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Chemical Structure| 1802220-02-5 Chemical Structure| 1802220-02-5

Structure of Repotrectinib
CAS No.: 1802220-02-5

Chemical Structure| 1802220-02-5

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TPX-0005 is a potent ALK/ROS1/TRK inhibitor, with IC50 of 5.3 nM, 1.01 nM, 1.26 nM and 1.08 nM for SRC, WT ALK, ALK G1202R and ALK L1196M, respectively.

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Product Details of Repotrectinib

CAS No. :1802220-02-5
Formula : C18H18FN5O2
M.W : 355.37
SMILES Code : O=C1NC[C@H](C)OC2=CC=C(F)C=C2[C@@H](C)NC3=NC4=C1C=NN4C=C3
MDL No. :MFCD31544350
InChI Key :FIKPXCOQUIZNHB-WDEREUQCSA-N
Pubchem ID :135565923

Safety of Repotrectinib

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of Repotrectinib

RTK

Isoform Comparison

Biological Activity

Target
  • Src

    Src, IC50:5.3 nM

  • ALK

    ALK(G1202R), IC50:1.26 nM

    ALK(L1196M), IC50:1.01 nM

In Vitro:

Cell Line
Concentration Treated Time Description References
KM12SM cells 1 μM 72 h KM12SM cells were sensitive to repotrectinib, IC50 of 1.2 nM Cancer Sci. 2022 Jul;113(7):2323-2335.
IRC and KM12 cells 1-5000 nM 72 hours To assess the effect of Selpercatinib on the growth inhibition and TRK-mediated signaling in NTRK fusion-positive tumor cells. Results showed that Selpercatinib significantly inhibited tumor cell growth and TRK signaling. Br J Cancer. 2024 Aug;131(3):601-610.
Ba/F3_G595R cells 1 μM 72 h Ba/F3_G595R cells were sensitive to repotrectinib Cancer Sci. 2022 Jul;113(7):2323-2335.
Ba/F3_WT cells 1 μM 72 h Ba/F3_WT cells were sensitive to repotrectinib Cancer Sci. 2022 Jul;113(7):2323-2335.
M3B cells 1 μM 72 h M3B cells were resistant to repotrectinib, IC50 of 295.7 nM Cancer Sci. 2022 Jul;113(7):2323-2335.
YU1079 0.097 μM 72 h To evaluate the anti-tumor activity of Repotrectinib in crizotinib-resistant ROS1 G2032R mutation models, results showed that Repotrectinib significantly inhibited the growth of YU1079 cells. Clin Cancer Res. 2020 Jul 1;26(13):3287-3295.
YU1078 0.021 µM 72 h To evaluate the anti-tumor activity of Repotrectinib in treatment-naïve ROS1-rearranged NSCLC models, results showed that Repotrectinib significantly inhibited the growth of YU1078 cells. Clin Cancer Res. 2020 Jul 1;26(13):3287-3295.
SK-N-BE 510.8 ± 16.94 nM 5 days Repotrectinib has a weaker inhibitory effect on the proliferation of non-ALK-addicted neuroblastoma cells SK-N-BE. Sci Rep. 2019 Dec 18;9(1):19353.
SK-N-AS 594.8 ± 47.3 nM 5 days Repotrectinib has a weaker inhibitory effect on the proliferation of non-ALK-addicted neuroblastoma cells SK-N-AS. Sci Rep. 2019 Dec 18;9(1):19353.
Kelly 310.9 ± 7.9 nM 5 days Repotrectinib inhibits proliferation of ALK-addicted neuroblastoma cells and reduces phosphorylation levels of pY1604-ALK, pERK5, pSTAT3, p-p70 S6K, pAKT, and pERK. Sci Rep. 2019 Dec 18;9(1):19353.
CLB-GE 259.4 ± 6.3 nM 5 days Repotrectinib inhibits proliferation of ALK-addicted neuroblastoma cells and reduces phosphorylation levels of pY1604-ALK, pERK5, pSTAT3, p-p70 S6K, pAKT, and pERK. Sci Rep. 2019 Dec 18;9(1):19353.
CLB-BAR 124.1 ± 4.89 nM 5 days Repotrectinib inhibits proliferation of ALK-addicted neuroblastoma cells and reduces phosphorylation levels of pY1604-ALK, pERK5, pSTAT3, p-p70 S6K, pAKT, and pERK. Sci Rep. 2019 Dec 18;9(1):19353.
NIH-3T3-tv-a cells 100 nM 5 days To evaluate the growth inhibitory effect of Repotrectinib on TPM3-NTRK1-G595R mutant spheroids, results showed that Repotrectinib significantly inhibited the growth of mutant spheroids. Cell Rep. 2024 Oct 22;43(10):114829.
NIH-3T3-tv-a cells 100 nM 5 days To evaluate the growth inhibitory effect of Repotrectinib on TPM3-NTRK1-F589L mutant spheroids, results showed that Repotrectinib significantly inhibited the growth of mutant spheroids. Cell Rep. 2024 Oct 22;43(10):114829.
NIH-3T3-tv-a cells 100 nM 5 days To evaluate the growth inhibitory effect of Repotrectinib on NTRK fusion-driven spheroids, results showed that Repotrectinib significantly inhibited the growth of spheroids. Cell Rep. 2024 Oct 22;43(10):114829.
KM12 cells <0.03 nM 4 h Repotrectinib was the most potent inhibitor of TRKA autophosphorylation, with an IC50 value less than 0.03 nM. Mol Cancer Ther. 2021 Dec;20(12):2446-2456.
Ba/F3 cells <0.2 nM 72 h Repotrectinib showed the highest potency against wild-type TRKA, TRKB, and TRKC fusions, with IC50 values less than 0.2 nM. Mol Cancer Ther. 2021 Dec;20(12):2446-2456.
HCC78 ROS1L2026M 1 - 5000 nM 120 h To evaluate the inhibitory effect of Repotrectinib on ROS1L2026M mutant cells, results showed significant resistance of ROS1L2026M cells to Repotrectinib J Transl Med. 2024 Mar 3;22(1):234.
HCC78 ROS1G2032R 1 - 5000 nM 120 h To evaluate the inhibitory effect of Repotrectinib on ROS1G2032R mutant cells, results showed significant resistance of ROS1G2032R cells to Repotrectinib J Transl Med. 2024 Mar 3;22(1):234.

