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 | |
|---|---|---|---|---|
| SCHEMBL17668147 | 0.83 | — | — | |
| SCHEMBL73703 | 0.83 | — | — | |
| Hydrochloric Acid SCHEMBL113844 | 0.79 | — | — | |
| SCHEMBL11168659 | 0.79 | — | — | |
| Fluoride SCHEMBL11279341 | 0.79 | TSHR (0.36) | — | |
| Ammonia Solution, Strong SCHEMBL23326264 | 0.79 | — | — | |
| SCHEMBL7779076 | 0.79 | — | — | |
| SCHEMBL2195741 | 0.79 | — | — | |
| SCHEMBL10386253 | 0.79 | — | — | |
| SCHEMBL102443 | 0.79 | — | — |
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 19 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2025072741-A1 | PRESERVATIVES FOR MOLECULAR SAMPLE ANALYSIS WITH SAMPLE COLLECTION DEVICES | BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) | 2025-04-03 | — | — | WO | claimed |
| US-20240352157-A1 | DISSOLUTION OF CHITOSAN IN APROTIC AQUEOUS MEDIUM COMPOSITION, PREPARATION METHODS AND BIOMEDICAL USES THEREOF | Oligo Médic Inc. (CA) | 2024-10-24 | — | — | US | claimed |
| WO-2022226633-A1 | NOVEL WATER-SOLUBLE CHITOSAN COMPOSITIONS AND METHOD TO PREPARE THE SAME | Oligo Médic Inc. (CA) | 2022-11-03 | — | — | WO | claimed |
| CN-105805426-B | Pipeline runs through device | 上海火克新材料有限公司 | 2017-10-27 | — | — | CN | claimed |
| CN-103509074-A | Synthesis method of nucleoside diphosphate 6-deoxy-L-pyranose | UNIV JIANGXI NORMAL SCI & TECH | 2014-01-15 | — | — | CN | claimed |
| WO-2025072741-A1 | PRESERVATIVES FOR MOLECULAR SAMPLE ANALYSIS WITH SAMPLE COLLECTION DEVICES | BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) | 2025-04-03 | — | — | WO | disclosed |
| US-20240352157-A1 | DISSOLUTION OF CHITOSAN IN APROTIC AQUEOUS MEDIUM COMPOSITION, PREPARATION METHODS AND BIOMEDICAL USES THEREOF | Oligo Médic Inc. (CA) | 2024-10-24 | — | — | US | disclosed |
| EP-4141122-A2 | CARBON-NEUTRAL AND CARBON-POSITIVE PHOTORESPIRATION BYPASS ROUTES SUPPORTING HIGHER PHOTOSYNTHETIC RATE AND YIELD | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) | 2023-03-01 | — | — | EP | disclosed |
| WO-2022226633-A1 | NOVEL WATER-SOLUBLE CHITOSAN COMPOSITIONS AND METHOD TO PREPARE THE SAME | Oligo Médic Inc. (CA) | 2022-11-03 | — | — | WO | disclosed |
| US-10781456-B2 | Carbon-neutral and carbon-positive photorespiration bypass routes supporting higher photosynthetic rate and yield | MAX-PLANCK-GESELLSCHAFT ZUR FÖRDERUNG DER WISSENSCHAFTEN E.V., (DE) | 2020-09-22 | — | — | US | disclosed |
| US-20180223302-A1 | CARBON-NEUTRAL AND CARBON-POSITIVE PHOTORESPIRATION BYPASS ROUTES SUPPORTING HIGHER PHOTOSYNTHETIC RATE AND YIELD | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) | 2018-08-09 | — | — | US | disclosed |
| EP-3313994-A1 | CARBON-NEUTRAL AND CARBON-POSITIVE PHOTORESPIRATION BYPASS ROUTES SUPPORTING HIGHER PHOTOSYNTHETIC RATE AND YIELD | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) | 2018-05-02 | — | — | EP | disclosed |
| WO-2016207219-A1 | CARBON-NEUTRAL AND CARBON-POSITIVE PHOTORESPIRATION BYPASS ROUTES SUPPORTING HIGHER PHOTOSYNTHETIC RATE AND YIELD | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) | 2016-12-29 | — | — | WO | disclosed |
| CN-103509067-B | By the method for hydrogen monophosphite intermediate synthesis sugar-1-monophosphate | JIANGXI SCIENCE & TECHNOLOGY NORMAL UNIVERSITY (CN) | 2016-02-17 | — | — | CN | disclosed |
| CN-103509074-A | Synthesis method of nucleoside diphosphate 6-deoxy-L-pyranose | UNIV JIANGXI NORMAL SCI & TECH | 2014-01-15 | — | — | CN | disclosed |
| CN-103509067-A | Method for synthesizing glycosyl-1-monophosphate by hydrogen phosphite monoester intermediate | UNIV JIANGXI NORMAL SCI & TECH | 2014-01-15 | — | — | CN | disclosed |
| CN-103509067-A | Method for synthesizing glycosyl-1-monophosphate by hydrogen phosphite monoester intermediate | UNIV JIANGXI NORMAL SCI & TECH | 2014-01-15 | — | — | CN | disclosed |
| CN-103509074-A | Synthesis method of nucleoside diphosphate 6-deoxy-L-pyranose | UNIV JIANGXI NORMAL SCI & TECH | 2014-01-15 | — | — | CN | disclosed |
| EP-0793668-B1 | DERIVATIVES OF CARBOHYDRATES AND COMPOSITIONS CONTAINING THEM | BIONERIS AB (SE) | 2004-03-31 | — | — | EP | disclosed |