Compile Data Set for Download or QSAR
Report error Found 104 Enz. Inhib. hit(s) with all data for entry = 10654
TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557412BDBM557412(US11358936, Compound 1-40 | 3-((4-(Aminomethyl)pyr...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557338BDBM557338(US11358936, Compound 1-39 | 3-((4-(Aminomethyl)pyr...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557447BDBM557447(US11358936, Compound 1-42 | 3-((4-(Aminomethyl)pyr...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 50266785BDBM50266785(CHEMBL4066192 | US11358936, Compound 1-41)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557559BDBM557559(US11358936, Compound 1-44 | 3-((4-(Aminomethyl)pyr...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557558BDBM557558(US11358936, Compound 1-43)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557560BDBM557560(US11358936, Compound 1-45 | 3-(((4-(Aminomethyl)py...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 50232693BDBM50232693(CHEMBL4072524 | US11358936, Compound 2-3)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557565BDBM557565(US11358936, Compound 2-4)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557574BDBM557574((2-(3-Phenoxyphenoxy)pyridin-4-yl)methanamine | U...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557323BDBM557323(US11358936, Compound 1-24 | 3-((4-Aminomethyl)pyri...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557322BDBM557322(US11358936, Compound 1-23 | 3-((4-Aminomethyl)pyri...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557325BDBM557325(US11358936, Compound 1-26 | Methyl 4-(3-((4-(amind...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557324BDBM557324(US11358936, Compound 1-25 | 3-((4-(Aminomethyl)pyr...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557327BDBM557327(US11358936, Compound 1-28 | 3-(3-((4-Aminomethyl)p...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557326BDBM557326(US11358936, Compound 1-27 | Ethyl 3-(3-((4-(aminom...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557329BDBM557329(US11358936, Compound 1-30 | 3-((4-(Aminomethyl)pyr...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557328BDBM557328(US11358936, Compound 1-29 | 4-(3-((4-(Aminomethyl)...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557331BDBM557331(US11358936, Compound 1-32 | 3-((4-(Aminomethyl)pyr...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557330BDBM557330(US11358936, Compound 1-31 | 3-((4-(Aminomethyl)pyr...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557333BDBM557333(US11358936, Compound 1-34 | 4-((3-((4-Aminomethyl)...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557332BDBM557332(US11358936, Compound 1-33 | Methyl 4-((3-((4-(amin...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557335BDBM557335(US11358936, Compound 1-36 | (R)-3-((4-Aminomethyl)...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557334BDBM557334(US11358936, Compound 1-35 | 3-((3-((4-Aminomethyl)...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557337BDBM557337(US11358936, Compound 1-38 | 3-((4-(Aminomethyl)pyr...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557336BDBM557336(US11358936, Compound 1-37 | 3-((4-(Aminomethyl)pyr...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557597BDBM557597(US11358936, Compound 2-27 | 2-(4-((4-(Aminomethyl)...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557596BDBM557596(US11358936, Compound 2-26 | 2-(4-((4-(Aminomethyl)...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557598BDBM557598(US11358936, Compound 2-28)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557601BDBM557601(US11358936, Compound 2-31 | 2-(4-((4-(Aminomethyl)...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557600BDBM557600(US11358936, Compound 2-30 | 2-(4-((4-(Aminomethyl)...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557603BDBM557603(US11358936, Compound 2-33 | (2-((1-(6-Fluorobenzo[...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557602BDBM557602(US11358936, Compound 2-32 | (2-((1H-Indol-4-yl)oxy...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557605BDBM557605(US11358936, Compound 2-36 | 5-((4-(Aminomethyl)pyr...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557604BDBM557604(US11358936, Compound 2-35)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557607BDBM557607(US11358936, Compound 2-38 | (S)-(3-((4-(Aminomethy...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557606BDBM557606(US11358936, Compound 2-37 | 5-((4-(Aminomethyl)pyr...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557609BDBM557609(US11358936, Compound 2-40 | Racemic-(4-(aminomethy...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557608BDBM557608(US11358936, Compound 2-39 | (A)-3-((4-(Aminomethyl...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557611BDBM557611(US11358936, Compound 2-41 | 4-(Aminomethyl)-N-benz...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557580BDBM557580(US11358936, Compound 2-11 | (2-((1-(2,4-Difluorobe...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557578BDBM557578(US11358936, Compound 2-10)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557582BDBM557582(US11358936, Compound 2-13)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557581BDBM557581(US11358936, Compound 2-12 | (2-((1-(2,4-Difluorobe...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557584BDBM557584(US11358936, Compound 2-15 | (2-((1-((5-Fluoropyrid...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557583BDBM557583(US11358936, Compound 2-14 | (2-((1-((6-Methoxypyri...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557586BDBM557586(US11358936, Compound 2-17 | (2-((1-((2-(Trifluorom...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557585BDBM557585(US11358936, Compound 2-16 | (2-((1-(Quinolin-2-ylm...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557589BDBM557589(US11358936, Compound 2-19 | (2-((1-(1-Methyl-1H-py...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

TargetLysyl oxidase homolog 2(Human)
Pharmakea

US Patent
LigandChemical structure of BindingDB Monomer ID 557587BDBM557587(US11358936, Compound 2-18 | (2-((1-(4-Fluorophenyl...)
Affinity DataIC50: 300nMAssay Description:LOXL2 amine oxidase activity is evaluated by measuring Amplex Red fluorescence using 10-20× concentrated conditioned media from CHO cells stably expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/19/2022
Entry Details
US Patent

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