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33 similar compounds to monomer 50382351

Compile data set for download or QSAR
Wt: 955.8
BDBM21732
Wt: 955.8
BDBM21733
Wt: 955.8
BDBM21734
Wt: 980.8
BDBM85108
Wt: 952.7
BDBM85111
Wt: 938.7
BDBM85112
Wt: 924.7
BDBM85113
Wt: 1032.8
BDBM50101693
Wt: 992.8
BDBM50101694
Wt: 965.7
BDBM50101695
Wt: 978.7
BDBM50101697
Wt: 1006.8
BDBM50101698
Wt: 1018.8
BDBM50101699
Wt: 992.8
BDBM50101700
Wt: 980.8
BDBM50101704
Displayed 1 to 15 (of 33 total )  |  Next  |  Last  >>

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 16 hits for monomerid = 21732,21733,21734,85108,85111,85112,85113,50101693,50101694,50101695,50101697,50101698,50101699,50101700,50101704   
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
Serotonin N-acetyltransferase


(Ovis aries)
BDBM50101694
PNG
(Bisubstrate Analogue | [5-(6-amino-9H-purin-9-yl)-...)
Show SMILES CC(CSCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP([O-])([O-])=O)n1cnc2c(N)ncnc12)C(=O)CCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C36H53N8O17P3S/c1-21(25(45)10-6-7-22-15-40-24-9-5-4-8-23(22)24)17-65-14-13-38-27(46)11-12-39-34(49)31(48)36(2,3)18-58-64(55,56)61-63(53,54)57-16-26-30(60-62(50,51)52)29(47)35(59-26)44-20-43-28-32(37)41-19-42-33(28)44/h4-5,8-9,15,19-21,26,29-31,35,40,47-48H,6-7,10-14,16-18H2,1-3H3,(H,38,46)(H,39,49)(H,53,54)(H,55,56)(H2,37,41,42)(H2,50,51,52)/p-2
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6n/an/an/an/an/an/an/an/a



Johns Hopkins University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of serotonin N-acetyl-transferase


J Med Chem 44: 2479-85 (2001)


Article DOI: 10.1021/jm010049v
BindingDB Entry DOI: 10.7270/Q2319WKP
More data for this
Ligand-Target Pair
Serotonin N-acetyltransferase


(Ovis aries)
BDBM50101699
PNG
(Bisubstrate Analogue | [5-(6-amino-9H-purin-9-yl)-...)
Show SMILES CC(C)(COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP([O-])([O-])=O)n1cnc2c(N)ncnc12)C(O)C(=O)NCCC(=O)NCCSC1CCCC1C(=O)CCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C38H55N8O17P3S/c1-38(2,19-60-66(57,58)63-65(55,56)59-18-27-32(62-64(52,53)54)31(49)37(61-27)46-21-45-30-34(39)43-20-44-35(30)46)33(50)36(51)41-14-13-29(48)40-15-16-67-28-12-6-9-24(28)26(47)11-5-7-22-17-42-25-10-4-3-8-23(22)25/h3-4,8,10,17,20-21,24,27-28,31-33,37,42,49-50H,5-7,9,11-16,18-19H2,1-2H3,(H,40,48)(H,41,51)(H,55,56)(H,57,58)(H2,39,43,44)(H2,52,53,54)/p-2
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7n/an/an/an/an/an/an/an/a



Johns Hopkins University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of serotonin N-acetyl-transferase


J Med Chem 44: 2479-85 (2001)


Article DOI: 10.1021/jm010049v
BindingDB Entry DOI: 10.7270/Q2319WKP
More data for this
Ligand-Target Pair
Serotonin N-acetyltransferase (AANAT)


