BDBM50012855 10H-Phenothiazin::10H-phenothiazine::CHEMBL828::cid_7108::dibenzo-1,4-thiazine::phenothiazine

SMILES N1c2ccccc2Sc2ccccc12

InChI Key InChIKey=WJFKNYWRSNBZNX-UHFFFAOYSA-N

Data  3 KI  6 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50012855   

TargetAlpha-synuclein(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50012855(10H-Phenothiazin | 10H-phenothiazine | CHEMBL828 |...)
Affinity DataKi: >500nMAssay Description:Binding affinity to human alpha-synuclein expressed in Escherichia coli BL21 (DE3) cells after 1 hr by thioflavin T fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1A) dopamine receptor(RAT)
UniversitÉ

Curated by PDSP Ki Database
LigandPNGBDBM50012855(10H-Phenothiazin | 10H-phenothiazine | CHEMBL828 |...)
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
UniversitÉ

Curated by PDSP Ki Database
LigandPNGBDBM50012855(10H-Phenothiazin | 10H-phenothiazine | CHEMBL828 |...)
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1/2(RAT)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50012855(10H-Phenothiazin | 10H-phenothiazine | CHEMBL828 |...)
Affinity DataIC50:  940nMAssay Description:In vitro inhibition of Prostaglandin G/H synthase pathway in rat basophilic leukemia (RBL-1) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-synuclein(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50012855(10H-Phenothiazin | 10H-phenothiazine | CHEMBL828 |...)
Affinity DataIC50:  2.60E+4nMAssay Description:Binding affinity to human alpha-synuclein expressed in Escherichia coli BL21 (DE3) cells after 1 hr by thioflavin T fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPleiotropic ABC efflux transporter of multiple drugs(Saccharomyces cerevisiae S288c)
Wroclaw Medical University

Curated by ChEMBL
LigandPNGBDBM50012855(10H-Phenothiazin | 10H-phenothiazine | CHEMBL828 |...)
Affinity DataIC50: >4.00E+5nMAssay Description:Inhibition of Pdr5p-mediated rhodamine 6G transport in Saccharomyces cerevisiae MKPDR5h plasma membrane by spectrofluorometric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNADPH oxidase 1(Homo sapiens (Human))
The Scripps Research Institute Molecular Screening Center

Curated by PubChem BioAssay
LigandPNGBDBM50012855(10H-Phenothiazin | 10H-phenothiazine | CHEMBL828 |...)
Affinity DataIC50:  369nMAssay Description:Data Source (MLPCN Center Name): The Scripps Research Institute Molecular Screening Center (SRIMSC) Center Affiliation: The Scripps Research Institut...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay
TargetNADPH oxidase 1(Homo sapiens (Human))
The Scripps Research Institute Molecular Screening Center

Curated by PubChem BioAssay
LigandPNGBDBM50012855(10H-Phenothiazin | 10H-phenothiazine | CHEMBL828 |...)
Affinity DataIC50:  349nMAssay Description:Data Source (MLPCN Center Name): The Scripps Research Institute Molecular Screening Center (SRIMSC) Center Affiliation: The Scripps Research Institut...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay
TargetPolyunsaturated fatty acid 5-lipoxygenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50012855(10H-Phenothiazin | 10H-phenothiazine | CHEMBL828 |...)
Affinity DataIC50:  1.40E+3nMAssay Description:In vitro inhibition of 5-lipoxygenase pathway in rat basophilic leukemia (RBL-1) cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed