BindingDB logo
myBDB logout
Compile Data Set for Download or QSAR

Found 44 hits with Last Name = 'lin' and Initial = 'cn'   
Target/Host
(Institution)		LigandTarget/Host
Links		Ligand
Links		Trg + Lig
Links		Ki
nM		ΔG°
kJ/mole		IC50
nM		Kd
nM		EC50/IC50
nM		koff
s-1		kon
M-1s-1		pHTemp
°C
Angiotensin-converting enzyme


(Homo sapiens (Human))		BDBM50292544
PNG
(3,4,6,7-tetrahydroxyxanthone | CHEMBL477740)
Show SMILES Oc1ccc2c(oc3cc(O)c(O)cc3c2=O)c1O
Show InChI InChI=1S/C13H8O6/c14-7-2-1-5-11(17)6-3-8(15)9(16)4-10(6)19-13(5)12(7)18/h1-4,14-16,18H
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
 1.42E+4n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of ACE by Lineweaver-Burk plot

J Nat Prod 55: 691-695 (1992)


Article DOI: 10.1021/np50083a025
BindingDB Entry DOI: 10.7270/Q21C1WXZ
More data for this
Ligand-Target Pair
Angiotensin-converting enzyme


(Homo sapiens (Human))		BDBM50292547
PNG
(1,3,5,6-tetrahydroxyxanthone | 1,3,5,6-tetrahydrox...)
Show SMILES Oc1cc(O)c2c(c1)oc1c(O)c(O)ccc1c2=O
Show InChI InChI=1S/C13H8O6/c14-5-3-8(16)10-9(4-5)19-13-6(11(10)17)1-2-7(15)12(13)18/h1-4,14-16,18H
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
 3.42E+4n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of ACE by Lineweaver-Burk plot

J Nat Prod 55: 691-695 (1992)


Article DOI: 10.1021/np50083a025
BindingDB Entry DOI: 10.7270/Q21C1WXZ
More data for this
Ligand-Target Pair
Angiotensin-converting enzyme


(Homo sapiens (Human))		BDBM50292546
PNG
(3,4,5,6-tetrahydroxyxanthone | CHEMBL477921 | US91...)
Show SMILES Oc1ccc2c(oc3c(O)c(O)ccc3c2=O)c1O
Show InChI InChI=1S/C13H8O6/c14-7-3-1-5-9(16)6-2-4-8(15)11(18)13(6)19-12(5)10(7)17/h1-4,14-15,17-18H
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
 1.26E+5n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of ACE by Lineweaver-Burk plot

J Nat Prod 55: 691-695 (1992)


Article DOI: 10.1021/np50083a025
BindingDB Entry DOI: 10.7270/Q21C1WXZ
More data for this
Ligand-Target Pair
Angiotensin-converting enzyme


(Homo sapiens (Human))		BDBM50155447
PNG
(1,3,6,7-Tetrahydroxy-xanthen-9-one | 1,3,6,7-tetra...)
Show SMILES Oc1cc(O)c2c(c1)oc1cc(O)c(O)cc1c2=O
Show InChI InChI=1S/C13H8O6/c14-5-1-9(17)12-11(2-5)19-10-4-8(16)7(15)3-6(10)13(12)18/h1-4,14-17H
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem

Patents

Similars
Article
PubMed
 2.50E+5n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of ACE by Lineweaver-Burk plot

J Nat Prod 55: 691-695 (1992)


Article DOI: 10.1021/np50083a025
BindingDB Entry DOI: 10.7270/Q21C1WXZ
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM35440
PNG
(ALLOPURINOL | MLS000069453 | SMR000059083 | cid_20...)
Show SMILES O=c1[nH]cnc2n[nH]cc12
Show InChI InChI=1S/C5H4N4O/c10-5-3-1-8-9-4(3)6-2-7-5/h1-2H,(H2,6,7,8,9,10)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
n/an/a 1.90E+3n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 mins

