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29 similar compounds to monomer 50405114

Wt: 348.2
BDBM19254
Purchase
Wt: 364.2
BDBM82540
Wt: 363.2
BDBM81822
Purchase
Wt: 361.2
BDBM92537
Purchase
Wt: 346.1
BDBM92539
Purchase
Wt: 362.1
BDBM92540
Wt: 362.1
BDBM50231945
Purchase
Wt: 363.2
BDBM50326433
Purchase
Wt: 362.2
BDBM50367210
Wt: 394.2
BDBM50369231
Wt: 380.2
BDBM50369232
Wt: 452.3
BDBM50369233
Wt: 396.6
BDBM50369234
Wt: 416.2
BDBM50369235
Wt: 450.3
BDBM50369236
Displayed 1 to 15 (of 29 total )  |  Next  |  Last  >>

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 27 hits for monomerid = 19254,82540,81822,92537,92539,92540,50231945,50326433,50367210,50369231,50369232,50369233,50369234,50369235,50369236   
Target
(Institution)
LigandTarget
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Adenosine Receptors A2a (A2a)


(Rattus norvegicus (rat))
BDBM82540
PNG
(CAS_146-80-5 | NSC_1190 | Xanthosine)
Show SMILES OC1C(COP(O)(O)=O)OC(C1O)n1cnc2c1[nH]c(=O)[nH]c2=O
Show InChI InChI=1S/C10H13N4O9P/c15-5-3(1-22-24(19,20)21)23-9(6(5)16)14-2-11-4-7(14)12-10(18)13-8(4)17/h2-3,5-6,9,15-16H,1H2,(H2,19,20,21)(H2,12,13,17,18)
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PubMed
8.5n/an/an/an/an/an/an/an/a



National Institute of Diabetes, Digestive and Kidney Diseases

Curated by PDSP Ki Database




Mol Pharmacol 45: 1101-11 (1994)

More data for this
Ligand-Target Pair
Adenosine receptor


(Rattus norvegicus (rat))
BDBM82540
PNG
(CAS_146-80-5 | NSC_1190 | Xanthosine)
Show SMILES OC1C(COP(O)(O)=O)OC(C1O)n1cnc2c1[nH]c(=O)[nH]c2=O
Show InChI InChI=1S/C10H13N4O9P/c15-5-3(1-22-24(19,20)21)23-9(6(5)16)14-2-11-4-7(14)12-10(18)13-8(4)17/h2-3,5-6,9,15-16H,1H2,(H2,19,20,21)(H2,12,13,17,18)
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9.10n/an/an/an/an/an/an/an/a



National Institute of Diabetes, Digestive and Kidney Diseases

Curated by PDSP Ki Database




Mol Pharmacol 45: 1101-11 (1994)

More data for this
Ligand-Target Pair
ADORA3


(RAT)
BDBM82540
PNG
(CAS_146-80-5 | NSC_1190 | Xanthosine)
Show SMILES OC1C(COP(O)(O)=O)OC(C1O)n1cnc2c1[nH]c(=O)[nH]c2=O
Show InChI InChI=1S/C10H13N4O9P/c15-5-3(1-22-24(19,20)21)23-9(6(5)16)14-2-11-4-7(14)12-10(18)13-8(4)17/h2-3,5-6,9,15-16H,1H2,(H2,19,20,21)(H2,12,13,17,18)
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23.4n/an/an/an/an/an/an/an/a



National Institute of Diabetes, Digestive and Kidney Diseases

Curated by PDSP Ki Database




Mol Pharmacol 45: 1101-11 (1994)

More data for this
Ligand-Target Pair
Cholecystokinin


(RAT)
BDBM81822
PNG
(CAS_6804 | GMP | Guanosine | NSC_6804)
Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)C1OC(COP(O)(O)=O)C(O)C1O
Show InChI InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)
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200n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche & Co., Ltd.

