⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL664500 | 1.00 | — | — | |
| SCHEMBL184638 | 1.00 | — | — | |
| Bromide SCHEMBL6735763 | 0.97 | TAAR1 (0.44) | — | |
| SCHEMBL28751595 | 0.87 | TSHR (0.48) | — | |
| SCHEMBL3174147 | 0.84 | PTGS2 (0.54) | — | |
| SCHEMBL332099 | 0.83 | ESR1 (0.38) | — | |
| SCHEMBL332300 | 0.79 | HDAC4 (0.37) | — | |
| SCHEMBL20216133 | 0.78 | LTA4H (0.52) | — | |
| SCHEMBL21524731 | 0.78 | ALDH1A1 (0.46) | — | |
| SCHEMBL1960097 | 0.77 | TAAR1 (0.50) | — |
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 32 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4198029-A1 | INHIBITORS OF PEPTIDYL ARGININE DEIMINASE (PAD) ENZYMES AND USES THEREOF | University Health Network (CA) | 2023-06-21 | — | — | EP | disclosed |
| WO-2020215267-A1 | USE OF NTCP INHIBITORS IN PREVENTING AND TREATING HEPATOCARCINOGENESIS | NATIONAL INSTITUTE OF BIOLOGICAL SCIENCES, BEIJING (CN) | 2020-10-29 | — | — | WO | disclosed |
| WO-2020194920-A1 | THERMOSETTING EPOXY RESIN COMPOSITION, LAYERED SHEET FOR CIRCUIT BOARD, METAL-BASED CIRCUIT BOARD, AND POWER MODULE | 日本発條株式会社 | 2020-10-01 | — | — | WO | disclosed |
| WO-2018182774-A1 | HERBICIDE | UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) | 2018-10-04 | — | — | WO | disclosed |
| US-9868729-B2 | Inhibitors of protein kinases | PORTOLA PHARMACEUTICALS, INC. (US) | 2018-01-16 | — | — | US | disclosed |
| EP-3062150-A2 | CHEMICALLY AMPLIFIED POSITIVE RESIST COMPOSITION AND PATTERN FORMING PROCESS | Shin-Etsu Chemical Co., Ltd. (JP) | 2016-08-31 | — | — | EP | disclosed |
| US-20160070174-A1 | PATTERN FORMING METHOD, ACTIVE LIGHT SENSITIVE OR RADIATION SENSITIVE RESIN COMPOSITION, ACTIVE LIGHT SENSITIVE OR RADIATION SENSITIVE FILM, METHOD FOR MANUFACTURING ELECTRONIC DEVICE, AND ELECTRONIC DEVICE | FUJIFILM CORPORATION (JP) | 2016-03-10 | — | — | US | disclosed |
| EP-2391600-B1 | INTERMEDIATES IN THE ENANTIOSELECTIVE SYNTHESIS OF 3-(AMINOMETHYL)-5-METHYL-HEXANOIC ACID | PROVOST FELLOWS & SCHOLARS COLLEGE OF THE HOLY UNDIVIDED TRINITY OF QUEEN ELIZABETH NEAR DUBLIN (IE) | 2016-01-06 | — | — | EP | disclosed |
| US-9223219-B2 | Pattern forming method, actinic ray-sensitive or radiation-sensitive resin composition and resist film | FUJIFILM CORPORATION (JP) | 2015-12-29 | — | — | US | disclosed |
| US-8877423-B2 | Actinic ray-sensitive or radiation-sensitive resin composition and pattern forming method using the same | FUJIFILM CORPORATION (JP) | 2014-11-04 | — | — | US | disclosed |
| EP-1385870-B1 | PEPTIDES AS NS3-SERINE PROTEASE INHIBITORS OF HEPATITIS C VIRUS | SCHERING CORP (US) | 2010-03-17 | — | — | EP | disclosed |
| US-7585535-B2 | Flavour and fragrance compositions | GIVAUDAN SA (CH) | 2009-09-08 | — | — | US | disclosed |
| EP-1392132-B1 | FLAVOUR AND FRAGRANCE COMPOSITIONS | GIVAUDAN SA (CH) | 2009-07-29 | — | — | EP | disclosed |
| US-20040253362-A1 | Flavour and fragrance compositions | GIVAUDAN SA (CH) | 2004-12-16 | — | — | US | disclosed |
| EP-1392132-A1 | FLAVOUR AND FRAGRANCE COMPOSITIONS | Givaudan SA (CH) | 2004-03-03 | — | — | EP | disclosed |
| WO-2002098241-A1 | FLAVOUR AND FRAGRANCE COMPOSITIONS | GIVAUDAN SA (CH) | 2002-12-12 | — | — | WO | disclosed |
| EP-1264547-A1 | Flavour and fragrance compositions | Givaudan SA (CH) | 2002-12-11 | — | — | EP | disclosed |
| EP-0083335-B1 | OPTICALLY ACTIVE CHIRAL COMPOUNDS, PROCESS FOR THEIR PREPARATION AND USE OF THESE COMPOUNDS IN THE PROTECTION OF FUNCTIONAL -OH, -SH, -NH- GROUPS, IN THE SEPARATION OF RACEMATES, IN THE PREPARATION OF OPTICALLY ACTIVE IMIDOESTER HYDROCHLORIDES AND OF OPTICALLY ACTIVE ESTERS, IN THE PREPARATION OF OPTICALLY ENRICHED ALCOHOLS AND IN THE PREPARATION OF OPTICALLY ACTIVE COMPOUNDS BY ASYMMETRIC INDUCTION | Noe, Christian, Dipl.-Ing. Dr. (AT) | 1987-08-12 | — | — | EP | disclosed |
| US-4497960-A | Chiral, optically active compounds useful as protective groups for hydroxy, thiol and amino compounds | NOE CHRISTIAN (AT) | 1985-02-05 | — | — | US | disclosed |
| EP-0083335-A1 | Optically active chiral compounds, process for their preparation and use of these compounds in the protection of functional -OH, -SH, -NH- groups, in the separation of racemates, in the preparation of optically active imidoester hydrochlorides and of optically active esters, in the preparation of optically enriched alcohols and in the preparation of optically active compounds by asymmetric induction | Noe, Christian, Dipl.-Ing. Dr. (AT) | 1983-07-06 | — | — | EP | disclosed |