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BDBM50279583 CHEMBL505581::N-[(1S,2S,4R,5R)-5-Guanidino-2,4-bis-(4-guanidino-naphthalen-1-yloxy)-cyclohexyl]-guanidine

SMILES: [#7]\[#6](-[#7])=[#7]\[#6@@H]-1-[#6]-[#6@H](\[#7]=[#6](\[#7])-[#7])-[#6@H](-[#6]-[#6@H]1-[#8]-c1ccc(\[#7]=[#6](\[#7])-[#7])c2ccccc12)-[#8]-c1ccc(\[#7]=[#6](\[#7])-[#7])c2ccccc12

InChI Key: InChIKey=LTXPGDDRGDRKKV-MNHALERFSA-N

Data: 1 KI

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50279583   
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
Homo sapiens furin (paired basic amino acid cleaving enzyme) (FURIN), mRNA


(Homo sapiens (Human))
BDBM50279583
PNG
(CHEMBL505581 | N-[(1S,2S,4R,5R)-5-Guanidino-2,4-bi...)
Show SMILES [#7]\[#6](-[#7])=[#7]\[#6@@H]-1-[#6]-[#6@H](\[#7]=[#6](\[#7])-[#7])-[#6@H](-[#6]-[#6@H]1-[#8]-c1ccc(\[#7]=[#6](\[#7])-[#7])c2ccccc12)-[#8]-c1ccc(\[#7]=[#6](\[#7])-[#7])c2ccccc12 |r|
Show InChI InChI=1S/C30H36N12O2/c31-27(32)39-19-9-11-23(17-7-3-1-5-15(17)19)43-25-14-26(22(42-30(37)38)13-21(25)41-29(35)36)44-24-12-10-20(40-28(33)34)16-6-2-4-8-18(16)24/h1-12,21-22,25-26H,13-14H2,(H4,31,32,39)(H4,33,34,40)(H4,35,36,41)(H4,37,38,42)/t21-,22+,25-,26+
PDB

KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
69n/an/an/an/an/an/an/an/a



Mahidol University

Curated by ChEMBL


Assay Description
Inhibition of human recombinant furin-dependent anthrax protective antigen processing


Eur J Med Chem 44: 1664-73 (2009)


Article DOI: 10.1016/j.ejmech.2008.09.028
BindingDB Entry DOI: 10.7270/Q2MK6CQ9
More data for this
Ligand-Target Pair