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11 similar compounds to monomer 50128294

Compile data set for download or QSAR
Wt: 514.6
BDBM36170
Purchase
Wt: 499.7
BDBM50236230
Purchase
Wt: 359.4
BDBM50037259
Wt: 575.7
BDBM50150345
Wt: 386.4
BDBM50236229
Wt: 451.3
BDBM50236211
Wt: 372.4
BDBM50236231
Wt: 407.3
BDBM50236232
Wt: 415.4
BDBM50236233
Wt: 2180.6
BDBM50236209
Wt: 2095.5
BDBM50236210

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 15 hits for monomerid = 36170,50236230,50037259,50150345,50236229,50236211,50236231,50236232,50236233,50236209,50236210   
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
Ileal bile acid transporter/bile acid cotransporter


(Homo sapiens (Human))
BDBM50236230
PNG
(2-((R)-4-((3R,5S,7S,8R,9S,10S,13R,14S,17R)-3,7-dih...)
Show SMILES C[C@H](CCC(=O)NCCS(O)(=O)=O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Show InChI InChI=1S/C26H45NO6S/c1-16(4-7-23(30)27-12-13-34(31,32)33)19-5-6-20-24-21(9-11-26(19,20)3)25(2)10-8-18(28)14-17(25)15-22(24)29/h16-22,24,28-29H,4-15H2,1-3H3,(H,27,30)(H,31,32,33)/t16-,17+,18-,19-,20+,21+,22+,24+,25+,26-/m1/s1
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2.80E+4n/an/an/an/an/an/an/an/a



Wake Forest University

Curated by ChEMBL


Assay Description
TP_TRANSPORTER: inhibition of Taurocholate uptake in ASBT-expressing COS cells


Am J Physiol 274: 157-69 (1998)


Article DOI: 10.1152/ajpgi.1998.274.1.G157
BindingDB Entry DOI: 10.7270/Q2B859C1
More data for this
Ligand-Target Pair
3',5'-cyclic phosphodiesterase


(Homo sapiens (Human))
BDBM50236229
PNG
(CHEMBL4074644)
Show SMILES Cc1cc(N2CCCC(C2)C(=O)Nc2ccc3ccccc3c2)n2ncnc2n1
Show InChI InChI=1S/C22H22N6O/c1-15-11-20(28-22(25-15)23-14-24-28)27-10-4-7-18(13-27)21(29)26-19-9-8-16-5-2-3-6-17(16)12-19/h2-3,5-6,8-9,11-12,14,18H,4,7,10,13H2,1H3,(H,26,29)
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n/an/a 140n/an/an/an/an/an/a



Dart Neuroscience LLC

Curated by ChEMBL


Assay Description
Inhibition of human full length GST-tagged PDE2a using FAM-labeled cAMP as substrate preincubated for 5 mins followed by substrate addition measured ...


J Med Chem 60: 2037-2051 (2017)

More data for this
Ligand-Target Pair
Calcitonin gene-related peptide (CGRP alpha)


(Homo sapiens (Human))
BDBM50150345
PNG
(CHEMBL3770044)
Show SMILES Cc1cc(C[C@@H](NC(=O)N2CCN(CC2)c2ccccc2F)C(=O)N2CCC(CC2)N2CCCCC2)cc2cn[nH]c12
Show InChI InChI=1S/C32H42FN7O2/c1-23-19-24(20-25-22-34-36-30(23)25)21-28(31(41)39-13-9-26(10-14-39)37-11-5-2-6-12-37)35-32(42)40-17-15-38(16-18-40)29-8-4-3-7-27(29)33/h3-4,7-8,19-20,22,26,28H,2,5-6,9-18,21H2,1H3,(H,34,36)(H,35,42)/t28-/m1/s1
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n/an/a 130n/an/an/an/an/an/a



Bristol-Myers Squibb Discovery

Curated by ChEMBL


Assay Description
Displacement of [125I]CGRP from alpha CGRP in human SK-N-MC cells after 2 hrs by scintillation counter


Bioorg Med Chem Lett 26: 1229-32 (2016)


Article DOI: 10.1016/j.bmcl.2016.01.026
BindingDB Entry DOI: 10.7270/Q2NG4SH3
More data for this
Ligand-Target Pair
Phospholipase A2


(Homo sapiens (Human))
BDBM50236230
PNG
(2-((R)-4-((3R,5S,7S,8R,9S,10S,13R,14S,17R)-3,7-dih...)
Show SMILES C[C@H](CCC(=O)NCCS(O)(=O)=O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Show InChI InChI=1S/C26H45NO6S/c1-16(4-7-23(30)27-12-13-34(31,32)33)19-5-6-20-24-21(9-11-26(19,20)3)25(2)10-8-18(28)14-17(25)15-22(24)29/h16-22,24,28-29H,4-15H2,1-3H3,(H,27,30)(H,31,32,33)/t16-,17+,18-,19-,20+,21+,22+,24+,25+,26-/m1/s1
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n/an/an/a 1.00E+4n/an/an/an/an/a



University of Delaware

Curated by ChEMBL


Assay Description
Binding affinity to human pancreatic recombinant 1B PLA2 expressed in Escherichia coli by resonance energy transfer assay in presence of trimethyl-am...


J Nat Prod 72: 24-8 (2009)


Article DOI: 10.1021/np8004453
BindingDB Entry DOI: 10.7270/Q2X34XG0
More data for this
Ligand-Target Pair
G-protein coupled bile acid receptor 1


(Homo sapiens (Human))
BDBM50236230
PNG
(2-((R)-4-((3R,5S,7S,8R,9S,10S,13R,14S,17R)-3,7-dih...)
Show SMILES C[C@H](CCC(=O)NCCS(O)(=O)=O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Show InChI InChI=1S/C26H45NO6S/c1-16(4-7-23(30)27-12-13-34(31,32)33)19-5-6-20-24-21(9-11-26(19,20)3)25(2)10-8-18(28)14-17(25)15-22(24)29/h16-22,24,28-29H,4-15H2,1-3H3,(H,27,30)(H,31,32,33)/t16-,17+,18-,19-,20+,21+,22+,24+,25+,26-/m1/s1
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n/an/an/an/a 3.00E+4n/an/an/an/a



INSERM

Curated by ChEMBL


Assay Description
Agonist activity at human TGR5 expressed in CHO cells by luciferase assay


J Med Chem 51: 1831-41 (2008)


Article DOI: 10.1021/jm7015864
BindingDB Entry DOI: 10.7270/Q2222VNJ
More data for this
Ligand-Target Pair
ADAM17


(Homo sapiens (Human))
BDBM50236210
PNG
(CHEMBL4078311)
Show SMILES CC[C@H](C)[C@@H]1NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H]2CSSC[C@H](NC1=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H]1CSSC[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H]3CSSC[C@H](NC(=O)[C@@H](NC1=O)[C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N3)C(=O)N[C@@H](CC(C)C)C(=O)N2
Show InChI InChI=1S/C83H139N33O19S6/c1-8-41(5)60-76(133)112-55-37-139-136-34-52(70(127)103-47(22-15-27-96-81(88)89)65(122)102-45(20-13-25-94-79(84)85)63(120)100-33-59(119)114-60)110-68(125)50(30-40(3)4)107-73(130)54-36-138-140-38-56(109-67(124)49(105-72(55)129)24-17-29-98-83(92)93)74(131)115-61(42(6)9-2)77(134)113-57-39-141-137-35-53(71(128)104-48(66(123)108-54)23-16-28-97-82(90)91)111-69(126)51(31-44-18-11-10-12-19-44)101-58(118)32-99-64(121)46(21-14-26-95-80(86)87)106-78(135)62(43(7)117)116-75(57)132/h10-12,18-19,40-43,45-57,60-62,117H,8-9,13-17,20-39H2,1-7H3,(H,99,121)(H,100,120)(H,101,118)(H,102,122)(H,103,127)(H,104,128)(H,105,129)(H,106,135)(H,107,130)(H,108,123)(H,109,124)(H,110,125)(H,111,126)(H,112,133)(H,113,134)(H,114,119)(H,115,131)(H,116,132)(H4,84,85,94)(H4,86,87,95)(H4,88,89,96)(H4,90,91,97)(H4,92,93,98)/t41-,42-,43+,45-,46-,47-,48-,49-,50-,51-,52-,53-,54-,55-,56-,57-,60-,61-,62-/m0/s1
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n/an/a 3.86E+3n/an/an/an/an/an/a



