⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL27283 | 1.00 | — | — | |
| SCHEMBL29004152 | 0.74 | — | — | |
| SCHEMBL7780990 | 0.71 | — | — | |
| SCHEMBL10524387 | 0.71 | — | — | |
| SCHEMBL28519075 | 0.71 | — | — | |
| SCHEMBL1891164 | 0.71 | — | — | |
| SCHEMBL15338800 | 0.71 | — | — | |
| SCHEMBL7780988 | 0.71 | — | — | |
| SCHEMBL1891166 | 0.71 | — | — | |
| SCHEMBL10524391 | 0.71 | — | — |
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 43 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118719009-B | Chromatography medium modification method | 山东微领生物有限公司 | 2025-02-14 | — | — | CN | claimed |
| CN-118719009-A | Novel chromatography medium modification method | 山东微领生物有限公司 | 2024-10-01 | — | — | CN | claimed |
| US-20250179066-A1 | ZWITTERIONIC ANTIBACTERIAL COMPOUNDS | HOFFMANN-LA ROCHE INC. (US) | 2025-06-05 | — | — | US | disclosed |
| CN-118719009-B | Chromatography medium modification method | 山东微领生物有限公司 | 2025-02-14 | — | — | CN | disclosed |
| CN-118719009-A | Novel chromatography medium modification method | 山东微领生物有限公司 | 2024-10-01 | — | — | CN | disclosed |
| CN-110551069-B | Synthesis method of 5-phenylpentanol compound and intermediate thereof | 中国科学院上海有机化学研究所 | 2022-10-04 | — | — | CN | disclosed |
| US-20220281871-A1 | Pyrazolo[1,5-A][1,3,5]Triazine and Pyrazolo[1,5-A]Pyrimidine Derivatives as CDK Inhibitors | AURIGENE DISCOVERY TECHNOLOGIES LIMITED (IN) | 2022-09-08 | — | — | US | disclosed |
| EP-2508521-B2 | Method for the production of amino crotonyl compounds | BOEHRINGER INGELHEIM INT (DE) | 2022-09-07 | — | — | EP | disclosed |
| EP-3981766-A1 | INDAZOLE DERIVATIVES USEFUL IN THE TREATMENT OF CANCER | Eisai R&D Management Co., Ltd. (JP) | 2022-04-13 | — | — | EP | disclosed |
| US-10851065-B2 | Tetrasubstituted alkene compounds and their use | EISAI R&D MANAGEMENT CO., LTD. (JP) | 2020-12-01 | — | — | US | disclosed |
| CN-105175331-B | A kind of preparation method of the molecular targeted anti-tumor drug of EGFR class | 江苏苏中药业集团股份有限公司 | 2019-04-26 | — | — | CN | disclosed |
| US-6379935-B1 | USING MICROORGANISMS | SHOWA DENKO KABUSHIKI KAISHA (JP) | 2002-04-30 | — | — | US | disclosed |
| US-20020031811-A1 | Method of producing alpha-halo-alpha, beta-saturated carbonyl compounds | SHOWA DENKO K.K. | 2002-03-14 | — | — | US | disclosed |
| US-20020028491-A1 | METHOD OF PRODUCING ALPHA-HALO-ALPHA, BETA-SATURATED CARBONYL COMPOUNDS FROM THE CORRESPONDING ALPHA, BETA UNSURATED COMPOUNDS | SHOWA DENKO KABUSHIKI KAISHA (JP) | 2002-03-07 | — | — | US | disclosed |
| EP-1091958-A1 | SALTS OF PAROXETINE | SMITHKLINE BEECHAM PLC (GB) | 2001-04-18 | — | — | EP | disclosed |
| US-6184415-B1 | ASYMMETRIC HYDROGENATION OF A 2-HALO(ELECTRONEGATIVE)ALKENOIC ACID/SALT (2-HALOACRYLIC ACID OR SALT), USING AN ENANTIOMETRICAL RICHED CATALYST OF 2,2'-BIS(DIARYLPHOSPHINO-PHINO-1,1'-BINAPHTHYL COMPLEX OF RUTHENIUM; HALIDE PROMOTERS | ALBEMARLE CORPORATION | 2001-02-06 | — | — | US | disclosed |
| EP-0979877-A2 | Method of producing alpha-halo-alpha, beta-saturated carbonyl compounds | SHOWA DENKO KABUSHIKI KAISHA (JP) | 2000-02-16 | — | — | EP | disclosed |
| WO-2000001692-A1 | SALTS OF PAROXETINE | SMITHKLINE BEECHAM PLC (GB) | 2000-01-13 | — | — | WO | disclosed |
| US-5717128-A | HEATING AN ESTER OF 2-HYDROXY-2-METHYL-3-BUTENOIC ACID WITH PHOSPHOROUS BROMIDE OR CHLORIDE; THEN WITH TRIALKYL ESTER OF PHOSPHOROUS ACID | BASF AKTIENGESELLSCHAFT (DE) | 1998-02-10 | — | — | US | disclosed |
| US-H327-H | Nematicidal alkenanilides | FMC CORPORATION (US) | 1987-09-01 | — | — | US | disclosed |