(Homo sapiens (Human))
BDBM85108
PNG
(AANAT bisubstrate analog, 3)
Show SMILES CC(C)(COP(O)(=O)OP(O)(=O)OC[C@H]1OC([C@@H](O)[C@@H]1OP(O)(O)=O)n1cnc2c(N)ncnc12)[C@@H](O)C(=O)NCCC(=O)NCCSCCC(=O)CCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C35H51N8O17P3S/c1-35(2,30(47)33(48)38-12-10-26(45)37-13-15-64-14-11-22(44)7-5-6-21-16-39-24-9-4-3-8-23(21)24)18-57-63(54,55)60-62(52,53)56-17-25-29(59-61(49,50)51)28(46)34(58-25)43-20-42-27-31(36)40-19-41-32(27)43/h3-4,8-9,16,19-20,25,28-30,34,39,46-47H,5-7,10-15,17-18H2,1-2H3,(H,37,45)(H,38,48)(H,52,53)(H,54,55)(H2,36,40,41)(H2,49,50,51)/t25-,28+,29-,30+,34?/m1/s1
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32 -10.4n/an/an/an/an/a6.830



Johns Hopkins University School of Medicine



Assay Description
AANAT activity was measured using a spectrophotometric assay in which the enzymatic product CoASH concentration were determined indirectly by monitor...


Bioorg Chem 31: 398-411 (2003)


Article DOI: 10.1016/S0045-2068(03)00081-6
BindingDB Entry DOI: 10.7270/Q2DB80CR
More data for this
Ligand-Target Pair
Serotonin N-acetyltransferase


(Ovis aries)
BDBM50101697
PNG
(Bisubstrate Analogue | [5-(6-amino-9H-purin-9-yl)-...)
Show SMILES CC(C)(COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP([O-])([O-])=O)n1cnc2c(N)ncnc12)C(O)C(=O)NCCC(=O)NCCSCCC(=O)CCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C35H51N8O17P3S/c1-35(2,30(47)33(48)38-12-10-26(45)37-13-15-64-14-11-22(44)7-5-6-21-16-39-24-9-4-3-8-23(21)24)18-57-63(54,55)60-62(52,53)56-17-25-29(59-61(49,50)51)28(46)34(58-25)43-20-42-27-31(36)40-19-41-32(27)43/h3-4,8-9,16,19-20,25,28-30,34,39,46-47H,5-7,10-15,17-18H2,1-2H3,(H,37,45)(H,38,48)(H,52,53)(H,54,55)(H2,36,40,41)(H2,49,50,51)/p-2
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32n/an/an/an/an/an/an/an/a



Johns Hopkins University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of serotonin N-acetyl-transferase


J Med Chem 44: 2479-85 (2001)


Article DOI: 10.1021/jm010049v
BindingDB Entry DOI: 10.7270/Q2319WKP
More data for this
Ligand-Target Pair
Serotonin N-acetyltransferase


(Ovis aries)
BDBM50101695
PNG
(Bisubstrate Analogue | [5-(6-amino-9H-purin-9-yl)-...)
Show SMILES CC(C)(COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP([O-])([O-])=O)n1cnc2c(N)ncnc12)C(O)C(=O)NCCC(=O)NCCSCC(=O)NCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C33H48N9O17P3S/c1-33(2,28(46)31(47)37-10-8-23(43)36-11-12-63-15-24(44)35-9-7-19-13-38-21-6-4-3-5-20(19)21)16-56-62(53,54)59-61(51,52)55-14-22-27(58-60(48,49)50)26(45)32(57-22)42-18-41-25-29(34)39-17-40-30(25)42/h3-6,13,17-18,22,26-28,32,38,45-46H,7-12,14-16H2,1-2H3,(H,35,44)(H,36,43)(H,37,47)(H,51,52)(H,53,54)(H2,34,39,40)(H2,48,49,50)/p-2
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48n/an/an/an/an/an/an/an/a



Johns Hopkins University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of serotonin N-acetyl-transferase


J Med Chem 44: 2479-85 (2001)


Article DOI: 10.1021/jm010049v
BindingDB Entry DOI: 10.7270/Q2319WKP
More data for this
Ligand-Target Pair
Serotonin N-acetyltransferase


