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 SCHEMBL118357 | 0.90 | — | — | |
| Phosphoric Acid SCHEMBL77419 | 0.90 | — | — | |
| Phosphoric Acid SCHEMBL8393696 | 0.90 | — | — | |
| Phosphoric Acid SCHEMBL753330 | 0.90 | — | — | |
| Phosphoric Acid SCHEMBL599013 | 0.90 | — | — | |
| Phosphoric Acid SCHEMBL3282346 | 0.90 | — | — | |
| Phosphoric Acid SCHEMBL118639 | 0.90 | — | — | |
| Phosphoric Acid SCHEMBL7455928 | 0.90 | — | — | |
| Phosphoric Acid SCHEMBL22022958 | 0.90 | SLC34A1 (0.73) | — | |
| Phosphoric Acid SCHEMBL4303638 | 0.90 | — | — |
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 5 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-5693805-A | SULFONAMIDATION OF CHLOROSULFONYLCAMPHOR WITH PIPERAZINE DERIVATIVE SALT, OXIMATION, REDUCTION, SELECTIVE AMIDATION OF ENDO AMINE ISOMER, SALT FORMATION; TOCOLYTIC AGENTS | MERCK & CO., INC. (US) | 1997-12-02 | — | — | US | disclosed |
| WO-1994020483-A1 | PROCESS TO DERIVATIVES OF PIPERIZINYLCAMPHORSULFONYL OXYTOCIN ANTAGONISTS | MERCK & CO., INC. (US) | 1994-09-15 | — | — | WO | disclosed |
| EP-0614894-A1 | Process for the synthesis of substituted amide derivatives of piperazinylcamphorsulfonyl oxytocin antagonists | MERCK & CO. INC. (US) | 1994-09-14 | — | — | EP | disclosed |
| US-4472308-A | Azo dyestuffs containing an amino or acylated amino naphthol monosulfonic acid radical and at least one reactive phosphoric or phosphonic acid group | ICI UNITED STATES, INC. (US) | 1984-09-18 | — | — | US | disclosed |
| US-4230618-A | CELLULOSE | ICI UNITED STATES, INC. (US) | 1980-10-28 | — | — | US | disclosed |