Eur J Med Chem 46: 1222-31 (2011)


Article DOI: 10.1016/j.ejmech.2011.01.043
BindingDB Entry DOI: 10.7270/Q2RB74X9
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM35440
PNG
(ALLOPURINOL | MLS000069453 | SMR000059083 | cid_20...)
Show SMILES O=c1[nH]cnc2n[nH]cc12
Show InChI InChI=1S/C5H4N4O/c10-5-3-1-8-9-4(3)6-2-7-5/h1-2H,(H2,6,7,8,9,10)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
n/an/a 2.00E+3n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase (unknown origin)

J Nat Prod 71: 1027-31 (2008)


Article DOI: 10.1021/np8001145
BindingDB Entry DOI: 10.7270/Q25T3K7R
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM35440
PNG
(ALLOPURINOL | MLS000069453 | SMR000059083 | cid_20...)
Show SMILES O=c1[nH]cnc2n[nH]cc12
Show InChI InChI=1S/C5H4N4O/c10-5-3-1-8-9-4(3)6-2-7-5/h1-2H,(H2,6,7,8,9,10)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
n/an/a 2.00E+3n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase (unknown origin)

Bioorg Med Chem 16: 7270-6 (2008)


Article DOI: 10.1016/j.bmc.2008.06.031
BindingDB Entry DOI: 10.7270/Q2S182BF
More data for this
Ligand-Target Pair
Beta-glucuronidase


(Rattus norvegicus)		BDBM7458
PNG
(5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one...)
Show SMILES Oc1ccc(cc1)-c1cc(=O)c2c(O)cc(O)cc2o1
Show InChI InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)13-7-12(19)15-11(18)5-10(17)6-14(15)20-13/h1-7,16-18H
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem

Patents

Similars
Article
PubMed
n/an/a 2.80E+3n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Beta-glucuronidase


(Rattus norvegicus)		BDBM50142192
PNG
(3-(2,4-Dihydroxy-phenyl)-5,7-dihydroxy-chromen-4-o...)
Show SMILES Oc1ccc(c(O)c1)-c1coc2cc(O)cc(O)c2c1=O
Show InChI InChI=1S/C15H10O6/c16-7-1-2-9(11(18)3-7)10-6-21-13-5-8(17)4-12(19)14(13)15(10)20/h1-6,16-19H
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
KEGG
PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
n/an/a 5.90E+3n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Beta-glucuronidase


(Rattus norvegicus)		BDBM79181
PNG
(10-[3-(4-methyl-1-piperazinyl)propyl]-2-(trifluoro...)
Show SMILES CN1CCN(CCCN2c3ccccc3Sc3ccc(cc23)C(F)(F)F)CC1
Show InChI InChI=1S/C21H24F3N3S/c1-25-11-13-26(14-12-25)9-4-10-27-17-5-2-3-6-19(17)28-20-8-7-16(15-18(20)27)21(22,23)24/h2-3,5-8,15H,4,9-14H2,1H3
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

DrugBank
KEGG
PC cid
PC sid
PDB
UniChem

Similars
Article
PubMed
n/an/a 7.80E+3n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Lysozyme C-1


(Rattus norvegicus)		BDBM79181
PNG
(10-[3-(4-methyl-1-piperazinyl)propyl]-2-(trifluoro...)
Show SMILES CN1CCN(CCCN2c3ccccc3Sc3ccc(cc23)C(F)(F)F)CC1
Show InChI InChI=1S/C21H24F3N3S/c1-25-11-13-26(14-12-25)9-4-10-27-17-5-2-3-6-19(17)28-20-8-7-16(15-18(20)27)21(22,23)24/h2-3,5-8,15H,4,9-14H2,1H3
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

DrugBank
KEGG
PC cid
PC sid
PDB
UniChem

Similars
Article
PubMed
n/an/a 9.00E+3n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Lysozyme C-1


