Predicted protein targets (top 8)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.80 |
| ▸ | CHRM4 | P08173 | 1/20 | 0.43 |
| ▸ | CHRM5 | P08912 | 1/20 | 0.43 |
| ▸ | CHRM1 | P11229 | 1/20 | 0.43 |
| ▸ | CHRM3 | P20309 | 1/20 | 0.43 |
| ▸ | SLC18A3 | Q16572 | 3/20 | 0.39 |
| ▸ | CHRNB4 | P30926 | 1/20 | 0.37 |
| ▸ | CHRNA3 | P32297 | 1/20 | 0.37 |
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 | |
|---|---|---|---|---|
| SCHEMBL23043270 | 1.00 | TDP1 (0.80) | TDP1CHRM4CHRM5CHRM1CHRM3 | |
| SCHEMBL19317460 | 1.00 | TDP1 (0.80) | TDP1CHRM4CHRM5CHRM1CHRM3 | |
| SCHEMBL1856334 | 1.00 | TDP1 (0.80) | TDP1CHRM4CHRM5CHRM1CHRM3 | |
| SCHEMBL29366521 | 1.00 | TDP1 (0.80) | TDP1CHRM4CHRM5CHRM1CHRM3 | |
| SCHEMBL9040301 | 0.93 | TDP1 (0.84) | TDP1CHRM4CHRM5CHRM1CHRM3 | |
| SCHEMBL16757274 | 0.93 | TDP1 (0.91) | TDP1 | |
| SCHEMBL31501784 | 0.93 | TDP1 (0.91) | TDP1 | |
| Lupinine SCHEMBL2633852 | 0.89 | TDP1 (1.00) | TDP1 | |
| Lupinine SCHEMBL914675 | 0.89 | TDP1 (1.00) | TDP1 | |
| Lupinine SCHEMBL177708 | 0.89 | TDP1 (1.00) | TDP1 |
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 |
|---|---|---|---|---|---|---|---|
| CN-119798265-A | Asymmetric synthetic pyrrole method for preparing lixivium alkaloid | 武汉大学深圳研究院 | 2025-04-11 | — | — | CN | claimed |
| US-4894179-A | Absorbent composition containing a tertiary amino azabicyclic alcohol and an amine salt | EXXON RESEARCH AND ENGINEERING COMPANY (US) | 1990-01-16 | — | — | US | claimed |
| CN-119798265-A | Asymmetric synthetic pyrrole method for preparing lixivium alkaloid | 武汉大学深圳研究院 | 2025-04-11 | — | — | CN | disclosed |
| WO-1993010883-A1 | LEAN ACID GAS ENRICHMENT WITH SELECTIVE HINDERED AMINES | EXXON RESEARCH AND ENGINEERING COMPANY (US) | 1993-06-10 | — | — | WO | disclosed |
| US-4894179-A | Absorbent composition containing a tertiary amino azabicyclic alcohol and an amine salt | EXXON RESEARCH AND ENGINEERING COMPANY (US) | 1990-01-16 | — | — | US | disclosed |
| EP-0087207-B1 | A PROCESS FOR REMOVAL OF H2S FROM GASEOUS STREAMS WITH AMINO COMPOUNDS | EXXON RESEARCH AND ENGINEERING COMPANY (US) | 1986-08-06 | — | — | EP | disclosed |
| US-4405580-A | Process for selective removal of H2 S from mixtures containing H22 with tertiary amino azabicyclic alcohols | EXXON RESEARCH AND ENGINEERING CO. (US) | 1983-09-20 | — | — | US | disclosed |
| EP-0087207-A1 | A process for removal of H2S from gaseous streams with amino compounds | EXXON RESEARCH AND ENGINEERING COMPANY (US) | 1983-08-31 | — | — | EP | disclosed |