(Ovis aries)
BDBM50101700
PNG
(Bisubstrate Analogue | [5-(6-amino-9H-purin-9-yl)-...)
Show SMILES CC(CC(=O)CCCc1c[nH]c2ccccc12)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP([O-])([O-])=O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C36H53N8O17P3S/c1-21(15-23(45)8-6-7-22-16-40-25-10-5-4-9-24(22)25)65-14-13-38-27(46)11-12-39-34(49)31(48)36(2,3)18-58-64(55,56)61-63(53,54)57-17-26-30(60-62(50,51)52)29(47)35(59-26)44-20-43-28-32(37)41-19-42-33(28)44/h4-5,9-10,16,19-21,26,29-31,35,40,47-48H,6-8,11-15,17-18H2,1-3H3,(H,38,46)(H,39,49)(H,53,54)(H,55,56)(H2,37,41,42)(H2,50,51,52)/p-2
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52n/an/an/an/an/an/an/an/a



Johns Hopkins University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of serotonin N-acetyl-transferase


J Med Chem 44: 2479-85 (2001)


Article DOI: 10.1021/jm010049v
BindingDB Entry DOI: 10.7270/Q2319WKP
More data for this
Ligand-Target Pair
Serotonin N-acetyltransferase


(Ovis aries)
BDBM50101699
PNG
(Bisubstrate Analogue | [5-(6-amino-9H-purin-9-yl)-...)
Show SMILES CC(C)(COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP([O-])([O-])=O)n1cnc2c(N)ncnc12)C(O)C(=O)NCCC(=O)NCCSC1CCCC1C(=O)CCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C38H55N8O17P3S/c1-38(2,19-60-66(57,58)63-65(55,56)59-18-27-32(62-64(52,53)54)31(49)37(61-27)46-21-45-30-34(39)43-20-44-35(30)46)33(50)36(51)41-14-13-29(48)40-15-16-67-28-12-6-9-24(28)26(47)11-5-7-22-17-42-25-10-4-3-8-23(22)25/h3-4,8,10,17,20-21,24,27-28,31-33,37,42,49-50H,5-7,9,11-16,18-19H2,1-2H3,(H,40,48)(H,41,51)(H,55,56)(H,57,58)(H2,39,43,44)(H2,52,53,54)/p-2
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65n/an/an/an/an/an/an/an/a



Johns Hopkins University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of serotonin N-acetyl-transferase


J Med Chem 44: 2479-85 (2001)


Article DOI: 10.1021/jm010049v
BindingDB Entry DOI: 10.7270/Q2319WKP
More data for this
Ligand-Target Pair
Serotonin N-acetyltransferase


(Ovis aries)
BDBM50101698
PNG
(Bisubstrate Analogue)
Show SMILES CC(C)(CC(=O)CCCc1c[nH]c2ccccc12)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP([O-])([O-])=O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C37H55N8O17P3S/c1-36(2,31(49)34(50)40-13-12-27(47)39-14-15-66-37(3,4)16-23(46)9-7-8-22-17-41-25-11-6-5-10-24(22)25)19-59-65(56,57)62-64(54,55)58-18-26-30(61-63(51,52)53)29(48)35(60-26)45-21-44-28-32(38)42-20-43-33(28)45/h5-6,10-11,17,20-21,26,29-31,35,41,48-49H,7-9,12-16,18-19H2,1-4H3,(H,39,47)(H,40,50)(H,54,55)(H,56,57)(H2,38,42,43)(H2,51,52,53)/p-2
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275n/an/an/an/an/an/an/an/a



Johns Hopkins University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of serotonin N-acetyl-transferase


J Med Chem 44: 2479-85 (2001)


Article DOI: 10.1021/jm010049v
BindingDB Entry DOI: 10.7270/Q2319WKP
More data for this
Ligand-Target Pair
Serotonin N-acetyltransferase (AANAT)


