Known targets — ChEMBL curated mechanism
The experimentally established mechanism targets of Oxalic 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 | |
|---|---|---|---|---|
| ▸ | CHRNB2 | P17787 | 6/20 | 0.83 |
| ▸ | CHRNB4 | P30926 | 6/20 | 0.83 |
| ▸ | CHRNA3 | P32297 | 6/20 | 0.83 |
| ▸ | CHRNB1 | P11230 | 5/20 | 0.83 |
| ▸ | CHRNB3 | Q05901 | 5/20 | 0.83 |
| ▸ | CHRNA4 | P43681 | 3/20 | 0.83 |
| ▸ | CHRNA1 | P02708 | 1/20 | 0.83 |
| ▸ | CHRNA7 | P36544 | 1/20 | 0.83 |
| ▸ | JAK2 | O60674 | 1/20 | 0.57 |
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 | |
|---|---|---|---|---|
| SCHEMBL8435491 | 0.93 | CHRNB2 (0.92) | CHRNB2CHRNB4CHRNA3CHRNB1CHRNB3 | |
| SCHEMBL8438369 | 0.93 | CHRNB2 (0.92) | CHRNB2CHRNB4CHRNA3CHRNB1CHRNB3 | |
| Hydrochloric Acid SCHEMBL7406679 | 0.91 | CHRNB2 (0.90) | CHRNB2CHRNB4CHRNA3CHRNB1CHRNB3 | |
| SCHEMBL12214039 | 0.91 | CHRNB2 (1.00) | CHRNB2CHRNB4CHRNA3CHRNB1CHRNB3 | |
| SCHEMBL676032 | 0.91 | CHRNB2 (1.00) | CHRNB2CHRNB4CHRNA3CHRNB1CHRNB3 | |
| SCHEMBL29484629 | 0.91 | CHRNB2 (1.00) | CHRNB2CHRNB4CHRNA3CHRNB1CHRNB3 | |
| SCHEMBL7372710 | 0.91 | CHRNB2 (1.00) | CHRNB2CHRNB4CHRNA3CHRNB1CHRNB3 | |
| Fumaric Acid SCHEMBL237911 | 0.91 | CHRNB2 (0.80) | CHRNB2CHRNB4CHRNA3CHRNB1CHRNB3 | |
| Fumaric Acid SCHEMBL237912 | 0.91 | CHRNB2 (0.80) | CHRNB2CHRNB4CHRNA3CHRNB1CHRNB3 | |
| Hydrochloric Acid SCHEMBL7839221 | 0.90 | CHRNB2 (0.97) | CHRNB2CHRNB4CHRNA3CHRNB1CHRNB3 |
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 4 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1047690-A1 | HETEROCYCLIC ETHER AND THIOETHER COMPOUNDS USEFUL IN CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION | Abbott Laboratories (US) | 2000-11-02 | — | — | EP | disclosed |
| US-5948793-A | 3-pyridyloxymethyl heterocyclic ether compounds useful in controlling neurotransmitter release | ABBOTT LABORATORIES (US) | 1999-09-07 | — | — | US | disclosed |
| WO-1999032480-A1 | HETEROCYCLIC ETHER AND THIOETHER COMPOUNDS USEFUL IN CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION | ABBOTT LABORATORIES (US) | 1999-07-01 | — | — | WO | disclosed |
| US-5914328-A | CONTROL DOPAMINE RELEASE, ACTIVATE CHOLINERGIC CHANNELS | ABBOTT LABORATORIES (US) | 1999-06-22 | — | — | US | disclosed |