null

SMILES NCCCNCCCCNCCCN

InChI Key InChIKey=PFNFFQXMRSDOHW-UHFFFAOYSA-N

PDB links: 210 PDB IDs match this monomer.

  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 30 hits for monomerid = 79403   

TargetCarbonic anhydrase 4(Homo sapiens (Human))
Universita degli Studi di Firenze

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  10nMAssay Description:Inhibition of human carbonic anhydrase 4 by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22N52FBPubMed
TargetCarbonic anhydrase 7(Homo sapiens (Human))
Universita degli Studi di Firenze

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  710nMAssay Description:Inhibition of human carbonic anhydrase 7 by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22N52FBPubMed
TargetCarbonic anhydrase 5B, mitochondrial(Homo sapiens (Human))
Universita degli Studi di Firenze

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  830nMAssay Description:Inhibition of human carbonic anhydrase 5B by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22N52FBPubMed
TargetCarbonic anhydrase 5A, mitochondrial(Homo sapiens (Human))
Universita degli Studi di Firenze

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  840nMAssay Description:Inhibition of human carbonic anhydrase 5A by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22N52FBPubMed
TargetCarbonic anhydrase 14(Homo sapiens (Human))
Universita degli Studi di Firenze

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  860nMAssay Description:Inhibition of human carbonic anhydrase 14 by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22N52FBPubMed
TargetCarbonic anhydrase 6(Homo sapiens (Human))
Universita degli Studi di Firenze

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  990nMAssay Description:Inhibition of human carbonic anhydrase 6 by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22N52FBPubMed
TargetGlutamate receptor ionotropic, NMDA 1(RAT)
F. Hoffmann-La Roche Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  2.00E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KP80Q7PubMed
TargetIonotropic glutamate receptor subunit Delta2(Xenopus)
State University of New York

Curated by PDSP Ki Database
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N878C5PubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
University of Calgary

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  1.33E+4nMAssay Description:Inhibition of human carbonic anhydrase 9 preincubated for 15 mins by CO2 hydration stopped-flow assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6RVDPubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
University of Calgary

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  1.33E+4nMAssay Description:Inhibition of human carbonic anhydrase 9 by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22N52FBPubMed
TargetCarbonic anhydrase 13(Mus musculus (mouse))
Universita degli Studi di Firenze

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  2.26E+4nMAssay Description:Inhibition of mouse carbonic anhydrase 13 by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22N52FBPubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
University of Calgary

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  2.76E+4nMAssay Description:Inhibition of human carbonic anhydrase 12 preincubated for 15 mins by CO2 hydration stopped-flow assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6RVDPubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
University of Calgary

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  2.76E+4nMAssay Description:Inhibition of human carbonic anhydrase 12 by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22N52FBPubMed
TargetCarbonic anhydrase 15(Mus musculus)
Universita degli Studi di Firenze

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  7.40E+4nMAssay Description:Inhibition of mouse carbonic anhydrase 15 by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22N52FBPubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universita degli Studi di Firenze

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  8.40E+4nMAssay Description:Inhibition of human carbonic anhydrase 2 by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universita degli Studi di Firenze

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  8.40E+4nMAssay Description:Inhibition of human carbonic anhydrase 2 preincubated for 15 mins by CO2 hydration stopped-flow assayMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 3(Homo sapiens (Human))
Universita degli Studi di Firenze

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  1.67E+5nMAssay Description:Inhibition of human carbonic anhydrase 3 by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22N52FBPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universita degli Studi di Firenze

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  2.31E+5nMAssay Description:Inhibition of human carbonic anhydrase 1 by stopped flow CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22N52FBPubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Universita degli Studi di Firenze

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataKi:  2.31E+5nMAssay Description:Inhibition of human carbonic anhydrase 1 preincubated for 15 mins by CO2 hydration stopped-flow assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6RVDPubMed
TargetGlutamate receptor ionotropic, NMDA 2B(Homo sapiens (Human))
University of Bristol

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataEC50:  1.25E+5nMAssay Description:Positive allosteric modulation of GluN2B receptor (unknown origin) in hippocampal neurons assessed as increase in glycine-induced channel current by ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N019RGPubMed
TargetGlutamate receptor ionotropic, NMDA 2B(Rattus norvegicus (Rat))
University of Bristol

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataEC50:  8.10E+4nMAssay Description:Positive allosteric modulation of GluN2B receptor in rat spinal cord neurons assessed as increase in glycine-induced channel current by two electrode...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N019RGPubMed
TargetGlutamate receptor ionotropic, NMDA 2B(Homo sapiens (Human))
University of Bristol

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataEC50:  1.27E+5nMAssay Description:Positive allosteric modulation of GluN2B receptor (unknown origin) expressed in xenopus laevis oocytes assessed as increase in glycine-induced channe...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N019RGPubMed
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+5nMAssay Description:Inhibition of bovine calmodulin-activated cAMP dependent phosphodiesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21Z4757PubMed
TargetDNA topoisomerase 2-alpha(Homo sapiens (Human))
Department of Pharmacy and Biotechnology, Alma Mater Studiorum-University of Bologna, Via Belmeloro 6, 40126 Bologna, Italy; Laboratory of Molecular Modeling and Drug Discovery, Istituto Italiano di

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of recombinant human topoisomerase-2alpha expressed in Saccharomyces cerevisiae JEL1 harboring topoisomerase1 deletion mutant assessed as ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21R6T0QPubMed
TargetGlutamate receptor ionotropic, NMDA 1/2B(Rattus norvegicus (Rat))
Emory University

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataEC50:  1.00E+5nMAssay Description:Positive allosteric modulation of recombinant rat GluN1/GluN2B receptor expressed in xenopus laevis oocyte assessed as potentiation of glycine-induce...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q298898HPubMed
TargetCaspase-2(Homo sapiens (Human))
University of Illinois

Curated by ChEMBL
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataEC50:  8.50E+3nMAssay Description:Activation of procaspase 2 after 24 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7H5FPubMed
TargetUbiquitin-conjugating enzyme E2 N(Homo sapiens (Human))
Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataIC50: 1.43E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego CA...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X34VX0PCBioAssay
TargetCoagulation factor XIII A chain [Q652E](Homo sapiens (Human))TBA
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin-conjugating enzyme E2 N(Homo sapiens (Human))
Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataIC50: 1.56E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego CA...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2SB4462PCBioAssay
TargetBcl-2-related protein A1(Mus musculus (Mouse))
Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM79403(3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;h...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego CA...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25D8Q92PCBioAssay