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TargetPeroxisome proliferator-activated receptor alpha(Human)
The University of Sydney

Curated by ChEMBL
LigandPNGBDBM50299413((3',5'-dimethoxy-7-hydroxyisoflavone) | CHEMBL5750...)
Affinity DataEC50:  2.46E+4nMAssay Description:Agonist activity at human PPARalpha assessed as induction of transactivation activity by cell based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/4/2020
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
The University of Sydney

Curated by ChEMBL
LigandPNGBDBM50299416(3'-methoxy-7-hydroxyisoflavone | CHEMBL573966)
Affinity DataEC50:  2.23E+4nMAssay Description:Agonist activity at human PPARgamma assessed as induction of transactivation activity by cell based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/4/2020
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
The University of Sydney

Curated by ChEMBL
LigandPNGBDBM50299413((3',5'-dimethoxy-7-hydroxyisoflavone) | CHEMBL5750...)
Affinity DataEC50:  1.89E+4nMAssay Description:Agonist activity at human PPARgamma assessed as induction of transactivation activity by cell based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/4/2020
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
The University of Sydney

Curated by ChEMBL
LigandPNGBDBM50299416(3'-methoxy-7-hydroxyisoflavone | CHEMBL573966)
Affinity DataEC50:  3.31E+4nMAssay Description:Agonist activity at human PPARalpha assessed as induction of transactivation activity by cell based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/4/2020
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
The University of Sydney

Curated by ChEMBL
LigandPNGBDBM50299415(4'-fluoro-7-hydroxyisoflavone | CHEMBL583378)
Affinity DataEC50:  2.31E+4nMAssay Description:Agonist activity at human PPARalpha assessed as induction of transactivation activity by cell based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/4/2020
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
The University of Sydney

Curated by ChEMBL
LigandPNGBDBM50299415(4'-fluoro-7-hydroxyisoflavone | CHEMBL583378)
Affinity DataEC50:  1.54E+4nMAssay Description:Agonist activity at human PPARgamma assessed as induction of transactivation activity by cell based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/4/2020
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
The University of Sydney

Curated by ChEMBL
LigandPNGBDBM50299414(psi-baptigenin | psedobaptigenin | pseudobaptogeni...)
Affinity DataEC50:  8.90E+3nMAssay Description:Agonist activity at human PPARalpha assessed as induction of transactivation activity by cell based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/4/2020
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
The University of Sydney

Curated by ChEMBL
LigandPNGBDBM50299414(psi-baptigenin | psedobaptigenin | pseudobaptogeni...)
Affinity DataEC50:  2.69E+4nMAssay Description:Agonist activity at human PPARgamma assessed as induction of transactivation activity by cell based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/4/2020
Entry Details Article
PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
Kunming Institute of Botany

Curated by ChEMBL
LigandPNGBDBM50596580(CHEMBL5173280)
Affinity DataKd:  1.66E+4nMAssay Description:Binding affinity to SARS-CoV-2 3CL protease at 1.875 to 50 uM by SPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/22/2023
Entry Details
PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
Kunming Institute of Botany

Curated by ChEMBL
LigandPNGBDBM50596581(CHEMBL5171650)
Affinity DataKd:  1.43E+4nMAssay Description:Binding affinity to SARS-CoV-2 3CL protease at 1.875 to 50 uM by SPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/22/2023
Entry Details
PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
Kunming Institute of Botany

Curated by ChEMBL
LigandPNGBDBM50009001(CHEMBL8260 | Baicalein | 5,6,7-Trihydroxyflavone |...)
Affinity DataKd:  3.13E+4nMAssay Description:Binding affinity to SARS-CoV-2 3CL protease at 1.875 to 50 uM by SPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/22/2023
Entry Details
PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
Kunming Institute of Botany

Curated by ChEMBL
LigandPNGBDBM50596580(CHEMBL5173280)
Affinity DataKd:  1.20E+4nMAssay Description:Binding affinity to SARS-CoV-2 3CL protease at 1.875 to 50 uM in presence of wallichins D by SPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/22/2023
Entry Details
PubMed
TargetReplicase polyprotein 1ab(2019-nCoV)
Kunming Institute of Botany

