BDBM50225900 CHEMBL270215::N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-acetylursolamide

SMILES CC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC=C4[C@@H]5[C@@H](C)[C@H](C)CC[C@]5(C(=O)NCCCN5CCN(CCCN)CC5)CC[C@@]4(C)[C@]3(C)CC[C@H]2C1(C)C

InChI Key InChIKey=IUJKWMKQXCXZKK-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 = 50225900   

TargetAromatase(Human)
Universidade Federal Do Rio Grande Do Sul (Ufrgs)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50225900BDBM50225900(N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-ace...)
Affinity DataIC50: 5.00E+5nMAssay Description:Inhibition of aromatase in human placental microsomes assessed as tritiated water release after 15 mins using [1-beta, 3H]androstenedione as substrat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetHistidine-rich protein PFHRP-II(malaria parasite P. falciparum)
Universidade Federal Do Rio Grande Do Sul (Ufrgs)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50225900BDBM50225900(N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-ace...)
Affinity DataIC50: 2.00E+7nMAssay Description:Inhibition of beta-hematin formationMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/21/2013
Entry Details Article
PubMed