Start with type 2 diabetes mellitus, then reuse UniProt P13866 as the stable protein anchor across project notes and exports.
CHEMBL4979 Target Snapshot
Sodium/glucose cotransporter 1 · 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 2026-09-13Sodium/glucose cotransporter 1 shows approved-linked disease relevance led by type 2 diabetes mellitus. 5 more disease programs remain visible in the same review block. 2 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt P13866. Start with type 2 diabetes mellitus, then reuse UniProt P13866 as the stable protein anchor across project notes and exports.
Sodium/glucose cotransporter 1 shows approved-linked disease relevance led by type 2 diabetes mellitus. 5 more disease programs remain visible in the same review block. 2 linked drugs remain visible in the same block.
Start review with type 2 diabetes mellitus because it currently carries approved-linked support. Linked drugs include LICOGLIFLOZIN, SOTAGLIFLOZIN. 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 proxySodium/glucose cotransporter 1
Review this target as Sodium/glucose cotransporter 1, mapped to UniProt P13866. Sequence length is 664 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 Sodium/glucose cotransporter 1 as ChEMBL target CHEMBL4979, mapped to UniProt P13866. 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 Sodium/glucose cotransporter 1 is the right protein anchor across sources, using UniProt P13866 as the stable mapping.
Jump to Protein ContextUse this block first when you need to confirm why type 2 diabetes mellitus is currently framed as approved-linked support. It currently carries 2 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 | Sodium/glucose cotransporter 1 |
| Target Type | SINGLE PROTEIN |
| Organism | Homo sapiens |
| UniProt | P13866 |
Next Actions
UniProt Target Context
Reviewable protein naming and mapping context for this target snapshot.
| Protein Label | Sodium/glucose cotransporter 1 |
| UniProt Accession | P13866 |
| Component Type | Protein |
| Sequence Length | 664 aa |
Sodium/glucose cotransporter 1
How to read this target
Review this target as Sodium/glucose cotransporter 1, mapped to UniProt P13866. Sequence length is 664 aa.
Disease Relevance & Evidence Level
Open Targets-ready disease context using the current target-indication evidence contract.
Sodium/glucose cotransporter 1 shows approved-linked disease relevance led by type 2 diabetes mellitus. 5 more disease programs remain visible in the same review block.
How to read disease relevance
Start review with type 2 diabetes mellitus because it currently carries approved-linked support. Linked drugs include LICOGLIFLOZIN, SOTAGLIFLOZIN. 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 |
|---|---|---|---|---|
| CHEMBL485830 | 9.8 | IC50 | 0.16 | Preclinical |
| CHEMBL521026 | 9.77 | IC50 | 0.17 | Preclinical |
| CHEMBL4297625 | 9.3 | IC50 | 0.5 | Clinical |
| CHEMBL5835461 | 9.24 | IC50 | 0.58 | Preclinical |
| CHEMBL3690855 | 9.15 | IC50 | 0.7 | Preclinical |
| CHEMBL3686477 | 9.05 | IC50 | 0.9 | Preclinical |
| CHEMBL5873761 | 9.01 | IC50 | 0.98 | Preclinical |
| CHEMBL3695107 | 8.96 | IC50 | 1.1 | Preclinical |
| CHEMBL3690821 | 8.96 | IC50 | 1.1 | Preclinical |
| CHEMBL3686485 | 8.96 | IC50 | 1.1 | Preclinical |
pChEMBL Value Distribution
Approved Drugs
Assay Landscape
Binding — 121 assays, 1,255 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell-based format | 70 | 482 | 6.0 |
| assay format | 31 | 732 | 7.7 |
| single protein format | 18 | 40 | 5.7 |
| cell membrane format | 2 | 1 | 5.1 |
ADME — 6 assays, 43 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell-based format | 6 | 43 | 5.5 |
Functional — 2 assays, 21 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell-based format | 2 | 21 | 5.5 |