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Chemical Structure| 1020172-07-9 Chemical Structure| 1020172-07-9

Structure of Rebastinib
CAS No.: 1020172-07-9

Chemical Structure| 1020172-07-9

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DCC-2036 is a conformational control Bcr-Abl inhibitor for Abl1 (WT) and Abl1 (T315I) with IC50 of 0.8 nM and 4 nM, also inhibits SRC, LYN, FGR, HCK, KDR, FLT3, and Tie-2.

Synonyms: DCC-2036

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Product Details of Rebastinib

CAS No. :1020172-07-9
Formula : C30H28FN7O3
M.W : 553.59
SMILES Code : O=C(NC)C1=NC=CC(OC2=CC=C(NC(NC3=CC(C(C)(C)C)=NN3C4=CC=C5N=CC=CC5=C4)=O)C(F)=C2)=C1
Synonyms :
DCC-2036
MDL No. :MFCD19443646
InChI Key :WVXNSAVVKYZVOE-UHFFFAOYSA-N
Pubchem ID :25066467

Safety of Rebastinib

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

Related Pathways of Rebastinib

RTK

Isoform Comparison

Biological Activity

Target
  • Abl

    p-Abl1 (native), IC50:0.75 nM

    u-Abl1 (T315I), IC50:5 nM

In Vitro:

Cell Line
Concentration Treated Time Description References
HBMVECs 1 μM Rebastinib inhibited CCM3 loss-induced EC sprouting and lumen formation PMC7835246
HeLa cells 10 μM Evaluated the selectivity of Rebastinib on kinases in HeLa cells, finding that 86% of kinases were efficiently competed PMC10072906
HEK 293 cells 0.5 μM 4 h Rebastinib does not hinder ligand-induced stimulation of ErbB1, ErbB2, and ErbB4 in HEK 293 cells. PMC10337807
HBMVECs 1 μM Rebastinib inhibited the increased EC sprouting and lumen formation induced by CCM3 knockdown, restoring normal vascular structure. PMC7835246
TIE-2+ M-MDSC 5 nM Rebastinib effectively restored the IFN-γ production by tumor-specific T cells inactivated by ANGPT2 exposition. PMC9353943
HUVECs 0.058 nM Inhibition of Ang1-stimulated Tie2 kinase activity PMC5669998
EA.hy926 0.091 nM Inhibition of Ang1-stimulated Tie2 kinase activity PMC5669998
iBMM Tie2Hi 0.26 nM Inhibition of Tie2 phosphorylation PMC5669998
CHO 2.0 nM Inhibition of Tie2 activity PMC5669998

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice Breast cancer model Oral 10 mg/kg Twice per week for 4 weeks Rebastinib inhibits TMEM doorway function, reducing TMEM Activity-MRI PMC9440218
Mouse Pdcd10BECKO mouse model Subcutaneous injection 10 μg/g Daily injection from P4 to P14, then weekly injection from P15 to P60 Rebastinib significantly reduced the number and size of CCM lesions and restored EC-pericyte interactions PMC7835246
mice Pdcd10BECKO mouse model subcutaneous injection 10 μg/g daily from P4 to P14, or daily from P8 to P18, and weekly from P19 to P60 Rebastinib significantly reduced the number and size of CCM lesions, restored EC-pericyte interactions, and improved vascular integrity. PMC7835246
Mouse MMTV-PyMT mouse mammary tumor model Oral 10 mg/kg Daily for 4 weeks Inhibition of tumor growth, metastasis, and extension of survival PMC5669998

Clinical Trial:

NCT Number Conditions Phases Recruitment Completion Date Locations
NCT00827138 Chronic Myeloid Leukemia PHASE1 COMPLETED 2025-01-13 City of Hope, Duarte, Californ... More >>ia, 91010, United States|H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida, 33612, United States|Emory University, Atlanta, Georgia, 30322, United States|University of Chicago, Chicago, Illinois, 60637, United States|The University of Kansas Cancer Center, Kansas City, Kansas, 66160, United States|Sidney Kimmel Cancer Center at Johns Hopkins, Baltimore, Maryland, 21287, United States|Tufts Medical Center, Boston, Massachusetts, 02111, United States|University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan, 48109, United States|MD Anderson Cancer Center, Houston, Texas, 77030, United States|Medical College of Wisconsin, Milwaukee, Wisconsin, 53226, United States Less <<

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.81mL

0.36mL

0.18mL

9.03mL

1.81mL

0.90mL

18.06mL

3.61mL

1.81mL

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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