BDBM50334048 (-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl-1,2,3,4-tetrahydroquinoline::5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl-1,2,3,4-tetrahydroquinoline::CHEMBL258191::racemic-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl-1,2,3,4-tetrahydroquinoline

SMILES CC1CC(C)(C)Nc2c(C)cc(c(Cl)c12)-c1cccc2cc[nH]c12

InChI Key InChIKey=ZAINQQRFGATLID-UHFFFAOYSA-N

Data  10 KI  6 IC50  3 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 19 hits for monomerid = 50334048   

TargetGlucocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataKi:  0.600nMAssay Description:Displacement of radiolabeled dexamethasone from glucocorticoid receptor expressed in baculovirusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataKi:  0.600nMAssay Description:Displacement of radiolabeled Dexamethasone from glucocorticoid receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataKi:  0.600nMAssay Description:Displacement of radiolabeled Dexamethasone from glucocorticoid receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProgesterone receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataKi:  8.20nMAssay Description:Binding affinity at progesterone receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProgesterone receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataKi:  8.20nMAssay Description:Binding affinity at progesterone receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProgesterone receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataKi:  13nMAssay Description:Binding affinity to progesterone receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMineralocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataKi:  21nMAssay Description:Binding affinity to mineralocorticoid receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMineralocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataKi:  21nMAssay Description:Binding affinity at mineralocorticoid receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataKi:  57nMAssay Description:Binding affinity to androgen receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataKi:  57nMAssay Description:Binding affinity at androgen receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataIC50:  59nMAssay Description:Transrepression activity at glucocorticoid receptor in IL-1beta-stimulated human HepG2 cells assessed as inhibition of AP1 response element-induced I...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataEC50:  20nMAssay Description:Agonist activity at glucocorticoid receptor in human HepG2 cells co-transfected with GRE assessed as transactivation activity by luciferase reporter ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataIC50:  9.40nMAssay Description:Transrepression activity at glucocorticoid receptor in TNFalpha/IL1beta-stimulated human HepG2 cells assessed as inhibition of NFkappaB-dependent E-s...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataEC50:  12nMAssay Description:Agonist activity at glucocorticoid receptor assessed as glucose repsponse element transcriptional transactivation by luciferase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataEC50:  12nMAssay Description:Agonist activity at glucocorticoid receptor assessed as glucose repsponse element transcriptional transactivation by luciferase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataIC50: >1.00E+3nMAssay Description:Antagonist activity at glucocorticoid receptor assessed as inhibition of dexamethasone-induced glucose response element transcriptional transactivati...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataIC50: >1.00E+3nMAssay Description:Antagonist activity at glucocorticoid receptor assessed as inhibition of dexamethasone-induced glucose response element transcriptional transactivati...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataIC50:  12nMAssay Description:Activity at glucocorticoid receptor assessed as repression of TNFalpha and IL1 beta-induced E-selectin expressionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucocorticoid receptor(Homo sapiens (Human))
Ligand Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50334048((-)-5-chloro-6-(1H-indol-7-yl)-2,2,4,8-tetramethyl...)
Affinity DataIC50:  12nMAssay Description:Activity at glucocorticoid receptor assessed as repression of TNFalpha and IL1 beta-induced E-selectin expressionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed