Phosphoric Acid

Phosphoric Acid

SCHEMBL6264338

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

nearest known ligand 0.58

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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 20)

geneUniProtsupporting neighboursconfidence
SLC34A1 Q06495 1/20 0.58
LMNA P02545 3/20 0.40
KDM4E B2RXH2 2/20 0.39
CYP2C19 P33261 1/20 0.39
KMT2A Q03164 1/20 0.39
CA2 P00918 1/20 0.39
TYMS P04818 1/20 0.38
BLM P54132 2/20 0.33
MMP2 P08253 1/20 0.33
THRB P10828 1/20 0.33
MAPK1 P28482 1/20 0.33
HSD17B10 Q99714 1/20 0.33
FDPS P14324 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
CA1 P00915 2/20 0.30
CA4 P22748 2/20 0.30
CA5A P35218 2/20 0.30
CA5B Q9Y2D0 2/20 0.30
CYP3A4 P08684 1/20 0.30
NFKB1 P19838 1/20 0.30

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 SCHEMBL18315376 0.95 SLC34A1 (0.54) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL18315375 0.95 SLC34A1 (0.54) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL8762980 0.95 SLC34A1 (0.54) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL403321 0.95 SLC34A1 (0.54) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL736577 0.95 SLC34A1 (0.54) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL3026198 0.95 SLC34A1 (0.67) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL4362914 0.95 SLC34A1 (0.67) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL310374 0.91 SLC34A1 (0.50) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL5160559 0.91 SLC34A1 (0.61) SLC34A1LMNAKDM4ECYP2C19KMT2A
Phosphoric Acid SCHEMBL8011743 0.91 SLC34A1 (0.50) SLC34A1LMNAKDM4ECYP2C19KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-104693147-A Method for preparation of ethylene oxide by ethylene epoxidation DALIAN CHEMICAL PHYSICS INST 2015-06-10 CN claimed
WO-2004010515-A2 METHOD OF SYNTHESIZING ELECTROCHEMICALLY ACTIVE MATERIALS FROM A SLURRY OF PRECURSORS VALENCE TECHNOLOGY, INC. (US) 2004-01-29 WO claimed
US-20040013943-A1 Liquid phase of slurry containing a solvent, alkali metal ions, and at least one anion selected from phosphate, hydrogen phosphate and dihydrogen phosphate; solid phase of slurry containg at least one transition metal LITHIUM WERKS TECHNOLOGY B.V. (NL) 2004-01-22 US claimed
WO-2023074372-A1 AQUEOUS AGROCHEMICAL SUSPENSION COMPOSITION, PLANT DISEASE CONTROL METHOD, AND SEED OF USEFUL PLANT クミアイ化学工業株式会社 2023-05-04 WO disclosed
WO-2023074370-A1 AQUEOUS AGROCHEMICAL SUSPENSION COMPOSITION, METHOD FOR PREVENTING CROP DAMAGE, AND SEED OF USEFUL PLANT クミアイ化学工業株式会社 2023-05-04 WO disclosed
EP-4084611-A1 GELLED HYDRATION MEDIUM Enhold B.V. (NL) 2022-11-09 EP disclosed
WO-2021136818-A1 GELLED HYDRATION MEDIUM ENHOLD B.V. (NL) 2021-07-08 WO disclosed
CN-104693147-A Method for preparation of ethylene oxide by ethylene epoxidation DALIAN CHEMICAL PHYSICS INST 2015-06-10 CN disclosed
EP-1342757-B1 Cathodic electrodeposition coating agents containing bismuth complexes, preparation and use thereof DU PONT (US) 2005-10-26 EP disclosed
EP-1342757-A1 Cathodic electrodeposition coating agents containing bismuth complexes, preparation and use thereof E.I. DU PONT DE NEMOURS AND COMPANY (US) 2003-09-10 EP disclosed
US-4038473-A PROCESS FOR CLEANING POLYMERIZATION REACTORS THE B. F. GOODRICH COMPANY (US) 1977-07-26 US disclosed