Predicted protein targets (top 10)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MMP1 | P03956 | 18/20 | 0.73 |
| ▸ | MMP3 | P08254 | 18/20 | 0.73 |
| ▸ | MMP13 | P45452 | 18/20 | 0.73 |
| ▸ | MMP2 | P08253 | 17/20 | 0.73 |
| ▸ | MMP8 | P22894 | 17/20 | 0.73 |
| ▸ | MMP9 | P14780 | 4/20 | 0.73 |
| ▸ | ADAM17 | P78536 | 2/20 | 0.73 |
| ▸ | MMP7 | P09237 | 1/20 | 0.73 |
| ▸ | MMP14 | P50281 | 1/20 | 0.73 |
| ▸ | USP19 | O94966 | 2/20 | 0.35 |
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 | |
|---|---|---|---|---|
| SCHEMBL7972567 | 1.00 | MMP1 (0.73) | MMP1MMP3MMP13MMP2MMP8 | |
| SCHEMBL7088211 | 0.87 | MMP1 (0.80) | MMP1MMP3MMP13MMP2MMP8 | |
| SCHEMBL7091833 | 0.87 | MMP1 (0.80) | MMP1MMP3MMP13MMP2MMP8 | |
| SCHEMBL10118168 | 0.85 | MMP1 (0.75) | MMP1MMP3MMP13MMP2MMP8 | |
| Cipemastat SCHEMBL10321896 | 0.85 | MMP1 (1.00) | MMP1MMP3MMP13MMP2MMP8 | |
| Cipemastat SCHEMBL7297038 | 0.85 | MMP1 (1.00) | MMP1MMP3MMP13MMP2MMP8 | |
| SCHEMBL7874423 | 0.85 | MMP1 (0.79) | MMP1MMP3MMP13MMP2MMP8 | |
| SCHEMBL7874425 | 0.85 | MMP1 (0.79) | MMP1MMP3MMP13MMP2MMP8 | |
| Cipemastat SCHEMBL7088217 | 0.85 | MMP1 (1.00) | MMP1MMP3MMP13MMP2MMP8 | |
| Cipemastat SCHEMBL7297043 | 0.85 | MMP1 (1.00) | MMP1MMP3MMP13MMP2MMP8 |
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 5 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-6222039-B1 | REACTING LACTONE COMPOUND CONTAINING NITROGEN HETEROCYCLE WITH CYCLIC AMINE; OXIDIZING TO FORM CARBOXYLIC ACID GROUP; INTRODUCING HYDROXYLAMINE GROUP AT HYDROXYL OF CARBOXYLIC ACID GROUP | HOFFMAN-LA ROCHE INC. | 2001-04-24 | — | — | US | claimed |
| EP-0974590-A1 | Process for the preparation of chiral lactones by asymetrical hydrogenation | F. HOFFMANN-LA ROCHE AG (CH) | 2000-01-26 | — | — | EP | claimed |
| US-6277997-B1 | HYDROGENATING ASYMMETRICALLY 2,5-DIHYDROFURAN DERIVATIVE IN PRESENCE OF CATALYST COMPRISING METAL DIPHOSPHINE COMPLEX TO PRODUCE LACTONE DERIVATIVE | HOFFMANN-LA ROCHE INC. | 2001-08-21 | — | — | US | disclosed |
| US-6222039-B1 | REACTING LACTONE COMPOUND CONTAINING NITROGEN HETEROCYCLE WITH CYCLIC AMINE; OXIDIZING TO FORM CARBOXYLIC ACID GROUP; INTRODUCING HYDROXYLAMINE GROUP AT HYDROXYL OF CARBOXYLIC ACID GROUP | HOFFMAN-LA ROCHE INC. | 2001-04-24 | — | — | US | disclosed |
| EP-0974590-A1 | Process for the preparation of chiral lactones by asymetrical hydrogenation | F. HOFFMANN-LA ROCHE AG (CH) | 2000-01-26 | — | — | EP | disclosed |