(Homo sapiens (Human))
BDBM85112
PNG
(AANAT bisubstrate analog, 5)
Show SMILES CC(C)(COP(O)(=O)OP(O)(=O)OC[C@H]1OC([C@@H](O)[C@@H]1OP(O)(O)=O)n1cnc2c(N)ncnc12)[C@@H](O)C(=O)NCCC(=O)NCCSCCCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C33H49N8O16P3S/c1-33(2,28(44)31(45)36-11-10-24(42)35-12-14-61-13-6-5-7-20-15-37-22-9-4-3-8-21(20)22)17-54-60(51,52)57-59(49,50)53-16-23-27(56-58(46,47)48)26(43)32(55-23)41-19-40-25-29(34)38-18-39-30(25)41/h3-4,8-9,15,18-19,23,26-28,32,37,43-44H,5-7,10-14,16-17H2,1-2H3,(H,35,42)(H,36,45)(H,49,50)(H,51,52)(H2,34,38,39)(H2,46,47,48)/t23-,26+,27-,28+,32?/m1/s1
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310 -9.02n/an/an/an/an/a6.830



Johns Hopkins University School of Medicine



Assay Description
AANAT activity was measured using a spectrophotometric assay in which the enzymatic product CoASH concentration were determined indirectly by monitor...


Bioorg Chem 31: 398-411 (2003)


Article DOI: 10.1016/S0045-2068(03)00081-6
BindingDB Entry DOI: 10.7270/Q2DB80CR
More data for this
Ligand-Target Pair
Serotonin N-acetyltransferase (AANAT)


(Homo sapiens (Human))
BDBM85111
PNG
(AANAT bisubstrate analog, 4)
Show SMILES CC(C)(COP(O)(=O)OP(O)(=O)OC[C@H]1OC([C@@H](O)[C@@H]1OP(O)(O)=O)n1cnc2c(N)ncnc12)[C@@H](O)C(=O)NCCC(=O)NCCSCCCCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C34H51N8O16P3S/c1-34(2,29(45)32(46)37-12-11-25(43)36-13-15-62-14-7-3-4-8-21-16-38-23-10-6-5-9-22(21)23)18-55-61(52,53)58-60(50,51)54-17-24-28(57-59(47,48)49)27(44)33(56-24)42-20-41-26-30(35)39-19-40-31(26)42/h5-6,9-10,16,19-20,24,27-29,33,38,44-45H,3-4,7-8,11-15,17-18H2,1-2H3,(H,36,43)(H,37,46)(H,50,51)(H,52,53)(H2,35,39,40)(H2,47,48,49)/t24-,27+,28-,29+,33?/m1/s1
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360 -8.93n/an/an/an/an/a6.830



Johns Hopkins University School of Medicine



Assay Description
AANAT activity was measured using a spectrophotometric assay in which the enzymatic product CoASH concentration were determined indirectly by monitor...


Bioorg Chem 31: 398-411 (2003)


Article DOI: 10.1016/S0045-2068(03)00081-6
BindingDB Entry DOI: 10.7270/Q2DB80CR
More data for this
Ligand-Target Pair
Serotonin N-acetyltransferase (AANAT)


(Homo sapiens (Human))
BDBM85113
PNG
(AANAT bisubstrate analog, 6)
Show SMILES CC(C)(COP(O)(=O)OP(O)(=O)OC[C@H]1OC([C@@H](O)[C@@H]1OP(O)(O)=O)n1cnc2c(N)ncnc12)[C@@H](O)C(=O)NCCC(=O)NCCSCCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C32H47N8O16P3S/c1-32(2,27(43)30(44)35-10-9-23(41)34-11-13-60-12-5-6-19-14-36-21-8-4-3-7-20(19)21)16-53-59(50,51)56-58(48,49)52-15-22-26(55-57(45,46)47)25(42)31(54-22)40-18-39-24-28(33)37-17-38-29(24)40/h3-4,7-8,14,17-18,22,25-27,31,36,42-43H,5-6,9-13,15-16H2,1-2H3,(H,34,41)(H,35,44)(H,48,49)(H,50,51)(H2,33,37,38)(H2,45,46,47)/t22-,25+,26-,27+,31?/m1/s1
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840 -8.42n/an/an/an/an/a6.830



Johns Hopkins University School of Medicine



Assay Description
AANAT activity was measured using a spectrophotometric assay in which the enzymatic product CoASH concentration were determined indirectly by monitor...


