SCHEMBL523990

SCHEMBL523990

O=C[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)COP(=O)(O)O[C@H](C=O)[C@@H](O)[C@H](O)[C@H](O)COP(=O)(O)O

nearest known ligand 0.58

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
MPI P34949 1/20 0.58
PGD P52209 3/20 0.39
PGK1 P00558 1/20 0.34
PGK2 P07205 1/20 0.34

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL9117419 1.00 MPI (0.58) MPIPGDPGK1PGK2
SCHEMBL987653 1.00 MPI (0.58) MPIPGDPGK1PGK2
Methoxyamine SCHEMBL6040178 0.93 MPI (0.51) MPIPGDPGK1PGK2
Methoxyamine SCHEMBL6040185 0.93 MPI (0.51) MPIPGDPGK1PGK2
Methoxyamine SCHEMBL6040149 0.93 MPI (0.51) MPIPGDPGK1PGK2
SCHEMBL3487364 0.90 MPI (0.45) MPI
SCHEMBL5921670 0.90 MPI (0.45) MPI
Mannose 6-Phosphate SCHEMBL9738212 0.87 MPI (0.75) MPIPGDPGK1PGK2
Mannose 6-Phosphate SCHEMBL1874195 0.87 MPI (0.75) MPIPGDPGK1PGK2
Mannose 6-Phosphate SCHEMBL9739836 0.87 MPI (0.75) MPIPGDPGK1PGK2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3679065-A1 SIGNALING AND ANTIGEN-PRESENTING BIFUNCTIONAL RECEPTORS (SABR) California Institute of Technology (US) 2020-07-15 EP disclosed
WO-2019051001-A1 SIGNALING AND ANTIGEN-PRESENTING BIFUNCTIONAL RECEPTORS (SABR) CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2019-03-14 WO disclosed
EP-2305314-B1 Remodelling and glycoconjugation of antibodies RATIOPHARM GMBH (DE) 2015-12-23 EP disclosed
EP-2760477-A1 DI-ALIPHATIC SUBSTITUTED PEGYLATED LIPIDS Alnylam Pharmaceuticals, Inc. (US) 2014-08-06 EP disclosed
WO-2013049328-A9 DI-ALIPHATIC SUBSTITUTED PEGYLATED LIPIDS ALNYLAM PHARMACEUTICALS, INC. (US) 2013-12-27 WO disclosed
EP-2663548-A1 PEGYLATED LIPIDS AND THEIR USE FOR DRUG DELIVERY Alnylam Pharmaceuticals, Inc. (US) 2013-11-20 EP disclosed
WO-2013049328-A1 DI-ALIPHATIC SUBSTITUTED PEGYLATED LIPIDS ALNYLAM PHARMACEUTICALS, INC. (US) 2013-04-04 WO disclosed
EP-2512449-A1 METHODS AND COMPOSITIONS FOR DELIVERY OF NUCLEIC ACIDS The University of British Columbia (CA) 2012-10-24 EP disclosed
WO-2012099755-A1 PEGYLATED LIPIDS AND THEIR USE FOR DRUG DELIVERY ALNYLAM PHARMACEUTICALS, INC. (US) 2012-07-26 WO disclosed
WO-2012016184-A2 METHODS AND COMPOSITIONS FOR DELIVERY OF ACTIVE AGENTS ALNYLAM PHARMACEUTICALS, INC. (US) 2012-02-02 WO disclosed
WO-2012016188-A2 METHODS AND COMPOSITIONS FOR DELIVERY OF ACTIVE AGENTS ALNYLAM PHARMACEUTICALS, INC. (US) 2012-02-02 WO disclosed
WO-2011143230-A1 METHODS AND COMPOSITIONS FOR DELIVERY OF ACTIVE AGENTS ALNYLAM PHARMACEUTICALS (US) 2011-11-17 WO disclosed
WO-2011100131-A9 MONOMERS AND OLIGONUCLEOTIDES COMPRISING CYCLOADDITION ADDUCT(S) ALNYLAM PHARMACUTICALS, INC. (US) 2011-10-20 WO disclosed
WO-2011100131-A2 MONOMERS AND OLIGONUCLEOTIDES COMPRISING CYCLOADDITION ADDUCT(S) ALNYLAM PHARMACUTICALS, INC. (US) 2011-08-18 WO disclosed
WO-2011094580-A2 CHELATED COPPER FOR USE IN THE PREPARATION OF CONJUGATED OLIGONUCLEOTIDES ALNYLAM PHARMACEUTICALS, INC. (US) 2011-08-04 WO disclosed
WO-2011075656-A1 METHODS AND COMPOSITIONS FOR DELIVERY OF NUCLEIC ACIDS THE UNIVERSITY OF BRITISH COLUMBIA (CA) 2011-06-23 WO disclosed
WO-2009142822-A9 2-F MODIFIED RNA INTERFERENCE AGENTS ALNYLAM PHARMACEUTICALS, INC. (US) 2010-01-14 WO disclosed
WO-2009142822-A2 2-F MODIFIED RNA INTERFERENCE AGENTS ALNYLAM PHARMACEUTICALS, INC. (US) 2009-11-26 WO disclosed
EP-1615611-A2 iRNA CONJUGATES Alnylam Pharmaceuticals Inc. (US) 2006-01-18 EP disclosed
WO-2004091515-A2 iRNA CONJUGATES ALNYLAM PHARMACEUTICALS, INC. (US) 2004-10-28 WO disclosed