Start with myocardial infarction, then reuse UniProt P00750 as the stable protein anchor across project notes and exports.
CHEMBL1873 Target Snapshot
Tissue-type plasminogen activator · SINGLE PROTEIN · Homo sapiens
Research home keeps recent targets
This target will appear in recent viewed items on this browser. Use the demo workspace to preview watch rules and decision queues.
Switch target
Move to another high-traffic target or paste a specific ChEMBL target ID.
Frame the target before identity details
Structured disease, protein, and project context should read before the lower-level identity rail.
As of 2026-09-14Tissue-type plasminogen activator shows approved-linked disease relevance led by myocardial infarction. 5 more disease programs remain visible in the same review block. 3 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt P00750. Start with myocardial infarction, then reuse UniProt P00750 as the stable protein anchor across project notes and exports.
Tissue-type plasminogen activator shows approved-linked disease relevance led by myocardial infarction. 5 more disease programs remain visible in the same review block. 3 linked drugs remain visible in the same block.
Start review with myocardial infarction because it currently carries approved-linked support. Linked drugs include ALTEPLASE, RETEPLASE, TENECTEPLASE. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.
Disease source · ChEMBL drug mechanism + indication proxyTissue-type plasminogen activator
Review this target as Tissue-type plasminogen activator, mapped to UniProt P00750. Sequence length is 562 aa.
Protein source · UniProt accession via ChEMBL component mappingCross-source identity
Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats Tissue-type plasminogen activator as ChEMBL target CHEMBL1873, mapped to UniProt P00750. Disease framing currently uses the Open Targets-ready proxy contract.
Reuse the same identifiers in notes, watch rules, exports, and review packs so provenance stays stable across surfaces.
Start with the right source
Choose the first block or source based on the question you are trying to answer.
Start here when your first question is whether Tissue-type plasminogen activator is the right protein anchor across sources, using UniProt P00750 as the stable mapping.
Jump to Protein ContextUse this block first when you need to confirm why myocardial infarction is currently framed as approved-linked support. It currently carries 3 linked drugs in the same disease frame.
Jump to Disease ContextOpen the one-page evidence card when you want the rationale, activity base, and attribution together.
Open Review-ready CardBasic Information
Verify identity, organism, and the fastest next research jumps from the same page.
| Preferred Name | Tissue-type plasminogen activator |
| Target Type | SINGLE PROTEIN |
| Organism | Homo sapiens |
| UniProt | P00750 |
Next Actions
UniProt Target Context
Reviewable protein naming and mapping context for this target snapshot.
| Protein Label | Tissue-type plasminogen activator |
| UniProt Accession | P00750 |
| Component Type | Protein |
| Sequence Length | 562 aa |
Tissue-type plasminogen activator
How to read this target
Review this target as Tissue-type plasminogen activator, mapped to UniProt P00750. Sequence length is 562 aa.
Disease Relevance & Evidence Level
Open Targets-ready disease context using the current target-indication evidence contract.
Tissue-type plasminogen activator shows approved-linked disease relevance led by myocardial infarction. 5 more disease programs remain visible in the same review block.
How to read disease relevance
Start review with myocardial infarction because it currently carries approved-linked support. Linked drugs include ALTEPLASE, RETEPLASE, TENECTEPLASE. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.
Clinical Phase Distribution
Activity Type Distribution
Top Inhibitors (by pChEMBL)
| ChEMBL ID | pChEMBL | Type | Value (nM) | Phase |
|---|---|---|---|---|
| CHEMBL439678 | 9.54 | Ki | 0.29 | Preclinical |
| CHEMBL105819 | 9.15 | IC50 | 0.7 | Preclinical |
| CHEMBL92615 | 8.52 | Ki | 3.0 | Preclinical |
| CHEMBL290376 | 8.24 | Ki | 5.7 | Preclinical |
| CHEMBL418965 | 8.22 | Ki | 6.0 | Preclinical |
| CHEMBL5901486 | 8.22 | IC50 | 6.0 | Preclinical |
| CHEMBL94952 | 8.22 | Ki | 6.0 | Preclinical |
| CHEMBL4457757 | 8.1 | IC50 | 8.0 | Preclinical |
| CHEMBL4460436 | 8.1 | IC50 | 8.0 | Preclinical |
| CHEMBL5964796 | 8.09 | IC50 | 8.2 | Preclinical |
pChEMBL Value Distribution
Approved Drugs
Assay Landscape
Binding — 239 assays, 870 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| single protein format | 237 | 411 | 5.4 |
| assay format | 1 | 459 | 7.5 |
| cell-free format | 1 | 0 | — |
Functional — 4 assays, 0 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| assay format | 4 | 0 | — |
ADME — 1 assays, 13 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| single protein format | 1 | 13 | 6.2 |