Curated by PDSP Ki Database




J Neurosci 4: 1021-33 (1984)

More data for this
Ligand-Target Pair
Orotidine phosphate decarboxylase


(Saccharomyces cerevisiae)
BDBM50231945
PNG
(CHEMBL253328 | xanthosine-5'-monophosphate disodiu...)
Show SMILES O[C@@H]1[C@@H](COP([O-])([O-])=O)O[C@H]([C@@H]1O)n1cnc2c1[nH]c(=O)[nH]c2=O
Show InChI InChI=1S/C10H13N4O9P/c15-5-3(1-22-24(19,20)21)23-9(6(5)16)14-2-11-4-7(14)12-10(18)13-8(4)17/h2-3,5-6,9,15-16H,1H2,(H2,19,20,21)(H2,12,13,17,18)/p-2/t3-,5-,6-,9-/m1/s1
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PubMed
400n/an/an/an/an/an/an/an/a



Toronto General Research Institute

Curated by ChEMBL


Assay Description
Inhibition of yeast ODCase


Citation and Details
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Cholecystokinin


(RAT)
BDBM81822
PNG
(CAS_6804 | GMP | Guanosine | NSC_6804)
Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)C1OC(COP(O)(O)=O)C(O)C1O
Show InChI InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)
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1.00E+3n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche & Co., Ltd.

Curated by PDSP Ki Database




J Neurosci 4: 1021-33 (1984)

More data for this
Ligand-Target Pair
Hypoxanthine-guanine phosphoribosyltransferase (HGPRT)


(Homo sapiens (Human))
BDBM19254
PNG
(IMP | Inosine | Inosinic acid | [(2R,3S,4R,5R)-3,4...)
Show SMILES O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)n1cnc2c1nc[nH]c2=O
Show InChI InChI=1S/C10H13N4O8P/c15-6-4(1-21-23(18,19)20)22-10(7(6)16)14-3-13-5-8(14)11-2-12-9(5)17/h2-4,6-7,10,15-16H,1H2,(H,11,12,17)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
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5.40E+3n/an/an/an/an/an/an/an/a



The University of Queensland

Curated by ChEMBL


Assay Description
Inhibition of human HGPRT


Citation and Details
More data for this
Ligand-Target Pair
ADORA3


(RAT)
BDBM81822
PNG
(CAS_6804 | GMP | Guanosine | NSC_6804)
Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)C1OC(COP(O)(O)=O)C(O)C1O
Show InChI InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)
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>1.00E+4n/an/an/an/an/an/an/an/a



National Institute of Diabetes, Digestive and Kidney Diseases

Curated by PDSP Ki Database




Mol Pharmacol 45: 1101-11 (1994)

More data for this
Ligand-Target Pair
ADORA3


(RAT)
BDBM19254
PNG
(IMP | Inosine | Inosinic acid | [(2R,3S,4R,5R)-3,4...)
Show SMILES O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)n1cnc2c1nc[nH]c2=O
Show InChI InChI=1S/C10H13N4O8P/c15-6-4(1-21-23(18,19)20)22-10(7(6)16)14-3-13-5-8(14)11-2-12-9(5)17/h2-4,6-7,10,15-16H,1H2,(H,11,12,17)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
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>1.00E+4n/an/an/an/an/an/an/an/a



National Institute of Diabetes, Digestive and Kidney Diseases

Curated by PDSP Ki Database




Mol Pharmacol 45: 1101-11 (1994)

More data for this
Ligand-Target Pair
Adenosine Receptors A2a (A2a)


(Rattus norvegicus (rat))
BDBM19254
PNG
(IMP | Inosine | Inosinic acid | [(2R,3S,4R,5R)-3,4...)
Show SMILES O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)n1cnc2c1nc[nH]c2=O
Show InChI InChI=1S/C10H13N4O8P/c15-6-4(1-21-23(18,19)20)22-10(7(6)16)14-3-13-5-8(14)11-2-12-9(5)17/h2-4,6-7,10,15-16H,1H2,(H,11,12,17)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
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>1.00E+4n/an/an/an/an/an/an/an/a



National Institute of Diabetes, Digestive and Kidney Diseases

Curated by PDSP Ki Database




Mol Pharmacol 45: 1101-11 (1994)

More data for this
Ligand-Target Pair
Adenosine receptor


(Rattus norvegicus (rat))
BDBM19254
PNG
(IMP | Inosine | Inosinic acid | [(2R,3S,4R,5R)-3,4...)
Show SMILES O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)n1cnc2c1nc[nH]c2=O
Show InChI InChI=1S/C10H13N4O8P/c15-6-4(1-21-23(18,19)20)22-10(7(6)16)14-3-13-5-8(14)11-2-12-9(5)17/h2-4,6-7,10,15-16H,1H2,(H,11,12,17)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
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>1.00E+4n/an/an/an/an/an/an/an/a



