Compile Data Set for Download or QSAR
Report error Found 19 of affinity data for UniProtKB/TrEMBL: P14927
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027963BDBM50027963(CHEMBL3360259)
Affinity DataIC50: 2.50E+3nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027960BDBM50027960(CHEMBL188279)
Affinity DataIC50: 5.00E+3nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028004BDBM50028004(CHEMBL3360267)
Affinity DataIC50: 5.00E+3nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028006BDBM50028006(CHEMBL186268)
Affinity DataIC50: 8.00E+3nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028005BDBM50028005(CHEMBL185823)
Affinity DataIC50: 8.00E+3nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027968BDBM50027968(CHEMBL3360264)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027969BDBM50027969(CHEMBL3360268)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027966BDBM50027966(CHEMBL3360262)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027967BDBM50027967(CHEMBL3360263)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027964BDBM50027964(CHEMBL3360260)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027965BDBM50027965(CHEMBL3360261)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027962BDBM50027962(CHEMBL3360258)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027961BDBM50027961(CHEMBL3360257 | US10849901, Compound 126)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027958BDBM50027958(CHEMBL3360255)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027959BDBM50027959(CHEMBL3360256)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028009BDBM50028009(CHEMBL2322452)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028007BDBM50028007(CHEMBL3360266)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028008BDBM50028008(CHEMBL3360265)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed
TargetCytochrome b-c1 complex subunit 7(Human)
Yonsei University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 60397BDBM60397(SMR000092793 | MLS000115777 | N-(4-hydroxyphenyl)-...)
Affinity DataIC50: 2.00E+4nMAssay Description:Modulation of UQCRB in human HepG2 cells assessed as inhibition of HIF-1alpha for 4 hrs under 1%O2 by Western blot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/8/2016
Entry Details Article
PubMed