(Rattus norvegicus)		BDBM50142192
PNG
(3-(2,4-Dihydroxy-phenyl)-5,7-dihydroxy-chromen-4-o...)
Show SMILES Oc1ccc(c(O)c1)-c1coc2cc(O)cc(O)c2c1=O
Show InChI InChI=1S/C15H10O6/c16-7-1-2-9(11(18)3-7)10-6-21-13-5-8(17)4-12(19)14(13)15(10)20/h1-6,16-19H
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
KEGG
PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
n/an/a 9.70E+3n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Beta-glucuronidase


(Rattus norvegicus)		BDBM50077323
PNG
(7,4'-Dihydroxyflavone | 7-hydroxy-2-(4-hydroxyphen...)
Show SMILES Oc1ccc(cc1)-c1cc(=O)c2ccc(O)cc2o1
Show InChI InChI=1S/C15H10O4/c16-10-3-1-9(2-4-10)14-8-13(18)12-6-5-11(17)7-15(12)19-14/h1-8,16-17H
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
KEGG
PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
n/an/a 1.37E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Lysozyme C-1


(Rattus norvegicus)		BDBM7458
PNG
(5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one...)
Show SMILES Oc1ccc(cc1)-c1cc(=O)c2c(O)cc(O)cc2o1
Show InChI InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)13-7-12(19)15-11(18)5-10(17)6-14(15)20-13/h1-7,16-18H
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem

Patents

Similars
Article
PubMed
n/an/a 1.77E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50263178
PNG
(2',5'-Diethoxy-2-(5-methylthienyl)chalcone | CHEMB...)
Show SMILES CCOc1ccc(OCC)c(c1)C(=O)\C=C\c1ccc(C)s1
Show InChI InChI=1S/C18H20O3S/c1-4-20-14-7-11-18(21-5-2)16(12-14)17(19)10-9-15-8-6-13(3)22-15/h6-12H,4-5H2,1-3H3/b10-9+
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 2.13E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase (unknown origin)

Bioorg Med Chem 16: 7270-6 (2008)


Article DOI: 10.1016/j.bmc.2008.06.031
BindingDB Entry DOI: 10.7270/Q2S182BF
More data for this
Ligand-Target Pair
Lysozyme C-1


(Rattus norvegicus)		BDBM50142193
PNG
(2'-hydroxydaidzein | 3-(2,4-dihydroxyphenyl)-7-hyd...)
Show SMILES Oc1ccc(c(O)c1)-c1coc2cc(O)ccc2c1=O
Show InChI InChI=1S/C15H10O5/c16-8-1-3-10(13(18)5-8)12-7-20-14-6-9(17)2-4-11(14)15(12)19/h1-7,16-18H
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
KEGG
PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
n/an/a 2.63E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Lysozyme C-1


(Rattus norvegicus)		BDBM50142191
PNG
(5,7-Dihydroxy-3-(4-hydroxy-2-methoxy-phenyl)-chrom...)
Show SMILES COc1cc(O)ccc1-c1coc2cc(O)cc(O)c2c1=O
Show InChI InChI=1S/C16H12O6/c1-21-13-5-8(17)2-3-10(13)11-7-22-14-6-9(18)4-12(19)15(14)16(11)20/h2-7,17-19H,1H3
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a>3.00E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Lysozyme C-1


(Rattus norvegicus)		BDBM50077323
PNG
(7,4'-Dihydroxyflavone | 7-hydroxy-2-(4-hydroxyphen...)
Show SMILES Oc1ccc(cc1)-c1cc(=O)c2ccc(O)cc2o1
Show InChI InChI=1S/C15H10O4/c16-10-3-1-9(2-4-10)14-8-13(18)12-6-5-11(17)7-15(12)19-14/h1-8,16-17H
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
KEGG
PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
n/an/a>3.00E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Lysozyme C-1