State University of New York

Curated by ChEMBL


Assay Description
Inhibition of recombinant human TACE extracellular domain (215 to 671 residues) assessed as inhibition of proteolytic activity preincubated for 30 mi...


J Med Chem 60: 1916-1927 (2017)

More data for this
Ligand-Target Pair
Antrax lethal toxin


(Bacillus anthracis)
BDBM50236210
PNG
(CHEMBL4078311)
Show SMILES CC[C@H](C)[C@@H]1NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H]2CSSC[C@H](NC1=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H]1CSSC[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H]3CSSC[C@H](NC(=O)[C@@H](NC1=O)[C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N3)C(=O)N[C@@H](CC(C)C)C(=O)N2
Show InChI InChI=1S/C83H139N33O19S6/c1-8-41(5)60-76(133)112-55-37-139-136-34-52(70(127)103-47(22-15-27-96-81(88)89)65(122)102-45(20-13-25-94-79(84)85)63(120)100-33-59(119)114-60)110-68(125)50(30-40(3)4)107-73(130)54-36-138-140-38-56(109-67(124)49(105-72(55)129)24-17-29-98-83(92)93)74(131)115-61(42(6)9-2)77(134)113-57-39-141-137-35-53(71(128)104-48(66(123)108-54)23-16-28-97-82(90)91)111-69(126)51(31-44-18-11-10-12-19-44)101-58(118)32-99-64(121)46(21-14-26-95-80(86)87)106-78(135)62(43(7)117)116-75(57)132/h10-12,18-19,40-43,45-57,60-62,117H,8-9,13-17,20-39H2,1-7H3,(H,99,121)(H,100,120)(H,101,118)(H,102,122)(H,103,127)(H,104,128)(H,105,129)(H,106,135)(H,107,130)(H,108,123)(H,109,124)(H,110,125)(H,111,126)(H,112,133)(H,113,134)(H,114,119)(H,115,131)(H,116,132)(H4,84,85,94)(H4,86,87,95)(H4,88,89,96)(H4,90,91,97)(H4,92,93,98)/t41-,42-,43+,45-,46-,47-,48-,49-,50-,51-,52-,53-,54-,55-,56-,57-,60-,61-,62-/m0/s1
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n/an/a 1.04E+3n/an/an/an/an/an/a



State University of New York

Curated by ChEMBL


Assay Description
Inhibition of Bacillus anthracis lethal factor protease preincubated for 30 mins prior to addition of substrate containing fluorescent proteins CyPet...


J Med Chem 60: 1916-1927 (2017)

