Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA2 | P00918 | 3/20 | 0.50 |
| ▸ | MEN1 | O00255 | 1/20 | 0.47 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.47 |
| ▸ | ESR1 | P03372 | 1/20 | 0.46 |
| ▸ | L3MBTL1 | Q9Y468 | 4/20 | 0.45 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.45 |
| ▸ | CA4 | P22748 | 2/20 | 0.44 |
| ▸ | CA5A | P35218 | 2/20 | 0.44 |
| ▸ | POLB | P06746 | 2/20 | 0.44 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.43 |
| ▸ | ACHE | P22303 | 1/20 | 0.42 |
| ▸ | HTT | P42858 | 2/20 | 0.41 |
| ▸ | PKM | P14618 | 2/20 | 0.41 |
| ▸ | CA12 | O43570 | 1/20 | 0.40 |
| ▸ | CA1 | P00915 | 1/20 | 0.40 |
| ▸ | CA7 | P43166 | 1/20 | 0.40 |
| ▸ | CA9 | Q16790 | 1/20 | 0.40 |
| ▸ | CA5B | Q9Y2D0 | 1/20 | 0.40 |
| ▸ | LMNA | P02545 | 1/20 | 0.39 |
| ▸ | CFTR | P13569 | 1/20 | 0.39 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
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 | |
|---|---|---|---|---|
| SCHEMBL8673873 | 0.82 | ESR1 (0.48) | CA2MEN1KMT2AESR1L3MBTL1 | |
| SCHEMBL13397677 | 0.81 | CA2 (0.67) | CA2MEN1KMT2AESR1L3MBTL1 | |
| SCHEMBL777146 | 0.79 | ACHE (0.56) | CA2MEN1KMT2AL3MBTL1ALDH1A1 | |
| SCHEMBL344018 | 0.78 | CA2 (0.54) | CA2MEN1KMT2AESR1L3MBTL1 | |
| SCHEMBL5483761 | 0.78 | HPGD (0.58) | MEN1KMT2AALDH1A1TDP1ACHE | |
| SCHEMBL28845469 | 0.78 | ESR1 (0.50) | CA2MEN1KMT2AESR1L3MBTL1 | |
| SCHEMBL18951487 | 0.78 | L3MBTL1 (0.48) | CA2MEN1KMT2AESR1L3MBTL1 | |
| SCHEMBL11652853 | 0.78 | CA2 (0.44) | CA2MEN1KMT2AESR1L3MBTL1 | |
| SCHEMBL499887 | 0.77 | L3MBTL1 (0.56) | CA2MEN1KMT2AESR1L3MBTL1 | |
| SCHEMBL332078 | 0.77 | L3MBTL1 (0.58) | CA2MEN1KMT2AESR1L3MBTL1 |
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 92 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117903195-A | Method for preparing (2-oxo-2-arylethyl) (phenyl) phosphonate alkyl ester compound | 湖南理工学院 | 2024-04-19 | — | — | CN | claimed |
| CN-114960227-B | High-strength automobile cover plate and processing technology thereof | 常熟新常泰汽车内饰科技有限公司 | 2023-07-21 | — | — | CN | claimed |
| CN-103254234-B | Methyl triazinyl triphenyl hypophosphite compound and preparation method thereof | UNIVERSITY OF SCIENCE AND TECHNOLOGY OF SUZHOU (CN) | 2016-04-27 | — | — | CN | claimed |
| CN-103360625-B | Flame retardant tetra (O-methyl-phenyl phosphinic) glycoluril compound and preparation method therefor | XIANGCHENG INSTITUTE OF SUZHOU UNIVERSITY OF SCIENCE AND TECHNOLOGY (CN) | 2014-10-15 | — | — | CN | claimed |
| CN-103360625-A | Flame retardant tetra (O-methyl-phenyl phosphinic) glycoluril compound and preparation method therefor | XIANGCHENG RES INST SUZHOU UNIV SCI & TECH | 2013-10-23 | — | — | CN | claimed |
| CN-103254234-A | Methyl triazinyl triphenyl hypophosphite compound and preparation method thereof | USTC UNIV SCIENCE TECH CN | 2013-08-21 | — | — | CN | claimed |
| US-12100809-B2 | Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery | MITSUBISHI CHEMICAL CORPORATION (JP) | 2024-09-24 | — | — | US | disclosed |
| CN-117916038-A | Metal paste for bonding, bonded body, and method for producing same | 株式会社力森诺科 | 2024-04-19 | — | — | CN | disclosed |
| CN-117903195-A | Method for preparing (2-oxo-2-arylethyl) (phenyl) phosphonate alkyl ester compound | 湖南理工学院 | 2024-04-19 | — | — | CN | disclosed |
| CN-114960227-B | High-strength automobile cover plate and processing technology thereof | 常熟新常泰汽车内饰科技有限公司 | 2023-07-21 | — | — | CN | disclosed |
| CN-114126677-B | Crosslinkable hydrogel composition | 苏黎世联邦理工学院 | 2023-06-06 | — | — | CN | disclosed |
| CN-112679708-B | Catalyst composition for preparing polyglycolic acid through continuous ring opening, method for preparing polyglycolic acid and polyglycolic acid | 中国石油化工股份有限公司 | 2023-04-07 | — | — | CN | disclosed |
| CN-115591007-A | Preparation method of tissue adhesive for repairing meniscus tear | 南京理工大学（CN） | 2023-01-13 | — | — | CN | disclosed |
| US-4294989-A | OPTICALLY ACTIVE HYDROGENATION CATALYSTS | MONSANTO COMPANY (US) | 1981-10-13 | — | — | US | disclosed |
| US-4265827-A | METHYLCYCOHEXYL-O-ANISYLARSINE OPTICALLY ACTIVE CATALYST | MONSANTO COMPANY (US) | 1981-05-05 | — | — | US | disclosed |
| US-4261919-A | OF BETA-SUBSTITUTED-ALPHA-ACYLAMIDO-ACRYLIC ACIDS TO YIELD OPTICALLY ACTIVE MIXTURE | MONSANTO COMPANY (US) | 1981-04-14 | — | — | US | disclosed |
| US-4168267-A | Phosphinylalkanoyl prolines | E. R. SQUIBB & SONS, INC. (US) | 1979-09-18 | — | — | US | disclosed |
| US-4124533-A | HYDROGENATION CATALYSTS | MONSANTO COMPANY (US) | 1978-11-07 | — | — | US | disclosed |
| US-4119652-A | HYDROGENATION CATALYSTS; COORDINATION COMPOUNDS OF IRIDIUM, RHODIUM OR RUTHENIUM WITH PHOSPHINE OR ARSINE LIGANDS; OPTICALLY ACTIVE | MONSANTO COMPANY (US) | 1978-10-10 | — | — | US | disclosed |
| US-4005127-A | L-Dopa process and intermediates | MONSANTO COMPANY (US) | 1977-01-25 | — | — | US | disclosed |