(Rattus norvegicus)		BDBM50366927
PNG
(CHEMBL1159471)
Show SMILES OC[C@H]1OC(Oc2cc(O)c3c(c2)oc(-c2ccc(O)cc2)c(O)c3=O)[C@H](O)[C@@H](O)[C@@H]1O |r|
Show InChI InChI=1S/C21H20O11/c22-7-13-15(25)17(27)19(29)21(32-13)30-10-5-11(24)14-12(6-10)31-20(18(28)16(14)26)8-1-3-9(23)4-2-8/h1-6,13,15,17,19,21-25,27-29H,7H2/t13-,15-,17+,19-,21?/m1/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a>3.00E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Beta-glucuronidase


(Rattus norvegicus)		BDBM50142193
PNG
(2'-hydroxydaidzein | 3-(2,4-dihydroxyphenyl)-7-hyd...)
Show SMILES Oc1ccc(c(O)c1)-c1coc2cc(O)ccc2c1=O
Show InChI InChI=1S/C15H10O5/c16-8-1-3-10(13(18)5-8)12-7-20-14-6-9(17)2-4-11(14)15(12)19/h1-7,16-18H
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
KEGG
PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
n/an/a>3.00E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Beta-glucuronidase


(Rattus norvegicus)		BDBM50366927
PNG
(CHEMBL1159471)
Show SMILES OC[C@H]1OC(Oc2cc(O)c3c(c2)oc(-c2ccc(O)cc2)c(O)c3=O)[C@H](O)[C@@H](O)[C@@H]1O |r|
Show InChI InChI=1S/C21H20O11/c22-7-13-15(25)17(27)19(29)21(32-13)30-10-5-11(24)14-12(6-10)31-20(18(28)16(14)26)8-1-3-9(23)4-2-8/h1-6,13,15,17,19,21-25,27-29H,7H2/t13-,15-,17+,19-,21?/m1/s1
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a>3.00E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Lysozyme C-1


(Rattus norvegicus)		BDBM50142190
PNG
(2-((11bR,12R)-9-Hydroxy-5b,11b-dihydro-6H-3,7,12-t...)
Show SMILES C[C@](O)(CO)c1cc2c3O[C@@H]4[C@@H](COc5cc(O)ccc45)c3ccc2o1
Show InChI InChI=1S/C20H18O6/c1-20(23,9-21)17-7-13-15(25-17)5-4-11-14-8-24-16-6-10(22)2-3-12(16)19(14)26-18(11)13/h2-7,14,19,21-23H,8-9H2,1H3/t14-,19-,20-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a>3.00E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Beta-glucuronidase


(Rattus norvegicus)		BDBM50142191
PNG
(5,7-Dihydroxy-3-(4-hydroxy-2-methoxy-phenyl)-chrom...)
Show SMILES COc1cc(O)ccc1-c1coc2cc(O)cc(O)c2c1=O
Show InChI InChI=1S/C16H12O6/c1-21-13-5-8(17)2-3-10(13)11-7-22-14-6-9(18)4-12(19)15(14)16(11)20/h2-7,17-19H,1H3
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a>3.00E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Beta-glucuronidase


(Rattus norvegicus)		BDBM50142190
PNG
(2-((11bR,12R)-9-Hydroxy-5b,11b-dihydro-6H-3,7,12-t...)
Show SMILES C[C@](O)(CO)c1cc2c3O[C@@H]4[C@@H](COc5cc(O)ccc45)c3ccc2o1
Show InChI InChI=1S/C20H18O6/c1-20(23,9-21)17-7-13-15(25-17)5-4-11-14-8-24-16-6-10(22)2-3-12(16)19(14)26-18(11)13/h2-7,14,19,21-23H,8-9H2,1H3/t14-,19-,20-/m0/s1
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a>3.00E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CB

Bioorg Med Chem Lett 14: 1011-4 (2004)


