⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL18760074 | 1.00 | — | — | |
| SCHEMBL27646 | 1.00 | — | — | |
| Methane SCHEMBL7940021 | 0.93 | — | — | |
| Methane SCHEMBL6180360 | 0.87 | — | — | |
| SCHEMBL18897676 | 0.82 | ALDH1A1 (0.89) | — | |
| Methyl Alcohol SCHEMBL3851435 | 0.82 | — | — | |
| SCHEMBL21841873 | 0.82 | ALDH1A1 (0.89) | — | |
| SCHEMBL22129611 | 0.82 | — | — | |
| Benzene SCHEMBL3778558 | 0.82 | ALDH1A1 (0.42) | — | |
| SCHEMBL22374 | 0.82 | — | — |
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 1480 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-120136654-A | Method for preparing bicyclopropyl high-energy fuel by catalyzing olefin with ionic liquid | 河南大学 | 2025-06-13 | — | — | CN | claimed |
| CN-119326166-A | Passion fruit flavor essence, electronic cigarette tobacco tar comprising same and application | 比亚迪精密制造有限公司 | 2025-01-21 | — | — | CN | claimed |
| EP-4431504-A1 | AROMATIC HETEROCYCLIC COMPOUND AND APPLICATION THEREOF | Shanghai Institute of Material Medica, Chinese Academy of Sciences (CN) | 2024-09-18 | — | — | EP | claimed |
| CN-118388307-A | Method for synthesizing bicyclopropenyl high-energy fuel with high selectivity | 龙子湖新能源实验室 | 2024-07-26 | — | — | CN | claimed |
| WO-2024146632-A1 | TETRAHYDROTHIOPHENE DERIVATIVE AND USE THEREOF IN MEDICINE | 西藏海思科制药有限公司 | 2024-07-11 | — | — | WO | claimed |
| CN-118146224-A | Nitrogen-containing tricyclic derivative and application thereof in medicine | 西藏海思科制药有限公司 | 2024-06-07 | — | — | CN | claimed |
| WO-2024109799-A1 | PYRIMIDINE DERIVATIVE AND APPLICATION THEREOF IN MEDICINE | 西藏海思科制药有限公司 | 2024-05-30 | — | — | WO | claimed |
| WO-2024105018-A1 | NOVEL PYRROLO[1,2-d][1,2,4]TRIAZINONE DERIVATIVES AS NEGATIVE ALLOSTERIC MODULATORS OF MGLU7 RECEPTORS | ADDEX PHARMA S.A. (CH) | 2024-05-23 | — | — | WO | claimed |
| US-20240051949-A1 | HETEROCYCLE DERIVATIVES FOR TREATING TRPM3 MEDIATED DISORDERS | UNIV LEUVEN KATH (BE) | 2024-02-15 | — | — | US | claimed |
| WO-2024012570-A1 | NITROGEN-CONTAINING HETEROCYCLIC DERIVATIVE, AND COMPOSITION AND PHARMACEUTICAL USE THEREOF | 西藏海思科制药有限公司 | 2024-01-18 | — | — | WO | claimed |
| US-5945557-A | PHENYL DERIVATIVES WHICH POSSESS A SUBSTITUTED CYCLOPROPYL MOIETY; USEFUL AGAINST POWDERY MILDEW, BLIGHT AND OTHER PLATN DISEASES; INSECTICIDES AGAINST SOUTHERN ARMYWORM, MEXICAN BEAN BEETLE AND SPIDER MITES, FOR EXAMPLE | ROHM AND HAAS COMPANY (US) | 1999-08-31 | — | — | US | claimed |
| EP-0924197-A1 | Substituted cyclopropyl phenoxymethyl phenyl carbamates and their use as fungicides | ROHM AND HAAS COMPANY (US) | 1999-06-23 | — | — | EP | claimed |
| EP-0889024-A1 | Benzyloxy substituted aromatics and their use as fungicides and insecticides | ROHM AND HAAS COMPANY (US) | 1999-01-07 | — | — | EP | claimed |
| CN-1034216-C | 7-(substituted)-9-[(substituted glycyl) amido]-6-demethyl-6-deoxytetracyclines | AMERICAN CYANAMID CO (US) | 1997-03-12 | — | — | CN | claimed |
| CN-1033971-C | 9-[(substituted glycyl) amido]-6-demethyl-6-deoxytetracyclines | AMERICAN CYANAMID CO (US) | 1997-02-05 | — | — | CN | claimed |
| CN-1033087-C | Novel 7-(substituted)-8-(substituted-9-[(substituted glycyl) amido]-6-demethyl-6-deoxytetracyclines | AMERICAN CYANAMID CO (US) | 1996-10-23 | — | — | CN | claimed |
| EP-0432132-B1 | A method for preparation of mono- and diisopropylnaphthalenes | TOSOH CORP (JP) | 1993-12-08 | — | — | EP | claimed |
| US-5026941-A | Catalytic alkylation of naphthalene and/or 2-isopropyl-naphthalene in the presence of a saturated polycarbocyclic compound to yield 2,6- and 2,7-diisopropylnaphthalene | TOSHO CORPORATION (JP) | 1991-06-25 | — | — | US | claimed |
| EP-0432132-A1 | A method for preparation of mono- and diisopropylnaphthalenes | Tosoh Corporation (JP) | 1991-06-12 | — | — | EP | claimed |
| EP-0338292-A1 | A Method for the Preparation of Diisopropyluaphthalenes | Tosoh Corporation (JP) | 1989-10-25 | — | — | EP | claimed |