← SynDRA
QUIZARTINIB
SynDRA canonical compound SYN0020171 — structure-anchored drug synonym record
| Clinical phase | Phase 3 |
| Approval status | Approved · Rx/OTC |
| Primary target(s) | RET |
| Mechanism of action | FLT3 inhibitor |
All known targets
- FLT3
- CSF1R
- KIT
- RET
- PDGFRB
- PDGFRA
- NTRK2
- MUSK
- MYH10
- MYLK
- MYLK3
- NTRK1
Mechanisms of action (all sources)
- FLT3 INHIBITOR
- CSF1R INHIBITOR
- Macrophage colony stimulating factor receptor inhibitor
- Tyrosine-protein kinase receptor FLT3 inhibitor
- KIT INHIBITOR
- Stem cell growth factor receptor inhibitor
- PDGFRB INHIBITOR
- Platelet-derived growth factor receptor inhibitor
- PDGFRA INHIBITOR
- RET INHIBITOR
- Tyrosine-protein kinase receptor RET inhibitor
Bioactivity evidence (ChEMBL activities table — not curator-asserted)
- MAPK14
- AURKB
- MAPK12
- MAP3K20
- MINK1
- IRAK4
- IRAK1
- PAK3
- RIPK3
- CDK7
- CAMKK1
- BLK
- MAPK9
- ULK3
- PHKG1
- PIM1
- PIKFYVE
- PIK3CG
- PIK3CD
- PIK3CB
- PIK3CA
- PIK3C3
- PIK3C2G
- PIK3C2B
- PI4KB
- PHKG2
- PGRMC1
- PIM3
- PFKP
- PEBP1
- PDXK
- PDPK1
- PASK
- PAK6
- PAK5
- PAK4
- WNK2
- PAK2
- PAK1
- PIM2
Screening evidence (raw PubChem HTS — uncurated, known false-positive rate)
Drug classes
- Antineoplastic Agents
- Tyrosine Kinase Inhibitors
ATC classes
- L01E · PROTEIN KINASE INHIBITORS
Cross-references
Synonyms
- VANFLYTA
- Vanflyta
- quizartinib hydrochloride
- quizartinib dihydrochloride
- vanflyta
- AC220
- AC010220
- AC-220
- AC-010220
- AC010220.2HCL
- AC220 (QUIZARTINIB)
- AC708
- ASP-2689
- QUIZARTINIB (AC220)
- Quizartinib dihydrochloride
- Quizartinib (AC220)
- AC 220
- Quizartinib HCl
- Quizartinib freebase
- 7LA4O6Q0D3
- CHEMBL576982
- CHEBI:90217
- 950769-58-1 (free base)
- 1132827-21-4 (HCl)
- CHEMBL2386811
- AC220 compound
- AC220,Quizartinib
- Quizartinib [USAN]
- Quizartinib [USAN:INN]
- quizartinibum
- UNII-7LA4O6Q0D3
- Quizartinib, 95%
- Quizartinib, ac220
- Quizartinib, Free Base
- AC220 - Quizartinib
- QUIZARTINIB [MI]
- Quizartinib; PLX3397
- QUIZARTINIB [INN]
Look up QUIZARTINIB in the interactive SynDRA portal →