BindingDB PrimarySearch

Found 39 Enz. Inhib. hit(s) with Target = 'Aromatase' and Ligand = 'BDBM8611'

Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

Ki: 0.0500nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

Ki: 0.600nMAssay Description:Inhibition constant for human aromatase cytochrome P450 19A1 activityMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

Ki: 1.5nMAssay Description:Inhibition of human placental microsome cytochrome P450 19A1More data for this Ligand-Target Pair

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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

Ki: 1.5nMAssay Description:Binding affinity was measured on Cytochrome P450 19A1More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

Ki: 1.60nMAssay Description:Inhibition of aromatase in human placental microsomesMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 0.00400nMAssay Description:Inhibition of aromatase (unknown origin) transfected in human MCF7 cellsMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 0.0300nMAssay Description:Aromatase inhibitor potency as iron-binding-related type II difference spectrumMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 3nMAssay Description:Inhibition of human aromatase using dibenzylfluorescein substrate preincubated for 30 mins measured after 30 mins by fluorescence assayMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 4.5nMAssay Description:Inhibition of human placental microsome CYP19More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 5nMAssay Description:Inhibition of human placental microsome CYP19More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 5nMAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta,2beta-3H]testosterone during aromatization. After incubation, the ...More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 6.40nMAssay Description:In vitro inhibition of cytochrome P450 19A1More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 29.5nMpH: 7.4Assay Description:The enzyme was obtained from the microsome fraction of fresh human placenta (St. Josephs Krankenhaus, Saarbrucken-Dudweiler, Germany) according to th...More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 30nMAssay Description:Inhibition of human placental CYP19 using [1beta-3H]androstenedione substrateMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 30nMAssay Description:Inhibition of human placental CYP19 using androstenedione as substrateMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 30nMAssay Description:Inhibition of human placental CYP19More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 30nMAssay Description:Inhibition of human placental CYP19More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 30nMAssay Description:Inhibition of human placental microsome CYP19More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 30nMAssay Description:Inhibition of aromatase in human placental microsomesMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 30nMAssay Description:Inhibition of human recombinant CYP19 using [1beta-3H]androstenedione as substrateMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 30nMpH: 7.4Assay Description:The enzyme was obtained from the microsome fraction of fresh human placenta (St. Josephs Krankenhaus, Saarbrucken-Dudweiler, Germany) according to th...More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

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Details US Patent

Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

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Details US Patent

Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 30nMAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta-3H] Androstenedione during aromatization. After incubation, the re...More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 30nMAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from 3H-labeled androstenedione during aromatization. After incubation, the re...More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 39nMAssay Description:In vitro inhibition of cytochrome P450 19A1More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 39nMAssay Description:In vitro inhibition of cytochrome P450 19A1More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 41nMAssay Description:Inhibition of human placental CYP19 using [1beta-3H]androstenedione as substrate by 3H2O-methodMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 41nMAssay Description:Inhibition of human CYP19 using [1beta-3H]androstenedione as substrate by 3H2O methodMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 41nMAssay Description:Inhibition of human placental CYP19 using androstenedione substrateMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 50nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 52nMAssay Description:Inhibition of human placental microsome cytochrome P450 19A1 aromataseMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 52nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 52nMAssay Description:Inhibition of human placental microsome CYP19 using [1beta-3H] androstenedione as a substrateMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 52nMAssay Description:Inhibition of CYP19 in human placental microsomesMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 52nMAssay Description:Inhibition of CYP19 in human placental microsomes using [1beta-3H]-androstendione as a substrateMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 52nMAssay Description:Inhibition of aromatase from human placental microsomesMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
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Aromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL

BDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)

IC50: 200nMAssay Description:Inhibition of human aromatase cytochrome P450 19A1 activityMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
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Filter my 39 hits

Targets 1▿
- Aromatase 39
Publications 30▿
- J Med Chem 34: 725-36 (1991) 5
- US Patent US9271963 (2016) 3
- J Med Chem 48: 1563-75 (2005) 2
- Bioorg Med Chem Lett 8: 1041-4 (1999) 2
- Bioorg Med Chem 20: 2427-34 (2012) 2
- Eur J Med Chem 241: (2022) 1
- J Med Chem 54: 2307-19 (2011) 1
- J Med Chem 56: 460-70 (2013) 1
- J Med Chem 50: 3420-2 (2007) 1
- Bioorg Med Chem Lett 20: 3050-64 (2010) 1
- J Med Chem 59: 5131-48 (2016) 1
- J Med Chem 51: 8077-87 (2008) 1
- Bioorg Med Chem Lett 21: 186-90 (2010) 1
- J Med Chem 44: 672-80 (2001) 1
- J Med Chem 54: 1613-25 (2011) 1
- J Med Chem 57: 5011-22 (2014) 1
- J Med Chem 56: 1723-9 (2013) 1
- J Med Chem 33: 2933-42 (1990) 1
- J Med Chem 55: 7080-9 (2012) 1
- J Med Chem 49: 4777-80 (2006) 1
- J Med Chem 53: 5347-51 (2010) 1
- J Med Chem 55: 6629-33 (2012) 1
- J Med Chem 51: 5064-74 (2008) 1
- Pharmacol Rev 49: 2222-31 (2006) 1
- J Med Chem 48: 1796-805 (2005) 1
- Bioorg Med Chem Lett 18: 4713-5 (2008) 1
- Eur J Med Chem 90: 788-96 (2015) 1
- Bioorg Med Chem 16: 8349-58 (2008) 1
- J Med Chem 51: 6138-49 (2008) 1
- J Med Chem 48: 6632-42 (2005) 1
Institutions 17▿
- Saarland University 10
- Ciba-Geigy 5
- University Of Bologna 4
- Universitat Des Saarlandes 3
- Centre D'Etudes Et De Recherche Sur Le MéDicament De Normandie 2
- Saarland University & Helmholtz Institute For Pharmaceutical Research Saarland (Hips) 2
- Purdue University 2
- Saarland University And Helmholtz Institute For Pharmaceutical Research Saarland (Hips) 2
- Université 1
- Saarland University & Helmholtz Institute For Pharmaceutical Research Saarland 1
- TBA 1
- Johns Hopkins University 1
- Università 1
- Universita` Degli Studi Di Bari Aldo Moro 1
- Johns Hopkins University School Of Medicine 1
- Zhejiang University 1
- State University Of New York Upstate Medical University 1
Affinity: 0.0040 to 2.0E+2 nM▿
- Ki 5
- IC50 34
- Affinity ≤ nM
Xtal structures: 0
Docked structures: 0
Catalog Cmpds: 1