Bioorg Chem 31: 398-411 (2003)


Article DOI: 10.1016/S0045-2068(03)00081-6
BindingDB Entry DOI: 10.7270/Q2DB80CR
More data for this
Ligand-Target Pair
Serotonin N-acetyltransferase


(Ovis aries)
BDBM50101693
PNG
(Bisubstrate Analogue | [5-(6-amino-9H-purin-9-yl)-...)
Show SMILES CC(C)(COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP([O-])([O-])=O)n1cnc2c(N)ncnc12)C(O)C(=O)NCCC(=O)NCCS[C@@H]1CCCCC1C(=O)CCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C39H57N8O17P3S/c1-39(2,20-61-67(58,59)64-66(56,57)60-19-28-33(63-65(53,54)55)32(50)38(62-28)47-22-46-31-35(40)44-21-45-36(31)47)34(51)37(52)42-15-14-30(49)41-16-17-68-29-13-6-4-10-25(29)27(48)12-7-8-23-18-43-26-11-5-3-9-24(23)26/h3,5,9,11,18,21-22,25,28-29,32-34,38,43,50-51H,4,6-8,10,12-17,19-20H2,1-2H3,(H,41,49)(H,42,52)(H,56,57)(H,58,59)(H2,40,44,45)(H2,53,54,55)/p-2/t25?,28?,29-,32?,33?,34?,38?/m1/s1
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942n/an/an/an/an/an/an/an/a



Johns Hopkins University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of serotonin N-acetyl-transferase


J Med Chem 44: 2479-85 (2001)


Article DOI: 10.1021/jm010049v
BindingDB Entry DOI: 10.7270/Q2319WKP
More data for this
Ligand-Target Pair
Serotonin N-acetyltransferase


(Ovis aries)
BDBM50101704
PNG
(Bisubstrate Analogue | [5-(6-amino-9H-purin-9-yl)-...)
Show SMILES CC(C)(COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP([O-])([O-])=O)n1cnc2c(N)ncnc12)C(O)C(=O)NCCC(=O)NCCSCCC(O)CCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C35H53N8O17P3S/c1-35(2,30(47)33(48)38-12-10-26(45)37-13-15-64-14-11-22(44)7-5-6-21-16-39-24-9-4-3-8-23(21)24)18-57-63(54,55)60-62(52,53)56-17-25-29(59-61(49,50)51)28(46)34(58-25)43-20-42-27-31(36)40-19-41-32(27)43/h3-4,8-9,16,19-20,22,25,28-30,34,39,44,46-47H,5-7,10-15,17-18H2,1-2H3,(H,37,45)(H,38,48)(H,52,53)(H,54,55)(H2,36,40,41)(H2,49,50,51)/p-2
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1.10E+3n/an/an/an/an/an/an/an/a



Johns Hopkins University School of Medicine

Curated by ChEMBL


Assay Description
Inhibition of serotonin N-acetyl-transferase


J Med Chem 44: 2479-85 (2001)


Article DOI: 10.1021/jm010049v
BindingDB Entry DOI: 10.7270/Q2319WKP
More data for this
Ligand-Target Pair
alpha-Methylacyl-CoA Racemase


