⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL12269670 | 0.81 | — | — | |
| SCHEMBL10035167 | 0.80 | — | — | |
| SCHEMBL10902184 | 0.77 | TSHR (0.38) | — | |
| SCHEMBL10931254 | 0.77 | TSHR (0.32) | — | |
| SCHEMBL20745216 | 0.77 | GPR55 (0.36) | — | |
| SCHEMBL10900500 | 0.77 | TSHR (0.38) | — | |
| SCHEMBL16889084 | 0.77 | GLRA1 (0.38) | — | |
| SCHEMBL20745215 | 0.77 | GPR55 (0.36) | — | |
| SCHEMBL6980204 | 0.75 | GAA (0.44) | — | |
| SCHEMBL919813 | 0.75 | LMNA (0.40) | — |
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 133 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-8658570-B2 | Use of anthranilamide derivatives for controlling insects and spider mites by drenching, soil mixing, furrow treatment, drip application, soil, stem or flower injection, in hydroponic systems, by planting hole treatment or dip application, floating or seedbox application or by treating seed, and also for enhancing the stress tolerance of plants to abiotic stress | BAYER CROPSCIENCE AG (DE) | 2014-02-25 | — | — | US | claimed |
| CN-102845415-A | Plant respiration inhibitor for tree transplanting and preparation method of plant respiration inhibitor | ZHONGTAI BRANCH ZHEJIANG XINLANTIAN GARDEN SEEDLINGS TECHNOLOGY CO LTD | 2013-01-02 | — | — | CN | claimed |
| EP-0708083-B1 | Process for preparing isopropylidene amino-oxy-acetic acid (methoxycarbonylmethylene) ester | BASF AG (DE) | 1998-08-19 | — | — | EP | claimed |
| EP-0708083-A1 | Process for preparing isopropylidene amino-oxy-acetic acid (methoxycarbonylmethylene) ester | BASF AKTIENGESELLSCHAFT (DE) | 1996-04-24 | — | — | EP | claimed |
| JP-8225505-A | — | — | None | — | — | JP | disclosed |
| CN-118684960-A | Low-smoke halogen-free polyolefin composition and preparation method and application thereof | 金发科技股份有限公司 | 2024-09-24 | — | — | CN | disclosed |
| CN-115895098-B | B1-level ultraviolet light crosslinking low-smoke halogen-free insulating composition and preparation method and application thereof | 金发科技股份有限公司 | 2024-07-12 | — | — | CN | disclosed |
| CN-115895098-A | B1-level ultraviolet crosslinking low-smoke halogen-free insulating composition and preparation method and application thereof | 金发科技股份有限公司 | 2023-04-04 | — | — | CN | disclosed |
| US-20220340893-A1 | BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES | NUEVOLUTION A/S (DK) | 2022-10-27 | — | — | US | disclosed |
| US-10435372-B2 | Use of phenylpyrazolin-3-carboxylates for improving plant yield | BAYER INTELLECTUAL PROPERTY GMBH (DE) | 2019-10-08 | — | — | US | disclosed |
| US-10426169-B2 | Heteroarylpiperidine and -piperazine derivatives as fungicides | BAYER INTELLECTUAL PROPERTY GMBH (DE) | 2019-10-01 | — | — | US | disclosed |
| EP-2964023-B1 | USE OF N-(2-METHOXYBENZOYL)-4-[METHYLAMINOCARBONYL)AMINO]BENZENESULFONAMIDE IN COMBINATION WITH AN INSECTICIDE OR FUNGICIDE FOR IMPROVING PLANT YIELD | BAYER CROPSCIENCE AG (DE) | 2019-08-07 | — | — | EP | disclosed |
| JP-H08225505-A | PRODUCTION OF METHYL ISOPROPYLIDENEAMINOOXYACETOXYACETATE | BASF AG | 1996-09-03 | — | — | JP | disclosed |
| EP-0708083-A1 | Process for preparing isopropylidene amino-oxy-acetic acid (methoxycarbonylmethylene) ester | BASF AKTIENGESELLSCHAFT (DE) | 1996-04-24 | — | — | EP | disclosed |
| EP-0708083-A1 | Process for preparing isopropylidene amino-oxy-acetic acid (methoxycarbonylmethylene) ester | BASF AKTIENGESELLSCHAFT (DE) | 1996-04-24 | — | — | EP | disclosed |
| US-5393921-A | Process for synthesizing O-substituted oxime compounds and conversion to the corresponding O-substituted hydroxylamine | THE GILLETTE COMPANY (US) | 1995-02-28 | — | — | US | disclosed |
| WO-1995001952-A1 | PROCESS FOR SYNTHESIZING O-SUBSTITUTED OXIME COMPOUNDS AND CONVERSION TO THE CORRESPONDING O-SUBSTITUTED HYDROXYLAMINE | THE GILLETTE COMPANY (US) | 1995-01-19 | — | — | WO | disclosed |
| US-5382685-A | Preparation of O-substituted hydroxylammonium salts | BASF AKTIENGESELLSCHAFT (DE) | 1995-01-17 | — | — | US | disclosed |
| EP-0417167-A1 | PROCESS FOR THE SYNTHESIS OF O-SUBSTITUTED OXIME COMPOUNDS | AlliedSignal Inc. (US) | 1991-03-20 | — | — | EP | disclosed |
| WO-1989011473-A1 | PROCESS FOR THE SYNTHESIS OF O-SUBSTITUTED OXIME COMPOUNDS | ALLIED-SIGNAL INC. (US) | 1989-11-30 | — | — | WO | disclosed |