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BDBM50268599 CHEMBL4078066

SMILES: COc1cc2CCN(CCn3cc(COc4ccccc4C(=O)Nc4ccc(OC(F)(F)F)cc4)nn3)Cc2cc1OC

InChI Key: InChIKey=HMFHTSHKRKYNII-UHFFFAOYSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50268599   
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
ATP-dependent translocase ABCB1


(Homo sapiens (Human))
BDBM50268599
PNG
(CHEMBL4078066)
Show SMILES COc1cc2CCN(CCn3cc(COc4ccccc4C(=O)Nc4ccc(OC(F)(F)F)cc4)nn3)Cc2cc1OC
Show InChI InChI=1S/C30H30F3N5O5/c1-40-27-15-20-11-12-37(17-21(20)16-28(27)41-2)13-14-38-18-23(35-36-38)19-42-26-6-4-3-5-25(26)29(39)34-22-7-9-24(10-8-22)43-30(31,32)33/h3-10,15-16,18H,11-14,17,19H2,1-2H3,(H,34,39)
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 4.5n/an/an/an/an/an/a



Center of Drug Discovery, State Key Laboratory of Natural Medicines, China Pharmaceutical University, 24 Tongjiaxiang, Nanjing 210009, PR China.

Curated by ChEMBL


Assay Description
Inhibition of ABCB1 in human K562/A02 cells assessed as potentiation of adriamycin-induced cytotoxicity by measuring ADR IC50 at 5 uM measured after ...


Bioorg Med Chem 25: 4194-4202 (2017)


Article DOI: 10.1016/j.bmc.2017.06.015
BindingDB Entry DOI: 10.7270/Q26H4KWV
More data for this
Ligand-Target Pair