PPADS   

GtoPdb Ligand ID: 1725

Compound class: Synthetic organic
Comment: The structure of this ligand was drawn from the image in [1]. There is some variation in representations of the structure elsewhere, which include CID 6093163.
2D Structure
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Physico-chemical Properties
Hydrogen bond acceptors 14
Hydrogen bond donors 5
Rotatable bonds 8
Topological polar surface area 276.98
Molecular weight 510.98
XLogP -1.2
No. Lipinski's rules broken 1
SMILES / InChI / InChIKey
Canonical SMILES O=Cc1c(COP(=O)(O)O)c(N=Nc2ccc(cc2S(=O)(=O)O)S(=O)(=O)O)nc(c1O)C
Isomeric SMILES O=Cc1c(COP(=O)(O)O)c(/N=N/c2ccc(cc2S(=O)(=O)O)S(=O)(=O)O)nc(c1O)C
InChI InChI=1S/C14H14N3O12PS2/c1-7-13(19)9(5-18)10(6-29-30(20,21)22)14(15-7)17-16-11-3-2-8(31(23,24)25)4-12(11)32(26,27)28/h2-5,19H,6H2,1H3,(H2,20,21,22)(H,23,24,25)(H,26,27,28)/b17-16+
InChI Key PNFZSRRRZNXSMF-WUKNDPDISA-N
Selectivity at GPCRs
Key to terms and symbols Click column headers to sort
Target Sp. Type Action Value Parameter Concentration range (M) Reference
P2Y6 receptor Hs Antagonist Antagonist 4.0 pKB - 3
pKB 4.0 (KB 1x10-4 M) [3]
P2Y1 receptor Hs Antagonist Antagonist 5.2 pKi - 4
pKi 5.2 [4]
P2Y4 receptor Hs Antagonist Antagonist 2.0 – 5.0 pEC50 - 1
pEC50 2.0 – 5.0 [1]
P2Y13 receptor Hs Antagonist Antagonist 4.9 pIC50 - 2
pIC50 4.9 [2]
Ligand mentioned in the following text fields