Compile Data Set for Download or QSAR
Found 435 with Last Name = 'fei' and Initial = 'f'
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495338(CHEMBL3110147)copy SMILEScopy InChI
Affinity DataKi:  133nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495344(CHEMBL3110154)copy SMILEScopy InChI
Affinity DataKi:  257nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495345(CHEMBL3110149)copy SMILEScopy InChI
Affinity DataKi:  297nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495339(CHEMBL3110146)copy SMILEScopy InChI
Affinity DataKi:  516nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495349(CHEMBL3110153)copy SMILEScopy InChI
Affinity DataKi:  598nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495343(CHEMBL3110145)copy SMILEScopy InChI
Affinity DataKi:  612nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495342(CHEMBL3110151)copy SMILEScopy InChI
Affinity DataKi:  641nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495349(CHEMBL3110153)copy SMILEScopy InChI
Affinity DataKi:  733nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495343(CHEMBL3110145)copy SMILEScopy InChI
Affinity DataKi:  802nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495341(CHEMBL3110150)copy SMILEScopy InChI
Affinity DataKi:  808nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495342(CHEMBL3110151)copy SMILEScopy InChI
Affinity DataKi:  815nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495347(CHEMBL3110152)copy SMILEScopy InChI
Affinity DataKi:  847nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495346(CHEMBL3110148)copy SMILEScopy InChI
Affinity DataKi:  3.24E+3nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495340(CHEMBL3110155)copy SMILEScopy InChI
Affinity DataKi:  3.81E+3nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495339(CHEMBL3110146)copy SMILEScopy InChI
Affinity DataKi:  2.79E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495347(CHEMBL3110152)copy SMILEScopy InChI
Affinity DataKi:  2.80E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495341(CHEMBL3110150)copy SMILEScopy InChI
Affinity DataKi:  4.70E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495338(CHEMBL3110147)copy SMILEScopy InChI
Affinity DataKi:  4.73E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495344(CHEMBL3110154)copy SMILEScopy InChI
Affinity DataKi:  4.76E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495340(CHEMBL3110155)copy SMILEScopy InChI
Affinity DataKi:  6.40E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495345(CHEMBL3110149)copy SMILEScopy InChI
Affinity DataKi:  7.22E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495346(CHEMBL3110148)copy SMILEScopy InChI
Affinity DataKi:  9.45E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495348(CHEMBL3110156)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495337(CHEMBL3110157)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495337(CHEMBL3110157)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar de Engenharia

Curated by ChEMBL
LigandPNGBDBM50495348(CHEMBL3110156)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28K7D2GPubMed
TargetType-1 angiotensin II receptor(Homo sapiens (Human))
Beijing Institute of Technology

Curated by ChEMBL
LigandPNGBDBM50493576(CHEMBL2435828)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PK0K32PubMed
TargetType-1 angiotensin II receptor(Homo sapiens (Human))
Beijing Institute of Technology

Curated by ChEMBL
LigandPNGBDBM50493578(CHEMBL2435824)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PK0K32PubMed
TargetType-1 angiotensin II receptor(Homo sapiens (Human))
Beijing Institute of Technology

Curated by ChEMBL
LigandPNGBDBM82258(CAS_114798-26-4 | Losartan | NSC_3961)copy SMILEScopy InChI
Affinity DataIC50: 0.330nMAssay Description:Inhibition of angiotensin AT1 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GT5P7JPubMed
TargetType-2 angiotensin II receptor(Homo sapiens (Human))
Beijing Institute of Technology

