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Gene Set: D4 : CTD - 2,2-bis(4-hydroxyphenyl)-1,1,1-trichloroethane


Collection D4 : CTD
Chemical Name 2,2-bis(4-hydroxyphenyl)-1,1,1-trichloroethane ( From PubChem : HYDROXYCHLOR )
FDA NPC WHO Indian Australia China Traditional
Herbal
Clinical
Trail
NotNotNotNotNotNotNotNot
Molecular
Weight
Hydrogen Bond
Donor Count
Hydrogen Bond
Acceptor Count
cLogP Lipinski Rule
317.595 g/mol 2 2 4.5999 True
Structure
InChI InChI=1S/C14H11Cl3O2/c15-14(16,17)13(9-1-5-11(18)6-2-9)10-3-7-12(19)8-4-10/h1-8,13,18-19H
InChIKey IUGDILGOLSSKNE-UHFFFAOYSA-N
Links

Gene (19 / 78)


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Source Type Unit Value Gene PMID Assay Other
CTDaffects(binding)AR
C404910
CTDdecreases(activity)AR
C404910
CTDaffects(binding)AR
C404910
CTDdecreases(reaction)AR
C404910
CTDincreases(activity)AR
C404910
CTDdecreases(reaction)AR
C404910
CTDincreases(activity)AR
C404910
CTDaffects(binding)AR
C404910
CTDdecreases(reaction)AR
C404910
CTDincreases(activity)AR
C404910
CTDdecreases(activity)AR
C404910
CTDincreases(expression)CXCL12
C404910
CTDaffects(response to substance)CXCL12
C404910
CTDdecreases(reaction)CXCL12
C404910
CTDdecreases(response to substance)CXCR4
C404910
CTDdecreases(activity)CYP17A1
C404910
CTDaffects(binding)CYP19A1
C404910
CTDdecreases(activity)CYP19A1
C404910
CTDdecreases(reaction)CYP19A1
C404910
CTDincreases(metabolic processing)CYP19A1
C404910
CTDdecreases(expression)CYP19A1
C404910
CTDaffects(binding)ESR1
C404910
CTDincreases(activity)ESR1
C404910
CTDaffects(binding)ESR1
C404910
CTDaffects(binding)ESR1
C404910
CTDdecreases(reaction)ESR1
C404910
CTDincreases(activity)ESR1
C404910
CTDincreases(reaction)ESR1
C404910
CTDincreases(activity)ESR1
C404910
CTDdecreases(reaction)ESR1
C404910
CTDincreases(expression)ESR1
C404910
CTDaffects(binding)ESR2
C404910
CTDdecreases(activity)ESR2
C404910
CTDaffects(binding)ESR2
C404910
CTDincreases(activity)ESR2
C404910
CTDaffects(binding)ESR2
C404910
CTDdecreases(reaction)ESR2
C404910
CTDincreases(activity)ESR2
C404910
CTDincreases(expression)GREB1
C404910
CTDdecreases(reaction)GREB1
C404910
CTDdecreases(activity)HSD11B1
C404910
CTDdecreases(activity)HSD11B2
C404910
CTDdecreases(activity)HSD17B3
C404910
CTDdecreases(reaction)HSD17B3
C404910
CTDincreases(expression)PGR
C404910
CTDdecreases(reaction)PGR
C404910
CTDincreases(expression)PRSS23
C404910
CTDdecreases(reaction)PRSS23
C404910
CTDincreases(expression)TFF1
C404910
CTDdecreases(reaction)TFF1
C404910
CTDincreases(expression)WISP2
C404910
CTDdecreases(reaction)WISP2
C404910
PubChem Potency-Replicate_1uM6.917AR-GI(Protien) :
PubChem Ratio Potency (uM)uM7.761AR-GI(Protien) :
PubChem Ratio Potency (uM)uM8.350AR-GI(Protien) :
PubChem Potency-Replicate_1uM9.735AR-GI(Protien) :
PubChem Potency-Replicate_1uM30.638AR-GI(Protien) :
PubChem Potency-Replicate_1uM48.360AR-GI(Protien) :
PubChem Potency-Replicate_1uM61.131CYP19A1-GI(Protien) :
PubChem Potency-Replicate_1uM0.077ESR1-GI(Protien) :
PubChem Potency-Replicate_1uM0.121ESR1-GI(Protien) :
PubChem Ratio Potency (uM)uM0.593ESR1-GI(Protien) :
PubChem Potency-Replicate_1uM0.614ESR1-GI(Protien) :
PubChem Ratio Potency (uM)uM0.804ESR1-GI(Protien) :
PubChem Potency-Replicate_1uM0.977ESR1-GI(Protien) :
PubChem ER Potency (uM)uM44.970ESR1-GI(Protien) :
PubChem Potency-Replicate_1uM48.558ESR1-GI(Protien) :
PubChem Potency-Replicate_1uM54.261ESR1-GI(Protien) :
PubChem Potency-Replicate_1uM54.941ESR1-GI(Protien) :
PubChem ER Potency (uM)uM57.476ESR1-GI(Protien) :
PubChem Ratio Potency (uM)uMESR1-GI(Protien) :
PubChem Ratio Potency (uM)uM57.090HSPB1-GI(Protien) :
PubChem Ratio Potency (uM)uM10.068NFE2L2-GI(Protien) :
PubChem PotencyuM54.483NFE2L2-GI(Protien) :
PubChem Potency-Replicate_1uM21.872NR3C1-GI(Protien) :
PubChem NoneuMNR3C1-GI(Protien) :
PubChem Potency-Replicate_1uM6.917PPARG-GI(Protien) :
PubChem NoneuMPPARG-GI(Protien) :
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