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 SCHEMBL28221616 | 1.00 | — | — | |
| Phosphoric Acid SCHEMBL7633600 | 0.94 | — | — | |
| Phosphoric Acid SCHEMBL28427133 | 0.94 | — | — | |
| Phosphoric Acid SCHEMBL28823328 | 0.94 | — | — | |
| Phosphoric Acid SCHEMBL8773587 | 0.94 | — | — | |
| Phosphoric Acid SCHEMBL28118395 | 0.94 | — | — | |
| Phosphoric Acid SCHEMBL29224025 | 0.94 | — | — | |
| Phosphoric Acid SCHEMBL1332284 | 0.93 | — | — | |
| Phosphoric Acid SCHEMBL3788505 | 0.93 | CA2 (0.56) | — | |
| Phosphoric Acid SCHEMBL5907 | 0.93 | CA2 (0.56) | — |
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 587 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-20260112549-A1 | HIGH-PERFORMANCE SOLID STATE ELECTROLYTE BASED ON SOLID ACID WITH LOW SELF-DISCHARGE AND EXCEPTIONAL IONIC CONDUCTIVITY | THE AMERICAN UNIV IN CAIRO (EG) | 2026-04-23 | — | — | US | 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 |
| 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-0393382-B1 | Device for the measurement of an electric field | ASEA BROWN BOVERI (CH) | 1994-06-01 | — | — | EP | 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-5053694-A | DEVICE FOR MEASURING AN ELECTRIC FIELD | ASEA BROWN BOVERI LTD. (CH) | 1991-10-01 | — | — | US | claimed |
| US-5029953-A | Ultraviolet optical isolator utilizing the KDP-isomorphs | THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY (US) | 1991-07-09 | — | — | US | claimed |
| US-3960901-A | Preparation of citraconic acid | PFIZER INC. (US) | 1976-06-01 | — | — | US | claimed |
| US-3954940-A | Process for surface work strain relief of electrooptic crystals | MCDONNELL DOUGLAS CORPORATION (US) | 1976-05-04 | — | — | US | claimed |