Start with chronic lymphocytic leukemia, then reuse UniProt P50750 as the stable protein anchor across project notes and exports.
CHEMBL3116 Target Snapshot
Cyclin-dependent kinase 9 · 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 2026-09-13Cyclin-dependent kinase 9 shows late clinical disease relevance led by chronic lymphocytic leukemia. 5 more disease programs remain visible in the same review block. 4 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt P50750. Start with chronic lymphocytic leukemia, then reuse UniProt P50750 as the stable protein anchor across project notes and exports.
Cyclin-dependent kinase 9 shows late clinical disease relevance led by chronic lymphocytic leukemia. 5 more disease programs remain visible in the same review block. 4 linked drugs remain visible in the same block.
Start review with chronic lymphocytic leukemia because it currently carries late clinical support. Linked drugs include ALVOCIDIB, BMS-387032, DINACICLIB, ZOTIRACICLIB. 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 proxyCyclin-dependent kinase 9
Review this target as Cyclin-dependent kinase 9, mapped to UniProt P50750. Sequence length is 372 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 Cyclin-dependent kinase 9 as ChEMBL target CHEMBL3116, mapped to UniProt P50750. 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 Cyclin-dependent kinase 9 is the right protein anchor across sources, using UniProt P50750 as the stable mapping.
Jump to Protein ContextUse this block first when you need to confirm why chronic lymphocytic leukemia is currently framed as late clinical support. It currently carries 4 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 | Cyclin-dependent kinase 9 |
| Target Type | SINGLE PROTEIN |
| Organism | Homo sapiens |
| UniProt | P50750 |
Next Actions
UniProt Target Context
Reviewable protein naming and mapping context for this target snapshot.
| Protein Label | Cyclin-dependent kinase 9 |
| UniProt Accession | P50750 |
| Component Type | Protein |
| Sequence Length | 372 aa |
Cyclin-dependent kinase 9
How to read this target
Review this target as Cyclin-dependent kinase 9, mapped to UniProt P50750. Sequence length is 372 aa.
Disease Relevance & Evidence Level
Open Targets-ready disease context using the current target-indication evidence contract.
Cyclin-dependent kinase 9 shows late clinical disease relevance led by chronic lymphocytic leukemia. 5 more disease programs remain visible in the same review block.
How to read disease relevance
Start review with chronic lymphocytic leukemia because it currently carries late clinical support. Linked drugs include ALVOCIDIB, BMS-387032, DINACICLIB, ZOTIRACICLIB. 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 |
|---|---|---|---|---|
| CHEMBL3694406 | 10.82 | IC50 | 0.015 | Preclinical |
| CHEMBL3694400 | 10.74 | IC50 | 0.018 | Preclinical |
| CHEMBL3694402 | 10.72 | IC50 | 0.019 | Preclinical |
| CHEMBL3694407 | 10.54 | IC50 | 0.029 | Preclinical |
| CHEMBL3694401 | 10.41 | IC50 | 0.039 | Preclinical |
| CHEMBL3694404 | 9.94 | IC50 | 0.116 | Preclinical |
| CHEMBL5197170 | 9.67 | Kd | 0.213 | Preclinical |
| CHEMBL4777844 | 9.3 | IC50 | 0.495 | Preclinical |
| CHEMBL422897 | 9.2 | Ki | 0.631 | Preclinical |
| CHEMBL2006674 | 9.1 | Ki | 0.7943 | Preclinical |
pChEMBL Value Distribution
Approved Drugs
Assay Landscape
Binding — 574 assays, 1,659 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| single protein format | 264 | 1,463 | 7.1 |
| cell-based format | 253 | 162 | 7.2 |
| assay format | 33 | 6 | 7.5 |
| subcellular format | 24 | 28 | 6.4 |
Functional — 6 assays, 187 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell-based format | 5 | 2 | 5.7 |
| assay format | 1 | 185 | 6.6 |
Toxicity — 1 assays, 0 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| assay format | 1 | 0 | — |