More data for this
Ligand-Target Pair
Antrax lethal toxin


(Bacillus anthracis)
BDBM50236209
PNG
(CHEMBL4067395)
Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CSSC[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H]3CSSC[C@H](NC1=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N3)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H]1CSSC[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC1=O)C(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2
Show InChI InChI=1S/C86H146N36O19S6/c1-8-43(6)62-79(140)119-59-40-147-143-36-55(117-71(132)53(33-45-18-10-9-11-19-45)106-60(124)34-105-64(125)46(20-12-26-99-81(87)88)112-80(141)63(44(7)123)122-77(59)138)73(134)110-49(23-15-29-102-84(93)94)67(128)114-56-37-144-146-39-58(76(137)121-62)115-68(129)50(24-16-30-103-85(95)96)111-74(135)57-38-145-142-35-54(116-70(131)52(32-41(2)3)113-75(56)136)72(133)109-48(22-14-28-101-83(91)92)66(127)107-47(21-13-27-100-82(89)90)65(126)108-51(25-17-31-104-86(97)98)69(130)120-61(42(4)5)78(139)118-57/h9-11,18-19,41-44,46-59,61-63,123H,8,12-17,20-40H2,1-7H3,(H,105,125)(H,106,124)(H,107,127)(H,108,126)(H,109,133)(H,110,134)(H,111,135)(H,112,141)(H,113,136)(H,114,128)(H,115,129)(H,116,131)(H,117,132)(H,118,139)(H,119,140)(H,120,130)(H,121,137)(H,122,138)(H4,87,88,99)(H4,89,90,100)(H4,91,92,101)(H4,93,94,102)(H4,95,96,103)(H4,97,98,104)/t43-,44+,46-,47-,48-,49-,50-,51-,52-,53-,54-,55-,56-,57-,58-,59-,61-,62-,63-/m0/s1
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n/an/a 262n/an/an/an/an/an/a



State University of New York

Curated by ChEMBL


Assay Description
Inhibition of Bacillus anthracis lethal factor protease preincubated for 30 mins prior to addition of substrate containing fluorescent proteins CyPet...


J Med Chem 60: 1916-1927 (2017)

More data for this
Ligand-Target Pair
ADAM17


(Homo sapiens (Human))
BDBM50236209
PNG
(CHEMBL4067395)
Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CSSC[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H]3CSSC[C@H](NC1=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N3)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H]1CSSC[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC1=O)C(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2
Show InChI InChI=1S/C86H146N36O19S6/c1-8-43(6)62-79(140)119-59-40-147-143-36-55(117-71(132)53(33-45-18-10-9-11-19-45)106-60(124)34-105-64(125)46(20-12-26-99-81(87)88)112-80(141)63(44(7)123)122-77(59)138)73(134)110-49(23-15-29-102-84(93)94)67(128)114-56-37-144-146-39-58(76(137)121-62)115-68(129)50(24-16-30-103-85(95)96)111-74(135)57-38-145-142-35-54(116-70(131)52(32-41(2)3)113-75(56)136)72(133)109-48(22-14-28-101-83(91)92)66(127)107-47(21-13-27-100-82(89)90)65(126)108-51(25-17-31-104-86(97)98)69(130)120-61(42(4)5)78(139)118-57/h9-11,18-19,41-44,46-59,61-63,123H,8,12-17,20-40H2,1-7H3,(H,105,125)(H,106,124)(H,107,127)(H,108,126)(H,109,133)(H,110,134)(H,111,135)(H,112,141)(H,113,136)(H,114,128)(H,115,129)(H,116,131)(H,117,132)(H,118,139)(H,119,140)(H,120,130)(H,121,137)(H,122,138)(H4,87,88,99)(H4,89,90,100)(H4,91,92,101)(H4,93,94,102)(H4,95,96,103)(H4,97,98,104)/t43-,44+,46-,47-,48-,49-,50-,51-,52-,53-,54-,55-,56-,57-,58-,59-,61-,62-,63-/m0/s1
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n/an/a 870n/an/an/an/an/an/a



State University of New York

Curated by ChEMBL


Assay Description
Inhibition of recombinant human TACE extracellular domain (215 to 671 residues) assessed as inhibition of proteolytic activity preincubated for 30 mi...