(Rattus norvegicus (rat))
BDBM21732
PNG
((R)-ibuprofenoyl-CoA, 20)
Show SMILES CCC(C)c1ccc(cc1)[C@@H](C)C(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C34H52N7O17P3S/c1-6-19(2)21-7-9-22(10-8-21)20(3)33(46)62-14-13-36-24(42)11-12-37-31(45)28(44)34(4,5)16-55-61(52,53)58-60(50,51)54-15-23-27(57-59(47,48)49)26(43)32(56-23)41-18-40-25-29(35)38-17-39-30(25)41/h7-10,17-20,23,26-28,32,43-44H,6,11-16H2,1-5H3,(H,36,42)(H,37,45)(H,50,51)(H,52,53)(H2,35,38,39)(H2,47,48,49)/t19?,20-,23-,26-,27-,28?,32-/m1/s1
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UniProtKB/SwissProt

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PC cid
PC sid
UniChem

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Article
PubMed
5.40E+3 -7.47n/an/an/an/an/a7.037



University of Liverpool



Assay Description
AMACR activity was determined by monitoring the interconversion of the (25R/S)-isomer of THC-CoA. Reaction product was analyzed by resolution of (25S...


J Med Chem 50: 2700-7 (2007)


Article DOI: 10.1021/jm0702377
BindingDB Entry DOI: 10.7270/Q2X065BT
More data for this
Ligand-Target Pair
alpha-Methylacyl-CoA Racemase


(Rattus norvegicus (rat))
BDBM21733
PNG
((S)-ibuprofenoyl-CoA, 20)
Show SMILES CCC(C)c1ccc(cc1)[C@H](C)C(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C34H52N7O17P3S/c1-6-19(2)21-7-9-22(10-8-21)20(3)33(46)62-14-13-36-24(42)11-12-37-31(45)28(44)34(4,5)16-55-61(52,53)58-60(50,51)54-15-23-27(57-59(47,48)49)26(43)32(56-23)41-18-40-25-29(35)38-17-39-30(25)41/h7-10,17-20,23,26-28,32,43-44H,6,11-16H2,1-5H3,(H,36,42)(H,37,45)(H,50,51)(H,52,53)(H2,35,38,39)(H2,47,48,49)/t19?,20-,23+,26+,27+,28?,32+/m0/s1
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UniProtKB/SwissProt

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PC cid
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UniChem

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Article
PubMed
1.92E+4 -6.69n/an/an/an/an/a7.037



University of Liverpool



Assay Description
AMACR activity was determined by monitoring the interconversion of the (25R/S)-isomer of THC-CoA. Reaction product was analyzed by resolution of (25S...


J Med Chem 50: 2700-7 (2007)


Article DOI: 10.1021/jm0702377
BindingDB Entry DOI: 10.7270/Q2X065BT
More data for this
Ligand-Target Pair
alpha-Methylacyl-CoA Racemase


(Rattus norvegicus (rat))
BDBM21734
PNG
((Rac)-ibuprofenoyl-CoA, 20 | racemic mixture)
Show SMILES CCC(C)c1ccc(cc1)C(C)C(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)n1cnc2c(N)ncnc12
Show InChI InChI=1S/C34H52N7O17P3S/c1-6-19(2)21-7-9-22(10-8-21)20(3)33(46)62-14-13-36-24(42)11-12-37-31(45)28(44)34(4,5)16-55-61(52,53)58-60(50,51)54-15-23-27(57-59(47,48)49)26(43)32(56-23)41-18-40-25-29(35)38-17-39-30(25)41/h7-10,17-20,23,26-28,32,43-44H,6,11-16H2,1-5H3,(H,36,42)(H,37,45)(H,50,51)(H,52,53)(H2,35,38,39)(H2,47,48,49)/t19?,20?,23-,26-,27-,28?,32-/m1/s1
KEGG

UniProtKB/SwissProt

GoogleScholar
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
5.60E+4 -6.03n/an/an/an/an/a7.037



University of Liverpool



Assay Description
AMACR activity was determined by monitoring the interconversion of the (25R/S)-isomer of THC-CoA. Reaction product was analyzed by resolution of (25S...


J Med Chem 50: 2700-7 (2007)


Article DOI: 10.1021/jm0702377
BindingDB Entry DOI: 10.7270/Q2X065BT
More data for this
Ligand-Target Pair