BDBM50136473 CHEMBL1269597::[(40-OH) MeLeu]4-CsA derivatives

SMILES [H][C@@]1([C@H](O)[C@H](C)C\C=C\C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](NC(=O)[C@H](CC(C)(C)O)N(C)C(=O)[C@@H](SCCN(C)C)N(C)C(=O)[C@H](CC)NC1=O)C(C)C

InChI Key InChIKey=AQHMBDAHQGYLIU-UHFFFAOYSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50136473   

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Centre De Recherche De Paris

Curated by ChEMBL
LigandPNGBDBM50136473([(40-OH) MeLeu]4-CsA derivatives | CHEMBL1269597)
Affinity DataIC50: 1.54E+3nMAssay Description:In vitro inhibitory activity against HIV-1 RT in CEM4 cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/9/2012
Entry Details Article
PubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Human)
Centre De Recherche De Paris

Curated by ChEMBL
LigandPNGBDBM50136473([(40-OH) MeLeu]4-CsA derivatives | CHEMBL1269597)
Affinity DataIC50: 1.55E+3nMAssay Description:Immunosuppressive activity was measured by inhibition of the IL-2 production in Jurkat cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/9/2012
Entry Details Article
PubMed