⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL1869849 | 0.74 | — | — | |
| SCHEMBL15616505 | 0.70 | — | — | |
| SCHEMBL16221486 | 0.70 | — | — | |
| SCHEMBL3690276 | 0.70 | — | — | |
| SCHEMBL8010637 | 0.70 | — | — | |
| SCHEMBL4394690 | 0.70 | — | — | |
| SCHEMBL6832917 | 0.70 | — | — | |
| SCHEMBL18360098 | 0.70 | — | — | |
| SCHEMBL9984 | 0.67 | — | — | |
| SCHEMBL14534759 | 0.67 | — | — |
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
Appears in 3664 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122079867-A | Synthesis method of chiral delta-caprolactam compound | — | 2026-05-26 | — | — | CN | claimed |
| CN-120137738-A | Compositions comprising iodofluorocarbons | 阿科玛法国公司 | 2025-06-13 | — | — | CN | claimed |
| EP-4567086-A1 | REFRIGERATION CYCLE WORKING MEDIUM AND REFRIGERATION CYCLE SYSTEM | Panasonic Intellectual Property Management Co., Ltd. (JP) | 2025-06-11 | — | — | EP | claimed |
| CN-119977753-A | Process for producing iodofluorocarbon compounds | 阿科玛法国公司 | 2025-05-13 | — | — | CN | claimed |
| CN-119954594-A | Process for producing iodofluorocarbon compounds | 阿科玛法国公司 | 2025-05-09 | — | — | CN | claimed |
| CN-119954592-A | Process for producing iodofluorocarbon compounds | 阿科玛法国公司 | 2025-05-09 | — | — | CN | claimed |
| CN-114349774-B | Preparation method of bicyclo [1.1.1] amyl angular borate compound | 凯美克(上海)医药科技有限公司 | 2024-06-04 | — | — | CN | claimed |
| WO-2024111308-A1 | COMPOSITION CONTAINING FLUOROIODOALKANE | 東ソー株式会社 | 2024-05-30 | — | — | WO | claimed |
| US-20240130361-A1 | NONFLAMMABLE LIQUID COMPOSITION AND ITS APPLICATIONS | TOSOH CORPORATION (JP) | 2024-04-25 | — | — | US | claimed |
| CN-115650990-B | Fluorine-containing near infrared absorption cationic phthalocyanine and preparation method thereof | 常州大学 | 2024-03-19 | — | — | CN | claimed |
| EP-0708087-A1 | Method for making a substituted benzene compound | ROHM AND HAAS COMPANY (US) | 1996-04-24 | — | — | EP | claimed |
| EP-0700953-A2 | Thermal insulating foamed material and method for manufacturing the same | MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) | 1996-03-13 | — | — | EP | claimed |
| EP-0649887-A2 | Water-repellant and antiseptic coating composition | DOW CORNING ASIA, Ltd. (JP) | 1995-04-26 | — | — | EP | claimed |
| EP-0493412-A1 | METHOD OF DISSOLVING CHOLESTEROL-RICH CALCULI WITH SHORT CHAIN HALOGENATED ORGANIC SOLVENTS AND COSOLVENTS | BAXTER INTERNATIONAL INC. (US) | 1992-07-08 | — | — | EP | claimed |
| WO-1991003146-A2 | METHOD OF DISSOLVING CHOLESTEROL-RICH CALCULI WITH SHORT CHAIN HALOGENATED ORGANIC SOLVENTS AND COSOLVENTS | BAXTER INTERNATIONAL INC. (US) | 1991-03-21 | — | — | WO | claimed |
| US-4994025-A | Dissolving solvent using halogenated solvent | BAXTER INTERNATIONAL INC. (US) | 1991-02-19 | — | — | US | claimed |
| CN-1045771-A | Toluylic acid trifluoro ethyl ester that replaces and preparation method thereof and the application on sterilant | SCHERING AG (DE) | 1990-10-03 | — | — | CN | claimed |
| EP-0070198-B1 | RADIATION-SENSITIVE COMPOSITION AND PATTERN-FORMATION METHOD USING THE SAME | Hitachi, Ltd. (JP) | 1985-06-19 | — | — | EP | claimed |
| EP-0070198-A1 | Radiation-sensitive composition and pattern-formation method using the same | Hitachi, Ltd. (JP) | 1983-01-19 | — | — | EP | claimed |
| US-4257860-A | Deuterium enrichment by selective photoinduced dissociation of a multihalogenated organic compound | THE UNITED STATES OF AMERICA AS REPRESENTED BY THE UNITED STATES DEPARTMENT OF ENERGY (US) | 1981-03-24 | — | — | US | claimed |