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SMILES: Cc1cn(C2OC(CNC(=O)CC(O)(CC(=O)OCC=C)C(=O)OCC=C)C=C2)c(=O)[nH]c1=O

InChI Key: InChIKey=YLVMQBPSTIXROC-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50288061   
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
Reverse transcriptase/RNaseH


(Human immunodeficiency virus 1)		BDBM50288061
PNG
(2-Hydroxy-2-({[5-(5-methyl-2,4-dioxo-3,4-dihydro-2...)
Show SMILES Cc1cn(C2OC(CNC(=O)CC(O)(CC(=O)OCC=C)C(=O)OCC=C)C=C2)c(=O)[nH]c1=O |c:27|
Show InChI InChI=1S/C22H27N3O9/c1-4-8-32-18(27)11-22(31,20(29)33-9-5-2)10-16(26)23-12-15-6-7-17(34-15)25-13-14(3)19(28)24-21(25)30/h4-7,13,15,17,31H,1-2,8-12H2,3H3,(H,23,26)(H,24,28,30)
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UniProtKB/TrEMBL

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PC cid
PC sid
UniChem

Similars
Article
n/an/a>1.00E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of HIV-1 reverse transcriptase.

Bioorg Med Chem Lett 6: 2405-2410 (1996)


Article DOI: 10.1016/0960-894X(96)00444-1
BindingDB Entry DOI: 10.7270/Q2Z31ZMC
More data for this
Ligand-Target Pair