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SMILES: [H][C@@]12O[C@]1(CO)[C@@H](O)[C@]1(O)[C@@H](OC(=O)c3ccccc3)[C@@H](C)[C@]3([H])[C@H](C)CCCCCC[C@@H](OC(=O)c4ccc5ccccc5c4)C45O[C@]6([H])[C@@]2([H])[C@](O4)([C@H](COC(=O)c2ccccc2)C[C@@]6(O5)C(C)=C)[C@@]13[H]

InChI Key: InChIKey=KQBHJVOLMIUMGJ-YPYKPGJWSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50519072   
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
O94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139


(Homo sapiens (Human))
BDBM50519072
PNG
(CHEMBL4580556)
Show SMILES [H][C@@]12O[C@]1(CO)[C@@H](O)[C@]1(O)[C@@H](OC(=O)c3ccccc3)[C@@H](C)[C@]3([H])[C@H](C)CCCCCC[C@@H](OC(=O)c4ccc5ccccc5c4)C45O[C@]6([H])[C@@]2([H])[C@](O4)([C@H](COC(=O)c2ccccc2)C[C@@]6(O5)C(C)=C)[C@@]13[H] |r,TLB:1:50:66.67:47,THB:71:52:66.67:47,54:52:66.67:47,65:66:52.50.53:47,32:46:54.66.65:50|
Show InChI InChI=1S/C55H60O13/c1-31(2)51-28-39(29-62-47(57)35-19-10-7-11-20-35)54-42-45(51)66-55(67-51,68-54)40(63-49(59)38-26-25-34-18-15-16-23-37(34)27-38)24-14-6-5-9-17-32(3)41-33(4)44(64-48(58)36-21-12-8-13-22-36)53(61,43(41)54)50(60)52(30-56)46(42)65-52/h7-8,10-13,15-16,18-23,25-27,32-33,39-46,50,56,60-61H,1,5-6,9,14,17,24,28-30H2,2-4H3/t32-,33+,39+,40-,41+,42-,43-,44+,45-,46+,50-,51-,52+,53-,54-,55?/m1/s1
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KEGG

UniProtKB/SwissProt

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PC cid
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UniChem
Article
PubMed
n/an/a>1n/an/an/an/an/an/a



Toho University

Curated by ChEMBL


Assay Description
Agonist activity at Protein kinase C in human MT4 cells infected with HIV-1 NL4-3 assessed as inhibition of viral replication measured on day 3 post-...


J Med Chem 62: 6958-6971 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00339
More data for this
Ligand-Target Pair