Curated by ChEMBL
LigandPNGBDBM50596581(CHEMBL5171650)
Affinity DataKd:  1.20E+4nMAssay Description:Binding affinity to SARS-CoV-2 3CL protease at 1.875 to 50 uM in presence of wallichins C by SPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/22/2023
Entry Details
PubMed
TargetSpike glycoprotein(2019-nCoV)
Kunming Institute of Botany

Curated by ChEMBL
LigandPNGBDBM50596580(CHEMBL5173280)
Affinity DataKd:  9.17E+4nMAssay Description:Binding affinity to SARS-CoV-2 Spike glycoprotein receptor-binding domain at 1.875 to 50 uM by SPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/22/2023
Entry Details
PubMed
TargetSpike glycoprotein(2019-nCoV)
Kunming Institute of Botany

Curated by ChEMBL
LigandPNGBDBM50596581(CHEMBL5171650)
Affinity DataKd:  6.79E+4nMAssay Description:Binding affinity to SARS-CoV-2 Spike glycoprotein receptor-binding domain at 1.875 to 50 uM by SPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/22/2023
Entry Details
PubMed
TargetSpike glycoprotein(2019-nCoV)
Kunming Institute of Botany

Curated by ChEMBL
LigandPNGBDBM50596580(CHEMBL5173280)
Affinity DataKd:  6.47E+4nMAssay Description:Binding affinity to SARS-CoV-2 Spike glycoprotein receptor-binding domain at 1.875 to 50 uM in presence of wallichins D by SPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/22/2023
Entry Details
PubMed
TargetSpike glycoprotein(2019-nCoV)
Kunming Institute of Botany