Article DOI: 10.1016/j.bmcl.2003.11.074
BindingDB Entry DOI: 10.7270/Q2C829VG
More data for this
Ligand-Target Pair
Angiotensin-converting enzyme


(Homo sapiens (Human))		BDBM50292544
PNG
(3,4,6,7-tetrahydroxyxanthone | CHEMBL477740)
Show SMILES Oc1ccc2c(oc3cc(O)c(O)cc3c2=O)c1O
Show InChI InChI=1S/C13H8O6/c14-7-2-1-5-11(17)6-3-8(15)9(16)4-10(6)19-13(5)12(7)18/h1-4,14-16,18H
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
n/an/a 3.54E+4n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of ACE

J Nat Prod 55: 691-695 (1992)


Article DOI: 10.1021/np50083a025
BindingDB Entry DOI: 10.7270/Q21C1WXZ
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50340832
PNG
(3-[3-(Piperidin-1-yl)-propoxy]xanthone | CHEMBL176...)
Show SMILES O=c1c2ccccc2oc2cc(OCCCN3CCCCC3)ccc12
Show InChI InChI=1S/C21H23NO3/c23-21-17-7-2-3-8-19(17)25-20-15-16(9-10-18(20)21)24-14-6-13-22-11-4-1-5-12-22/h2-3,7-10,15H,1,4-6,11-14H2
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 3.78E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 mins

Eur J Med Chem 46: 1222-31 (2011)


Article DOI: 10.1016/j.ejmech.2011.01.043
BindingDB Entry DOI: 10.7270/Q2RB74X9
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50244273
PNG
(CHEMBL470950 | CHEMBL511791 | Hyperielliptone HB)
Show SMILES [#6]-[#6]-[#6](-[#6])-[#6](=O)-[#6]-1-[#6](=O)[C@@]([#6])([#6]\[#6]=[#6](\[#6])-[#6])[#6](=O)[C@@]2([#6]-[#6@H]3-[#6@H](-[#6]-[#6][C@@]3([#6])[#8])[C@]([#6])([#8])[#6]2)[#6]-1=O |r|
Show InChI InChI=1S/C27H40O6/c1-8-16(4)20(28)19-21(29)24(5,11-9-15(2)3)23(31)27(22(19)30)13-18-17(26(7,33)14-27)10-12-25(18,6)32/h9,16-19,32-33H,8,10-14H2,1-7H3/t16?,17-,18-,19?,24+,25+,26+,27+/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 4.21E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase (unknown origin)

J Nat Prod 71: 1027-31 (2008)


Article DOI: 10.1021/np8001145
BindingDB Entry DOI: 10.7270/Q25T3K7R
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50244273
PNG
(CHEMBL470950 | CHEMBL511791 | Hyperielliptone HB)
Show SMILES [#6]-[#6]-[#6](-[#6])-[#6](=O)-[#6]-1-[#6](=O)[C@@]([#6])([#6]\[#6]=[#6](\[#6])-[#6])[#6](=O)[C@@]2([#6]-[#6@H]3-[#6@H](-[#6]-[#6][C@@]3([#6])[#8])[C@]([#6])([#8])[#6]2)[#6]-1=O |r|
Show InChI InChI=1S/C27H40O6/c1-8-16(4)20(28)19-21(29)24(5,11-9-15(2)3)23(31)27(22(19)30)13-18-17(26(7,33)14-27)10-12-25(18,6)32/h9,16-19,32-33H,8,10-14H2,1-7H3/t16?,17-,18-,19?,24+,25+,26+,27+/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 4.21E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase (unknown origin)

J Nat Prod 71: 1027-31 (2008)


Article DOI: 10.1021/np8001145
BindingDB Entry DOI: 10.7270/Q25T3K7R
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50340843
PNG
(3-Hydroxy-6-[3-(methylpiperazylamino)-propoxy]xant...)
Show SMILES CN1CCN(CCCOc2ccc3c(c2)oc2cc(O)ccc2c3=O)CC1
Show InChI InChI=1S/C21H24N2O4/c1-22-8-10-23(11-9-22)7-2-12-26-16-4-6-18-20(14-16)27-19-13-15(24)3-5-17(19)21(18)25/h3-6,13-14,24H,2,7-12H2,1H3
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 4.43E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 mins

