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 SCHEMBL1079610 | 0.94 | — | — | |
| Phosphoric Acid SCHEMBL7633607 | 0.94 | SLC34A1 (0.42) | — | |
| Phosphoric Acid SCHEMBL8773583 | 0.94 | — | — | |
| Phosphoric Acid SCHEMBL28378331 | 0.88 | SLC34A1 (0.39) | — | |
| Phosphoric Acid SCHEMBL7918310 | 0.88 | — | — | |
| Phosphoric Acid SCHEMBL28378329 | 0.88 | — | — | |
| Phosphoric Acid SCHEMBL31005001 | 0.88 | — | — | |
| Phosphoric Acid SCHEMBL8773619 | 0.88 | SLC34A1 (0.39) | — | |
| Phosphoric Acid SCHEMBL25395731 | 0.86 | — | — | |
| Phosphoric Acid SCHEMBL21951285 | 0.86 | SLC34A1 (0.46) | — |
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 481 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117143592-B | Mn (Mn)4+Activated fluoride (oxide) red fluorescent material and preparation method thereof | 华南理工大学 | 2026-05-22 | — | — | CN | claimed |
| US-20250214952-A1 | NOVEL TAFAMIDIS SYNTHESIS METHOD | KOREA UNIVERSITY RESEARCH AND BUSINESS FOUNDATION (KR) | 2025-07-03 | — | — | US | claimed |
| CN-115888772-B | Catalyst for decarbonylation and carbonylation coupling reaction and preparation method and application thereof | 中国石油化工股份有限公司 | 2025-05-30 | — | — | CN | claimed |
| CN-120040296-A | Method for purifying 4,4' -diaminodiphenyl methane | 同创化学(山东)有限公司 | 2025-05-27 | — | — | CN | claimed |
| CN-115260015-B | Method for producing methacrolein and methacrylic acid | 中国石油化工股份有限公司 | 2025-05-06 | — | — | CN | claimed |
| CN-119909664-A | Preparation method of doped rutile titanium dioxide with {101} and {110} crystal faces selectively exposed and low defect concentration | 中国科学院金属研究所 | 2025-05-02 | — | — | CN | claimed |
| CN-119874536-A | Purification method of 3,3 '-dichloro-4, 4' -diaminodiphenyl methane | 同创化学(山东)有限公司 | 2025-04-25 | — | — | CN | claimed |
| WO-2025081799-A1 | NEGATIVE ELECTRODE SHEET, SECONDARY BATTERY, AND ELECTRIC DEVICE | 宁德时代新能源科技股份有限公司 | 2025-04-24 | — | — | WO | claimed |
| CN-119798095-A | Purification method of 3,3 '-dimethyl-4, 4' -diaminodiphenyl methane | 同创化学(山东)有限公司 | 2025-04-11 | — | — | CN | claimed |
| CN-119409554-A | Preparation method of cardanol | 烟台皓元生物医药科技有限公司 | 2025-02-11 | — | — | CN | claimed |
| EP-0874798-B1 | METHOD FOR MODIFYING CATALYST PERFORMANCE DURING THE GAS PHASE SYNTHESIS OF VINYL ACETATE | DU PONT (US) | 2001-08-29 | — | — | EP | claimed |
| EP-0874798-A1 | METHOD FOR MODIFYING CATALYST PERFORMANCE DURING THE GAS PHASE SYNTHESIS OF VINYL ACETATE | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1998-11-04 | — | — | EP | claimed |
| US-5688993-A | USING CATALYST MIXTURE | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1997-11-18 | — | — | US | claimed |
| WO-1997023442-A1 | METHOD FOR MODIFYING CATALYST PERFORMANCE DURING THE GAS PHASE SYNTHESIS OF VINYL ACETATE | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1997-07-03 | — | — | WO | claimed |
| EP-0518475-B1 | Analysis of samples utilizing capillary electrophoresis | BECKMAN INSTRUMENTS INC (US) | 1997-04-09 | — | — | EP | claimed |
| US-5409617-A | High speed pre-decomposition the waste materials by heating waste materials with an aqueous solution comprising one or more salts of silica, alkali or alkaline earth metal silicate, borate, phosphate, bi- or triphosphates | SRI INTERNATIONAL (US) | 1995-04-25 | — | — | US | claimed |
| WO-1995002556-A1 | ENVIRONMENTALLY ACCEPTABLE WASTE DISPOSAL BY HYDROTHERMAL DECOMPOSITION OF LABILE COMPOUNDS | SRI INTERNATIONAL (US) | 1995-01-26 | — | — | WO | claimed |
| EP-0518475-A1 | Analysis of samples utilizing capillary electrophoresis | BECKMAN INSTRUMENTS, INC. (US) | 1992-12-16 | — | — | EP | claimed |
| US-5120413-A | Using electrolyte buffer comprising agent which complexes with sugar moieties of glycoproteins | BECKMAN INSTRUMENTS, INC. (US) | 1992-06-09 | — | — | US | claimed |
| US-3960901-A | Preparation of citraconic acid | PFIZER INC. (US) | 1976-06-01 | — | — | US | claimed |