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice YU1078 xenograft model Oral 15 mg/kg Twice daily, for 21 days To evaluate the anti-tumor activity of Repotrectinib in the YU1078 xenograft model, results showed that Repotrectinib significantly inhibited tumor growth and delayed tumor recurrence. Clin Cancer Res. 2020 Jul 1;26(13):3287-3295.
Mice Neuroblastoma xenograft model Oral 20 mg/kg, twice daily Twice daily for 14 days Repotrectinib significantly inhibits tumor growth in a neuroblastoma xenograft model, with a tumor growth inhibition (TGI) of 87.07%, and animals gained weight. Sci Rep. 2019 Dec 18;9(1):19353.
Mice NTRK fusion-driven glioma models Intraperitoneal (i.p.) injection 20 mg/kg Twice a day for 25 hours To evaluate the therapeutic effect of Repotrectinib on NTRK fusion-driven gliomas, results showed that Repotrectinib significantly reduced p-ERK and p-S6 levels in tumor tissue and induced apoptosis. Cell Rep. 2024 Oct 22;43(10):114829.
Nude mice NIH3T3 LMNA–TRKA xenograft model Oral 3 mg/kg, 10 mg/kg, 30 mg/kg Twice daily, continuous treatment Repotrectinib demonstrated significant antitumor activity in the LMNA–TRKAG595R xenograft model, achieving 95% tumor growth inhibition, 19% tumor regression, and 46% tumor regression at doses of 3 mg/kg, 10 mg/kg, and 30 mg/kg, respectively. Mol Cancer Ther. 2021 Dec;20(12):2446-2456.
SHO mice Brain metastasis model Oral 15 mg/kg Daily, continuous treatment Single-agent repotrectinib treatment significantly inhibited tumor growth, and the combination with Gefitinib and Trametinib further prolonged mouse survival Cancer Sci. 2022 Jul;113(7):2323-2335.

Clinical Trial:

NCT Number Conditions Phases Recruitment Completion Date Locations
NCT06352528 Hepatic Impairment|Healthy Vol... More >>unteers Less << PHASE1 RECRUITING 2025-07-24 Local Institution - 0006, Miam... More >>i Lakes, Florida, 33014-2811, United States|Panax Clinical Research, Miami Lakes, Florida, 33014, United States|Local Institution - 0005, Orlando, Florida, 32809-3017, United States|Orlando Clinical Research Center, Orlando, Florida, 32809, United States|Local Institution - 0004, San Antonio, Texas, 78215, United States|Texas Liver Institute, San Antonio, Texas, 78215, United States Less <<
NCT06552234 NSCLC Stage IV|NSCLC, Stage II... More >>I Less << PHASE2 RECRUITING 1931-09-01 CH Aix-en-Provence, Aix-en-Pro... More >>vence, Bouches Du Rh?ne, France|AP-HM, Marseille, Bouches Du Rh?ne, France|HIA Sainte Anne, Toulon, Var, France|CHU Angers, Angers, France|CHU Bordeaux, Bordeaux, France|CHU Brest, Brest, France|Centre Fran?ois Baclesse, Caen, France|CH Chambéry, Chambéry, France|H?pitaux civils de Colmar, Colmar, France|CHI Créteil, Créteil, France|CHD Vendée, La Roche-sur-Yon, France|CHRU Lille, Lille, France|CHU Limoges, Limoges, France|Hospices Civils de Lyon, Lyon, France|CH Cornouaille, Quimper, France|CHU Rennes, Rennes, France|CHU Rouen, Rouen, France|H?pital Foch, Suresnes, France|CHU Toulouse, Toulouse, France|H?pitaux Nord-Ouest, Villefranche-sur-Sa?ne, France Less <<
NCT05926232 - AVAILABLE - -
NCT06315010 NSCLC|Brain Metastases|ROS1 Ge... More >>ne Rearrangement Less << PHASE2 NOT_YET_RECRUITING 2025-04-28 -

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.81mL

0.56mL

0.28mL

14.07mL

2.81mL

1.41mL

28.14mL

5.63mL

2.81mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

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