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BDBM108432 US8609688, 10

SMILES: CCN(CC)C(=O)C1CCN(CC1)c1cccc(c1)-c1ccc2nc(-c3cccnc3N)n(-c3ccc(cc3)C3(N)CCC3)c2n1

InChI Key: InChIKey=BXMVUEBGZCWIKD-UHFFFAOYSA-N

Data: 2 IC50  2 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 4 hits for monomerid = 108432   
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
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM108432
PNG
(US8609688, 10)
Show SMILES CCN(CC)C(=O)C1CCN(CC1)c1cccc(c1)-c1ccc2nc(-c3cccnc3N)n(-c3ccc(cc3)C3(N)CCC3)c2n1
Show InChI InChI=1S/C37H42N8O/c1-3-43(4-2)36(46)25-17-22-44(23-18-25)29-9-5-8-26(24-29)31-15-16-32-35(41-31)45(34(42-32)30-10-6-21-40-33(30)38)28-13-11-27(12-14-28)37(39)19-7-20-37/h5-6,8-16,21,24-25H,3-4,7,17-20,22-23,39H2,1-2H3,(H2,38,40)
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

US Patent
n/an/an/a 0.200n/an/an/a7.580



ArQule, Inc.

US Patent


Assay Description
Protein-ligand binding was identified with the thermal shift assay which is based on the ligand-induced stabilization of the protein tertiary structu...


US Patent US8609688 (2013)


BindingDB Entry DOI: 10.7270/Q2H41Q2M
More data for this
Ligand-Target Pair
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM108432
PNG
(US8609688, 10)
Show SMILES CCN(CC)C(=O)C1CCN(CC1)c1cccc(c1)-c1ccc2nc(-c3cccnc3N)n(-c3ccc(cc3)C3(N)CCC3)c2n1
Show InChI InChI=1S/C37H42N8O/c1-3-43(4-2)36(46)25-17-22-44(23-18-25)29-9-5-8-26(24-29)31-15-16-32-35(41-31)45(34(42-32)30-10-6-21-40-33(30)38)28-13-11-27(12-14-28)37(39)19-7-20-37/h5-6,8-16,21,24-25H,3-4,7,17-20,22-23,39H2,1-2H3,(H2,38,40)
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

US Patent
n/an/a 4.15n/an/an/an/an/an/a



ArQule, Inc.

US Patent


Assay Description
AKT1 activity was assayed using the GSK3-derived biotinylated peptide substrate, crosstide (biotin-GRPRTSSFAEG), and AlphaScreen (Amplified Luminesce...


US Patent US8962619 (2015)


BindingDB Entry DOI: 10.7270/Q2W957W7
More data for this
Ligand-Target Pair
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM108432
PNG
(US8609688, 10)
Show SMILES CCN(CC)C(=O)C1CCN(CC1)c1cccc(c1)-c1ccc2nc(-c3cccnc3N)n(-c3ccc(cc3)C3(N)CCC3)c2n1
Show InChI InChI=1S/C37H42N8O/c1-3-43(4-2)36(46)25-17-22-44(23-18-25)29-9-5-8-26(24-29)31-15-16-32-35(41-31)45(34(42-32)30-10-6-21-40-33(30)38)28-13-11-27(12-14-28)37(39)19-7-20-37/h5-6,8-16,21,24-25H,3-4,7,17-20,22-23,39H2,1-2H3,(H2,38,40)
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

US Patent
n/an/an/a 0.200n/an/an/an/an/a



ArQule, Inc.

US Patent


Assay Description
Binding analysis. Protein-ligand binding was identified with the thermal shift assay which is based on the ligand-induced stabilization of the protei...


US Patent US8962619 (2015)


BindingDB Entry DOI: 10.7270/Q2W957W7
More data for this
Ligand-Target Pair
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM108432
PNG
(US8609688, 10)
Show SMILES CCN(CC)C(=O)C1CCN(CC1)c1cccc(c1)-c1ccc2nc(-c3cccnc3N)n(-c3ccc(cc3)C3(N)CCC3)c2n1
Show InChI InChI=1S/C37H42N8O/c1-3-43(4-2)36(46)25-17-22-44(23-18-25)29-9-5-8-26(24-29)31-15-16-32-35(41-31)45(34(42-32)30-10-6-21-40-33(30)38)28-13-11-27(12-14-28)37(39)19-7-20-37/h5-6,8-16,21,24-25H,3-4,7,17-20,22-23,39H2,1-2H3,(H2,38,40)
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

US Patent
n/an/a 4.15n/an/an/an/a8.025



ArQule, Inc.

US Patent


Assay Description
AKT1 activity was assayed using the GSK3-derived biotinylated peptide substrate, crosstide (biotin-GRPRTSSFAEG), and AlphaScreen™ (Amplified Lum...


US Patent US8609688 (2013)


BindingDB Entry DOI: 10.7270/Q2H41Q2M
More data for this
Ligand-Target Pair