National Institute of Diabetes, Digestive and Kidney Diseases

Curated by PDSP Ki Database




Mol Pharmacol 45: 1101-11 (1994)

More data for this
Ligand-Target Pair
Adenosine receptor


(Rattus norvegicus (rat))
BDBM81822
PNG
(CAS_6804 | GMP | Guanosine | NSC_6804)
Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)C1OC(COP(O)(O)=O)C(O)C1O
Show InChI InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)
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>1.00E+4n/an/an/an/an/an/an/an/a



National Institute of Diabetes, Digestive and Kidney Diseases

Curated by PDSP Ki Database




Mol Pharmacol 45: 1101-11 (1994)

More data for this
Ligand-Target Pair
PACAP


(RAT)
BDBM81822
PNG
(CAS_6804 | GMP | Guanosine | NSC_6804)
Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)C1OC(COP(O)(O)=O)C(O)C1O
Show InChI InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)
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>1.00E+4n/an/an/an/an/an/an/an/a



Georg-August-University

Curated by PDSP Ki Database




Eur J Biochem 202: 951-8 (1991)

More data for this
Ligand-Target Pair
Adenosine Receptors A2a (A2a)


(Rattus norvegicus (rat))
BDBM81822
PNG
(CAS_6804 | GMP | Guanosine | NSC_6804)
Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)C1OC(COP(O)(O)=O)C(O)C1O
Show InChI InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)
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>1.00E+4n/an/an/an/an/an/an/an/a



National Institute of Diabetes, Digestive and Kidney Diseases

Curated by PDSP Ki Database




Mol Pharmacol 45: 1101-11 (1994)

More data for this
Ligand-Target Pair
Deoxyribonucleoside 5'-monophosphate N-glycosidase (Rcl)


(Rattus norvegicus (Rat))
BDBM92537
PNG
(GMP)
Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)C1OC(COP([O-])([O-])=O)C(O)C1O
Show InChI InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)/p-2
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PubMed
2.00E+4n/an/an/an/an/an/an/an/a



Institut Pasteur



Assay Description
Rcl inhibition by nucleotides.


Citation and Details
More data for this
Ligand-Target Pair
Deoxyribonucleoside 5'-monophosphate N-glycosidase (Rcl)


(Rattus norvegicus (Rat))
BDBM92539
PNG
(IMP)
Show SMILES OC1C(COP([O-])([O-])=O)OC(C1O)n1cnc2c1nc[nH]c2=O
Show InChI InChI=1S/C10H13N4O8P/c15-6-4(1-21-23(18,19)20)22-10(7(6)16)14-3-13-5-8(14)11-2-12-9(5)17/h2-4,6-7,10,15-16H,1H2,(H,11,12,17)(H2,18,19,20)/p-2
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4.90E+4n/an/an/an/an/an/an/an/a



Institut Pasteur



Assay Description
Rcl inhibition by nucleotides.


Citation and Details
More data for this
Ligand-Target Pair
Deoxyribonucleoside 5'-monophosphate N-glycosidase (Rcl)


(Rattus norvegicus (Rat))
BDBM92540
PNG
(XMP)
Show SMILES OC1C(COP([O-])([O-])=O)OC(C1O)n1cnc2c1[nH]c(=O)[nH]c2=O
Show InChI InChI=1S/C10H13N4O9P/c15-5-3(1-22-24(19,20)21)23-9(6(5)16)14-2-11-4-7(14)12-10(18)13-8(4)17/h2-3,5-6,9,15-16H,1H2,(H2,19,20,21)(H2,12,13,17,18)/p-2
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5.40E+4n/an/an/an/an/an/an/an/a



Institut Pasteur



Assay Description
Rcl inhibition by nucleotides.


