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Found 120 Enz. Inhib. hit(s) with Target = 'UDP-glucuronosyltransferase 2B7'
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211740((1R)-phenyl-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricy...)
Affinity DataKi:  18.4nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM19264((4E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dih...)
Affinity DataKi:  1.50E+3nMAssay Description:Uncompetitive substrate inhibition of UGT2B7 in diabetic human kidney microsomes assessed as reduction in enzyme-mediated mycophenolic acid phenolic ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM19264((4E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dih...)
Affinity DataKi:  1.50E+3nMAssay Description:Uncompetitive substrate inhibition of UGT2B7 in diabetic human liver microsomes assessed as reduction in enzyme-mediated mycophenolic acid phenolic 7...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM19264((4E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dih...)
Affinity DataKi:  1.50E+3nMAssay Description:Uncompetitive substrate inhibition of UGT2B7 in non-diabetic human kidney microsomes assessed as reduction in enzyme-mediated mycophenolic acid pheno...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM19264((4E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dih...)
Affinity DataKi:  1.50E+3nMAssay Description:Uncompetitive substrate inhibition of UGT2B7 in non-diabetic human liver microsomes assessed as reduction in enzyme-mediated mycophenolic acid phenol...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM19264((4E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dih...)
Affinity DataKi:  2.00E+3nMAssay Description:Uncompetitive substrate inhibition of UGT2B7 in diabetic human liver microsomes assessed as reduction in enzyme-mediated mycophenolic acid acyl glucu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM19264((4E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dih...)
Affinity DataKi:  2.00E+3nMAssay Description:Uncompetitive substrate inhibition of UGT2B7 in diabetic human kidney microsomes assessed as reduction in enzyme-mediated mycophenolic acid acyl gluc...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM19264((4E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dih...)
Affinity DataKi:  2.00E+3nMAssay Description:Uncompetitive substrate inhibition of UGT2B7 in non-diabetic human liver microsomes assessed as reduction in enzyme-mediated mycophenolic acid acyl g...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM19264((4E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dih...)
Affinity DataKi:  2.00E+3nMAssay Description:Uncompetitive substrate inhibition of UGT2B7 in non-diabetic human kidney microsomes assessed as reduction in enzyme-mediated mycophenolic acid acyl ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183611((rac)-5,7-dimethyl-1,2,3,4-tetrahydronaphthalen-1-...)
Affinity DataKi:  1.01E+5nMAssay Description:Competitive inhibition of UGT2B7-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183598((rac)-6-methyl-3,4-dihydro-2H-chromen-4-ol | CHEMB...)
Affinity DataKi:  1.13E+5nMAssay Description:Competitive inhibition of UGT2B7-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50002692((AZT) 1-(4-Azido-5-hydroxymethyl-tetrahydro-furan-...)
Affinity DataKi:  1.50E+5nMAssay Description:Uncompetitive substrate inhibition of UGT2B7 in non-diabetic human kidney microsomes assessed as reduction in enzyme-mediated zidovudine glucuronide ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50002692((AZT) 1-(4-Azido-5-hydroxymethyl-tetrahydro-furan-...)
Affinity DataKi:  1.50E+5nMAssay Description:Uncompetitive substrate inhibition of UGT2B7 in diabetic human kidney microsomes assessed as reduction in enzyme-mediated zidovudine glucuronide form...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50088511(CHEBI:87620 | Epiestriol | Epioestriol)
Affinity DataKi:  1.62E+5nMAssay Description:Inhibition of recombinant human C-terminal His-tagged UGT2B7 after 15 to 60 mins by Michaelis-Menten equation analysis in presence of UDPGAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183611((rac)-5,7-dimethyl-1,2,3,4-tetrahydronaphthalen-1-...)
Affinity DataKi:  1.92E+5nMAssay Description:Non competitive inhibition of UGT2B7-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50002692((AZT) 1-(4-Azido-5-hydroxymethyl-tetrahydro-furan-...)
