Compile Data Set for Download or QSAR
Report error Found 103 Enz. Inhib. hit(s) with all data for entry = 8027
TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791819BDBM791819(US12544382, Example D28)
Affinity DataIC50: 1nMAssay Description:NMDA receptors are ion channels that are highly permeable to Ca2+ ions, rendering it possible to monitor NMDA receptor function using cell-based calc...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791760BDBM791760(US12544382, Example D6)
Affinity DataIC50: 1nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791790BDBM791790(US12544382, Example D17)
Affinity DataIC50: 1nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791799BDBM791799(US12544382, Example D20)
Affinity DataIC50: 1nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791796BDBM791796(US12544382, Example D19)
Affinity DataIC50: 1nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791763BDBM791763(US12544382, Example D7)
Affinity DataIC50: 1nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791778BDBM791778(US12544382, Example D13)
Affinity DataIC50: 1nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791793BDBM791793(US12544382, Example D18)
Affinity DataIC50: 1nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791791BDBM791791(US12544382, Example D52)
Affinity DataIC50: 2nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791802BDBM791802(US12544382, Example D21)
Affinity DataIC50: 2nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791782BDBM791782(US12544382, Example D49)
Affinity DataIC50: 2nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791779BDBM791779(US12544382, Example D48)
Affinity DataIC50: 2nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791775BDBM791775(US12544382, Example D12)
Affinity DataIC50: 3nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791803BDBM791803(US12544382, Example D55)
Affinity DataIC50: 3nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791769BDBM791769(US12544382, Example D10)
Affinity DataIC50: 3nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791785BDBM791785(US12544382, Example D50)
Affinity DataIC50: 3nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791752BDBM791752(US12544382, Example D39)
Affinity DataIC50: 3nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791766BDBM791766(US12544382, Example D8)
Affinity DataIC50: 3nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791811BDBM791811(US12544382, Example D24)
Affinity DataIC50: 3nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791797BDBM791797(US12544382, Example D54a)
Affinity DataIC50: 4nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791747BDBM791747(US12544382, Example A16)
Affinity DataIC50: 4nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791794BDBM791794(US12544382, Example D53)
Affinity DataIC50: 4nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791776BDBM791776(US12544382, Example D47)
Affinity DataIC50: 5nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791740BDBM791740(US12544382, Example D35)
Affinity DataIC50: 5nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791755BDBM791755(US12544382, Example D40)
Affinity DataIC50: 5nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791719BDBM791719(US12544382, Example D29)
Affinity DataIC50: 5nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791749BDBM791749(US12544382, Example D38)
Affinity DataIC50: 5nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791745BDBM791745(US12544382, Example D1)
Affinity DataIC50: 5nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791773BDBM791773(US12544382, Example D46)
Affinity DataIC50: 6nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791754BDBM791754(US12544382, Example D4)
Affinity DataIC50: 6nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791748BDBM791748(US12544382, Example D2)
Affinity DataIC50: 6nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791808BDBM791808(US12544382, Example D23)
Affinity DataIC50: 8nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791772BDBM791772(US12544382, Example D11)
Affinity DataIC50: 8nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791817BDBM791817(US12544382, Example D27)
Affinity DataIC50: 8nMAssay Description:NMDA receptors are ion channels that are highly permeable to Ca2+ ions, rendering it possible to monitor NMDA receptor function using cell-based calc...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791806BDBM791806(US12544382, Example D56)
Affinity DataIC50: 9nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791770BDBM791770(US12544382, Example D45)
Affinity DataIC50: 10nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791818BDBM791818(US12544382, Example A41)
Affinity DataIC50: 11nMAssay Description:NMDA receptors are ion channels that are highly permeable to Ca2+ ions, rendering it possible to monitor NMDA receptor function using cell-based calc...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791815BDBM791815(US12544382, Example D26)
Affinity DataIC50: 12nMAssay Description:NMDA receptors are ion channels that are highly permeable to Ca2+ ions, rendering it possible to monitor NMDA receptor function using cell-based calc...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791800BDBM791800(US12544382, Example D54b)
Affinity DataIC50: 13nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791734BDBM791734(US12544382, Example D33)
Affinity DataIC50: 13nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791768BDBM791768(US12544382, Example A23)
Affinity DataIC50: 14nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791743BDBM791743(US12544382, Example D36)
Affinity DataIC50: 15nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791732BDBM791732(US12544382, Example A11)
Affinity DataIC50: 15nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791805BDBM791805(US12544382, Example D22)
Affinity DataIC50: 16nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791722BDBM791722(US12544382, Example D30a)
Affinity DataIC50: 16nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791809BDBM791809(US12544382, Example D57)
Affinity DataIC50: 16nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791784BDBM791784(US12544382, Example D15)
Affinity DataIC50: 17nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791756BDBM791756(US12544382, Example A19)
Affinity DataIC50: 18nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791764BDBM791764(US12544382, Example D43)
Affinity DataIC50: 19nMAssay Description:Inhibition of cAMP Activity of GPR6 In Vitro AssayThis cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity o...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

TargetSerine/threonine-protein kinase ATR(Human)
Beijing Tide Pharmaceutical Co.

US Patent
LigandChemical structure of BindingDB Monomer ID 791744BDBM791744(US12544382, Example A15)
Affinity DataIC50: 21nMAssay Description:This cell based assay measures the ability of compounds to inhibit the constitutive cAMP activity of GPR6 receptor expressed in CHO-K1 cells. CHO cel...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/22/2026
Entry Details US Patent

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