Drug intelligence / Profile preview

BB3103

Development stage
Discontinued
Lead developer
British Biotech
Modality
Small Molecules
Administration
Intratumoral, Parenteral
01

Overview

BB3103 is a synthetic, water-soluble, broad-spectrum hydroxamic acid-based metalloproteinase inhibitor originally developed by British Biotech. It acts as a potent inhibitor of matrix metalloproteinases (MMPs), including MMP-1, MMP-2, MMP-3, MMP-7, MMP-9, MMP-12, MMP-13, and MMP-14, as well as a disintegrin and metalloproteinase (ADAM) family proteins, particularly ADAM10 and ADAM17 (TACE). BB3103 has been widely used in preclinical research to study the role of metalloproteinases in processes such as tumor invasion, metastasis, angiogenesis, wound healing, and ectodomain shedding of cell surface proteins (e.g., TNF-alpha, APP, and L1). Development of BB3103 for cancer was discontinued in the preclinical stage.

02

Targets

MMP-2 (Matrix metalloproteinase-2)MMP3 (Matrix metalloproteinase-3)ADAM10 (Disintegrin and metalloproteinase domain-containing protein 10)MMP1 (Matrix metalloproteinase-1)MMP7 (Matrix metallopeptidase 7)ADAM17 (A disintegrin and metalloprotease 17)MMP14 (Matrix metalloproteinase 14)MMP12 (Macrophage Metalloelastase)MMP13 (Matrix metalloproteinase-13)MMP9 (Matrix metalloproteinase-9)

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