BDBM50407447 CHEMBL5285729

SMILES CC(C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](N)CC(O)=O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O

InChI Key InChIKey=LCDWSUSRECLAGB-GYABJUTGSA-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 = 50407447   

Target7-dehydrocholesterol reductase(Human)
Gitam (Deemed To Be University)

Curated by ChEMBL
LigandPNGBDBM50407447(CHEMBL5285729)
Affinity DataIC50:  5.00E+4nMAssay Description:Histamine-induced inhibition of forskolin- stimulated cAMP accumulation in SK-N-MC cells overexpressing the human Histamine H3 receptorMore data for this Ligand-Target Pair
In DepthDetails PubMed
Target3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase(Human)
Gitam (Deemed To Be University)

Curated by ChEMBL
LigandPNGBDBM50407447(CHEMBL5285729)
Affinity DataIC50:  303nMAssay Description:Antagonistic affinity tested against isolated Rat Prostatic Vas Deferens Alpha-1A adrenergic receptorMore data for this Ligand-Target Pair
In DepthDetails PubMed