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 SCHEMBL1864261 | 0.82 | — | — | |
| Phosphoric Acid SCHEMBL8633021 | 0.82 | — | — | |
| Trimethyl Phosphate SCHEMBL1426174 | 0.80 | LMNA (0.43) | — | |
| Trimethyl Phosphate SCHEMBL28203085 | 0.77 | LMNA (0.42) | — | |
| Phosphoric Acid SCHEMBL17700975 | 0.77 | CA2 (0.55) | — | |
| Phosphoric Acid SCHEMBL1656818 | 0.77 | CA2 (0.55) | — | |
| Phosphoric Acid SCHEMBL19347379 | 0.77 | — | — | |
| Phosphoric Acid SCHEMBL295473 | 0.77 | — | — | |
| Phosphoric Acid SCHEMBL5493690 | 0.77 | CA2 (0.55) | — | |
| Phosphoric Acid SCHEMBL11261943 | 0.77 | CA2 (0.55) | — |
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 14 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-113372363-B | Preparation method of descarbamoyl cefuroxime | 广东立国制药有限公司 | 2022-11-25 | — | — | CN | claimed |
| CN-113372363-A | Preparation method of descarbamoyl cefuroxime | 深圳市立国药物研究有限公司 | 2021-09-10 | — | — | CN | claimed |
| WO-2008110507-A1 | METHOD OF SCAVENGING OXYGEN IN AQUEOUS SYSTEMS | ARKEMA FRANCE (FR) | 2008-09-18 | — | — | WO | claimed |
| CN-113372363-B | Preparation method of descarbamoyl cefuroxime | 广东立国制药有限公司 | 2022-11-25 | — | — | CN | disclosed |
| CN-113372363-A | Preparation method of descarbamoyl cefuroxime | 深圳市立国药物研究有限公司 | 2021-09-10 | — | — | CN | disclosed |
| CN-103063763-A | High performance liquid chromatography detection method for residual quantity of multiple ultraviolet absorbents in cosmetics | LIN WEIXUAN | 2013-04-24 | — | — | CN | disclosed |
| WO-2008110507-A1 | METHOD OF SCAVENGING OXYGEN IN AQUEOUS SYSTEMS | ARKEMA FRANCE (FR) | 2008-09-18 | — | — | WO | disclosed |
| US-20030053927-A1 | Controlled Rellease of oxygen scavengers in cooling systems | DOBER CHEMICAL CORPORATION | 2003-03-20 | — | — | US | disclosed |
| EP-0297916-B1 | CONTROL OF CORROSION IN AQUEOUS SYSTEMS | W.R. Grace & Co.-Conn. (US) | 1992-05-13 | — | — | EP | disclosed |
| US-4847001-A | DIHYDROXYBENZENE SULFONIC ACIDS AND SALTS | W. R. GRACE & CO.-CONN. (US) | 1989-07-11 | — | — | US | disclosed |
| EP-0297916-A1 | Control of corrosion in aqueous systems | W.R. Grace & Co.-Conn. (US) | 1989-01-04 | — | — | EP | disclosed |
| US-4626411-A | Composition and method for deoxygenation | DEARBORN CHEMICAL COMPANY, LIMITED (CA) | 1986-12-02 | — | — | US | disclosed |
| EP-0161822-A2 | Composition and method for deoxygenation of aqueous systems | DEARBORN CHEMICAL COMPANY LIMITED (CA) | 1985-11-21 | — | — | EP | disclosed |
| US-4067690-A | HYDROXYLAMINE DERIVATIVES AS OXYGEN SCAVENGERS TO REDUCE CORROSION | CHEMED CORPORATION (US) | 1978-01-10 | — | — | US | disclosed |