⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL2109116 | 0.92 | TDP1 (0.47) | — | |
| SCHEMBL3681605 | 0.88 | TDP1 (0.44) | — | |
| Butane SCHEMBL7265784 | 0.87 | TDP1 (0.37) | — | |
| SCHEMBL94190 | 0.82 | — | — | |
| SCHEMBL6303961 | 0.78 | TDP1 (0.50) | — | |
| Hydrogen Peroxide SCHEMBL1086229 | 0.78 | TDP1 (0.50) | — | |
| SCHEMBL4449694 | 0.77 | TSHR (0.39) | — | |
| SCHEMBL1042991 | 0.74 | — | — | |
| SCHEMBL8368422 | 0.74 | TSHR (0.37) | — | |
| SCHEMBL3688120 | 0.72 | LMNA (0.38) | — |
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 52 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2024060640-A1 | MODIFIED EPOXIDIZED RUBBER, PREPARATION METHOD THEREFOR, AND USE THEREOF | 江苏麒祥高新材料有限公司 | 2024-03-28 | — | — | WO | claimed |
| CN-114028578-A | Preparation method of stearic acid modified camptothecin-based liposome | 北京化工大学 | 2022-02-11 | — | — | CN | claimed |
| US-9404029-B2 | Rheology modifiers | CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) | 2016-08-02 | — | — | US | claimed |
| EP-2844715-B1 | RHEOLOGY MODIFIERS | CHEVRON PHILLIPS CHEMICAL CO (US) | 2016-03-09 | — | — | EP | claimed |
| US-20150159075-A1 | Rheology Modifiers | CHEVRON PHILLIPS CHEMICAL COMPANY LP | 2015-06-11 | — | — | US | claimed |
| EP-2844715-A1 | RHEOLOGY MODIFIERS | Chevron Phillips Chemical Company LP (US) | 2015-03-11 | — | — | EP | claimed |
| WO-2013165728-A1 | RHEOLOGY MODIFIERS | CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) | 2013-11-07 | — | — | WO | claimed |
| US-20130288933-A1 | Rheology Modifiers | CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) | 2013-10-31 | — | — | US | claimed |
| US-8158726-B2 | Poly(thioesters), their applications and derivatives | POLYMERIGHT, INC. (US) | 2012-04-17 | — | — | US | claimed |
| US-20070015902-A1 | Poly(thioesters), their applications and derivatives | CHEVRON PHILLIPS CHEMICAL COMPANY LP | 2007-01-18 | — | — | US | claimed |
| JP-57192466-A | — | — | None | — | — | JP | disclosed |
| CN-118253343-A | Synthesis method of symmetrical trisulfide compound and high-efficiency catalyst used by same | 常州大学 | 2024-06-28 | — | — | CN | disclosed |
| WO-2024060640-A1 | MODIFIED EPOXIDIZED RUBBER, PREPARATION METHOD THEREFOR, AND USE THEREOF | 江苏麒祥高新材料有限公司 | 2024-03-28 | — | — | WO | disclosed |
| US-11421223-B2 | Processes and host cells for genome, pathway, and biomolecular engineering | ENEVOLV, INC. (US) | 2022-08-23 | — | — | US | disclosed |
| CN-114028578-A | Preparation method of stearic acid modified camptothecin-based liposome | 北京化工大学 | 2022-02-11 | — | — | CN | disclosed |
| US-4284483-A | Hydroxyl-terminated liquid polymers and process for preparation thereof using a mixture of at least one hydroxyl-containing disulfide and at least one hydroxyl-containing trisulfide | THE B.F. GOODRICH COMPANY (US) | 1981-08-18 | — | — | US | disclosed |
| US-4238397-A | Hydroxyl-terminated liquid polymers and process for preparation thereof using a mixture of at least one hydroxyl-containing disulfide and at least one hydroxyl-containing trisulfide | THE B. F. GOODRICH COMPANY (US) | 1980-12-09 | — | — | US | disclosed |
| US-4214061-A | FROM AN ACRYLATE POLYMER, ISOCYANATE-TERMINATED POLYURETHANE PREPOLYMER, AND AN ALKANEDIOL; CURED | THE B. F. GOODRICH COMPANY (US) | 1980-07-22 | — | — | US | disclosed |
| US-4207238-A | Hydroxyl-terminated liquid polymers and process for preparation thereof using a mixture of at least one hydroxyl-containing disulfide and at least one hydroxyl-containing trisulfide | THE B. F. GOODRICH COMPANY (US) | 1980-06-10 | — | — | US | disclosed |
| EP-0001092-A2 | Process for the preparation of hydroxyl-terminated liquid polymers | The B.F. GOODRICH Company (US) | 1979-03-21 | — | — | EP | disclosed |