Affinity DataKi:  2.00E+5nMAssay Description:Uncompetitive substrate inhibition of UGT2B7 in non-diabetic human liver microsomes assessed as reduction in enzyme-mediated zidovudine glucuronide f...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50002692((AZT) 1-(4-Azido-5-hydroxymethyl-tetrahydro-furan-...)
Affinity DataKi:  2.00E+5nMAssay Description:Uncompetitive substrate inhibition of UGT2B7 in diabetic human liver microsomes assessed as reduction in enzyme-mediated zidovudine glucuronide forma...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183598((rac)-6-methyl-3,4-dihydro-2H-chromen-4-ol | CHEMB...)
Affinity DataKi:  2.58E+5nMAssay Description:Non competitive inhibition of UGT2B7-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183609((rac)-6-methyl-2,3-dihydro-1H-inden-1-ol | CHEMBL2...)
Affinity DataKi:  3.01E+5nMAssay Description:Competitive inhibition of UGT2B7-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM21398(4-[4-(4-Chloro-phenyl)-4-hydroxy-piperidin-1-yl]-1...)
Affinity DataKi:  5.90E+5nMAssay Description:Drug metabolism assessed as recombinant human UGT2B7 assessed as O-glucuronidation measured as inhibition constant at 10 to 400 uM incubated for 60 m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183609((rac)-6-methyl-2,3-dihydro-1H-inden-1-ol | CHEMBL2...)
Affinity DataKi:  6.24E+5nMAssay Description:Non competitive inhibition of UGT2B7-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50003616(2-n-propyl-n-valeric acid | CHEMBL109 | DPA | Di-n...)
Affinity DataKi:  1.60E+6nMAssay Description:Inhibition of AZT glucuronidation by human recombinant UGT2B7More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211740((1R)-phenyl-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricy...)
Affinity DataIC50:  47nMAssay Description:Inhibition of human UGT2B7 by substrate-independent inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211740((1R)-phenyl-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricy...)
Affinity DataIC50:  54nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211775(((1S,3aR,4S,8aR,9S)-4,8,8-trimethyl-decahydro-1,4-...)
Affinity DataIC50:  100nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211777((1S)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  200nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211764((1R)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  200nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211762((1S)-2-chloro-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethylt...)
Affinity DataIC50:  200nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211763((1R)-2-chloro-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethylt...)
Affinity DataIC50:  200nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211780((1S)-2,2-dimethyl-1-[(1R,2S,7S,8S,9S)-3,3,7-trimet...)
Affinity DataIC50:  200nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211782((1R)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  300nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211778((1S)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  300nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211765(CHEMBL226344 | ethyl (3S)-3-hydroxy-3-[(1R,2S,7S,8...)
Affinity DataIC50:  300nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211753((1R)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  400nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211739((1R)-2-methyl-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethylt...)
Affinity DataIC50:  400nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211741((1S)-2-methyl-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethylt...)
Affinity DataIC50:  400nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211749(CHEMBL390574 | ethyl (3R)-3-hydroxy-3-[(1R,2S,7S,8...)
Affinity DataIC50:  400nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211750((1S)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  500nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211743(2-[(1R,2S,7R,8S,9R)-3,3,7-trimethyltricyclo[5.4.0....)
Affinity DataIC50:  500nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211773((1R)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  500nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211769((1R)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  500nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211781((1S)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  600nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211744((2Z)-3-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  700nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211766((1S)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  700nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211748((1R)-2,2-dimethyl-1-[(1R,2S,7S,8S,9S)-3,3,7-trimet...)
Affinity DataIC50:  800nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211752((2E)-3-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  800nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211761(3-[(1R,2S,7R,8S,9R)-3,3,7-trimethyltricyclo[5.4.0....)
Affinity DataIC50:  900nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211759((3R)-3-hydroxy-3-[(1R,2S,7S,8S,9S)-3,3,7-trimethyl...)
Affinity DataIC50:  900nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211786((1S)-phenyl-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricy...)
Affinity DataIC50:  900nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211756((3S)-3-hydroxy-3-[(1R,2S,7S,8S,9S)-3,3,7-trimethyl...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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