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Chemical Structure| 917111-44-5 Chemical Structure| 917111-44-5

Structure of Lexibulin
CAS No.: 917111-44-5

Chemical Structure| 917111-44-5

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Lexibulin can potently inhibit microtubule polymerization with vascular-disrupting, and potential antineoplastic activities.

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Product Details of Lexibulin

CAS No. :917111-44-5
Formula : C24H30N6O2
M.W : 434.53
SMILES Code : O=C(NC1=CC=C(C2=NC=C(C)C(N[C@H](C3=CC=CN=C3)CCC)=N2)C=C1OC)NCC
MDL No. :MFCD18206787
InChI Key :MTJHLONVHHPNSI-IBGZPJMESA-N
Pubchem ID :11351021

Safety of Lexibulin

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

Related Pathways of Lexibulin

cytoskeleton

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
MG63 0, 20, 40, 80, 160, 320 nM 24 and 48 h CYT997 significantly inhibits OS cell proliferation and induces apoptosis and autophagy. PMC6357486
U2OS 0, 20, 40, 80, 160, 320 nM 24 and 48 h CYT997 significantly inhibits OS cell proliferation and induces apoptosis and autophagy. PMC6357486
SJSA 0, 20, 40, 80, 160, 320 nM 24 and 48 h CYT997 significantly inhibits OS cell proliferation and induces apoptosis and autophagy. PMC6357486
143B 0, 20, 40, 80, 160, 320 nM 24 and 48 h CYT997 significantly inhibits OS cell proliferation and induces apoptosis and autophagy. PMC6357486
HeLa S3 cells 50 µM 5 min Measurement of Lexibulin uptake in ENT1 and ENT2 cells showed that Lexibulin is a nontransported inhibitor of ENT1, and in ENT2 cells, Lexibulin uptake increased in the presence of NBMPR, indicating it is also a nontransported inhibitor of ENT2 PMC7816041

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
BALB/c-nu mice 143B osteosarcoma xenograft model Intraperitoneal injection 15 mg/kg Once daily for 28 days CYT997 significantly inhibits tumor growth, and the combination with 3-MA enhances the anti-tumor effect. PMC6357486

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.30mL

0.46mL

0.23mL

11.51mL

2.30mL

1.15mL

23.01mL

4.60mL

2.30mL

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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