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SMILES: Cc1nc(nc(C(N)=O)c1-c1cccc(Cl)c1Cl)N1C[C@@H]2CCC(N)[C@H]2C1

InChI Key:

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 = 503374   
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
Tyrosine-protein phosphatase non-receptor type 11


(Homo sapiens (Human))
BDBM503374
PNG
(2-((3aR,6aR)-4-Amino-hexahydro- cyclopenta-[c]pyrr...)
Show SMILES Cc1nc(nc(C(N)=O)c1-c1cccc(Cl)c1Cl)N1C[C@@H]2CCC(N)[C@H]2C1 |r,wU:25.28,wD:20.22,(-2.25,3.29,;-1.48,1.95,;.06,1.95,;.83,.62,;.06,-.71,;-1.48,-.71,;-2.25,-2.05,;-1.16,-3.14,;-3.79,-2.05,;-2.25,.62,;-3.79,.62,;-4.56,-.71,;-6.1,-.71,;-6.87,.62,;-6.1,1.95,;-6.87,3.29,;-4.56,1.95,;-3.79,3.29,;2.37,.62,;3.61,1.53,;4.86,.62,;6.4,.62,;6.87,-.84,;5.63,-1.75,;5.63,-3.29,;4.38,-.84,;2.84,-.84,)|
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/a 1.00E+3n/an/an/an/an/an/a


TBA



Citation and Details

BindingDB Entry DOI: 10.7270/Q2JS9VKW
More data for this
Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 11


(Homo sapiens (Human))
BDBM503374
PNG
(2-((3aR,6aR)-4-Amino-hexahydro- cyclopenta-[c]pyrr...)
Show SMILES Cc1nc(nc(C(N)=O)c1-c1cccc(Cl)c1Cl)N1C[C@@H]2CCC(N)[C@H]2C1 |r,wU:25.28,wD:20.22,(-2.25,3.29,;-1.48,1.95,;.06,1.95,;.83,.62,;.06,-.71,;-1.48,-.71,;-2.25,-2.05,;-1.16,-3.14,;-3.79,-2.05,;-2.25,.62,;-3.79,.62,;-4.56,-.71,;-6.1,-.71,;-6.87,.62,;-6.1,1.95,;-6.87,3.29,;-4.56,1.95,;-3.79,3.29,;2.37,.62,;3.61,1.53,;4.86,.62,;6.4,.62,;6.87,-.84,;5.63,-1.75,;5.63,-3.29,;4.38,-.84,;2.84,-.84,)|
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1.00E+3n/an/an/an/an/an/a


TBA

Assay Description
The inhibition of SHP2 by compounds of the invention was monitored using the surrogate substrate DiFMUP after protein activation by a peptide bearing...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2930X9N
More data for this
Ligand-Target Pair