1. Antibody-drug Conjugate/ADC Related Protein Tyrosine Kinase/RTK
  2. Antibody-Drug Conjugates (ADCs) TAM Receptor
  3. Mecbotamab vedotin

Mecbotamab vedotin  (Synonyms: BA3011; CAB-Axl-ADC; CAB-anti-Axl-ADC)

Cat. No.: HY-145622
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Mecbotamab vedotin (BA3011) is a pH dependent antibody drug conjugate (ADC) targeting AXL. Mecbotamab vedotin can significantly inhibit AXL in DU145 cells and LCLC-103H cells and kills cells. Mecbotamab vedotin can be used for research on cancer such as lung cancer, pancreatic cancer and prostate cancer. The antibody component is Mecbotamab (HY-P9988), and the ADC toxin molecule is Vedotin (HY-15162).

For research use only. We do not sell to patients.

Mecbotamab vedotin

Mecbotamab vedotin Chemical Structure

CAS No. : 2460400-64-8

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Description

Mecbotamab vedotin (BA3011) is a pH dependent antibody drug conjugate (ADC) targeting AXL. Mecbotamab vedotin can significantly inhibit AXL in DU145 cells and LCLC-103H cells and kills cells. Mecbotamab vedotin can be used for research on cancer such as lung cancer, pancreatic cancer and prostate cancer. The antibody component is Mecbotamab (HY-P9988), and the ADC toxin molecule is Vedotin (HY-15162)[1].

IC50 & Target

AXL; BA301 γ1[1]

In Vitro

Mecbotamab vedotin (0.1-10000 ng/mL) efficiently binds to AXL at pH 6.0 in DU145 cells (EC50 = 16 ng/mL), LCLC-103H cells (EC50 = 37 ng/mL), 293-huAXL (EC50 = 56 ng/mL) and 293-cynoAXL (EC50 = 20 ng/mL)[1].
Mecbotamab vedotin (0.01-10000 ng/mL, 3 days) exhibits significant cytotoxicity at pH 6.0 in DU145 cells (IC50 = 1466 ng/mL) and LCLC-103H cells (IC50 = 474 ng/mL) but is non-toxic to 293-F cells[1].

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

Cell Cytotoxicity Assay[1]

Cell Line: DU145 cells, LCLC-103H cells and 293-F cells
Concentration: 0.01-10000 ng/mL
Incubation Time: 3 days
Result: Significantly killed the DU145 cells (IC50 = 1466 ng/mL) and LCLC-103H cells (IC50 = 474 ng/mL) at pH 6.0.
Effectively killed the DU145 cells (IC50 = 5069 ng/mL) and LCLC-103H cells (IC50 = 1095 ng/mL) at pH 7.4.
Had no significant toxicity to 293-F cells.
In Vivo

Mecbotamab vedotin (1-6 mg/kg, i.v., once every 4 days, for 6 times) significantly inhibits tumor growth in female NOD/SCID mice bearing LCLC-103H tumors[1].
Mecbotamab vedotin (1-10 mg/kg, i.v., once every 4 days, for 4 times) significantly inhibits tumor growth in female NOD/SCID mice bearing MIA PaCa-2 tumors[1].
Mecbotamab vedotin (6-15 mg/kg, i.v., once every 4 days, for 6 times) significantly delayed tumor growth in male BALB/c nude mice bearing DU145 tumors[1].

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

Animal Model: 1×106 LCLC-103H cells injected female NOD/SCID mice[1]
Dosage: 1, 3 and 6 mg/kg
Administration: Intravenous injection (i.v.), once every 4 days, for 6 times
Result: Significantly inhibited tumor growth (TGI range of 114-115%) and the efficacy of the 3 and 6 mg/kg groups persisted until 57 days.
Animal Model: 1×106 MIA PaCa-2 cells injected female NOD/SCID mice[1]
Dosage: 1, 3, 6 and 10 mg/kg
Administration: Intravenous injection (i.v.), once every 4 days, for 4 times
Result: Resulted in a TGI of 59% in the 6 mg/kg group and complete tumor regression in the 10 mg/kg group.
Animal Model: 5×106 DU145 cells injected female NOD/SCID mice[1]
Dosage: 6, 10 and 15 mg/kg
Administration: Intravenous injection (i.v.), once every 4 days, for 6 times
Result: Showed persistent anti-tumor activity in the 10 and 15 mg/kg groups.
Clinical Trial
CAS No.
Appearance

Liquid

Color

Colorless to light yellow

SMILES

[Mecbotamab 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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