null

SMILES CCCC(O)=O

InChI Key InChIKey=FERIUCNNQQJTOY-UHFFFAOYSA-N

PDB links: 32 PDB IDs match this monomer. 6178 PDB IDs contain this monomer as substructures.

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 18 hits for monomerid = 26109   

TargetSolute carrier family 22 member 20(Mus musculus)
University of California

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataKi:  8.20E+4nMAssay Description:Inhibition of mouse Oat6-mediated [3H]ES uptake in Xenopus oocytes after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W95B35PubMed
TargetHistone deacetylase(Homo sapiens (Human))
Hacettepe University

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataKi:  1.36E+5nMAssay Description:Inhibition of HDAC in human Hela cells nuclear extracts by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22F7R82PubMed
TargetSolute carrier family 22 member 6(Mus musculus)
University of California

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataKi:  3.50E+6nMAssay Description:Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W95B35PubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 9.00E+3nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibition of human recombinant HDAC8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC7More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetFree fatty acid receptor 3(Homo sapiens (Human))
Department of Pharmacy and Biotechnology, University of Bologna , Via Belmeloro 6, 40126 Bologna, Italy.

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataEC50:  1.20E+4nMAssay Description:Agonist activity at human GPCR41 transfected in HEK293 cells assessed as [35S]GTPgammaS binding by scintillation counting methodMore data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+5nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XD15PJPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+5nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XD15PJPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+5nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XD15PJPubMed
TargetLysine-specific demethylase 4E(Homo sapiens (Human))
University of Oxford

LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+7nMpH: 7.5 T: 2°CAssay Description:A coupled-assay for JMJD2E activity employing formaldehyde dehydrogenase (FDH) from Pseudomonas putida was developed. Formaldehyde release by demethy...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959FV4PubMed
TargetMethyl-accepting chemotaxis protein NahY(Pseudomonas putida (Arthrobacter siderocapsulatus))
CSIC

LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataKd:  9.20E+4nMT: 2°CAssay Description:Measurements were done on a VP-microcalorimeter (MicroCal, Amherst, MA).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K64GNSPubMed

Activity Spreadsheet -- ITC Data from BindingDB

Found 1 hit for monomerid = 26109   

CellMethyl-accepting chemotaxis protein (McpS)(Pseudomonas putida (Arthrobacter siderocapsulatus))
CSIC

SyringePNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)
ITC DataΔG°: -5.41kcal/mole −TΔS°: 2.80kcal/mole ΔH°: -7.88kcal/mole logk: 1.09E+4
T: 20.00°C 
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K64GNSPubMed