⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL28204570 | 0.81 | — | — | |
| SCHEMBL38438 | 0.81 | — | — | |
| SCHEMBL27559008 | 0.78 | — | — | |
| SCHEMBL2162560 | 0.78 | — | — | |
| SCHEMBL18730920 | 0.78 | — | — | |
| Methacrylic Acid SCHEMBL5879314 | 0.77 | FFAR3 (0.32) | — | |
| SCHEMBL6885496 | 0.76 | TSHR (0.31) | — | |
| SCHEMBL11698960 | 0.76 | — | — | |
| SCHEMBL11698965 | 0.76 | — | — | |
| Vinyl Chloride SCHEMBL10468846 | 0.74 | TSHR (0.30) | — |
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 26 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-116925413-A | Anticoagulant biological material and preparation method thereof | 上海鸿脉医疗科技有限公司 | 2023-10-24 | — | — | CN | claimed |
| US-20060246564-A1 | Immobilized biological material with improved functionality and method for producing the same | CO2 SOLUTION INC. (CA) | 2006-11-02 | — | — | US | claimed |
| CN-116925413-A | Anticoagulant biological material and preparation method thereof | 上海鸿脉医疗科技有限公司 | 2023-10-24 | — | — | CN | disclosed |
| US-20230279016-A1 | Tetrahydropyrazolopyrimidines and Related Analogs for Inhibiting YAP/TAZ-TEAD | CISTIM LEUVEN VZW (BE) | 2023-09-07 | — | — | US | disclosed |
| US-20220340893-A1 | BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES | NUEVOLUTION A/S (DK) | 2022-10-27 | — | — | US | disclosed |
| US-8946144-B2 | Phosphonated glycopeptide and lipoglycopeptide antibiotics and uses thereof for the prevention and treatment of bone and joint infections | THE MEDICINES COMPANY (US) | 2015-02-03 | — | — | US | disclosed |
| CN-103429318-A | C02 treatments using enzymatic particles sized according to reactive liquid film thickness for enhanced catalysis | CO2 SOLUTION INC | 2013-12-04 | — | — | CN | disclosed |
| WO-2012103653-A1 | C02 TREATMENTS USING ENZYMATIC PARTICLES SIZED ACCORDING TO REACTIVE LIQUID FILM THICKNESS FOR ENHANCED CATALYSIS | CO2 SOLUTIONS INC. (CA) | 2012-08-09 | — | — | WO | disclosed |
| US-7723522-B2 | Pyridine derivative production method | FUJIFILM FINECHEMICALS CO., LTD (JP) | 2010-05-25 | — | — | US | disclosed |
| US-7723522-B2 | Pyridine derivative production method | FUJIFILM FINECHEMICALS CO., LTD (JP) | 2010-05-25 | — | — | US | disclosed |
| US-7723522-B2 | Pyridine derivative production method | FUJIFILM FINECHEMICALS CO., LTD (JP) | 2010-05-25 | — | — | US | disclosed |
| EP-1559711-A1 | PREPARATION OF PYRIDINE DERIVATIVES USING PYRIMIDINIUM DERIVATIVES AS INTERMEDIATES | Sankio Chemical Co., Ltd. (JP) | 2005-08-03 | — | — | EP | disclosed |
| US-5424323-A | An antiseptic aqueous concentrate solution comsisting of two quaternary ammonium compounds, one dialdehyde and at least one aliphatic hydroxyl compound; microbiocides for nonabsorbent surfaces such as metal, ceramics, wood, medical equipment | CETYLITE INDUSTRIES, INC. (US) | 1995-06-13 | — | — | US | disclosed |
| US-5407949-A | Biocide for killing bacteria, spores, fungi and viruses having two heterocyclic quaternary compounds, a dialdehyde and alcohol | CETYLITE INDUSTRIES, INC. (US) | 1995-04-18 | — | — | US | disclosed |
| US-5344838-A | Quaternary ammonium compounds, dialdehyde, alcohol | CETYLITE INDUSTRIES, INC. (US) | 1994-09-06 | — | — | US | disclosed |
| US-5338748-A | Storage stable aqueous mixture of heterocyclic and aliphatic quaternary ammonium compounds, aliphatic dialdehydes and aliphatic hydroxyl compounds | CETYLITE INDUSTRIES, INC. (US) | 1994-08-16 | — | — | US | disclosed |
| US-5124359-A | At least one quaternary ammonium compound, aliphatic dialdehyde, and aliphatic hydroxyl compound; nonabsorbent surfaces; medical equipment | CETYLITE INDUSTRIES, INC. (US) | 1992-06-23 | — | — | US | disclosed |
| EP-0168761-B1 | PROCESS FOR THE PRODUCTION OF 2-METHYL-2-ALKENALS FROM DIHYDROPYRANES | BASF Aktiengesellschaft (DE) | 1987-04-01 | — | — | EP | disclosed |
| EP-0168761-A1 | Process for the production of 2-methyl-2-alkenals from dihydropyranes | BASF Aktiengesellschaft (DE) | 1986-01-22 | — | — | EP | disclosed |
| US-4220795-A | MODIFIERS OF SMOOTH MUSCLE ACTIVITY, PLATELET ANTIAGGREGATING AGENTS, GASTRIC ANTISCRETORY AGENTS, BRONCHODILATORS | MILES LABORATORIES, INC. (US) | 1980-09-02 | — | — | US | disclosed |