Compile Data Set for Download or QSAR
Report error Found 389 Enz. Inhib. hit(s) with all data for entry = 11321
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607107BDBM607107(US11685745, Example 64)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607106BDBM607106(US11685745, Example 51)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607105BDBM607105(US11685745, Example 43)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607104BDBM607104(US11685745, Example 37)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607111BDBM607111(US11685745, Example 189)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607110BDBM607110(US11685745, Example 176)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607109BDBM607109(US11685745, Example 123)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607108BDBM607108(US11685745, Example 79)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607115BDBM607115(US11685745, Example 334)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607114BDBM607114(US11685745, Example 332)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607112BDBM607112(US11685745, Example 225)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607119BDBM607119(US11685745, Example 427)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607118BDBM607118(US11685745, Example 378)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607116BDBM607116(US11685745, Example 336)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607123BDBM607123(US11685745, Example 557)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607122BDBM607122(US11685745, Example 545)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607121BDBM607121(US11685745, Example 492)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607124BDBM607124(US11685745, Example 581 | US11685745, Example 576)
Affinity DataIC50: 10nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607131BDBM607131(US11685745, Example 16)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607130BDBM607130(US11685745, Example 15)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607129BDBM607129(US11685745, Example 7)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607128BDBM607128(US11685745, Example 6)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607135BDBM607135(US11685745, Example 21)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607134BDBM607134(US11685745, Example 20)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607133BDBM607133(US11685745, Example 19)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607132BDBM607132(US11685745, Example 17)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607139BDBM607139(US11685745, Example 28)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607138BDBM607138(US11685745, Example 27)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607137BDBM607137(US11685745, Example 26)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607136BDBM607136(US11685745, Example 22)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607143BDBM607143(US11685745, Example 35)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607142BDBM607142(US11685745, Example 34)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607141BDBM607141(US11685745, Example 31)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607140BDBM607140(US11685745, Example 30)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607127BDBM607127(US11685745, Example 5)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607126BDBM607126(US11685745, Example 4)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607125BDBM607125(US11685745, Example 2)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607163BDBM607163(US11685745, Example 60)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607162BDBM607162(US11685745, Example 58)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607161BDBM607161(US11685745, Example 57)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607160BDBM607160(US11685745, Example 56)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607167BDBM607167(US11685745, Example 66)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607166BDBM607166(US11685745, Example 65)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607165BDBM607165(US11685745, Example 62)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607164BDBM607164(US11685745, Example 61)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607171BDBM607171(US11685745, Example 74)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607170BDBM607170(US11685745, Example 73)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607169BDBM607169(US11685745, Example 71)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607168BDBM607168(US11685745, Example 67)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Dart Neuroscience

US Patent
LigandChemical structure of BindingDB Monomer ID 607175BDBM607175(US11685745, Example 78)
Affinity DataIC50: 55nMAssay Description:PDE7 inhibition was determined by an IMAP TR-FRET assay using PDE7B. The IMAP TR-FRET PDE assay was optimized for concentration of enzyme, FAM-cAMP s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/31/2023
Entry Details
US Patent

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