⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL857124 | 1.00 | — | — | |
| SCHEMBL22708 | 1.00 | — | — | |
| Water SCHEMBL28084183 | 0.97 | — | — | |
| Cyclohexanone SCHEMBL28845315 | 0.93 | ALDH1A1 (0.50) | — | |
| SCHEMBL14066006 | 0.92 | — | — | |
| SCHEMBL105656 | 0.92 | — | — | |
| SCHEMBL9490715 | 0.91 | TRIM24 (0.38) | — | |
| SCHEMBL24304032 | 0.90 | KMT2A (0.54) | — | |
| SCHEMBL2196645 | 0.90 | KMT2A (0.54) | — | |
| SCHEMBL230871 | 0.90 | KMT2A (0.54) | — |
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 295 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-114317624-B | Method for synthesizing poly- (R) -5-methyl-epsilon-caprolactone by utilizing micro-channel reaction device through three-enzyme catalysis | 南京工业大学 | 2024-05-07 | — | — | CN | claimed |
| CN-114317624-A | Method for synthesizing poly- (R) -5-methyl-epsilon-caprolactone by three-enzyme catalysis by using microchannel reaction device | 南京工业大学 | 2022-04-12 | — | — | CN | claimed |
| EP-1015415-B1 | NOVEL STEREOSELECTIVE PROCESSES FOR THE PREPARATION OF GABAPENTIN ANALOGUES | WARNER LAMBERT CO (US) | 2003-05-07 | — | — | EP | claimed |
| JP-8245668-A | — | — | None | — | — | JP | disclosed |
| US-20260043010-A1 | ENONE REDUCTASES | CODEXIS, INC. (US) | 2026-02-12 | — | — | US | disclosed |
| US-12371674-B2 | Enone reductases | CODEXIS, INC. (US) | 2025-07-29 | — | — | US | disclosed |
| US-20250171431-A1 | HETEROCYCLIC INHIBITORS OF IGF-1R FOR TREATMENT OF DISEASE | HORIZON THERAPEUTICS IRELAND DAC (IE) | 2025-05-29 | — | — | US | disclosed |
| WO-2025030163-A1 | HETEROCYCLIC INHIBITORS OF IGF-1R FOR TREATMENT OF DISEASE | HORIZON THERAPEUTICS IRELAND DAC (IE) | 2025-02-06 | — | — | WO | disclosed |
| US-20240218002-A1 | PHOSPHINE-UREA LIGANDS FOR TRANSITION METAL CATALYZED CROSS-COUPLING REACTIONS | THE TEXAS A&M UNIVERSITY SYSTEM (US) | 2024-07-04 | — | — | US | disclosed |
| CN-114317624-B | Method for synthesizing poly- (R) -5-methyl-epsilon-caprolactone by utilizing micro-channel reaction device through three-enzyme catalysis | 南京工业大学 | 2024-05-07 | — | — | CN | disclosed |
| WO-2023250316-A1 | COMPOUNDS FOR TREATING SPINOCEREBELLAR ATAXIA TYPE 3 | PTC THERAPEUTICS, INC. (US) | 2023-12-28 | — | — | WO | disclosed |
| US-5162586-A | Catalyst complex containing copper, a disubstituted aminetroponeimine chelating ligand and an organometallic reagent | MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) | 1992-11-10 | — | — | US | disclosed |
| EP-0479970-A1 | ANTIMALARIAL ANALOGS OF ARTEMISININ | SRI INTERNATIONAL (US) | 1992-04-15 | — | — | EP | disclosed |
| WO-1991014689-A1 | ANTIMALARIAL ANALOGS OF ARTEMISININ | SRI INTERNATIONAL (US) | 1991-10-03 | — | — | WO | disclosed |
| US-4962214-A | COPPER AMINOTROPONEIMINE COMPLEX CATALYSTS | MASSACHUSETTES INSTITUTE OF TECHNOLOGY (US) | 1990-10-09 | — | — | US | disclosed |
| WO-1989010916-A1 | ENANTIOSELECTIVE ADDITION OF HYDROCARBONS TO ALPHA,BETA-UNSATURATED CARBONYL COMPOUNDS | MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) | 1989-11-16 | — | — | WO | disclosed |
| WO-1989009209-A1 | PIPERIDINE RING MODIFIED PHENCYCLIDINE ANALOGS AS ANTICONVULSANTS | MARION LABORATORIES, INC. (US) | 1989-10-05 | — | — | WO | disclosed |
| EP-0067517-B1 | PROCESS FOR THE PREPARATION OF AN ENANTIOMER OF A BETA-LACTAM DERIVATIVE | BEECHAM GROUP PLC (GB) | 1986-02-26 | — | — | EP | disclosed |
| US-4443599-A | 8-Oxo-3-oxa-1-azabicyclo[4.2.0]octanes containing a chiral center | BEECHAM GROUP P.L.C. (GB) | 1984-04-17 | — | — | US | disclosed |
| EP-0067517-A1 | Process for the preparation of an enantiomer of a beta-lactam derivative | BEECHAM GROUP PLC (GB) | 1982-12-22 | — | — | EP | disclosed |