1. Antibody-drug Conjugate/ADC Related Protein Tyrosine Kinase/RTK Apoptosis
  2. Antibody-Drug Conjugates (ADCs) VEGFR Apoptosis
  3. Bevacizumab vedotin

Bevacizumab vedotin is an antibody-drug conjugate (ADC). Bevacizumab vedotin blocks the VEGF/VEGFR pathway to exert anti-angiogenic effects. Bevacizumab vedotin exhibits anti-proliferative effects on cancer cells, promotes cancer cell apoptosis (Apoptosis), induces cancer cell cycle arrest, and possesses anti-migratory activity against breast cancer cells. Bevacizumab vedotin can be used in research related to glioma, hepatocellular carcinoma, and breast cancer.

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Bevacizumab vedotin

Bevacizumab vedotin Chemical Structure

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Description

Bevacizumab vedotin is an antibody-drug conjugate (ADC). Bevacizumab vedotin blocks the VEGF/VEGFR pathway to exert anti-angiogenic effects. Bevacizumab vedotin exhibits anti-proliferative effects on cancer cells, promotes cancer cell apoptosis (Apoptosis), induces cancer cell cycle arrest, and possesses anti-migratory activity against breast cancer cells. Bevacizumab vedotin can be used in research related to glioma, hepatocellular carcinoma, and breast cancer[1].

In Vitro

Bevacizumab vedotin (1 mg; 72-120 h) exhibits high serum stability[1].
Bevacizumab vedotin (30-165 min) rapidly and completely releases its MMAE payload under the mediation of cathepsin B[1].
Bevacizumab vedotin (0-10 μg/mL; 48 h) potently inhibits the proliferation of U87, HepG2 and MCF-7 cells, with IC50 values of 14.1712 μg/mL, 0.6483 μg/mL and 0.1442 μg/mL, respectively[1].
Bevacizumab vedotin (1 μg/mL; 48 h) induces apoptosis in U87, HepG2 and MCF-7 cells after 48 h of treatment[1].
Treatment with Bevacizumab vedotin (0.1-20 μg/mL; 48 h) induces G1-phase cell cycle arrest in U87 and HepG2 cells[1].
Bevacizumab vedotin (0.01-0.1 μg/mL; 12-48 h) inhibits the migration of MCF-7 cells in a concentration- and time-dependent manner, and downregulates the expression of VEGF-A in MCF-7 cells[1].
Bevacizumab vedotin (0.1-1 μg/mL; 4-48 h) exhibits anti-angiogenic activity, reduces tube formation (junctions and branches) in HUVECs, downregulates VEGF-A expression, and upregulates VEGFR-2 expression in HUVECs[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Proliferation Assay[1]

Cell Line: U87 , HepG2 , MCF-7 cells
Concentration: 0, 0.01, 0.05, 0.1, 0.2, 0.5, 1, 5, 10 μg/mL
Incubation Time: 48 h
Result: Inhibited proliferation of all three cell lines.
Reached an IC50 of 14.1712 μg/mL for U87 cells.
Reached an IC50 of 0.6483 μg/mL for HepG2 cells.
Reached an IC50 of 0.1442 μg/mL for MCF-7 cells.

Apoptosis Analysis[1]

Cell Line: U87 , HepG2 , MCF-7 cells
Concentration: 1 μg/mL
Incubation Time: 48 h
Result: Promoted apoptosis in all three cell lines.
Achieved a pro-apoptotic rate of 113% relative to the control group for U87 cells.
Achieved a pro-apoptotic rate of 304% relative to the control group for HepG2 cells.
Achieved a pro-apoptotic rate of 288% relative to the control group for MCF-7 cells.

Cell Cycle Analysis[1]

Cell Line: U87 , HepG2 cells
Concentration: 0.1-20 μg/mL
Incubation Time: 48 h
Result: Induced G1 phase cell cycle arrest in U87 and HepG2 cells.

Cell Migration Assay [1]

Cell Line: MCF-7 cells
Concentration: 0, 0.01, 0.02, 0.05, 0.1 μg/mL
Incubation Time: 0 h, 12 h, 24 h, 36 h and 48 h
Result: Enhanced concentration-dependent inhibition of MCF-7 cell migration with increasing incubation time.

Western Blot Analysis[1]

Cell Line: MCF-7 cells
Concentration: 0.01, 0.05, 0.1 μg/mL
Incubation Time: 48 h
Result: Caused concentration-dependent downregulation of VEGF-A expression in MCF-7 cells.

Western Blot Analysis[1]

Cell Line: HUVEC cells
Concentration: 0.1, 0.5, 1 μg/mL
Incubation Time: 48 h
Result: Caused concentration-dependent downregulation of VEGF-A expression in HUVEC cells.
Caused concentration-dependent upregulation of VEGFR-2 expression in HUVEC cells.
Molecular Weight

149114 (average)

Appearance

Liquid

Color

Colorless to light yellow

SMILES

[Bevacizumab vedotin]

Shipping

Shipping with dry ice.

Storage

-80°C, protect from light

Purity & Documentation
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Bevacizumab vedotin
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