⚠ 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 | |
|---|---|---|---|---|
| Trifluoromethanesulfonic Acid SCHEMBL28299326 | 1.00 | ALDH1A1 (0.47) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL28098241 | 0.96 | ALDH1A1 (0.45) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL39465 | 0.96 | ALDH1A1 (0.50) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL295 | 0.96 | — | — | |
| Trifluoromethanesulfonic Acid SCHEMBL3950101 | 0.96 | — | — | |
| Trifluoromethanesulfonic Acid SCHEMBL3507077 | 0.96 | — | — | |
| Trifluoromethanesulfonic Acid SCHEMBL28295055 | 0.93 | ALDH1A1 (0.43) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL25293989 | 0.92 | — | — | |
| Trifluoromethanesulfonic Acid SCHEMBL25292879 | 0.92 | — | — | |
| Trifluoromethanesulfonic Acid SCHEMBL23094034 | 0.92 | ALDH1A1 (0.47) | — |
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 67 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-113543706-B | Electrode comprising a conductive acrylate-based pressure sensitive adhesive | 汉高股份有限及两合公司 | 2024-07-23 | — | — | CN | claimed |
| CN-118235027-A | Ion conductive composition for thermal sensor | 汉高股份有限及两合公司 | 2024-06-21 | — | — | CN | claimed |
| CN-115989294-A | Dry stimulating electrode | 汉高股份有限及两合公司 | 2023-04-18 | — | — | CN | claimed |
| EP-4042471-A1 | METHOD FOR DIRECTED SELF-ASSEMBLY LITHOGRAPHY | ARKEMA FRANCE (FR) | 2022-08-17 | — | — | EP | claimed |
| CN-114746383-A | Improved process for the preparation of bromochloromethane | 赛拓有限责任公司 | 2022-07-12 | — | — | CN | claimed |
| CN-113557281-A | Dry electrode binder | 汉高股份有限及两合公司 | 2021-10-26 | — | — | CN | claimed |
| CN-113543706-A | Electrode comprising a conductive acrylate-based pressure sensitive adhesive | 汉高股份有限及两合公司 | 2021-10-22 | — | — | CN | claimed |
| CN-101880228-A | Clean preparation method for butyl acetate | LANZHOU INST OF CHEMISTRY PHYSICS CHINESE ACADEMY OF SCIENCES | 2010-11-10 | — | — | CN | claimed |
| EP-0650478-A1 | METHOD OF FORMING N-PROTECTED AMINO ACID THIOHYDANTOINS | THE PERKIN-ELMER CORPORATION (US) | 1995-05-03 | — | — | EP | claimed |
| US-5304497-A | Method of forming N-protected amino acid thiohydantoins | APPLIED BIOSYSTEMS, INC. (US) | 1994-04-19 | — | — | US | claimed |
| WO-1994002468-A1 | METHOD OF FORMING N-PROTECTED AMINO ACID THIOHYDANTOINS | APPLIED BIOSYSTEMS, INC. (US) | 1994-02-03 | — | — | WO | claimed |
| CN-115745934-B | Preparation method of 1-deuterated-2-deoxidized-D-glucose | 北京瑞博奥医药科技有限公司 | 2024-12-13 | — | — | CN | disclosed |
| CN-119119063-A | Pyridine derivatives having N-linked cyclic substituents as cGAS inhibitors | 勃林格殷格翰国际有限公司 | 2024-12-13 | — | — | CN | disclosed |
| CN-119119062-A | Pyridine derivatives having N-linked cyclic substituents as cGAS inhibitors | 勃林格殷格翰国际有限公司 | 2024-12-13 | — | — | CN | disclosed |
| EP-3623394-B1 | METALLACYCLOALKYLENE COMPLEXES AND USE FOR ALKYNE POLYMERIZATION TO CYCLIC POLYACETYLENES | UNIV FLORIDA (US) | 2024-07-24 | — | — | EP | disclosed |
| EP-0736052-A1 | PROCESS TO REACT EPOXIDE-CONTAINING COMPOUNDS AND ALIPHATIC ALCOHOLS | THE DOW CHEMICAL COMPANY (US) | 1996-10-09 | — | — | EP | disclosed |
| WO-1995017445-A1 | PROCESS TO REACT EPOXIDE-CONTAINING COMPOUNDS AND ALIPHATIC ALCOHOLS | THE DOW CHEMICAL COMPANY (US) | 1995-06-29 | — | — | WO | disclosed |
| EP-0650478-A1 | METHOD OF FORMING N-PROTECTED AMINO ACID THIOHYDANTOINS | THE PERKIN-ELMER CORPORATION (US) | 1995-05-03 | — | — | EP | disclosed |
| US-5304497-A | Method of forming N-protected amino acid thiohydantoins | APPLIED BIOSYSTEMS, INC. (US) | 1994-04-19 | — | — | US | disclosed |
| WO-1994002468-A1 | METHOD OF FORMING N-PROTECTED AMINO ACID THIOHYDANTOINS | APPLIED BIOSYSTEMS, INC. (US) | 1994-02-03 | — | — | WO | disclosed |