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SMILES: C[C@@H](O)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O

InChI Key: InChIKey=AKHSKKCXQXMJGT-OKYODGFXSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50269904   
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
Furin


(Homo sapiens (Human))
BDBM50269904
PNG
(CHEMBL527041 | TPRARRRKKRW)
Show SMILES C[C@@H](O)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O |r,wU:1.1,15.15,31.31,53.53,73.73,93.93,wD:3.3,11.12,26.27,42.42,64.64,82.82,(-6,-47.73,;-6.29,-46.22,;-7.75,-45.72,;-5.14,-45.22,;-5.43,-43.7,;-3.68,-45.71,;-2.52,-44.7,;-3.48,-47.24,;-4.6,-48.49,;-3.78,-49.94,;-2.13,-49.61,;-2.22,-48.06,;-.88,-47.29,;-.88,-45.75,;.45,-48.06,;1.78,-47.29,;1.78,-45.74,;3.11,-44.98,;3.11,-43.43,;4.44,-42.67,;4.44,-41.12,;3.1,-40.35,;5.76,-40.36,;3.11,-48.05,;3.11,-49.59,;4.45,-47.28,;5.77,-48.05,;5.77,-49.58,;7.11,-47.28,;7.11,-45.73,;8.44,-48.04,;9.77,-47.27,;9.77,-45.74,;11.1,-44.97,;11.1,-43.43,;12.44,-42.66,;12.44,-41.11,;11.1,-40.34,;13.76,-40.35,;11.1,-48.05,;11.1,-49.58,;12.44,-47.28,;13.77,-48.04,;13.77,-49.58,;15.1,-50.35,;15.1,-51.88,;16.44,-52.65,;16.44,-54.19,;15.11,-54.96,;17.78,-54.96,;15.1,-47.27,;15.1,-45.73,;16.44,-48.04,;17.77,-47.26,;17.77,-45.73,;19.1,-44.95,;19.1,-43.42,;20.43,-42.65,;20.43,-41.11,;19.09,-40.33,;21.77,-40.34,;19.1,-48.03,;19.1,-49.57,;20.44,-47.27,;21.77,-48.03,;21.77,-49.57,;23.1,-50.34,;23.1,-51.87,;24.44,-52.65,;24.44,-54.18,;23.1,-47.26,;23.1,-45.72,;24.43,-48.03,;25.77,-47.26,;25.77,-45.71,;27.1,-44.95,;27.1,-43.4,;28.43,-42.63,;28.43,-41.09,;27.1,-48.02,;27.1,-49.56,;28.43,-47.25,;29.77,-48.02,;29.77,-49.56,;31.1,-50.32,;31.1,-51.86,;32.43,-52.64,;32.43,-54.17,;31.11,-54.94,;33.77,-54.94,;31.1,-47.25,;31.1,-45.71,;32.43,-48.02,;33.77,-47.25,;33.77,-45.7,;35.1,-44.94,;36.5,-45.55,;37.53,-44.41,;36.75,-43.08,;37.23,-41.62,;36.2,-40.47,;34.69,-40.8,;34.22,-42.26,;35.26,-43.4,;35.1,-48.01,;36.43,-47.24,;35.1,-49.55,)|
Show InChI InChI=1S/C65H116N30O12/c1-35(86-52(99)42(19-9-27-80-61(70)71)93-59(106)48-24-14-32-95(48)60(107)49(68)36(2)96)51(98)87-43(20-10-28-81-62(72)73)55(102)90-45(22-12-30-83-64(76)77)57(104)91-44(21-11-29-82-63(74)75)56(103)89-40(17-5-7-25-66)53(100)88-41(18-6-8-26-67)54(101)92-46(23-13-31-84-65(78)79)58(105)94-47(50(69)97)33-37-34-85-39-16-4-3-15-38(37)39/h3-4,15-16,34-36,40-49,85,96H,5-14,17-33,66-68H2,1-2H3,(H2,69,97)(H,86,99)(H,87,98)(H,88,100)(H,89,103)(H,90,102)(H,91,104)(H,92,101)(H,93,106)(H,94,105)(H4,70,71,80)(H4,72,73,81)(H4,74,75,82)(H4,76,77,83)(H4,78,79,84)/t35-,36+,40-,41-,42-,43-,44-,45-,46-,47-,48-,49-/m0/s1
PDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
59n/an/an/an/an/an/an/an/a



Institute for Medical Research

Curated by ChEMBL


Assay Description
Inhibition of human recombinant furin assessed as fluorescent Pyr-RTKR-AMC substrate cleavage


J Biol Chem 282: 20847-53 (2007)


Article DOI: 10.1074/jbc.M703847200
BindingDB Entry DOI: 10.7270/Q2057FPB
More data for this
Ligand-Target Pair