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BDBM50242406 CHEMBL448652::SNEWIQPRLPQH

SMILES: CC[C@H](C)[C@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](N)CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc1cnc[nH]1)C(O)=O

InChI Key: InChIKey=BMZQNOXMUPLPCR-PBLORMCUSA-N

Data: 1 IC50  1 Kd

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50242406   
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
Ephrin type-B receptor 2


(Mus musculus)
BDBM50242406
PNG
(CHEMBL448652 | SNEWIQPRLPQH)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](N)CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc1cnc[nH]1)C(O)=O |r,wU:22.29,4.4,73.75,88.91,wD:39.41,31.37,8.20,2.2,46.47,58.61,62.64,84.88,97.100,(6.11,-.72,;6.16,-2.26,;7.52,-2.99,;8.83,-2.19,;7.56,-4.54,;6.25,-5.35,;4.9,-4.62,;4.85,-3.07,;3.59,-5.43,;3.63,-6.97,;4.99,-7.7,;6.37,-7.03,;7.44,-8.15,;6.7,-9.49,;7.23,-10.95,;6.23,-12.12,;4.71,-11.85,;4.2,-10.39,;5.19,-9.22,;2.23,-4.7,;.91,-5.5,;.96,-7.04,;-.45,-4.77,;-.49,-3.23,;.82,-2.42,;.78,-.88,;-.58,-.15,;2.09,-.07,;-1.75,-5.58,;-3.11,-4.85,;-3.15,-3.31,;-4.42,-5.66,;-4.38,-7.2,;-3.02,-7.93,;-1.7,-7.12,;-2.97,-9.47,;-5.78,-4.92,;-7.09,-5.74,;-7.05,-7.27,;-8.44,-5,;-8.49,-3.47,;-9.75,-5.81,;-11.11,-5.08,;8.92,-5.27,;8.96,-6.81,;10.23,-4.46,;11.59,-5.19,;11.64,-6.73,;10.32,-7.54,;10.37,-9.08,;11.72,-9.81,;9.05,-9.89,;12.9,-4.38,;12.85,-2.84,;14.25,-5.11,;14.6,-6.76,;16.28,-6.94,;16.97,-5.41,;15.65,-4.56,;15.81,-3.04,;14.57,-2.14,;17.22,-2.4,;18.52,-3.23,;18.46,-4.76,;19.76,-5.59,;19.7,-7.12,;21.01,-7.95,;20.95,-9.49,;19.59,-10.2,;22.25,-10.31,;19.89,-2.51,;19.94,-.96,;21.19,-3.33,;22.55,-2.62,;22.62,-1.07,;23.98,-.35,;24.04,1.18,;25.28,-1.18,;23.85,-3.43,;25.22,-2.71,;23.8,-4.98,;22.47,-6.01,;23.05,-7.6,;24.72,-7.54,;24.9,-6.01,;26.35,-5.46,;26.59,-3.94,;27.53,-6.44,;28.97,-5.9,;29.22,-4.39,;30.68,-3.83,;30.92,-2.33,;29.74,-1.36,;32.37,-1.78,;30.18,-6.88,;29.92,-8.42,;31.6,-6.34,;32.81,-7.32,;32.56,-8.86,;33.74,-9.82,;33.63,-11.38,;35.06,-11.95,;36.04,-10.76,;35.22,-9.46,;34.23,-6.78,;35.44,-7.77,;34.48,-5.28,)|
Show InChI InChI=1S/C67H101N21O19/c1-5-34(4)54(86-60(100)44(26-35-29-76-39-12-7-6-11-37(35)39)83-57(97)42(18-21-53(93)94)78-59(99)45(28-52(71)92)82-55(95)38(68)31-89)63(103)81-43(17-20-51(70)91)64(104)87-23-9-14-48(87)61(101)79-40(13-8-22-75-67(72)73)56(96)84-46(25-33(2)3)65(105)88-24-10-15-49(88)62(102)80-41(16-19-50(69)90)58(98)85-47(66(106)107)27-36-30-74-32-77-36/h6-7,11-12,29-30,32-34,38,40-49,54,76,89H,5,8-10,13-28,31,68H2,1-4H3,(H2,69,90)(H2,70,91)(H2,71,92)(H,74,77)(H,78,99)(H,79,101)(H,80,102)(H,81,103)(H,82,95)(H,83,97)(H,84,96)(H,85,98)(H,86,100)(H,93,94)(H,106,107)(H4,72,73,75)/t34-,38-,40-,41-,42-,43-,44-,45-,46-,47-,48-,49-,54-/m0/s1
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Article
PubMed
n/an/a 1.50E+4n/an/an/an/an/an/a



The Scripps Research Institute

Curated by ChEMBL


Assay Description
Binding affinity at mouse EphB2 receptor by ELISA


J Biol Chem 282: 36505-13 (2007)


