Compile Data Set for Download or QSAR
Report error Found 21 Enz. Inhib. hit(s) with all data for entry = 50022871
TargetEndothelial PAS domain-containing protein 1(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50655402BDBM50655402(CHEMBL6133742)
Affinity DataKd:  0.240nMAssay Description:Binding affinity to HIF-2alpha (unknown origin) assessed as dissociation constantMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetOrexin/Hypocretin receptor type 1(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 334973BDBM334973(US9732075, Example 5.36 | [(S)-2-(5-Chloro-4-methy...)
Affinity DataIC50: 0.600nMAssay Description:Antagonist activity at OX1 receptor (unknown origin) expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetDipeptidyl peptidase 4(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50225074BDBM50225074(CHEMBL385517 | BMS-477118 | (1S,6S)-2-(2-adamantan...)
Affinity DataKi:  0.600nMAssay Description:Binding affinity to DPP-4 (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetOrexin receptor type 2(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 334973BDBM334973(US9732075, Example 5.36 | [(S)-2-(5-Chloro-4-methy...)
Affinity DataIC50: 0.900nMAssay Description:Antagonist activity at OX2 receptor (unknown origin) expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetRenin(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50655404BDBM50655404(CHEMBL6141922)
Affinity DataIC50: 2nMAssay Description:Inhibition of renin (unknown origin) using Arg-Glu(EDANS)-lle-His-Pro-Phe-His-Leu-Val-lle-His-Thr-Lys(dabcyl)-Arg as substrate incubated for 10 mins ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
LigandChemical structure of BindingDB Monomer ID 25150BDBM25150(Belinostat | (2E)-N-hydroxy-3-[3-(phenylsulfamoyl)...)
Affinity DataIC50: 2.90nMAssay Description:Inhibition of PI3Kalpha (unknown origin) using PIP2 as substrate measured after 30 mins by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetEndothelial PAS domain-containing protein 1(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50655403BDBM50655403(CHEMBL6145373)
Affinity DataKd:  3.10nMAssay Description:Binding affinity to HIF-2alpha (unknown origin) assessed as dissociation constantMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetDipeptidyl peptidase 4(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 171268BDBM171268(US9085555, 698)
Affinity DataKi:  6nMAssay Description:Binding affinity to DPP-4 (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetDipeptidyl peptidase 4(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50628586BDBM50628586(CHEMBL5398220)
Affinity DataKi:  7nMAssay Description:Binding affinity to DPP-4 (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetDipeptidyl peptidase 4(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50151003BDBM50151003(CHEMBL1627303 | CHEMBL363250 | (S)-1-((S)-2-Amino-...)
Affinity DataKi:  8nMAssay Description:Binding affinity to DPP-4 (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50247539BDBM50247539(N-((3S,5S)-1-((E)-3-(3,4-dimethoxyphenyl)acryloyl)...)
Affinity DataIC50: 9nMAssay Description:Inhibition of SARS-CoV-2 main protease extracted from Escherichia coli BL21 (DE3) cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50009331BDBM50009331(CHEMBL3233843 | US9346814, Cmpd No 24 Example 28)
Affinity DataIC50: 9nMAssay Description:Inhibition of SARS-CoV-2 main proteaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50239948BDBM50239948(US9850225, Example 1166 | CHEMBL4071326)
Affinity DataIC50: 11nMAssay Description:Inhibition of SARS-CoV-2 main proteaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetEndothelial PAS domain-containing protein 1(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50655401BDBM50655401(CHEMBL6160361)
Affinity DataKd:  11nMAssay Description:Binding affinity to HIF-2alpha (unknown origin) assessed as dissociation constantMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetOrexin receptor type 2(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 154947BDBM154947(US9000029, 26)
Affinity DataIC50: 11nMAssay Description:Antagonist activity at OX2 receptor (unknown origin) expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetEndothelial PAS domain-containing protein 1(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50655399BDBM50655399(CHEMBL6161996)
Affinity DataKd:  12nMAssay Description:Binding affinity to HIF-2alpha (unknown origin) assessed as dissociation constantMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetHistone deacetylase 6(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 25150BDBM25150(Belinostat | (2E)-N-hydroxy-3-[3-(phenylsulfamoyl)...)
Affinity DataIC50: 26nMAssay Description:Inhibition of HDAC6 (unknown origin) using Ac-Leu-Gly-Lys (Ac)-AMC as substrate measured for 60 mins by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetEndothelial PAS domain-containing protein 1(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50655400BDBM50655400(CHEMBL6120402)
Affinity DataKd:  52nMAssay Description:Binding affinity to HIF-2alpha (unknown origin) assessed as dissociation constantMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetOrexin/Hypocretin receptor type 1(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 154947BDBM154947(US9000029, 26)
Affinity DataIC50: 60nMAssay Description:Antagonist activity at OX1 receptor (unknown origin) expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetReplicase polyprotein 1ab(2019-nCoV)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50655405BDBM50655405(CHEMBL6141747)
Affinity DataIC50: 182nMAssay Description:Inhibition of SARS-CoV-2 main protease extracted from Escherichia coli BL21 (DE3) cellsMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
Target72 kDa type IV collagenase(Human)
Enamine Ltd.

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50420291BDBM50420291(CHEMBL2088991)
Affinity DataIC50: 450nMAssay Description:Inhibition of MMP-2 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed