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Expanding GOSTARᵀᴹ TPD with 10K+ New Degraders for Smarter Drug Design and Strategic Decisions

Between April and July 2025, the GOSTARᵀᴹ TPD database added 20% more content. More than 10,000 new degrader structures were added with 70,000 structure-activity relationships. Additionally, GOSTARᵀᴹ TPD substantially expanded its ADMET data, as well as new coverage for modality and ligase. The update helps support degrader design, IP analysis, and target-ligase prioritization.

GOSTARᵀᴹ TPD database content growth summary

Metric April, 2025 July, 2025 Growth (Q1–Q2)
Unique Structures 51,023 61,312 +10,289
Structure-Activity Relationships (SAR) 152,773 223,645 +70,872
Bivalent Degraders 33,932 42,773 +8,841
Monovalent Degraders 5,371 7,240 +1,869
ADMET Data Points 8,816 37,305 +28,489
Patents 408 1,522 +1,114
Journal Articles 158 4,754 +4,596
Other Data Source 21 220 +199

Newly covered degrader types

  • Antibody-targeted chimeras – ATACs
  • Regulated induced proximity targeting chimeras – RIPTACs
  • Covalent degraders

Newly curated E3 ligases

  • DDB1 And CUL4 Associated Factor 16 (DCAF16)
  • Beta-transducin repeats-containing proteins (β-TrCP)
  • Adhesion-regulating molecule 1 (ADRM1)
  • Baculoviral IAP repeat-containing protein 2 (BIRC2)

Value to our users

This content release extends GOSTARᵀᴹ TPDs coverage in ways that support both design and strategy. New ADMET profiles help guide the selection of compounds for further development. Latest patent coverage improves visibility into competitive and IP landscapes. The updated dataset also supports SAR-based design and machine learning applications.

Try It yourself

Log in to your GOSTARᵀᴹ TPD account to explore the latest data, or contact our team for access to high-quality curated degrader datasets.

More innovations coming soon—stay tuned!

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