1. Immunology/Inflammation
  2. CD276/B7-H3
  3. Omburtamab

Omburtamab is a humanized monoclonal antibody targeting B7-H3 (CD276). Omburtamab selectively binds to B7-H3 highly expressed on the surface of tumor cells and activates anti-tumor immune responses mediated by T cells and natural killer (NK) cells. Omburtamab can promote the specific infiltration of CAR-T cells into tumors, enhance the killing function of NK cells through the CD16 signaling pathway, and regulate tumor cell glucose metabolism (such as inhibiting the Warburg effect). Omburtamab has the potential to inhibit solid tumors such as non-small cell lung cancer (NSCLC).

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CAS No. : 1895083-75-6

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Based on 1 publication(s) in Google Scholar

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Description

Omburtamab is a humanized monoclonal antibody targeting B7-H3 (CD276). Omburtamab selectively binds to B7-H3 highly expressed on the surface of tumor cells and activates anti-tumor immune responses mediated by T cells and natural killer (NK) cells. Omburtamab can promote the specific infiltration of CAR-T cells into tumors, enhance the killing function of NK cells through the CD16 signaling pathway, and regulate tumor cell glucose metabolism (such as inhibiting the Warburg effect). Omburtamab has the potential to inhibit solid tumors such as non-small cell lung cancer (NSCLC)[1][2].

Isotype

Human IgG1(K214R) kappa

Recommend Isotype Controls
Species

Human

In Vitro

Omburtamab (anti-B7-H3 mAb, 8H9) (100 nM; 24 h) significantly inhibits the viability of B7-H3-positive tumor cells (such as A549 and HCT116) and induces cell apoptosis in vitro, and can enhance natural killer cell-mediated tumor cell lysis[1].

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

Cell Viability Assay[1]

Cell Line: A549, HCT 116, OVCAR-3, SK-OV-3, DLD-1, BT-474
Concentration: 100 nM
Incubation Time: 24 h
Result: Significantly reduced cell viability in B7-H3-positive tumor cell lines, with a dose-dependent decrease in metabolic activity compared to control groups.

Cell Cytotoxicity Assay[1]

Cell Line: A549, HCT 116, OVCAR-3, SK-OV-3, DLD-1, BT-474
Concentration: 100 nM
Incubation Time: 24 h
Result: Resulted a notable increase in apoptosis (Annexin V+/7-AAD+ cells) in A549 and HCT 116 cells, indicating caspase-dependent cell death induction.

Cell Cytotoxicity Assay[1]

Cell Line: A549, HCT 116, OVCAR-3, SK-OV-3, DLD-1, BT-474
Concentration: 100 nM
Incubation Time: 24 h
Result: Co-culture with peripheral blood mononuclear cells (PBMCs) revealed enhanced cytotoxicity against target cells, with specific lysis ratios increasing by 30–50% compared to untreated controls, mediated by CD16 signaling activation.
In Vivo

Omburtamab is derived into B7-H3 CAR and B7-H3/CD16 BiKE antibodies. B7-H3 CAR and B7-H3/CD16 BiKE (100 μg/mouse; intravenous injection; twice a week; a total of 4 times) significantly inhibit tumor growth and prolong mouse survival in NOD/SCID mouse subcutaneous transplantation non-small cell lung cancer (A549) and colorectal cancer (HCT 116) models without obvious systemic toxicity[1].

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

Clinical Trial
Molecular Weight

144980.00

CAS No.
Appearance

Liquid

Color

Colorless to light yellow

SMILES

[Omburtamab]

Shipping

Shipping with dry ice.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Format
  • IgG1-kappa
Purity & Documentation

Purity: 98.27%

References
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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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Omburtamab
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HY-P99157
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