BDBM63064 4-nitro-N-[3-nitro-5-(4-methoxyphenoxy)phenyl]-1-methyl-1H-pyrazole-3-carboxamide::MLS000324579::N-[3-(4-methoxyphenoxy)-5-nitro-phenyl]-1-methyl-4-nitro-pyrazole-3-carboxamide::N-[3-(4-methoxyphenoxy)-5-nitrophenyl]-1-methyl-4-nitro-3-pyrazolecarboxamide::N-[3-(4-methoxyphenoxy)-5-nitrophenyl]-1-methyl-4-nitropyrazole-3-carboxamide::SMR000160125::cid_4576185
SMILES COc1ccc(Oc2cc(NC(=O)c3nn(C)cc3[N+]([O-])=O)cc(c2)[N+]([O-])=O)cc1
InChI Key InChIKey=FRZIAIPAFVZFID-UHFFFAOYSA-N
Data 3 EC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 63064
Affinity DataEC50: 8.90E+3nMAssay Description:Keywords: Heat Shock Factor-1 (HSF-1), Stress Response, MG132, NIH3T3, Luminescence Assay Overview: Modified NIH3T3, transformed to express firefly...More data for this Ligand-Target Pair
Affinity DataEC50: 7.21E+4nMAssay Description:Keywords: apoptosis, BH3 domain, Bcl2-A1, BIM, caspase, cancer Primary Collaborator: Todd Golub, Broad Institute, golub@broadinstitute.org Assay Over...More data for this Ligand-Target Pair
TargetNeurotensin receptor type 1(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataEC50: 8.91E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair