Predicted protein targets (top 13)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MPI | P34949 | 1/20 | 0.50 |
| ▸ | PGK1 | P00558 | 1/20 | 0.48 |
| ▸ | PGK2 | P07205 | 1/20 | 0.48 |
| ▸ | PGD | P52209 | 4/20 | 0.46 |
| ▸ | LPAR1 | Q92633 | 7/20 | 0.39 |
| ▸ | LPAR4 | Q99677 | 3/20 | 0.39 |
| ▸ | LPAR5 | Q9H1C0 | 3/20 | 0.39 |
| ▸ | LPAR2 | Q9HBW0 | 3/20 | 0.39 |
| ▸ | LPAR3 | Q9UBY5 | 3/20 | 0.39 |
| ▸ | ENPP2 | Q13822 | 3/20 | 0.39 |
| ▸ | LPAR6 | P43657 | 2/20 | 0.39 |
| ▸ | CES2 | O00748 | 1/20 | 0.37 |
| ▸ | TRPV1 | Q8NER1 | 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 | |
|---|---|---|---|---|
| SCHEMBL28125367 | 0.87 | MPI (0.63) | MPIPGK1PGK2PGDLPAR1 | |
| SCHEMBL328992 | 0.87 | MPI (0.63) | MPIPGK1PGK2PGDLPAR1 | |
| SCHEMBL10709491 | 0.87 | MPI (0.63) | MPIPGK1PGK2PGDLPAR1 | |
| SCHEMBL1395698 | 0.87 | MPI (0.63) | MPIPGK1PGK2PGDLPAR1 | |
| SCHEMBL34088 | 0.87 | MPI (0.63) | MPIPGK1PGK2PGDLPAR1 | |
| Phosphoric Acid SCHEMBL11331805 | 0.86 | MPI (0.50) | MPIPGK1PGK2PGDLPAR1 | |
| Phosphoric Acid SCHEMBL7132362 | 0.86 | MPI (0.50) | MPIPGK1PGK2PGDLPAR1 | |
| Phosphoric Acid SCHEMBL615772 | 0.86 | MPI (0.50) | MPIPGK1PGK2PGDLPAR1 | |
| Phosphoric Acid SCHEMBL17103808 | 0.85 | MPI (0.61) | MPIPGK1PGK2PGDLPAR1 | |
| Phosphoric Acid SCHEMBL6754811 | 0.85 | MPI (0.61) | MPIPGK1PGK2PGDLPAR1 |
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 45 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-110914441-B | Improved process for producing isobutene from 3-methylcrotonic acid | 环球生物能源公司 | 2024-06-28 | — | — | CN | disclosed |
| EP-3622080-B1 | IMPROVED METHODS FOR PRODUCING ISOBUTENE FROM 3-METHYLCROTONIC ACID | GLOBAL BIOENERGIES (FR) | 2024-03-27 | — | — | EP | disclosed |
| CN-108779477-B | Method for producing isobutene from 3-methylcrotonyl-CoA | 环球生物能源公司 | 2022-12-13 | — | — | CN | disclosed |
| EP-3090043-B1 | 3-HYDROXYISOVALERATE (HIV) SYNTHASE VARIANTS | GLOBAL BIOENERGIES (FR) | 2022-02-02 | — | — | EP | disclosed |
| US-20210403956-A1 | METHODS FOR PRODUCING ISOBUTENE FROM 3-METHYLCROTONIC ACID | GLOBAL BIOENERGIES (FR) | 2021-12-30 | — | — | US | disclosed |
| US-11124806-B2 | Methods for producing isobutene from 3-methylcrotonic acid | GLOBAL BIOENERGIES (FR) | 2021-09-21 | — | — | US | disclosed |
| US-20210277425-A1 | IMPROVED METHODS FOR PRODUCING lSOBUTENE FROM 3-METHYLCROTONIC ACID | GLOBAL BIOENERGIES (FR) | 2021-09-09 | — | — | US | disclosed |
| CN-107075536-B | Process for producing 3-hydroxy-3-methylbutyric acid | 环球生物能源公司 | 2021-07-02 | — | — | CN | disclosed |
| CN-107075530-B | Method for producing isobutene from 3-methylcrotonyl-CoA | 环球生物能源公司 | 2021-06-01 | — | — | CN | disclosed |
| US-10941423-B2 | Method for the production of isoamyl alcohol | GLOBAL BIOENERGIES (FR) | 2021-03-09 | — | — | US | disclosed |
| WO-2015101493-A1 | 3-HYDROXYISOVALERATE (HIV) SYNTHASE VARIANTS | GLOBAL BIOENERGIES (FR) | 2015-07-09 | — | — | WO | disclosed |
| US-9017977-B2 | Method for the enzymatic production of 3-hydroxy-3-methylbutyric acid from acetone and acetyl-coa | SCIENTIST OF FORTUNE S.A. (LU) | 2015-04-28 | — | — | US | disclosed |
| EP-2478109-B1 | Method for the enzymatic production of 3-hydroxy-3-methylbutyric acid from acetone and acetyl-CoA | SCIENTIST OF FORTUNE SA (LU) | 2015-04-01 | — | — | EP | disclosed |
| US-20120220001-A1 | METHOD FOR THE ENZYMATIC PRODUCTION OF 3-HYDROXY-S-METHYLBUTYRIC ACID FROM ACETONE AND ACETYL-COA | SCIENTIST OF FORTUNE S.A. (LU) | 2012-08-30 | — | — | US | disclosed |
| EP-2478109-A1 | METHOD FOR THE ENZYMATIC PRODUCTION OF 3-HYDROXY-S-METHYLBUTYRIC ACID FROM ACETONE AND ACETYL-COA | Marlière, Philippe (BE) | 2012-07-25 | — | — | EP | disclosed |
| WO-2011032934-A1 | METHOD FOR THE ENZYMATIC PRODUCTION OF 3-HYDROXY-S-METHYLBUTYRIC ACID FROM ACETONE AND ACETYL-COA | MARLIERE PHILIPPE (FR) | 2011-03-24 | — | — | WO | disclosed |
| EP-2295593-A1 | Method for the enymatic production of 3-hydroxy-3-methylbutyric acid from acetone and acetyl-CoA | Marliere, Philippe (FR) | 2011-03-16 | — | — | EP | disclosed |
| US-7286973-B1 | Method of screening inhibitors of mevalonate-independent isoprenoid biosynthetic pathway | THE SALK INSTITUTE FOR BIOLOGICAL STUDIES (US) | 2007-10-23 | — | — | US | disclosed |
| WO-2001083769-A9 | CRYSTALLIZATION OF 4-DIPHOSPHOCYTIDYL-2-C-METHYLERYTHRITOL SYNTHESIS | SALK INST FOR BIOLOGICAL STUDI (US) | 2003-02-06 | — | — | WO | disclosed |
| WO-2001083769-A2 | CRYSTALLIZATION OF 4-DIPHOSPHOCYTIDYL-2-C-METHYLERYTHRITOL SYNTHESIS | THE SALK INSTITUTE FOR BIOLOGICAL STUDIES (US) | 2001-11-08 | — | — | WO | disclosed |