cancers. It shares the same tumor-agnostic mechanism as the parent compound.
Masse moléculaire
526,5000 g/mol
TPSA
169,00 Ų
Aires thérapeutiques
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Structure 2D
Cite this structure
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SMILES
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cc(F)ccc3F)nc12)N1CC[C@H](O)C1.O=S(=O)(O)O
InChI
InChI=1S/C21H22F2N6O2.H2O4S/c22-13-3-4-16(23)15(10-13)18-2-1-7-28(18)19-6-9-29-20(26-19)17(11-24-29)25-21(31)27-8-5-14(30)12-27;1-5(2,3)4/h3-4,6,9-11,14,18,30H,1-2,5,7-8,12H2,(H,25,31);(H2,1,2,3,4)/t14-,18+;/m0./s1
Molecular Formula
C21H24F2N6O6S
HBD / HBA
4 / 11
Liaisons Rotatives
3
Atomes Lourds
36
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.
Foire aux questions
The sulfate salt form of larotrectinib, a TRK kinase inhibitor used to treat cancers with NTRK gene fusions including colorectal and breast cancers. It shares the same tumor-agnostic mechanism as the parent compound.
Yes, Larotrectinib 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). CHEMBL3989939. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 67330085. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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