⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL7719583 | 0.97 | GPR84 (0.55) | — | |
| SCHEMBL19382202 | 0.97 | GPR84 (0.55) | — | |
| SCHEMBL2514471 | 0.97 | GPR84 (0.55) | — | |
| SCHEMBL2745492 | 0.97 | GPR84 (0.55) | — | |
| SCHEMBL49642 | 0.97 | — | — | |
| SCHEMBL18823640 | 0.97 | GPR84 (0.55) | — | |
| SCHEMBL4558847 | 0.97 | GPR84 (0.55) | — | |
| SCHEMBL805230 | 0.97 | GPR84 (0.55) | — | |
| SCHEMBL18619738 | 0.97 | GPR84 (0.55) | — | |
| SCHEMBL5317211 | 0.97 | GPR84 (0.55) | — |
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 36 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20260049264-A1 | CHEMICAL SOLUTION AND CHEMICAL SOLUTION-HOUSING ARTICLE | FUJIFILM CORP (JP) | 2026-02-19 | — | — | US | disclosed |
| US-20250151740-A1 | COMPOSITION FOR PREVENTING FUNGAL SPOILAGE IN POST-HARVEST FRUITS, VEGETABLES AND FLOWERS, METHOD AND USE THEREOF | BIOBAB R&D, S.L. (ES) | 2025-05-15 | — | — | US | disclosed |
| CN-116199806-B | Coordination precipitation polymerization method for olefin polymerization and obtained polyolefin | 中国石油化工股份有限公司 | 2025-05-06 | — | — | CN | disclosed |
| CN-116217759-B | Coordination precipitation polymerization method for olefin polymerization and obtained polyolefin | 中国石油化工股份有限公司 | 2025-02-28 | — | — | CN | disclosed |
| US-20250011274-A1 | USE OF 1-(4- TERT- BUTYL CYCLOHEXYL) PROPYL ACETATE AS AROMA INGREDIENT | BASF SE (DE) | 2025-01-09 | — | — | US | disclosed |
| WO-2024237109-A1 | CHEMICAL SOLUTION AND CHEMICAL-SOLUTION-ACCOMMODATING BODY | 富士フイルム株式会社 | 2024-11-21 | — | — | WO | disclosed |
| US-20240334945-A1 | FLAXSEED PLANT MILK WITH GOOD FLAVOR, SELF-STABILIZATION AND FUNCTIONAL ACTIVITY BASED ON INTERFACE CONTROL AND PREPARATION METHOD AND APPLICATION THEREOF | OIL CROPS RESEARCH INSTITUTE, CHINESE ACADEMY OF AGRICULTURAL SCIENCES (CN) | 2024-10-10 | — | — | US | disclosed |
| CN-116831117-A | Mountain Mao Ding moth sex pheromone attractant and application thereof | 中国林业科学研究院森林生态环境与自然保护研究所(国家林业和草原局世界自然遗产保护研究中心) | 2023-10-03 | — | — | CN | disclosed |
| US-11744273-B2 | Sweetness enhancing volatile compositions and methods of increasing perceived sweetness of a comestible | UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED (US) | 2023-09-05 | — | — | US | disclosed |
| EP-3253752-B1 | [9,10-DIMETHOXY-3-(2-METHYLPROPYL)-1H,2H,3H,4H,6H,7H,11BH-PYRIDO-[2,1-A]ISOQUINOLIN-2-YL]METHANOL AND COMPOUNDS, COMPOSITIONS AND METHODS RELATING THERETO | NEUROCRINE BIOSCIENCES INC (US) | 2023-08-16 | — | — | EP | disclosed |
| US-7588828-B2 | Preparation of nanoparticle materials | NANOCO TECHNOLOGIES LIMITED (GB) | 2009-09-15 | — | — | US | disclosed |
| EP-1828240-B1 | NOVEL MULTIMERIC CD40 LIGANDS, METHOD FOR PREPARING SAME AND USE THEREOF FOR PREPARING DRUGS | CENTRE NAT RECH SCIENT (FR) | 2009-07-29 | — | — | EP | disclosed |
| WO-2009047343-A1 | BENZOCYCLOHEPTENE DERIVATIVES AS ESTROGENS HAVING SELECTIVE ACTIVITY | BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) | 2009-04-16 | — | — | WO | disclosed |
| EP-1987808-A1 | Composition for care and/or make-up removal of keratinous material(s) | L'OREAL (FR) | 2008-11-05 | — | — | EP | disclosed |
| EP-1962792-A1 | COSMETIC AGENTS HAVING INCREASED FRAGRANCE INTENSITY AND PERSISTENCE | Henkel AG & Co. KGaA (DE) | 2008-09-03 | — | — | EP | disclosed |
| US-20080160306-A1 | Conversion of a precursor composition to nanoparticles is effected in the presence of a molecular cluster compound where molecules of cluster compound act as seed or nucleation point upon which nanoparticle growth may be initiated; high-temperature nucleation step is not required | NANOCO TECHNOLOGIES LIMITED (GB) | 2008-07-03 | — | — | US | disclosed |
| WO-2007068339-A1 | COSMETIC AGENTS HAVING INCREASED FRAGRANCE INTENSITY AND PERSISTENCE | HENKEL AG & CO. KGAA (DE) | 2007-06-21 | — | — | WO | disclosed |
| US-4397779-A | RADIOIMMUNOASSAY OF THEOPHYLLINE AND DERIVATIVES; IODINATION | BAXTER TRAVENOL LABORATORIES, INC. (US) | 1983-08-09 | — | — | US | disclosed |
| US-4297494-A | Xanthine tracers | BAXTER TRAVENOL LABORATORIES, INC. (US) | 1981-10-27 | — | — | US | disclosed |
| US-4244939-A | RADIOIMMUNOASSAY | BAXTER TRAVENOL LABORATORIES, INC. (US) | 1981-01-13 | — | — | US | disclosed |