Compile Data Set for Download or QSAR
maximum 50k data
Found 183 with Last Name = 'shan' and Initial = 'z'
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Binzhou Medical University

Curated by ChEMBL
LigandPNGBDBM50607777(CHEMBL5220392)
Affinity DataKi:  1.21E+3nMAssay Description:Mixed type inhibition of N-terminal His-tagged recombinant human PTP1B expressed in Escherichia coli using pNPP as substrate assessed as inhibition c...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Binzhou Medical University

Curated by ChEMBL
LigandPNGBDBM50607780(CHEMBL5220593)
Affinity DataKi:  3.02E+3nMAssay Description:Mixed type inhibition of N-terminal His-tagged recombinant human PTP1B expressed in Escherichia coli using pNPP as substrate assessed as inhibition c...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338624((R)-3-amino-1-(3-(4-(methoxycarbonyl)phenyl)-6,7-d...)
Affinity DataIC50:  12.4nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338635((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(3-(methox...)
Affinity DataIC50:  15.1nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338619((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(3-(furan-...)
Affinity DataIC50:  15.8nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Affinity DataIC50:  16nMAssay Description:In vitro inhibitory concentration against rat cortex acetylcholinesteraseMore data for this Ligand-Target Pair
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338615((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(6,7-dihyd...)
Affinity DataIC50:  17.8nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM11162((1R)-3-oxo-3-[3-(trifluoroethyl)-5,6-dihydro[1,2,4...)
Affinity DataIC50:  19.4nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50403921(CHEMBL309664)
Affinity DataIC50:  20nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liver; (observed value)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50403921(CHEMBL309664)
Affinity DataIC50:  20nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338637((R)-3-amino-1-(3-(difluoromethyl)-6,7-dihydro-[1,2...)
Affinity DataIC50:  22.5nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338617((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(6,7-dihyd...)
Affinity DataIC50:  22.8nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338618((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(3-(furan-...)
Affinity DataIC50:  26.2nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338625((R)-3-amino-1-(3-(4-(dimethyamide)phenyl)-6,7-dihy...)
Affinity DataIC50:  26.6nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338621((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(6,7-dihyd...)
Affinity DataIC50:  28.6nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338634((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(3-(amide)...)
Affinity DataIC50:  29.9nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50403929(CHEMBL76394)
Affinity DataIC50:  30nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50089165(CHEMBL23622 | Cyclopropanecarboxylic acid 3-oxo-cy...)
Affinity DataIC50:  30nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liver; (observed value)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50403929(CHEMBL76394)
Affinity DataIC50:  30nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liver; (observed value)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50089165(CHEMBL23622 | Cyclopropanecarboxylic acid 3-oxo-cy...)
Affinity DataIC50:  30nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338628((R)-3-amino-1-(3-(4-(cyano)phenyl)-6,7-dihydro-[1,...)
Affinity DataIC50:  30.0nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338622((R)-3-amino-1-(3-(4-(mesyl)phenyl)-6,7-dihydro-[1,...)
Affinity DataIC50:  33.2nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338620((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(6,7-dihyd...)
Affinity DataIC50:  33.3nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338623((R)-3-amino-1-(3-(4-(carboxyl)phenyl)-6,7-dihydro-...)
Affinity DataIC50:  33.8nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338626((R)-3-amino-1-(3-(4-(amide)phenyl)-6,7-dihydro-[1,...)
Affinity DataIC50:  36.4nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338632((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(3-(4-phen...)
Affinity DataIC50:  37.5nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50075319(2-{HYDROXY[2-NITRO-4-(TRIFLUOROMETHYL)PHENYL]METHY...)
Affinity DataIC50:  40nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liver; (observed value)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50075319(2-{HYDROXY[2-NITRO-4-(TRIFLUOROMETHYL)PHENYL]METHY...)
Affinity DataIC50:  40nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50124366(4-Cyclopropanecarbonyl-3-cyclopropanecarbonyloxy-5...)
Affinity DataIC50:  40nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liver; (observed value)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50124366(4-Cyclopropanecarbonyl-3-cyclopropanecarbonyloxy-5...)
Affinity DataIC50:  40nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50075318(2-(2-Chloro-4-methanesulfonyl-benzoyl)-3-hydroxy-c...)
Affinity DataIC50:  45nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liver; (observed value)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338631((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(3-(4-fluo...)
Affinity DataIC50:  45.2nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338627((R)-3-amino-1-(3-(3-(methoxycarbonyl)phenyl)-6,7-d...)
Affinity DataIC50:  46.6nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338630((R)-3-amino-1-(3-(4-chlorophenyl)-6,7-dihydro-[1,2...)
Affinity DataIC50:  46.9nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338616((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(6,7-dihyd...)
Affinity DataIC50:  47.3nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50075318(2-(2-Chloro-4-methanesulfonyl-benzoyl)-3-hydroxy-c...)
Affinity DataIC50:  50nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50169850(5,6-Dimethoxy-2-(4-pyrrolidin-1-ylmethyl-phenoxy)-...)
Affinity DataIC50:  50nMAssay Description:In vitro inhibitory concentration against rat cortex acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338636((R)-3-amino-1-(3-(trifluoromethyl)-6,7-dihydro-[1,...)
Affinity DataIC50:  50.7nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338633((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(3-(dimeth...)
Affinity DataIC50:  52.3nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50199522((+)-huperzine A | (+-)-HA | (-)-1-Amino-13-ethylid...)
Affinity DataIC50:  53nMAssay Description:In vitro inhibitory concentration against rat cortex acetylcholinesteraseMore data for this Ligand-Target Pair
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50403933(CHEMBL72081)
Affinity DataIC50:  70nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50403933(CHEMBL72081)
Affinity DataIC50:  71nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liver; (observed value)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338629((R)-3-amino-1-(3-(4-(trifluoromethyl)phenyl)-6,7-d...)
Affinity DataIC50:  75.3nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338638((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(6,7-dihyd...)
Affinity DataIC50:  77.1nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50403928(CHEMBL307048)
Affinity DataIC50:  89nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liver; (observed value)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDipeptidyl peptidase 4(Homo sapiens (Human))
Shandong University Of Traditional Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50338639((R)-3-amino-4-(2,4,5-trifluorophenyl)-1-(6,7-dihyd...)
Affinity DataIC50:  89.5nMAssay Description:Inhibition of human DPP4 assessed as hydrolytic reaction of Ala-Pro-AMCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50403928(CHEMBL307048)
Affinity DataIC50:  90nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50169857(2-(4-Diethylaminomethyl-phenoxy)-5,6-dimethoxy-ind...)
Affinity DataIC50:  100nMAssay Description:In vitro inhibitory concentration against rat cortex acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50089168(CHEMBL26162 | Propionic acid 3-oxo-cyclohex-1-enyl...)
Affinity DataIC50:  110nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxyphenylpyruvate dioxygenase(Sus scrofa)
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50089168(CHEMBL26162 | Propionic acid 3-oxo-cyclohex-1-enyl...)
Affinity DataIC50:  110nMAssay Description:Concentration required to achieve 50% inhibition against 4-Hydroxyphenylpyruvate dioxygenase (HPPD) from pig liver; (observed value)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Displayed 1 to 50 (of 183 total ) | Next | Last >>
Jump to: