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42 similar compounds to monomer 50396017

Compile data set for download or QSAR
Wt: 381.4
BDBM28428
Wt: 367.4
BDBM28430
Wt: 339.3
BDBM28431
Purchase
Wt: 351.3
BDBM28435
Wt: 366.3
BDBM28437
Wt: 337.3
BDBM28441
Wt: 323.3
BDBM28442
Wt: 366.3
BDBM28451
Wt: 294.3
BDBM28453
Wt: 294.3
BDBM92643
Wt: 322.3
BDBM92644
Wt: 322.3
BDBM50003268
Wt: 336.3
BDBM50003267
Wt: 376.4
BDBM50454902
Wt: 362.4
BDBM50454905
Displayed 1 to 15 (of 42 total )  |  Next  |  Last  >>

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 23 hits for monomerid = 28428,28430,28431,28435,28437,28441,28442,28451,28453,92643,92644,50003268,50003267,50454902,50454905   
Target/Host
(Institution)
LigandTarget/Host
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 receptor A1


(Rattus norvegicus (rat))
BDBM50454905
PNG
(CHEMBL2113466)
Show SMILES CCNC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NC3CCCC3)ncnc12
Show InChI InChI=1S/C17H26N6O3/c1-2-18-7-11-13(24)14(25)17(26-11)23-9-21-12-15(19-8-20-16(12)23)22-10-5-3-4-6-10/h8-11,13-14,17-18,24-25H,2-7H2,1H3,(H,19,20,22)/t11-,13-,14-,17-/m1/s1
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2.41E+3n/an/an/an/an/an/an/an/a



Leiden/Amsterdam Center for Drug Research

Curated by ChEMBL


Assay Description
Binding affinity against adenosine A1 receptor using [3H]DPCPX in rat cortical membranes in the absence of GTP


J Med Chem 41: 102-8 (1998)


Article DOI: 10.1021/jm970508l
BindingDB Entry DOI: 10.7270/Q2MK6DKX
More data for this
Ligand-Target Pair
Adenosine receptor A1


(Rattus norvegicus (rat))
BDBM50454902
PNG
(CHEMBL2113472)
Show SMILES CCCNC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NC3CCCC3)ncnc12
Show InChI InChI=1S/C18H28N6O3/c1-2-7-19-8-12-14(25)15(26)18(27-12)24-10-22-13-16(20-9-21-17(13)24)23-11-5-3-4-6-11/h9-12,14-15,18-19,25-26H,2-8H2,1H3,(H,20,21,23)/t12-,14-,15-,18-/m1/s1
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4.64E+3n/an/an/an/an/an/an/an/a



Leiden/Amsterdam Center for Drug Research

Curated by ChEMBL


Assay Description
Binding affinity against adenosine A1 receptor using [3H]DPCPX in rat cortical membranes in the absence of GTP


J Med Chem 41: 102-8 (1998)


Article DOI: 10.1021/jm970508l
BindingDB Entry DOI: 10.7270/Q2MK6DKX
More data for this
Ligand-Target Pair
Adenosine receptor A1


(Rattus norvegicus (rat))
BDBM50454905
PNG
(CHEMBL2113466)
Show SMILES CCNC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NC3CCCC3)ncnc12
Show InChI InChI=1S/C17H26N6O3/c1-2-18-7-11-13(24)14(25)17(26-11)23-9-21-12-15(19-8-20-16(12)23)22-10-5-3-4-6-10/h8-11,13-14,17-18,24-25H,2-7H2,1H3,(H,19,20,22)/t11-,13-,14-,17-/m1/s1
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8.56E+3n/an/an/an/an/an/an/an/a



Leiden/Amsterdam Center for Drug Research

Curated by ChEMBL


Assay Description
Binding affinity against adenosine A1 receptor using [3H]DPCPX in rat cortical membranes in the presence of GTP.


J Med Chem 41: 102-8 (1998)


Article DOI: 10.1021/jm970508l
BindingDB Entry DOI: 10.7270/Q2MK6DKX
More data for this
Ligand-Target Pair
Histone-lysine N-methyltransferase, H3 lysine-79 specific


(Homo sapiens (Human))
BDBM92644
PNG
(EPZ002446)
Show SMILES CC(C)N(C)CC1OC([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C14H22N6O3/c1-7(2)19(3)4-8-10(21)11(22)14(23-8)20-6-18-9-12(15)16-5-17-13(9)20/h5-8,10-11,14,21-22H,4H2,1-3H3,(H2,15,16,17)/t8?,10-,11-,14?/m1/s1
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1.20E+4n/an/an/an/an/an/an/an/a



Epizyme Inc.



Assay Description
Assay of DOT1L enzymatic activity were performed under balanced conditions using a radiometric assay.


Chem Biol Drug Des 80: 971-80 (2012)


Article DOI: 10.1111/cbdd.12050
BindingDB Entry DOI: 10.7270/Q2Z89B12
More data for this
Ligand-Target Pair
Adenosine receptor A1


(Rattus norvegicus (rat))
BDBM50454902
PNG
(CHEMBL2113472)
Show SMILES CCCNC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NC3CCCC3)ncnc12
Show InChI InChI=1S/C18H28N6O3/c1-2-7-19-8-12-14(25)15(26)18(27-12)24-10-22-13-16(20-9-21-17(13)24)23-11-5-3-4-6-11/h9-12,14-15,18-19,25-26H,2-8H2,1H3,(H,20,21,23)/t12-,14-,15-,18-/m1/s1
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1.43E+4n/an/an/an/an/an/an/an/a



Leiden/Amsterdam Center for Drug Research

Curated by ChEMBL


Assay Description
Binding affinity against adenosine A1 receptor using [3H]DPCPX in rat cortical membranes in the presence of GTP.


J Med Chem 41: 102-8 (1998)


Article DOI: 10.1021/jm970508l
BindingDB Entry DOI: 10.7270/Q2MK6DKX
More data for this
Ligand-Target Pair
Adenosine Receptors A2a (A2a)


(Rattus norvegicus (rat))
BDBM50454902
PNG
(CHEMBL2113472)
Show SMILES CCCNC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NC3CCCC3)ncnc12
Show InChI InChI=1S/C18H28N6O3/c1-2-7-19-8-12-14(25)15(26)18(27-12)24-10-22-13-16(20-9-21-17(13)24)23-11-5-3-4-6-11/h9-12,14-15,18-19,25-26H,2-8H2,1H3,(H,20,21,23)/t12-,14-,15-,18-/m1/s1
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1.45E+4n/an/an/an/an/an/an/an/a



Leiden/Amsterdam Center for Drug Research

Curated by ChEMBL


Assay Description
Binding affinity against Adenosine A2A receptor using [3H]-CGS- 21680 as the radioligand in rat striatal membranes


J Med Chem 41: 102-8 (1998)


Article DOI: 10.1021/jm970508l
BindingDB Entry DOI: 10.7270/Q2MK6DKX
More data for this
Ligand-Target Pair
Histone-lysine N-methyltransferase, H3 lysine-79 specific


(Homo sapiens (Human))
BDBM28453
PNG
((2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-[(dimeth...)
Show SMILES CN(C)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C12H18N6O3/c1-17(2)3-6-8(19)9(20)12(21-6)18-5-16-7-10(13)14-4-15-11(7)18/h4-6,8-9,12,19-20H,3H2,1-2H3,(H2,13,14,15)/t6-,8-,9-,12-/m1/s1
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3.80E+4n/an/an/an/an/an/an/an/a



Baylor College of Medicine

Curated by ChEMBL


Assay Description
Competitive inhibition of recombinant human DOT1L using adenosine/deazaadenosine as substrate and SAM cofactor


J Med Chem 56: 8972-83 (2013)


Article DOI: 10.1021/jm4007752
BindingDB Entry DOI: 10.7270/Q2D50PDQ
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Histone-lysine N-methyltransferase, H3 lysine-79 specific


(Homo sapiens (Human))
BDBM92643
PNG
(EPZ000004)
Show SMILES CN(C)CC1OC([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C12H18N6O3/c1-17(2)3-6-8(19)9(20)12(21-6)18-5-16-7-10(13)14-4-15-11(7)18/h4-6,8-9,12,19-20H,3H2,1-2H3,(H2,13,14,15)/t6?,8-,9-,12?/m1/s1
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3.80E+4n/an/an/an/an/an/an/an/a



Epizyme Inc.



Assay Description
Assay of DOT1L enzymatic activity were performed under balanced conditions using a radiometric assay.


Chem Biol Drug Des 80: 971-80 (2012)


Article DOI: 10.1111/cbdd.12050
BindingDB Entry DOI: 10.7270/Q2Z89B12
More data for this
Ligand-Target Pair
Adenosine Receptors A2a (A2a)


(Rattus norvegicus (rat))
BDBM50454905
PNG
(CHEMBL2113466)
Show SMILES CCNC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NC3CCCC3)ncnc12
Show InChI InChI=1S/C17H26N6O3/c1-2-18-7-11-13(24)14(25)17(26-11)23-9-21-12-15(19-8-20-16(12)23)22-10-5-3-4-6-10/h8-11,13-14,17-18,24-25H,2-7H2,1H3,(H,19,20,22)/t11-,13-,14-,17-/m1/s1
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4.25E+4n/an/an/an/an/an/an/an/a



Leiden/Amsterdam Center for Drug Research

Curated by ChEMBL


Assay Description
Binding affinity against Adenosine A2A receptor using [3H]-CGS- 21680 as the radioligand in rat striatal membranes


J Med Chem 41: 102-8 (1998)


Article DOI: 10.1021/jm970508l
BindingDB Entry DOI: 10.7270/Q2MK6DKX
More data for this
Ligand-Target Pair
S-adenosylmethionine decarboxylase 1


(Rattus norvegicus)
BDBM28441
PNG
((2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-{[(3-ami...)
Show SMILES CN(CCCN)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C14H23N7O3/c1-20(4-2-3-15)5-8-10(22)11(23)14(24-8)21-7-19-9-12(16)17-6-18-13(9)21/h6-8,10-11,14,22-23H,2-5,15H2,1H3,(H2,16,17,18)/t8-,10-,11-,14-/m1/s1
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6.00E+4n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of H-Ras-mediated farnesylation expressed in mouse NIH3T3 cells


J Med Chem 25: 550-6 (1982)


Article DOI: 10.1021/jm00347a014
BindingDB Entry DOI: 10.7270/Q2VX0H37
More data for this
Ligand-Target Pair
S-adenosylmethionine decarboxylase 1


(Rattus norvegicus)
BDBM28441
PNG
((2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-{[(3-ami...)
Show SMILES CN(CCCN)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C14H23N7O3/c1-20(4-2-3-15)5-8-10(22)11(23)14(24-8)21-7-19-9-12(16)17-6-18-13(9)21/h6-8,10-11,14,22-23H,2-5,15H2,1H3,(H2,16,17,18)/t8-,10-,11-,14-/m1/s1
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3.80E+5n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against S-adenosyl-L-methionine decarboxylase using liver from rat in absence of putrescine


J Med Chem 25: 550-6 (1982)


Article DOI: 10.1021/jm00347a014
BindingDB Entry DOI: 10.7270/Q2VX0H37
More data for this
Ligand-Target Pair
S-adenosylmethionine decarboxylase 1


(Homo sapiens (Human))
BDBM28451
PNG
(3-({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-d...)
Show SMILES CN(CCC(=N)NO)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C14H22N8O4/c1-21(3-2-8(15)20-25)4-7-10(23)11(24)14(26-7)22-6-19-9-12(16)17-5-18-13(9)22/h5-7,10-11,14,23-25H,2-4H2,1H3,(H2,15,20)(H2,16,17,18)/t7-,10-,11-,14-/m1/s1
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n/an/a 1.57E+5n/an/an/an/an/an/a



Cornell University



Assay Description
The C-terminal his-tagged AdoMetDC was assayed by measuring the release of 14CO2 from S-adenosyl-L-[carboxy-14C]methionine (Amersham Pharmacia Biotec...


J Med Chem 52: 1388-407 (2009)


Article DOI: 10.1021/jm801126a
BindingDB Entry DOI: 10.7270/Q2222S3J
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Adenosine receptor A1


(Rattus norvegicus (rat))
BDBM50454902
PNG
(CHEMBL2113472)
Show SMILES CCCNC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NC3CCCC3)ncnc12
Show InChI InChI=1S/C18H28N6O3/c1-2-7-19-8-12-14(25)15(26)18(27-12)24-10-22-13-16(20-9-21-17(13)24)23-11-5-3-4-6-11/h9-12,14-15,18-19,25-26H,2-8H2,1H3,(H,20,21,23)/t12-,14-,15-,18-/m1/s1
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n/an/an/an/a 1.39E+4n/an/an/an/a



Leiden/Amsterdam Center for Drug Research

Curated by ChEMBL


Assay Description
Effective concentration for [35S]GTP-gamma-S, binding to adenosine A1 receptor in rat brain membranes


J Med Chem 41: 102-8 (1998)


Article DOI: 10.1021/jm970508l
BindingDB Entry DOI: 10.7270/Q2MK6DKX
More data for this
Ligand-Target Pair
S-adenosylmethionine decarboxylase 1


(Homo sapiens (Human))
BDBM28442
PNG
((2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-{[(2-ami...)
Show SMILES CN(CCN)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C13H21N7O3/c1-19(3-2-14)4-7-9(21)10(22)13(23-7)20-6-18-8-11(15)16-5-17-12(8)20/h5-7,9-10,13,21-22H,2-4,14H2,1H3,(H2,15,16,17)/t7-,9-,10-,13-/m1/s1
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n/an/an/an/an/an/an/a6.822



Cornell University



Assay Description
The C-terminal his-tagged AdoMetDC was assayed by measuring the release of 14CO2 from S-adenosyl-L-[carboxy-14C]methionine (Amersham Pharmacia Biotec...


J Med Chem 52: 1388-407 (2009)


Article DOI: 10.1021/jm801126a
BindingDB Entry DOI: 10.7270/Q2222S3J
More data for this
Ligand-Target Pair
S-adenosylmethionine decarboxylase 1


(Homo sapiens (Human))
BDBM28441
PNG
((2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-{[(3-ami...)
Show SMILES CN(CCCN)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C14H23N7O3/c1-20(4-2-3-15)5-8-10(22)11(23)14(24-8)21-7-19-9-12(16)17-6-18-13(9)21/h6-8,10-11,14,22-23H,2-5,15H2,1H3,(H2,16,17,18)/t8-,10-,11-,14-/m1/s1
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n/an/a 5.00E+5n/an/an/an/a6.822



Cornell University



Assay Description
The C-terminal his-tagged AdoMetDC was assayed by measuring the release of 14CO2 from S-adenosyl-L-[carboxy-14C]methionine (Amersham Pharmacia Biotec...


J Med Chem 52: 1388-407 (2009)


Article DOI: 10.1021/jm801126a
BindingDB Entry DOI: 10.7270/Q2222S3J
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
S-adenosylmethionine decarboxylase 1


(Homo sapiens (Human))
BDBM28437
PNG
(3-({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-d...)
Show SMILES CN(CCC(=O)NN)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C14H22N8O4/c1-21(3-2-8(23)20-16)4-7-10(24)11(25)14(26-7)22-6-19-9-12(15)17-5-18-13(9)22/h5-7,10-11,14,24-25H,2-4,16H2,1H3,(H,20,23)(H2,15,17,18)/t7-,10-,11-,14-/m1/s1
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n/an/a 1.50E+3n/an/an/an/a6.822



Cornell University



Assay Description
The C-terminal his-tagged AdoMetDC was assayed by measuring the release of 14CO2 from S-adenosyl-L-[carboxy-14C]methionine (Amersham Pharmacia Biotec...


J Med Chem 52: 1388-407 (2009)


Article DOI: 10.1021/jm801126a
BindingDB Entry DOI: 10.7270/Q2222S3J
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
S-adenosylmethionine decarboxylase 1


(Homo sapiens (Human))
BDBM28453
PNG
((2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-[(dimeth...)
Show SMILES CN(C)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C12H18N6O3/c1-17(2)3-6-8(19)9(20)12(21-6)18-5-16-7-10(13)14-4-15-11(7)18/h4-6,8-9,12,19-20H,3H2,1-2H3,(H2,13,14,15)/t6-,8-,9-,12-/m1/s1
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n/an/a 9.00E+3n/an/an/an/an/an/a



Cornell University



Assay Description
The C-terminal his-tagged AdoMetDC was assayed by measuring the release of 14CO2 from S-adenosyl-L-[carboxy-14C]methionine (Amersham Pharmacia Biotec...


J Med Chem 52: 1388-407 (2009)


Article DOI: 10.1021/jm801126a
BindingDB Entry DOI: 10.7270/Q2222S3J
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
S-adenosylmethionine decarboxylase 1


(Homo sapiens (Human))
BDBM28431
PNG
((2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-({[2-(am...)
Show SMILES CN(CCON)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C13H21N7O4/c1-19(2-3-23-15)4-7-9(21)10(22)13(24-7)20-6-18-8-11(14)16-5-17-12(8)20/h5-7,9-10,13,21-22H,2-4,15H2,1H3,(H2,14,16,17)/t7-,9-,10-,13-/m1/s1
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n/an/a 55n/an/an/an/a6.822



Cornell University



Assay Description
The C-terminal his-tagged AdoMetDC was assayed by measuring the release of 14CO2 from S-adenosyl-L-[carboxy-14C]methionine (Amersham Pharmacia Biotec...


J Med Chem 52: 1388-407 (2009)


Article DOI: 10.1021/jm801126a
BindingDB Entry DOI: 10.7270/Q2222S3J
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
S-adenosylmethionine decarboxylase 1


(Homo sapiens (Human))
BDBM28430
PNG
((2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-({[4-(am...)
Show SMILES CN(CCCCON)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C15H25N7O4/c1-21(4-2-3-5-25-17)6-9-11(23)12(24)15(26-9)22-8-20-10-13(16)18-7-19-14(10)22/h7-9,11-12,15,23-24H,2-6,17H2,1H3,(H2,16,18,19)/t9-,11-,12-,15-/m1/s1
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n/an/a 18n/an/an/an/a6.822



Cornell University



Assay Description
The C-terminal his-tagged AdoMetDC was assayed by measuring the release of 14CO2 from S-adenosyl-L-[carboxy-14C]methionine (Amersham Pharmacia Biotec...


J Med Chem 52: 1388-407 (2009)


Article DOI: 10.1021/jm801126a
BindingDB Entry DOI: 10.7270/Q2222S3J
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Adenosine receptor A2b


(Homo sapiens (Human))
BDBM50003267
PNG
(6-guanidino- NECA | CHEMBL405144)
Show SMILES CCNC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NC(N)=N)ncnc12
Show InChI InChI=1S/C13H20N8O3/c1-2-16-3-6-8(22)9(23)12(24-6)21-5-19-7-10(20-13(14)15)17-4-18-11(7)21/h4-6,8-9,12,16,22-23H,2-3H2,1H3,(H4,14,15,17,18,20)/t6-,8-,9-,12-/m1/s1
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n/an/an/an/a 1.84E+7n/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL


Assay Description
Agonist activity at human adenosine A2B receptor expressed in CHO cells assessed as stimulation of adenylate cyclase


J Med Chem 51: 2088-99 (2008)


Article DOI: 10.1021/jm701442d
BindingDB Entry DOI: 10.7270/Q2R49RNV
More data for this
Ligand-Target Pair
Adenosine receptor A2b


(Homo sapiens (Human))
BDBM50003268
PNG
(CHEMBL407502)
Show SMILES CCNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(NC)ncnc12
Show InChI InChI=1S/C13H18N6O4/c1-3-15-12(22)9-7(20)8(21)13(23-9)19-5-18-6-10(14-2)16-4-17-11(6)19/h4-5,7-9,13,20-21H,3H2,1-2H3,(H,15,22)(H,14,16,17)/t7-,8+,9-,13+/m0/s1
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n/an/an/an/a 4.17E+4n/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL


Assay Description
Agonist activity at human adenosine A2B receptor expressed in CHO cells assessed as stimulation of adenylate cyclase


J Med Chem 51: 2088-99 (2008)


Article DOI: 10.1021/jm701442d
BindingDB Entry DOI: 10.7270/Q2R49RNV
More data for this
Ligand-Target Pair
S-adenosylmethionine decarboxylase 1


(Homo sapiens (Human))
BDBM28428
PNG
((2R,3R,4S,5R)-2-(6-amino-8-methyl-9H-purin-9-yl)-5...)
Show SMILES CN(CCCCON)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1c(C)nc2c(N)ncnc12
Show InChI InChI=1S/C16H27N7O4/c1-9-21-11-14(17)19-8-20-15(11)23(9)16-13(25)12(24)10(27-16)7-22(2)5-3-4-6-26-18/h8,10,12-13,16,24-25H,3-7,18H2,1-2H3,(H2,17,19,20)/t10-,12-,13-,16-/m1/s1
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n/an/a 5n/an/an/an/a6.822



Cornell University



Assay Description
The C-terminal his-tagged AdoMetDC was assayed by measuring the release of 14CO2 from S-adenosyl-L-[carboxy-14C]methionine (Amersham Pharmacia Biotec...


J Med Chem 52: 1388-407 (2009)


Article DOI: 10.1021/jm801126a
BindingDB Entry DOI: 10.7270/Q2222S3J
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
S-adenosylmethionine decarboxylase 1


(Homo sapiens (Human))
BDBM28435
PNG
(3-({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-d...)
Show SMILES CN(CCC(N)=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C14H21N7O4/c1-20(3-2-8(15)22)4-7-10(23)11(24)14(25-7)21-6-19-9-12(16)17-5-18-13(9)21/h5-7,10-11,14,23-24H,2-4H2,1H3,(H2,15,22)(H2,16,17,18)/t7-,10-,11-,14-/m1/s1
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n/an/a 7.00E+3n/an/an/an/a6.822



Cornell University



Assay Description
The C-terminal his-tagged AdoMetDC was assayed by measuring the release of 14CO2 from S-adenosyl-L-[carboxy-14C]methionine (Amersham Pharmacia Biotec...


J Med Chem 52: 1388-407 (2009)


Article DOI: 10.1021/jm801126a
BindingDB Entry DOI: 10.7270/Q2222S3J
More data for this
Ligand-Target Pair
3D
3D Structure (docked)