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 3)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | GGPS1 | O95749 | 9/20 | 0.35 |
| ▸ | FDPS | P14324 | 11/20 | 0.32 |
| ▸ | ENPP2 | Q13822 | 1/20 | 0.31 |
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 SCHEMBL30381493 | 0.95 | GGPS1 (0.32) | GGPS1 | |
| Phosphoric Acid SCHEMBL7993142 | 0.94 | GGPS1 (0.41) | GGPS1FDPSENPP2 | |
| SCHEMBL2327534 | 0.91 | GGPS1 (0.30) | GGPS1 | |
| SCHEMBL15922028 | 0.89 | — | — | |
| Phosphoric Acid SCHEMBL31027757 | 0.89 | GPR84 (0.38) | GGPS1FDPSENPP2 | |
| SCHEMBL3470871 | 0.87 | — | — | |
| SCHEMBL107551 | 0.87 | HRH3 (0.34) | — | |
| Diethyl Hydrogen Phosphate SCHEMBL6005556 | 0.85 | LMNA (0.31) | — | |
| SCHEMBL535081 | 0.85 | HRH3 (0.30) | — | |
| SCHEMBL535453 | 0.85 | HRH3 (0.32) | — |
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 7 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2558102-A1 | SYNERGISTIC INTERACTION OF AT LEAST ONE VITAMIN E COMPONENT AND TYROSINASE INHIBITORS FOR DERMATOLOGICAL APPLICATIONS | Davos Life Science Pte. Ltd. (SG) | 2013-02-20 | — | — | EP | disclosed |
| WO-2011129765-A1 | SYNERGISTIC INTERACTION OF AT LEAST ONE VITAMIN E COMPONENT AND TYROSINASE INHIBITORS FOR DERMATOLOGICAL APPLICATIONS | DAVOS LIFE SCIENCE PTE. LTD. (SG) | 2011-10-20 | — | — | WO | disclosed |
| EP-2376448-A2 | IMPROVED METHOD FOR THE PREPARATION OF 1-ACETYL-6-AMINO-3,3-DIMETHYL-2,3-DIHYDROINDOLE | Amgen, Inc (US) | 2011-10-19 | — | — | EP | disclosed |
| WO-2010071828-A2 | IMPROVED METHOD FOR THE PREPARATION OF 1-ACETYL-6-AMINO-3,3-DIMETHYL-2,3-DIHYDROINDOLE | AMGEN INC. (US) | 2010-06-24 | — | — | WO | disclosed |
| EP-1456435-A4 | ELECTROCHEMICAL PROCESS FOR PRODUCING IONIC LIQUIDS | SACHEM INC (US) | 2006-10-25 | — | — | EP | disclosed |
| EP-1456435-A1 | ELECTROCHEMICAL PROCESS FOR PRODUCING IONIC LIQUIDS | SACHEM, INC. (US) | 2004-09-15 | — | — | EP | disclosed |
| WO-2003046257-A1 | ELECTROCHEMICAL PROCESS FOR PRODUCING IONIC LIQUIDS | SACHEM, INC. (US) | 2003-06-05 | — | — | WO | disclosed |