Curated by ChEMBL
LigandPNGBDBM50596581(CHEMBL5171650)
Affinity DataKd:  6.47E+4nMAssay Description:Binding affinity to SARS-CoV-2 Spike glycoprotein receptor-binding domain at 1.875 to 50 uM in presence of wallichins C by SPR assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/22/2023
Entry Details
PubMed
TargetRNA demethylase ALKBH5(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50631032(CHEMBL5401284)
Affinity DataKd:  6.62E+3nMAssay Description:Binding affinity to biotinylated ALKBH5 (66 to 292 residues)(unknown origin) expressed in Escherichia coli BL21(DE3) assessed as equilibrium dissocia...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/21/2024
Entry Details
PubMed
TargetRNA demethylase ALKBH5(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50631032(CHEMBL5401284)
Affinity DataKd:  1.12E+4nMAssay Description:Binding affinity to NT-647-NHS fluorescent dye-labeled wild-type ALKBH5 (66 to 292 residues)(unknown origin) expressed in Escherichia coli BL21(DE3) ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/21/2024
Entry Details
PubMed
TargetRNA demethylase ALKBH5(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50631032(CHEMBL5401284)
Affinity DataKd:  3.73E+5nMAssay Description:Binding affinity to NT-647-NHS fluorescent dye-labeled ALKBH5 R130A mutant (unknown origin) expressed in Escherichia coli BL21(DE3) using m6A-ssDNA a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/21/2024
Entry Details
PubMed
TargetRNA demethylase ALKBH5(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50631032(CHEMBL5401284)
Affinity DataKd:  5.30E+4nMAssay Description:Binding affinity to NT-647-NHS fluorescent dye-labeled ALKBH5 K132A mutant (unknown origin) expressed in Escherichia coli BL21(DE3) using m6A-ssDNA a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/21/2024
Entry Details
PubMed
TargetRNA demethylase ALKBH5(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50631032(CHEMBL5401284)
Affinity DataKd:  2.90E+5nMAssay Description:Binding affinity to NT-647-NHS fluorescent dye-labeled ALKBH5 Y139A mutant (unknown origin) expressed in Escherichia coli BL21(DE3) using m6A-ssDNA a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/21/2024
Entry Details
PubMed
TargetRNA demethylase ALKBH5(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50631032(CHEMBL5401284)
Affinity DataKd:  1.58E+4nMAssay Description:Binding affinity to NT-647-NHS fluorescent dye-labeled ALKBH5 Y139A/R277A mutant (unknown origin) expressed in Escherichia coli BL21(DE3) using m6A-s...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/21/2024
Entry Details
PubMed
TargetMast/stem cell growth factor receptor Kit(Human)
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50521626(CHEMBL4448433)
Affinity DataIC50: 0.0200nMAssay Description:Inhibition of human c-KIT A loop exon 17 D820Y single mutant using poly (Glu,Tyr) 4:1 as substrate in presence of 33P-gamma-ATP by hotspot kinase ass...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Human)
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50519725(CHEMBL4513768)
Affinity DataIC50: 0.100nMAssay Description:Inhibition of wild type FLT3 (unknown origin) expressed in HEK293T cells assessed as decrease in FLT3 phosphorylation at 0.1 to 1000 nM after 1 hr by...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Human)
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50519725(CHEMBL4513768)
Affinity DataIC50: 0.100nMAssay Description:Inhibition of wild type FLT3 D835Y mutant (unknown origin) expressed in HEK293T cells assessed as decrease in FLT3 D835Y phosphorylation at 0.1 to 10...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Human)
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50519725(CHEMBL4513768)
Affinity DataIC50: 0.100nMAssay Description:Inhibition of wild type FLT3 ITD mutant (unknown origin) expressed in HEK293T cells assessed as decrease in FLT3 ITD phosphorylation at 0.1 to 1000 n...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetMast/stem cell growth factor receptor Kit(Human)
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50521626(CHEMBL4448433)
Affinity DataIC50: 0.120nMAssay Description:Inhibition of human c-KIT A loop exon 17 Y823D single mutant using poly (Glu,Tyr) 4:1 as substrate in presence of 33P-gamma-ATP by hotspot kinase ass...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetMast/stem cell growth factor receptor Kit(Human)
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50521626(CHEMBL4448433)
Affinity DataIC50: 0.180nMAssay Description:Inhibition of human c-KIT A loop exon 11/17 V560G/N822K double mutant using poly (Glu,Tyr) 4:1 as substrate in presence of 33P-gamma-ATP by hotspot k...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetAurora kinase B(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50565411(CHEMBL4799738)
Affinity DataIC50: 0.316nMAssay Description:Inhibition of recombinant human full-length His-tagged Aurora B expressed in baculovirus expression system using 5-FAM-LRRASLG-CONH2 as substrate pre...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/30/2022
Entry Details Article
PubMed
TargetTGF-beta receptor type-1(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50579200(CHEMBL4852453)
Affinity DataIC50: 0.320nMAssay Description:Inhibition of human TGFbeta receptor 1 in human HEK293 cells preincubated for 24 hrs followed by addition of TGFbeta1 and measured after 24 hrs by lu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/24/2022
Entry Details Article
PubMed
TargetAurora kinase B(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50466808(AZD-1152-HQPA | Barasertib)
Affinity DataIC50: 0.326nMAssay Description:Inhibition of recombinant human full-length His-tagged Aurora B expressed in baculovirus expression system using 5-FAM-LRRASLG-CONH2 as substrate pre...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/30/2022
Entry Details Article
PubMed
TargetAurora kinase B(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50565427(CHEMBL4784002)
Affinity DataIC50: 0.336nMAssay Description:Inhibition of recombinant human full-length His-tagged Aurora B expressed in baculovirus expression system using 5-FAM-LRRASLG-CONH2 as substrate pre...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/30/2022
Entry Details Article
PubMed
TargetTGF-beta receptor type-1(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50579201(CHEMBL4858177)
Affinity DataIC50: 0.340nMAssay Description:Inhibition of human TGFbeta receptor 1 in human HEK293 cells preincubated for 24 hrs followed by addition of TGFbeta1 and measured after 24 hrs by lu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/24/2022
Entry Details Article
PubMed
TargetTGF-beta receptor type-1(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50579196(CHEMBL4877947)
Affinity DataIC50: 0.350nMAssay Description:Inhibition of human TGFbeta receptor 1 in human HEK293 cells preincubated for 24 hrs followed by addition of TGFbeta1 and measured after 24 hrs by lu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/24/2022
Entry Details Article
PubMed
TargetHigh affinity nerve growth factor receptor(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM374727(US10246466, Example 93 | (7S,13R)-11-fluoro-7,13-d...)
Affinity DataIC50: 0.400nMAssay Description:Inhibition of TRKA G595R mutant (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/19/2021
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetTyrosine-protein kinase BTK(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50357312(IBRUTINIB | US9181263, 1 | US9108973, Ref 1 | US92...)
Affinity DataIC50: 0.5nMAssay Description:Inhibition of BTK (unknown origin) after 60 mins by FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50322823((S)-N-(4-(3-chloro-4-fluorophenylamino)-7-(tetrahy...)
Affinity DataIC50: 0.5nMAssay Description:Irreversible inhibition of wild type EGFR (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetTGF-beta receptor type-1(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50579206(CHEMBL4846578)
Affinity DataIC50: 0.510nMAssay Description:Inhibition of human TGFbeta receptor 1 in human HEK293 cells preincubated for 24 hrs followed by addition of TGFbeta1 and measured after 24 hrs by lu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/24/2022
Entry Details Article
PubMed
TargetTGF-beta receptor type-1(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50579194(CHEMBL4872884)
Affinity DataIC50: 0.540nMAssay Description:Inhibition of human TGFbeta receptor 1 in human HEK293 cells preincubated for 24 hrs followed by addition of TGFbeta1 and measured after 24 hrs by lu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/24/2022
Entry Details Article
PubMed
TargetAurora kinase A(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50004205(MK-0457 | MK-045 | VX-680 | VX-68 | TOZASERTIB | U...)
Affinity DataIC50: 0.600nMAssay Description:Inhibition of Aurora A (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/30/2022
Entry Details Article
PubMed
TargetTGF-beta receptor type-1(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50579171(CHEMBL4861887)
Affinity DataIC50: 0.620nMAssay Description:Inhibition of human TGFbeta receptor 1 in human HEK293 cells preincubated for 24 hrs followed by addition of TGFbeta1 and measured after 24 hrs by lu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/24/2022
Entry Details Article
PubMed
TargetTGF-beta receptor type-1(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50579198(CHEMBL4872045)
Affinity DataIC50: 0.630nMAssay Description:Inhibition of human TGFbeta receptor 1 in human HEK293 cells preincubated for 24 hrs followed by addition of TGFbeta1 and measured after 24 hrs by lu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/24/2022
Entry Details Article
PubMed
TargetTGF-beta receptor type-1(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50579188(CHEMBL4874893)
Affinity DataIC50: 0.650nMAssay Description:Inhibition of human TGFbeta receptor 1 in human HEK293 cells preincubated for 24 hrs followed by addition of TGFbeta1 and measured after 24 hrs by lu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/24/2022
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Naples Federico II

