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BDBM50292295 2-hydroxy-5-(5-(((1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl)amino)methyl)furan-2-yl)benzoic acid::CHEMBL390576

SMILES: CC1(C)CC(CC(C)(C)N1[O])NCc1ccc(o1)-c1ccc(O)c(c1)C(O)=O

InChI Key: InChIKey=RNZFFIHMOKKHKH-UHFFFAOYSA-N

Data: 5 IC50

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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50292295   
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
Protein-tyrosine phosphatase 1B


(Homo sapiens (Human))
BDBM50292295
PNG
(2-hydroxy-5-(5-(((1-hydroxy-2,2,6,6-tetramethylpip...)
Show SMILES CC1(C)CC(CC(C)(C)N1[O])NCc1ccc(o1)-c1ccc(O)c(c1)C(O)=O |^1:10|
Show InChI InChI=1S/C21H27N2O5/c1-20(2)10-14(11-21(3,4)23(20)27)22-12-15-6-8-18(28-15)13-5-7-17(24)16(9-13)19(25)26/h5-9,14,22,24H,10-12H2,1-4H3,(H,25,26)
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PubMed
n/an/a>1.00E+6n/an/an/an/an/an/a



Institute for Medical Research

Curated by ChEMBL


Assay Description
Inhibition of PTP1B


J Med Chem 50: 2137-43 (2007)


Article DOI: 10.1021/jm061481l
BindingDB Entry DOI: 10.7270/Q2BG2NP4
More data for this
Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 2


(Homo sapiens (Human))
BDBM50292295
PNG
(2-hydroxy-5-(5-(((1-hydroxy-2,2,6,6-tetramethylpip...)
Show SMILES CC1(C)CC(CC(C)(C)N1[O])NCc1ccc(o1)-c1ccc(O)c(c1)C(O)=O |^1:10|
Show InChI InChI=1S/C21H27N2O5/c1-20(2)10-14(11-21(3,4)23(20)27)22-12-15-6-8-18(28-15)13-5-7-17(24)16(9-13)19(25)26/h5-9,14,22,24H,10-12H2,1-4H3,(H,25,26)
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PubMed
n/an/a 6.85E+5n/an/an/an/an/an/a



Institute for Medical Research

Curated by ChEMBL


Assay Description
Inhibition of TCPTP


J Med Chem 50: 2137-43 (2007)


Article DOI: 10.1021/jm061481l
BindingDB Entry DOI: 10.7270/Q2BG2NP4
More data for this
Ligand-Target Pair
Dual specificity protein phosphatase (VHR)


(Homo sapiens (Human))
BDBM50292295
PNG
(2-hydroxy-5-(5-(((1-hydroxy-2,2,6,6-tetramethylpip...)
Show SMILES CC1(C)CC(CC(C)(C)N1[O])NCc1ccc(o1)-c1ccc(O)c(c1)C(O)=O |^1:10|
Show InChI InChI=1S/C21H27N2O5/c1-20(2)10-14(11-21(3,4)23(20)27)22-12-15-6-8-18(28-15)13-5-7-17(24)16(9-13)19(25)26/h5-9,14,22,24H,10-12H2,1-4H3,(H,25,26)
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n/an/a 2.41E+5n/an/an/an/an/an/a



Institute for Medical Research

Curated by ChEMBL


Assay Description
Inhibition of VHR


J Med Chem 50: 2137-43 (2007)


Article DOI: 10.1021/jm061481l
BindingDB Entry DOI: 10.7270/Q2BG2NP4
More data for this
Ligand-Target Pair
Hematopoietic protein-tyrosine phosphatase (HEPTP)


(Homo sapiens (Human))
BDBM50292295
PNG
(2-hydroxy-5-(5-(((1-hydroxy-2,2,6,6-tetramethylpip...)
Show SMILES CC1(C)CC(CC(C)(C)N1[O])NCc1ccc(o1)-c1ccc(O)c(c1)C(O)=O |^1:10|
Show InChI InChI=1S/C21H27N2O5/c1-20(2)10-14(11-21(3,4)23(20)27)22-12-15-6-8-18(28-15)13-5-7-17(24)16(9-13)19(25)26/h5-9,14,22,24H,10-12H2,1-4H3,(H,25,26)
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n/an/a>1.00E+6n/an/an/an/an/an/a



Institute for Medical Research

Curated by ChEMBL


Assay Description
Inhibition of HePTP


J Med Chem 50: 2137-43 (2007)


Article DOI: 10.1021/jm061481l
BindingDB Entry DOI: 10.7270/Q2BG2NP4
More data for this
Ligand-Target Pair
Leukocyte common antigen


(Homo sapiens (Human))
BDBM50292295
PNG
(2-hydroxy-5-(5-(((1-hydroxy-2,2,6,6-tetramethylpip...)
Show SMILES CC1(C)CC(CC(C)(C)N1[O])NCc1ccc(o1)-c1ccc(O)c(c1)C(O)=O |^1:10|
Show InChI InChI=1S/C21H27N2O5/c1-20(2)10-14(11-21(3,4)23(20)27)22-12-15-6-8-18(28-15)13-5-7-17(24)16(9-13)19(25)26/h5-9,14,22,24H,10-12H2,1-4H3,(H,25,26)
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Article
PubMed
n/an/a>1.00E+6n/an/an/an/an/an/a



Institute for Medical Research

Curated by ChEMBL


Assay Description
Inhibition of CD45


J Med Chem 50: 2137-43 (2007)


Article DOI: 10.1021/jm061481l
BindingDB Entry DOI: 10.7270/Q2BG2NP4
More data for this
Ligand-Target Pair