1. Antibody-drug Conjugate/ADC Related Immunology/Inflammation
  2. ADC Antibody TROP2
  3. Sacituzumab (powder)

Sacituzumab (powder) is a humanized IgG1 monoclonal antibody targeting Trophoblast cell surface antigen 2 (TROP2). Sacituzumab (powder) demonstrates a lack of antitumor effects alone and does not inhibit the function of TROP-2 during tumor metastasis, binding to the linear epitopes of TROP-2 protein. Sacituzumab (powder) can be used for the synthesis of antibody-drug conjugates (ADC) drug Sacituzumab govitecan (HY-132254). Sacituzumab govitecan can be used in the field of triple-negative breast cancer.

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

Sacituzumab (powder) Chemical Structure

Sacituzumab (powder) Chemical Structure

CAS No. : 1796566-95-4

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Description

Sacituzumab (powder) is a humanized IgG1 monoclonal antibody targeting Trophoblast cell surface antigen 2 (TROP2). Sacituzumab (powder) demonstrates a lack of antitumor effects alone and does not inhibit the function of TROP-2 during tumor metastasis, binding to the linear epitopes of TROP-2 protein. Sacituzumab (powder) can be used for the synthesis of antibody-drug conjugates (ADC) drug Sacituzumab govitecan (HY-132254). Sacituzumab govitecan can be used in the field of triple-negative breast cancer[1][2][3][4].

In Vitro

Sacituzumab (0.5 nM, 800 s) possesses non-competitive binding sites and recognized distinct epitopes of TROP-2 on the antigen. Additionally, the binding to cancer cell lines activities of Sacituzumab and hIMB1636 is similar[1].
Sacituzumab (5 mg/mL, 48 h) binds to a linear epitope within TROP-2, which might not interrupt the assembly of TROP-2 molecules on the cell surface in HEK-293T cells[2].

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

Cell Viability Assay[2]

Cell Line: HEK-293T cells
Concentration: 5 mg/mL
Incubation Time: 48 h
Result: Bound to the linear epitopes of denatured TROP-2 proteins in HEK 293T cells.
In Vivo

Sacituzumab (50 mg/kg, i.v., every 5 days for four times) exhibits a weak antitumor effect without significant weight loss in MDA-MB-468 xenograft mouse model[1].

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

Animal Model: MDA-MB-468 xenograft model of 6-week-old female BALB/c nude mice[1]
Dosage: 50 mg/kg
Administration: i.v., intervals of 5 days and repeated a total of four times
Result: Decreased the tumor inhibition rate to 29.1% at 50 mg/kg in MDA-MB-468 xenograft model.
Molecular Weight

145.52 kDa

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[Sacituzumab (powder)]

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    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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Sacituzumab (powder)
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HY-P99045A
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