Predicted protein targets (top 10)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | RAB9A | P51151 | 3/20 | 0.45 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.43 |
| ▸ | MAPT | P10636 | 1/20 | 0.43 |
| ▸ | MAOB | P27338 | 2/20 | 0.41 |
| ▸ | MAOA | P21397 | 1/20 | 0.41 |
| ▸ | NPC1 | O15118 | 1/20 | 0.40 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.40 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.40 |
| ▸ | ATM | Q13315 | 1/20 | 0.39 |
| ▸ | IDO1 | P14902 | 1/20 | 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 | |
|---|---|---|---|---|
| SCHEMBL11337101 | 0.84 | RAB9A (0.48) | RAB9AALDH1A1MAPTMAOBMAOA | |
| SCHEMBL11200759 | 0.78 | RAB9A (0.54) | RAB9AALDH1A1MAPTMAOBMAOA | |
| SCHEMBL10334788 | 0.74 | RAB9A (0.50) | RAB9AALDH1A1MAPTMAOBMAOA | |
| SCHEMBL11195351 | 0.72 | RAB9A (0.48) | RAB9AALDH1A1MAPTMAOBMAOA | |
| SCHEMBL6151831 | 0.71 | RAB9A (0.61) | RAB9AALDH1A1MAPTNPC1TDP1 | |
| SCHEMBL8716892 | 0.71 | RAB9A (0.61) | RAB9AALDH1A1MAPTNPC1TDP1 | |
| SCHEMBL6645015 | 0.71 | RAB9A (0.61) | RAB9AALDH1A1MAPTNPC1TDP1 | |
| SCHEMBL9976430 | 0.70 | ALDH1A1 (0.55) | RAB9AALDH1A1MAPTMAOBMAOA | |
| SCHEMBL8533970 | 0.70 | IDO1 (0.53) | RAB9AALDH1A1MAPTMAOBMAOA | |
| SCHEMBL9044754 | 0.69 | ALDH1A1 (0.53) | RAB9AALDH1A1MAPTMAOBIDO1 |
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 1 patent. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2015131100-A1 | LIGAND-CONTROLLED C(SP3)-H ARYLATION AND OLEFINATION IN SYNTHESIS OF UNNATURAL CHIRAL ALPHA AMINO ACIDS | THE SCRIPPS RESEARCH INSTITUTE (US) | 2015-09-03 | — | — | WO | disclosed |