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BDBM23493 hydroxamate deriv., 84::methyl (1R,2S)-2-(hydroxycarbamoyl)-1-({4-[2-(naphthalen-2-yl)ethoxy]phenyl}methyl)cyclopropane-1-carboxylate

SMILES: COC(=O)[C@@]1(Cc2ccc(OCCc3ccc4ccccc4c3)cc2)C[C@@H]1C(=O)NO

InChI Key: InChIKey=IXTZZWZMRYIHAU-RDGATRHJSA-N

Data: 1 KI

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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 23493   
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
TNF-alpha-Converting Enzyme


(Homo sapiens (Human))
BDBM23493
PNG
(hydroxamate deriv., 84 | methyl (1R,2S)-2-(hydroxy...)
Show SMILES COC(=O)[C@@]1(Cc2ccc(OCCc3ccc4ccccc4c3)cc2)C[C@@H]1C(=O)NO |r|
Show InChI InChI=1S/C25H25NO5/c1-30-24(28)25(16-22(25)23(27)26-29)15-18-7-10-21(11-8-18)31-13-12-17-6-9-19-4-2-3-5-20(19)14-17/h2-11,14,22,29H,12-13,15-16H2,1H3,(H,26,27)/t22-,25+/m1/s1
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MMDB

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Similars

Article
PubMed
>1.00E+5n/an/an/an/an/an/an/an/a



Schering-Plough Research Institute



Assay Description
Enzyme activity was determined by a kinetic assay measuring the rate of increase in fluorescent intensity generated by the cleavage of an internally ...


J Med Chem 51: 725-36 (2008)


Article DOI: 10.1021/jm070376o
BindingDB Entry DOI: 10.7270/Q2Q23XKR
More data for this
Ligand-Target Pair