| Identification | Back Directory | [Name]
LOXO-101 (sulfate) | [CAS]
1223405-08-0 | [Synonyms]
LOX-101
Loxo-101（S）
LOX-101(sulfate)
ARRY 470) sulfate
LOXO-101 (sulfate)
Larotrectinib sulfate
Larotrectinib(LOXO 101
ARRY-470, Larotrectinib
Larotrectinib sulfate salt
Larotrectinib sulfate（LOXO101）
Larotrectinib (LOXO-101) sulfate
Larotrectinib/LOXO 101/ARRY 470 sulfate
(S)-N-(5-((R)-2-(2,5-difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide sulfate
(3S)-N-[5-[(2R)-2-(2,5-Difluorophenyl)-1-pyrrolidinyl]pyrazolo[1,5-a]pyrimidin-3-yl]-3-hydroxy-1-pyrrolidinecarboxamide sulfate
(3S)-N-[5-[(2R)-2-(2,5-Difluorophenyl)-1-pyrrolidinyl]pyrazolo[1,5-a]pyrimidin-3-yl]-3-hydroxy-1-pyrrolidinecarboxamide sulfate (1:1)
1-Pyrrolidinecarboxamide, N-[5-[(2R)-2-(2,5-difluorophenyl)-1-pyrrolidinyl]pyrazolo[1,5-a]pyrimidin-3-yl]-3-hydroxy-, (3S)-, sulfate (1:1) | [EINECS(EC#)]
232-655-5 | [Molecular Formula]
C21H22F2N6O2.H2SO4 | [MDL Number]
MFCD29472286 | [MOL File]
1223405-08-0.mol | [Molecular Weight]
526.52 |
| Chemical Properties | Back Directory | [storage temp. ]
Store at -20°C | [solubility ]
≥18.47 mg/mL in DMSO; ≥2.14 mg/mL in EtOH; ≥29.65 mg/mL in H2O | [form ]
solid | [Stability:]
Hygroscopic |
| Hazard Information | Back Directory | [Description]
LOXO-101 (sulfate) is an orally bioavailable, potent, ATP-competitive inhibitor of TRKA, TRKB, and TRKC. LOXO-101 has IC50 values in the low nanomolar range for inhibition of all three TRK family members in binding and cellular assays, with 100x selectivity over other kinases, and has shown acceptable pharmaceutical properties and safety in nonclinical models. The TRK family of neurotrophin receptors, TRKA, TRKB, and TRKC (encoded by NTRK1, NTRK2, and NTRK3 genes, respectively) and their neurotrophin ligands regulate growth, differentiation and survival of neurons. | [Uses]
Larotrectinib Sulfate is a potent and selective oral ATP-competitive inhibitor of tropomyosin receptor kinases (TRK). | [in vitro]
in previous study, loxo-101 was evaluated for off-target kinase enzyme inhibition against a panel of non-trk kinases at a concentration of 1,000 nm and atp concentrations around the km. results showed that loxo-101 had greater than 50% inhibition for only one non-trk kinase, which was tnk2 with ic50 of 576 nm. moreover, there were neither relevant herg inhibition nor prolonged qt observation [1]. | [in vivo]
animal study found that loxo-101 was able to inhibit in vivo tumor growth. athymic nude mice injected with km12 cells were orally treated with loxo-101 daily for 2 weeks, and dose-dependent tumor inhibition was observed, indicating the ability of loxo-101 to inhibit in-vivo tumor growth [1]. | [IC 50]
low nanomolar range for inhibition of all trk family members | [References]
[1] doebele rc et al. an oncogenic ntrk fusion in a patient with soft-tissue sarcoma with response to the tropomyosin-related kinase inhibitor loxo-101. cancer discov.2015 oct;5(10):1049-57. |
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