Curated by ChEMBL
LigandPNGBDBM50043280(4'-((1,4'-dimethyl-2'-propyl(2,6'-bi-1H-benzimidaz...)copy SMILEScopy InChI
Affinity DataIC50: 0.330nMAssay Description:Displacement of [125I]Sar1 Ile8-Ang 2 from angiotensin 2 AT2 receptor after 180 mins by gamma countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29K4BPWPubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50591330(CHEMBL5197431)copy SMILES
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6VHVPubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50591331(CHEMBL5197282)copy SMILES
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6VHVPubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50591334(CHEMBL5191146)copy SMILES
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6VHVPubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50591327(CHEMBL5177544)copy SMILES
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6VHVPubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM158481(US9029401, 1728 (t-TUCB))copy SMILEScopy InChI
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM409005(US10377744, Compound No. 26 | US11123311, Compound...)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6VHVPubMed
TargetBifunctional epoxide hydrolase 2(Rattus norvegicus)TBA
LigandPNGBDBM50581728(CHEMBL5093683)copy SMILES
Affinity DataIC50: 0.400nMAssay Description:Inhibition of rat recombinant sEH using CMNPC as substrate incubated for 5 mins by fluorescent based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KPPPubMed
TargetBifunctional epoxide hydrolase 2(Rattus norvegicus)TBA
LigandPNGBDBM50581727(CHEMBL5084744)copy SMILES
Affinity DataIC50: 0.400nMAssay Description:Inhibition of rat recombinant sEH using CMNPC as substrate incubated for 5 mins by fluorescent based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KPPPubMed
TargetBifunctional epoxide hydrolase 2(Rattus norvegicus)TBA
LigandPNGBDBM50581725(CHEMBL5081862)copy SMILES
Affinity DataIC50: 0.400nMAssay Description:Inhibition of rat recombinant sEH using CMNPC as substrate incubated for 5 mins by fluorescent based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KPPPubMed
TargetBifunctional epoxide hydrolase 2(Mus musculus (Mouse))TBA
LigandPNGBDBM50581727(CHEMBL5084744)copy SMILES
Affinity DataIC50: 0.400nMAssay Description:Inhibition of mouse recombinant sEH using CMNPC as substrate incubated for 5 mins by fluorescent based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KPPPubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM409005(US10377744, Compound No. 26 | US11123311, Compound...)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMAssay Description:Inhibition of human recombinant sEH using CMNPC as substrate incubated for 5 mins by fluorescent based assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KPPPubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50581727(CHEMBL5084744)copy SMILES
Affinity DataIC50: 0.400nMAssay Description:Inhibition of human recombinant sEH using CMNPC as substrate incubated for 5 mins by fluorescent based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70KPPPubMed
TargetType-1 angiotensin II receptor(Homo sapiens (Human))
Beijing Institute of Technology

Curated by ChEMBL
LigandPNGBDBM50493577(CHEMBL2435823)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMAssay Description:Displacement of [125I]-Sar1Ile8-angiotensin 2 from angiotensin 2 AT1 receptor (unknown origin) after 180 mins by gamma counting analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PK0K32PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50604191(CHEMBL5207628)copy SMILES
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76HMMPubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50604188(CHEMBL5204900)copy SMILES
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76HMMPubMed
TargetBifunctional epoxide hydrolase 2(Mus musculus (Mouse))TBA
LigandPNGBDBM50591345(CHEMBL5196519)copy SMILES
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6VHVPubMed
TargetBifunctional epoxide hydrolase 2(Mus musculus (Mouse))TBA
LigandPNGBDBM50591344(CHEMBL5208857)copy SMILES
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6VHVPubMed
TargetBifunctional epoxide hydrolase 2(Mus musculus (Mouse))TBA
LigandPNGBDBM50591341(CHEMBL5177372)copy SMILES
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6VHVPubMed
TargetBifunctional epoxide hydrolase 2(Mus musculus (Mouse))TBA
LigandPNGBDBM50591337(CHEMBL5192445)copy SMILES
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6VHVPubMed
TargetBifunctional epoxide hydrolase 2(Mus musculus (Mouse))TBA
LigandPNGBDBM50591336(CHEMBL5179027)copy SMILES
Affinity DataIC50: 0.400nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6VHVPubMed
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