⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL17030340 | 0.84 | ALDH1A1 (0.44) | — | |
| SCHEMBL27848826 | 0.82 | ALDH1A1 (0.44) | — | |
| SCHEMBL22341413 | 0.80 | ALDH1A1 (0.43) | — | |
| SCHEMBL17054357 | 0.79 | — | — | |
| SCHEMBL3046216 | 0.77 | TSHR (0.42) | — | |
| SCHEMBL1170397 | 0.77 | — | — | |
| SCHEMBL27551301 | 0.76 | — | — | |
| SCHEMBL29041503 | 0.76 | — | — | |
| SCHEMBL28415354 | 0.76 | — | — | |
| SCHEMBL5828545 | 0.76 | — | — |
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 40 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20040054216-A1 | Method for producing lysine derivative | AJINOMOTO CO., INC. (JP) | 2004-03-18 | — | — | US | claimed |
| US-6664412-B2 | Protecting amino group or amino group and carboxyl group of optically active 2-amino-6-methyl-6-nitroheptanoic acid with protecting group, reducing nitro group to synthesize 6,6-dimethyllysine and reacting this with acetic acid | AJINOMOTO CO., INC. (JP) | 2003-12-16 | — | — | US | claimed |
| US-20030105351-A1 | Method for producing lysine derivative | AJINOMOTO CO. INC (JP) | 2003-06-05 | — | — | US | claimed |
| US-20020042537-A1 | Method for producing lysine derivative | AJINOMOTO CO., INC. (JP) | 2002-04-11 | — | — | US | claimed |
| EP-1179599-A2 | Method for producing lysine derivative | Ajinomoto Co., Inc. (JP) | 2002-02-13 | — | — | EP | claimed |
| WO-2024143106-A1 | STABILIZED ALKYL-BROMIDE-COMPOUND-CONTAINING LIQUID COMPOSITION AND USE FOR SAME | 東ソー株式会社 | 2024-07-04 | — | — | WO | disclosed |
| EP-2201360-B1 | DETECTION OF CHEMICALS WITH INFRARED LIGHT | THE GOVERNMENT OF THE U S A AS REPRESENTED BY THE SECRETARY OF THE NAVY (US) | 2021-06-30 | — | — | EP | disclosed |
| EP-3134410-B1 | INHIBITING THE TRANSIENT RECEPTOR POTENTIAL A1 ION CHANNEL | LILLY CO ELI (US) | 2021-03-10 | — | — | EP | disclosed |
| US-20170158702-A1 | MULTIVALENT RAS BINDING COMPOUNDS | KYRAS THERAPEUTICS, INC. | 2017-06-08 | — | — | US | disclosed |
| EP-3045565-B1 | Method for increasing adhesion between a chromium surface and a lacquer | ATOTECH DEUTSCHLAND GMBH (DE) | 2017-03-08 | — | — | EP | disclosed |
| US-9394297-B2 | Amides as pim inhibitors | AMGEN INC. (US) | 2016-07-19 | — | — | US | disclosed |
| US-20150329538-A1 | AMIDES AS PIM INHIBITORS | AMGEN INC. (US) | 2015-11-19 | — | — | US | disclosed |
| US-4785131-A | Substituted cyanonaphthalene process | ETHYL CORPORATION (US) | 1988-11-15 | — | — | US | disclosed |
| US-4764635-A | Aromatization process | ETHYL CORPORATION (US) | 1988-08-16 | — | — | US | disclosed |
| US-4762943-A | Aromatization process | ETHYL CORPORATION (US) | 1988-08-09 | — | — | US | disclosed |
| EP-0256849-A1 | Aromatization process | ETHYL CORPORATION (US) | 1988-02-24 | — | — | EP | disclosed |
| US-4727148-A | Certain aromatization process for preparing 1-alkyl-1,4-dihydro-4-oxo-7-(4-pyridyl)-3-quinoline carboxylic acid | ETHYL CORPORATION (US) | 1988-02-23 | — | — | US | disclosed |
| EP-0254422-A1 | Aromatization process | ETHYL CORPORATION (US) | 1988-01-27 | — | — | EP | disclosed |
| US-4649202-A | Brominative aromatization of 4-cyclohexenylpyridines | ETHYL CORPORATION (US) | 1987-03-10 | — | — | US | disclosed |
| US-4154658-A | CODISTILLATION WITH A SOLVENT | THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY (US) | 1979-05-15 | — | — | US | disclosed |