Eur J Med Chem 46: 1222-31 (2011)


Article DOI: 10.1016/j.ejmech.2011.01.043
BindingDB Entry DOI: 10.7270/Q2RB74X9
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50340834
PNG
(3-[3-(4-Methylpiperazino)-propoxy]xanthone | CHEMB...)
Show SMILES CN1CCN(CCCOc2ccc3c(c2)oc2ccccc2c3=O)CC1
Show InChI InChI=1S/C21H24N2O3/c1-22-10-12-23(13-11-22)9-4-14-25-16-7-8-18-20(15-16)26-19-6-3-2-5-17(19)21(18)24/h2-3,5-8,15H,4,9-14H2,1H3
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 4.73E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 mins

Eur J Med Chem 46: 1222-31 (2011)


Article DOI: 10.1016/j.ejmech.2011.01.043
BindingDB Entry DOI: 10.7270/Q2RB74X9
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50340841
PNG
(3-[3-(Diethylamino)-propoxy]-6-hydroxyxanthone | C...)
Show SMILES CCN(CC)CCCOc1ccc2c(c1)oc1cc(O)ccc1c2=O
Show InChI InChI=1S/C20H23NO4/c1-3-21(4-2)10-5-11-24-15-7-9-17-19(13-15)25-18-12-14(22)6-8-16(18)20(17)23/h6-9,12-13,22H,3-5,10-11H2,1-2H3
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 5.35E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 mins

Eur J Med Chem 46: 1222-31 (2011)


Article DOI: 10.1016/j.ejmech.2011.01.043
BindingDB Entry DOI: 10.7270/Q2RB74X9
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50340836
PNG
(3-[3-(Diethylamino)-propoxy]xanthone | CHEMBL17612...)
Show SMILES CCN(CC)CCCOc1ccc2c(c1)oc1ccccc1c2=O
Show InChI InChI=1S/C20H23NO3/c1-3-21(4-2)12-7-13-23-15-10-11-17-19(14-15)24-18-9-6-5-8-16(18)20(17)22/h5-6,8-11,14H,3-4,7,12-13H2,1-2H3
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 5.65E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 mins

Eur J Med Chem 46: 1222-31 (2011)


Article DOI: 10.1016/j.ejmech.2011.01.043
BindingDB Entry DOI: 10.7270/Q2RB74X9
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50340839
PNG
(3-[3-(Cyclopropylamino)-propoxy]-6-hydroxyxanthone...)
Show SMILES Oc1ccc2c(c1)oc1cc(OCCCNC3CC3)ccc1c2=O
Show InChI InChI=1S/C19H19NO4/c21-13-4-6-15-17(10-13)24-18-11-14(5-7-16(18)19(15)22)23-9-1-8-20-12-2-3-12/h4-7,10-12,20-21H,1-3,8-9H2
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 6.30E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 mins

Eur J Med Chem 46: 1222-31 (2011)


Article DOI: 10.1016/j.ejmech.2011.01.043
BindingDB Entry DOI: 10.7270/Q2RB74X9
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50340833
PNG
(3-[3-(Pyrrolidin-1-yl)-propoxy]xanthone | CHEMBL17...)
Show SMILES O=c1c2ccccc2oc2cc(OCCCN3CCCC3)ccc12
Show InChI InChI=1S/C20H21NO3/c22-20-16-6-1-2-7-18(16)24-19-14-15(8-9-17(19)20)23-13-5-12-21-10-3-4-11-21/h1-2,6-9,14H,3-5,10-13H2
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 6.55E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 mins

Eur J Med Chem 46: 1222-31 (2011)


