null

SMILES C[C@H]([C@@H](N1CCN(CCCc2ccccc2)C1=O)C(=O)NC[C@H]1OC[C@H](N)CO1)c1c[nH]c2ccccc12

InChI Key InChIKey=WSNROJRGRINVPX-IFAMKMIRSA-N

  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 = 50075284   

TargetSomatostatin receptor type 2(Homo sapiens (Human))TBA
LigandPNGBDBM50075284((2R,3S)-N-(5-Amino-[1,3]dioxan-2-ylmethyl)-3-(1H-i...)copy SMILEScopy InChI
Affinity DataKi:  18nMMore data for this Ligand-Target Pair
In DepthDetails
TargetSomatostatin receptor type 2(Homo sapiens (Human))TBA
LigandPNGBDBM50075284((2R,3S)-N-(5-Amino-[1,3]dioxan-2-ylmethyl)-3-(1H-i...)copy SMILEScopy InChI
Affinity DataKi:  18nMAssay Description:In vitro binding affinity was evaluated against human Somatostatin receptor type 2 (hSSTR-2)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FB5235PubMed