Article DOI: 10.1074/jbc.M706340200
BindingDB Entry DOI: 10.7270/Q29C6X7S
More data for this
Ligand-Target Pair
Ephrin type-B receptor 2


(Homo sapiens (Human))
BDBM50242406
PNG
(CHEMBL448652 | SNEWIQPRLPQH)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](N)CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc1cnc[nH]1)C(O)=O |r,wU:22.29,4.4,73.75,88.91,wD:39.41,31.37,8.20,2.2,46.47,58.61,62.64,84.88,97.100,(6.11,-.72,;6.16,-2.26,;7.52,-2.99,;8.83,-2.19,;7.56,-4.54,;6.25,-5.35,;4.9,-4.62,;4.85,-3.07,;3.59,-5.43,;3.63,-6.97,;4.99,-7.7,;6.37,-7.03,;7.44,-8.15,;6.7,-9.49,;7.23,-10.95,;6.23,-12.12,;4.71,-11.85,;4.2,-10.39,;5.19,-9.22,;2.23,-4.7,;.91,-5.5,;.96,-7.04,;-.45,-4.77,;-.49,-3.23,;.82,-2.42,;.78,-.88,;-.58,-.15,;2.09,-.07,;-1.75,-5.58,;-3.11,-4.85,;-3.15,-3.31,;-4.42,-5.66,;-4.38,-7.2,;-3.02,-7.93,;-1.7,-7.12,;-2.97,-9.47,;-5.78,-4.92,;-7.09,-5.74,;-7.05,-7.27,;-8.44,-5,;-8.49,-3.47,;-9.75,-5.81,;-11.11,-5.08,;8.92,-5.27,;8.96,-6.81,;10.23,-4.46,;11.59,-5.19,;11.64,-6.73,;10.32,-7.54,;10.37,-9.08,;11.72,-9.81,;9.05,-9.89,;12.9,-4.38,;12.85,-2.84,;14.25,-5.11,;14.6,-6.76,;16.28,-6.94,;16.97,-5.41,;15.65,-4.56,;15.81,-3.04,;14.57,-2.14,;17.22,-2.4,;18.52,-3.23,;18.46,-4.76,;19.76,-5.59,;19.7,-7.12,;21.01,-7.95,;20.95,-9.49,;19.59,-10.2,;22.25,-10.31,;19.89,-2.51,;19.94,-.96,;21.19,-3.33,;22.55,-2.62,;22.62,-1.07,;23.98,-.35,;24.04,1.18,;25.28,-1.18,;23.85,-3.43,;25.22,-2.71,;23.8,-4.98,;22.47,-6.01,;23.05,-7.6,;24.72,-7.54,;24.9,-6.01,;26.35,-5.46,;26.59,-3.94,;27.53,-6.44,;28.97,-5.9,;29.22,-4.39,;30.68,-3.83,;30.92,-2.33,;29.74,-1.36,;32.37,-1.78,;30.18,-6.88,;29.92,-8.42,;31.6,-6.34,;32.81,-7.32,;32.56,-8.86,;33.74,-9.82,;33.63,-11.38,;35.06,-11.95,;36.04,-10.76,;35.22,-9.46,;34.23,-6.78,;35.44,-7.77,;34.48,-5.28,)|
Show InChI InChI=1S/C67H101N21O19/c1-5-34(4)54(86-60(100)44(26-35-29-76-39-12-7-6-11-37(35)39)83-57(97)42(18-21-53(93)94)78-59(99)45(28-52(71)92)82-55(95)38(68)31-89)63(103)81-43(17-20-51(70)91)64(104)87-23-9-14-48(87)61(101)79-40(13-8-22-75-67(72)73)56(96)84-46(25-33(2)3)65(105)88-24-10-15-49(88)62(102)80-41(16-19-50(69)90)58(98)85-47(66(106)107)27-36-30-74-32-77-36/h6-7,11-12,29-30,32-34,38,40-49,54,76,89H,5,8-10,13-28,31,68H2,1-4H3,(H2,69,90)(H2,70,91)(H2,71,92)(H,74,77)(H,78,99)(H,79,101)(H,80,102)(H,81,103)(H,82,95)(H,83,97)(H,84,96)(H,85,98)(H,86,100)(H,93,94)(H,106,107)(H4,72,73,75)/t34-,38-,40-,41-,42-,43-,44-,45-,46-,47-,48-,49-,54-/m0/s1
PDB
MMDB

NCI pathway
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UniProtKB/SwissProt

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Article
PubMed
n/an/an/a 6.00E+3n/an/an/an/an/a



The Scripps Research Institute

Curated by ChEMBL


Assay Description
Binding affinity at human EphB2 receptor by isothermal titration calorimetry


J Biol Chem 282: 36505-13 (2007)


Article DOI: 10.1074/jbc.M706340200
BindingDB Entry DOI: 10.7270/Q29C6X7S
More data for this
Ligand-Target Pair