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Gene Set: D4 : CTD - fexofenadine


Collection D4 : CTD
Chemical Name fexofenadine ( From PubChem : FEXOFENADINE HYDROCHLORIDE )
FDA NPC WHO Indian Australia China Traditional
Herbal
Clinical
Trail
ApprovedNotNotNotNotNotNotNot
Molecular
Weight
Hydrogen Bond
Donor Count
Hydrogen Bond
Acceptor Count
cLogP Lipinski Rule
538.117 g/mol 4 5 6.2504 False(2/4)
Structure
InChI InChI=1S/C32H39NO4.ClH/c1-31(2,30(35)36)25-17-15-24(16-18-25)29(34)14-9-21-33-22-19-28(20-23-33)32(37,26-10-5-3-6-11-26)27-12-7-4-8-13-27;/h3-8,10-13,15-18,28-29,34,37H,9,14,19-23H2,1-2H3,(H,35,36);1H
InChIKey RRJFVPUCXDGFJB-UHFFFAOYSA-N
Links

Gene (25 / 62)


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Source Type Unit Value Gene PMID Assay Other
CTDaffects(response to substance)ABCB1
C093230
CTDaffects(response to substance)ABCB1
C093230
CTDincreases(reaction)ABCB1
C093230
CTDincreases(reaction)ABCB1
C093230
CTDincreases(transport)ABCB1
C093230
CTDincreases(reaction)ABCB11
C093230
CTDincreases(uptake)ABCB11
C093230
CTDaffects(cotreatment)ABCC2
C093230
CTDincreases(uptake)ABCC2
C093230
CTDdecreases(reaction)CCL11
C093230
CTDincreases(expression)CCL11
C093230
CTDdecreases(expression)CCL17
C093230
CTDdecreases(expression)CCL22
C093230
CTDdecreases(reaction)CCL5
C093230
CTDincreases(expression)CCL5
C093230
CTDaffects(binding)GUSB
C093230
CTDdecreases(reaction)GUSB
C093230
CTDincreases(activity)GUSB
C093230
CTDincreases(expression)GUSB
C093230
CTDaffects(binding)HRH1
C093230
CTDdecreases(activity)HRH1
C093230
CTDdecreases(reaction)HRH1
C093230
CTDincreases(abundance)HRH1
C093230
CTDincreases(activity)HRH1
C093230
CTDincreases(expression)HRH1
C093230
CTDdecreases(expression)ICAM1
C093230
CTDdecreases(reaction)IL6
C093230
CTDincreases(expression)IL6
C093230
CTDdecreases(reaction)KCNH2
C093230
CTDincreases(activity)KCNH2
C093230
CTDdecreases(phosphorylation)MAPK1
C093230
CTDdecreases(phosphorylation)MAPK3
C093230
CTDdecreases(reaction)MMP2
C093230
CTDincreases(activity)MMP2
C093230
CTDincreases(expression)MMP2
C093230
CTDdecreases(reaction)MMP9
C093230
CTDincreases(activity)MMP9
C093230
CTDincreases(expression)MMP9
C093230
CTDdecreases(reaction)NFKB1
C093230
CTDincreases(activity)NFKB1
C093230
CTDaffects(cotreatment)NR1I2
C093230
CTDincreases(activity)NR1I2
C093230
CTDdecreases(reaction)RELA
C093230
CTDincreases(activity)RELA
C093230
CTDaffects(cotreatment)SLCO1B1
C093230
CTDincreases(uptake)SLCO1B1
C093230
CTDincreases(uptake)SLCO1B1
C093230
CTDdecreases(reaction)SLCO1B3
C093230
CTDincreases(uptake)SLCO1B3
C093230
CTDaffects(cotreatment)SLCO1B3
C093230
CTDincreases(uptake)SLCO1B3
C093230
CTDdecreases(reaction)TIMP1
C093230
CTDincreases(expression)TIMP1
C093230
CTDdecreases(reaction)TIMP2
C093230
CTDincreases(expression)TIMP2
C093230
CTDdecreases(reaction)TNF
C093230
CTDincreases(activity)TNF
C093230
CTDdecreases(reaction)TNF
C093230
CTDincreases(expression)TNF
C093230
CTDincreases(expression)TNF
C093230
PubChem PotencyuM19.953ALOX15-GI(Protien) :
ChEMBLPotencynM19952.600ALOX15
-Target : CHEMBL2903
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12801 East 17th Avenue
Division of Medical Oncology , Department of Medicine
University of Colorado School of Medicine
Aurora, CO 80045, USA

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