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.
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Phosphoric Acid SCHEMBL4310890 | 1.00 | — | — | |
| Phosphoric Acid SCHEMBL7743392 | 0.94 | SLC34A1 (0.46) | — | |
| Phosphoric Acid SCHEMBL9099370 | 0.94 | SLC34A1 (0.46) | — | |
| Phosphoric Acid SCHEMBL217686 | 0.94 | SLC34A1 (0.46) | — | |
| Phosphoric Acid SCHEMBL436 | 0.94 | — | — | |
| Phosphoric Acid SCHEMBL15066667 | 0.88 | — | — | |
| Phosphoric Acid SCHEMBL2989706 | 0.88 | — | — | |
| Phosphoric Acid SCHEMBL1979287 | 0.88 | SLC34A1 (0.42) | — | |
| Phosphoric Acid SCHEMBL1291546 | 0.88 | — | — | |
| Phosphoric Acid SCHEMBL2181871 | 0.88 | — | — |
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 57 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20250249440-A1 | PROCESS AND CATALYST FOR CATALYTIC CRACKING OF NAPHTHA TO LIGHT OLEFINS AND AROMATICS | HINDUSTAN PETROLEUM CORPORATION LIMITED (IN) | 2025-08-07 | — | — | US | claimed |
| CN-119433594-A | Lignin derived carbon-alloy-metal oxide heterojunction catalyst and preparation method thereof | 广西大学 | 2025-02-14 | — | — | CN | claimed |
| CN-118806880-A | CGAS-STING activated mineralized vaccine and preparation method and application thereof | 苏州大学 | 2024-10-22 | — | — | CN | claimed |
| CN-117399038-A | Indium zinc sulfide photocatalyst modified by sub-nanoscale clusters, and preparation and application thereof | 中国矿业大学 | 2024-01-16 | — | — | CN | claimed |
| CN-113023704-A | Preparation method of coralline cobalt pyrophosphate supercapacitor electrode material | 重庆大学 | 2021-06-25 | — | — | CN | claimed |
| US-20150349343-A1 | Low-Cost Method for Making Lithium Transition Metal Olivines with High Energy Density | DOW GLOBAL TECHNOLOGIES LLC | 2015-12-03 | — | — | US | claimed |
| EP-2867161-A2 | LOW-COST METHOD FOR MAKING LITHIUM TRANSITION METAL OLIVINES WITH HIGH ENERGY DENSITY | Dow Global Technologies LLC (US) | 2015-05-06 | — | — | EP | claimed |
| WO-2014004386-A2 | LOW-COST METHOD FOR MAKING LITHIUM TRANSITION METAL OLIVINES WITH HIGH ENERGY DENSITY | DOW GLOBAL TECHNOLOGIES LLC (US) | 2014-01-03 | — | — | WO | claimed |
| US-4895821-A | MOISTURE RESISTANT, EXHAUST SYSTEM REDUCTION OF NITROGEN OXIDES | DIDIER-WERKE AG (DE) | 1990-01-23 | — | — | US | claimed |
| US-12454461-B1 | Fabrication of CaB2O4/Co3(BO3)2/PbO2/Co3O4 nanocomposite material using Pechini sol-gel method | IMAM MOHAMMAD IBN SAUD ISLAMIC UNIVERSITY (SA) | 2025-10-28 | — | — | US | disclosed |
| US-20250249440-A1 | PROCESS AND CATALYST FOR CATALYTIC CRACKING OF NAPHTHA TO LIGHT OLEFINS AND AROMATICS | HINDUSTAN PETROLEUM CORPORATION LIMITED (IN) | 2025-08-07 | — | — | US | disclosed |
| US-12357962-B1 | Fabrication of Ca3Co4O9/MgO nanocomposite materials using pechini sol-gel method | IMAM MOHAMMAD IBN SAUD ISLAMIC UNIVERSITY (SA) | 2025-07-15 | — | — | US | disclosed |
| CN-119433594-A | Lignin derived carbon-alloy-metal oxide heterojunction catalyst and preparation method thereof | 广西大学 | 2025-02-14 | — | — | CN | disclosed |
| EP-3661893-B1 | TWO-COMPONENT COMPOSITION FOR THE PREPARATION OF AN AQUEOUS COATING MASS | HERAEUS ELECTRONICS GMBH & CO KG (DE) | 2025-01-22 | — | — | EP | disclosed |
| WO-2014100529-A1 | LMFP CATHODE MATERIALS WITH IMPROVED ELECTROCHEMICAL PERFORMANCE | DOW GLOBAL TECHNOLOGIES LLC (US) | 2014-06-26 | — | — | WO | disclosed |
| WO-2014098934-A1 | CO-SOLVENT ASSISTED MICROWAVE-SOLVOTHERMAL PROCESS FOR MAKING OLIVINE LITHIUM TRANSITION METAL PHOSPHATE ELECTRODE MATERIALS | DOW GLOBAL TECHNOLOGIES LLC (US) | 2014-06-26 | — | — | WO | disclosed |
| WO-2014004386-A2 | LOW-COST METHOD FOR MAKING LITHIUM TRANSITION METAL OLIVINES WITH HIGH ENERGY DENSITY | DOW GLOBAL TECHNOLOGIES LLC (US) | 2014-01-03 | — | — | WO | disclosed |
| CN-102093199-A | Method for reclaiming cobalt acetate in reaction waste residue | WUXI JINMIN KEXIN SHANHE PHARMACEUTICAL INDUSTRY CO LTD | 2011-06-15 | — | — | CN | disclosed |
| US-5508173-A | REAGENT LAYER CONTAINS PYRUVIC ACID OXIDASE; SPREADING LAYER HAS SPECIFIC VOID VOLUME AND CONTAINS AN ALPHA-KETOGLUTARIC ACID AND L-ALANINE | FUJI PHOTO FILM CO., LTD. (JP) | 1996-04-16 | — | — | US | disclosed |
| US-4503145-A | DIAGNOSIS OF LIVER DISORDERS | FUJI PHOTO FILM CO., LTD. (JP) | 1985-03-05 | — | — | US | disclosed |