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BDBM50430346 CHEMBL2333886

SMILES: C[N+]1(C)C[C@H]([C@@H](C1)c1nc2ccc(cc2c(=O)[nH]1)-c1cn[nH]c1)c1ccccc1

InChI Key: InChIKey=NKPRLPJLIAJOCL-VQTJNVASSA-O

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50430346   
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
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50430346
PNG
(CHEMBL2333886)
Show SMILES C[N+]1(C)C[C@H]([C@@H](C1)c1nc2ccc(cc2c(=O)[nH]1)-c1cn[nH]c1)c1ccccc1 |r|
Show InChI InChI=1S/C23H23N5O/c1-28(2)13-19(15-6-4-3-5-7-15)20(14-28)22-26-21-9-8-16(17-11-24-25-12-17)10-18(21)23(29)27-22/h3-12,19-20H,13-14H2,1-2H3,(H-,24,25,26,27,29)/p+1/t19-,20+/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 4n/an/an/an/an/an/a



Translational Research Institute

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 6-His-tagged ROCK2 expressed in baculovirus-infected Sf9 cells using LCB-AKRRRLSSLRA-NH2 as substrate after 25 mins b...


Bioorg Med Chem Lett 23: 1592-9 (2013)


Article DOI: 10.1016/j.bmcl.2013.01.109
BindingDB Entry DOI: 10.7270/Q2TD9ZQM
More data for this
Ligand-Target Pair