Citation and Details
More data for this
Ligand-Target Pair
Inosine Monophosphate Dehydrogenase Type 2 (IMPDH2)


(Homo sapiens (human))
BDBM50369232
PNG
(CHEMBL607643)
Show SMILES O[C@H]1[C@H](COP(O)(O)=O)OC([C@H]1O)n1cnc2c1nc(CF)[nH]c2=O
Show InChI InChI=1S/C11H14FN4O8P/c12-1-5-14-9-6(10(19)15-5)13-3-16(9)11-8(18)7(17)4(24-11)2-23-25(20,21)22/h3-4,7-8,11,17-18H,1-2H2,(H,14,15,19)(H2,20,21,22)/t4-,7-,8-,11?/m0/s1
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n/an/a 1.20E+3n/an/an/an/an/an/a



University of Chicago

Curated by ChEMBL


Assay Description
Concentration required for 50% inhibition of human Inosine-5'-monophosphate dehydrogenase 2 using Spectrophotometric assay


Citation and Details
More data for this
Ligand-Target Pair
Inosine Monophosphate Dehydrogenase Type 2 (IMPDH2)


(Homo sapiens (human))
BDBM50369233
PNG
(CHEMBL607940)
Show SMILES O[C@H]1[C@H](COP(O)(O)=O)OC([C@H]1O)n1cnc2c1nc(CCc1ccccc1)[nH]c2=O
Show InChI InChI=1S/C18H21N4O8P/c23-14-11(8-29-31(26,27)28)30-18(15(14)24)22-9-19-13-16(22)20-12(21-17(13)25)7-6-10-4-2-1-3-5-10/h1-5,9,11,14-15,18,23-24H,6-8H2,(H,20,21,25)(H2,26,27,28)/t11-,14-,15-,18?/m0/s1
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n/an/a 4.60E+5n/an/an/an/an/an/a



University of Chicago

Curated by ChEMBL


Assay Description
Concentration required for 50% inhibition of human Inosine-5'-monophosphate dehydrogenase 2 using Spectrophotometric assay


Citation and Details
More data for this
Ligand-Target Pair
Inosine Monophosphate Dehydrogenase Type 2 (IMPDH2)


(Homo sapiens (human))
BDBM50369234
PNG
(CHEMBL608491)
Show SMILES O[C@H]1[C@H](COP(O)(O)=O)OC([C@H]1O)n1cnc2c1nc(CCl)[nH]c2=O
Show InChI InChI=1S/C11H14ClN4O8P/c12-1-5-14-9-6(10(19)15-5)13-3-16(9)11-8(18)7(17)4(24-11)2-23-25(20,21)22/h3-4,7-8,11,17-18H,1-2H2,(H,14,15,19)(H2,20,21,22)/t4-,7-,8-,11?/m0/s1
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n/an/a 1.32E+3n/an/an/an/an/an/a



University of Chicago

Curated by ChEMBL


Assay Description
Concentration required for 50% inhibition of human Inosine-5'-monophosphate dehydrogenase 2 using Spectrophotometric assay


Citation and Details
More data for this
Ligand-Target Pair
Inosine Monophosphate Dehydrogenase Type 2 (IMPDH2)


(Homo sapiens (human))
BDBM50369235
PNG
(CHEMBL610231)
Show SMILES O[C@H]1[C@H](COP(O)(O)=O)OC([C@H]1O)n1cnc2c1nc([nH]c2=O)C(F)(F)F
Show InChI InChI=1S/C11H12F3N4O8P/c12-11(13,14)10-16-7-4(8(21)17-10)15-2-18(7)9-6(20)5(19)3(26-9)1-25-27(22,23)24/h2-3,5-6,9,19-20H,1H2,(H,16,17,21)(H2,22,23,24)/t3-,5-,6-,9?/m0/s1
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n/an/a>1.00E+6n/an/an/an/an/an/a



University of Chicago

Curated by ChEMBL


Assay Description
Concentration required for 50% inhibition of human Inosine-5'-monophosphate dehydrogenase 2 using Spectrophotometric assay


Citation and Details
More data for this
Ligand-Target Pair
Inosine Monophosphate Dehydrogenase Type 2 (IMPDH2)


(Homo sapiens (human))
BDBM50367210
PNG
(CHEMBL610157)
Show SMILES Cc1nc2n(cnc2c(=O)[nH]1)C1O[C@@H](COP(O)(O)=O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C11H15N4O8P/c1-4-13-9-6(10(18)14-4)12-3-15(9)11-8(17)7(16)5(23-11)2-22-24(19,20)21/h3,5,7-8,11,16-17H,2H2,1H3,(H,13,14,18)(H2,19,20,21)/t5-,7-,8-,11?/m0/s1
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n/an/a>1.00E+6n/an/an/an/an/an/a



