Compile Data Set for Download or QSAR
Report error Found 90 Enz. Inhib. hit(s) with all data for entry = 13590
TargetTyrosine-protein kinase SYK(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808969BDBM808969(US12637469, Compound 10)
Affinity DataIC50: 11nMAssay Description:Table 1: Experimental steps and methods:a) Compound dilution and plate making1) The compound powder is weighed, dissolved in a certain amount of DMSO...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 12nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase SYK(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 15nMAssay Description:Table 1: Experimental steps and methods:a) Compound dilution and plate making1) The compound powder is weighed, dissolved in a certain amount of DMSO...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase SYK(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808964BDBM808964(US12637469, Compound 5)
Affinity DataIC50: 17nMAssay Description:Table 1: Experimental steps and methods:a) Compound dilution and plate making1) The compound powder is weighed, dissolved in a certain amount of DMSO...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetVascular endothelial growth factor receptor 2(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808964BDBM808964(US12637469, Compound 5)
Affinity DataIC50: 19nMAssay Description:In Vitro Test of the Compound's Inhibitory Effect on VEGFR2 Kinase Experimental Methods and Procedures: The ADP-GLO Kinase Assay is an analytical rea...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetVascular endothelial growth factor receptor 2(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808968BDBM808968(US12637469, Compound 9)
Affinity DataIC50: 22nMAssay Description:In Vitro Test of the Compound's Inhibitory Effect on VEGFR2 Kinase Experimental Methods and Procedures: The ADP-GLO Kinase Assay is an analytical rea...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase SYK(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808968BDBM808968(US12637469, Compound 9)
Affinity DataIC50: 23nMAssay Description:Table 1: Experimental steps and methods:a) Compound dilution and plate making1) The compound powder is weighed, dissolved in a certain amount of DMSO...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetVascular endothelial growth factor receptor 2(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 23nMAssay Description:In Vitro Test of the Compound's Inhibitory Effect on VEGFR2 Kinase Experimental Methods and Procedures: The ADP-GLO Kinase Assay is an analytical rea...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase SYK(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808967BDBM808967(US12637469, Compound 8)
Affinity DataIC50: 30nMAssay Description:Table 1: Experimental steps and methods:a) Compound dilution and plate making1) The compound powder is weighed, dissolved in a certain amount of DMSO...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetVascular endothelial growth factor receptor 2(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808963BDBM808963(US12637469, Compound 2)
Affinity DataIC50: 31nMAssay Description:In Vitro Test of the Compound's Inhibitory Effect on VEGFR2 Kinase Experimental Methods and Procedures: The ADP-GLO Kinase Assay is an analytical rea...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetVascular endothelial growth factor receptor 2(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808967BDBM808967(US12637469, Compound 8)
Affinity DataIC50: 31nMAssay Description:In Vitro Test of the Compound's Inhibitory Effect on VEGFR2 Kinase Experimental Methods and Procedures: The ADP-GLO Kinase Assay is an analytical rea...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase SYK(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808966BDBM808966(US12637469, Compound 7)
Affinity DataIC50: 34nMAssay Description:Table 1: Experimental steps and methods:a) Compound dilution and plate making1) The compound powder is weighed, dissolved in a certain amount of DMSO...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase SYK(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808970BDBM808970(US12637469, Compound 11)
Affinity DataIC50: 34nMAssay Description:Table 1: Experimental steps and methods:a) Compound dilution and plate making1) The compound powder is weighed, dissolved in a certain amount of DMSO...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetVascular endothelial growth factor receptor 2(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808969BDBM808969(US12637469, Compound 10)
Affinity DataIC50: 41nMAssay Description:In Vitro Test of the Compound's Inhibitory Effect on VEGFR2 Kinase Experimental Methods and Procedures: The ADP-GLO Kinase Assay is an analytical rea...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetVascular endothelial growth factor receptor 2(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808966BDBM808966(US12637469, Compound 7)
Affinity DataIC50: 42nMAssay Description:In Vitro Test of the Compound's Inhibitory Effect on VEGFR2 Kinase Experimental Methods and Procedures: The ADP-GLO Kinase Assay is an analytical rea...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetVascular endothelial growth factor receptor 2(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808965BDBM808965(US12637469, Compound 6)
Affinity DataIC50: 44nMAssay Description:In Vitro Test of the Compound's Inhibitory Effect on VEGFR2 Kinase Experimental Methods and Procedures: The ADP-GLO Kinase Assay is an analytical rea...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetCytochrome P450 1A2(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 50nMAssay Description:Table 3: Experimental methods and procedures1) Prepare test compound and standard inhibitor working solution (100×);2) Take the microsomes out of the...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetCytochrome P450 2C9(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 50nMAssay Description:Table 3: Experimental methods and procedures1) Prepare test compound and standard inhibitor working solution (100×);2) Take the microsomes out of the...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase SYK(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808965BDBM808965(US12637469, Compound 6)