J Med Chem 60: 1916-1927 (2017)

More data for this
Ligand-Target Pair
Factor D


(Homo sapiens (Human))
BDBM50236211
PNG
(CHEMBL4065974)
Show SMILES COC(=O)c1cccc(NC(=O)N2CCC[C@H]2C(=O)Nc2cccc(OC(F)(F)F)c2)c1
Show InChI InChI=1S/C21H20F3N3O5/c1-31-19(29)13-5-2-6-14(11-13)26-20(30)27-10-4-9-17(27)18(28)25-15-7-3-8-16(12-15)32-21(22,23)24/h2-3,5-8,11-12,17H,4,9-10H2,1H3,(H,25,28)(H,26,30)/t17-/m0/s1
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n/an/a>3.00E+4n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of recombinant human complement factor D catalytic domain (G24 to A253 residues) expressed in Escherichia coli Rosetta using Z-Lys-thioben...


J Med Chem 60: 1946-1958 (2017)

More data for this
Ligand-Target Pair
3',5'-cyclic phosphodiesterase


(Homo sapiens (Human))
BDBM50236231
PNG
(CHEMBL4087945)
Show SMILES Cc1cc(C2CCCN(C2)C(=O)c2ccc3ncccc3c2)n2ncnc2n1
Show InChI InChI=1S/C21H20N6O/c1-14-10-19(27-21(25-14)23-13-24-27)17-5-3-9-26(12-17)20(28)16-6-7-18-15(11-16)4-2-8-22-18/h2,4,6-8,10-11,13,17H,3,5,9,12H2,1H3
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n/an/a 2n/an/an/an/an/an/a



Dart Neuroscience LLC

Curated by ChEMBL


Assay Description
Tested for the inhibitory activity against pepsin (Second pure eluting diastereomer )


J Med Chem 60: 2037-2051 (2017)

More data for this
Ligand-Target Pair
3',5'-cyclic phosphodiesterase


(Homo sapiens (Human))
BDBM50236232
PNG
(CHEMBL4062668)
Show SMILES Cc1cc([C@@H]2CN(CC(F)(F)C2)C(=O)c2cc(C)c(F)c(F)c2)n2ncnc2n1
Show InChI InChI=1S/C19H17F4N5O/c1-10-3-12(5-14(20)16(10)21)17(29)27-7-13(6-19(22,23)8-27)15-4-11(2)26-18-24-9-25-28(15)18/h3-5,9,13H,6-8H2,1-2H3/t13-/m0/s1
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n/an/a 62n/an/an/an/an/an/a



Dart Neuroscience LLC

Curated by ChEMBL


Assay Description
Inhibition of human full length GST-tagged PDE2a using FAM-labeled cAMP as substrate preincubated for 5 mins followed by substrate addition measured ...


J Med Chem 60: 2037-2051 (2017)

More data for this
Ligand-Target Pair
3',5'-cyclic phosphodiesterase


(Homo sapiens (Human))
BDBM50236233
PNG
(CHEMBL4077469)
Show SMILES Cc1cc([C@@H]2CN(CC(F)(F)C2)C(=O)c2ccc(F)c(c2)C2CC2)n2ncnc2n1
Show InChI InChI=1S/C21H20F3N5O/c1-12-6-18(29-20(27-12)25-11-26-29)15-8-21(23,24)10-28(9-15)19(30)14-4-5-17(22)16(7-14)13-2-3-13/h4-7,11,13,15H,2-3,8-10H2,1H3/t15-/m0/s1
PDB
MMDB

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UniProtKB/SwissProt

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DrugBank
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MMDB
PC cid
PC sid
UniChem

Patents


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PubMed
n/an/a 23n/an/an/an/an/an/a



Dart Neuroscience LLC

Curated by ChEMBL


Assay Description
Inhibition of human full length GST-tagged PDE2a using FAM-labeled cAMP as substrate preincubated for 5 mins followed by substrate addition measured ...


