⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL15395937 | 1.00 | — | — | |
| SCHEMBL8024507 | 1.00 | — | — | |
| SCHEMBL3103329 | 0.76 | — | — | |
| SCHEMBL20381047 | 0.76 | — | — | |
| SCHEMBL8377003 | 0.76 | — | — | |
| SCHEMBL25784943 | 0.74 | — | — | |
| SCHEMBL405356 | 0.72 | — | — | |
| SCHEMBL8271203 | 0.72 | DGAT1 (0.33) | — | |
| SCHEMBL5792271 | 0.72 | DGAT1 (0.33) | — | |
| SCHEMBL391370 | 0.72 | — | — |
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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0979814-B1 | Improved synthesis of haloformimine compounds | ROHM & HAAS (US) | 2003-10-22 | — | — | EP | claimed |
| US-6207863-B1 | MAINTAINING A PH BETWEEN 2 AND 5 DURING THE HALOGENATION OF FORMIMINES GREATLY INCREASES THE YIELDS OF HALOFORMIMINES AND GREATLY DECREASES THE RATE OF BY-PRODUCT FORMATION. | ROHM AND HAAS COMPANY | 2001-03-27 | — | — | US | claimed |
| CN-1245795-A | Improved method for synthesizing halogenated methylenimine compound | ROHM & HAAS (US) | 2000-03-01 | — | — | CN | claimed |
| EP-0979814-A1 | Improved synthesis of haloformimine compounds | ROHM AND HAAS COMPANY (US) | 2000-02-16 | — | — | EP | claimed |
| EP-0464381-B1 | 2-Methoxyiminocarboxylic acid esters | BAYER AG (DE) | 1995-07-26 | — | — | EP | claimed |
| US-20230232827-A1 | METHOD FOR CONTROLLING SOYBEAN RUST FUNGUS RESISTANT TO QoI FUNGICIDES | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2023-07-27 | — | — | US | disclosed |
| US-20230232827-A1 | METHOD FOR CONTROLLING SOYBEAN RUST FUNGUS RESISTANT TO QoI FUNGICIDES | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2023-07-27 | — | — | US | disclosed |
| CN-111116582-B | mGluR2 antagonist | 大连大学 | 2022-07-29 | — | — | CN | disclosed |
| CN-111116582-A | mGluR2 antagonist | 大连大学 | 2020-05-08 | — | — | CN | disclosed |
| US-20050079979-A1 | Substituted benzoylisoxazoles and the use thereof as herbicides | MULLER KLAUS-HELMUT (DE) | 2005-04-14 | — | — | US | disclosed |
| US-6838415-B1 | Substituted benzoylisoxazoles and the use thereof as herbicides | BAYER AKTIENGESELLSCHAFT (DE) | 2005-01-04 | — | — | US | disclosed |
| EP-0979814-B1 | Improved synthesis of haloformimine compounds | ROHM & HAAS (US) | 2003-10-22 | — | — | EP | disclosed |
| EP-0562382-B1 | Process for the preparation of isoxazole-3,4-dicarboxylic acid derivatives | BASF AG (DE) | 1998-01-21 | — | — | EP | disclosed |
| US-5464809-A | Fungicidal 2-methoximinocarboxylic esters | BAYER AKTIENGESELLSCHAFT (DE) | 1995-11-07 | — | — | US | disclosed |
| EP-0418667-B1 | Carboxylic acid amides | BASF AG (DE) | 1995-08-16 | — | — | EP | disclosed |
| US-5380914-A | Plants, intermediates | BAYER AKTIENGESELLSCHAFT (DE) | 1995-01-10 | — | — | US | disclosed |
| US-5312960-A | Fungicidal 2-methoximinocarboxylic esters | BAYER AKTIENGESELLSCHAFT (DE) | 1994-05-17 | — | — | US | disclosed |
| US-5264580-A | Reaction of hydroximyl chlorides and beta-keto acids or esters, cyclization | BASF AKTIENGESELLSCHAFT (DE) | 1993-11-23 | — | — | US | disclosed |
| EP-0562382-A1 | Process for the preparation of isoxazole-3,4-dicarboxylic acid derivatives | BASF Aktiengesellschaft (DE) | 1993-09-29 | — | — | EP | disclosed |
| US-5201932-A | Herbicides | BASF AKTIENGESELLSCHAFT (DE) | 1993-04-13 | — | — | US | disclosed |