Cell membrane · SUBCELLULAR · Homo sapiens
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Structured disease, protein, and project context should read before the lower-level identity rail.
As of 2026-09-13Cell membrane shows late clinical disease relevance led by HIV infection. 5 more disease programs remain visible in the same review block. 1 linked drug keeps the current disease frame grounded. Use HIV infection as the disease frame, then confirm a stable protein accession before cross-source reuse.
Use HIV infection as the disease frame, then confirm a stable protein accession before cross-source reuse.
Cell membrane shows late clinical disease relevance led by HIV infection. 5 more disease programs remain visible in the same review block. 1 linked drug remains visible in the same block.
Start review with HIV infection because it currently carries late clinical support. Linked drugs include NONOXYNOL 9. 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 proxyCell membrane
Review this target as Cell membrane.
Protein source · UniProt accession via ChEMBL component mappingKeep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats Cell membrane as ChEMBL target CHEMBL3390826. 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.
Choose the first block or source based on the question you are trying to answer.
Start here when your first question is whether Cell membrane still has a stable protein naming contract across sources.
Jump to Protein ContextUse this block first when you need to confirm why HIV infection is currently framed as late clinical support. It currently carries 1 linked drug 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 CardVerify identity, organism, and the fastest next research jumps from the same page.
| Preferred Name | Cell membrane |
| Target Type | SUBCELLULAR |
| Organism | Homo sapiens |
Reviewable protein naming and mapping context for this target snapshot.
Review this target as Cell membrane.
Open Targets-ready disease context using the current target-indication evidence contract.
Cell membrane shows late clinical disease relevance led by HIV infection. 5 more disease programs remain visible in the same review block.
Start review with HIV infection because it currently carries late clinical support. Linked drugs include NONOXYNOL 9. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell membrane format | 121 | 0 | — |
| subcellular format | 32 | 0 | — |
| mitochondrion format | 10 | 0 | — |