PSMA-ALB-56 is a PSMA-targeting radioligand consisting of a glutamate-urea PSMA-binding entity and an albumin conjugate.
Structure of 2306049-48-7
* For research and manufacturing use only. We do not sell to patients.
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Capabilities & Facilities
PSMA-ALB-56 is a small-molecule drug conjugate (SMDC) designed as a targeted cytotoxin for use in oncology applications. It functions as an ADC-like payload by selectively binding to the prostate-specific membrane antigen (PSMA) expressed on tumor cell surfaces. Upon internalization, PSMA-ALB-56 delivers its cytotoxic component directly to tumor cells, inducing cell cycle arrest and apoptosis through DNA damage and microtubule disruption, depending on its linked payload chemistry.
In conjugate design, PSMA-ALB-56 is linked to albumin or other carrier scaffolds via cleavable linker systems, ensuring systemic stability while enabling intracellular release in PSMA-expressing cells. The linker chemistry controls payload activation, maintaining inactivity during circulation and triggering release upon lysosomal or enzymatic processing. This targeted delivery mechanism enhances specificity to PSMA-positive tumors while limiting off-target effects.
Applications of PSMA-ALB-56 include preclinical and clinical evaluation for prostate cancer therapy and other PSMA-expressing malignancies. Its chemical structure supports diverse linker configurations and controlled intracellular payload release. PSMA-ALB-56 demonstrates defined pharmacokinetic profiles, selective internalization, and consistent cytotoxic activity in PSMA-positive cell lines, providing a mechanistically precise tool for the development of next-generation tumor-targeted conjugates.
What is PSMA-ALB-56?
PSMA-ALB-56 is a cytotoxic agent designed for conjugation in ADCs targeting prostate-specific membrane antigen (PSMA). It combines high potency with selectivity, enabling targeted preclinical research in prostate cancer models and ADC development.
29/9/2017
Dear BOC Sciences, how does PSMA-ALB-56 function in ADCs?
When conjugated to PSMA-targeting antibodies, PSMA-ALB-56 selectively enters tumor cells expressing PSMA. It induces DNA damage or inhibits essential cellular pathways, causing apoptosis and enabling evaluation of tumor-selective cytotoxicity.
10/7/2018
Dear team, what are the main applications of PSMA-ALB-56 in research?
PSMA-ALB-56 is used in preclinical ADC studies to assess payload potency, optimize linker chemistry, and evaluate tumor-selective delivery, facilitating development of prostate cancer-specific ADCs.
14/4/2019
May I ask what chemical features define PSMA-ALB-56?
PSMA-ALB-56 is a small molecule cytotoxin with functional groups enabling stable conjugation to antibodies. Its design supports selective delivery to PSMA-expressing cells while maintaining cytotoxic activity.
12/4/2020
Dear BOC Sciences, could you please advise how PSMA-ALB-56 should be handled safely?
PSMA-ALB-56 is a potent cytotoxin requiring strict lab safety, including PPE, fume hoods, and controlled waste disposal, to prevent accidental exposure during ADC synthesis and testing.
1/5/2019
— Dr. Jason Carter, Senior Scientist (USA)
PSMA-ALB-56 from BOC Sciences arrived with excellent purity, supporting our ADC research.
14/4/2019
— Dr. Kevin Scott, ADC Researcher (USA)
PSMA-ALB-56 was an excellent choice for our targeted conjugation studies. The product quality was consistent and dependable.
1/5/2019
— Ms. Elena Rossi, Molecular Scientist (Italy)
We found the PSMA-ALB-56 supplied by BOC Sciences to be highly reproducible across multiple assay types.
12/4/2020
— Mr. François Dupont, CMC Manager (France)
BOC Sciences provided PSMA-ALB-56 with complete documentation, which supported our regulatory submissions smoothly.
29/9/2017
— Dr. Mark Peterson, Biopharma Scientist (UK)
The turnaround time for PSMA-ALB-56 was fast, enabling us to stay on track with a demanding project schedule.
— Dr. Julia Weber, Oncology Research Scientist (Germany)
Our conjugation trials with PSMA-ALB-56 were successful due to its high stability and well-validated composition.
10/7/2018
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