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SMILES: Clc1ccc(cc1)-c1[nH]oc(=O)c1C=C1C=CC(=O)C=C1

InChI Key: InChIKey=ZWIUQXJARFWPRY-UHFFFAOYSA-N

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 = 66575   
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
Bcl-2-like protein 11


(Homo sapiens (Human))
BDBM66575
PNG
((4Z)-3-(4-chlorophenyl)-4-(4-hydroxybenzylidene)is...)
Show SMILES Clc1ccc(cc1)-c1[nH]oc(=O)c1C=C1C=CC(=O)C=C1 |c:17,21,(5.23,-5.36,;5.23,-3.82,;6.57,-3.05,;6.57,-1.51,;5.23,-.74,;3.9,-1.51,;3.9,-3.05,;5.23,.8,;3.99,1.71,;4.46,3.17,;6,3.17,;6.91,4.42,;6.48,1.71,;7.94,1.23,;9.09,2.26,;8.77,3.77,;9.91,4.8,;11.38,4.33,;12.52,5.36,;11.7,2.82,;10.55,1.79,)|
Show InChI InChI=1S/C16H10ClNO3/c17-12-5-3-11(4-6-12)15-14(16(20)21-18-15)9-10-1-7-13(19)8-2-10/h1-9,18H
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n/an/an/an/a>3.50E+5n/an/an/an/a



Broad Institute

Curated by PubChem BioAssay


Assay Description
Keywords: apoptosis, BH3 domain, Bcl2-A1, BIM, caspase, cancer Primary Collaborator: Todd Golub, Broad Institute, golub@broadinstitute.org Assay Over...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q24J0CKJ
More data for this
Ligand-Target Pair
Perilipin-5


(Homo sapiens (Human))
BDBM66575
PNG
((4Z)-3-(4-chlorophenyl)-4-(4-hydroxybenzylidene)is...)
Show SMILES Clc1ccc(cc1)-c1[nH]oc(=O)c1C=C1C=CC(=O)C=C1 |c:17,21,(5.23,-5.36,;5.23,-3.82,;6.57,-3.05,;6.57,-1.51,;5.23,-.74,;3.9,-1.51,;3.9,-3.05,;5.23,.8,;3.99,1.71,;4.46,3.17,;6,3.17,;6.91,4.42,;6.48,1.71,;7.94,1.23,;9.09,2.26,;8.77,3.77,;9.91,4.8,;11.38,4.33,;12.52,5.36,;11.7,2.82,;10.55,1.79,)|
Show InChI InChI=1S/C16H10ClNO3/c17-12-5-3-11(4-6-12)15-14(16(20)21-18-15)9-10-1-7-13(19)8-2-10/h1-9,18H
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n/an/a 3.10E+3n/an/an/an/an/an/a



The Scripps Research Institute Molecular Screening Center

Curated by PubChem BioAssay


Assay Description
Source (MLPCN Center Name): The Scripps Research Institute Molecular Screening Center (SRIMSC) Affiliation: The Scripps Research Institute, TSRI Assa...


PubChem Bioassay (2011)


BindingDB Entry DOI: 10.7270/Q2D21W3H
More data for this
Ligand-Target Pair
Perilipin-1


(Homo sapiens (Human))
BDBM66575
PNG
((4Z)-3-(4-chlorophenyl)-4-(4-hydroxybenzylidene)is...)
Show SMILES Clc1ccc(cc1)-c1[nH]oc(=O)c1C=C1C=CC(=O)C=C1 |c:17,21,(5.23,-5.36,;5.23,-3.82,;6.57,-3.05,;6.57,-1.51,;5.23,-.74,;3.9,-1.51,;3.9,-3.05,;5.23,.8,;3.99,1.71,;4.46,3.17,;6,3.17,;6.91,4.42,;6.48,1.71,;7.94,1.23,;9.09,2.26,;8.77,3.77,;9.91,4.8,;11.38,4.33,;12.52,5.36,;11.7,2.82,;10.55,1.79,)|
Show InChI InChI=1S/C16H10ClNO3/c17-12-5-3-11(4-6-12)15-14(16(20)21-18-15)9-10-1-7-13(19)8-2-10/h1-9,18H
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n/an/a 2.28E+3n/an/an/an/an/an/a



The Scripps Research Institute Molecular Screening Center

Curated by PubChem BioAssay


Assay Description
Source (MLPCN Center Name): The Scripps Research Institute Molecular Screening Center (SRIMSC) Affiliation: The Scripps Research Institute, TSRI Assa...


PubChem Bioassay (2011)


BindingDB Entry DOI: 10.7270/Q2HT2MS2
More data for this
Ligand-Target Pair
Neurotensin receptor type 1


(Homo sapiens (Human))
BDBM66575
PNG
((4Z)-3-(4-chlorophenyl)-4-(4-hydroxybenzylidene)is...)
Show SMILES Clc1ccc(cc1)-c1[nH]oc(=O)c1C=C1C=CC(=O)C=C1 |c:17,21,(5.23,-5.36,;5.23,-3.82,;6.57,-3.05,;6.57,-1.51,;5.23,-.74,;3.9,-1.51,;3.9,-3.05,;5.23,.8,;3.99,1.71,;4.46,3.17,;6,3.17,;6.91,4.42,;6.48,1.71,;7.94,1.23,;9.09,2.26,;8.77,3.77,;9.91,4.8,;11.38,4.33,;12.52,5.36,;11.7,2.82,;10.55,1.79,)|
Show InChI InChI=1S/C16H10ClNO3/c17-12-5-3-11(4-6-12)15-14(16(20)21-18-15)9-10-1-7-13(19)8-2-10/h1-9,18H
PDB

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n/an/an/an/a 8.29E+3n/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...


PubChem Bioassay (2011)


BindingDB Entry DOI: 10.7270/Q22N50RJ
More data for this
Ligand-Target Pair