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.
Predicted protein targets (top 9)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MEN1 | O00255 | 2/20 | 0.44 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.44 |
| ▸ | ALOX15 | P16050 | 2/20 | 0.44 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.44 |
| ▸ | MAPT | P10636 | 2/20 | 0.42 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.42 |
| ▸ | UGT1A1 | P22309 | 1/20 | 0.42 |
| ▸ | BTN3A1 | O00481 | 3/20 | 0.41 |
| ▸ | GGPS1 | O95749 | 8/20 | 0.38 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
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 SCHEMBL10336339 | 1.00 | MEN1 (0.44) | MEN1CYP3A4ALOX15KMT2AMAPT | |
| Pyrophosphoric Acid SCHEMBL7743852 | 0.85 | BTN3A1 (0.55) | MEN1CYP3A4ALOX15KMT2AMAPT | |
| SCHEMBL115620 | 0.84 | — | — | |
| SCHEMBL8813968 | 0.84 | KMT2A (0.55) | MEN1CYP3A4ALOX15KMT2AMAPT | |
| Formaldehyde SCHEMBL8208771 | 0.81 | — | — | |
| Bromide SCHEMBL9843003 | 0.81 | — | — | |
| Hydrogen Peroxide SCHEMBL31511442 | 0.81 | — | — | |
| Geraniol SCHEMBL20481327 | 0.79 | KMT2A (0.79) | MEN1CYP3A4ALOX15KMT2AMAPT | |
| Geraniol SCHEMBL20481326 | 0.79 | KMT2A (0.79) | MEN1CYP3A4ALOX15KMT2AMAPT | |
| Geraniol SCHEMBL27699074 | 0.79 | KMT2A (0.79) | MEN1CYP3A4ALOX15KMT2AMAPT |
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 8 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20080318227-A1 | Intermediates and enzymes of the non-mevalonate isoprenoid pathway | BACHER ADELBERT | 2008-12-25 | — | — | US | disclosed |
| US-20080300222-A1 | Phosphoantigen Salts Of Organic Bases And Methods For Their Crystallization | INNATE PHARMA (FR) | 2008-12-04 | — | — | US | disclosed |
| EP-1933848-A2 | PHOSPHOANTIGEN SALTS OF ORGANIC BASES AND METHODS FOR THEIR CRYSTALLIZATION | Innate Pharma (FR) | 2008-06-25 | — | — | EP | disclosed |
| US-7297509-B2 | Intermediates and enzymes of the non-mevalonate isoprenoid pathway | Bacher, Adelbert (DE) | 2007-11-20 | — | — | US | disclosed |
| WO-2007039635-A2 | PHOSPHOANTIGEN SALTS OF ORGANIC BASES AND METHODS FOR THEIR CRYSTALLIZATION | INNATE PHARMA (FR) | 2007-04-12 | — | — | WO | disclosed |
| US-20040176570-A1 | Intermediates and enzymes of the non-mevalonate isoprenoid pathway | ROHDICH, FELIX (DE) | 2004-09-09 | — | — | US | disclosed |
| EP-1377663-A2 | INTERMEDIATES AND ENZYMES OF THE NON-MEVALONATE ISOPRENOID PATHWAY | Bacher, Adelbert (DE) | 2004-01-07 | — | — | EP | disclosed |
| WO-2002083720-A2 | INTERMEDIATES AND ENZYMES OF THE NON-MEVALONATE ISOPRENOID PATHWAY | BACHER ADELBERT (DE) | 2002-10-24 | — | — | WO | disclosed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20040176570-A1 | Intermediates and enzymes of the non-mevalonate isoprenoid pathway | FDPS, DHPS, COASY | MEN1 1622/4885CYP3A4 244/4885ALOX15 2054/4885 |
| US-20080300222-A1 | Phosphoantigen Salts Of Organic Bases And Methods For Their Crystallization | HLA-B, LCK, HLA-A | MEN1 3785/4885CYP3A4 4004/4885ALOX15 1720/4885 |
| US-20080318227-A1 | Intermediates and enzymes of the non-mevalonate isoprenoid pathway | FDPS, DHPS, COASY | MEN1 1731/4885CYP3A4 311/4885ALOX15 1870/4885 |
“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.