Phosphoric Acid

Phosphoric Acid

SCHEMBL615772

CC(=O)C(O)O.O=C[C@H](O)COP(=O)(O)O.O=P(O)(O)O

nearest known ligand 0.50

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Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Phosphoric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
MPI P34949 1/20 0.50
PGK1 P00558 1/20 0.44
PGK2 P07205 1/20 0.44
PGD P52209 3/20 0.42
LPAR1 Q92633 7/20 0.39
LPAR4 Q99677 3/20 0.39
LPAR5 Q9H1C0 3/20 0.39
LPAR2 Q9HBW0 3/20 0.39
LPAR3 Q9UBY5 3/20 0.39
ENPP2 Q13822 3/20 0.39
LPAR6 P43657 2/20 0.39
CES2 O00748 1/20 0.37
TRPV1 Q8NER1 1/20 0.37

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
Phosphoric Acid SCHEMBL11331805 1.00 MPI (0.50) MPIPGK1PGK2PGDLPAR1
Phosphoric Acid SCHEMBL7132362 1.00 MPI (0.50) MPIPGK1PGK2PGDLPAR1
Phosphoric Acid SCHEMBL6754811 0.89 MPI (0.61) MPIPGK1PGK2PGDLPAR1
Phosphoric Acid SCHEMBL17103808 0.89 MPI (0.61) MPIPGK1PGK2PGDLPAR1
SCHEMBL328992 0.87 MPI (0.63) MPIPGK1PGK2PGDLPAR1
SCHEMBL1395698 0.87 MPI (0.63) MPIPGK1PGK2PGDLPAR1
SCHEMBL28125367 0.87 MPI (0.63) MPIPGK1PGK2PGDLPAR1
SCHEMBL10709491 0.87 MPI (0.63) MPIPGK1PGK2PGDLPAR1
SCHEMBL34088 0.87 MPI (0.63) MPIPGK1PGK2PGDLPAR1
Pyruvate SCHEMBL1409133 0.86 MPI (0.50) MPIPGK1PGK2PGDLPAR1

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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20130288313-A1 Method of Producing L-Amino Acid AJINOMOTO CO., INC. (JP) 2013-10-31 US disclosed
US-8512987-B2 culturing an Escherichia coli modified to increase the glycerol dehydrogenase and dihydroxyacetone kinase activities; useful as additives in animal feeds, health food, amino acid infusions AJINOMOTO CO., INC. (JP) 2013-08-20 US disclosed
US-20120040415-A1 METHOD FOR PRODUCING AN L-AMINO ACID AJINOMOTO CO., INC. (JP) 2012-02-16 US disclosed
US-20100047878-A1 METHOD OF PRODUCING L-AMINO ACID AJINOMOTO CO., INC. (JP) 2010-02-25 US disclosed
EP-2113570-A1 METHOD OF PRODUCING L-AMINO ACID Ajinomoto Co., Inc. (JP) 2009-11-04 EP disclosed