⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
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 | |
|---|---|---|---|---|
| SCHEMBL30972500 | 1.00 | — | — | |
| SCHEMBL2687087 | 1.00 | — | — | |
| SCHEMBL1405707 | 1.00 | — | — | |
| Bicarbonate SCHEMBL17054410 | 0.97 | SLC22A6 (0.63) | — | |
| SCHEMBL30641549 | 0.87 | SLC22A6 (0.57) | — | |
| SCHEMBL17204173 | 0.87 | SLC22A6 (0.57) | — | |
| SCHEMBL2227091 | 0.87 | SLC22A6 (0.57) | — | |
| SCHEMBL1135965 | 0.87 | SLC22A6 (0.57) | — | |
| SCHEMBL8893904 | 0.87 | SLC22A6 (0.57) | — | |
| SCHEMBL3371887 | 0.87 | SLC22A6 (0.57) | — |
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 709 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-112143688-B | Construction and application of recombinant escherichia coli | 鲁南制药集团股份有限公司 | 2024-05-07 | — | — | CN | claimed |
| CN-117843473-A | Preparation method of levocarnitine impurity | 常州寅盛药业有限公司 | 2024-04-09 | — | — | CN | claimed |
| CN-117843509-A | Preparation method of levocarnitine impurity | 常州寅盛药业有限公司 | 2024-04-09 | — | — | CN | claimed |
| CN-117757826-A | Recombinant expression plasmid of short-chain dehydrogenase, recombinant genetically engineered bacterium and application thereof | 浙江工业大学 | 2024-03-26 | — | — | CN | claimed |
| CN-117757690-A | Burkholderia cepacia (Burkholderia cepacia) WZ-5 and application thereof | 浙江工业大学 | 2024-03-26 | — | — | CN | claimed |
| CN-113652408-B | Carbonyl reductase mutant and application thereof in synthesis of (R) -4-chloro-3-hydroxybutyrate ethyl ester | 华东理工大学 | 2024-02-20 | — | — | CN | claimed |
| CN-117402843-A | Ketoreductase from schizosaccharomyces japonica yFS275 and application thereof | 万华化学集团股份有限公司 | 2024-01-16 | — | — | CN | claimed |
| CN-117402839-A | Ketoreductase and application thereof in preparation of (R) -4-chloro-3-hydroxybutyrate | 万华化学集团股份有限公司 | 2024-01-16 | — | — | CN | claimed |
| CN-117384868-A | Engineered ketoreductase and method for preparing chiral alcohol compounds | 宁波酶赛生物工程有限公司 | 2024-01-12 | — | — | CN | claimed |
| CN-114380706-B | Method and device for continuously preparing L-carnitine at low cost | 浙江财和生物科技有限公司 | 2024-01-09 | — | — | CN | claimed |
| US-5700670-A | TREATING MICROORGANISM CULTURE WITH ALKYL ESTER OF GAMMA-SUBSTITUTED ACETOACETIC ACID FOR STEREOSPECIFIC REDUCTION OF CARBONYL GROUP TO HYDROXYL GROUP YIELDS GAMMA-SUBSTITUTED 3-HYDROXYBUTYRIC ACID | MITSUBISHI CHEMICAL CORPORATION (JP) | 1997-12-23 | — | — | US | claimed |
| US-5614641-A | USING A PHOSPHINO-CONTAINING RUTHENIUM COMPLEX AS CATALYST | ELF AQUITAINE (FR) | 1997-03-25 | — | — | US | claimed |
| EP-0648201-B1 | ENANTIOSELECTIVE HYDROGENATION OF THE CARBONYL BOND USING RUTHENIUM COMPLEXES WITH BIPHOSPHINE LIGANDS | ELF AQUITAINE (FR) | 1997-01-22 | — | — | EP | claimed |
| EP-0737751-A2 | Method for producing optically active ester of gamma-substituted-beta-hydroxybutyric acid | Mitsubishi Chemical Corporation (JP) | 1996-10-16 | — | — | EP | claimed |
| EP-0648201-A1 | Enantioselective hydrogenation of the carbonyl bond using ruthenium complexes with biphosphine ligands. | ELF AQUITAINE (FR) | 1995-04-19 | — | — | EP | claimed |
| WO-1994001390-A1 | ENANTIOSELECTIVE CARBONYL GROUP HYDROGENATION METHOD USING RUTHENIUM/DIPHOSPHINE LIGAND COMPLEXES | ELF AQUITAINE (FR) | 1994-01-20 | — | — | WO | claimed |
| EP-0288994-B1 | PROCESS FOR PRODUCING OPTICALLY ACTIVE COMPOUNDS | Chisso Corporation (JP) | 1992-07-22 | — | — | EP | claimed |
| EP-0223328-B1 | PROCESS FOR PRODUCING OXIRACETAM | DENKI KAGAKU KOGYO KABUSHIKI KAISHA (JP) | 1992-01-29 | — | — | EP | claimed |
| US-4962031-A | SPECIFIC COMPOUNDS HAVING HYDROXYL GROUPS REACTED WITH ESTERS IN PRESENCE OF HYDROLASES | CHISSO CORPORATION (JP) | 1990-10-09 | — | — | US | claimed |
| EP-0288994-A2 | Process for producing optically active compounds | Chisso Corporation (JP) | 1988-11-02 | — | — | EP | claimed |