Repositioning Candidate Details
Candidate ID: | R0809 |
Source ID: | DB05470 |
Source Type: | investigational |
Compound Type: | small molecule |
Compound Name: | VX-702 |
Synonyms: | -- |
Molecular Formula: | C19H12F4N4O2 |
SMILES: | NC(=O)N(C1=CC=C(C(N)=O)C(=N1)C1=CC=C(F)C=C1F)C1=C(F)C=CC=C1F |
Structure: |
|
DrugBank Description: | VX-702 is a small molecule investigational oral anti-cytokine therapy for treatment of inflammatory diseases, specifically rheumatoid arthritis (RA). It acts as a p38 MAP kinase inhibitor. In the future, VX-702 may be investigated for combination with methotrexate, a commonly used therapy for RA. |
CAS Number: | 745833-23-2 |
Molecular Weight: | 404.325 |
DrugBank Indication: | Investigated for use/treatment in coronary artery disease, inflammatory disorders (unspecified), and rheumatoid arthritis. |
DrugBank Pharmacology: | VX-703 is an anti-cytokine therapy in which p38 MAP kinase inhibitor effectively inhibits LPS-stimulated TNF||, IL-6 and IL-1|| production. |
DrugBank MoA: | This p38 MAP kinase inhibitor effectively inhibits LPS-stimulated TNF||, IL-6 and IL-1|| production. |
Targets: | Mitogen-activated protein kinase 14; Tumor necrosis factor; Interleukin-1 beta; Interleukin-6 |
Inclusion Criteria: | Target associated |

Strategy ID | Strategy | Synonyms | Related Targets | Related Drugs | |
---|---|---|---|---|---|
S05 | Anti-inflammatory | inflammatory | Bile acid; TNF-a inhibitor; Dual PPAR-α and -δ agonists; Toll-Like Receptor; (TLR)-4 antagonist; Caspase inhibitor; ASK-1 inhibitor | Ursodeoxycholic Acid; Pentoxifylline; Elafibranor; JKB-121; Emricasan; Selonsertib; | Details |
Diseases ID | DO ID | Disease Name | Definition | Class | |
---|---|---|---|---|---|
I15 | 1290 | Bone disease | A connective tissue disease that affects the structure or development of bone or causes an impairment of normal bone function. http://en.wikipedia.org/wiki/Bone_disease | disease of anatomical entity/ musculoskeletal system disease/connective tissue disease | Details |