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ZANDELISIB
SynDRA canonical compound SYN0040101 — structure-anchored drug synonym record
| Clinical phase | Phase 2 |
| Primary target(s) | PIK3CD |
| Mechanism of action | pi3k inhibitor |
| Indication | non-hodgkin lymphoma (nhl) |
| Disease area | oncology |
All known targets
- PIK3CD
- MTOR
- PIK3CA
- PIK3CB
- PIK3CG
Mechanisms of action (all sources)
- PIK3CD INHIBITOR
- PI3-kinase p110-delta subunit inhibitor
- MTOR inhibitor
- PIK3CA INHIBITOR
- PIK3CB INHIBITOR
- PIK3CG INHIBITOR
- PI3K inhibitor
Cross-references
Synonyms
- ME-401
- PWT-143
- ACC-524
- PW-143
- PWT143
- UNII-8Z28M5SX0X
- 8Z28M5SX0X
- 4-yl)-1,3,5-triazin-2-amine
- [2-(1-methylpiperidin-4-yl)phenyl]propan-2-yl}-6-(morpholin-
- 4-[2-(difluoromethyl)-1H-benzimidazol-1-yl]-N-{2-methyl-1-
- Zandelisib [INN]
- Zandelisib [USAN]
- SCHEMBL12936730
- GTPL10627
- ME401
- WHO 11202
- ZINC148868634
- Example 51 [WO2012135160A1]
- HY-109198
- CS-0119144
- A35 [WO2012135160A1]
- 1,3,5-Triazin-2-amine, 4-(2-(difluoromethyl)-1H-benzimidazol-1-yl)-N-(1,1-dimethyl-2-(2-(1-methyl-4-piperidinyl)phenyl)ethyl)-6-(4-morpholinyl)-
- 4-(2-(Difluoromethyl)benzimidazol-1-yl)-N-(1,1-dimethyl-2-(2-(1-methyl-4-piperidyl)phenyl)ethyl)-6-morpholino-1,3,5-triazin-2-amine
- 4-[2-(difluoromethyl)benzimidazol-1-yl]-N-[2-methyl-1-[2-(1-methylpiperidin-4-yl)phenyl]propan-2-yl]-6-morpholin-4-yl-1,3,5-triazin-2-amine
- Me-401
- RefChem:195844
- PI3K-delta Inhibitor PWT143
- Zandelisib?
- ZANDELISIB [JAN]
- Zandelisib [USAN:INN]
- ZANDELISIB [WHO-DD]
- Zandelisib (JAN/USAN/INN)
- orb1308922
- SCHEMBL29366620
- SCHEMBL30089332
- SCHEMBL30165731
- C31H38F2N8O
- WPFUFWIHMYZXSF-UHFFFAOYSA-N
- A1L62
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