J Med Chem 60: 2037-2051 (2017)

More data for this
Ligand-Target Pair
Mast/stem cell growth factor receptor Kit


(Homo sapiens (Human))
BDBM50037259
PNG
(CHEMBL3356289)
Show SMILES C=CC(=O)N1CCN(CC1)c1ccc(\C=C2/C(=O)Nc3ccccc23)cc1
Show InChI InChI=1S/C22H21N3O2/c1-2-21(26)25-13-11-24(12-14-25)17-9-7-16(8-10-17)15-19-18-5-3-4-6-20(18)23-22(19)27/h2-10,15H,1,11-14H2,(H,23,27)/b19-15-
PDB

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PC sid
UniChem

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Article
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n/an/a 128n/an/an/an/an/an/a



Wenzhou Medical University

Curated by ChEMBL


Assay Description
Inhibition of recombinant c-Kit (unknown origin) after 1 hr by microfluidic assay


Bioorg Med Chem 22: 6953-60 (2014)


Article DOI: 10.1016/j.bmc.2014.10.017
BindingDB Entry DOI: 10.7270/Q2W37XW6
More data for this
Ligand-Target Pair
Aurora kinase B


(Homo sapiens (Human))
BDBM50037259
PNG
(CHEMBL3356289)
Show SMILES C=CC(=O)N1CCN(CC1)c1ccc(\C=C2/C(=O)Nc3ccccc23)cc1
Show InChI InChI=1S/C22H21N3O2/c1-2-21(26)25-13-11-24(12-14-25)17-9-7-16(8-10-17)15-19-18-5-3-4-6-20(18)23-22(19)27/h2-10,15H,1,11-14H2,(H,23,27)/b19-15-
PDB

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n/an/a 2.21E+3n/an/an/an/an/an/a



Wenzhou Medical University

Curated by ChEMBL


Assay Description
Inhibition of recombinant Aur B (unknown origin) after 1 hr by microfluidic assay


Bioorg Med Chem 22: 6953-60 (2014)


Article DOI: 10.1016/j.bmc.2014.10.017
BindingDB Entry DOI: 10.7270/Q2W37XW6
More data for this
Ligand-Target Pair

Activity Spreadsheet -- ITC Data from BindingDB

Found 7 hits for monomerid = 36170,50236230,50037259,50150345,50236229,50236211,50236231,50236232,50236233,50236209,50236210
Cell (A)Syringe (B)Cell
Links
Syringe
Links
Cell + Syr
Links
ΔG°
kcal/mole
-TΔS°
kcal/mole
ΔH°
kcal/mole
log KpHTemp
°C
BDBM11
JPEG
BDBM36170
JPEG
CHEBI
KEGG
MMDB
PC cid
PC sid
KEGG
PC cid
PC sid
n/a1.10-5.683.367.2025



Nankai University





J Org Chem 70: 8703-11 (2005)

BDBM36166
JPEG
BDBM36170
JPEG
PC cid
PC sid
KEGG
PC cid
PC sid
n/a1.39-5.523.037.2025



Nankai University





J Org Chem 70: 8703-11 (2005)

BDBM36167
JPEG
BDBM36170
JPEG
PC cid
PC sid
KEGG
PC cid
PC sid
n/a1.48-5.803.177.2025



Nankai University





J Org Chem 70: 8703-11 (2005)

BDBM11
JPEG
BDBM36170
JPEG
CHEBI
KEGG
MMDB
PC cid
PC sid
KEGG
PC cid
PC sid
-4.581.10-5.683.367.2025



Nankai University





J Phys Chem B 107: 14130 (2003)

BDBM36127
JPEG
BDBM36170
JPEG
CHEBI
PC cid
PC sid
KEGG
PC cid
PC sid
-4.591.84-6.423.367.2025



Nankai University





J Phys Chem B 107: 14130 (2003)

BDBM36171
JPEG
BDBM36170
JPEG
PC cid
PC sid
KEGG
PC cid
PC sid
-4.263.57-7.823.127.2025



Nankai University





J Phys Chem B 107: 14130 (2003)

BDBM36172
JPEG
BDBM36170
JPEG
PC cid
PC sid
KEGG
PC cid
PC sid
-4.700.164-4.873.457.2025



Nankai University





J Phys Chem B 107: 14130 (2003)