University of Chicago

Curated by ChEMBL


Assay Description
Concentration required for 50% inhibition of human Inosine-5'-monophosphate dehydrogenase 2 using Spectrophotometric assay


Citation and Details
More data for this
Ligand-Target Pair
Protein kinase C-interacting protein 1


(Rattus norvegicus)
BDBM50326433
PNG
(((2R,3R,4S,5R)-5-(2-amino-6-oxo-1H-purin-9(6H)-yl)...)
Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)[C@@H]1O[C@H](COP(O)(O)=O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)/t3-,5+,6+,9-/m1/s1
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n/an/an/a 6.70E+4n/an/an/an/an/a



University of Maryland

Curated by ChEMBL


Assay Description
Binding affinity to mouse HINT1 by fluorescence quenching assay


Citation and Details
More data for this
Ligand-Target Pair
Protein kinase C-interacting protein 1


(Rattus norvegicus)
BDBM50326433
PNG
(((2R,3R,4S,5R)-5-(2-amino-6-oxo-1H-purin-9(6H)-yl)...)
Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)[C@@H]1O[C@H](COP(O)(O)=O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)/t3-,5+,6+,9-/m1/s1
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n/an/an/a 6.00E+4n/an/an/an/an/a



University of Maryland

Curated by ChEMBL


Assay Description
Binding affinity to mouse HINT1 by NMR analysis


Citation and Details
More data for this
Ligand-Target Pair
Inosine-5'-monophosphate dehydrogenase


(Escherichia coli (strain K12))
BDBM50369236
PNG
(CHEMBL611912)
Show SMILES O[C@H]1[C@H](COP(O)(O)=O)OC([C@H]1O)n1cnc2c1nc(C=Cc1ccccc1)[nH]c2=O
Show InChI InChI=1S/C18H19N4O8P/c23-14-11(8-29-31(26,27)28)30-18(15(14)24)22-9-19-13-16(22)20-12(21-17(13)25)7-6-10-4-2-1-3-5-10/h1-7,9,11,14-15,18,23-24H,8H2,(H,20,21,25)(H2,26,27,28)/t11-,14-,15-,18?/m0/s1
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n/an/a 6.90E+4n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Ability to inhibit Inosine-5'-monophosphate dehydrogenase isolated from Escherichia coli


J Med Chem 27: 429-32 (1984)

More data for this
Ligand-Target Pair
Inosine Monophosphate Dehydrogenase Type 2 (IMPDH2)


(Homo sapiens (human))
BDBM50369231
PNG
(CHEMBL610230)
Show SMILES OC(O)c1nc2n(cnc2c(=O)[nH]1)C1O[C@@H](COP(O)(O)=O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C11H15N4O10P/c16-5-3(1-24-26(21,22)23)25-10(6(5)17)15-2-12-4-8(15)13-7(11(19)20)14-9(4)18/h2-3,5-6,10-11,16-17,19-20H,1H2,(H,13,14,18)(H2,21,22,23)/t3-,5-,6-,10?/m0/s1
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n/an/a 440n/an/an/an/an/an/a



University of Chicago

Curated by ChEMBL


Assay Description
Concentration required for 50% inhibition of human Inosine-5'-monophosphate dehydrogenase 2 using Spectrophotometric assay


Citation and Details
More data for this
Ligand-Target Pair
Inosine Monophosphate Dehydrogenase Type 2 (IMPDH2)


(Homo sapiens (human))
BDBM50369236
PNG
(CHEMBL611912)
Show SMILES O[C@H]1[C@H](COP(O)(O)=O)OC([C@H]1O)n1cnc2c1nc(C=Cc1ccccc1)[nH]c2=O
Show InChI InChI=1S/C18H19N4O8P/c23-14-11(8-29-31(26,27)28)30-18(15(14)24)22-9-19-13-16(22)20-12(21-17(13)25)7-6-10-4-2-1-3-5-10/h1-7,9,11,14-15,18,23-24H,8H2,(H,20,21,25)(H2,26,27,28)/t11-,14-,15-,18?/m0/s1
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n/an/a 3.70E+4n/an/an/an/an/an/a



University of Chicago

Curated by ChEMBL


Assay Description
Concentration required for 50% inhibition of human Inosine-5'-monophosphate dehydrogenase 2 using Spectrophotometric assay


Citation and Details
More data for this
Ligand-Target Pair