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Gene Set: D4 : CTD - Loratadine


Collection D4 : CTD
Chemical Name Loratadine ( From PubChem : LORATADINE )
FDA NPC WHO Indian Australia China Traditional
Herbal
Clinical
Trail
ApprovedNotNotApprovedNotApprovedNotNot
Molecular
Weight
Hydrogen Bond
Donor Count
Hydrogen Bond
Acceptor Count
cLogP Lipinski Rule
382.883 g/mol 0 4 4.8257 True
Structure
InChI InChI=1S/C22H23ClN2O2/c1-2-27-22(26)25-12-9-15(10-13-25)20-19-8-7-18(23)14-17(19)6-5-16-4-3-11-24-21(16)20/h3-4,7-8,11,14H,2,5-6,9-10,12-13H2,1H3
InChIKey JCCNYMKQOSZNPW-UHFFFAOYSA-N
Links

Gene (43 / 81)


⊖ Less

Source Type Unit Value Gene PMID Assay Other
CTDincreases(export)ABCB1
D017336
CTDdecreases(reaction)ABCB11
D017336
CTDincreases(transport)ABCB11
D017336
CTDdecreases(activity)ABCB11
D017336
CTDdecreases(response to substance)ABCC1
D017336
CTDdecreases(reaction)ABCC2
D017336
CTDincreases(export)ABCC2
D017336
CTDdecreases(activity)ALOX5
D017336
CTDdecreases(expression)AP1S1
D017336
CTDincreases(expression)ASNS
D017336
CTDincreases(activity)CASP3
D017336
CTDincreases(reaction)CASP3
D017336
CTDincreases(activity)CASP3
D017336
CTDincreases(cleavage)CASP3
D017336
CTDincreases(activity)CASP3
D017336
CTDincreases(reaction)CASP3
D017336
CTDincreases(activity)CASP7
D017336
CTDincreases(reaction)CASP7
D017336
CTDincreases(cleavage)CASP8
D017336
CTDincreases(cleavage)CASP9
D017336
CTDdecreases(activity)CYP2C8
D017336
CTDaffects(metabolic processing)CYP2D6
D017336
CTDdecreases(activity)CYP3A4
D017336
CTDincreases(expression)FABP1
D017336
CTDincreases(expression)GDPD3
D017336
CTDincreases(expression)HPN
D017336
CTDaffects(binding)HRH1
D017336
CTDincreases(expression)INHBE
D017336
CTDaffects(activity)KCNH2
D017336
CTDaffects(binding)KCNH2
D017336
CTDdecreases(activity)KCNH2
D017336
CTDdecreases(reaction)KCNH2
D017336
CTDincreases(transport)KCNH2
D017336
CTDdecreases(activity)KCNH2
D017336
CTDincreases(expression)LSS
D017336
CTDincreases(expression)NR0B2
D017336
CTDincreases(expression)NUPR1
D017336
CTDdecreases(expression)RPS6
D017336
CTDincreases(expression)SERPINA3
D017336
CTDdecreases(expression)SLC2A3
D017336
CTDdecreases(expression)TAGLN
D017336
PubChem Potency-Replicate_1uM17.374AR-GI(Protien) :
PubChem AR Potency (uM)uM27.644AR-GI(Protien) :
PubChem Potency-Replicate_1uM61.131AR-GI(Protien) :
PubChem NoneuMCACNA1H-GI(Protien) :
PubChem PotencyuM0.398CYP2C19-GI(Protien) :
PubChem PotencyuM15.849CYP2C9-GI(Protien) :
PubChem NoneuMCYP2C9-GI(Protien) :
PubChem PotencyuM31.623CYP2D6-GI(Protien) :
PubChem NoneuMDRD3-GI(Protien) :
PubChem NoneuMDRD3-GI(Protien) :
PubChem Ratio Potency (uM)uM22.577ESR1-GI(Protien) :
PubChem Potency-Replicate_1uM26.832ESR1-GI(Protien) :
PubChem Potency-Replicate_1uM61.131ESR1-GI(Protien) :
PubChem ER Potency (uM)uM61.131ESR1-GI(Protien) :
PubChem PotencyuM23.109GMNN-GI(Protien) :
PubChem PotencyuM15.849HIF1A-GI(Protien) :
PubChem PotencyuM19.953MAPK1-GI(Protien) :
PubChem Ratio Potency (uM)uM6.188NFE2L2-GI(Protien) :
PubChem Ratio Potency (uM)uM6.601NFE2L2-GI(Protien) :
PubChem PotencyuM7.943NPSR1-GI(Protien) :
PubChem PotencyuM12.589NPSR1-GI(Protien) :
PubChem IC50uMPHOSPHO1-GI(Protien) :
PubChem Ratio Potency (uM)uM59.324PPARD-GI(Protien) :
PubChem Potency-Replicate_1uM13.332PPARG-GI(Protien) :
PubChem NoneuMPPARG-GI(Protien) :
PubChem PotencyuM2.661TDP1-GI(Protien) :
PubChem PotencyuM11.886TDP1-GI(Protien) :
PubChem PotencyuM12.995TDP1-GI(Protien) :
PubChem PotencyuM14.963TDP1-GI(Protien) :
PubChem PotencyuM20.596TDP1-GI(Protien) :
PubChem PotencyuM39.811TSHR-GI(Protien) :
ChEMBLPotencynM398.100CYP2C19
-Target : CHEMBL3622
ChEMBLPotencynM15848.900CYP2C9
-Target : CHEMBL3397
ChEMBLAC50nM15848.900CYP2C9
-Target : CHEMBL3397
ChEMBLPotencynM31622.800CYP2D6
-Target : CHEMBL289
ChEMBLPotencynM15848.900HIF1A
-Target : CHEMBL4261
ChEMBLPotencynM19952.600MAPK1
-Target : CHEMBL4040
ChEMBLPotencynM7943.300NPSR1
-Target : CHEMBL5162
ChEMBLPotencynM12589.300NPSR1
-Target : CHEMBL5162
ChEMBLPotencynM39810.700TSHR
-Target : CHEMBL1963
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