Article DOI: 10.1016/j.ejmech.2011.01.043
BindingDB Entry DOI: 10.7270/Q2RB74X9
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50340838
PNG
(3-Hydroxy-6-[3-(pyrrolidin-1-yl)-propoxy]xanthone ...)
Show SMILES Oc1ccc2c(c1)oc1cc(OCCCN3CCCC3)ccc1c2=O
Show InChI InChI=1S/C20H21NO4/c22-14-4-6-16-18(12-14)25-19-13-15(5-7-17(19)20(16)23)24-11-3-10-21-8-1-2-9-21/h4-7,12-13,22H,1-3,8-11H2
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 6.88E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 mins

Eur J Med Chem 46: 1222-31 (2011)


Article DOI: 10.1016/j.ejmech.2011.01.043
BindingDB Entry DOI: 10.7270/Q2RB74X9
More data for this
Ligand-Target Pair
Angiotensin-converting enzyme


(Homo sapiens (Human))		BDBM50292547
PNG
(1,3,5,6-tetrahydroxyxanthone | 1,3,5,6-tetrahydrox...)
Show SMILES Oc1cc(O)c2c(c1)oc1c(O)c(O)ccc1c2=O
Show InChI InChI=1S/C13H8O6/c14-5-3-8(16)10-9(4-5)19-13-6(11(10)17)1-2-7(15)12(13)18/h1-4,14-16,18H
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
n/an/a 6.92E+4n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of ACE

J Nat Prod 55: 691-695 (1992)


Article DOI: 10.1021/np50083a025
BindingDB Entry DOI: 10.7270/Q21C1WXZ
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50340840
PNG
(3-[3-(Cyclohexylamino)-propoxy]-6-hydroxyxanthone ...)
Show SMILES Oc1ccc2c(c1)oc1cc(OCCCNC3CCCCC3)ccc1c2=O
Show InChI InChI=1S/C22H25NO4/c24-16-7-9-18-20(13-16)27-21-14-17(8-10-19(21)22(18)25)26-12-4-11-23-15-5-2-1-3-6-15/h7-10,13-15,23-24H,1-6,11-12H2
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 7.29E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 mins

Eur J Med Chem 46: 1222-31 (2011)


Article DOI: 10.1016/j.ejmech.2011.01.043
BindingDB Entry DOI: 10.7270/Q2RB74X9
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50340837
PNG
(3-Hydroxy-6-[3-(piperidin-1-yl)-propoxy]xanthone |...)
Show SMILES Oc1ccc2c(c1)oc1cc(OCCCN3CCCCC3)ccc1c2=O
Show InChI InChI=1S/C21H23NO4/c23-15-5-7-17-19(13-15)26-20-14-16(6-8-18(20)21(17)24)25-12-4-11-22-9-2-1-3-10-22/h5-8,13-14,23H,1-4,9-12H2
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 8.23E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 mins

Eur J Med Chem 46: 1222-31 (2011)


Article DOI: 10.1016/j.ejmech.2011.01.043
BindingDB Entry DOI: 10.7270/Q2RB74X9
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50340842
PNG
(3-Hydroxy-6-[3-(piperazino)-propoxy]xanthone | CHE...)
Show SMILES Oc1ccc2c(c1)oc1cc(OCCCN3CCNCC3)ccc1c2=O
Show InChI InChI=1S/C20H22N2O4/c23-14-2-4-16-18(12-14)26-19-13-15(3-5-17(19)20(16)24)25-11-1-8-22-9-6-21-7-10-22/h2-5,12-13,21,23H,1,6-11H2
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 9.19E+4n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 mins

Eur J Med Chem 46: 1222-31 (2011)


