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BDBM50407487 CHEMBL2373330

SMILES: [H][C@]12O[C@]11CCC3C4CC[C@H](O)[C@@]4(C)CCC3[C@@]1(C)CC(C2=O)S(C)(=O)=O

InChI Key: InChIKey=FELAYLQGNMVPPT-UINGLUMGSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50407487   
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
Human immunodeficiency virus type 1 Tat protein


(Human immunodeficiency virus type 1 (isolate PCV12...)
BDBM50407487
PNG
(CHEMBL2373330)
Show SMILES [H][C@]12O[C@]11CCC3C4CC[C@H](O)[C@@]4(C)CCC3[C@@]1(C)CC(C2=O)S(C)(=O)=O
Show InChI InChI=1S/C20H30O5S/c1-18-8-7-13-11(12(18)4-5-15(18)21)6-9-20-17(25-20)16(22)14(26(3,23)24)10-19(13,20)2/h11-15,17,21H,4-10H2,1-3H3/t11?,12?,13?,14?,15-,17?,18-,19+,20+/m0/s1
PDB
MMDB

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PC sid
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PubMed
n/an/a 8.40E+3n/an/an/an/an/an/a



Sterling Winthrop Pharmaecuticals Research Division

Curated by ChEMBL


Assay Description
The compound was tested for inhibition of HIV-1 replication in SW480 cells using HIV tat assay


J Med Chem 38: 3197-206 (1995)


BindingDB Entry DOI: 10.7270/Q27D2WBX
More data for this
Ligand-Target Pair