⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL15392061 | 0.91 | CA2 (0.35) | — | |
| SCHEMBL6057097 | 0.87 | — | — | |
| SCHEMBL26034551 | 0.86 | ALDH1A1 (0.32) | — | |
| SCHEMBL2452477 | 0.84 | MEN1 (0.33) | — | |
| SCHEMBL13309715 | 0.80 | ALDH1A1 (0.39) | — | |
| SCHEMBL6241122 | 0.79 | — | — | |
| SCHEMBL19214405 | 0.76 | — | — | |
| SCHEMBL251442 | 0.76 | ALDH1A1 (0.33) | — | |
| SCHEMBL1154 | 0.76 | — | — | |
| SCHEMBL17333164 | 0.73 | — | — |
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 1389 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117820389-A | Preparation method of 5'-O-DMTr-2' -O-MOE-5-methyluridine | 康羽生命科学技术(苏州)有限公司 | 2024-04-05 | — | — | CN | claimed |
| CN-114122259-A | Perovskite thin-film solar cell and preparation method thereof | 杭州纤纳光电科技有限公司 | 2022-03-01 | — | — | CN | claimed |
| CN-122081865-A | Evaporation boat, preparation method thereof and application of evaporation boat in preparation of current collector | — | 2026-05-26 | — | — | CN | disclosed |
| CN-122061108-A | Evaporation boat suitable for preparing current collector, and preparation method and application thereof | 扬州纳力新材料科技股份有限公司 | 2026-05-19 | — | — | CN | disclosed |
| CN-117820389-A | Preparation method of 5'-O-DMTr-2' -O-MOE-5-methyluridine | 康羽生命科学技术(苏州)有限公司 | 2024-04-05 | — | — | CN | disclosed |
| CN-117820389-A | Preparation method of 5'-O-DMTr-2' -O-MOE-5-methyluridine | 康羽生命科学技术(苏州)有限公司 | 2024-04-05 | — | — | CN | disclosed |
| CN-108341951-B | Dynamic polymer with hybrid cross-linked structure and application thereof | 厦门天策材料科技有限公司 | 2023-06-20 | — | — | CN | disclosed |
| CN-111386118-B | Combination pharmaceutical agents as RSV inhibitors | 英安塔制药有限公司 | 2023-05-09 | — | — | CN | disclosed |
| CN-114835765-B | Synthesis process of 2' -O- (2-methoxyethyl) guanosine | 奥锐特药业(天津)有限公司 | 2022-11-08 | — | — | CN | disclosed |
| CN-114835765-A | 2 a , Synthesis process of (E) -O- (2-methoxyethyl) guanosine | 奥锐特药业(天津)有限公司 | 2022-08-02 | — | — | CN | disclosed |
| CN-108200760-B | Benzodiazepine derivatives as RSV inhibitors | 英安塔制药有限公司 | 2022-04-01 | — | — | CN | disclosed |
| WO-1998026028-A1 | FUEL COMPOSITIONS EXHIBITING IMPROVED FUEL STABILITY | ORR WILLIAM C (US) | 1998-06-18 | — | — | WO | disclosed |
| EP-0813539-A1 | IMPROVED PROCESS FOR THE SYNTHESIS OF 2'-O-SUBSTITUTED PYRIMIDINES AND OLIGOMERIC COMPOUNDS THEREFROM | ISIS PHARMACEUTICALS, INC. (US) | 1997-12-29 | — | — | EP | disclosed |
| WO-1997030067-A1 | SUGAR-MODIFIED GAPPED OLIGONUCLEOTIDES | ISIS PHARMACEUTICALS, INC. (US) | 1997-08-21 | — | — | WO | disclosed |
| WO-1997029780-A1 | METHOXYETHOXY OLIGONUCLEOTIDES FOR MODULATION OF PROTEIN KINASE C EXPRESSION | ISIS PHARMACEUTICALS, INC. (US) | 1997-08-21 | — | — | WO | disclosed |
| WO-1996027606-A1 | IMPROVED PROCESS FOR THE SYNTHESIS OF 2'-O-SUBSTITUTED PYRIMIDINES AND OLIGOMERIC COMPOUNDS THEREFROM | ISIS PHARMACEUTICALS, INC. (US) | 1996-09-12 | — | — | WO | disclosed |
| US-5004789-A | Prepreg Mats Containing Phenolic Resin And An Additive Of Triethanolamine Borate Or An Amine And Boric Acid Or Anhydride Mixture | SOCIETE CHIMIQUES DES CHARBONNAGES S.A. (FR) | 1991-04-02 | — | — | US | disclosed |
| EP-0249517-A1 | Use of resinous compositions based on phenolic resins | CRAY VALLEY SA (FR) | 1987-12-16 | — | — | EP | disclosed |
| EP-0145518-A1 | Derivatives of polycarbons, their manufacture and their use in chemistry and electrochemistry | CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) | 1985-06-19 | — | — | EP | disclosed |
| EP-0031537-A1 | Process for preparing oxiranes | BAYER AG (DE) | 1981-07-08 | — | — | EP | disclosed |