Phosphoric Acid

Phosphoric Acid

SCHEMBL9063702

CCCC[P+](CCCC)(CCCC)CCCC.CCCC[P+](CCCC)(CCCC)CCCC.CCCC[P+](CCCC)(CCCC)CCCC.CCCC[P+](CCCC)(CCCC)CCCC.CCCC[P+](CCCC)(CCCC)CCCC.CCCC[P+](CCCC)(CCCC)CCCC.O=P([O-])([O-])[O-].O=P([O-])([O-])[O-]

nearest known ligand 0.60

Full drug profile on Sugi Atlas →

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 10)

geneUniProtsupporting neighboursconfidence
DNM1 Q05193 2/20 0.60
FDPS P14324 6/20 0.50
CYP3A4 P08684 1/20 0.41
L3MBTL1 Q9Y468 1/20 0.41
GGPS1 O95749 2/20 0.39
LAP3 P28838 2/20 0.39
CA2 P00918 2/20 0.39
TRPM8 Q7Z2W7 2/20 0.39
TSHR P16473 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39

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 SCHEMBL266936 1.00 DNM1 (0.60) DNM1FDPSCYP3A4L3MBTL1GGPS1
Phosphoric Acid SCHEMBL7172651 0.97 DNM1 (0.57) DNM1FDPSCYP3A4L3MBTL1GGPS1
Phosphoric Acid SCHEMBL7178325 0.97 DNM1 (0.57) DNM1FDPSCYP3A4L3MBTL1GGPS1
Methyl Phosphonate SCHEMBL7181529 0.95 DNM1 (0.55) DNM1FDPSCYP3A4L3MBTL1GGPS1
Phosphoric Acid SCHEMBL10532007 0.92 DNM1 (0.75) DNM1FDPSGGPS1LAP3CA2
Phosphoric Acid SCHEMBL6908898 0.92 FDPS (0.56) DNM1FDPSGGPS1LAP3
SCHEMBL5070634 0.92 DNM1 (0.52) DNM1FDPSCYP3A4L3MBTL1GGPS1
SCHEMBL7892230 0.92 DNM1 (0.52) DNM1FDPSCYP3A4L3MBTL1GGPS1
Phosphoric Acid SCHEMBL6909609 0.92 FDPS (0.56) DNM1FDPSGGPS1LAP3
Methyl Phosphonate SCHEMBL7180319 0.92 DNM1 (0.52) DNM1FDPSCYP3A4L3MBTL1GGPS1

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
EP-0299421-B1 Imide modified epoxy resins DOW CHEMICAL CO (US) 1996-03-13 EP disclosed
EP-0399351-A2 Epoxy resin and water borne coatings therefrom THE DOW CHEMICAL COMPANY (US) 1990-11-28 EP disclosed
US-4946911-A CONTAINING UNSATURATED IMIDE THE DOW CHEMICAL COMPANY (US) 1990-08-07 US disclosed
US-4847348-A BINDERS, COATINGS THE DOW CHEMICAL COMPANY (US) 1989-07-11 US disclosed
EP-0299421-A2 Imide modified epoxy resins THE DOW CHEMICAL COMPANY (US) 1989-01-18 EP disclosed