Article DOI: 10.1016/j.ejmech.2011.01.043
BindingDB Entry DOI: 10.7270/Q2RB74X9
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50340835
PNG
(3-[3-(Piperazino)-propoxy]xanthone | CHEMBL1761211)
Show SMILES O=c1c2ccccc2oc2cc(OCCCN3CCNCC3)ccc12
Show InChI InChI=1S/C20H22N2O3/c23-20-16-4-1-2-5-18(16)25-19-14-15(6-7-17(19)20)24-13-3-10-22-11-8-21-9-12-22/h1-2,4-7,14,21H,3,8-13H2
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.09E+5n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 mins

Eur J Med Chem 46: 1222-31 (2011)


Article DOI: 10.1016/j.ejmech.2011.01.043
BindingDB Entry DOI: 10.7270/Q2RB74X9
More data for this
Ligand-Target Pair
Xanthine dehydrogenase/oxidase


(Homo sapiens (Human))		BDBM50263222
PNG
(2'-Ethoxy-5'-methoxy-2-(5-methylthienyl)chalcone |...)
Show SMILES CCOc1ccc(OC)cc1C(=O)\C=C\c1ccc(C)s1
Show InChI InChI=1S/C17H18O3S/c1-4-20-17-10-6-13(19-3)11-15(17)16(18)9-8-14-7-5-12(2)21-14/h5-11H,4H2,1-3H3/b9-8+
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 1.31E+5n/an/an/an/an/an/a



Kaohsiung Medical University

Curated by ChEMBL


Assay Description
Inhibition of xanthine oxidase (unknown origin)

Bioorg Med Chem 16: 7270-6 (2008)


Article DOI: 10.1016/j.bmc.2008.06.031
BindingDB Entry DOI: 10.7270/Q2S182BF
More data for this
Ligand-Target Pair
Angiotensin-converting enzyme


(Homo sapiens (Human))		BDBM50292546
PNG
(3,4,5,6-tetrahydroxyxanthone | CHEMBL477921 | US91...)
Show SMILES Oc1ccc2c(oc3c(O)c(O)ccc3c2=O)c1O
Show InChI InChI=1S/C13H8O6/c14-7-3-1-5-9(16)6-2-4-8(15)11(18)13(6)19-12(5)10(7)17/h1-4,14-15,17-18H
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
n/an/a 2.39E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of ACE

J Nat Prod 55: 691-695 (1992)


Article DOI: 10.1021/np50083a025
BindingDB Entry DOI: 10.7270/Q21C1WXZ
More data for this
Ligand-Target Pair
Angiotensin-converting enzyme


(Homo sapiens (Human))		BDBM50155447
PNG
(1,3,6,7-Tetrahydroxy-xanthen-9-one | 1,3,6,7-tetra...)
Show SMILES Oc1cc(O)c2c(c1)oc1cc(O)c(O)cc1c2=O
Show InChI InChI=1S/C13H8O6/c14-5-1-9(17)12-11(2-5)19-10-4-8(16)7(15)3-6(10)13(12)18/h1-4,14-17H
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem

Patents

Similars
Article
PubMed
n/an/a 5.31E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of ACE

J Nat Prod 55: 691-695 (1992)


Article DOI: 10.1021/np50083a025
BindingDB Entry DOI: 10.7270/Q21C1WXZ
More data for this
Ligand-Target Pair
Angiotensin-converting enzyme


(Homo sapiens (Human))		BDBM50292545
PNG
(2,3,6,7-Tethrahydroxyxanthone | CHEMBL12700)
Show SMILES Oc1cc2oc3cc(O)c(O)cc3c(=O)c2cc1O
Show InChI InChI=1S/C13H8O6/c14-7-1-5-11(3-9(7)16)19-12-4-10(17)8(15)2-6(12)13(5)18/h1-4,14-17H
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents

Similars
Article
PubMed
n/an/a 7.69E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of ACE

J Nat Prod 55: 691-695 (1992)


Article DOI: 10.1021/np50083a025
BindingDB Entry DOI: 10.7270/Q21C1WXZ
More data for this
Ligand-Target Pair