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Drug Targets
🎯 Drug Targets
Browse 6 drug targets with druggability analysis, composite scores, and clinical context
6
Targets
0
High Druggability
0.60
Avg Score
15
Target Classes
Druggability Distribution
High:
0
Medium:
0
Low:
6
Unknown:
0
Avg druggability score:
0.404
Clinical Pipeline
Approved:
2
Phase III:
2
Phase II:
2
Phase I:
0
Preclinical:
0
Total compounds:
14
· Approved:
0
Search
Class
All Classes
Enzyme
(35)
Signaling Protein
(25)
Structural Protein
(17)
Protein
(16)
Gpcr
(13)
Ion Channel
(12)
Transcription Factor
(11)
Receptor
(11)
Ligand
(10)
Transporter
(8)
Epigenetic Regulator
(8)
Kinase
(7)
Protease
(4)
Other
(4)
Chaperone
(4)
Druggability
All Druggability
Low
(100)
Medium
(62)
High
(14)
Undruggable
(6)
other
(3)
Sort
Score
Druggability
Gene A-Z
Market Price
Filtered by: class=receptor, druggability=Low — 6 results
TFR1
Transferrin receptor protein 1
Phase 4
Receptor
Low Druggability
Score
0.66
Drug.
0.44
Safety
0.50
Drugs
2
Hyps
4
Papers
34
Monoclonal antibodies targeting receptor or iron chelation affecting iron uptake
TLR4
Toll-like receptor 4
Phase 3
Receptor
Low Druggability
Score
0.66
Drug.
0.41
Safety
0.30
Drugs
1
Hyps
6
Papers
0
Small molecule antagonist or antibody blocking TLR4-mediated neuroinflammatory signaling
TREM2
Triggering receptor expressed on myeloid cells 2
Phase 2
Receptor
Low Druggability
Score
0.65
Drug.
0.42
Safety
0.60
Drugs
4
Hyps
35
Papers
25
Agonist antibodies that enhance TREM2 signaling to promote microglial function
SDC1
Syndecan-1
Phase 2
Receptor
Low Druggability
Score
0.58
Drug.
0.38
Safety
0.60
Drugs
1
Hyps
1
Papers
26
Small molecule modulation of heparan sulfate interactions or shedding
LRP1
LDL receptor related protein 1
Phase 3
Receptor
Low Druggability
Score
0.53
Drug.
0.39
Safety
0.40
Drugs
2
Hyps
12
Papers
51
Modulation of receptor-mediated endocytosis and clearance pathways
IGF2R
Insulin-like growth factor 2 receptor
Phase 4
Receptor
Low Druggability
Score
0.50
Drug.
0.39
Safety
0.40
Drugs
4
Hyps
1
Papers
28
Drugs targeting IGF2R typically work by blocking IGF2 binding and signaling through the IGF1R/IGF2R axis, thereby inhibiting mitogenic and anti-apoptotic effects in cancer cells. Alternatively, agents may enhance IGF2 clearance through IGF2R-mediated endocytosis to reduce circulating IGF2 levels and downstream signaling.