Affinity DataIC50: 50nMAssay Description:Table 1: Experimental steps and methods:a) Compound dilution and plate making1) The compound powder is weighed, dissolved in a certain amount of DMSO...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetCytochrome P450 2C19(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 50nMAssay Description:Table 3: Experimental methods and procedures1) Prepare test compound and standard inhibitor working solution (100×);2) Take the microsomes out of the...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetCytochrome P450 2D6(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 50nMAssay Description:Table 3: Experimental methods and procedures1) Prepare test compound and standard inhibitor working solution (100×);2) Take the microsomes out of the...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 50nMAssay Description:Table 3: Experimental methods and procedures1) Prepare test compound and standard inhibitor working solution (100×);2) Take the microsomes out of the...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetVascular endothelial growth factor receptor 2(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808970BDBM808970(US12637469, Compound 11)
Affinity DataIC50: 56nMAssay Description:In Vitro Test of the Compound's Inhibitory Effect on VEGFR2 Kinase Experimental Methods and Procedures: The ADP-GLO Kinase Assay is an analytical rea...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetMitogen-activated protein kinase kinase kinase kinase 4 (MAP4K4)(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 63nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetVascular endothelial growth factor receptor 2(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808971BDBM808971(US12637469, Compound 12)
Affinity DataIC50: 88nMAssay Description:In Vitro Test of the Compound's Inhibitory Effect on VEGFR2 Kinase Experimental Methods and Procedures: The ADP-GLO Kinase Assay is an analytical rea...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetSerine/threonine-protein kinase B-raf(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 91nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetVascular endothelial growth factor receptor 1 (Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 104nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetHigh affinity nerve growth factor receptor (TrkA)(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 112nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetNon-receptor tyrosine-protein kinase TYK2(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 117nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase SYK(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808963BDBM808963(US12637469, Compound 2)
Affinity DataIC50: 125nMAssay Description:Table 1: Experimental steps and methods:a) Compound dilution and plate making1) The compound powder is weighed, dissolved in a certain amount of DMSO...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase JAK2(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 141nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase ABL1(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 152nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase Yes(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 204nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase TXK(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 227nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetAurora kinase B(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 232nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetMitogen-activated protein kinase 10(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 279nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase SYK(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808971BDBM808971(US12637469, Compound 12)
Affinity DataIC50: 315nMAssay Description:Table 1: Experimental steps and methods:a) Compound dilution and plate making1) The compound powder is weighed, dissolved in a certain amount of DMSO...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetProto-oncogene tyrosine-protein kinase Src(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 367nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase Fyn(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 373nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetCasein kinase I isoform epsilon(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 385nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase HCK(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 418nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetFocal adhesion kinase 1(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 469nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetRho-associated protein kinase 2 (ROCK2)(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 499nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase JAK3(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 550nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase JAK1(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 663nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 756nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetProtein BRICK1(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 775nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetProto-oncogene tyrosine-protein kinase Src [1-530](Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 827nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetFibroblast growth factor receptor 1(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 847nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

TargetTyrosine-protein kinase Lyn(Human)
Ocumension Therapeutics (Suzhou) Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 808962BDBM808962(US12637469, Compound 1)
Affinity DataIC50: 934nMAssay Description:Table 2: Purpose: In order to investigate the specificity of compounds for target inhibition, this study tested the activity and selectivity of test ...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
10/12/2026
Entry Details
US Patent

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