Phosphoric Acid

Phosphoric Acid

SCHEMBL1133239

O.O.O.O.O.O.O.O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].[Mg+2].[Mg+2].[Mg+2]

nearest known ligand 0.42

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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 2)

geneUniProtsupporting neighboursconfidence
SLC34A1 Q06495 1/20 0.42
LMNA P02545 2/20 0.36

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 SCHEMBL5179411 1.00 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL29020585 1.00 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL2455597 1.00 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL735373 1.00 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL736220 1.00 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL844683 1.00 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL5921833 1.00 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL2590425 1.00 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL23722691 0.94 SLC34A1 (0.50) SLC34A1LMNA
Phosphoric Acid SCHEMBL2225189 0.94

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 30 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119776150-B Chlorella extracellular fluid and preparation method and application thereof 滨州医学院 2025-06-24 CN claimed
CN-119776150-A Chlorella extracellular fluid and preparation method and application thereof 滨州医学院 2025-04-08 CN claimed
CN-119776150-B Chlorella extracellular fluid and preparation method and application thereof 滨州医学院 2025-06-24 CN disclosed
CN-118726439-B Method for constructing bacillus subtilis chassis strain with improved recombinant protein expression capability 江南大学 2025-04-15 CN disclosed
CN-119776150-A Chlorella extracellular fluid and preparation method and application thereof 滨州医学院 2025-04-08 CN disclosed
CN-118726439-A Method for constructing bacillus subtilis chassis strain with improved recombinant protein expression capability 江南大学 2024-10-01 CN disclosed
CN-117203326-A Proliferation promoter for lactic acid coccus 麒麟控股株式会社 2023-12-08 CN disclosed
US-11659839-B2 Resistance inducing agent for plants PANAC CO., LTD. (JP) 2023-05-30 US disclosed
CN-112334006-B Resistance inducer for plants 日本凡纳克株式会社 2022-03-04 CN disclosed
US-20210360935-A1 RESISTANCE INDUCING AGENT FOR PLANTS PANAC CO., LTD. (JP) 2021-11-25 US disclosed
EP-3777539-A1 RESISTANCE INDUCING AGENT FOR PLANTS Panac Co., Ltd. (JP) 2021-02-17 EP disclosed
EP-1584690-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE a-METHYLCYSTEINE DERIVATIVE KANEKA CORPORATION (JP) 2005-10-12 EP disclosed
US-20050186654-A1 Method for producing dipeptide AJINOMOTO CO., INC. (JP) 2005-08-25 US disclosed
EP-1559789-A2 Method for producing dipeptide Ajinomoto Co., Ltd. (JP) 2005-08-03 EP disclosed
EP-1550725-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE alpha-METHYLCYSTEINE DERIVATIVE KANEKA CORPORATION (JP) 2005-07-06 EP disclosed
US-6606822-B2 Nodule fromation, nitrogen fixation; microorganisms of Rhizobium, alkali metal molybdate and amide, imine, or amine polymer; stability, viability SINTESIS QUIMICA S.A.I.C. (AR) 2003-08-19 US disclosed
US-20020050096-A1 Aqueous base inoculant composition for seeds, coated seeds and method for storing the composition SINTESIS QUIMICA S.A.I.C. (AR) 2002-05-02 US disclosed
EP-0690131-B1 Non-reducing saccharide and its production and use HAYASHIBARA BIOCHEM LAB (JP) 2001-12-19 EP disclosed
US-5908767-A CULTURING MICROORGANISMS CAPABLE OF FORMING AN ENZYME; REDUCTION OF STARCH HYDROLYZATE KABUSHIKI KAISHA HAYASHIBARA SEIBUTSU KAGAKU KENKYUJO (JP) 1999-06-01 US disclosed
EP-0690131-A1 Non-reducing saccharide and its production and use KABUSHIKI KAISHA HAYASHIBARA SEIBUTSU KAGAKU KENKYUJO (JP) 1996-01-03 EP disclosed