Curated by ChEMBL
LigandPNGBDBM50514844(CHEMBL4473213)
Affinity DataIC50: 0.670nMAssay Description:Inhibition of RET isoform 9 M918T mutant in human MZ-CRC-1 cells assessed as reduction in cell proliferation supplemented with fresh medium containin...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details Article
PubMed
TargetCoiled-coil domain-containing protein 6(Human)
University of Naples Federico II

Curated by ChEMBL
LigandPNGBDBM50514844(CHEMBL4473213)
Affinity DataIC50: 0.670nMAssay Description:Inhibition of CCDC6/RET in human TPC1 cells assessed as reduction in cell proliferation supplemented with fresh medium containing compound for every ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
University of Naples Federico II

Curated by ChEMBL
LigandPNGBDBM50514844(CHEMBL4473213)
Affinity DataIC50: 0.670nMAssay Description:Inhibition of RET isoform 9 C634W mutant in human TT cells assessed as reduction in cell proliferation supplemented with fresh medium containing comp...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details Article
PubMed
TargetCoiled-coil domain-containing protein 6(Human)
University of Naples Federico II

Curated by ChEMBL
LigandPNGBDBM50514844(CHEMBL4473213)
Affinity DataIC50: 0.670nMAssay Description:Inhibition of CCDC6/RET in human LC2/ad cells assessed as reduction in cell proliferation supplemented with fresh medium containing compound for ever...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details Article
PubMed
TargetMast/stem cell growth factor receptor Kit(Human)
National Health Research Institutes

Curated by ChEMBL
LigandPNGBDBM50521626(CHEMBL4448433)
Affinity DataIC50: 0.670nMAssay Description:Inhibition of human c-KIT A loop exon 17 D816H single mutant using poly (Glu,Tyr) 4:1 as substrate in presence of 33P-gamma-ATP by hotspot kinase ass...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/23/2021
Entry Details Article
PubMed
TargetTGF-beta receptor type-1(Human)
University of Arkansas For Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50579185(CHEMBL4867170)
Affinity DataIC50: 0.670nMAssay Description:Inhibition of human TGFbeta receptor 1 in human HEK293 cells preincubated for 24 hrs followed by addition of TGFbeta1 and measured after 24 hrs by lu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/24/2022
Entry Details Article
PubMed
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