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- ChemComp-CPB: 2-(2-CHLORO-PHENYL)-5,7-DIHYDROXY-8-(3-HYDROXY-1-METHYL-PIPERIDIN... -
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Open data
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Basic information
Entry | ![]() | ||
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Name | Name: Synonyms: FLAVOPIRIDOL Comment | inhibitor, alkaloid*YM | |
-Chemical information
Composition | |||||||||
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Others | Type: NON-POLYMER / PDB classification: HETAIN / Three letter code: CPB / Model coordinates PDB-ID: 1C8K | ||||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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-Details
-SMILES
ACDLabs 10.04 | CACTVS 3.341 | OpenEye OEToolkits 1.5.0 | |
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-SMILES CANONICAL
CACTVS 3.341 | OpenEye OEToolkits 1.5.0 | |
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-InChI
InChI 1.03 |
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-InChIKey
InChI 1.03 |
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-SYSTEMATIC NAME
ACDLabs 10.04 | OpenEye OEToolkits 1.5.0 | |
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-PDB entries
Showing all 5 items
![](data/pdb/img/1c8k.jpg)
PDB-1c8k:
FLAVOPIRIDOL INHIBITS GLYCOGEN PHOSPHORYLASE BY BINDING AT THE INHIBITOR SITE
![](data/pdb/img/1e1y.jpg)
PDB-1e1y:
Flavopiridol inhibits glycogen phosphorylase by binding at the inhibitor site
![](data/pdb/img/3blr.jpg)
PDB-3blr:
Crystal Structure of Human CDK9/cyclinT1 in complex with Flavopiridol
![](data/pdb/img/3ebp.jpg)
PDB-3ebp:
Glycogen Phosphorylase b/flavopiridol complex
![](data/pdb/img/4o71.jpg)
PDB-4o71:
Crystal structure of the first bromodomain of human BRD4 in complex with FLAVOPIRIDOL