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Gene Set: D4 : CTD - 6,7-dimethoxy-3-phenylquinoxaline


Collection D4 : CTD
Chemical Name 6,7-dimethoxy-3-phenylquinoxaline ( From PubChem : TYRPHOSTIN AG 1296 )
FDA NPC WHO Indian Australia China Traditional
Herbal
Clinical
Trail
NotNotNotNotNotNotNotNot
Molecular
Weight
Hydrogen Bond
Donor Count
Hydrogen Bond
Acceptor Count
cLogP Lipinski Rule
266.295 g/mol 0 4 3.314 True
Structure
InChI InChI=1S/C16H14N2O2/c1-19-15-8-12-13(9-16(15)20-2)18-14(10-17-12)11-6-4-3-5-7-11/h3-10H,1-2H3
InChIKey QNOXYUNHIGOWNY-UHFFFAOYSA-N
Links

Gene (9 / 22)


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Source Type Unit Value Gene PMID Assay Other
CTDdecreases(phosphorylation)AKT1
C106250
CTDaffects(cotreatment)MAPK1
C106250
CTDdecreases(activity)MAPK1
C106250
CTDaffects(cotreatment)MAPK3
C106250
CTDdecreases(activity)MAPK3
C106250
CTDdecreases(reaction)PDGFB
C407689
CTDincreases(expression)PDGFB
C407689
CTDincreases(secretion)PDGFB
C407689
CTDdecreases(reaction)PDGFRB
C407689
CTDincreases(expression)PDGFRB
C407689
CTDdecreases(reaction)PDGFRB
C106250
CTDincreases(activity)PDGFRB
C106250
CTDincreases(phosphorylation)PDGFRB
C106250
PubChem irf1 Inhibition [HEL cells] (IC50)uM0.690JAK2-GI(Protien) :
PubChem PotencyuM15.849SMN2-GI(Protien) :
PubChem PotencyuM28.184SMN2-GI(Protien) :
PubChem PotencyuM20.596TDP1-GI(Protien) :
PubChem PotencyuM25.119TDP1-GI(Protien) :
PubChem PotencyuM35.481TDP1-GI(Protien) :
ChEMBLActivityum0.690JAK2
-Target : CHEMBL2971
ChEMBLPotencynM28183.800SMN1; SMN2
-Target : CHEMBL1293232
ChEMBLPotencynM15848.900SMN1; SMN2
-Target : CHEMBL1293232
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